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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Scmh1
sex comb on midleg homolog 1
MGI:1352762
24 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Scmh1tm1e.1(EUCOMM)Hmgu/Scmh1tm1e.1(EUCOMM)Hmgu
C57BL/6N-Scmh1tm1e.1(EUCOMM)Hmgu/Ieg
abnormal auditory brainstem response J:211773
abnormal liver morphology J:211773
enlarged cecum J:211773
Scmh1tm1Hko/Scmh1tm1Hko
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal seminiferous tubule morphology J:119909
abnormal spermatogenesis J:119909
abnormal sternocostal joint morphology J:119909
abnormal testis morphology J:119909
arrest of male meiosis J:119909
azoospermia J:119909
cervical vertebral fusion J:119909
cervical vertebral transformation J:119909
early cellular replicative senescence J:119909
increased rib number J:119909
male infertility J:119909
multinucleated giant male germ cells J:119909
vertebral transformation J:119909
Scmh1tm1Yota/Scmh1tm1Yota
involves: 129X1/SvJ * C57BL/6
abnormal fetal liver hematopoietic progenitor cell morphology J:194424
abnormal hematopoietic stem cell morphology J:194424
decreased B cell number J:194424
decreased T cell number J:194424
increased hematopoietic stem cell number J:194424
myeloid hyperplasia J:194424
normal reproductive system phenotype J:194424
normal skeleton phenotype J:194424

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