GOLGA8M
gene geneOn this page
Summary
GOLGA8M (golgin A8 family member M, HGNC:44404) is a protein-coding gene on chromosome 15q13.1, encoding Golgin subfamily A member 8M (H3BSY2). It is a selective cancer dependency (DepMap: 14.5% of cell lines).
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 653720 — RefSeq curated summary.
At a glance
- Clinical variants (ClinVar): 12 total
- Cancer dependency (DepMap): dependent in 14.5% of screened cell lines
- MANE Select transcript:
NM_001282468
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:44404 |
| Approved symbol | GOLGA8M |
| Name | golgin A8 family member M |
| Location | 15q13.1 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000188626 |
| Ensembl biotype | protein_coding |
| Entrez | 653720 |
Gene structure
Transcript identifiers
Ensembl transcripts: 2 — 1 protein_coding, 1 protein_coding_CDS_not_defined
ENST00000563027, ENST00000563213
RefSeq mRNA: 1 — MANE Select: NM_001282468
NM_001282468
CCDS: CCDS61572
Canonical transcript exons
ENST00000563027 — 19 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001597346 | 28705483 | 28705739 |
| ENSE00001759101 | 28706116 | 28706203 |
| ENSE00002213610 | 28706399 | 28706506 |
| ENSE00002235947 | 28706613 | 28706699 |
| ENSE00002311899 | 28707953 | 28708037 |
| ENSE00002313715 | 28707748 | 28707857 |
| ENSE00002577222 | 28703842 | 28703917 |
| ENSE00002577898 | 28702465 | 28702562 |
| ENSE00002586034 | 28698583 | 28702129 |
| ENSE00002595393 | 28705159 | 28705227 |
| ENSE00002598353 | 28712276 | 28712421 |
| ENSE00002598481 | 28708126 | 28708173 |
| ENSE00002598874 | 28703319 | 28703410 |
| ENSE00002606367 | 28702214 | 28702369 |
| ENSE00002618297 | 28702645 | 28702745 |
| ENSE00002620954 | 28708375 | 28708413 |
| ENSE00003513022 | 28710487 | 28710606 |
| ENSE00003571383 | 28709267 | 28709347 |
| ENSE00003668175 | 28709529 | 28709588 |
Expression profiles
Bgee: expression breadth ubiquitous, 128 present calls, max score 86.93.
Top tissues by expression
133 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| sural nerve | UBERON:0015488 | 86.93 | gold quality |
| right lobe of thyroid gland | UBERON:0001119 | 86.73 | gold quality |
| thyroid gland | UBERON:0002046 | 85.13 | gold quality |
| left lobe of thyroid gland | UBERON:0001120 | 84.81 | gold quality |
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 83.39 | gold quality |
| left ovary | UBERON:0002119 | 74.32 | gold quality |
| right ovary | UBERON:0002118 | 73.51 | gold quality |
| ovary | UBERON:0000992 | 73.44 | gold quality |
| bone marrow cell | CL:0002092 | 72.81 | gold quality |
| subcutaneous adipose tissue | UBERON:0002190 | 71.64 | gold quality |
| adipose tissue | UBERON:0001013 | 71.31 | gold quality |
| right lobe of liver | UBERON:0001114 | 71.19 | gold quality |
| omental fat pad | UBERON:0010414 | 70.94 | gold quality |
| liver | UBERON:0002107 | 70.88 | gold quality |
| bone marrow | UBERON:0002371 | 69.61 | gold quality |
| left testis | UBERON:0004533 | 68.92 | gold quality |
| testis | UBERON:0000473 | 68.85 | gold quality |
| right testis | UBERON:0004534 | 68.77 | gold quality |
| thoracic mammary gland | UBERON:0005200 | 68.17 | gold quality |
| apex of heart | UBERON:0002098 | 67.30 | gold quality |
| tibial nerve | UBERON:0001323 | 65.06 | gold quality |
| endocervix | UBERON:0000458 | 64.88 | gold quality |
| right coronary artery | UBERON:0001625 | 64.82 | gold quality |
| pituitary gland | UBERON:0000007 | 64.70 | gold quality |
| descending thoracic aorta | UBERON:0002345 | 64.45 | gold quality |
| adenohypophysis | UBERON:0002196 | 64.29 | gold quality |
| right uterine tube | UBERON:0001302 | 63.01 | gold quality |
| placenta | UBERON:0001987 | 62.81 | gold quality |
| right atrium auricular region | UBERON:0006631 | 62.75 | gold quality |
| body of uterus | UBERON:0009853 | 62.61 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.98 |
Regulation
Is transcription factor: no
miRNA regulators (miRDB)
132 targeting GOLGA8M, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):
| miRNA | Max score | Avg score | miRNA target_count |
|---|---|---|---|
| HSA-MIR-4262 | 100.00 | 73.26 | 3931 |
| HSA-MIR-656-3P | 100.00 | 72.15 | 2788 |
| HSA-MIR-3646 | 100.00 | 73.56 | 5283 |
| HSA-MIR-4795-3P | 100.00 | 74.62 | 4024 |
| HSA-MIR-3662 | 99.99 | 73.82 | 5684 |
| HSA-MIR-4282 | 99.99 | 75.36 | 6408 |
| HSA-MIR-181A-5P | 99.99 | 72.96 | 2995 |
| HSA-MIR-181B-5P | 99.99 | 72.97 | 2996 |
| HSA-MIR-181C-5P | 99.99 | 72.95 | 2996 |
| HSA-MIR-181D-5P | 99.99 | 73.04 | 2997 |
| HSA-MIR-4531 | 99.99 | 69.70 | 3181 |
| HSA-MIR-6077 | 99.99 | 68.04 | 2299 |
| HSA-MIR-520D-5P | 99.98 | 73.34 | 4883 |
| HSA-MIR-524-5P | 99.98 | 73.43 | 4882 |
| HSA-MIR-4482-3P | 99.98 | 72.50 | 3147 |
| HSA-LET-7F-2-3P | 99.98 | 70.98 | 2588 |
| HSA-MIR-1185-1-3P | 99.98 | 71.04 | 2593 |
| HSA-MIR-1185-2-3P | 99.98 | 71.04 | 2593 |
| HSA-MIR-32-5P | 99.98 | 75.21 | 1964 |
| HSA-MIR-92A-3P | 99.98 | 75.21 | 1960 |
| HSA-MIR-92B-3P | 99.98 | 75.25 | 1955 |
| HSA-MIR-25-3P | 99.98 | 74.60 | 1817 |
| HSA-MIR-363-3P | 99.98 | 74.72 | 1821 |
| HSA-MIR-367-3P | 99.98 | 74.83 | 1819 |
| HSA-MIR-607 | 99.97 | 73.62 | 5593 |
| HSA-MIR-3148 | 99.97 | 75.06 | 6478 |
| HSA-MIR-493-5P | 99.96 | 72.47 | 2382 |
| HSA-MIR-3910 | 99.95 | 71.13 | 2227 |
| HSA-LET-7C-3P | 99.95 | 73.42 | 2862 |
| HSA-MIR-144-3P | 99.94 | 73.98 | 2698 |
Functional genomics
DepMap (CRISPR cell-line fitness): dependent in 14.5% of screened cell lines.
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), GOLGA8G (ENSG00000183629), GOLGA8R (ENSG00000186399), GOLGA8O (ENSG00000206127), GOLGA6B (ENSG00000215186), GOLGA8B (ENSG00000215252), GOLGA8N (ENSG00000232653), GOLGA8K (ENSG00000249931), GOLGA8T (ENSG00000261247), GOLGA8S (ENSG00000261739), GOLGA8H (ENSG00000261794)
Protein
Protein identifiers
Golgin subfamily A member 8M — H3BSY2 (reviewed: H3BSY2)
All UniProt accessions (1): H3BSY2
UniProt curated annotations — full annotation on UniProt →
Similarity. Belongs to the GOLGA8 family.
Isoforms (3)
| UniProt ID | Names | Canonical? |
|---|---|---|
| H3BSY2-1 | 1 | yes |
| H3BSY2-2 | 2 | |
| H3BSY2-3 | 3 |
RefSeq proteins (1): NP_001269397* (*=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 (15 total): splice variant 5, region of interest 4, compositionally biased region 3, coiled-coil region 2, chain 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-H3BSY2-F1 | 67.68 | 0.26 |
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 36 (showing top):
chr15q13, GOBP_ENDOMEMBRANE_SYSTEM_ORGANIZATION, GOBP_GOLGI_ORGANIZATION, GOCC_GOLGI_STACK, GOCC_GOLGI_CISTERNA, GOCC_CIS_GOLGI_NETWORK, GOCC_GOLGI_CISTERNA_MEMBRANE, GOCC_ORGANELLE_SUBCOMPARTMENT, GOCC_GOLGI_CIS_CISTERNA, MIR3662, MIR520D_5P, MIR524_5P, MIR4262, MIR181A_5P_MIR181B_5P, MIR181D_5P
GO Biological Process (1): Golgi organization (GO:0007030)
GO Molecular Function (1): protein binding (GO:0005515)
GO Cellular Component (4): Golgi cis cisterna (GO:0000137), cis-Golgi network (GO:0005801), Golgi cisterna membrane (GO:0032580), Golgi apparatus (GO:0005794)
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| Golgi cisterna | 2 |
| intracellular membrane-bounded organelle | 2 |
| organelle organization | 1 |
| endomembrane system organization | 1 |
| binding | 1 |
| Golgi apparatus | 1 |
| organelle membrane | 1 |
| cytoplasm | 1 |
| endomembrane system | 1 |
Protein interactions and networks
STRING
176 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| GOLGA8M | SMIM31 | A0A1B0GVY4 | 665 |
| GOLGA8M | LRRC9 | Q6ZRR7 | 621 |
| GOLGA8M | UROC1 | Q96N76 | 506 |
| GOLGA8M | POTEB3 | A0JP26 | 476 |
| GOLGA8M | ARPC1A | Q92747 | 397 |
| GOLGA8M | OR4M2 | Q8NGB6 | 367 |
| GOLGA8M | HHLA1 | C9JL84 | 357 |
| GOLGA8M | APBA2 | Q99767 | 333 |
| GOLGA8M | SLC39A8 | Q9C0K1 | 290 |
| GOLGA8M | UGT2B10 | P36537 | 288 |
| GOLGA8M | OC90 | Q02509 | 269 |
| GOLGA8M | ITSN2 | Q9NZM3 | 238 |
| GOLGA8M | CDC45 | O75419 | 232 |
| GOLGA8M | HERC2 | O95714 | 224 |
| GOLGA8M | CHRFAM7A | Q494W8 | 220 |
IntAct
0 interactions, top by confidence:
BioGRID (3): GOLGA8M (Proximity Label-MS), TBRG4 (Cross-Linking-MS (XL-MS)), UBXN1 (Cross-Linking-MS (XL-MS))
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
12 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 0 |
| Likely benign | 12 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
2787 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 15:28702210:TCACC:T | donor_loss | 1.0000 |
| 15:28702211:CACCA:C | donor_loss | 1.0000 |
| 15:28702212:A:AC | donor_gain | 1.0000 |
| 15:28702212:ACC:A | donor_loss | 1.0000 |
| 15:28702213:C:CC | donor_gain | 1.0000 |
| 15:28702213:CCA:C | donor_gain | 1.0000 |
| 15:28702365:TTCAC:T | acceptor_gain | 1.0000 |
| 15:28702366:TCAC:T | acceptor_gain | 1.0000 |
| 15:28702367:CAC:C | acceptor_gain | 1.0000 |
| 15:28702367:CACC:C | acceptor_gain | 1.0000 |
| 15:28702368:AC:A | acceptor_gain | 1.0000 |
| 15:28702369:CC:C | acceptor_gain | 1.0000 |
| 15:28702370:C:CC | acceptor_gain | 1.0000 |
| 15:28702463:A:T | donor_loss | 1.0000 |
| 15:28702464:CC:C | donor_loss | 1.0000 |
| 15:28702476:C:CA | donor_gain | 1.0000 |
| 15:28702643:A:AC | donor_gain | 1.0000 |
| 15:28702644:C:CC | donor_gain | 1.0000 |
| 15:28703314:CTCA:C | donor_loss | 1.0000 |
| 15:28703315:TCA:T | donor_loss | 1.0000 |
| 15:28703316:CACCA:C | donor_loss | 1.0000 |
| 15:28703317:A:AC | donor_gain | 1.0000 |
| 15:28703317:ACCA:A | donor_loss | 1.0000 |
| 15:28703318:C:CC | donor_gain | 1.0000 |
| 15:28703327:C:A | donor_gain | 1.0000 |
| 15:28703412:T:C | acceptor_loss | 1.0000 |
| 15:28703869:G:C | donor_gain | 1.0000 |
| 15:28704055:T:TA | donor_gain | 1.0000 |
| 15:28704068:G:C | donor_gain | 1.0000 |
| 15:28704080:G:C | donor_gain | 1.0000 |
AlphaMissense
4179 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 15:28705649:A:G | L322P | 0.864 |
| 15:28709289:A:G | L96P | 0.823 |
| 15:28702299:G:C | F546L | 0.815 |
| 15:28702299:G:T | F546L | 0.815 |
| 15:28702301:A:G | F546L | 0.815 |
| 15:28705670:A:G | L315P | 0.809 |
| 15:28706429:C:A | W252C | 0.807 |
| 15:28706429:C:G | W252C | 0.807 |
| 15:28707830:A:G | L170P | 0.804 |
| 15:28702674:G:C | F480L | 0.802 |
| 15:28702674:G:T | F480L | 0.802 |
| 15:28702676:A:G | F480L | 0.802 |
| 15:28712287:C:G | A13P | 0.794 |
| 15:28706431:A:G | W252R | 0.778 |
| 15:28706431:A:T | W252R | 0.778 |
| 15:28708030:A:G | L135P | 0.777 |
| 15:28712282:C:A | K14N | 0.774 |
| 15:28712282:C:G | K14N | 0.774 |
| 15:28705682:A:G | L311P | 0.770 |
| 15:28710601:T:A | K18N | 0.767 |
| 15:28710601:T:G | K18N | 0.767 |
| 15:28710605:A:G | L17S | 0.759 |
| 15:28708382:A:G | L114P | 0.748 |
| 15:28701987:A:C | F622L | 0.735 |
| 15:28701987:A:T | F622L | 0.735 |
| 15:28701989:A:G | F622L | 0.735 |
| 15:28709268:A:G | L103S | 0.732 |
| 15:28706417:C:A | M256I | 0.722 |
| 15:28706417:C:G | M256I | 0.722 |
| 15:28706417:C:T | M256I | 0.722 |
dbSNP variants (sampled 300 via entrez): RS1000124177 (15:28701707 G>A), RS1000496296 (15:28704604 G>A,C), RS1000569765 (15:28704357 T>G), RS1000626697 (15:28698738 C>G,T), RS1000713115 (15:28710132 C>A,T), RS1000808933 (15:28699039 G>T), RS1000840244 (15:28715190 A>G), RS1001078427 (15:28710813 T>G), RS1001797580 (15:28698261 T>A), RS1001887628 (15:28709734 C>G,T), RS1001897859 (15:28703947 T>C,G), RS1001976716 (15:28698660 T>C), RS1002054150 (15:28714784 C>A,G), RS1002148917 (15:28715083 G>C,T), RS1002529927 (15:28709503 C>G)
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
0 associations (top):
Drugs & pharmacology
Drug and pharmacology data
Is drug target: no
PharmGKB: 1 entry (VIP=true, CPIC=false)
CTD chemical–gene interactions
2 total (human), top 2 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| Benzo(a)pyrene | decreases expression | 1 |
| Okadaic Acid | decreases 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.