GOLGA8G
gene geneOn this page
Also known as DKFZp434K052
Summary
GOLGA8G (golgin A8 family member G, HGNC:25328) is a protein-coding gene on chromosome 15q13.1, encoding Golgin subfamily A member 8G (P0DX53).
Predicted to be involved in Golgi organization. Predicted to be located in Golgi apparatus. Predicted to be active in Golgi cis cisterna; Golgi cisterna membrane; and cis-Golgi network.
Source: NCBI Gene 283768 — RefSeq curated summary.
At a glance
- GWAS associations: 1
- Clinical variants (ClinVar): 1 total
- MANE Select transcript:
NM_001350919
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:25328 |
| Approved symbol | GOLGA8G |
| Name | golgin A8 family member G |
| Location | 15q13.1 |
| Locus type | gene with protein product |
| Status | Approved |
| Aliases | DKFZp434K052 |
| Ensembl gene | ENSG00000183629 |
| Ensembl biotype | protein_coding |
| Entrez | 283768 |
Gene structure
Transcript identifiers
Ensembl transcripts: 8 — 7 retained_intron, 1 protein_coding
ENST00000382949, ENST00000524859, ENST00000525590, ENST00000561497, ENST00000562627, ENST00000568534, ENST00000569308, ENST00000570018
RefSeq mRNA: 3 — MANE Select: NM_001350919
NM_001350919, NM_001368078, NM_001368080
CCDS: CCDS86439
Canonical transcript exons
ENST00000525590 — 19 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001655749 | 28528886 | 28528933 |
| ENSE00001730921 | 28529207 | 28529245 |
| ENSE00002603788 | 28519611 | 28522757 |
| ENSE00003458494 | 28526902 | 28526989 |
| ENSE00003476031 | 28522843 | 28522995 |
| ENSE00003508519 | 28530100 | 28530180 |
| ENSE00003528127 | 28523085 | 28523185 |
| ENSE00003537410 | 28527185 | 28527292 |
| ENSE00003545668 | 28528508 | 28528617 |
| ENSE00003547131 | 28526255 | 28526511 |
| ENSE00003581121 | 28532826 | 28532971 |
| ENSE00003587272 | 28523943 | 28524034 |
| ENSE00003594757 | 28523268 | 28523368 |
| ENSE00003598116 | 28530364 | 28530423 |
| ENSE00003636710 | 28531009 | 28531128 |
| ENSE00003665792 | 28525919 | 28525987 |
| ENSE00003670326 | 28524472 | 28524547 |
| ENSE00003680072 | 28527399 | 28527488 |
| ENSE00003685356 | 28528713 | 28528797 |
Expression profiles
Bgee: expression breadth broad, 81 present calls, max score 87.60.
Top tissues by expression
108 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| right testis | UBERON:0004534 | 87.60 | gold quality |
| left testis | UBERON:0004533 | 87.43 | gold quality |
| testis | UBERON:0000473 | 86.39 | gold quality |
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 79.40 | gold quality |
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 74.98 | gold quality |
| stromal cell of endometrium | CL:0002255 | 58.52 | gold quality |
| putamen | UBERON:0001874 | 53.97 | gold quality |
| cortical plate | UBERON:0005343 | 50.35 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 48.54 | gold quality |
| caudate nucleus | UBERON:0001873 | 45.72 | gold quality |
| sural nerve | UBERON:0015488 | 44.97 | gold quality |
| cortex of kidney | UBERON:0001225 | 44.69 | gold quality |
| prefrontal cortex | UBERON:0000451 | 44.13 | silver quality |
| liver | UBERON:0002107 | 43.37 | silver quality |
| right coronary artery | UBERON:0001625 | 43.27 | silver quality |
| urinary bladder | UBERON:0001255 | 43.25 | gold quality |
| right lobe of liver | UBERON:0001114 | 43.11 | silver quality |
| left lobe of thyroid gland | UBERON:0001120 | 42.34 | silver quality |
| vermiform appendix | UBERON:0001154 | 42.33 | gold quality |
| right lobe of thyroid gland | UBERON:0001119 | 42.18 | gold quality |
| ectocervix | UBERON:0012249 | 41.77 | gold quality |
| thyroid gland | UBERON:0002046 | 41.66 | silver quality |
| right atrium auricular region | UBERON:0006631 | 41.57 | gold quality |
| body of pancreas | UBERON:0001150 | 41.52 | silver quality |
| right adrenal gland cortex | UBERON:0035827 | 41.36 | gold quality |
| nucleus accumbens | UBERON:0001882 | 41.05 | gold quality |
| duodenum | UBERON:0002114 | 40.87 | gold quality |
| frontal cortex | UBERON:0001870 | 40.37 | silver quality |
| muscle of leg | UBERON:0001383 | 40.36 | gold quality |
| primary visual cortex | UBERON:0002436 | 40.36 | silver quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.49 |
Regulation
Is transcription factor: no
Cross-species orthologs
5 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| danio_rerio | golga2 | ENSDARG00000063197 |
| mus_musculus | Golga2 | ENSMUSG00000002546 |
| rattus_norvegicus | Golga2l1 | ENSRNOG00000050262 |
| drosophila_melanogaster | GM130 | FBGN0034697 |
| caenorhabditis_elegans | WBGENE00018017 |
Paralogs (18): GOLGA6D (ENSG00000140478), GOLGA8F (ENSG00000153684), GOLGA6A (ENSG00000159289), GOLGA2 (ENSG00000167110), GOLGA6C (ENSG00000167195), GOLGA8A (ENSG00000175265), GOLGA8Q (ENSG00000178115), GOLGA8J (ENSG00000179938), GOLGA8R (ENSG00000186399), GOLGA8M (ENSG00000188626), GOLGA8O (ENSG00000206127), GOLGA6B (ENSG00000215186), GOLGA8B (ENSG00000215252), GOLGA8N (ENSG00000232653), GOLGA8K (ENSG00000249931), GOLGA8T (ENSG00000261247), GOLGA8S (ENSG00000261739), GOLGA8H (ENSG00000261794)
Protein
Protein identifiers
Golgin subfamily A member 8G — P0DX53 (reviewed: P0DX53)
All UniProt accessions (2): P0DX53, A0A0G2JP48
UniProt curated annotations — full annotation on UniProt →
Miscellaneous. May be produced at very low levels due to a premature stop codon in the mRNA, leading to nonsense-mediated mRNA decay. May be produced at very low levels due to a premature stop codon in the mRNA, leading to nonsense-mediated mRNA decay.
Similarity. Belongs to the GOLGA8 family.
Isoforms (3)
| UniProt ID | Names | Canonical? |
|---|---|---|
| P0DX53-1 | 1 | yes |
| P0DX53-4 | 4 | |
| P0DX53-5 | 5 |
RefSeq proteins (3): NP_001337848, NP_001355007, NP_001355009 (=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR024858 | GOLGA | Family |
| IPR043937 | GOLGA_C | Conserved_site |
| IPR043976 | GOLGA_cons_dom | Domain |
Pfam: PF15070, PF19046
UniProt features (20 total): region of interest 6, compositionally biased region 5, splice variant 4, coiled-coil region 3, chain 1, sequence conflict 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-P0DX53-F1 | 69.25 | 0.39 |
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 16 (showing top):
chr15q13, NAKAMURA_TUMOR_ZONE_PERIPHERAL_VS_CENTRAL_DN, AACTGGA_MIR145, GOCC_CIS_GOLGI_NETWORK, KIM_WT1_TARGETS_DN, WILCOX_RESPONSE_TO_PROGESTERONE_UP, CAGTATT_MIR200B_MIR200C_MIR429, CTACTGT_MIR199A, MEBARKI_HCC_PROGENITOR_WNT_UP, MEBARKI_HCC_PROGENITOR_WNT_UP_CTNNB1_DEPENDENT, MEBARKI_HCC_PROGENITOR_WNT_UP_BLOCKED_BY_FZD8CRD, MEBARKI_HCC_PROGENITOR_WNT_UP_CTNNB1_DEPENDENT_BLOCKED_BY_FZD8CRD, TTGCCAA_MIR182, GTGCAAT_MIR25_MIR32_MIR92_MIR363_MIR367, TGAATGT_MIR181A_MIR181B_MIR181C_MIR181D
GO Biological Process (0):
GO Molecular Function (1): protein binding (GO:0005515)
GO Cellular Component (2): cis-Golgi network (GO:0005801), Golgi apparatus (GO:0005794)
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| intracellular membrane-bounded organelle | 2 |
| binding | 1 |
| Golgi apparatus | 1 |
| cytoplasm | 1 |
| endomembrane system | 1 |
Protein interactions and networks
STRING
0 interactions, top by confidence (×1000):
IntAct
2 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| GOLGA8G | GOLGA8J | psi-mi:“MI:0914”(association) | 0.350 |
ESM2 similar proteins: A2AHC3, A2AMT1, A6NCC3, A6NN73, D3Z8E6, D6RF30, E7F5E1, H3BPF8, H3BQL2, H3BSY2, O15061, O35668, P0DX52, P0DX53, P53814, P54256, P54257, P62025, P97434, Q02435, Q06002, Q06637, Q0D2H9, Q0VF96, Q12934, Q3UHU5, Q3V0F0, Q5DU05, Q5T5Y3, Q5TF21, Q60664, Q62627, Q63312, Q6AW69, Q6NZL0, Q6PHN1, Q6WCQ1, Q70IV5, Q80VC9, Q80Y56
Diamond homologs: A0A1B0GV03, A1IH00, A6NC78, A6NCC3, A6NDK9, A6NDN3, A6NEF3, A6NEM1, A6NI86, A6NN73, A7E2F4, A8MQT2, A8MZA4, F8WBI6, H0YKK7, H0YM25, H3BPF8, H3BSY2, H3BV12, I6L899, P0CG33, P0CJ92, P0DX00, P0DX01, P0DX02, P0DX52, P0DX53, Q08379, Q62839, Q8N7Z2, Q8N9W4, Q921M4, Q9NYA3, A6NMD2, D6RF30, H3BQL2, Q0D2H9, Q9HBQ8
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
1 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 0 |
| Likely benign | 1 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
2593 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 15:28522840:CACCA:C | donor_loss | 1.0000 |
| 15:28522841:A:AC | donor_gain | 1.0000 |
| 15:28522841:A:T | donor_loss | 1.0000 |
| 15:28522841:ACCAC:A | donor_gain | 1.0000 |
| 15:28522842:C:CC | donor_gain | 1.0000 |
| 15:28522842:CCA:C | donor_gain | 1.0000 |
| 15:28522842:CCACC:C | donor_gain | 1.0000 |
| 15:28522991:TTCAC:T | acceptor_gain | 1.0000 |
| 15:28522992:TCAC:T | acceptor_gain | 1.0000 |
| 15:28522993:CAC:C | acceptor_gain | 1.0000 |
| 15:28522993:CACC:C | acceptor_gain | 1.0000 |
| 15:28522994:AC:A | acceptor_gain | 1.0000 |
| 15:28522995:CC:C | acceptor_gain | 1.0000 |
| 15:28522995:CCTG:C | acceptor_loss | 1.0000 |
| 15:28522996:C:CA | acceptor_loss | 1.0000 |
| 15:28522996:C:CC | acceptor_gain | 1.0000 |
| 15:28523080:TCTA:T | donor_loss | 1.0000 |
| 15:28523081:CTAC:C | donor_loss | 1.0000 |
| 15:28523082:TACCT:T | donor_loss | 1.0000 |
| 15:28523083:ACCT:A | donor_loss | 1.0000 |
| 15:28523096:C:CA | donor_gain | 1.0000 |
| 15:28523181:CTTTC:C | acceptor_gain | 1.0000 |
| 15:28523263:CTCA:C | donor_gain | 1.0000 |
| 15:28523266:A:AC | donor_gain | 1.0000 |
| 15:28523267:C:CA | donor_gain | 1.0000 |
| 15:28523267:CTG:C | donor_gain | 1.0000 |
| 15:28523267:CTGA:C | donor_gain | 1.0000 |
| 15:28523267:CTGAT:C | donor_gain | 1.0000 |
| 15:28523290:A:AC | donor_gain | 1.0000 |
| 15:28523291:C:CC | donor_gain | 1.0000 |
AlphaMissense
4259 scored. Top likely-pathogenic:
dbSNP variants (sampled 300 via entrez): RS1000122938 (15:28533729 C>T), RS1000237674 (15:28532845 A>G), RS1001337827 (15:28531952 A>G), RS1001450788 (15:28531321 A>G), RS1003122738 (15:28519153 G>A), RS1003417812 (15:28520091 G>A), RS1006029503 (15:28526156 C>G,T), RS1007147800 (15:28523622 C>T), RS1007263787 (15:28520374 A>G), RS1009259774 (15:28520230 T>C), RS1010150317 (15:28533438 G>A), RS1010210943 (15:28531519 T>A), RS1010679738 (15:28532073 G>C), RS1012237377 (15:28522241 C>T), RS1016091987 (15:28531302 GA>G,GAA)
Disease associations
OMIM: gene `` | disease phenotypes:
GenCC curated gene-disease
Mondo (0):
Orphanet (0):
HPO phenotypes
0 total (0 of 0 shown, HPO-id order):
GWAS associations
1 associations (top):
| Study | Trait | p-value |
|---|---|---|
| GCST009391_1967 | Metabolite levels | 1.000000e-06 |
EFO canonical traits (1, from GWAS)
| EFO ID | Trait name |
|---|---|
| EFO:0010541 | trimethylamine-N-oxide measurement |
Drugs & pharmacology
Drug and pharmacology data
Is drug target: no
PharmGKB: 1 entry (VIP=true, CPIC=false)
CTD chemical–gene interactions
1 total (human), top 1 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| Progesterone | increases expression | 1 |
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.