Show pageOld revisionsBacklinksFold/unfold allBack to top This page is read only. You can view the source, but not change it. Ask your administrator if you think this is wrong. ======= MYO3A ======= == Gene Information == * **<color #00a2e8>Official Symbol</color>**: MYO3A * **<color #00a2e8>Official Name</color>**: myosin IIIA * **<color #00a2e8>Aliases and Previous Symbols</color>**: N/A * **<color #00a2e8>Entrez ID</color>**: [[https://www.ncbi.nlm.nih.gov/gene/?term=53904|53904]] * **<color #00a2e8>UniProt</color>**: [[https://www.uniprot.org/uniprot/Q8NEV4|Q8NEV4]] * **<color #00a2e8>Interactions</color>**: [[https://thebiogrid.org/search.php?search=MYO3A&organism=9606|BioGRID]] * **<color #00a2e8>PubMed articles</color>**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20MYO3A|Open PubMed]] * **<color #00a2e8>OMIM</color>**: [[https://omim.org/entry/606808|Open OMIM]] == Function Summary == * **<color #00a2e8>Entrez Summary</color>**: The protein encoded by this gene belongs to the myosin superfamily. Myosins are actin-dependent motor proteins and are categorized into conventional myosins (class II) and unconventional myosins (classes I and III through XV) based on their variable C-terminal cargo-binding domains. Class III myosins, such as this one, have a kinase domain N-terminal to the conserved N-terminal motor domains and are expressed in photoreceptors. The protein encoded by this gene plays an important role in hearing in humans. Three different recessive, loss of function mutations in the encoded protein have been shown to cause nonsyndromic progressive hearing loss. Expression of this gene is highly restricted, with the strongest expression in retina and cochlea. [provided by RefSeq, Jul 2008]. * **<color #00a2e8>UniProt Summary</color>**: Probable actin-based motor with a protein kinase activity. Probably plays a role in vision and hearing (PubMed:12032315). Required for normal cochlear hair bundle development and hearing. Plays an important role in the early steps of cochlear hair bundle morphogenesis. Influences the number and lengths of stereocilia to be produced and limits the growth of microvilli within the forming auditory hair bundles thereby contributing to the architecture of the hair bundle, including its staircase pattern. Involved in the elongation of actin in stereocilia tips by transporting the actin regulatory factor ESPN to the plus ends of actin filaments (By similarity). {ECO:0000250|UniProtKB:Q8K3H5, ECO:0000269|PubMed:12032315}. <button type='primary' size='sm' modal='Pfam_Domains'>Pfam Domains</button> <button type='primary' size='sm' modal='GO_terms'>GO Terms</button> <modal id='Pfam_Domains' size='lg' title='Pfam Domains'> |Pkinase Tyr| |Pkinase| |Myosin head| </modal> <modal id='GO_terms' size='lg' title='GO Terms'> |plus-end directed microfilament motor activity| |actin-dependent ATPase activity| |stereocilium tip| |filopodium tip| |microfilament motor activity| |cochlea morphogenesis| |myosin complex| |filamentous actin| |ADP binding| |cochlea development| |filopodium| |inner ear morphogenesis| |ear morphogenesis| |sensory perception of sound| |sensory perception of mechanical stimulus| |protein autophosphorylation| |inner ear development| |calmodulin binding| |visual perception| |ear development| |sensory perception of light stimulus| |protein kinase activity| |sensory organ morphogenesis| |actin binding| |embryonic organ morphogenesis| |protein serine/threonine kinase activity| |embryonic organ development| |sensory organ development| |embryonic morphogenesis| |animal organ morphogenesis| |sensory perception| |protein phosphorylation| |embryo development| |phosphorylation| |nervous system process| |ATP binding| |system process| </modal> \\ === CRISPR Data === <button type='primary' size='small' modal='Compound_Hit'>Compound Hit</button> <button type='default' size='small' modal='Most_Correlated_Genes'>Most Correlated Genes in Chemogenomics</button> <button type='primary' size='small' modal='Essential_Avana'>Tissues where Essential in the Avana Dataset (DepMap 20Q1)</button> <modal id='Compound_Hit' size='lg' title='Compound Hit'> ^Screen^Score^ |[[:results:exp40|2-Methoxyestradiol 0.2μM R01 exp40]]|-2.14| |[[:results:exp26|Oligomycin-A 20μM R00 exp26]]|-2.02| </modal> <modal id='Most_Correlated_Genes' size='lg' title='Most Correlated Genes in Chemogenomics'> No correlation found to any other genes in chemogenomics. </modal> <modal id='Essential_Avana' size='lg' title='Tissues where Essential in the Avana Dataset (DepMap 20Q1)'> Global Fraction of Cell Lines Where Essential: 0/739 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|0/28| |blood|0/28| |bone|0/26| |breast|0/33| |central nervous system|0/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|0/16| |kidney|0/21| |liver|0/20| |lung|0/75| |lymphocyte|0/16| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|0/15| |prostate|0/1| |skin|0/24| |soft tissue|0/9| |thyroid|0/2| |upper aerodigestive|0/22| |urinary tract|0/29| |uterus|0/5| </modal> == Essentiality in NALM6 == * **<color #00a2e8>Essentiality Rank</color>**: 12882 * **<color #00a2e8>Expression level (log2 read counts)</color>**: -1.49 <button type='primary' size='small' modal='Dist_expr'>Expression Distribution</button> <modal id='Dist_expr' size='lg' title='MYO3A Expression in NALM6 Cells: -1.49'> {{:chemogenomics:nalm6 dist.png?nolink |}} </modal> Last modified: 2025/12/10 20:19by 127.0.0.1