ENSMUSG00000021779


Mus musculus

Features
Gene ID: ENSMUSG00000021779
  
Biological name :Thrb
  
Synonyms : P37242 / Thrb / Thyroid hormone receptor beta
  
Possible biological names infered from orthology : P10828
  
Species: Mus musculus
  
Chr. number: 14
Strand: 1
Band: A2
Gene start: 17660261
Gene end: 18038090
  
Corresponding Affymetrix probe sets: 10412882 (MoGene1.0st)   1422202_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000153055
Ensembl peptide - ENSMUSP00000089053
Ensembl peptide - ENSMUSP00000153230
Ensembl peptide - ENSMUSP00000153355
Ensembl peptide - ENSMUSP00000022303
Ensembl peptide - ENSMUSP00000022304
NCBI entrez gene - 21834     See in Manteia.
MGI - MGI:98743
RefSeq - XM_017315948
RefSeq - XM_011244741
RefSeq - XM_011244742
RefSeq - XM_011244743
RefSeq - XM_011244745
RefSeq - XM_017315946
RefSeq - XM_017315947
RefSeq - NM_001113417
RefSeq - NM_009380
RefSeq - XM_006517966
RefSeq - XM_006517967
RefSeq - XM_006517968
RefSeq - XM_006517970
RefSeq - XM_006517971
RefSeq - XM_006517972
RefSeq - XM_011244737
RefSeq - XM_011244738
RefSeq - XM_011244739
RefSeq - XM_011244740
RefSeq Peptide - NP_001106888
RefSeq Peptide - NP_033406
swissprot - A0A286YDB1
swissprot - A0A286YD21
swissprot - P37242
swissprot - A0A286YCM0
Ensembl - ENSMUSG00000021779
  

This gene has been taged as a transcription factor by TFT
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 thrbENSDARG00000021163Danio rerio
 THRBENSGALG00000011294Gallus gallus
 THRBENSG00000151090Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Thra / P63058 / Thyroid hormone receptor alpha / P10827*ENSMUSG0000005875661
Rara / P11416 / retinoic acid receptor, alpha / P10276*ENSMUSG0000003799227
Rarb / P22605 / retinoic acid receptor, beta / P10826*ENSMUSG0000001749127
Rarg / P18911 / Retinoic acid receptor gamma / P13631*ENSMUSG0000000128827
Nr1h4 / Q60641 / Bile acid receptor / Q96RI1* / nuclear receptor subfamily 1 group H member 4*ENSMUSG0000004763825
Nr1i2 / O54915 / Nuclear receptor subfamily 1 group I member 2 / O75469*ENSMUSG0000002280924
Nr1h5ENSMUSG0000004893824
Nr1h3 / Q9Z0Y9 / Mus musculus nuclear receptor subfamily 1, group H, member 3 (Nr1h3), transcript variant 3, mRNA. / Q13133* / nuclear receptor subfamily 1 group H member 3*ENSMUSG0000000210824
Nr1h2 / Q60644 / Oxysterols receptor LXR-beta / P55055* / nuclear receptor subfamily 1 group H member 2*ENSMUSG0000006060124
Vdr / P48281 / vitamin D (1,25-dihydroxyvitamin D3) receptor / P11473* / vitamin D receptor*ENSMUSG0000002247923
Nr1i3 / O35627 / Nuclear receptor subfamily 1 group I member 3 / Q14994*ENSMUSG0000000567722


Protein motifs (from Interpro)
Interpro ID Name
 IPR000536  Nuclear hormone receptor, ligand-binding domain
 IPR001628  Zinc finger, nuclear hormone receptor-type
 IPR001723  Nuclear hormone receptor
 IPR001728  Thyroid hormone receptor
 IPR013088  Zinc finger, NHR/GATA-type
 IPR035500  Nuclear hormone receptor-like domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0000122 negative regulation of transcription by RNA polymerase II IGI
 biological_processGO:0006351 transcription, DNA-templated IEA
 biological_processGO:0006355 regulation of transcription, DNA-templated TAS
 biological_processGO:0006357 regulation of transcription by RNA polymerase II IGI
 biological_processGO:0007165 signal transduction IEA
 biological_processGO:0007605 sensory perception of sound IMP
 biological_processGO:0007621 negative regulation of female receptivity IMP
 biological_processGO:0008016 regulation of heart contraction IMP
 biological_processGO:0008050 female courtship behavior IMP
 biological_processGO:0009887 animal organ morphogenesis IMP
 biological_processGO:0030522 intracellular receptor signaling pathway IEA
 biological_processGO:0043401 steroid hormone mediated signaling pathway IEA
 biological_processGO:0045892 negative regulation of transcription, DNA-templated IDA
 biological_processGO:0045944 positive regulation of transcription by RNA polymerase II IGI
 biological_processGO:0060509 type I pneumocyte differentiation IGI
 cellular_componentGO:0000790 nuclear chromatin IDA
 cellular_componentGO:0005634 nucleus TAS
 cellular_componentGO:0016604 nuclear body IEA
 molecular_functionGO:0003677 DNA binding IEA
 molecular_functionGO:0003700 DNA-binding transcription factor activity TAS
 molecular_functionGO:0003707 steroid hormone receptor activity IEA
 molecular_functionGO:0004887 thyroid hormone receptor activity TAS
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0008270 zinc ion binding IEA
 molecular_functionGO:0019899 enzyme binding IEA
 molecular_functionGO:0031490 chromatin DNA binding IDA
 molecular_functionGO:0043565 sequence-specific DNA binding IEA
 molecular_functionGO:0046872 metal ion binding IEA
 molecular_functionGO:0070324 thyroid hormone binding IEA


Pathways (from Reactome)
Pathway description
Nuclear Receptor transcription pathway
SUMOylation of intracellular receptors


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000031 abnormal cochlea morphology "any anomaly, deformity, malformation, impairment or dysfunction of the cochlea" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, cml:Cathleen M. Lutz , Mouse Genome Informatics Curator, J:21484]
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Allelic Composition: Sp4tm1Krc/Sp4tm1Krc
Genetic Background: involves: 129S4/SvJae * Black Swiss

Allelic Composition: Thrbtm4Few/Thrbtm4Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss

 MP:0000042 abnormal organ of Corti "abnormalities associated with the highly specialized epithelium in the floor of the ductus cochlearis; also referred to a spiral organ (organum spirale), or acoustic papilla" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Tsta3tm1Jbl/Tsta3+
Genetic Background: involves: 129S2/SvPas * C57BL/6J

Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/c * C57BL/6J

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss

 MP:0000043 organ of Corti degeneration "a retrogressive impairment of function or destruction of the highly specialized epithelium in the floor of the ductus cochlearis" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss

 MP:0000066 osteoporosis "reduction in bone mass or atrophy of skeletal tissue; may lead to skeletal fragility" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:57315]
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Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

 MP:0000081 premature suture closure "early fusion of the bones of the skull" [J:26513]
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Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss

 MP:0000130 abnormal cancellous bone morphology "structural anomaly of bone that has a latticelike or spongy structure" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Cacna2d2du/Cacna2d2du
Genetic Background: TKDU

 MP:0000135 reduced cortical bone thickness "thinner than normal superficial layer of compact bone " [J:61509]
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Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

 MP:0000165 abnormal hypertrophic chondrocyte zone "anomaly of the cartilage cell matrix layer " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:58795]
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Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

 MP:0000438 abnormal skull morphology "anomalous structure or development of the cranium" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Suprmam1BALB/cMed/Suprmam1BALB/cMed,Trp53tm1Tyj/Trp53+
Genetic Background: involves: 129S2/SvPas * BALB/cMed * C57BL/6 * C57BL/6J

 MP:0000478 delayed intestine development "slowed progression to a structurally mature intestine" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Thratm1Jas/Thratm1Jas,Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ

 MP:0000496 abnormal small intestine morphology "structural or developmental anomalies of the intestinum tenue " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Thratm1Jas/Thratm1Jas,Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ

 MP:0000547 short limbs "reduced average length of the extremities" [MGI:CLS, J:61509]
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Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

 MP:0000592 short tail "reduced length of tail compared to control " [J:55583]
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Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

 MP:0000636 enlarged pituitary gland "increased size of pituitary gland" [J:50053]
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Allelic Composition: Cr2tm1Hmo/Cr2tm1Hmo
Genetic Background: B6.129S7-Cr2tm1Hmo

 MP:0000745 tremors "repetitive, cyclical movements of the body or a body part; usually involuntary, but can also manifest in response to an attempt at movement" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Tcf7tm1a(EUCOMM)Wtsi/Tcf7tm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Tcf7tm1a(EUCOMM)Wtsi/Ics

 MP:0000852 small cerebellum "reduced size of cerebellum" [MGI:CLS, J:17203, J:67524]
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Allelic Composition: Cxadrtm1Dvst/Cxadrtm1Dvst
Genetic Background: involves: 129X1/SvJ * C57BL/6

Allelic Composition: Thrbtm2Few/Thrb+
Genetic Background: involves: 129X1/SvJ * C57BL/6

 MP:0000875 abnormal cerebellar Purkinje cell layer "any malformation or absence of the cell layer that lies just underneath the molecular layer of the cerebellar cortex; it contains the neuronal cell bodies of the Purkinje cells that are arranged side by side in a single layer, and candelabrum interneurons are vertically oriented between the Purkinje cells" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Cxadrtm1Dvst/Cxadrtm1Dvst
Genetic Background: involves: 129X1/SvJ * C57BL/6

Allelic Composition: Thrbtm2Few/Thrb+
Genetic Background: involves: 129X1/SvJ * C57BL/6

 MP:0000877 abnormal Purkinje cell "any structural anomaly of the neurons located at the interface of the molecular and internal granule layers of the cerebellar cortex; these inhibitory neurons provide the output of the cerebellar cortex through axons that project into the white matter, and extensive dendritic trees from the Purkinje cells extend upward in a single plane into the molecular layer where they synapse with parallel fibers of granule cells" [J:46140, Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3]
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Allelic Composition: Cxadrtm1Dvst/Cxadrtm1Dvst
Genetic Background: involves: 129X1/SvJ * C57BL/6

Allelic Composition: Thrbtm2Few/Thrb+
Genetic Background: involves: 129X1/SvJ * C57BL/6

 MP:0000880 decreased Purkinje cell number "fewer than normal neuronal cells that are located in the interface of the molecular and granular layers of the cerebellar cortex" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:45302]
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Allelic Composition: Cxadrtm1Dvst/Cxadrtm1Dvst
Genetic Background: involves: 129X1/SvJ * C57BL/6

Allelic Composition: Thrbtm2Few/Thrb+
Genetic Background: involves: 129X1/SvJ * C57BL/6

 MP:0000890 thin cerebellar molecular layer "reduced width of the outer of the three cortical layers of the cerebellum" [J:46854]
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Allelic Composition: Cxadrtm1Dvst/Cxadrtm1Dvst
Genetic Background: involves: 129X1/SvJ * C57BL/6

Allelic Composition: Thrbtm2Few/Thrb+
Genetic Background: involves: 129X1/SvJ * C57BL/6

 MP:0001006 abnormal cone morphology "structural or developmental anomaly of the retinal receptors that give rise to color vision" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Dnmt1tm2Enl/Dnmt1tm2Enl
Genetic Background: involves: 129S4/SvJae

Allelic Composition: Thrbtm3Few/Thrbtm3Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm4Few/Thrbtm4Few
Genetic Background: involves: 129 * C57BL/6

 MP:0001258 decreased body length "decreased crown to tail distance compared to controls" [cwg:Carroll W. Goldsmith, Mouse Genome Informatics Curator]
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Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

 MP:0001262 decreased body weight "lower than normal average weight " [J:61295]
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Allelic Composition: Thratm2Ven/Thratm3Ven
Genetic Background: involves: 129P2/OlaHsd * C57BL/6NCrl

Allelic Composition: Thratm3Ven/Thra+,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6NCrl

Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: B6.129-Thratm1Ven Thrbtm1Df

Allelic Composition: Thrbtm6.1Few/Thrbtm6.1Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm6.1Few/Thrb+
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

Allelic Composition: Thratm1Jas/Thratm1Jas,Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ

 MP:0001265 reduced body size "smaller than average body weight, height and/or length of an organism compared to controls" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:23170]
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Allelic Composition: Ddb1tm1Spg/Ddb1tm1Spg,Trp53tm1Tyj/Trp53tm1Tyj,Tg(Nes-cre)1Kln/0
Genetic Background: involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

 MP:0001399 hyperactivity "general restlessness or excessive movement; more frequent movement from one place to another" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60409, J:57125]
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Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks
Genetic Background: involves: C57BL/6J

 MP:0001463 abnormal spatial learning "defects in the abilibity to navigate using behavioraly meaningful locations" [CFG:Center for Functional Genomics , Northwestern University]
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Allelic Composition: Cxadrtm1Dvst/Cxadrtm1Dvst
Genetic Background: involves: 129X1/SvJ * C57BL/6

Allelic Composition: Thrbtm2Few/Thrb+
Genetic Background: involves: 129X1/SvJ * C57BL/6

 MP:0001473 reduced long term potentiation "less than the normal persistent robust synaptic response induced by synchronous stimulation of pre- and postsynaptic cells " [Principles of Neural Science:ISBN 0-8385-8034-3]
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Allelic Composition: Mir34atm1.2Arte/Mir34atm1.2Arte,Tg(Neurod2-Smo*A1)199Jols/0
Genetic Background: involves: C57BL/6 * C57BL/6N

 MP:0001496 audiogenic seizures "a reflex seizure triggered by loud noises" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Sh3bp2tm1Bjro/Sh3bp2tm1Bjro,Tnftm1Gkl/Tnftm1Gkl
Genetic Background: involves: 129S/SvEv * 129S4/SvJae * BALB/cJ * C57BL/6J

 MP:0001541 abnormal osteoclast function "reduced ability or inability of osteoclasts to absorb and remove osseous tissue" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:58795]
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Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

 MP:0001731 abnormal postnatal growth "anomaly in reaching a developmental stage or stages after birth" [il:Ira Lu, Mouse Genome Informatics Curator]
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Allelic Composition: Thratm3Ven/Thra+,Thrbtm1Df/Thrb+
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6NCrl

 MP:0001732 postnatal growth retardation "slow or limited development after birth " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Thratm2Ven/Thratm2Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * BALB/c * C57BL/6J

Allelic Composition: Thratm2Ven/Thra+,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * BALB/c * C57BL/6J

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

Allelic Composition: Thratm1Jas/Thratm1Jas,Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ

Allelic Composition: Thratm1Jas/Thra+,Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ

 MP:0001900 impaired synaptic plasticity "decreased or inability of the nervous system to change its reactivity as a result of successive activations " [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Mir34atm1.2Arte/Mir34atm1.2Arte,Tg(Neurod2-Smo*A1)199Jols/0
Genetic Background: involves: C57BL/6 * C57BL/6N

 MP:0001926 female infertility "inability of female to produce live offspring" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:34193]
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Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: B6.129-Thratm1Ven Thrbtm1Df

Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/c * C57BL/6J

 MP:0001954 respiratory distress "physical difficulty or inability to breathe" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:54931]
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Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0001967 deafness "inability to hear" [J:57651]
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Allelic Composition: Tsta3tm1Jbl/Tsta3+
Genetic Background: involves: 129S2/SvPas * C57BL/6J

Allelic Composition: Thrbtm1Df/Thrbtm1Df
Genetic Background: either: B6.129S1-Thrbtm1Df or (involves: 129S1/Sv * C57BL/6J)

 MP:0002041 pituitary adenoma "appearance of benign neoplasms of the pituitary" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:33042]
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Allelic Composition: Cr2tm1Hmo/Cr2tm1Hmo
Genetic Background: B6.129S7-Cr2tm1Hmo

 MP:0002083 premature death "death after 3 weeks of age, but before normal life span" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * C57BL/6J

Allelic Composition: Thratm1Jas/Thratm1Jas,Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ

 MP:0002109 abnormal limb morphology "abnormal development of limbs resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Suprmam1BALB/cMed/Suprmam1BALB/cMed,Trp53tm1Tyj/Trp53+
Genetic Background: involves: 129S2/SvPas * BALB/cMed * C57BL/6 * C57BL/6J

 MP:0002113 abnormal skeleton development "anomalous differentiation or remodeling of bone tissue resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

Allelic Composition: Thratm1Jas/Thratm1Jas,Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ

 MP:0002626 increased heart rate "greater than average resting heart beats per minute" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator]
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Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

 MP:0002674 abnormal sperm motility "anomalies in the mobility of the spermatozoa" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: B6.129-Thratm1Ven Thrbtm1Df

 MP:0002757 reduced vertical activity "lesser than average time spent jumping or rearing" [J:82829, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator]
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Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks
Genetic Background: involves: C57BL/6J

 MP:0002764 short tibia " reduced length of the medial and larger bone of the lower leg" [J:12736, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator]
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Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

Allelic Composition: Thrbtm1.1Syc/Thrb+
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss

Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

 MP:0002874 decreased hemoglobin content "decrease in the total hemoglobin content in the circulating blood" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Tcf7tm1a(EUCOMM)Wtsi/Tcf7tm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Tcf7tm1a(EUCOMM)Wtsi/Ics

 MP:0002876 abnormal thyroid physiology "anomalous function of this endocrine gland that normally produces hormones that regulate the metabolic rate of the body " [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Thrbtm1Few/Thrbtm1Few
Genetic Background: involves: 129S4/SvJae

 MP:0002896 abnormal bone mineralization "defect in the process by which minerals are deposited into bone" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

 MP:0003055 abnormal epiphyseal plate morphology "malformed or absent cartilagenous center of ossification on the long bones permitting growth of the bone in both directions during development" [MeSH:National Library of Medicine - Medical Subject Headings, 2003]
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Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

Allelic Composition: Thratm1Jas/Thratm1Jas,Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ

 MP:0003109 short femur "reduced length of the long bone of the thigh" [ava:Anna V. Anagnostopoulos, Mouse Genome Informatics Curator, Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

Allelic Composition: Thrbtm1.1Syc/Thrb+
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

 MP:0003149 abnormal tectorial membrane morphology "malformation, malfunction or absence of the overlaying membrane of cochlear duct, an extracellular matrix of the inner ear that contacts the stereocilia bundles of specialized sensory hair cells; sound induces movement of these hair cells relative to the tectorial membrane, deflects the stereocilia, and leads to fluctuations in hair cell membrane potential, transducing sound into electrical signals" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator, J:77634]
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Allelic Composition: Thrbtm4Few/Thrbtm4Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/c * C57BL/6J

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss

 MP:0003150 detached tectorial membrane "tectorial membrane is abnormally detached from the cochlear epithelium or spiral limbus" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator, J:77634]
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Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss

 MP:0003350 increased circulating levels of thyroid hormone 
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Allelic Composition: Thrbtm1Mkni/Thrbtm1Mkni,Hprttm1(TG-cre)1Sasr/Y
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0003417 premature endochondral bone ossification "early onset of bone formation in bones that form from cartilage" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:94631]
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Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss

Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

 MP:0003418 premature intramembranous bone ossification "early onset of bone formation in bones that form without a cartilagenous intermediate including the cranium and clavicle" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss

 MP:0003442 decreased circulating glycerol level "lower than normal concentration of glycerol in the blood" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Tcf7tm1a(EUCOMM)Wtsi/Tcf7tm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Tcf7tm1a(EUCOMM)Wtsi/Ics

 MP:0003498 thyroid hyperplasia 
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Allelic Composition: Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129S1/Sv * C57BL/6J

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

Allelic Composition: Thratm1Jas/Thratm1Jas,Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ

 MP:0003502 increased activity of thyroid 
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Allelic Composition: Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129S1/Sv * C57BL/6J

Allelic Composition: Thrbtm3Few/Thrbtm3Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

 MP:0003638 abnormal response/metabolism to endogenous compounds "altered ability or inability to metabolize or respond to substances normally present in the body" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Oca2p-un+J/Oca2p-un+J
Genetic Background: C57BL/6J-Oca2p-un

Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

Allelic Composition: Ncoa1tm1Bwo/Ncoa1tm1Bwo,Thrbtm1Olc/Thrbtm1Olc
Genetic Background: B6.129-Ncoa1tm1Bwo Thrbtm1Olc

Allelic Composition: Thrbtm3.1Df/Thrbtm3.1Df
Genetic Background: B6J.Cg-Thrbtm3.1Df

 MP:0003662 abnormal proliferative zone "germinal layer of the epiphyseal plate where cells are actively dividing as well as producing extracellular matrix" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:96254]
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Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

 MP:0003795 abnormal bone structure 
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Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

 MP:0003825 abnormal pillar cell morphology "abnormalities of the supporting cells that form the inner and outer walls of the tunnel in the organ of Corti " [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
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Allelic Composition: Thrbtm3Few/Thrbtm3Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm4Few/Thrbtm4Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/c * C57BL/6J

 MP:0003965 abnormal pituitary hormone level "aberration in the blood or tissue concentration of any of the hormones secreted by the pituitary" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: B6.129-Thratm1Ven Thrbtm1Df

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6

 MP:0004022 abnormal cone electrophysiology "anomaly in the function of light adapted vision mediated by the cones" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Dnmt1tm2Enl/Dnmt1tm2Enl
Genetic Background: involves: 129S4/SvJae

 MP:0004148 increased cortical bone thickness "thicker than normal superficial layer of compact bone" [brs:Beverly Richards-Smith, Mouse Genome Informatics Curator]
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Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

 MP:0004197 abnormal fetal growth/weight/body size "limited or accelerated growth or development apparent during the fetal period (sensu Mus: from E14 through birth)" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

 MP:0004362 cochlear hair cell degeneration "degeneration or loss of the sensory epithelial cells of the cochlea; these cells are in synaptic contact with the auditory nerve" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss

 MP:0004402 decreased cochlear outer hair cell number "decreased number (or less than the expected 3 rows) of the columnar outer hair sensory cells of the organ of Corti" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Thrbtm4Few/Thrbtm4Few
Genetic Background: involves: 129 * C57BL/6

 MP:0004404 cochlear outer hair cell degeneration "degeneration or loss of the columnar outer hair sensory cells of the organ of Corti" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Thrbtm3Few/Thrbtm3Few
Genetic Background: involves: 129 * C57BL/6

 MP:0004411 decreased endocochlear potential "reduction of the electrical potential difference between the endolymphatic and perilymphatic compartments of the cochlea" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/c * C57BL/6J

 MP:0004414 decreased cochlear microphonics "reduction of the bioelectric potentials produced by the hair cells of the organ of Corti in response to sound" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Thrbtm1Df/Thrbtm1Mkni,Tg(Pres-cre)1Jnz/0
Genetic Background: involves: 129S1/Sv * C57BL/6J * FVB/NJ

 MP:0004415 abnormal cochlear nerve compound action potential "anomaly in the combined potentials resulting from activation of the auditory division of the eighth cranial nerve; these potentials represent the summed activity of multiple cochlear afferent fibers discharging synchronously and thus assess the combined functional state of OHCs, IHCs, and their primary afferent innervation" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Thrbtm1Df/Thrbtm1Mkni,Tg(Pres-cre)1Jnz/0
Genetic Background: involves: 129S1/Sv * C57BL/6J * FVB/NJ

 MP:0004433 abnormal cochlear inner hair cell physiology "anomalies in processes pertinent to the function of cochlear IHCs which constitute the true sensory cell type sending impulses via the cochlear (auditory) nerve" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129S1/Sv * C57BL/6J

Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/c * C57BL/6J

Allelic Composition: Thrbtm1Df/Thrbtm1Df
Genetic Background: B6J.129S1-Thrbtm1Df

Allelic Composition: Thrbtm1Df/Thrbtm1Mkni,Tg(Pres-cre)1Jnz/0
Genetic Background: involves: 129S1/Sv * C57BL/6J * FVB/NJ

 MP:0004434 abnormal cochlear outer hair cell physiology "anomalies in processes pertinent to the function of cochlear OHCs which are known to enhance the performance of the cochlea, both qualitatively (increased selectivity) and quantitatively (increased sensitivity); in addition to the mechanoelectric transduction required for auditory sensation, OHCs also perform electromechanical transduction, whereby transmembrane voltage drives rapid changes in the length and stiffness of OHCs at audio frequencies in vitro (electromotility)" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129S1/Sv * C57BL/6J

Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/c * C57BL/6J

 MP:0004437 decreased cochlear outer hair cell electromotility "reduced motility of the cochlear OHCs in response to electrical stimulation" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129S1/Sv * C57BL/6J

Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/c * C57BL/6J

 MP:0004465 degeneration of supporting cells "degeneration or loss of the highly differentiated epithelial cells with distinctive morphological features that surround all hair cells in the organ of Corti" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Thrbtm4Few/Thrbtm4Few
Genetic Background: involves: 129 * C57BL/6

 MP:0004466 short cochlear outer hair cells 
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Allelic Composition: Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129S1/Sv * C57BL/6J

 MP:0004591 enlarged tectorial membrane "increased size of the overlaying membrane of cochlear duct, an extracellular matrix of the inner ear that contacts the stereocilia bundles of specialized sensory hair cells" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129S1/Sv * C57BL/6J

Allelic Composition: Thrbtm3Few/Thrbtm3Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm4Few/Thrbtm4Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/c * C57BL/6J

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss

Allelic Composition: Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129S1/Sv * C57BL/6J * FVB/NJ

 MP:0004664 delayed inner ear development "slowed progression to structurally mature components of the labyrinth, including the semicircular canals, vestibule and cochlea" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129S1/Sv * C57BL/6J

Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/c * C57BL/6J

 MP:0004696 abnormal thyroid follicle morphology "any structural abnormality of the small spherical vesicular components of the thyroid gland that are lined with epithelium and contain a colloid substance that both serves as a reservoir of materials for thyroid hormone production and stores thyroid hormones" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129S1/Sv * C57BL/6J

Allelic Composition: Thratm2Ven/Thratm2Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * BALB/c * C57BL/6J

Allelic Composition: Thrbtm1.1Syc/Thrb+
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

Allelic Composition: Thratm1Jas/Thratm1Jas,Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ

 MP:0004701 decreased circulating insulin-like growth factor I level "reduced blood concentration of this polypeptide hormone with growth-regulating, insulin-like, and mitogenic activities" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

 MP:0004736 abnormal distortion product otoacoustic emission "any abnormality in the sound produced by the cochlea in response to stimulation with 2 simultaneous tones of different frequencies; this measurement is particularly useful in assessing the functional state of OHCs" [eMedicine:http://www.emedicine.com/ent/topic372.htm, MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Thrbtm3Few/Thrbtm3Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm4Few/Thrbtm4Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129S1/Sv * C57BL/6J * FVB/NJ

 MP:0004737 absent distortion product otoacoustic emissions "failure to create mechanical distortions in the inner ear when two primary tones are presented, indicating failure of outer hair cells to amplify basilar membrane motion" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Thrbtm4Few/Thrbtm4Few
Genetic Background: involves: 129 * C57BL/6

 MP:0004738 abnormal brainstem auditory evoked potential "anomaly in the electrical activity generated in response to short tone bursts; may be used to evaluate sensorineural hearing function" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator", MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: B6.129-Thratm1Ven Thrbtm1Df

 MP:0004740 sensorineural hearing loss "a form of progressive hearing loss due to a lesion of the auditory division of cranial nerve VIII or the inner ear" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Thrbtm3Few/Thrbtm3Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm4Few/Thrbtm4Few
Genetic Background: involves: 129 * C57BL/6

 MP:0004852 decreased testis weight "reduced average weight of the male reproductive glands" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: B6.129-Thratm1Ven Thrbtm1Df

 MP:0004864 spiral ligament degeneration "degeneration or loss of the thickened periosteal lining of the bony cochlea that forms the outer wall of the cochlear duct to which the basal lamina attaches" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Thrbtm4Few/Thrbtm4Few
Genetic Background: involves: 129 * C57BL/6

 MP:0004984 increased osteoclast cell number "greater than average number of the bone resorpting cells that remove bone tissue by degrading the mineralized matrix" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

 MP:0005119 decreased circulating thyroid-stimulating hormone level "less than expected blood concentration of the hormone that stimulates the growth and function of the thyroid gland" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Ppargc1atm2.1Brsp/Ppargc1atm2.1Brsp,Tg(Myog-cre)1Eno/0
Genetic Background: involves: 129 * BALB/c * C57BL/6J * C57BL/6N

 MP:0005122 increased circulating thyroid-stimulating hormone level "greater than expected blood concentration of the hormone that stimulates the growth and function of the thyroid gland" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Dnmt1tm2Enl/Dnmt1tm2Enl
Genetic Background: involves: 129S4/SvJae

Allelic Composition: Thrbtm3Few/Thrbtm3Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm4Few/Thrbtm4Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm1Few/Thrbtm1Few
Genetic Background: involves: 129S4/SvJae

Allelic Composition: Thrbtm2Few/Thrbtm2Few
Genetic Background: involves: 129X1/SvJ * C57BL/6

Allelic Composition: Thrbtm2Few/Thrb+
Genetic Background: involves: 129X1/SvJ * C57BL/6

Allelic Composition: Thrbtm5Few/Thrbtm5Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

Allelic Composition: Thrbtm1.1Syc/Thrb+
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6

Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6

Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

Allelic Composition: Thratm1Jas/Thratm1Jas,Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ

Allelic Composition: Ncoa1tm1Bwo/Ncoa1tm1Bwo,Thrbtm1Olc/Thrbtm1Olc
Genetic Background: B6.129-Ncoa1tm1Bwo Thrbtm1Olc

 MP:0005130 decreased follicle stimulating hormone level "less than expected concentration of the hormone that, in females, stimulates the graafian follicles of the ovary and assists in follicular maturation and the secretion of estradiol; in the male it stimulates the epithelium of the seminiferous tubules and is partly responsible for spermatogenesis " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: B6.129-Thratm1Ven Thrbtm1Df

 MP:0005132 decreased luteinizing hormone level "lower than normal concentration of LH " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: B6.129-Thratm1Ven Thrbtm1Df

 MP:0005135 increased thyroid-stimulating hormone level "less than expected concentration of the hormone that stimulates the growth and function of the thyroid gland" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Tsta3tm1Jbl/Tsta3+
Genetic Background: involves: 129S2/SvPas * C57BL/6J

Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: B6.129-Thratm1Ven Thrbtm1Df

Allelic Composition: Thrbtm1Df/Thrbtm1Df
Genetic Background: either: B6.129S1-Thrbtm1Df or (involves: 129S1/Sv * C57BL/6J)

 MP:0005136 decreased growth hormone level "less than the expected concentration of the hormone that promotes body growth, fat mobilization, and inhibition of glucose utilization" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: B6.129-Thratm1Ven Thrbtm1Df

 MP:0005138 decreased prolactin level "less than expected concentration of the hormone that stimulates milk secretion " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: B6.129-Thratm1Ven Thrbtm1Df

 MP:0005355 enlarged thyroid gland "increased size of the endocrine gland located in the front and to the sides of the upper part of the trachea, and which secretes thyroid hormone and calcitonin " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:85158, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator]
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Allelic Composition: Tsta3tm1Jbl/Tsta3+
Genetic Background: involves: 129S2/SvPas * C57BL/6J

Allelic Composition: Thrbtm3Few/Thrbtm3Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm4Few/Thrbtm4Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

Allelic Composition: Thrbtm1.1Syc/Thrb+
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

Allelic Composition: Thrbtm1Df/Thrbtm1.1Syc
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * C57BL/6J

 MP:0005361 small pituitary gland "reduced size of the pituitary gland, the compound gland suspended from the base of the hypothalamus, which secretes somatotropins, prolactin, TSH (thyroid-stimulating hormone), gonadotropins, adrenal corticotropin" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6

 MP:0005418 abnormal circulating hormone level "anomalous blood concentration of any of the chemical substances that have specific regulatory effects on the activity of a certain organ or organs; originally applied to substances secreted by various endocrine glands and transported in the bloodstream to the target organs, it is sometimes extended to include substances that are not produced by the endocrine glands but that have similar effects" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

 MP:0005468 abnormal thyroid hormone level "aberrant concentration of any of the hormones secreted by the thryoid gland" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, J:13923, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Thratm2Ven/Thratm2Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * BALB/c * C57BL/6J

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6

Allelic Composition: Thrbtm1Mkni/Thrbtm1Mkni,Hprttm1(TG-cre)1Sasr/Y
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0005470 increased thyroxine level "greater than the normal concentration of the major hormone dervied from the thryoid gland; it normally affects cellular metabolism" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Thrbtm1Few/Thrbtm1Few
Genetic Background: involves: 129S4/SvJae

Allelic Composition: Thrbtm2Few/Thrbtm2Few
Genetic Background: involves: 129X1/SvJ * C57BL/6

Allelic Composition: Thrbtm2Few/Thrb+
Genetic Background: involves: 129X1/SvJ * C57BL/6

Allelic Composition: Thrbtm1Mkni/Thrbtm1Mkni,Hprttm1(TG-cre)1Sasr/Y
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0005474 increased triiodothyronine level "greater than the normal concentration of this hormone synthesized and secreted by the thyroid; normally, this is the main thyroid hormone used by the tissues " [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Thrbtm1Few/Thrbtm1Few
Genetic Background: involves: 129S4/SvJae

Allelic Composition: Thrbtm2Few/Thrbtm2Few
Genetic Background: involves: 129X1/SvJ * C57BL/6

Allelic Composition: Thrbtm2Few/Thrb+
Genetic Background: involves: 129X1/SvJ * C57BL/6

Allelic Composition: Thratm1Jas/Thratm1Jas,Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ

 MP:0005477 increased circulating thyroxine level "greater than the normal blood concentration of the major hormone dervied from the thryoid gland; it normally affects cellular metabolism" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Tsta3tm1Jbl/Tsta3+
Genetic Background: involves: 129S2/SvPas * C57BL/6J

Allelic Composition: Thrbtm3Few/Thrbtm3Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm5Few/Thrbtm5Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm5Few/Thrb+
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm1Df/Thrbtm1Df
Genetic Background: either: B6.129S1-Thrbtm1Df or (involves: 129S1/Sv * C57BL/6J)

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

Allelic Composition: Thrbtm1.1Syc/Thrb+
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6

Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6

Allelic Composition: Thrbtm6.1Few/Thrbtm6.1Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm6.1Few/Thrb+
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

Allelic Composition: Thratm1Jas/Thratm1Jas,Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ

Allelic Composition: Ncoa1tm1Bwo/Ncoa1tm1Bwo,Thrbtm1Olc/Thrbtm1Olc
Genetic Background: B6.129-Ncoa1tm1Bwo Thrbtm1Olc

Allelic Composition: Thrbtm1Mkni/Thrbtm1Mkni,Hprttm1(TG-cre)1Sasr/Y
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0005478 decreased circulating thyroxine level "less than the normal blood concentration of the major hormone dervied from the thryoid gland; it normally affects cellular metabolism" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Tsta3tm1Jbl/Tsta3+
Genetic Background: involves: 129S2/SvPas * C57BL/6J

Allelic Composition: Thratm2Ven/Thratm2Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * BALB/c * C57BL/6J

 MP:0005479 decreased circulating triiodothyronine level "less than the normal blood concentration of this hormone synthesized and secreted by the thyroid; normally, this is the main thyroid hormone used by the tissues " [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Thratm2Ven/Thratm2Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * BALB/c * C57BL/6J

 MP:0005480 increased circulating triiodothyronine level "greater than the normal blood concentration of this hormone synthesized and secreted by the thyroid; normally, this is the main thyroid hormone used by the tissues " [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Dnmt1tm2Enl/Dnmt1tm2Enl
Genetic Background: involves: 129S4/SvJae

Allelic Composition: Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129S1/Sv * C57BL/6J

Allelic Composition: Thrbtm3Few/Thrbtm3Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm5Few/Thrbtm5Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm1Df/Thrbtm1Df
Genetic Background: either: B6.129S1-Thrbtm1Df or (involves: 129S1/Sv * C57BL/6J)

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

Allelic Composition: Thrbtm1.1Syc/Thrb+
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6

Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6

Allelic Composition: Thrbtm6.1Few/Thrbtm6.1Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm6.1Few/Thrb+
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

Allelic Composition: Ncoa1tm1Bwo/Ncoa1tm1Bwo,Thrbtm1Olc/Thrbtm1Olc
Genetic Background: B6.129-Ncoa1tm1Bwo Thrbtm1Olc

 MP:0005646 abnormal pituitary gland physiology "anmalous function of this unpaired compound gland suspended from the base of the hypothalamus by a short extension of the infundibulum, the infundibular or pituitary stalk" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Thrbtm3Few/Thrbtm3Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm4Few/Thrbtm4Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

Allelic Composition: Thrbtm1.1Syc/Thrb+
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

 MP:0006325 impaired hearing "reduced ability to percieve auditory stimuli" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss

 MP:0006395 abnormal epiphyseal plate morphology "any structural anomaly of the cartilaginous center of ossification on the bones permitting growth of the bone in both directions during development" [MESH:A02.835.232.251.352]
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Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

 MP:0006396 decreased long bone epiphyseal plate size "reduced size of the cartilaginous center of ossification on the long bones permitting growth of the bone in both directions during development" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

 MP:0008142 decreased small intestinal villus size "reduced size of the tiny hair-like projections that protrude from the inside of the small intestine that contain blood vessels that capture digested nutrients that are absorbed through the intestinal wall; the villi increase the absorptive surface area of the small intestine by approximately 30-fold" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", MGI:rbabiuk "Randall Babiuk, Mouse Genome Informatics Curator"]
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Allelic Composition: Thratm1Jas/Thratm1Jas,Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ

 MP:0008337 increased thyrotroph cell number "greater number of an anterior pituitary cell that produces thyroid-stimulating hormone" [MESH:A06.407.747.608.968]
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Allelic Composition: Thrbtm3Few/Thrbtm3Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm4Few/Thrbtm4Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

 MP:0009346 decreased cancellous bone thickness "thinner than normal bone with a lattice-like or spongy structure" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

 MP:0009766 increased sensitivity to xenobiotic induced morbidity/mortality "decrease in the amount of a foreign compound required to cause death or diseased state" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/c * C57BL/6J

 MP:0009780 abnormal chondrocyte physiology "any functional anomaly of nondividing cartilage cells" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
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Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

 MP:0010346 increased thyroid carcinioma incidence "greater than the expected number of a malignant epithelial neoplasms of the thyroid gland, occurring in a specific population in a given time period" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Thrbtm1Df/Thrbtm1.1Syc
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * C57BL/6J

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * C57BL/6J

 MP:0011100 complete preweaning lethality "death of all organisms of a given genotype in a population between fertilization and weaning age (Mus: approximately 3-4 weeks of age)" [MGI:csmith]
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Allelic Composition: Thratm2Ven/Thratm3Ven
Genetic Background: involves: 129P2/OlaHsd * C57BL/6NCrl

 MP:0011270 decreased excitatory postsynaptic current amplitude "reduction in the size (height or maximum displacement) of the evoked excitatory postsynaptic current wave" [MGI:csmith]
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Allelic Composition: Mir34atm1.2Arte/Mir34atm1.2Arte,Tg(Neurod2-Smo*A1)199Jols/0
Genetic Background: involves: C57BL/6 * C57BL/6N

 MP:0011617 abnormal habituation "anomaly in the process in which there is a progressive decline of behavioral response probability with a repetitive stimulus" [GO:0046959, PMID:16774787]
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Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks
Genetic Background: involves: C57BL/6J

Allelic Composition: Thrbtm1.1Syc/Thrb+
Genetic Background: involves: 129S6/SvEvTac * NIH Black Swiss

 MP:0011967 increased or absent threshold for auditory brainstem response "increase in the value at which one or more sound frequencies or broadband clicks first elicits a recordable response generated by electrical activity of neurons in the ascending auditory system, or complete lack of a recordable response at any frequency or broadband click" [MGI:csmith]
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Allelic Composition: Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129S1/Sv * C57BL/6J

Allelic Composition: Thrbtm3Few/Thrbtm3Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm4Few/Thrbtm4Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thratm1Ven/Thra+,Thrbtm1Df/Thrbtm1Df
Genetic Background: B6.129-Thratm1Ven Thrbtm1Df

Allelic Composition: Thrbtm1Df/Thrbtm1Df
Genetic Background: either: B6.129S1-Thrbtm1Df or (involves: 129S1/Sv * C57BL/6J)

Allelic Composition: Thrbtm1Df/Thrbtm1Df
Genetic Background: B6J.129S1-Thrbtm1Df

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss

Allelic Composition: Thrbtm1Df/Thrbtm1Mkni,Tg(Pres-cre)1Jnz/0
Genetic Background: involves: 129S1/Sv * C57BL/6J * FVB/NJ

Allelic Composition: Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129S1/Sv * C57BL/6J * FVB/NJ

 MP:0012315 impaired learning "impaired ability to aquire lasting change in behavior that is the result of experience" [http:psychology.about.com/od/lindex/g/learning.htm]
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Allelic Composition: Fcer1gtm1Tks/Fcer1gtm1Tks
Genetic Background: involves: C57BL/6J

Allelic Composition: Thrbtm1.1Syc/Thrb+
Genetic Background: involves: 129S6/SvEvTac * NIH Black Swiss

 MP:0014091 abnormal tectorial membrane striated-sheet matrix morphology "any structural anomaly of the laminated, striated-sheet matrix within which collagen fibrils of the TM are imbedded; the striated sheet matrix is formed by two types of fine-diameter collagen filaments, a light and a dark staining type that lie in parallel within the plane of each sheet and are extensively linked along their length by staggered cross bridges; it originates medially within the sulcal zone, extends to the marginal band and is particularly evident in apical regions of the cochlea, where it has a less compressed appearance" [PMID:18797289, PMID:24363064]
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Allelic Composition: Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129S1/Sv * C57BL/6J

Allelic Composition: Thratm1Ven/Thratm1Ven,Thrbtm1Df/Thrbtm1Df
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/c * C57BL/6J

 MP:0020168 decreased thyroid gland weight "lower than average weight of the thyroid gland" [GOC:NV]
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Allelic Composition: Thrbtm1Mkni/Thrbtm1Mkni,Hprttm1(TG-cre)1Sasr/Y
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Thrbtm1Mkni/Thrb+,Hprttm1(TG-cre)1Sasr/Y
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0020169 increased thyroid gland weight "higher than average weight of the thyroid gland" [GOC:NV]
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Allelic Composition: Thrbtm5Few/Thrbtm5Few
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm5Few/Thrb+
Genetic Background: involves: 129 * C57BL/6

Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * C57BL/6J

 MP:0030018 increased cardiac cell glucose uptake "increased ability of the cells of the heart to take in glucose" [MGI:anna]
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Allelic Composition: Thratm1Syc/Thra+
Genetic Background: involves: 129S6/SvEvTac

 MP:0030389 small fontanelles "an abnormally decreased size of one or more fontanelles for age-related norms" [HP:0005486, MGI:anna]
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Allelic Composition: Thrbtm1.1Syc/Thrbtm1.1Syc
Genetic Background: involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

Allelic Composition: Thrbtm1Olc/Thrbtm1Olc
Genetic Background: involves: 129/Sv

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSMUSG00000015120 Ube2i / P63280 / ubiquitin-conjugating enzyme E2I / P63279*  / reaction
 ENSMUSG00000020265 Sumo3 / Q9Z172 / small ubiquitin-like modifier 3 / P55854*  / reaction
 ENSMUSG00000026021 Sumo1 / P63166 / Small ubiquitin-related modifier 1 / P63165* / small ubiquitin-like modifier 1*  / reaction / complex






 

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