Myo5a Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Myo5a
myosin VA
MGI:105976

49 phenotypes from 54 alleles in 30 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Myo5a^d+2J/Myo5a^d+2J DBA/2J-Myo5a^d+2J	abnormal coat/hair pigmentation	J:26019
	phenotypic reversion	J:7092
	reversion by viral sequence excision	J:7092
Myo5a^d+16J/Myo5a^d+16J DBA/1J-Myo5a^d+16J	reversion by viral sequence excision	J:7092
Myo5a^d+17J/Myo5a^d+17J DBA/2J-Myo5a^d+17J	reversion by viral sequence excision	J:7092
Myo5a^d+18J/Myo5a^d+18J DBA/J-Myo5a^d+18J	reversion by viral sequence excision	J:7092
Myo5a^d+Ha/Myo5a^d+Ha DBA/2Ha-Myo5a^d+Ha	reversion by viral sequence excision	J:7092
Myo5a^d-2Btlr/Myo5a^d-2Btlr C57BL/6J-Myo5a^d-2Btlr	normal behavior/neurological phenotype	J:133118
	diluted coat color	J:133118
	normal immune system phenotype	J:133118
Myo5a^d-15H/Myo5a^d-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
Myo5a^d-50H/Myo5a^d-50H involves: 101/H * C3H/HeH	opisthotonus	J:178968
Myo5a^d-51H/Myo5a^d-51H involves: 101/H * C3H/HeH	opisthotonus	J:178968
Myo5a^d-52H/Myo5a^d-52H involves: 101/H * C3H/HeH	no abnormal phenotype detected	J:178968
Myo5a^d-53H/Myo5a^d-53H involves: 101/H * C3H/HeH	opisthotonus	J:178968
Myo5a^d-61H/Myo5a^d-61H involves: 101/H * C3H/HeH	no abnormal phenotype detected	J:178968
Myo5a^d-78H/Myo5a^d-78H involves: 101/H * C3H/HeH	no abnormal phenotype detected	J:178968
Myo5a^d-80H/Myo5a^d-80H involves: 101/H * C3H/HeH	opisthotonus	J:178968
Myo5a^d-82H/Myo5a^d-82H involves: 101/H * C3H/HeH	opisthotonus	J:178968
Myo5a^d-83H/Myo5a^d-83H involves: C3H/HeH	opisthotonus	J:178968
Myo5a^d-84H/Myo5a^d-84H involves: 101/H	opisthotonus	J:178968
Myo5a^d-85H/Myo5a^d-85H involves: 101/H * C3H/HeH	opisthotonus	J:169366
Myo5a^d-86H/Myo5a^d-86H involves: 101/H * C3H/HeH	opisthotonus	J:178968
Myo5a^d-86H/Myo5a^d-97H involves: 101/H * C3H/HeH	opisthotonus	J:178968
Myo5a^d-90H/Myo5a^d-l involves: 101/H * C3H/HeH * C57BL/Gr	opisthotonus	J:179353
Myo5a^d-93H/Myo5a^d-l involves: 101/H * C3H/HeH * C57BL/Gr	opisthotonus	J:179353
Myo5a^d-105H/Myo5a^d-105H involves: 101/H * C3H/HeH	abnormal coat/hair pigmentation	J:179353
Myo5a^d-Btlr/Myo5a^d-Btlr C57BL/6J-Myo5a^d-Btlr	diluted coat color	J:133117
Myo5a^d-Btlr/Myo5a^d-Btlr C57BL/6J-Myo5a^d-Btlr	normal immune system phenotype	J:133117
Myo5a^d-J/Myo5a^d-J involves: C57BL/6J	abnormal coat/hair pigmentation	J:24230
Myo5a^d-J/Myo5a^d-J involves: C57BL/6J	diluted coat color	J:24230
Myo5a^d-l20J/Myo5a^d-l20J involves: C57BL/6J	normal immune system phenotype	J:111253
Myo5a^d-l20J/Myo5a^d-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
Myo5a^d-l31J/Myo5a^d-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
Myo5a^d-l32J/Myo5a^d-l32J B6.Cg-Myo5a^d-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
Myo5a^d-l33J/Myo5a^d-l33J involves: C57BL/6J	ataxia	J:169214
	diluted coat color	J:169214
	postnatal lethality, incomplete penetrance	J:169214
	premature death	J:169214
Myo5a^d-l34J/Myo5a^d-l34J BALB/cJ-Myo5a^d-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
Myo5a^d-l34J/Myo5a^d-l34J involves: BALB/cJ * CAST/EiJ	diluted coat color	J:216055
Myo5a^d-l35J/Myo5a^d-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
Myo5a^d-l/Myo5a^d-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
Myo5a^d-n2Btlr/Myo5a^d-n2Btlr C57BL/6J-Myo5a^d-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
Myo5a^d-n2J/Myo5a^d-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
Myo5a^d-n3Btlr/Myo5a^d-n3Btlr C57BL/6J-Myo5a^d-n3Btlr	diluted coat color	J:201726
	impaired righting response	J:201726
	opisthotonus	J:201726
Myo5a^d-n/Myo5a^d-n B10.D2-H2^d/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
Myo5a^d-nBtlr/Myo5a^d-nBtlr C57BL/6J-Myo5a^d-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
Myo5a^d/Myo5a^d-15H Not Specified	normal behavior/neurological phenotype	J:13409
Myo5a^d/Myo5a^d-15H Not Specified	diluted coat color	J:13409
Myo5a^d/Myo5a^d-50H involves: 101/H * C3H/HeH	abnormal coat/hair pigmentation	J:178968
Myo5a^d/Myo5a^d-51H involves: 101/H * C3H/HeH	abnormal coat/hair pigmentation	J:178968
Myo5a^d/Myo5a^d-52H involves: 101/H * C3H/HeH	abnormal coat/hair pigmentation	J:178968
Myo5a^d/Myo5a^d-53H involves: 101/H * C3H/HeH	abnormal coat/hair pigmentation	J:178968
Myo5a^d/Myo5a^d-78H involves: 101/H * C3H/HeH	abnormal coat/hair pigmentation	J:178968
Myo5a^d/Myo5a^d-80H involves: 101/H * C3H/HeH	abnormal coat/hair pigmentation	J:178968
Myo5a^d/Myo5a^d-82H involves: 101/H * C3H/HeH	abnormal coat/hair pigmentation	J:178968
Myo5a^d/Myo5a^d-83H involves: C3H/HeH	abnormal coat/hair pigmentation	J:178968
Myo5a^d/Myo5a^d-84H involves: 101/H	abnormal coat/hair pigmentation	J:178968
Myo5a^d/Myo5a^d-85H involves: 101/H * C3H/HeH	abnormal coat/hair pigmentation	J:169366
Myo5a^d/Myo5a^d-86H involves: 101/H * C3H/HeH	abnormal coat/hair pigmentation	J:178968
Myo5a^d/Myo5a^d-89H involves: 101/H * C3H/HeH	abnormal coat/hair pigmentation	J:169366
Myo5a^d/Myo5a^d-93H involves: 101/H * C3H/HeH	abnormal coat/hair pigmentation	J:179353
Myo5a^d/Myo5a^d-97H involves: 101/H * C3H/HeH	no abnormal phenotype detected	J:178968
Myo5a^d/Myo5a^d-105H involves: 101/H * C3H/HeH	no abnormal phenotype detected	J:179353
Myo5a^d/Myo5a^d involves: C57BL/6J	abnormal melanocyte morphology	J:37976
Myo5a^m1163Lja/Myo5a^m1163Lja C57BL/6J-Myo5a^m1163Lja	ataxia	J:179895
Myo5a^rgsc11/Myo5a^rgsc11 involves: C57BL/6JJcl * DBA/2JJcl	diluted coat color	J:133634
Myo5a^rgsc52/Myo5a^rgsc52 involves: C57BL/6JJcl * DBA/2JJcl	diluted coat color	J:133634
Myo5a^rgsc152/Myo5a^rgsc152 involves: C57BL/6JJcl * DBA/2JJcl	diluted coat color	J:133634
Myo5a^rgsc229/Myo5a^rgsc229 involves: C57BL/6JJcl * DBA/2JJcl	diluted coat color	J:133634
Myo5a^rgsc235/Myo5a^rgsc235 involves: C57BL/6JJcl * DBA/2JJcl	diluted coat color	J:133634
Myo5a^rgsc379/Myo5a^rgsc379 involves: C57BL/6JJcl * DBA/2JJcl	diluted coat color	J:133634
Myo5a^rgsc388/Myo5a^rgsc388 involves: C57BL/6JJcl * DBA/2JJcl	diluted coat color	J:133634
Myo5a^rgsc432/Myo5a^rgsc432 involves: C57BL/6JJcl * DBA/2JJcl	diluted coat color	J:133634
Myo5a^rgsc450/Myo5a^rgsc450 involves: C57BL/6JJcl * DBA/2JJcl	diluted coat color	J:133634
Myo5a^rgsc593/Myo5a^rgsc593 involves: C57BL/6JJcl * DBA/2JJcl	diluted coat color	J:133634
Myo5a^rgsc705/Myo5a^rgsc705 involves: C57BL/6JJcl * DBA/2JJcl	diluted coat color	J:133634
Myo5a^rgsc940/Myo5a^rgsc940 involves: C57BL/6JJcl * DBA/2JJcl	diluted coat color	J:133634
Myo5a^{tm1a(KOMP)Wtsi}/Myo5a^{tm1a(KOMP)Wtsi} B6Brd;B6N-Tyr^c-Brd Myo5a^{tm1a(KOMP)Wtsi}/Wtsi	abnormal coat/hair pigmentation	J:232539
	diluted coat color	J:232539
Myo5a^{tm1a(KOMP)Wtsi}/Myo5a^{tm1a(KOMP)Wtsi} B6JTyr;B6N-Myo5a^{tm1a(KOMP)Wtsi}/Wtsi	abnormal behavior	J:175295
	abnormal coat/hair pigmentation	J:175295
	hyperactivity	J:175295
Myo5a^{tm1a(KOMP)Wtsi}/Myo5a^{tm1a(KOMP)Wtsi} C57BL/6-Myo5a^{tm1a(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
Myo5a^{tm1e(KOMP)Wtsi}/Myo5a^{tm1e(KOMP)Wtsi} B6Brd;B6N-Tyr^c-Brd Myo5a^{tm1e(KOMP)Wtsi}/Wtsi	abnormal hair cycle	J:232539
Myo5a^{tm1e(KOMP)Wtsi}/Myo5a^{tm1e(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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