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MYH9
HPA
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  • MYH9
PROTEIN SUMMARY GENE INFORMATION RNA DATA ANTIBODY DATA
GENERAL INFORMATIONi

General description of the gene and the encoded protein(s) using information from HGNC and Ensembl, as well as predictions made by the Human Protein Atlas project.

Gene namei

Official gene symbol, which is typically a short form of the gene name, according to HGNC.

MYH9
Synonyms DFNA17, EPSTS, FTNS, MHA, NMHC-II-A, NMMHCA
Gene descriptioni

Full gene name according to HGNC.

Myosin heavy chain 9
Protein classi

Assigned HPA protein class(es) for the encoded protein(s).

Cancer-related genes
Disease related genes
Human disease related genes
Plasma proteins
Predicted locationi

All transcripts of all genes have been analyzed regarding the location(s) of corresponding protein based on prediction methods for signal peptides and transmembrane regions.

  • Genes with at least one transcript predicted to encode a secreted protein, according to prediction methods or to UniProt location data, have been further annotated and classified with the aim to determine if the corresponding protein(s) are secreted or actually retained in intracellular locations or membrane-attached.

  • Remaining genes, with no transcript predicted to encode a secreted protein, will be assigned the prediction-based location(s).

The annotated location overrules the predicted location, so that a gene encoding a predicted secreted protein that has been annotated as intracellular will have intracellular as the final location.

Intracellular
Protein evidence Evidence at protein level (all genes)
GENE INFORMATIONi

Gene information from Ensembl and Entrez, as well as links to available gene identifiers are displayed here. Information was retrieved from Ensembl if not indicated otherwise.

Chromosome 22
Cytoband q12.3
Chromosome location (bp) 36281280 - 36388010
Number of transcriptsi

Number of protein-coding transcripts from the gene as defined by Ensembl.

6
Ensembl ENSG00000100345 (version 109)
Entrez gene 4627
HGNC HGNC:7579
UniProt P35579 (UniProt - Evidence at protein level)
neXtProt NX_P35579
GeneCards MYH9
Antibodypedia MYH9 antibodies


PROTEIN FUNCTION
Protein function (UniProt)i

Useful information about the protein provided by UniProt.

Cellular myosin that appears to play a role in cytokinesis, cell shape, and specialized functions such as secretion and capping. Required for cortical actin clearance prior to oocyte exocytosis (By similarity). Promotes cell motility in conjunction with S100A4 1. During cell spreading, plays an important role in cytoskeleton reorganization, focal contact formation (in the margins but not the central part of spreading cells), and lamellipodial retraction; this function is mechanically antagonized by MYH10 2.... show less
Molecular function (UniProt)i

Keywords assigned by UniProt to proteins due to their particular molecular function.

Actin-binding, Calmodulin-binding, Motor protein, Myosin
Biological process (UniProt)i

Keywords assigned by UniProt to proteins because they are involved in a particular biological process.

Cell adhesion, Cell shape
Ligand (UniProt)i

Keywords assigned by UniProt to proteins because they bind, are associated with, or whose activity is dependent of some molecule.

ATP-binding, Nucleotide-binding
Gene summary (Entrez)i

Useful information about the gene from Entrez

This gene encodes a conventional non-muscle myosin; this protein should not be confused with the unconventional myosin-9a or 9b (MYO9A or MYO9B). The encoded protein is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain which is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in this gene have been associated with non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness. [provided by RefSeq, Dec 2011]... show less
PROTEIN INFORMATIONi

The protein information section displays alternative protein-coding transcripts (splice variants) encoded by this gene according to the Ensembl database.

The Splice variant identifier links to the Ensembl website protein summary for the selected splice variant. The data in the Swissprot and TrEMBL columns links to corresponding pages in the UniProt database.

The protein classes assigned to this protein are shown if expanding the data in the protein class column. Parent protein classes are in bold font and subclasses are listed under the parent class.

The length of the protein (amino acid residues according to Ensembl), molecular mass (kDalton), predicted signal peptide and number of predicted transmembrane region(s) according to in-house majority decision methods based on sets of predictors are also reported.
Splice variant SwissProt TrEMBL Protein class Gene ontology Length & mass Signal peptide
(predicted)
Transmembrane regions
(predicted)
MYH9-201
ENSP00000216181
ENST00000216181
P35579
[Direct mapping] Myosin-9
Show all
A0A024R1N1
[Target identity:100%; Query identity:100%] Myosin, heavy polypeptide 9, non-muscle, isoform CRA_a
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Plasma proteins
Cancer-related genes
   Mutational cancer driver genes
   COSMIC somatic mutations in cancer genes
   COSMIC Somatic Mutations
   COSMIC Translocations
Disease related genes
Human disease related genes
   Cardiovascular diseases
   Hematologic diseases
   Nervous system diseases
   Ear disease
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0000146 [microfilament motor activity]
GO:0000166 [nucleotide binding]
GO:0000212 [meiotic spindle organization]
GO:0000904 [cell morphogenesis involved in differentiation]
GO:0001525 [angiogenesis]
GO:0001701 [in utero embryonic development]
GO:0001725 [stress fiber]
GO:0001726 [ruffle]
GO:0001768 [establishment of T cell polarity]
GO:0001772 [immunological synapse]
GO:0001778 [plasma membrane repair]
GO:0001931 [uropod]
GO:0003723 [RNA binding]
GO:0003774 [cytoskeletal motor activity]
GO:0003779 [actin binding]
GO:0005178 [integrin binding]
GO:0005515 [protein binding]
GO:0005516 [calmodulin binding]
GO:0005524 [ATP binding]
GO:0005634 [nucleus]
GO:0005737 [cytoplasm]
GO:0005819 [spindle]
GO:0005826 [actomyosin contractile ring]
GO:0005829 [cytosol]
GO:0005856 [cytoskeleton]
GO:0005886 [plasma membrane]
GO:0005903 [brush border]
GO:0005912 [adherens junction]
GO:0005925 [focal adhesion]
GO:0005938 [cell cortex]
GO:0006509 [membrane protein ectodomain proteolysis]
GO:0006911 [phagocytosis, engulfment]
GO:0007155 [cell adhesion]
GO:0007229 [integrin-mediated signaling pathway]
GO:0007520 [myoblast fusion]
GO:0008180 [COP9 signalosome]
GO:0008360 [regulation of cell shape]
GO:0009898 [cytoplasmic side of plasma membrane]
GO:0015031 [protein transport]
GO:0015629 [actin cytoskeleton]
GO:0016020 [membrane]
GO:0016459 [myosin complex]
GO:0016460 [myosin II complex]
GO:0016604 [nuclear body]
GO:0019904 [protein domain specific binding]
GO:0030048 [actin filament-based movement]
GO:0030220 [platelet formation]
GO:0030224 [monocyte differentiation]
GO:0030863 [cortical cytoskeleton]
GO:0031032 [actomyosin structure organization]
GO:0031252 [cell leading edge]
GO:0031410 [cytoplasmic vesicle]
GO:0031532 [actin cytoskeleton reorganization]
GO:0031594 [neuromuscular junction]
GO:0032154 [cleavage furrow]
GO:0032418 [lysosome localization]
GO:0032506 [cytokinetic process]
GO:0032796 [uropod organization]
GO:0032982 [myosin filament]
GO:0032991 [protein-containing complex]
GO:0042641 [actomyosin]
GO:0042802 [identical protein binding]
GO:0042803 [protein homodimerization activity]
GO:0043495 [protein-membrane adaptor activity]
GO:0043531 [ADP binding]
GO:0043534 [blood vessel endothelial cell migration]
GO:0045055 [regulated exocytosis]
GO:0045296 [cadherin binding]
GO:0050900 [leukocyte migration]
GO:0051015 [actin filament binding]
GO:0051295 [establishment of meiotic spindle localization]
GO:0060471 [cortical granule exocytosis]
GO:0060473 [cortical granule]
GO:0070062 [extracellular exosome]
GO:0070527 [platelet aggregation]
GO:0097513 [myosin II filament]
GO:0098609 [cell-cell adhesion]
GO:1903919 [negative regulation of actin filament severing]
GO:1903923 [positive regulation of protein processing in phagocytic vesicle]
GO:1905684 [regulation of plasma membrane repair]
Show all
1960 aa
226.5 kDa
No 0
MYH9-202
ENSP00000384631
ENST00000401701
Q5BKV1
[Direct mapping] MYH9 protein; Myosin-9
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Cancer-related genes
   Mutational cancer driver genes
   COSMIC somatic mutations in cancer genes
   COSMIC Somatic Mutations
   COSMIC Translocations
Human disease related genes
   Cardiovascular diseases
   Hematologic diseases
   Nervous system diseases
   Ear disease
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0000166 [nucleotide binding]
GO:0003774 [cytoskeletal motor activity]
GO:0003779 [actin binding]
GO:0005524 [ATP binding]
GO:0016459 [myosin complex]
GO:0051015 [actin filament binding]
Show all
218 aa
24.8 kDa
No 0
MYH9-203
ENSP00000414852
ENST00000456729
B1AH99
[Direct mapping] Myosin-9
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Cancer-related genes
   Mutational cancer driver genes
   COSMIC somatic mutations in cancer genes
   COSMIC Somatic Mutations
   COSMIC Translocations
Human disease related genes
   Cardiovascular diseases
   Hematologic diseases
   Nervous system diseases
   Ear disease
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0000166 [nucleotide binding]
GO:0003774 [cytoskeletal motor activity]
GO:0003779 [actin binding]
GO:0005524 [ATP binding]
GO:0016459 [myosin complex]
GO:0051015 [actin filament binding]
Show all
103 aa
11.6 kDa
No 0
MYH9-215
ENSP00000510688
ENST00000685801
A0A8I5KWT8
[Direct mapping] Myosin-9
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Cancer-related genes
   Mutational cancer driver genes
   COSMIC somatic mutations in cancer genes
   COSMIC Somatic Mutations
   COSMIC Translocations
Human disease related genes
   Cardiovascular diseases
   Hematologic diseases
   Nervous system diseases
   Ear disease
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0000166 [nucleotide binding]
GO:0003774 [cytoskeletal motor activity]
GO:0003779 [actin binding]
GO:0005515 [protein binding]
GO:0005524 [ATP binding]
GO:0016459 [myosin complex]
GO:0051015 [actin filament binding]
Show all
1981 aa
229.2 kDa
No 0
MYH9-218
ENSP00000510189
ENST00000688137
A0A8I5KU92
[Direct mapping] Myosin-9
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Cancer-related genes
   Mutational cancer driver genes
   COSMIC somatic mutations in cancer genes
   COSMIC Somatic Mutations
   COSMIC Translocations
Human disease related genes
   Cardiovascular diseases
   Hematologic diseases
   Nervous system diseases
   Ear disease
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0000166 [nucleotide binding]
GO:0003774 [cytoskeletal motor activity]
GO:0003779 [actin binding]
GO:0005524 [ATP binding]
GO:0016459 [myosin complex]
GO:0051015 [actin filament binding]
Show all
224 aa
25.3 kDa
No 0
MYH9-221
ENSP00000509816
ENST00000691296
A0A8I5KYI1
[Direct mapping] Myosin-9
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Cancer-related genes
   Mutational cancer driver genes
   COSMIC somatic mutations in cancer genes
   COSMIC Somatic Mutations
   COSMIC Translocations
Human disease related genes
   Cardiovascular diseases
   Hematologic diseases
   Nervous system diseases
   Ear disease
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0000166 [nucleotide binding]
GO:0003774 [cytoskeletal motor activity]
GO:0003779 [actin binding]
GO:0005524 [ATP binding]
GO:0016459 [myosin complex]
GO:0051015 [actin filament binding]
Show all
207 aa
23.6 kDa
No 0

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