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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
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Allelic Composition
Genetic Background
Annotated Term Reference
Pmelsi/Pmelsi
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
Pmelsi/Pmelsi
STOCK a Tyrp1b Pmelsi/J
normal pigmentation phenotype J:141035
Pmeltm1.1Sson/Pmeltm1.1Sson
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
Pmeltm1b(EUCOMM)Wtsi/Pmeltm1b(EUCOMM)Wtsi
C57BL/6N-Pmeltm1b(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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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory