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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Myo5a
myosin VA
MGI:105976
27 phenotypes from multigenic genotypes
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
a/a
Myo5ad/Myo5a+
Oca2p/Oca2+
Tyrp1B-lt/Tyrp1+
involves: C58 * CT/Ch
diluted coat color J:13094
a/a
Myo5ad/Myo5ad
involves: DBA/2J
abnormal choroid melanin granule morphology J:5346
abnormal hair follicle melanin granule distribution J:5346
a/a
Myo5ad/Myo5ad
Not Specified
abnormal coat/hair pigmentation J:12958
abnormal eye pigmentation J:12958
abnormal hair shaft melanin granule distribution J:12958
abnormal hair shaft morphology J:12958
abnormal melanocyte morphology J:12970
diluted coat color J:12958
d-58H/Myo5ad
involves: 101/H * C3H/HeH
abnormal coat/hair pigmentation J:178968
d-100H/Myo5ad
involves: C3H/HeH
no abnormal phenotype detected J:178968
Gnb5flr/Gnb5flr
Myo5aflr/Myo5aflr
involves: C57BL/6J * C57BL/10J * CBA/Ca
abnormal cerebellum morphology J:61324
abnormal motor capabilities/coordination/movement J:42513, J:61324
abnormal Purkinje cell dendrite morphology J:61324
ataxia J:42513, J:61324
convulsive seizures J:61324
impaired balance J:61324
impaired coordination J:61324
impaired righting response J:42513, J:61324
opisthotonus J:61324
normal pigmentation phenotype J:61324
postnatal lethality J:42513
Hps3coa/Hps3coa
Myo5ad/Myo5ad
Mregdsu/Mregdsu
involves: C57BL/10J
abnormal eye pigmentation J:29467
diluted coat color J:29467
Lystbg-slt/Lystbg-slt
Myo5ad/Myo5ad
involves: CT/Ch * YZ57/Ch
diluted coat color J:25388
normal vision/eye phenotype J:25388
Lystbg-slt/Lystbg-slt
Myo5ad/Myo5ad
Oca2p/Oca2p
Tyrp1b/Tyrp1b
involves: CT/Ch * YZ57/Ch
abnormal hair cycle J:83269
delayed hair regrowth J:83269
diluted coat color J:83269
premature hair loss J:83269
MitfMi-wh/Mitf+
Myo5ad/Myo5ad
involves: C57BL * DBA
decreased eye pigmentation J:13058
diluted coat color J:13058
Mregdsu/Mregdsu
Myo5ad-l20J/Myo5ad-l20J
involves: C57BL/6J
opisthotonus J:20299
normal pigmentation phenotype J:20299
Mregdsu/Mregdsu
Myo5ad/Myo5ad
involves: DBA/2J
abnormal melanocyte morphology J:7171
normal nervous system phenotype J:7171
normal pigmentation phenotype J:7171
Mregdsu/Mregdsu
Myo5ad/Myo5ad
STOCK a Myo5ad Hephl1cw
normal pigmentation phenotype J:9309
Myo5ad-l/d-100H
involves: C3H/HeH * C57BL/Gr
abnormal survival J:181531
opisthotonus J:181531
Myo5ad/Myo5a+
Rgsc80/Rgsc80+
involves: C57BL/6JJcl * DBA/2JJcl
diluted coat color J:133634

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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
04/09/2024
MGI 6.23
The Jackson Laboratory