Gene Gene information from NCBI Gene database.
Entrez ID 169981
Gene name Spindlin family member 3
Gene symbol SPIN3
Synonyms (NCBI Gene)
SPIN-3TDRD27bA445O16.1
Chromosome X
Chromosome location Xp11.21
miRNA miRNA information provided by mirtarbase database.
91
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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
7
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 identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
5
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ANDROGENETIC ALOPECIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HEPATITIS B VIRUS INFECTION GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HYPOGONADISM GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
NEUROTIC DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations