Pmel Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Pmel
premelanosome protein
MGI:98301

13 phenotypes from 3 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Pmel^si/Pmel^si Not Specified	normal hematopoietic system phenotype	J:29151
	normal homeostasis/metabolism phenotype	J:29151
	irregular coat pigmentation	J:13051, J:78801
	reduced hair shaft melanin granule number	J:13051
Pmel^si/Pmel^si STOCK a Tyrp1^b Pmel^si/J	normal pigmentation phenotype	J:141035
Pmel^tm1.1Sson/Pmel^tm1.1Sson involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6	abnormal choroid melanin granule morphology	J:177116
	abnormal melanosome morphology	J:177116
	abnormal retina melanin granule morphology	J:177116
	abnormal tail hair pigmentation	J:177116
	diluted coat color	J:177116
Pmel^{tm1b(EUCOMM)Wtsi}/Pmel^{tm1b(EUCOMM)Wtsi} C57BL/6N-Pmel^{tm1b(EUCOMM)Wtsi}/Ieg	decreased total body fat amount	J:211773
	increased circulating bilirubin level	J:211773
	increased startle reflex	J:211773

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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