Myo15a Gene Search Result

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14 records found for search term Myo15a

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RGD ID	Symbol	Name	Description	Chr	Start	Stop	Species	Annotations	Match	Type
1343693	MYO15A	myosin XVA	This gene encodes an unconventional myosin. This protein differs from other myosins in that it has a long N-terminal extension preceding the conserved motor domain. Studies in mice suggest that this protein is necessary for actin organization in the hair cells of the cochlea. Mutations in this gene ... (more) have been associated with profound, congenital, neurosensory, nonsyndromal deafness. This gene is located within the Smith-Magenis syndrome region on chromosome 17. Read-through transcripts containing an upstream gene and this gene have been identified, but they are not thought to encode a fusion protein. Several alternatively spliced transcript variants have been described, but their full length sequences have not been determined. [provided by RefSeq, Jul 2008]	17	18108756	18179800	Human	354	symbol , COSMIC , Human Proteome Map	gene, protein-coding, REVIEWED [RefSeq]
1561873	Myo15a	myosin XVA	ENCODES a protein that exhibits actin binding (inferred); ATP binding (inferred); cytoskeletal motor activity (inferred); INVOLVED IN response to light stimulus; inner ear morphogenesis (ortholog); locomotory behavior (ortholog); PARTICIPATES IN auditory mechanotransduction pathway; ASSOCIATED WITH ... (more) abnormal a-wave implicit time; abnormal b-wave implicit time; abnormal vision; ASSOCIATED WITH blindness; Alport syndrome (ortholog); autosomal recessive nonsyndromic deafness (ortholog); FOUND IN stereocilium (ortholog); stereocilium bundle (ortholog); INTERACTS WITH bisphenol A; methoxychlor; perfluorooctanoic acid	10	45776907	45835473	Rat	93	symbol , PhenoGen	gene, protein-coding, VALIDATED [RefSeq]
1615958	Myo15a	myosin XVA	Predicted to enable actin filament binding activity and microfilament motor activity. Acts upstream of or within inner ear morphogenesis; locomotory behavior; and sensory perception of sound. Located in stereocilium. Is expressed in several structures, including brain; heart; inner ear; liver; and m ... (more) etanephros. Used to study autosomal recessive nonsyndromic deafness 3. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness 3 and sensorineural hearing loss. Orthologous to human MYO15A (myosin XVA). [provided by Alliance of Genome Resources, Jul 2025]	11	60360165	60419195	Mouse	159	symbol , PhenoGen , description	gene, protein-coding, VALIDATED [RefSeq]
8710978	Myo15a	myosin XVA	INVOLVED IN inner ear morphogenesis (ortholog); locomotory behavior (ortholog); response to light stimulus (ortholog); PARTICIPATES IN auditory mechanotransduction pathway; ASSOCIATED WITH Alport syndrome (ortholog); autosomal recessive nonsyndromic deafness (ortholog); autosomal recessive nonsyndro ... (more) mic deafness 3 (ortholog); FOUND IN stereocilium (ortholog); stereocilium bundle (ortholog)	NW_004955478	11131908	11186465	Chinchilla	21	symbol	gene, protein-coding, MODEL [RefSeq]
12354057	MYO15A	myosin XVA	ENCODES a protein that exhibits actin binding (inferred); INVOLVED IN inner ear morphogenesis (ortholog); locomotory behavior (ortholog); response to light stimulus (ortholog); PARTICIPATES IN auditory mechanotransduction pathway; ASSOCIATED WITH Alport syndrome (ortholog); autosomal recessive nonsy ... (more) ndromic deafness (ortholog); autosomal recessive nonsyndromic deafness 3 (ortholog); FOUND IN stereocilium (ortholog); stereocilium bundle (ortholog)	5	41369484	41421303	Dog	24	symbol	gene, protein-coding, MODEL [RefSeq]
12590855	Myo15a	myosin XVA	ENCODES a protein that exhibits actin binding (inferred); ATP binding (inferred); cytoskeletal motor activity (inferred); INVOLVED IN inner ear morphogenesis (ortholog); locomotory behavior (ortholog); response to light stimulus (ortholog); PARTICIPATES IN auditory mechanotransduction pathway; ASSOC ... (more) IATED WITH Alport syndrome (ortholog); autosomal recessive nonsyndromic deafness (ortholog); autosomal recessive nonsyndromic deafness 3 (ortholog); FOUND IN cytoskeleton (inferred); myosin complex (inferred); stereocilium (inferred)	NW_004936741	1669680	1724929	Squirrel	35	symbol	gene, protein-coding, MODEL [RefSeq]
18690773	MYO15A	myosin XVA	ENCODES a protein that exhibits actin binding (inferred); ATP binding (inferred); cytoskeletal motor activity (inferred); INVOLVED IN inner ear morphogenesis (ortholog); locomotory behavior (ortholog); response to light stimulus (ortholog); PARTICIPATES IN auditory mechanotransduction pathway; ASSOC ... (more) IATED WITH Alport syndrome (ortholog); autosomal recessive nonsyndromic deafness (ortholog); autosomal recessive nonsyndromic deafness 3 (ortholog); FOUND IN cytoskeleton (inferred); myosin complex (inferred); stereocilium (inferred)				Green Monkey	35	symbol	gene, protein-coding, MODEL [RefSeq]
150657803	MYO15A		ENCODES a protein that exhibits actin binding (inferred); FOUND IN cytoplasm (inferred); cytoskeleton (inferred)				Dog	3	symbol	gene, protein-coding
14164235	MYO15A	myosin XVA	INVOLVED IN inner ear morphogenesis (ortholog); locomotory behavior (ortholog); response to light stimulus (ortholog); PARTICIPATES IN auditory mechanotransduction pathway; ASSOCIATED WITH Alport syndrome (ortholog); autosomal recessive nonsyndromic deafness (ortholog); autosomal recessive nonsyndro ... (more) mic deafness 3 (ortholog); FOUND IN stereocilium (ortholog); stereocilium bundle (ortholog); INTERACTS WITH deoxynivalenol				Pig	22	symbol	gene, protein-coding, MODEL [RefSeq]
18917658	Myo15a	myosin XVA	ENCODES a protein that exhibits actin binding (inferred); ATP binding (inferred); cytoskeletal motor activity (inferred); INVOLVED IN inner ear morphogenesis (ortholog); locomotory behavior (ortholog); response to light stimulus (ortholog); PARTICIPATES IN auditory mechanotransduction pathway; ASSOC ... (more) IATED WITH Alport syndrome (ortholog); autosomal recessive nonsyndromic deafness (ortholog); autosomal recessive nonsyndromic deafness 3 (ortholog); FOUND IN stereocilium bundle (ortholog)				Naked Mole-Rat	34	symbol	gene, protein-coding, MODEL [RefSeq]
287300382	myo15a						Tropical Clawed Frog		symbol	gene, null
287299558	myo15a.L						African Clawed Frog		symbol	gene, null
150404269	Myo15a^ci2	myosin XVA; ci2 mutant	ASSOCIATED WITH abnormal a-wave implicit time; abnormal b-wave implicit time; abnormal vision; ASSOCIATED WITH blindness				Rat	6	symbol , description	gene, allele
12041568	LOC100971960	unconventional myosin-XV	INVOLVED IN inner ear morphogenesis (ortholog); locomotory behavior (ortholog); response to light stimulus (ortholog); PARTICIPATES IN auditory mechanotransduction pathway; ASSOCIATED WITH Alport syndrome (ortholog); autosomal recessive nonsyndromic deafness (ortholog); autosomal recessive nonsyndro ... (more) mic deafness 3 (ortholog); FOUND IN stereocilium (ortholog); stereocilium bundle (ortholog)	17	32661499	32723320	Bonobo	21	old_gene_symbol	gene, protein-coding, MODEL [RefSeq]