MYH15 (myosin heavy chain 15)

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Gene miRNA Gene ontology Other IDs Protein Pathways Associated diseases Related genes Diseases linked via similar genes

Gene

• Entrez ID: 22989
• Gene name: Myosin heavy chain 15
• Gene symbol: MYH15
• Synonyms (NCBI Gene): -
• Chromosome: 3
• Chromosome location: 3q13.13

miRNA Show/Hide all (26)

miRTarBase ID	miRNA	Experiments	Reference
MIRT711480	hsa-miR-7161-3p	HITS-CLIP	19536157
MIRT711479	hsa-miR-6888-5p	HITS-CLIP	19536157
MIRT711478	hsa-miR-617	HITS-CLIP	19536157
MIRT711477	hsa-miR-6505-3p	HITS-CLIP	19536157
MIRT711476	hsa-miR-4683	HITS-CLIP	19536157
MIRT711480	hsa-miR-7161-3p	HITS-CLIP	19536157
MIRT711479	hsa-miR-6888-5p	HITS-CLIP	19536157
MIRT711478	hsa-miR-617	HITS-CLIP	19536157
MIRT711477	hsa-miR-6505-3p	HITS-CLIP	19536157
MIRT711476	hsa-miR-4683	HITS-CLIP	19536157
MIRT1168321	hsa-miR-3152-5p	CLIP-seq
MIRT1168322	hsa-miR-3671	CLIP-seq
MIRT1168323	hsa-miR-4666-5p	CLIP-seq
MIRT1168324	hsa-miR-4774-3p	CLIP-seq
MIRT1168325	hsa-miR-607	CLIP-seq
MIRT2048511	hsa-miR-4663	CLIP-seq
MIRT2048512	hsa-miR-4689	CLIP-seq
MIRT2048513	hsa-miR-579	CLIP-seq
MIRT2048514	hsa-miR-664	CLIP-seq
MIRT2277374	hsa-miR-3179	CLIP-seq
MIRT2048511	hsa-miR-4663	CLIP-seq
MIRT2048513	hsa-miR-579	CLIP-seq
MIRT2391249	hsa-miR-1236	CLIP-seq
MIRT2391250	hsa-miR-3663-5p	CLIP-seq
MIRT2391251	hsa-miR-593	CLIP-seq
MIRT2391252	hsa-miR-626	CLIP-seq

Gene ontology (GO) Show/Hide all (17)

GO ID	Ontology	Definition	Evidence	Reference
GO:0000146	Function	Microfilament motor activity	IBA
GO:0000166	Function	Nucleotide binding	IEA
GO:0002074	Process	Extraocular skeletal muscle development	IEA
GO:0003774	Function	Cytoskeletal motor activity	IEA
GO:0003779	Function	Actin binding	IEA
GO:0005516	Function	Calmodulin binding	IEA
GO:0005524	Function	ATP binding	IEA
GO:0005737	Component	Cytoplasm	IBA
GO:0005737	Component	Cytoplasm	IEA
GO:0005829	Component	Cytosol	IDA
GO:0016459	Component	Myosin complex	IEA
GO:0016460	Component	Myosin II complex	IBA
GO:0030016	Component	Myofibril	IEA
GO:0032982	Component	Myosin filament	IBA
GO:0032982	Component	Myosin filament	IEA
GO:0051015	Function	Actin filament binding	IBA
GO:0051015	Function	Actin filament binding	IEA

Other IDs

• MIM: 609929
• HGNC: 31073
• e!Ensembl: ENSG00000144821

Protein

• UniProt ID: Q9Y2K3
• Protein name: Myosin-15 (Myosin heavy chain 15)
• Protein function: Muscle contraction.
• Family and domains:

  Pfam

  Accession	ID	Position in sequence	Description	Type
  PF00063	Myosin_head	105 → 778	Myosin head (motor domain)	Domain
  PF01576	Myosin_tail_1	856 → 1936	Myosin tail	Coiled-coil
  PF02736	Myosin_N	51 → 91	Myosin N-terminal SH3-like domain	Domain

• Sequence:

  MVESCLLTFRAFFWWIALIKMDLSDLGEAAAFLRRSEAELLLLQATALDGKKKCWIPDGE
  NAYIEAEVKGSEDDGTVIVETADGESLSIKEDKIQQMNPPEFEMIEDMAMLTHLNEASVL
  HTLKRRYGQWMIYTYSGLFCVTINPYKWLPVYQKEVMAAYKGKRRSEAPPHIFAVANNAF
  QDMLHNRENQSILFTGESGAGKTVNSKHIIQYFATIAAMIESRKKQGALEDQIMQANTIL
  EAFGNAKTLRNDNSSRFGKFIRMHFGARGMLSSVDIDIYLLEKSRVIFQQAGERNYHIFY
  QILSGQKELHDLLLVSANPSDFHFCSCGAVTVESLDDAEELLATEQAMDILGFLPDEKYG
  CYKLTGAIMHFGNMKFKQKPREEQLEADGTENADKAAFLMGINSSELVKCLIHPRIKVGN
  EYVTRGQTIEQVTCAVGALSKSMYERMFKWLVARINRALDAKLSRQFFIGILDITGFEIL
  EYNSLEQLCINFTNEKLQQFFNWHMFVLEQEEYKKESIEWVSIGFGLDLQACIDLIEKPM
  GILSILEEECMFPKATDLTFKTKLFDNHFGKSVHLQKPKPDKKKFEAHFELVHYAGVVPY
  NISGWLEKNKDLLNETVVAVFQKSSNRLLASLFENYMSTDSAIPFGEKKRKKGASFQTVA
  SLHKENLNKLMTNLKSTAPHFVRCINPNVNKIPGILDPYLVLQQLRCNGVLEGTRICREG
  FPNRLQYADFKQRYCILNPRTFPKSKFVSSRKAAEELLGSLEIDHTQYRFGITKVFFKAG
  FLGQLEAIRDERLSKVFTLFQARAQGKLMRIKFQKILEERDALILIQWNIRAFMAVKNWP
  WMRLFFKIKPLVKSSEVGEEVAGLKEECAQLQKALEKSEFQREELKAKQVSLTQEKNDLI
  LQLQAEQETLANVEEQCEWLIKSKIQLEARVKELSERVEEEEEINSELTARGRKLEDECF
  ELKKEIDDLETMLVKSEKEKRTTEHKVKNLTEEVEFLNEDISKLNRAAKVVQEAHQQTLD
  DLHMEEEKLSSLSKANLKLEQQVDELEGALEQERKARMNCERELHKLEGNLKLNRESMEN
  LESSQRHLAEELRKKELELSQMNSKVENEKGLVAQLQKTVKELQTQIKDLKEKLEAERTT
  RAKMERERADLTQDLADLNERLEEVGGSSLAQLEITKKQETKFQKLHRDMEEATLHFETT
  SASLKKRHADSLAELEGQVENLQQVKQKLEKDKSDLQLEVDDLLTRVEQMTRAKANAEKL
  CTLYEERLHEATAKLDKVTQLANDLAAQKTKLWSESGEFLRRLEEKEALINQLSREKSNF
  TRQIEDLRGQLEKETKSQSALAHALQKAQRDCDLLREQYEEEQEVKAELHRTLSKVNAEM
  VQWRMKYENNVIQRTEDLEDAKKELAIRLQEAAEAMGVANARNASLERARHQLQLELGDA
  LSDLGKVRSAAARLDQKQLQSGKALADWKQKHEESQALLDASQKEVQALSTELLKLKNTY
  EESIVGQETLRRENKNLQEEISNLTNQVREGTKNLTEMEKVKKLIEEEKTEVQVTLEETE
  GALERNESKILHFQLELLEAKAELERKLSEKDEEIENFRRKQQCTIDSLQSSLDSEAKSR
  IEVTRLKKKMEEDLNEMELQLSCANRQVSEATKSLGQLQIQIKDLQMQLDDSTQLNSDLK
  EQVAVAERRNSLLQSELEDLRSLQEQTERGRRLSEEELLEATERINLFYTQNTSLLSQKK
  KLEADVARMQKEAEEVVQECQNAEEKAKKAAIEAANLSEELKKKQDTIAHLERTRENMEQ
  TITDLQKRLAEAEQMALMGSRKQIQKLESRVRELEGELEGEIRRSAEAQRGARRLERCIK
  ELTYQAEEDKKNLSRMQTQMDKLQLKVQNYKQQVEVAETQANQYLSKYKKQQHELNEVKE
  RAEVAESQVNKLKIKAREFGKKVQEE

• Sequence length: 1946

Pathways

KEGG Pathway

Motor proteins

Cytoskeleton in muscle cells

Associated diseases

Evidence Score:

• ★☆☆☆☆  Gene-disease association found in Text Mining only
• ★★☆☆☆  Found in Text Mining and Unknown/Other Associations
• ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources
• ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
• ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)

Unknown / Other Associations Show/Hide Unknown Diseases (14)
Phenotype Name	Clinical Significance	Source	Reference	Evidence Score
ANXIETY DISORDER	—	GWAS catalog	31748690	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
BIPOLAR DISORDER	—	GWAS catalog	31926635	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Cervical cancer	Benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Clear cell carcinoma of kidney	not provided; Benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Gastric cancer	Benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
HYPOTHYROIDISM	—	GWAS catalog	30595370, 36093044	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
INSOMNIA	—	GWAS catalog	35835914	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Lung cancer	Benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
MAJOR DEPRESSIVE DISORDER	—	GWAS catalog	31926635, 38177345	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Malignant tumor of esophagus	Benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
METABOLIC SYNDROME	—	GWAS catalog	39349817	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY	—	Disgenet	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Ovarian serous cystadenocarcinoma	Benign	ClinVar	—	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
TYPE 2 DIABETES MELLITUS	—	GWAS catalog	39349817	★★☆☆☆ Found in Text Mining + Unknown/Other Associations

Associations from Text Mining Show/Hide Text Mining Associations (11)
Disease Name	Disease (Merged)	Source	PMID	Relationship Type	Evidence Score
Amyotrophic Lateral Sclerosis	Amyotrophic Lateral Sclerosis	BEFREE	30985904		★☆☆☆☆ Found in Text Mining only
Arteriosclerosis	Arteriosclerosis	BEFREE	18073581		★☆☆☆☆ Found in Text Mining only
Asthma	Asthma	BEFREE	30906771		★☆☆☆☆ Found in Text Mining only
Asthma	Asthma	Pubtator	30906771	Associate	★☆☆☆☆ Found in Text Mining only
Atherosclerosis	Atherosclerosis	BEFREE	18073581		★☆☆☆☆ Found in Text Mining only
Cerebrovascular accident	Stroke	BEFREE	19752551		★☆☆☆☆ Found in Text Mining only
Coronary Disease	Coronary artery disease	Pubtator	18073581, 24736300	Associate	★☆☆☆☆ Found in Text Mining only
Hypothyroidism	Hypothyroidism	GWASCAT_DG	30595370		★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Nonsyndromic Deafness	Nonsyndromic Deafness	BEFREE	30579064		★☆☆☆☆ Found in Text Mining only
Stroke	Stroke	Pubtator	19752551	Stimulate	★☆☆☆☆ Found in Text Mining only
Stroke	Stroke	Pubtator	19752551	Associate	★☆☆☆☆ Found in Text Mining only

Related Genes

Sort by: Blended Diseases Pathways Evidence source

TRAIP 2 shared diseasesAnxiety disorder, Microcephaly 2 shared evidence sourcesGWAS catalog (Anxiety disorder), Disgenet (Microcephaly) Related via 2 shared diseases including Anxiety disorder, Microcephaly — evidence mostly GWAS catalog. MYH1 2 shared pathwaysMotor proteins, Cytoskeleton in muscle cells Related via 2 shared pathways including Motor proteins, Cytoskeleton in muscle cells. MYH4 2 shared pathwaysMotor proteins, Cytoskeleton in muscle cells Related via 2 shared pathways including Motor proteins, Cytoskeleton in muscle cells. MYH7B 2 shared pathwaysMotor proteins, Cytoskeleton in muscle cells Related via 2 shared pathways including Motor proteins, Cytoskeleton in muscle cells. MYH13 2 shared pathwaysMotor proteins, Cytoskeleton in muscle cells Related via 2 shared pathways including Motor proteins, Cytoskeleton in muscle cells.

Related Gene	Shared Diseases	Shared Disease Names	Shared Pathways	Shared Pathway Names	Shared Evidence Sources	Shared Evidence Names
TRAIP	2	["Anxiety disorder","Microcephaly"]	0	[]	2	["GWAS catalog (Anxiety disorder)","Disgenet (Microcephaly)"]
MYH1	0	[]	2	["Motor proteins","Cytoskeleton in muscle cells"]	0	[]
MYH4	0	[]	2	["Motor proteins","Cytoskeleton in muscle cells"]	0	[]
MYH7B	0	[]	2	["Motor proteins","Cytoskeleton in muscle cells"]	0	[]
MYH13	0	[]	2	["Motor proteins","Cytoskeleton in muscle cells"]	0	[]

Diseases Linked via Similar Genes

Coronary artery disease Linked via 2 of 5 related genesTRAIP, MYH13 Alzheimer disease Linked via 1 of 5 related genesTRAIP Attention deficit hyperactivity disorder Linked via 1 of 5 related genesTRAIP Autism Linked via 1 of 5 related genesTRAIP Hepatocellular carcinoma Linked via 1 of 5 related genesTRAIP

Disease	Linked Via (Gene Count)	Linked Via (Gene Names)
Coronary artery disease	2	["TRAIP","MYH13"]
Alzheimer disease	1	["TRAIP"]
Attention deficit hyperactivity disorder	1	["TRAIP"]
Autism	1	["TRAIP"]
Hepatocellular carcinoma	1	["TRAIP"]