GOLGA8M

gene
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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

FieldValue
HGNC IDHGNC:44404
Approved symbolGOLGA8M
Namegolgin A8 family member M
Location15q13.1
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000188626
Ensembl biotypeprotein_coding
Entrez653720

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

ExonStartEnd
ENSE000015973462870548328705739
ENSE000017591012870611628706203
ENSE000022136102870639928706506
ENSE000022359472870661328706699
ENSE000023118992870795328708037
ENSE000023137152870774828707857
ENSE000025772222870384228703917
ENSE000025778982870246528702562
ENSE000025860342869858328702129
ENSE000025953932870515928705227
ENSE000025983532871227628712421
ENSE000025984812870812628708173
ENSE000025988742870331928703410
ENSE000026063672870221428702369
ENSE000026182972870264528702745
ENSE000026209542870837528708413
ENSE000035130222871048728710606
ENSE000035713832870926728709347
ENSE000036681752870952928709588

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):

TissueAnatomy IDExpression scoreQuality
sural nerveUBERON:001548886.93gold quality
right lobe of thyroid glandUBERON:000111986.73gold quality
thyroid glandUBERON:000204685.13gold quality
left lobe of thyroid glandUBERON:000112084.81gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047383.39gold quality
left ovaryUBERON:000211974.32gold quality
right ovaryUBERON:000211873.51gold quality
ovaryUBERON:000099273.44gold quality
bone marrow cellCL:000209272.81gold quality
subcutaneous adipose tissueUBERON:000219071.64gold quality
adipose tissueUBERON:000101371.31gold quality
right lobe of liverUBERON:000111471.19gold quality
omental fat padUBERON:001041470.94gold quality
liverUBERON:000210770.88gold quality
bone marrowUBERON:000237169.61gold quality
left testisUBERON:000453368.92gold quality
testisUBERON:000047368.85gold quality
right testisUBERON:000453468.77gold quality
thoracic mammary glandUBERON:000520068.17gold quality
apex of heartUBERON:000209867.30gold quality
tibial nerveUBERON:000132365.06gold quality
endocervixUBERON:000045864.88gold quality
right coronary arteryUBERON:000162564.82gold quality
pituitary glandUBERON:000000764.70gold quality
descending thoracic aortaUBERON:000234564.45gold quality
adenohypophysisUBERON:000219664.29gold quality
right uterine tubeUBERON:000130263.01gold quality
placentaUBERON:000198762.81gold quality
right atrium auricular regionUBERON:000663162.75gold quality
body of uterusUBERON:000985362.61gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no0.98

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):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-4262100.0073.263931
HSA-MIR-656-3P100.0072.152788
HSA-MIR-3646100.0073.565283
HSA-MIR-4795-3P100.0074.624024
HSA-MIR-366299.9973.825684
HSA-MIR-428299.9975.366408
HSA-MIR-181A-5P99.9972.962995
HSA-MIR-181B-5P99.9972.972996
HSA-MIR-181C-5P99.9972.952996
HSA-MIR-181D-5P99.9973.042997
HSA-MIR-453199.9969.703181
HSA-MIR-607799.9968.042299
HSA-MIR-520D-5P99.9873.344883
HSA-MIR-524-5P99.9873.434882
HSA-MIR-4482-3P99.9872.503147
HSA-LET-7F-2-3P99.9870.982588
HSA-MIR-1185-1-3P99.9871.042593
HSA-MIR-1185-2-3P99.9871.042593
HSA-MIR-32-5P99.9875.211964
HSA-MIR-92A-3P99.9875.211960
HSA-MIR-92B-3P99.9875.251955
HSA-MIR-25-3P99.9874.601817
HSA-MIR-363-3P99.9874.721821
HSA-MIR-367-3P99.9874.831819
HSA-MIR-60799.9773.625593
HSA-MIR-314899.9775.066478
HSA-MIR-493-5P99.9672.472382
HSA-MIR-391099.9571.132227
HSA-LET-7C-3P99.9573.422862
HSA-MIR-144-3P99.9473.982698

Functional genomics

DepMap (CRISPR cell-line fitness): dependent in 14.5% of screened cell lines.

Cross-species orthologs

5 orthologs

OrganismSymbolGene ID
danio_reriogolga2ENSDARG00000063197
mus_musculusGolga2ENSMUSG00000002546
rattus_norvegicusGolga2l1ENSRNOG00000050262
drosophila_melanogasterGM130FBGN0034697
caenorhabditis_elegansWBGENE00018017

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 8MH3BSY2 (reviewed: H3BSY2)

All UniProt accessions (1): H3BSY2

UniProt curated annotations — full annotation on UniProt →

Similarity. Belongs to the GOLGA8 family.

Isoforms (3)

UniProt IDNamesCanonical?
H3BSY2-11yes
H3BSY2-22
H3BSY2-33

RefSeq proteins (1): NP_001269397* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR024858GOLGAFamily
IPR043937GOLGA_CConserved_site
IPR043976GOLGA_cons_domDomain

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)

ModelpLDDTFraction very-high
AF-H3BSY2-F167.680.26

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:

CategoryTerms
Golgi cisterna2
intracellular membrane-bounded organelle2
organelle organization1
endomembrane system organization1
binding1
Golgi apparatus1
organelle membrane1
cytoplasm1
endomembrane system1

Protein interactions and networks

STRING

176 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
GOLGA8MSMIM31A0A1B0GVY4665
GOLGA8MLRRC9Q6ZRR7621
GOLGA8MUROC1Q96N76506
GOLGA8MPOTEB3A0JP26476
GOLGA8MARPC1AQ92747397
GOLGA8MOR4M2Q8NGB6367
GOLGA8MHHLA1C9JL84357
GOLGA8MAPBA2Q99767333
GOLGA8MSLC39A8Q9C0K1290
GOLGA8MUGT2B10P36537288
GOLGA8MOC90Q02509269
GOLGA8MITSN2Q9NZM3238
GOLGA8MCDC45O75419232
GOLGA8MHERC2O95714224
GOLGA8MCHRFAM7AQ494W8220

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):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance0
Likely benign12
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

2787 predictions. Top by Δscore:

VariantEffectΔscore
15:28702210:TCACC:Tdonor_loss1.0000
15:28702211:CACCA:Cdonor_loss1.0000
15:28702212:A:ACdonor_gain1.0000
15:28702212:ACC:Adonor_loss1.0000
15:28702213:C:CCdonor_gain1.0000
15:28702213:CCA:Cdonor_gain1.0000
15:28702365:TTCAC:Tacceptor_gain1.0000
15:28702366:TCAC:Tacceptor_gain1.0000
15:28702367:CAC:Cacceptor_gain1.0000
15:28702367:CACC:Cacceptor_gain1.0000
15:28702368:AC:Aacceptor_gain1.0000
15:28702369:CC:Cacceptor_gain1.0000
15:28702370:C:CCacceptor_gain1.0000
15:28702463:A:Tdonor_loss1.0000
15:28702464:CC:Cdonor_loss1.0000
15:28702476:C:CAdonor_gain1.0000
15:28702643:A:ACdonor_gain1.0000
15:28702644:C:CCdonor_gain1.0000
15:28703314:CTCA:Cdonor_loss1.0000
15:28703315:TCA:Tdonor_loss1.0000
15:28703316:CACCA:Cdonor_loss1.0000
15:28703317:A:ACdonor_gain1.0000
15:28703317:ACCA:Adonor_loss1.0000
15:28703318:C:CCdonor_gain1.0000
15:28703327:C:Adonor_gain1.0000
15:28703412:T:Cacceptor_loss1.0000
15:28703869:G:Cdonor_gain1.0000
15:28704055:T:TAdonor_gain1.0000
15:28704068:G:Cdonor_gain1.0000
15:28704080:G:Cdonor_gain1.0000

AlphaMissense

4179 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
15:28705649:A:GL322P0.864
15:28709289:A:GL96P0.823
15:28702299:G:CF546L0.815
15:28702299:G:TF546L0.815
15:28702301:A:GF546L0.815
15:28705670:A:GL315P0.809
15:28706429:C:AW252C0.807
15:28706429:C:GW252C0.807
15:28707830:A:GL170P0.804
15:28702674:G:CF480L0.802
15:28702674:G:TF480L0.802
15:28702676:A:GF480L0.802
15:28712287:C:GA13P0.794
15:28706431:A:GW252R0.778
15:28706431:A:TW252R0.778
15:28708030:A:GL135P0.777
15:28712282:C:AK14N0.774
15:28712282:C:GK14N0.774
15:28705682:A:GL311P0.770
15:28710601:T:AK18N0.767
15:28710601:T:GK18N0.767
15:28710605:A:GL17S0.759
15:28708382:A:GL114P0.748
15:28701987:A:CF622L0.735
15:28701987:A:TF622L0.735
15:28701989:A:GF622L0.735
15:28709268:A:GL103S0.732
15:28706417:C:AM256I0.722
15:28706417:C:GM256I0.722
15:28706417:C:TM256I0.722

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.

ChemicalActions (top 5)PubMed papers
Benzo(a)pyrenedecreases expression1
Okadaic Aciddecreases expression1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.