Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
221150
Gene name Gene Name - the full gene name approved by the HGNC.
Spindle and kinetochore associated complex subunit 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SKA3
Synonyms (NCBI Gene) Gene synonyms aliases
C13orf3, RAMA1
Chromosome Chromosome number
13
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
13q12.11
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a component of the spindle and kinetochore-associated protein complex that regulates microtubule attachment to the kinetochores during mitosis. The encoded protein localizes to the outer kinetechore and may be required for normal chromos
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT052469 hsa-let-7a-5p CLASH 23622248
MIRT041438 hsa-miR-193b-3p CLASH 23622248
MIRT739086 hsa-miR-148b HITS-CLIP 33718276
MIRT739088 hsa-miR-148a HITS-CLIP 33718276
MIRT1350847 hsa-miR-1206 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000070 Process Mitotic sister chromatid segregation IMP 19289083
GO:0000278 Process Mitotic cell cycle IBA
GO:0000775 Component Chromosome, centromeric region IEA
GO:0000776 Component Kinetochore IBA
GO:0000776 Component Kinetochore IDA 20813266
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
619247 20262 ENSG00000165480
Protein
UniProt ID Q8IX90
Protein name Spindle and kinetochore-associated protein 3
Protein function Component of the SKA1 complex, a microtubule-binding subcomplex of the outer kinetochore that is essential for proper chromosome segregation (PubMed:19289083, PubMed:19360002, PubMed:23085020). The SKA1 complex is a direct component of the kinet
PDB 4AJ5
Family and domains
Sequence
MDPIRSFCGKLRSLASTLDCETARLQRALDGEESDFEDYPMRILYDLHSEVQTLKDDVNI
LLDKARLENQEGIDFIKATKVLMEKNSMDIMKIREYFQKYGYSPRVKKNSVHEQEAINSD
PELSNCENFQKTDVKDDLSDPPVASSCISEKSPRSPQLSDFGLERYIVSQVLPNPPQAVN
NYKEEPVIVTPPTKQSLVKVLKTPKCALKMDDFECVTPKLEHFGISEYTMCLNEDYTMGL
KNARNNKSEEAIDTESRLNDNVFATPSPIIQQLEKSDAEYTNSPLVPTFCTPGLKIPSTK
NSIALVSTNYPLSKTNSSSNDLEVEDRTSLVLNSDTCFENLTDPSSPTISSYENLLRTPT
PPEVTKIPEDILQLLSKYNSNLATPIAIKAVPPSKRFLKHGQNIRDVSNKEN
Sequence length 412
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
Oligodendroglioma Oligodendroglioma N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Associate 23496902, 32799774, 37180139
Carcinogenesis Associate 30402980, 35546682
Carcinoma Hepatocellular Associate 34045512
Cardiotoxicity Associate 34544967
Cholangiocarcinoma Associate 37821935
Chromosomal Instability Stimulate 27329586
Colorectal Neoplasms Associate 27329586
Drug Related Side Effects and Adverse Reactions Associate 34544967
Heart Failure Associate 34544967
Hypoxia Stimulate 37821935