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Symbol
Name
ID
Acvrl1
activin A receptor, type II-like 1
MGI:1338946
Phenotype annotations related to mortality/aging
Darker colors indicate more annotations
Human Phenotypes
Miscarriage
Disease(s) Associated with ACVRL1
hereditary hemorrhagic telangiectasia

Mouse Phenotypes
moribund
premature death
lethality throughout fetal growth and development, complete penetrance
postnatal lethality
embryonic lethality during organogenesis, complete penetrance
Availability Mouse Genotype
Acvrl1tm1Dgen/Acvrl1tm1Dgen
Acvrl1tm1Dyl/Acvrl1tm1Dyl
Acvrl1tm1Enl/Acvrl1tm1Enl
Acvrl1tm1Spo/Acvrl1tm1Spo
Acvrl1tm2.2Spo/Acvrl1tm2.2Spo
Acvrl1tm1Enl/Acvrl1+
Acvrl1tm1Spo/Acvrl1tm1Enl
Acvrl1tm2.1Spo/Acvrl1tm2.1Spo
Tg(Acvrl1-cre)L1Spo/0  (conditional)
Acvrl1tm2.1Spo/Acvrl1tm2.1Spo
Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+  (conditional)
Acvrl1tm2.1Spo/Acvrl1tm2.1Spo
Tg(Tal1-cre/ERT)1Jrg/0  (conditional)
Acvrl1tm2Spo/Acvrl1tm2Spo
Tg(Acvrl1-cre)L1Spo/0  (conditional)

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
04/09/2024
MGI 6.23
The Jackson Laboratory