ENSMUSG00000063972


Mus musculus

Features
Gene ID: ENSMUSG00000063972
  
Biological name :Nr6a1
  
Synonyms : Nr6a1 / Nuclear receptor subfamily 6 group A member 1 / Q64249
  
Possible biological names infered from orthology : Q15406
  
Species: Mus musculus
  
Chr. number: 2
Strand: -1
Band: B
Gene start: 38723370
Gene end: 38927688
  
Corresponding Affymetrix probe sets: 10482249 (MoGene1.0st)   1421515_at (Mouse Genome 430 2.0 Array)   1421516_at (Mouse Genome 430 2.0 Array)   1428825_at (Mouse Genome 430 2.0 Array)   1428826_at (Mouse Genome 430 2.0 Array)   1445872_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000108498
Ensembl peptide - ENSMUSP00000121234
Ensembl peptide - ENSMUSP00000126009
Ensembl peptide - ENSMUSP00000075624
Ensembl peptide - ENSMUSP00000115164
NCBI entrez gene - 14536     See in Manteia.
MGI - MGI:1352459
RefSeq - NM_001159548
RefSeq - NM_001159549
RefSeq - NM_010264
RefSeq - XM_011239025
RefSeq Peptide - NP_001153020
RefSeq Peptide - NP_001153021
RefSeq Peptide - NP_034394
swissprot - A0A0A0MQG4
swissprot - Q64249
swissprot - Z4YMW4
Ensembl - ENSMUSG00000063972
  

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
 nr6a1aENSDARG00000101508Danio rerio
 NR6A1ENSGALG00000001073Gallus gallus
 NR6A1ENSG00000148200Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Nr5a2 / P45448 / Nuclear receptor subfamily 5 group A member 2 / O00482*ENSMUSG0000002639822
Nr1d2 / Q60674 / nuclear receptor subfamily 1, group D, member 2 / Q14995*ENSMUSG0000002177522
Nr1d1 / Q3UV55 / Nuclear receptor subfamily 1 group D member 1 / P20393*ENSMUSG0000002088920
Rorc / P51450 / Nuclear receptor ROR-gamma / P51449* / RAR related orphan receptor C*ENSMUSG0000002815018
Nr5a1 / P33242 / Steroidogenic factor 1 / Q13285* / nuclear receptor subfamily 5 group A member 1*ENSMUSG0000002675118
Rora / P51448 / RAR-related orphan receptor alpha / P35398* / RAR related orphan receptor A*ENSMUSG0000003223818
Ppara / P23204 / peroxisome proliferator activated receptor alpha / Q07869*ENSMUSG0000002238317
Rorb / Q8R1B8 / Nuclear receptor ROR-beta / Q92753* / RAR related orphan receptor B*ENSMUSG0000003619217
Ppard / P35396 / Peroxisome proliferator-activated receptor delta / Q03181*ENSMUSG0000000225017
Pparg / peroxisome proliferator activated receptor gamma / P37231*ENSMUSG0000000044016


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
 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 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:0007275 multicellular organism development IEA
 biological_processGO:0007276 gamete generation IEP
 biological_processGO:0007283 spermatogenesis IEA
 biological_processGO:0030154 cell differentiation IEA
 biological_processGO:0030518 intracellular steroid hormone receptor signaling pathway IBA
 biological_processGO:0043401 steroid hormone mediated signaling pathway IEA
 biological_processGO:0045944 positive regulation of transcription by RNA polymerase II IDA
 cellular_componentGO:0005634 nucleus IBA
 cellular_componentGO:0005667 transcription factor complex IDA
 molecular_functionGO:0000978 RNA polymerase II proximal promoter sequence-specific DNA binding IMP
 molecular_functionGO:0001077 transcriptional activator activity, RNA polymerase II proximal promoter sequence-specific DNA binding IMP
 molecular_functionGO:0003677 DNA binding IDA
 molecular_functionGO:0003700 DNA-binding transcription factor activity IEA
 molecular_functionGO:0003707 steroid hormone receptor activity IEA
 molecular_functionGO:0004879 nuclear receptor activity IBA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0008270 zinc ion binding IEA
 molecular_functionGO:0042803 protein homodimerization activity IDA
 molecular_functionGO:0043565 sequence-specific DNA binding IDA
 molecular_functionGO:0046872 metal ion binding IEA


Pathways (from Reactome)
Pathway description
Nuclear Receptor transcription pathway


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000266 abnormal cardiac morphology "anomalies in the hollow, muscular organ that maintains the circulation of the blood" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Nr6a1tm1b(EUCOMM)Wtsi/Nr6a1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Nr6a1tm1b(EUCOMM)Wtsi/Bay

 MP:0000269 abnormal looping morphogenesis "atypical bending of the primitive heart tube during early development" [J:27443]
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Allelic Composition: Nr6a1tm1b(EUCOMM)Wtsi/Nr6a1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Nr6a1tm1b(EUCOMM)Wtsi/Bay

 MP:0000288 abnormal pericardium morphology "malformation of the fibroserous membrane covering the heart and beginning of the great vessels" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cml, J:54408]
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Allelic Composition: Nr6a1tm1b(EUCOMM)Wtsi/Nr6a1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Nr6a1tm1b(EUCOMM)Wtsi/Bay

 MP:0000292 distended pericardial sacs "stretched outer parietal layer of the pericardium" [J:25248]
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Allelic Composition: Mapk8ip3tm1.1Ysok/Mapk8ip3tm1.1Ysok
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

Allelic Composition: Nr6a1tm1Coo/Nr6a1tm1Coo
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0000913 abnormal brain development "malformed or incomplete differentiation of the brain" [MGI:cls, J:49840]
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Allelic Composition: Nr6a1tm1Coo/Nr6a1tm1Coo
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0000928 incomplete cephalic closure "arrest of the fusion of the cephalic neural folds" [J:12622]
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Allelic Composition: Mapk8ip3tm1.1Ysok/Mapk8ip3tm1.1Ysok
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

 MP:0001056 abnormal cranial nerve morphology "any anomaly, deformity, or malformation of any of the twelve nerves that emerge from the cranium as opposed to the spinal nerves" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:45302]
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Allelic Composition: Nr6a1tm1Coo/Nr6a1tm1Coo
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0001061 abnormal oculomotor nerve morphology "malformation or misprojection of the 3rd cranial nerve, which normally sends motor fibers to the levator muscles of the eyelid and to the superior rectus, inferior rectus, and inferior oblique muscles of the eye; and also sends parasympathetic efferents to the muscles controlling pupillary constriction and accommodation" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Nr6a1tm1Coo/Nr6a1tm1Coo
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0001063 abnormal trochlear nerve morphology "any malformation or misprojection of the 4th cranial nerve, which normally carries the motor innervation of the superior oblique muscles of the eye " [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Nr6a1tm1Coo/Nr6a1tm1Coo
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0001125 abnormal oocytes "anomalous structure of immature ova" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Ctnnb1tm1Mmt/Ctnnb1+,Tg(Fabp1-cre)1Mmt/?
Genetic Background: involves: 129X1/SvJ

 MP:0001289 persistence of hyaloid capillary system "failure of the degeneration of the transient vascular system of the eye during development" [J:49840]
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Allelic Composition: Npc1tm1b(EUCOMM)Hmgu/Npc1+
Genetic Background: C57BL/6N-Npc1tm1b(EUCOMM)Hmgu/H

 MP:0001672 abnormal embryogenesis/ development "anomaly in the establishment of the characteristic configuration of the embryonic body" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Tyrc-15R145M/Tyrc
Genetic Background: involves: 101/Rl * C3H/Rl

Allelic Composition: Nr6a1Gt(RRA042)Byg/Nr6a1Gt(RRA042)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Nr6a1tm1d(EUCOMM)Wtsi/Nr6a1tm1d(EUCOMM)Wtsi
Genetic Background: involves: 129S/SvEv * C57BL/6 * C57BL/6N * SJL

Allelic Composition: Nr6a1tm1b(EUCOMM)Wtsi/Nr6a1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Nr6a1tm1b(EUCOMM)Wtsi/Bay

 MP:0001689 incomplete somite formation "arrest of differentiation or patterning of the somites" [J:62882]
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Allelic Composition: Mapk8ip3tm1.1Ysok/Mapk8ip3tm1.1Ysok
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

Allelic Composition: Nr6a1tm1Coo/Nr6a1tm1Coo
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0001691 abnormal somite shape "atypical characteristic surface configuration of a segmental mass along the notochord of the developing embryo" [J:37888]
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Allelic Composition: Nr6a1tm1b(EUCOMM)Wtsi/Nr6a1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Nr6a1tm1b(EUCOMM)Wtsi/Bay

 MP:0001697 abnormal embryo size "anomalous proportions of embryo compared to littermates" [cwg:Carroll W. Goldsmith, Mouse Genome Informatics Curator]
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Allelic Composition: Nr6a1tm1b(EUCOMM)Wtsi/Nr6a1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Nr6a1tm1b(EUCOMM)Wtsi/Bay

 MP:0001698 reduced embryo size "smaller proportions of embryo compared to littermates" [J:61790]
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Allelic Composition: Nr6a1tm1d(EUCOMM)Wtsi/Nr6a1tm1d(EUCOMM)Wtsi
Genetic Background: involves: 129S/SvEv * C57BL/6 * C57BL/6N * SJL

 MP:0001700 abnormal embryo turning "atypical axial rotation of the germ layers of the embryo during the primitive streak/early somite stage (Mus:E8.5-E9.5) such that the curvature of the entire trunk region is reversed and the neural ectoderm moves to the convex region and the midgut region becomes located in the concave region" [The Atlas of Mouse Development:ISBN 0-12-402035-6, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Nr6a1tm1b(EUCOMM)Wtsi/Nr6a1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Nr6a1tm1b(EUCOMM)Wtsi/Bay

 MP:0001701 incomplete embryo turning "arrest of the axial rotation of the germ layers of the embryo during the primitive streak/early somite stage (E8.5-E9.5)" [J:62571]
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Allelic Composition: Nr6a1tm1d(EUCOMM)Wtsi/Nr6a1tm1d(EUCOMM)Wtsi
Genetic Background: involves: 129S/SvEv * C57BL/6 * C57BL/6N * SJL

 MP:0001718 abnormal yolk sac "malformed extraembryonic tissue which contributes to hematopoietic circulation" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:12623]
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Allelic Composition: Nr6a1tm1b(EUCOMM)Wtsi/Nr6a1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Nr6a1tm1b(EUCOMM)Wtsi/Bay

 MP:0001722 pale yolk sac "bloodless yolk sac" [J:62571]
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Allelic Composition: Nr6a1tm1b(EUCOMM)Wtsi/Nr6a1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Nr6a1tm1b(EUCOMM)Wtsi/Bay

 MP:0001726 abnormal allantois "malformed fetal membrane which contributes to the formation of the umbilical cord and placenta" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:12622]
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Allelic Composition: Mapk8ip3tm1.1Ysok/Mapk8ip3tm1.1Ysok
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

Allelic Composition: Nr6a1tm1Coo/Nr6a1tm1Coo
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Nr6a1tm1b(EUCOMM)Wtsi/Nr6a1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Nr6a1tm1b(EUCOMM)Wtsi/Bay

 MP:0001923 reduced female fertility "reduced ability of female to produce live offspring" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60409]
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Allelic Composition: Ctnnb1tm1Mmt/Ctnnb1+,Tg(Fabp1-cre)1Mmt/?
Genetic Background: involves: 129X1/SvJ

 MP:0001935 reduced litter size "fewer live born pups in a litter compared to average" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Ctnnb1tm1Mmt/Ctnnb1+,Tg(Fabp1-cre)1Mmt/?
Genetic Background: involves: 129X1/SvJ

 MP:0002084 abnormal developmental patterning "abnormal systematic arrangement of the developing body along an axis" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Mapk8ip3tm1.1Ysok/Mapk8ip3tm1.1Ysok
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

Allelic Composition: Nr6a1tm1Coo/Nr6a1tm1Coo
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0002085 abnormal embryonic tissue morphology "structural abnormality or development of any embryonic tissue resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Nr6a1tm1Coo/Nr6a1tm1Coo
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0002086 abnormal extraembryonic tissue morphology "structural abnormality or development of the membranes involved with embryonic protection and nutrition" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, J:40594, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Mapk8ip3tm1.1Ysok/Mapk8ip3tm1.1Ysok
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

Allelic Composition: Nr6a1tm1Coo/Nr6a1tm1Coo
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0002151 abnormal neural tube morphology/development "anomalous structure of or development of the embryonic neural tube resulting in structural anomaly" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Nr6a1tm1b(EUCOMM)Wtsi/Nr6a1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Nr6a1tm1b(EUCOMM)Wtsi/Bay

 MP:0002231 abnormal primitive streak morphology "anomaly in the midline ridge of the embryonic epiblast that later develops into mesoderm and endoderm" [The Atlas of Mouse Development:ISBN 0-12-402035-6, csmith:Cynthia L. Smith, Mouse Genome Informatics Curator]
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Allelic Composition: Mapk8ip3tm1.1Ysok/Mapk8ip3tm1.1Ysok
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

Allelic Composition: Nr6a1tm1Coo/Nr6a1tm1Coo
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0002780 decreased circulating testosterone level "less than the normal blood concentration of this most potent androgen" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Ctnnb1tm1Mmt/Ctnnb1+,Tg(Fabp1-cre)1Mmt/?
Genetic Background: involves: 129X1/SvJ

 MP:0002790 decreased circulating follicle stimulating hormone level "less than expected blood 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: Ctnnb1tm1Mmt/Ctnnb1+,Tg(Fabp1-cre)1Mmt/?
Genetic Background: involves: 129X1/SvJ

 MP:0002824 abnormal chorioallantoic fusion "abnormal process of or failure of the formation of the membrane that forms the fetal portion of the placenta; derived from the fusion of the chorion and the allantois" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, hdene:Howard Dene , Mouse Genome Informatics Curator]
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Allelic Composition: Nr6a1tm1b(EUCOMM)Wtsi/Nr6a1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Nr6a1tm1b(EUCOMM)Wtsi/Bay

 MP:0002836 abnormal chorion "malformations of the outermost extraembryonic membrane" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Mapk8ip3tm1.1Ysok/Mapk8ip3tm1.1Ysok
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

Allelic Composition: Nr6a1tm1Coo/Nr6a1tm1Coo
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0002861 abnormal tail bud morphology "anomalous formation of the primordial region of the embryo that arises to form the tail of the adult; appears approximately ten days following conception as a short stump, and then initiates elongation and thinning in normal development" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Mapk8ip3tm1.1Ysok/Mapk8ip3tm1.1Ysok
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

Allelic Composition: Nr6a1tm1b(EUCOMM)Wtsi/Nr6a1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Nr6a1tm1b(EUCOMM)Wtsi/Bay

 MP:0002884 abnormal branchial arches "malformation or anomaly in the transient structures of the embryo that develop into regions of the head, neck and ears" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Nr6a1tm1b(EUCOMM)Wtsi/Nr6a1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Nr6a1tm1b(EUCOMM)Wtsi/Bay

 MP:0003232 abnormal forebrain development "anomaly in the formation or patterning of the anterior primitive cerebral vesicle; most rostral of three primary vesicles of the embryonic neural tube" [J:93081, smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Nr6a1tm1b(EUCOMM)Wtsi/Nr6a1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Nr6a1tm1b(EUCOMM)Wtsi/Bay

 MP:0003384 abnormal ventral body wall "malformation in the anterior portion of a human body or the lower surface of an animal body comprised of ectoderm and mesoderm layers that encloses the body cavity" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
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Allelic Composition: Nr6a1tm1Coo/Nr6a1tm1Coo
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 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]
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Allelic Composition: Nr6a1tm1b(EUCOMM)Wtsi/Nr6a1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Nr6a1tm1b(EUCOMM)Wtsi/Bay

 MP:0003720 abnormal neural tube closure "abnormal invagination and fusion of the neuroepithelial layer in early development" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator, J:99099]
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Allelic Composition: Nr6a1tm1Coo/Nr6a1tm1Coo
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

Allelic Composition: Nr6a1tm1b(EUCOMM)Wtsi/Nr6a1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Nr6a1tm1b(EUCOMM)Wtsi/Bay

 MP:0003864 abnormal midbrain development "anomaly in the formation of or the patterning of the part of the brainstem developing from the middle of the three primary cerebral vesicles of the embryo" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Nr6a1tm1b(EUCOMM)Wtsi/Nr6a1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Nr6a1tm1b(EUCOMM)Wtsi/Bay

 MP:0003984 embryonic growth retardation "slow or limited development before birth" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Nr6a1tm1b(EUCOMM)Wtsi/Nr6a1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Nr6a1tm1b(EUCOMM)Wtsi/Bay

 MP:0004073 caudal body truncation "caudal part of body truncated with anterior portion relatively normal" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Nr6a1tm1Coo/Nr6a1tm1Coo
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0004174 abnormal spine curvature "deviation from the typical S-shape of the spine" [smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Nr6a1tm1Coo/Nr6a1tm1Coo
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0004180 failure of initiation of embryo turning "failure to begin the axial rotation of the germ layers of the embryo during the primitive streak/early somite stage (E8.5-E9.5)" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator]
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Allelic Composition: Mapk8ip3tm1.1Ysok/Mapk8ip3tm1.1Ysok
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

Allelic Composition: Nr6a1tm1Coo/Nr6a1tm1Coo
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0004556 enlarged allantois "increased size of the fetal membrane which contributes to the formation of the umbilical cord and placental blood vessels" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Mapk8ip3tm1.1Ysok/Mapk8ip3tm1.1Ysok
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

Allelic Composition: Nr6a1tm1Coo/Nr6a1tm1Coo
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0005181 decreased circulating estradiol level "less than the normal blood concentration of this most potent naturally occurring estrogen in mammals" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Ctnnb1tm1Mmt/Ctnnb1+,Tg(Fabp1-cre)1Mmt/?
Genetic Background: involves: 129X1/SvJ

 MP:0005185 decreased circulating progesterone level "less than the normal blood concentration of this antiestrogenic steroid" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:66817]
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Allelic Composition: Ctnnb1tm1Mmt/Ctnnb1+,Tg(Fabp1-cre)1Mmt/?
Genetic Background: involves: 129X1/SvJ

 MP:0006108 abnormal hindbrain development "anomaly in the formation or pattering of the caudal region of the brain" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:93573]
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Allelic Composition: Nr6a1tm1b(EUCOMM)Wtsi/Nr6a1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Nr6a1tm1b(EUCOMM)Wtsi/Bay

 MP:0008786 abnormal hindgut morphology "any structural anomaly of the caudal portion of the primitive digestive tube of the embryo" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"]
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Allelic Composition: Nr6a1tm1Coo/Nr6a1tm1Coo
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0009006 prolonged estrous cycle "increase in the length of the sexual cycle of female animals" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Ctnnb1tm1Mmt/Ctnnb1+,Tg(Fabp1-cre)1Mmt/?
Genetic Background: involves: 129X1/SvJ

 MP:0009010 abnormal diestrus "any anomaly or aberrant timing of the last phase of the estrous cycle, during which unfertilized eggs are eliminated, the vagina and vulva are at a minimum size, and new follicles begin to undergo a rapid growth for the next ovulation; if pregnancy does not occur, the metestrous phase is ultimately followed by the diestrous phase" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Ctnnb1tm1Mmt/Ctnnb1+,Tg(Fabp1-cre)1Mmt/?
Genetic Background: involves: 129X1/SvJ

 MP:0009011 prolonged diestrus "increase in the length of the diestrous phase of the estrous cycle in female animals" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Ctnnb1tm1Mmt/Ctnnb1+,Tg(Fabp1-cre)1Mmt/?
Genetic Background: involves: 129X1/SvJ

 MP:0009433 polyovular ovarian follicle "an ovarian follicle containing more than one oocyte (ovum)" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Ctnnb1tm1Mmt/Ctnnb1+,Tg(Fabp1-cre)1Mmt/?
Genetic Background: involves: 129X1/SvJ

 MP:0009657 failure of chorioallantoic fusion "failure to initiate and/or complete the formation of a highly vascularized extra-embryonic fetal membrane by fusion of the chorion and allantois" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Mapk8ip3tm1.1Ysok/Mapk8ip3tm1.1Ysok
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

Allelic Composition: Nr6a1tm1Coo/Nr6a1tm1Coo
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0009768 impaired somite development "atypical process of somite formation with the result of fewer or none of these cell masses being formed" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Nr6a1tm1d(EUCOMM)Wtsi/Nr6a1tm1d(EUCOMM)Wtsi
Genetic Background: involves: 129S/SvEv * C57BL/6 * C57BL/6N * SJL

 MP:0010378 increased respiratory quotient "increase in the ratio of the volume of carbon dioxide released to oxygen consumed by a body tissue or an organism compared to controls" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Npc1tm1b(EUCOMM)Hmgu/Npc1+
Genetic Background: C57BL/6N-Npc1tm1b(EUCOMM)Hmgu/H

 MP:0011092 complete embryonic lethality "death of all organisms of a given genotype in a population within the embryonic period prior to organogenesis (Mus: prior to E14)" [MGI:csmith]
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Allelic Composition: Nr6a1Gt(RRA042)Byg/Nr6a1Gt(RRA042)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Nr6a1tm1d(EUCOMM)Wtsi/Nr6a1tm1d(EUCOMM)Wtsi
Genetic Background: involves: 129S/SvEv * C57BL/6 * C57BL/6N * SJL

 MP:0011097 complete embryonic lethality before turning of embryo "death of all organisms of a given genotype in a population between somite formation and the initiation of embryo turning (Mus: E8 to less than E9)" [MGI:csmith]
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Allelic Composition: Mapk8ip3tm1.1Ysok/Mapk8ip3tm1.1Ysok
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

 MP:0011098 complete embryonic lethality during organogenesis "death of all organisms of a given genotype in a population between embryo turning and the completion of organogenesis (Mus: E9 to less than E14)" [MGI:csmith]
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Allelic Composition: Nr6a1tm1Coo/Nr6a1tm1Coo
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 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: Nr6a1tm1b(EUCOMM)Wtsi/Nr6a1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Nr6a1tm1b(EUCOMM)Wtsi/Bay

 MP:0012086 absent hindgut "absence of the caudal portion of the primitive digestive tube of the embryo" [MGI:anna]
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Allelic Composition: Mapk8ip3tm1.1Ysok/Mapk8ip3tm1.1Ysok
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

 MP:0012544 abnormal caudal neuropore morphology "any structural anomaly of the temporary opening at the extreme caudal end of the neural tube in early embryos; the posterior neuropore appears before the process of neural tube closure is complete" [MGI:anna]
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Allelic Composition: Nr6a1tm1Coo/Nr6a1tm1Coo
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6

 MP:0013293 embryonic lethality prior to tooth bud stage "death prior to the appearance of tooth buds (Mus: E12-E12.5)" [MGI:smb]
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Allelic Composition: Nr6a1tm1b(EUCOMM)Wtsi/Nr6a1tm1b(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Nr6a1tm1b(EUCOMM)Wtsi/Bay

  


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






 

0 s.

 
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