ENSMUSG00000000247


Mus musculus

Features
Gene ID: ENSMUSG00000000247
  
Biological name :Lhx2
  
Synonyms : Lhx2 / LIM/homeobox protein Lhx2 / Q9Z0S2
  
Possible biological names infered from orthology : LIM homeobox 2 / P50458
  
Species: Mus musculus
  
Chr. number: 2
Strand: 1
Band: B
Gene start: 38339281
Gene end: 38369733
  
Corresponding Affymetrix probe sets: 10471833 (MoGene1.0st)   1418317_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000114797
Ensembl peptide - ENSMUSP00000121462
Ensembl peptide - ENSMUSP00000135402
Ensembl peptide - ENSMUSP00000000253
Ensembl peptide - ENSMUSP00000115179
NCBI entrez gene - 16870     See in Manteia.
MGI - MGI:96785
RefSeq - XM_006497739
RefSeq - NM_001290646
RefSeq - NM_010710
RefSeq - XM_006497733
RefSeq - XM_006497734
RefSeq - XM_006497735
RefSeq - XM_006497736
RefSeq - XM_006497738
RefSeq Peptide - NP_001277575
RefSeq Peptide - NP_034840
swissprot - H3BKI3
swissprot - F6SM03
swissprot - Q543C6
swissprot - A0A0A0MQK9
swissprot - Q9Z0S2
swissprot - F6Z9H5
Ensembl - ENSMUSG00000000247
  

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
 LHX2ENSG00000106689Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Lhx9 / Q9WUH2 / LIM/homeobox protein Lhx9 / Q9NQ69* / LIM homeobox 9*ENSMUSG0000001923068
Lhx5 / P61375 / LIM homeobox protein 5 / Q9H2C1* / LIM homeobox 5*ENSMUSG0000002959527
Lhx6 / Q9R1R0 / Mus musculus LIM homeobox protein 6 (Lhx6), transcript variant 5, mRNA. / Q9UPM6* / LIM homeobox 6*ENSMUSG0000002689027
Lhx8 / O35652 / LIM/homeobox protein Lhx8 / Q68G74* / LIM homeobox 8*ENSMUSG0000009622525
Lhx3 / P50481 / LIM homeobox protein 3 / Q9UBR4* / LIM homeobox 3*ENSMUSG0000002693425
Lhx1 / P63006 / LIM/homeobox protein Lhx1 / P48742* / LIM homeobox 1*ENSMUSG0000001869825
Isl2 / Q9CXV0 / Insulin enhancer protein ISL-2 / Q96A47* / ISL LIM homeobox 2*ENSMUSG0000003231824
Isl1 / P61372 / Insulin enhancer protein ISL-1 / P61371* / ISL LIM homeobox 1*ENSMUSG0000004225823
Lmx1b / LIM homeobox transcription factor 1 beta / O60663*ENSMUSG0000003876522
Lhx4 / P53776 / LIM/homeobox protein Lhx4 / Q969G2* / LIM homeobox 4*ENSMUSG0000002646822
Lmx1a / Q9JKU8 / LIM homeobox transcription factor 1-alpha / Q8TE12*ENSMUSG0000002668622
Lmo3 / Q8BZL8 / Mus musculus LIM domain only 3 (Lmo3), transcript variant 2, mRNA. / Q8TAP4* / LIM domain only 3*ENSMUSG0000003022615
Lmo4 / P61969 / LIM domain transcription factor LMO4 / P61968* / LIM domain only 4*ENSMUSG0000002826615
Lmo1 / Q924W9 / Rhombotin-1 / P25800* / LIM domain only 1*ENSMUSG0000003611115
Lmo2 / P25801 / Rhombotin-2 / P25791* / LIM domain only 2*ENSMUSG0000003269812


Protein motifs (from Interpro)
Interpro ID Name
 IPR001356  Homeobox domain
 IPR001781  Zinc finger, LIM-type
 IPR009057  Homeobox-like domain superfamily
 IPR017970  Homeobox, conserved site


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001843 neural tube closure IMP
 biological_processGO:0001942 hair follicle development IMP
 biological_processGO:0006351 transcription, DNA-templated IEA
 biological_processGO:0006355 regulation of transcription, DNA-templated IEA
 biological_processGO:0006366 transcription by RNA polymerase II IEA
 biological_processGO:0007399 nervous system development IMP
 biological_processGO:0007411 axon guidance IMP
 biological_processGO:0007420 brain development IMP
 biological_processGO:0007498 mesoderm development IMP
 biological_processGO:0009953 dorsal/ventral pattern formation IMP
 biological_processGO:0021537 telencephalon development IMP
 biological_processGO:0021772 olfactory bulb development IMP
 biological_processGO:0021978 telencephalon regionalization IMP
 biological_processGO:0021987 cerebral cortex development IMP
 biological_processGO:0022008 neurogenesis IDA
 biological_processGO:0030182 neuron differentiation IMP
 biological_processGO:0045199 maintenance of epithelial cell apical/basal polarity IMP
 biological_processGO:0045893 positive regulation of transcription, DNA-templated IMP
 biological_processGO:0045944 positive regulation of transcription by RNA polymerase II IGI
 biological_processGO:0048646 anatomical structure formation involved in morphogenesis IMP
 biological_processGO:0048675 axon extension IDA
 biological_processGO:0060041 retina development in camera-type eye IGI
 biological_processGO:2000678 negative regulation of transcription regulatory region DNA binding IGI
 cellular_componentGO:0005622 intracellular IDA
 cellular_componentGO:0005634 nucleus IDA
 cellular_componentGO:0005654 nucleoplasm TAS
 molecular_functionGO:0000978 RNA polymerase II proximal promoter sequence-specific DNA binding IMP
 molecular_functionGO:0001076 transcription factor activity, RNA polymerase II transcription factor binding IPI
 molecular_functionGO:0001077 transcriptional activator activity, RNA polymerase II proximal promoter sequence-specific DNA binding IMP
 molecular_functionGO:0003677 DNA binding IEA
 molecular_functionGO:0003682 chromatin binding IDA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0043565 sequence-specific DNA binding IDA
 molecular_functionGO:0046872 metal ion binding IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000208 decreased hematocrit "less than the average percentage of a volume of a blood sample occupied by red blood cells" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
Show

Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

 MP:0000245 abnormal erythropoiesis "atypical process of red blood cell formation" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, tc:Teresa Chu , Mouse Genome Informatics Curator]
Show

Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

 MP:0000379 reduced hair follicle number "fewer number of the epidermal invaginations from which the hair shaft develops" [J:15108]
Show

Allelic Composition: Lhx2tm1Monu/Lhx2tm1Monu,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * CBA

 MP:0000382 underdeveloped hair follicles "arrest of or retarded differentiation of the epidermal invaginations from which the hair shaft develops" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:61790]
Show

Allelic Composition: Lhx2tm1Lcar/Lhx2tm1Lcar
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0000600 liver hypoplasia "reduced size of liver due to decreased cell number " [J:57631]
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Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

 MP:0000601 small liver "reduced size of the liver" [J:23170]
Show

Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

 MP:0000784 forebrain hypoplasia "reduced cell number in the anterior primitive cerebral vesicle; most rostral of three primary vesicles of the embryonic neural tube" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

 MP:0000785 telencephalon hypoplasia "reduced cell number in cerebral cortex and basal ganglia" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:45302]
Show

Allelic Composition: Emx1tm1(cre)Krj/Emx1+,Lhx2tm1.1Ddmo/Lhx2tm1.2Ddmo
Genetic Background: involves: 129S2/SvPas * C57BL/6 * SJL

Allelic Composition: Emx1tm1(cre)Krj/Emx1+,Lhx2tm1.1Ddmo/Lhx2tm1.1Ddmo
Genetic Background: involves: 129S2/SvPas * C57BL/6 * SJL

 MP:0000787 abnormal telencephalon morphology "any malformation or absence of the paired anteriolateral division of the prosencephalon plus the lamina terminalis from which the olfactory lobes, cerebral cortex, and subcortical nuclei are derived " [MeSH:National Library of Medicine - Medical Subject Headings , 2003, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

Allelic Composition: Emx1tm1(cre)Krj/Emx1+,Lhx2tm1.1Ddmo/Lhx2tm1.2Ddmo
Genetic Background: involves: 129S2/SvPas * C57BL/6 * SJL

Allelic Composition: Emx1tm1(cre)Krj/Emx1+,Lhx2tm1.1Ddmo/Lhx2tm1.1Ddmo
Genetic Background: involves: 129S2/SvPas * C57BL/6 * SJL

 MP:0000788 abnormal cerebral cortex morphology "malformed gray cellular mantle covering the surface of the brain" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:38857]
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Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

Allelic Composition: Lhx2tm1.1Monu/Lhx2tm1.1Monu
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Lhx2tm1Dra/Lhx2tm1.1Monu
Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6

Allelic Composition: Lhx2tm1Dra/Lhx2tm1Dra
Genetic Background: involves: 129S4/SvJae * C57BL/6

Allelic Composition: Lhx2tm1Monu/Lhx2tm1Monu,Tmem163Tg(ACTB-cre)2Mrt/0
Genetic Background: involves: 129P2/OlaHsd * CD-1 * FVB/N

Allelic Composition: Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+,Lhx2tm1Monu/Lhx2tm1Monu
Genetic Background: involves: 129 * 129P2/OlaHsd * C57BL/6

Allelic Composition: Emx1tm1(cre)Yql/Emx1+,Lhx2tm1Monu/Lhx2tm1Monu
Genetic Background: involves: 129P2/OlaHsd * 129S2/SvPas

 MP:0000809 absent hippocampus "missing convoluted brain structure below the cerebral hemispheres; forms part of the limbic system" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:59284]
Show

Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

 MP:0000819 abnormal olfactory bulb morphology "malformation or absence of the forebrain region that coordinates neuronal signaling involved in the perception of smell; it receives input from the sensory neurons and outputs to the olfactory cortex" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, Principles of Neural Science:ISBN 0-8385-8034-3, J:16461]
Show

Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

Allelic Composition: Lhx2tm1Dra/Lhx2tm1Dra,Olfr78tm1Jgst/Olfr78+
Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ

Allelic Composition: Emx1tm1(cre)Krj/Emx1+,Lhx2tm1.1Ddmo/Lhx2tm1.2Ddmo
Genetic Background: involves: 129S2/SvPas * C57BL/6 * SJL

Allelic Composition: Emx1tm1(cre)Krj/Emx1+,Lhx2tm1.1Ddmo/Lhx2tm1.1Ddmo
Genetic Background: involves: 129S2/SvPas * C57BL/6 * SJL

 MP:0000934 abnormal telencephalon development "malformed or incomplete differentiation of the anterior division of the embryonic prosencephalon " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:49840]
Show

Allelic Composition: Lhx2tm1Dra/Lhx2tm1Dra
Genetic Background: involves: 129S4/SvJae * C57BL/6

Allelic Composition: Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+,Lhx2tm1Monu/Lhx2tm1Monu
Genetic Background: involves: 129 * 129P2/OlaHsd * C57BL/6

 MP:0001286 abnormal eye development "malformation or arrest of differentiation of the visual organ" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:49840]
Show

Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

 MP:0001293 anophthalmia "congenital absence of all tissues of the eyes" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CML, J:71979]
Show

Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

Allelic Composition: Lhx2tm1Lcar/Lhx2tm1Lcar
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Lhx2tm1.1Lcar/Lhx2tm1.1Lcar,Tg(Lhx2-cre)1Lcar/0
Genetic Background: involves: 129P2/OlaHsd

 MP:0001577 anemia "less than normal levels of red blood cells, hemoglobin or volume of packed red blood cells " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:53370]
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Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

Allelic Composition: Lhx2tm1Lcar/Lhx2tm1Lcar
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0002073 abnormal hair growth "absence or reduced amount of hair or abnormal onset of hair growth cycle or development" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Ltbrtm1Kpf/Ltbrtm1Kpf
Genetic Background: B6.129P2-Ltbrtm1Kpf

Allelic Composition: Lhx2tm1Monu/Lhx2tm1Dra,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * CBA

Allelic Composition: Lhx2tm1.1Lcar/Lhx2tm1.1Lcar,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129S4/SvJae * C57BL/6 * CBA

Allelic Composition: Lhx2tm1Monu/Lhx2tm1Monu,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * CBA

 MP:0002192 hydrops fetalis "an abnormal accumulation of serous fluid in fetal tissues" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

 MP:0003078 aphakia "absence of the crystalline lens of the eye" [Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8, ava:Anna V. Anagnostopoulos, Mouse Genome Informatics Curator]
Show

Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

 MP:0003425 abnormal optic vesicle formation "anomalous formation of the hollow outgrowth from the lateral aspects of the embryonic forebrain from which the retina and optic nerve develop" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:94391]
Show

Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

Allelic Composition: Lhx2tm1.1Lcar/Lhx2tm1.1Lcar,Tg(Lhx2-cre)1Lcar/0
Genetic Background: involves: 129P2/OlaHsd

 MP:0003717 pallor "an unnatural paleness to the skin, generally attributable to anemia" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

 MP:0004100 abnormal spinal cord interneuron morphology "malformation or absence of neurons that exclusively interact with other neurons in the spinal cord" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Igf1tm2Arge/Igf1tm2.1Arge
Genetic Background: involves: 129S/SvEv * C57BL/6J * CBA

Allelic Composition: Lhx2tm1Dra/Lhx2+,Lhx9tm1Dodd/Lhx9tm1Dodd
Genetic Background: Not Specified

Allelic Composition: Lhx2tm1Dra/Lhx2tm1Dra,Lhx9tm1Dodd/Lhx9+
Genetic Background: Not Specified

Allelic Composition: Lhx2tm1Dra/Lhx2+,Lhx9tm1Dodd/Lhx9tm1Dodd,Robo3tm1Matl/Robo3+
Genetic Background: Not Specified

 MP:0005267 abnormal olfactory cortex morphology "anomalous structure of piriform cortex, part of the olfactory tract, which receives its major afferents from the olfactory bulb, and is primarily responsible for the identification of odors" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:83884]
Show

Allelic Composition: Emx1tm1(cre)Krj/Emx1+,Lhx2tm1.1Ddmo/Lhx2tm1.2Ddmo
Genetic Background: involves: 129S2/SvPas * C57BL/6 * SJL

Allelic Composition: Emx1tm1(cre)Krj/Emx1+,Lhx2tm1.1Ddmo/Lhx2tm1.1Ddmo
Genetic Background: involves: 129S2/SvPas * C57BL/6 * SJL

 MP:0006007 abnormal basal ganglion morphology "malformation or absence of any of a group of nuclei associated with the ability to carry out willed movements, including the caudate, putamen, nucleus accumbens, globus pallidus, substantia nigra, and subthalamic nucleus" [smb:Susan M Bello, Mouse Genome Informatics Curator]
Show

Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

 MP:0006092 abnormal olfactory neuron morphology "malformation in the neurons that are activated by specific odorants" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:92950]
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Allelic Composition: Lhx2tm1Dra/Lhx2tm1Dra,Olfr78tm1Jgst/Olfr78+
Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ

 MP:0008439 abnormal cortical plate morphology "any strucutral anomaly of the outer neural tube region in which post-mitotic neuroblasts migrate along radial glia to form the adult cortical layers" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", PMID:1812236]
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Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

 MP:0008547 abnormal neocortex morphology "any structural anomaly of the larger part of the mammalian cerebral cortex, distinguished from the allocortex by being composed of a larger number of nerve cells arranged in six layers" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition", MESH:A08.186.211.730.885.213.420]
Show

Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

Allelic Composition: Emx1tm1(cre)Krj/Emx1+,Lhx2tm1.1Ddmo/Lhx2tm1.2Ddmo
Genetic Background: involves: 129S2/SvPas * C57BL/6 * SJL

Allelic Composition: Emx1tm1(cre)Krj/Emx1+,Lhx2tm1.1Ddmo/Lhx2tm1.1Ddmo
Genetic Background: involves: 129S2/SvPas * C57BL/6 * SJL

Allelic Composition: Lhx2tm1.1Ddmo/Lhx2tm1.1Ddmo,Tg(Nes-cre)1Kln/0
Genetic Background: involves: C57BL/6 * SJL

 MP:0008858 abnormal hair cycle anagen phase "anomaly in the growth phase of the hair cycle" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Ltbrtm1Kpf/Ltbrtm1Kpf
Genetic Background: B6.129P2-Ltbrtm1Kpf

Allelic Composition: Lhx2tm1Monu/Lhx2tm1Dra,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * CBA

Allelic Composition: Lhx2tm1.1Lcar/Lhx2tm1.1Lcar,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129S4/SvJae * C57BL/6 * CBA

Allelic Composition: Lhx2tm1Monu/Lhx2tm1Monu,Tg(CAG-cre/Esr1*)5Amc/0
Genetic Background: involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * CBA

 MP:0008973 decreased erythroid progenitor cell number "reduced numbers of progenitors of the erythrocyte lineage" [CL:0000038, MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

 MP:0009773 absent retina "absence of the nerve layer lining the back of the eye that senses light, and creates impulses that travel through the optic nerve to the brain" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
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Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

 MP:0011099 complete lethality throughout fetal growth and development "death of all organisms of a given genotype in a population between the completion of organogenesis and birth (Mus: E14 to approximately E18.5)" [MGI:csmith]
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Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

 MP:0012170 absent optic placodes "absence of the paired thickenings of surface ectoderm that normally become invaginated to form the embryonic lens vesicles" [MGI:anna]
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Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

 MP:0030047 flat forehead "abnormal flatness of the forehead" [MGI:anna]
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Allelic Composition: Atmtm1Mfl/Atmtm1Mfl
Genetic Background: involves: 129T2/SvEms * C57BL/6J

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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