Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4651
Gene name Gene Name - the full gene name approved by the HGNC.
Myosin X
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MYO10
Synonyms (NCBI Gene) Gene synonyms aliases
MyoX
Chromosome Chromosome number
5
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
5p15.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the myosin superfamily. The protein represents an unconventional myosin; it should not be confused with the conventional non-muscle myosin-10 (MYH10). Unconventional myosins contain the basic domains of conventional myosins a
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT001532 hsa-miR-155-5p Luciferase reporter assay, qRT-PCR, Western blot 20427544
MIRT005212 hsa-miR-30a-5p pSILAC 18668040
MIRT001532 hsa-miR-155-5p pSILAC 18668040
MIRT001532 hsa-miR-155-5p Proteomics 18668040
MIRT005212 hsa-miR-30a-5p Proteomics;Other 18668040
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001726 Component Ruffle IEA
GO:0005515 Function Protein binding IPI 18570893, 21321230, 21642953, 25416956
GO:0005516 Function Calmodulin binding IEA
GO:0005524 Function ATP binding IEA
GO:0005547 Function Phosphatidylinositol-3,4,5-trisphosphate binding ISS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601481 7593 ENSG00000145555
Protein
UniProt ID Q9HD67
Protein name Unconventional myosin-X (Unconventional myosin-10)
Protein function Myosins are actin-based motor molecules with ATPase activity. Unconventional myosins serve in intracellular movements. MYO10 binds to actin filaments and actin bundles and functions as a plus end-directed motor. Moves with higher velocity and ta
PDB 2LW9 , 3AU4 , 3AU5 , 3PZD , 5I0H , 5I0I , 5KG8
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF18597 SH3_19 7 58 Myosin X N-terminal SH3 domain Domain
PF00063 Myosin_head 65 727 Myosin head (motor domain) Domain
PF00612 IQ 743 763 IQ calmodulin-binding motif Motif
PF00612 IQ 767 786 IQ calmodulin-binding motif Motif
PF00612 IQ 789 809 IQ calmodulin-binding motif Motif
PF16735 MYO10_CC 882 933 Unconventional myosin-X coiled coil domain Coiled-coil
PF00169 PH 1213 1310 PH domain Domain
PF00169 PH 1393 1497 PH domain Domain
PF00784 MyTH4 1586 1694 MyTH4 domain Family
PF00788 RA 1700 1769 Ras association (RalGDS/AF-6) domain Domain
PF00373 FERM_M 1793 1958 FERM central domain Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitous. {ECO:0000269|PubMed:10984435}.
Sequence
MDNFFTEGTRVWLRENGQHFPSTVNSCAEGIVVFRTDYGQVFTYKQSTITHQKVTAMHPT
NEEGVDDMASLTELHGGSIMYNLFQRYKRNQIYTYIGSILASVNPYQPIAGLYEPATMEQ
YSRRHLGELPPHIFAIANECYRCLWKRHDNQCILISGESGAGKTESTKLILKFLSVISQQ
SLELSLKEKTSCVERAILESSPIMEAFGNAKTVYNNNSSRFGKFVQLNICQKGNIQGGRI
VDYLLEKNRVVRQNPGERNYHIFYALLAGLEHEEREEFYLSTPENYHYLNQSGCVEDKTI
SDQESFREVITAMDVMQFSKEEVREVSRLLAGILHLGNIEFITAGGAQVSFKTALGRSAE
LLGLDPTQLTDALTQRSMFLRGEEILTPLNVQQAVDSRDSLAMALYACCFEWVIKKINSR
IKGNEDFKSIGILDIFGFENFEVNHFEQFNINYANEKLQEYFNKHIFSLEQLEYSREGLV
WEDIDWIDNGECLDLIEKKLGLLALINEESHFPQATDSTLLEKLHSQHANNHFYVKPRVA
VNNFGVKHYAGEVQYDVRGILEKNRDTFRDDLLNLLRESRFDFIYDLFEHVSSRNNQDTL
KCGSKHRRPTVSSQFKDSLHSLMATLSSSNPFFVRCIKPNMQKMPDQFDQAVVLNQLRYS
GMLETVRIRKAGYAVRRPFQDFYKRYKVLMRNLALPEDVRGKCTSLLQLYDASNSEWQLG
KTKVFLR
ESLEQKLEKRREEEVSHAAMVIRAHVLGFLARKQYRKVLYCVVIIQKNYRAFL
LRRRFL
HLKKAAIVFQKQLRGQIARRVYRQLLAEKREQEEKKKQEEEEKKKREEEERERE
RERREAELRAQQEEETRKQQELEALQKSQKEAELTRELEKQKENKQVEEILRLEKEIEDL
QRMKEQQELSLTEASLQKLQERRDQELRRLEEE
ACRAAQEFLESLNFDEIDECVRNIERS
LSVGSEFSSELAESACEEKPNFNFSQPYPEEEVDEGFEADDDAFKDSPNPSEHGHSDQRT
SGIRTSDDSSEEDPYMNDTVVPTSPSADSTVLLAPSVQDSGSLHNSSSGESTYCMPQNAG
DLPSPDGDYDYDQDDYEDGAITSGSSVTFSNSYGSQWSPDYRCSVGTYNSSGAYRFSSEG
AQSSFEDSEEDFDSRFDTDDELSYRRDSVYSCVTLPYFHSFLYMKGGLMNSWKRRWCVLK
DETFLWFRSKQEALKQGWLHKKGGGSSTLSRRNWKKRWFVLRQSKLMYFENDSEEKLKGT
VEVRTAKEIIDNTTKENGIDIIMADRTFHLIAESPEDASQWFSVLSQVHA
STDQEIQEMH
DEQANPQNAVGTLDVGLIDSVCASDSPDRPNSFVIITANRVLHCNADTPEEMHHWITLLQ
RSKGDTRVEGQEFIVRGWLHKEVKNSPKMSSLKLKKRWFVLTHNSLDYYKSSEKNALKLG
TLVLNSLCSVVPPDEKIFKETGYWNVTVYGRKHCYRLYTKLLNEATRWSSAIQNVTD
TKA
PIDTPTQQLIQDIKENCLNSDVVEQIYKRNPILRYTHHPLHSPLLPLPYGDINLNLLKDK
GYTTLQDEAIKIFNSLQQLESMSDPIPIIQGILQTGHDLRPLRDELYCQLIKQTNKVPHP
GSVGNLYSWQILTCLSCTFLPSRGILKYLKFHLKRIREQFPGSEMEKYALFTYESLKKTK
CREFVPSRDEIEAL
IHRQEMTSTVYCHGGGSCKITINSHTTAGEVVEKLIRGLAMEDSRN
MFALFEYNGHVDKAIESRTVVADVLAKFE
KLAATSEVGDLPWKFYFKLYCFLDTDNVPKD
SVEFAFMFEQAHEAVIHGHHPAPEENLQVLAALRLQYLQGDYTLHAAIPPLEEVYSLQRL
KARISQSTKTFTPCERLEKRRTSFLEGTLRRSFRTGSVVRQKVEEEQMLDMWIKEEVSSA
RASIIDKWRKFQGMNQEQAMAKYMALIKEWPGYGSTLF
DVECKEGGFPQELWLGVSADAV
SVYKRGEGRPLEVFQYEHILSFGAPLANTYKIVVDERELLFETSEVVDVAKLMKAYISMI
VKKRYSTTRSASSQGSSR
Sequence length 2058
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Fc gamma R-mediated phagocytosis
Motor proteins
Pathogenic Escherichia coli infection
  Regulation of actin dynamics for phagocytic cup formation
FCGR3A-mediated phagocytosis
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Cholelithiasis Cholelithiasis rs121918440, rs72552778, rs387906528, rs759202962, rs377160065, rs1051861187, rs757693457, rs752563752 17632509
Unknown
Disease term Disease name Evidence References Source
Mental depression Major Depressive Disorder 23377640 ClinVar
Mental Depression Mental Depression GWAS
Frontal Fibrosing Alopecia Frontal Fibrosing Alopecia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 23874428
Adenoma Associate 31675075
Alzheimer Disease Associate 36928034
Apraxias Associate 27120335
Breast Neoplasms Associate 36283390
Carcinogenesis Associate 32618228
Carcinoma Intraductal Noninfiltrating Stimulate 36283390
Depressive Disorder Major Associate 36928034
Inflammation Associate 37200188
Metabolic Syndrome Associate 23628382