GOLGA8H (golgin A8 family member H)

Gene Gene information from NCBI Gene database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID 728498
Gene name Golgin A8 family member H
Gene symbol GOLGA8H
Synonyms (NCBI Gene)
GOLGA6L11
Chromosome 15
Chromosome location 15q13.2
miRNA miRNA information provided by mirtarbase database.
44
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all (44)
miRTarBase ID miRNA Experiments Reference
MIRT444014 hsa-miR-548u PAR-CLIP 22100165
MIRT444013 hsa-miR-7161-5p PAR-CLIP 22100165
MIRT444012 hsa-miR-8087 PAR-CLIP 22100165
MIRT444011 hsa-miR-4424 PAR-CLIP 22100165
MIRT444010 hsa-miR-4434 PAR-CLIP 22100165
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
6
Gene miRNA 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 miRNA Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P0CJ92
Protein name Golgin subfamily A member 8H
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15070 GOLGA2L5 226 → 374 Putative golgin subfamily A member 2-like protein 5 Coiled-coil
PF15070 GOLGA2L5 365 → 515 Putative golgin subfamily A member 2-like protein 5 Coiled-coil
PF19046 GM130_C 593 → 632 GM130 C-terminal binding motif Motif
Sequence 
MAEETQHNKLAAAKKKLKEYWQKNSPRVPAGANRNRKTNGSVPEKATSGGCQPPGDSATG
FHREGPTSSATLKDLESPCQERAVVLDSRSVEISQLKNTIKSLKQQKKQVEHQLEEEKKA
NNKKQKAKRVLEVQIQTLNIQKGKLNTDLYHMKRSLRYFEEKSKDLAVCLQHSLQRKGEL
ESVLSNVMATQKKKANQLSSRSKARTEWKLEQSMREEALLKVQLTQLKESFQQVQLERDE
CAEHLKGERARWQQRMRKMSQEICTLKKEKQQDMRRVEKLERSLSKLKNQMAEPLPPEPP
AVPSEVELQHLRKELERVAGELQAQVKKNQRISLLNQRQEERIQEQEERLRKQEERIQEQ
HKSLQQLAKPQSVFEEPNNENKNALQLEQQVKELQEKLGEEHLEAASQQNQQLTAQLSLM
ALPGEGHGGEHLDSEGEEAPRPMPSVPEDPESREAMSSFMDHLEEKADLSELVKKKELCF
IHHWRDRCHQKTHHLLSEPGGRAKDAALGGGHHQAGAQGGDEGEAAGAAADGIAAYSNYN
NGHRKFLAAAHNSADEPGPGAPAPQELGAADKHGDLCEVSLTSSAQGEAREDPLLDKPTA
QPIVQDHQEHPGLGSNCCVPLLCWAWLPRRRR
Sequence length 632
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Gene miRNA 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
EPILEPSY — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations