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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Myo5a
myosin VA
MGI:105976
49 phenotypes from 54 alleles in 30 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background		 Annotated Term Reference
Myo5ad+2J/Myo5ad+2J
DBA/2J-Myo5ad+2J 		abnormal coat/hair pigmentation J:26019
phenotypic reversion J:7092
reversion by viral sequence excision J:7092
Myo5ad+16J/Myo5ad+16J
DBA/1J-Myo5ad+16J 		reversion by viral sequence excision J:7092
Myo5ad+17J/Myo5ad+17J
DBA/2J-Myo5ad+17J 		reversion by viral sequence excision J:7092
Myo5ad+18J/Myo5ad+18J
DBA/J-Myo5ad+18J 		reversion by viral sequence excision J:7092
Myo5ad+Ha/Myo5ad+Ha
DBA/2Ha-Myo5ad+Ha 		reversion by viral sequence excision J:7092
Myo5ad-2Btlr/Myo5ad-2Btlr
C57BL/6J-Myo5ad-2Btlr 		normal behavior/neurological phenotype J:133118
diluted coat color J:133118
normal immune system phenotype J:133118
Myo5ad-15H/Myo5ad-15H
Not Specified 		normal behavior/neurological phenotype J:13409
diluted coat color J:13409
opisthotonus J:13409
postnatal lethality, complete penetrance J:13409
seizures J:13409
Myo5ad-50H/Myo5ad-50H
involves: 101/H * C3H/HeH 		opisthotonus J:178968
Myo5ad-51H/Myo5ad-51H
involves: 101/H * C3H/HeH 		opisthotonus J:178968
Myo5ad-52H/Myo5ad-52H
involves: 101/H * C3H/HeH 		no abnormal phenotype detected J:178968
Myo5ad-53H/Myo5ad-53H
involves: 101/H * C3H/HeH 		opisthotonus J:178968
Myo5ad-61H/Myo5ad-61H
involves: 101/H * C3H/HeH 		no abnormal phenotype detected J:178968
Myo5ad-78H/Myo5ad-78H
involves: 101/H * C3H/HeH 		no abnormal phenotype detected J:178968
Myo5ad-80H/Myo5ad-80H
involves: 101/H * C3H/HeH 		opisthotonus J:178968
Myo5ad-82H/Myo5ad-82H
involves: 101/H * C3H/HeH 		opisthotonus J:178968
Myo5ad-83H/Myo5ad-83H
involves: C3H/HeH 		opisthotonus J:178968
Myo5ad-84H/Myo5ad-84H
involves: 101/H 		opisthotonus J:178968
Myo5ad-85H/Myo5ad-85H
involves: 101/H * C3H/HeH 		opisthotonus J:169366
Myo5ad-86H/Myo5ad-86H
involves: 101/H * C3H/HeH 		opisthotonus J:178968
Myo5ad-86H/Myo5ad-97H
involves: 101/H * C3H/HeH 		opisthotonus J:178968
Myo5ad-90H/Myo5ad-l
involves: 101/H * C3H/HeH * C57BL/Gr 		opisthotonus J:179353
Myo5ad-93H/Myo5ad-l
involves: 101/H * C3H/HeH * C57BL/Gr 		opisthotonus J:179353
Myo5ad-105H/Myo5ad-105H
involves: 101/H * C3H/HeH 		abnormal coat/hair pigmentation J:179353
Myo5ad-Btlr/Myo5ad-Btlr
C57BL/6J-Myo5ad-Btlr 		diluted coat color J:133117
normal immune system phenotype J:133117
Myo5ad-J/Myo5ad-J
involves: C57BL/6J 		abnormal coat/hair pigmentation J:24230
diluted coat color J:24230
Myo5ad-l20J/Myo5ad-l20J
involves: C57BL/6J 		normal immune system phenotype J:111253
Myo5ad-l20J/Myo5ad-l20J
involves: C57BL/6J * DBA/2J 		abnormal coat/hair pigmentation J:20299
abnormal involuntary movement J:20299
abnormal motor capabilities/coordination/movement J:20299
diluted coat color J:20299
opisthotonus J:20299
postnatal lethality J:20299
Myo5ad-l31J/Myo5ad-l31J
involves: A.B6-Tyr+ 		abnormal coat/hair pigmentation J:87349
abnormal gait J:87349
decreased body size J:87349
impaired balance J:87349
premature death J:87349
Myo5ad-l32J/Myo5ad-l32J
B6.Cg-Myo5ad-l32J/GrsrJ 		ataxia J:169210
clonic seizures J:169210
diluted coat color J:169210
impaired balance J:169210
opisthotonus J:169210
postnatal lethality, incomplete penetrance J:169210
premature death J:169210
Myo5ad-l33J/Myo5ad-l33J
involves: C57BL/6J 		ataxia J:169214
diluted coat color J:169214
postnatal lethality, incomplete penetrance J:169214
premature death J:169214
Myo5ad-l34J/Myo5ad-l34J
BALB/cJ-Myo5ad-l34J/GrsrJ 		ataxia J:216055
circling J:216055
decreased body size J:216055
impaired balance J:216055
opisthotonus J:216055
postnatal lethality, incomplete penetrance J:216055
premature death J:216055
Myo5ad-l34J/Myo5ad-l34J
involves: BALB/cJ * CAST/EiJ 		diluted coat color J:216055
Myo5ad-l35J/Myo5ad-l35J
involves: C57BL/6J 		ataxia J:216347
decreased body size J:216347
diluted coat color J:216347
impaired balance J:216347
impaired righting response J:216347
lethality at weaning, complete penetrance J:216347
Myo5ad-l/Myo5ad-l
involves: C57BL 		clonic seizures J:12978
diluted coat color J:12978
impaired balance J:12978
impaired limb coordination J:12978
impaired righting response J:12978
opisthotonus J:12978
Myo5ad-n2Btlr/Myo5ad-n2Btlr
C57BL/6J-Myo5ad-n2Btlr 		abnormal ear pigmentation J:133120
abnormal foot pigmentation J:133120
abnormal limb posture J:133120
abnormal tail pigmentation J:133120
diluted coat color J:133120
impaired righting response J:133120
lethality at weaning, complete penetrance J:133120
myoclonus J:133120
opisthotonus J:133120
Myo5ad-n2J/Myo5ad-n2J
involves: C57BL/6J * DBA/2J 		abnormal coat/hair pigmentation J:47547
abnormal motor capabilities/coordination/movement J:47547
diluted coat color J:47547
premature death J:47547
Myo5ad-n3Btlr/Myo5ad-n3Btlr
C57BL/6J-Myo5ad-n3Btlr 		diluted coat color J:201726
impaired righting response J:201726
opisthotonus J:201726
Myo5ad-n/Myo5ad-n
B10.D2-H2d/nSnJ 		abnormal cerebellum morphology J:171603
abnormal coat/hair pigmentation J:47547
abnormal eye blink conditioning behavior J:171603
abnormal gait J:171603
abnormal locomotor coordination J:171603
abnormal motor capabilities/coordination/movement J:47547
abnormal Purkinje cell dendrite morphology J:171603
ataxia J:171603
normal behavior/neurological phenotype J:171603
clonic seizures J:171603
diluted coat color J:47547, J:171603
impaired coordination J:171603
reduced long-term depression J:171603
slow postnatal weight gain J:171603
Myo5ad-nBtlr/Myo5ad-nBtlr
C57BL/6J-Myo5ad-nBtlr 		abnormal ear pigmentation J:133119
abnormal foot pigmentation J:133119
abnormal limb posture J:133119
abnormal tail pigmentation J:133119
diluted coat color J:133119
impaired righting response J:133119
lethality at weaning, complete penetrance J:133119
myoclonus J:133119
normal nervous system phenotype J:133119
opisthotonus J:133119
Myo5ad/Myo5ad-15H
Not Specified 		normal behavior/neurological phenotype J:13409
diluted coat color J:13409
Myo5ad/Myo5ad-50H
involves: 101/H * C3H/HeH 		abnormal coat/hair pigmentation J:178968
Myo5ad/Myo5ad-51H
involves: 101/H * C3H/HeH 		abnormal coat/hair pigmentation J:178968
Myo5ad/Myo5ad-52H
involves: 101/H * C3H/HeH 		abnormal coat/hair pigmentation J:178968
Myo5ad/Myo5ad-53H
involves: 101/H * C3H/HeH 		abnormal coat/hair pigmentation J:178968
Myo5ad/Myo5ad-78H
involves: 101/H * C3H/HeH 		abnormal coat/hair pigmentation J:178968
Myo5ad/Myo5ad-80H
involves: 101/H * C3H/HeH 		abnormal coat/hair pigmentation J:178968
Myo5ad/Myo5ad-82H
involves: 101/H * C3H/HeH 		abnormal coat/hair pigmentation J:178968
Myo5ad/Myo5ad-83H
involves: C3H/HeH 		abnormal coat/hair pigmentation J:178968
Myo5ad/Myo5ad-84H
involves: 101/H 		abnormal coat/hair pigmentation J:178968
Myo5ad/Myo5ad-85H
involves: 101/H * C3H/HeH 		abnormal coat/hair pigmentation J:169366
Myo5ad/Myo5ad-86H
involves: 101/H * C3H/HeH 		abnormal coat/hair pigmentation J:178968
Myo5ad/Myo5ad-89H
involves: 101/H * C3H/HeH 		abnormal coat/hair pigmentation J:169366
Myo5ad/Myo5ad-93H
involves: 101/H * C3H/HeH 		abnormal coat/hair pigmentation J:179353
Myo5ad/Myo5ad-97H
involves: 101/H * C3H/HeH 		no abnormal phenotype detected J:178968
Myo5ad/Myo5ad-105H
involves: 101/H * C3H/HeH 		no abnormal phenotype detected J:179353
Myo5ad/Myo5ad
involves: C57BL/6J 		abnormal melanocyte morphology J:37976
Myo5am1163Lja/Myo5am1163Lja
C57BL/6J-Myo5am1163Lja 		ataxia J:179895
Myo5argsc11/Myo5argsc11
involves: C57BL/6JJcl * DBA/2JJcl 		diluted coat color J:133634
Myo5argsc52/Myo5argsc52
involves: C57BL/6JJcl * DBA/2JJcl 		diluted coat color J:133634
Myo5argsc152/Myo5argsc152
involves: C57BL/6JJcl * DBA/2JJcl 		diluted coat color J:133634
Myo5argsc229/Myo5argsc229
involves: C57BL/6JJcl * DBA/2JJcl 		diluted coat color J:133634
Myo5argsc235/Myo5argsc235
involves: C57BL/6JJcl * DBA/2JJcl 		diluted coat color J:133634
Myo5argsc379/Myo5argsc379
involves: C57BL/6JJcl * DBA/2JJcl 		diluted coat color J:133634
Myo5argsc388/Myo5argsc388
involves: C57BL/6JJcl * DBA/2JJcl 		diluted coat color J:133634
Myo5argsc432/Myo5argsc432
involves: C57BL/6JJcl * DBA/2JJcl 		diluted coat color J:133634
Myo5argsc450/Myo5argsc450
involves: C57BL/6JJcl * DBA/2JJcl 		diluted coat color J:133634
Myo5argsc593/Myo5argsc593
involves: C57BL/6JJcl * DBA/2JJcl 		diluted coat color J:133634
Myo5argsc705/Myo5argsc705
involves: C57BL/6JJcl * DBA/2JJcl 		diluted coat color J:133634
Myo5argsc940/Myo5argsc940
involves: C57BL/6JJcl * DBA/2JJcl 		diluted coat color J:133634
Myo5atm1a(KOMP)Wtsi/Myo5atm1a(KOMP)Wtsi
B6Brd;B6N-Tyrc-Brd Myo5atm1a(KOMP)Wtsi/Wtsi 		abnormal coat/hair pigmentation J:232539
diluted coat color J:232539
Myo5atm1a(KOMP)Wtsi/Myo5atm1a(KOMP)Wtsi
B6JTyr;B6N-Myo5atm1a(KOMP)Wtsi/Wtsi 		abnormal behavior J:175295
abnormal coat/hair pigmentation J:175295
hyperactivity J:175295
Myo5atm1a(KOMP)Wtsi/Myo5atm1a(KOMP)Wtsi
C57BL/6-Myo5atm1a(KOMP)Wtsi 		abnormal coat/hair pigmentation J:209956
abnormal epidermal melanocyte morphology J:209956
abnormal epidermal pigmentation J:209956
abnormal hair follicle melanin granule morphology J:209956
abnormal hair follicle melanocyte morphology J:209956
abnormal melanosome morphology J:209956
Myo5atm1e(KOMP)Wtsi/Myo5atm1e(KOMP)Wtsi
B6Brd;B6N-Tyrc-Brd Myo5atm1e(KOMP)Wtsi/Wtsi 		abnormal hair cycle J:232539
Myo5atm1e(KOMP)Wtsi/Myo5atm1e(KOMP)Wtsi
involves: C57BL/6J * C57BL/6N 		diluted coat color J:195694
normal hematopoietic system phenotype J:195694
hypopigmentation J:195694
preweaning lethality, incomplete penetrance J:195694
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04/09/2024
MGI 6.23 		The Jackson Laboratory