ZFIN Gene: myh14

ZFIN ID: ZDB-GENE-100921-1

ZFIN ID: ZDB-GENE-100921-1

Gene Name:

myosin, heavy chain 14, non-muscle

Gene Symbol:

myh14

Sequence Ontology ID :

SO:0001217

Previous Names:

si:ch211-120k19.2, si:ch211-120k19.3

Location:

Chr: 16 Mapping Details/Browsers

Nomenclature History

AUTOMATED DESCRIPTION

Predicted to have ATP binding activity; actin filament binding activity; and motor activity. Predicted to localize to the myosin complex. Human ortholog(s) of this gene implicated in autosomal ...

GENE EXPRESSION No data available

MUTATIONS AND SEQUENCE TARGETING REAGENTS

Allele	Type	Localization	Consequence	Mutagen	Suppliers
sa15579	Point Mutation	Unknown	Splice Site	ENU	European Zebrafish Resource Center (EZRC) (order this) Zebrafish International Resource Center (ZIRC) (order this)
sa16888	Point Mutation	Unknown	Premature Stop	ENU	European Zebrafish Resource Center (EZRC) (order this) Zebrafish International Resource Center (ZIRC) (order this)
sa17178	Point Mutation	Unknown	Premature Stop	ENU	European Zebrafish Resource Center (EZRC) (order this) Zebrafish International Resource Center (ZIRC) (order this)
sa22798	Point Mutation	Unknown	Splice Site	ENU	European Zebrafish Resource Center (EZRC) (order this) Zebrafish International Resource Center (ZIRC) (order this)
sa36084	Point Mutation	Unknown	Splice Site	ENU	European Zebrafish Resource Center (EZRC) (order this) Zebrafish International Resource Center (ZIRC) (order this)
sa36085	Point Mutation	Unknown	Premature Stop	ENU	European Zebrafish Resource Center (EZRC) (order this) Zebrafish International Resource Center (ZIRC) (order this)
sa44846	Point Mutation	Unknown	Unknown	ENU
sa45571	Point Mutation	Unknown	Splice Site	ENU	Zebrafish International Resource Center (ZIRC) (order this)

PHENOTYPE No data available

DISEASE ASSOCIATED WITH myh14 HUMAN ORTHOLOG

Disease Ontology Term	OMIM Term	OMIM Phenotype ID
autosomal dominant nonsyndromic deafness 4A	Deafness, autosomal dominant 4A	600652
	?Peripheral neuropathy, myopathy, hoarseness, and hearing loss	614369

DISEASE ASSOCIATED WITH myh14 VIA EXPERIMENTAL MODELS No data available

GENE ONTOLOGY

Ontology	GO Term
Cellular Component	myosin complex (more)
Molecular Function	actin binding (more)

GO Terms (all 6)

PROTEIN FAMILIES, DOMAINS AND SITES
InterPro:IPR000048 (1) InterPro:IPR001609 (1) InterPro:IPR002928 (1) InterPro:IPR004009 (1) InterPro:IPR008989 (1) InterPro:IPR027401 (1) InterPro:IPR027417 (1) InterPro:IPR036961 (1)	PROSITE:PS50096 (1) PROSITE:PS51456 (1) PROSITE:PS51844 (1)	Pfam:PF00063 (1) Pfam:PF01576 (1) Pfam:PF02736 (1)

TRANSCRIPTS
Type	Name	Length (bp)	Analysis
ncRNA	myh14-002 (1)	529	Select Tool ZFIN BLAST NCBI BLAST Ensembl UCSC BLAT
mRNA	myh14-203 (1)	12826	Select Tool ZFIN BLAST NCBI BLAST Ensembl UCSC BLAT
	myh14-204 (1)	446	Select Tool ZFIN BLAST NCBI BLAST Ensembl UCSC BLAT

Withdrawn Transcripts
mRNA	si:ch211-120k19.3-002 (1)	529	Select Tool ZFIN BLAST NCBI BLAST Ensembl UCSC BLAT

GENE PRODUCT DESCRIPTION

INTERACTIONS AND PATHWAYS

ANTIBODIES No data available

PLASMIDS No data available

CONSTRUCTS WITH SEQUENCES FROM myh14 No data available

MARKER RELATIONSHIPS

myh14 Contained in:

[BAC] CH211-120K19 (1) (order this)

SEQUENCE INFORMATION

Type	Accession #	Length (bp/aa)	Analysis
RNA	RefSeq:XM_005157931 (1)	7884 bp	Select Tool ZFIN BLAST NCBI BLAST Ensembl UCSC BLAT
Genomic	GenBank:AL929505 (1)	178839 bp	Select Tool MegaBLAST Ensembl
Polypeptide	UniProtKB:E9QFE1 (1)	2020 aa	Select Tool ZFIN BLAST SIB BLAST Ensembl Protein Blast

Sequence Information (all 17)

OTHER myh14 GENE PAGES

Alliance (1)

Gene:563011 (1)

VEGA:OTTDARG00000032971 (1)

Ensembl(GRCz11):ENSDARG00000073732 (2)

ORTHOLOGY for myh14 ( Chr: 16 )

CITATIONS (13)

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