Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
169981
Gene name Gene Name - the full gene name approved by the HGNC.
Spindlin family member 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SPIN3
Synonyms (NCBI Gene) Gene synonyms aliases
SPIN-3, TDRD27, bA445O16.1
Chromosome Chromosome number
X
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
Xp11.21
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT023137 hsa-miR-124-3p Proteomics;Microarray 18668037
MIRT645472 hsa-miR-6777-3p HITS-CLIP 23824327
MIRT645471 hsa-miR-6814-5p HITS-CLIP 23824327
MIRT645470 hsa-miR-4301 HITS-CLIP 23824327
MIRT645469 hsa-miR-130b-5p HITS-CLIP 23824327
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 28514442, 29061846, 33961781
GO:0005654 Component Nucleoplasm IBA
GO:0005829 Component Cytosol IBA
GO:0006325 Process Chromatin organization IEA
GO:0006355 Process Regulation of DNA-templated transcription IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID Q5JUX0
Protein name Spindlin-3 (Spindlin-like protein 3) (SPIN-3)
Protein function Exhibits H3K4me3-binding activity.
PDB 5A1H
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02513 Spin-Ssty 50 99 Spin/Ssty Family Repeat
PF02513 Spin-Ssty 129 178 Spin/Ssty Family Repeat
PF02513 Spin-Ssty 210 255 Spin/Ssty Family Repeat
Sequence
MKTPFGKAAAGQRSRTGAGHGSVSVTMIKRKAAHKKHRSRPTSQPRGNIVGCRIQHGWKD
GDEPLTQWKGTVLDQVPVNPSLYLIKYDGFDCVYGLELH
RDERVSSLEVLPNRVASSRIS
DTHLAEIMVGKAVEHIFETEEGSKNEWRGMVLAQAPVMNTWFYITYEKDPVLYMYQLLDD
YKDGDLRILQDSNDSPLAEREPGEVIDSLVGKQVEYAKDDGSKRTGMVIHQVEAKPSVYF
IKFDDDFHIYVYDLV
KTS
Sequence length 258
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Hypogonadism Hypogonadism N/A N/A GWAS
Neuroticism Neuroticism N/A N/A GWAS
Systemic lupus erythematosus Systemic lupus erythematosus N/A N/A GWAS