GOLGA8S (golgin A8 family member S)

Gene Gene information from NCBI Gene database.
Gene Gene ontology Other IDs Protein Associated diseases
Entrez ID 653061
Gene name Golgin A8 family member S
Gene symbol GOLGA8S
Synonyms (NCBI Gene)
-
Chromosome 15
Chromosome location 15q11.2
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
6
Gene Gene ontology Other IDs Protein Associated diseases
Show/Hide all (6)
GO ID Ontology Definition Evidence Reference
GO:0000137 Component Golgi cis cisterna IBA
GO:0005794 Component Golgi apparatus IEA
GO:0005801 Component Cis-Golgi network IBA
GO:0005801 Component Cis-Golgi network IEA
GO:0007030 Process Golgi organization IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
Gene Gene ontology Other IDs Protein Associated diseases
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
H3BPF8
Protein name Golgin subfamily A member 8S
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15070 GOLGA2L5 226 → 366 Putative golgin subfamily A member 2-like protein 5 Coiled-coil
PF15070 GOLGA2L5 371 → 517 Putative golgin subfamily A member 2-like protein 5 Coiled-coil
PF19046 GM130_C 586 → 625 GM130 C-terminal binding motif Motif
Sequence 
MAEETRQSKLAAAKRKLKEYWQRNSPGVPAGAKRNRKTNGSIHETATSGGCHSPGDSATG
IHGESPTSSATLKDLESPCQELAVVPDSRSVKVSQLKNTIKSLKQQKKQVVHQLEEEKKA
NNEKQKAERELEVQIQRLNIQKGKLNTDLYHTKRSLRYFEEESKDLAVRLQHSLQRKGEL
ERALSAVTATQKKKAERFSSRSKARTEWKLEQSMREQALLKAQLTQLKESLKEVQLERDE
YAEHLKGERARWQQRMRKMSQEVCSLKKEKKHDKYRVETLERSLSKLKNQMAEPLPPEPP
AVPSEAELQHLRKELERVAGALQAQVEYNQRISLLNEGQKERLREQQERLPEQEERLQQL
AEPQNSFKELNNENKSVLQLEQQVKELQEKLGKERLEAASQQKQQLTAQLSLMALPGEGD
GGGHLDSEGEEAPRPIPSIPQDLESREAMSSFMDHLEEKADLSELVKKQELRFIQYWQER
CHQKIHHLLSEPGGRAKDAALGGGHHQAGAQGGDEDEAAGAAADGIAAYSNYNNGHRKFL
AAAHNPADEPGPGAPAPQELGAADKHGDLCEVSLTSSAQGEAREDPLLDKPTAQPIVQDH
QEHPGLGNNCCVPFFCWAWLPRRRR
Sequence length 625
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Gene Gene ontology Other IDs Protein Associated diseases
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)
Show/Hide Unknown Diseases (1)
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
BIPOLAR DISORDER — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations