Gene
|
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
|
29115 |
Gene nameGene Name - the full gene name approved by the HGNC.
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SAP30 binding protein |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
|
SAP30BP |
SynonymsGene synonyms aliases
|
HCNGP, HTRG, HTRP |
ChromosomeChromosome number
|
17 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
|
17q25.1 |
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
|
UniProt ID |
Q9UHR5 |
Protein name |
SAP30-binding protein (Transcriptional regulator protein HCNGP) |
Protein function |
Plays a role in transcriptional repression by promoting histone deacetylase activity, leading to deacetylation of histone H3 (PubMed:21221920). May be involved in the regulation of beta-2-microglobulin genes (By similarity). {ECO:0000250|UniProt |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF07818 |
HCNGP |
119 → 213 |
HCNGP-like protein |
Family |
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Sequence |
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Sequence length |
308 |
Interactions |
View interactions |
Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Schizophrenia |
Schizophrenia |
rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 |
21822266 |
|
Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Rotator cuff syndrome |
Rotator cuff syndrome |
|
26350878 |
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