Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6665
Gene name Gene Name - the full gene name approved by the HGNC.
SRY-box transcription factor 15
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SOX15
Synonyms (NCBI Gene) Gene synonyms aliases
SOX20, SOX26, SOX27
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17p13.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after for
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT2336842 hsa-miR-1323 CLIP-seq
MIRT2336843 hsa-miR-200b CLIP-seq
MIRT2336844 hsa-miR-200c CLIP-seq
MIRT2336845 hsa-miR-374c CLIP-seq
MIRT2336846 hsa-miR-429 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IBA 21873635
GO:0000122 Process Negative regulation of transcription by RNA polymerase II ISS 17363903
GO:0000785 Component Chromatin ISA
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IBA 21873635
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601297 11196 ENSG00000129194
Protein
UniProt ID O60248
Protein name Transcription factor SOX-15 (Protein SOX-12) (Protein SOX-20) (SRY-box transcription factor 15)
Protein function Transcription factor that binds to DNA at the 5'-AACAATG-3' consensus sequence (By similarity). Acts as a transcriptional activator and repressor (By similarity). Binds synergistically with POU5F1 (OCT3/4) to gene promoters (By similarity). Bind
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00505 HMG_box 49 117 HMG (high mobility group) box Domain
Tissue specificity TISSUE SPECIFICITY: Widely expressed in fetal and adult tissues examined, highest level found in fetal spinal cord and adult brain and testis. {ECO:0000269|PubMed:8978787, ECO:0000269|PubMed:9880678}.
Sequence
MALPGSSQDQAWSLEPPAATAAASSSSGPQEREGAGSPAAPGTLPLEKVKRPMNAFMVWS
SAQRRQMAQQNPKMHNSEISKRLGAQWKLLDEDEKRPFVEEAKRLRARHLRDYPDYK
YRP
RRKAKSSGAGPSRCGQGRGNLASGGPLWGPGYATTQPSRGFGYRPPSYSTAYLPGSYGSS
HCKLEAPSPCSLPQSDPRLQGELLPTYTHYLPPGSPTPYNPPLAGAPMPLTHL
Sequence length 233
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Atrial fibrillation Atrial Fibrillation rs120074192, rs121908590, rs121908593, rs121434558, rs587776851, rs387906612, rs387906613, rs387906614, rs387906615, rs199472687, rs199472705, rs199473324, rs587777336, rs587777339, rs587777557
View all (6 more)
30061737
Unknown
Disease term Disease name Evidence References Source
Paroxysmal atrial fibrillation Paroxysmal atrial fibrillation 30061737 ClinVar
Associations from Text Mining
Disease Name Relationship Type References
Abnormalities Drug Induced Associate 36672963
Adenocarcinoma Associate 35328735
Campomelic Dysplasia Associate 36672963
Carcinoma Embryonal Associate 18182846
Cardiovascular Diseases Associate 36672963
Central Nervous System Diseases Associate 36672963
Endometrial Neoplasms Associate 27881125, 28821564, 30935961
Endometriosis Associate 27881125
Infertility Male Associate 36446526
Intellectual Disability Associate 36672963