Fam83h Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Fam83h
family with sequence similarity 83, member H
MGI:2145900

30 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fam83h^{em1(IMPC)Ccpcz}/Fam83h⁺ C57BL/6N-Fam83h^{em1(IMPC)Ccpcz}/Ccpcz	abnormal gallbladder morphology	J:211773
	abnormal seminal vesicle morphology	J:211773
Fam83h^{em1(IMPC)Ccpcz}/Fam83h^{em1(IMPC)Ccpcz} C57BL/6N-Fam83h^{em1(IMPC)Ccpcz}/Ccpcz	abnormal behavior	J:211773
	abnormal cholesterol homeostasis	J:211773
	abnormal coat appearance	J:211773
	abnormal coat/ hair morphology	J:211773
	abnormal heart morphology	J:211773
	abnormal kidney morphology	J:211773
	abnormal mammary gland morphology	J:211773
	abnormal testis morphology	J:211773
	decreased exploration in new environment	J:211773
	decreased grip strength	J:211773
	decreased locomotor activity	J:211773
	increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number	J:211773
	increased circulating potassium level	J:211773
	no spontaneous movement	J:211773
	preweaning lethality, incomplete penetrance	J:211773
	small heart	J:211773
	small testis	J:211773
Fam83h^tm1.1Jpsi/Fam83h^tm1.1Jpsi involves: C57BL/6	abnormal oral cavity morphology	J:257948
	normal craniofacial phenotype	J:257948
	decreased body size	J:257948
	decreased locomotor activity	J:257948
	delayed tooth eruption	J:257948
	disheveled coat	J:257948
	periodontal pocket	J:257948
	postnatal lethality, incomplete penetrance	J:257948
	premature death	J:257948
	scaly skin	J:257948
	sparse hair	J:257948
	weakness	J:257948

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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