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. ======= SIM1 ======= == Gene Information == * **<color #00a2e8>Official Symbol</color>**: SIM1 * **<color #00a2e8>Official Name</color>**: SIM bHLH transcription factor 1 * **<color #00a2e8>Aliases and Previous Symbols</color>**: N/A * **<color #00a2e8>Entrez ID</color>**: [[https://www.ncbi.nlm.nih.gov/gene/?term=6492|6492]] * **<color #00a2e8>UniProt</color>**: [[https://www.uniprot.org/uniprot/P81133|P81133]] * **<color #00a2e8>Interactions</color>**: [[https://thebiogrid.org/search.php?search=SIM1&organism=9606|BioGRID]] * **<color #00a2e8>PubMed articles</color>**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20SIM1|Open PubMed]] * **<color #00a2e8>OMIM</color>**: [[https://omim.org/entry/603128|Open OMIM]] == Function Summary == * **<color #00a2e8>Entrez Summary</color>**: SIM1 and SIM2 genes are Drosophila single-minded (sim) gene homologs. SIM1 transcript was detected only in fetal kidney out of various adult and fetal tissues tested. Since the sim gene plays an important role in Drosophila development and has peak levels of expression during the period of neurogenesis,it was proposed that the human SIM gene is a candidate for involvement in certain dysmorphic features (particularly the facial and skull characteristics), abnormalities of brain development, and/or cognitive disability of Down syndrome. [provided by RefSeq, Jul 2008]. * **<color #00a2e8>UniProt Summary</color>**: Transcriptional factor that may have pleiotropic effects during embryogenesis and in the adult. <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'> |PAS| |PAS 3| |SIM C| </modal> <modal id='GO_terms' size='lg' title='GO Terms'> |ureteric bud development| |mesonephric epithelium development| |mesonephric tubule development| |mesonephros development| |kidney epithelium development| |kidney development| |renal system development| |urogenital system development| |protein heterodimerization activity| |DNA-binding transcription factor activity| |tube development| |epithelium development| |DNA binding| |DNA-binding transcription factor activity, RNA polymerase II-specific| |tissue development| </modal> \\ === CRISPR Data === <button type='default' 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'> No hits were found. </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>**: 5579 * **<color #00a2e8>Expression level (log2 read counts)</color>**: -1.34 <button type='primary' size='small' modal='Dist_expr'>Expression Distribution</button> <modal id='Dist_expr' size='lg' title='SIM1 Expression in NALM6 Cells: -1.34'> {{:chemogenomics:nalm6 dist.png?nolink |}} </modal> Last modified: 2026/01/07 22:37by 127.0.0.1