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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Brd4
bromodomain containing 4
MGI:1888520
31 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Brd4Gt(pGT1.8TM)ST132Nimr/Brd4+
involves: 129P2/Ola * C57BL/6J
abnormal craniofacial bone morphology J:76662
abnormal epididymis epithelium morphology J:76662
abnormal hepatocyte morphology J:76662
abnormal seminiferous tubule morphology J:76662
abnormal spermatogenesis J:76662
abnormal vas deferens morphology J:76662
cataract J:76662
embryonic growth retardation J:76662
microphthalmia J:76662
mixed cellular infiltration to dermis J:76662
postnatal growth retardation J:76662
postnatal lethality, incomplete penetrance J:76662
short mandible J:76662
short nasal bone J:76662
short premaxilla J:76662
thick epidermis J:76662
Brd4Gt(pGT1.8TM)ST132Nimr/Brd4Gt(pGT1.8TM)ST132Nimr
involves: 129P2/Ola * C57BL/6J
embryonic lethality, complete penetrance J:76662
inner cell mass degeneration J:76662
Brd4M1Rvt/Brd4+
involves: BALB/cAnNCrl * C3H/HeH
normal homeostasis/metabolism phenotype J:277882
nephrocalcinosis J:277882
Brd4tm1b(EUCOMM)Wtsi/Brd4+
C57BL/6N-Brd4tm1b(EUCOMM)Wtsi/Bay
abnormal cranium morphology J:211773
abnormal eye posterior chamber depth J:211773
abnormal retina blood vessel morphology J:211773
abnormal retina inner nuclear layer morphology J:211773
abnormal retina outer nuclear layer morphology J:211773
decreased prepulse inhibition J:211773
decreased total retina thickness J:211773
increased grip strength J:211773
short tibia J:211773
Brd4tm1b(EUCOMM)Wtsi/Brd4tm1b(EUCOMM)Wtsi
C57BL/6N-Brd4tm1b(EUCOMM)Wtsi/Bay
embryonic lethality prior to organogenesis J:211773
preweaning lethality, complete penetrance J:211773

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory