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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Acvr1b
activin A receptor, type 1B
MGI:1338944
40 phenotypes from 5 alleles in 5 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Acvr1btm1.1(KOMP)Vlcg/Acvr1b+
C57BL/6N-Acvr1btm1.1(KOMP)Vlcg/Ucd
abnormal coat/ hair morphology J:211773
abnormal uterus morphology J:211773
enlarged lymph nodes J:211773
small adrenal glands J:211773
small testis J:211773
Acvr1btm1.1(KOMP)Vlcg/Acvr1btm1.1(KOMP)Vlcg
C57BL/6N-Acvr1btm1.1(KOMP)Vlcg/Ucd
embryonic lethality prior to tooth bud stage J:211773
preweaning lethality, complete penetrance J:211773
Acvr1btm1.1Gsu/Acvr1btm1.1Gsu
Tg(KRT14-cre)8Brn/0
involves: 129 * C57BL/6J * FVB
abnormal epidermal layer morphology J:171766
abnormal hair cycle J:171766
abnormal hair follicle morphology J:171766
abnormal hair follicle regression J:171766
abnormal hair growth J:171766
abnormal incisor color J:171766
abnormal lower incisor morphology J:171766
abnormal skin adnexa physiology J:171766
abnormal skin physiology J:171766
abnormal skin sebaceous gland morphology J:171766
alopecia J:171766
normal digestive/alimentary phenotype J:171766
dilated hair follicle J:171766
enlarged sebaceous gland J:171766
epidermal cyst J:171766
hairless J:171766
postnatal growth retardation J:171766
normal reproductive system phenotype J:171766
thick epidermis J:171766
thick epidermis stratum basale J:171766
Acvr1btm1.1Gsu/Acvr1btm1.1Gsu
Tg(KRT14-cre)8Brn/Tg(KRT14-cre)8Brn
involves: 129 * C57BL/6J * FVB
alopecia J:171766
postnatal growth retardation J:171766
Acvr1btm1.1Pbe/Acvr1btm1.1Pbe
involves: 129S2/SvPas * C57BL/6 * FVB/N * SJL
embryonic lethality, complete penetrance J:188629
Acvr1btm1Enl/Acvr1btm1Enl
either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)
abnormal cell differentiation J:46637
abnormal distal visceral endoderm morphology J:46637
abnormal embryonic epiblast morphology J:46637
abnormal extraembryonic ectoderm morphology J:46637
abnormal visceral endoderm morphology J:46637
absent egg cylinders J:46637
absent mesoderm J:46637
disorganized extraembryonic tissue J:46637
embryonic growth arrest J:46637
embryonic lethality during organogenesis, complete penetrance J:46637
failure of primitive streak formation J:46637
Acvr1btm2.1Vlcg/Acvr1btm2.1Vlcg
involves: 129S6/SvEvTac * C57BL/6NTac
no abnormal phenotype detected J:200671

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
04/16/2024
MGI 6.23
The Jackson Laboratory