MYHAS (myosin heavy chain gene cluster antisense RNA)

Gene

• Entrez ID: 100128560
• Gene name: Myosin heavy chain gene cluster antisense RNA
• Gene symbol: MYHAS
• Synonyms (NCBI Gene): linc-MYH
• Chromosome: 17
• Chromosome location: 17p13.1

Other IDs

• MIM: HGNC
• HGNC: N/A
• e!Ensembl: HGNC

Associated diseases

Causal
Disease term	Disease name	dbSNP ID	References
Carney complex	Carney Complex Variant	rs281864790, rs281864785, rs281864799, rs281864779, rs281864798, rs281864801, rs387906692, rs281864782, rs281864783, rs281864797, rs281864800, rs281864792, rs281864784, rs727503379, rs886041228, rs886041351, rs141913727, rs1085307672, rs1555815121, rs1555814100, rs1555813578, rs1555813217, rs1555814477, rs1555811753, rs1568702458, rs1568698487, rs1568698504, rs1568701362, rs2085693506
Hecht syndrome	Hecht syndrome (disorder)	rs121434590
Myopathy	Myopathy	rs137854521, rs386834236, rs121908557, rs121909092, rs111033570, rs104894299, rs104894294, rs121909273, rs121909274, rs121909275, rs199474699, rs199476140, rs118192165, rs118192169, rs118192166, rs193922856, rs281865489, rs397514675, rs397514676, rs397514677, rs367543058, rs118192117, rs193922837, rs118192129, rs118192143, rs118192153, rs118192133, rs118192156, rs118192149, rs118192148, rs118192183, rs118192147, rs118192123, rs118192127, rs118192142, rs118192144, rs118192178, rs118192151, rs118192150, rs118192184, rs118192154, rs118192134, rs118192155, rs193922893, rs118192132, rs118192146, rs193922867, rs193922884, rs587777528, rs527236030, rs587777672, rs587777673, rs587777674, rs587777675, rs587783343, rs2754158, rs786204796, rs748277951, rs797046047, rs797046064, rs797046060, rs797045479, rs797045931, rs797045932, rs797045934, rs797045935, rs797045477, rs797045478, rs1057518851, rs1057518855, rs1057518773, rs1057518866, rs1555322610, rs1555806119, rs761483896, rs144071404, rs1198364572, rs1568614042, rs978984063, rs1568604308, rs1332371891, rs1601842249, rs777176261, rs1249621033, rs1278804520, rs1568613962, rs1568510406, rs1597512576, rs193922887, rs371455345, rs1603452200, rs1599634685, rs1575065895, rs1575201712, rs139715157, rs1974129338

Unknown
Disease term	Disease name	Evidence	References	Source
Inclusion body myopathy	INCLUSION BODY MYOPATHY 3, AUTOSOMAL DOMINANT		22349865, 20418530, 24193343, 23388406	ClinVar
Mental Depression	Mental Depression			GWAS
Neuroblastoma	Neuroblastoma	Loss of SNAI2 function reduces self-renewal, 3D invasion as well as metastatic spread in vivo, while strongly sensitizing neuroblastoma cells to RA-induced growth inhibition.		GWAS, CBGDA

Associations from Text Mining
Disease Name	Relationship Type	References
Laryngeal Neoplasms	Associate	31416476