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SAP30BP (SAP30 binding protein)

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.
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.
miRTarBase ID miRNA Experiments Reference
MIRT048958 hsa-miR-92a-3p CLASH 23622248
MIRT048958 hsa-miR-92a-3p CLASH 23622248
MIRT043616 hsa-miR-151a-3p CLASH 23622248
MIRT043246 hsa-miR-324-5p CLASH 23622248
MIRT1325799 hsa-miR-1207-5p CLIP-seq
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 9651585, 16189514, 18255255, 21516116, 22365833, 25416956, 31515488, 32296183, 32814053
GO:0005634 Component Nucleus IBA 21873635
GO:0005634 Component Nucleus IDA 9651585
GO:0005654 Component Nucleoplasm IDA
GO:0006355 Process Regulation of transcription, DNA-templated IEA
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
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
Sequence
MAGKKNVLSSLAVYAEDSEPESDGEAGIEAVGSAAEEKGGLVSDAYGEDDFSRLGGDEDG
YEEEEDENSRQSEDDDSETEKPEADDPKDNTEAEKRDPQELVASFSERVRNMSPDEIKIP
PEPPGRCSNHLQDKIQKLYERKIKEGMDMNYIIQRKKEFRNPSIYEKLIQFCAIDELGTN
YPKDMFDPHGWSEDSYYEALAKAQKIEMDKLEK
AKKERTKIEFVTGTKKGTTTNATSTTT
TTASTAVADAQKRKSKWDSAIPVTTIAQPTILTTTATLPAVVTVTTSASGSKTTVISAVG
TIVKKAKQ
Sequence length 308
Interactions View interactions
Associated diseases
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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