Slc24a5 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc24a5
solute carrier family 24, member 5
MGI:2677271

21 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc24a5^{tm1b(KOMP)Mbp}/Slc24a5^{tm1b(KOMP)Mbp} C57BL/6N-Slc24a5^{tm1b(KOMP)Mbp}/J	abnormal coat/hair pigmentation	J:211773
	abnormal iris transillumination	J:211773
	abnormal retina morphology	J:211773
	decreased fasting circulating glucose level	J:211773
	impaired righting response	J:211773
	increased circulating sodium level	J:211773
	increased grip strength	J:211773
Slc24a5^tm1Lex/Slc24a5^tm1Lex involves: 129S5/SvEvBrd * C57BL/6	abnormal ciliary body pigmentation	J:137416
	abnormal dermal pigmentation	J:137416
	abnormal ear pigmentation	J:137416
	abnormal epidermal pigmentation	J:137416
	abnormal hair shaft melanin granule morphology	J:137416
	abnormal hair shaft melanin granule shape	J:137416
	abnormal iris pigmentation	J:137416
	abnormal melanosome morphology	J:137416
	abnormal ocular fundus morphology	J:137416
	abnormal retina pigment epithelium morphology	J:137416
	abnormal retina pigmentation	J:137416
	hypopigmentation	J:137416
	iris hypoplasia	J:137416
	ocular albinism	J:137416

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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