Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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6603 |
Gene nameGene Name - the full gene name approved by the HGNC.
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SWI/SNF related BAF chromatin remodeling complex subunit D2 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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SMARCD2 |
SynonymsGene synonyms aliases
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BAF60B, CRACD2, PRO2451, Rsc6p, SGD2 |
ChromosomeChromosome number
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17 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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17q23.3 |
SummarySummary of gene provided in NCBI Entrez Gene.
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The protein encoded by this gene is a member of the SWI/SNF family of proteins, whose members display helicase and ATPase activities and which are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. T |
SNPsSNP information provided by dbSNP.
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miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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UniProt ID |
Q92925 |
Protein name |
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 2 (60 kDa BRG-1/Brm-associated factor subunit B) (BRG1-associated factor 60B) (BAF60B) |
Protein function |
Involved in transcriptional activation and repression of select genes by chromatin remodeling (alteration of DNA-nucleosome topology). Component of SWI/SNF chromatin remodeling complexes that carry out key enzymatic activities, changing chromati |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF02201 |
SWIB |
309 → 381 |
SWIB/MDM2 domain |
Domain |
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Sequence |
MSGRGAGGFPLPPLSPGGGAVAAALGAPPPPAGPGMLPGPALRGPGPAGGVGGPGAAAFR PMGPAGPAAQYQRPGMSPGNRMPMAGLQVGPPAGSPFGAAAPLRPGMPPTMMDPFRKRLL VPQAQPPMPAQRRGLKRRKMADKVLPQRIRELVPESQAYMDLLAFERKLDQTIARKRMEI QEAIKKPLTQKRKLRIYISNTFSPSKAEGDSAGTAGTPGGTPAGDKVASWELRVEGKLLD DPSKQKRKFSSFFKSLVIELDKELYGPDNHLVEWHRMPTTQETDGFQVKRPGDLNVKCTL LLMLDHQPPQYKLDPRLARLLGVHTQTRAAIMQALWLYIKHNQLQDGHEREYINCNRYFR QIFSCGRLRFSEIPMKLAGLLQHPDPIVINHVISVDPNDQKKTACYDIDVEVDDPLKAQM SNFLASTTNQQEIASLDVKIHETIESINQLKTQRDFMLSFSTDPQDFIQEWLRSQRRDLK IITDVIGNPEEERRAAFYHQPWAQEAVGRHIFAKVQQRRQELEQVLGIRLT
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Sequence length |
531 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Brachydactyly |
Brachydactyly |
rs121908949, rs28937580, rs121909082, rs104894122, rs863223289, rs863223290, rs104894121, rs1587657302, rs863223292, rs74315386, rs74315387, rs28936397, rs753691079, rs121909348, rs121917852, rs121917853, rs121917854, rs121917855, rs121917859, rs121917861, rs267606873, rs267606872, rs267606985, rs267606986, rs267606987, rs267606988, rs28933082, rs397514519, rs869025613, rs869025614, rs886039878, rs1553540620, rs1057518333, rs1948841937, rs1948868228, rs1948842030, rs1948842142 |
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Myelodysplasia |
Myelodysplasia |
rs141601766, rs1261178797 |
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Myelodysplastic syndrome |
MYELODYSPLASTIC SYNDROME |
rs193303018, rs387906631, rs1576745225, rs373145711, rs752746786, rs377023736, rs373221034, rs1576749014, rs1600586587 |
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Neutropenia |
Neutropenia |
rs879253882 |
28369036 |
Specific granule deficiency |
Specific granule deficiency, SPECIFIC GRANULE DEFICIENCY 2, SPECIFIC GRANULE DEFICIENCY 1 |
rs2140292116, rs2140291802, rs1057518731, rs1555580263, rs1057518733, rs760325316, rs112986541 |
28369034, 28369036, 28369036 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Monocytic leukemia |
Leukemia, Monocytic, Chronic |
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28369036 |
Myeloid leukemia |
Myeloid Leukemia |
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28369036 |
Osteopenia |
Osteopenia |
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Otitis media |
Recurrent otitis media |
rs601338, rs1047781, rs1800028 |
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