GOLGA6L26

gene
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Summary

GOLGA6L26 (golgin A6 family like 26, HGNC:56306) is a protein-coding gene on chromosome 15q11.2, encoding Golgin subfamily A member 6-like protein 26 (P0DX02).

At a glance

  • MANE Select transcript: NM_001382446

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:56306
Approved symbolGOLGA6L26
Namegolgin A6 family like 26
Location15q11.2
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000273756
Ensembl biotypeprotein_coding
Entrez102723623

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000618455

RefSeq mRNA: 1 — MANE Select: NM_001382446 NM_001382446

CCDS: CCDS91963

Canonical transcript exons

ENST00000618455 — 9 exons

ExonStartEnd
ENSE000017728412333401623334196
ENSE000037190962332693523328158
ENSE000037193202332928423329342
ENSE000037322712333110523331155
ENSE000037365862333092323331016
ENSE000037392872333072123330827
ENSE000037528632332881223328953
ENSE000037548422333224123332369
ENSE000039359422332453523326278

Expression profiles

Bgee: expression breadth broad, 18 present calls, max score 82.76.

Top tissues by expression

94 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047382.76gold quality
left testisUBERON:000453372.15gold quality
testisUBERON:000047371.98gold quality
right testisUBERON:000453469.34gold quality
sural nerveUBERON:001548844.34silver quality
ventricular zoneUBERON:000305340.11gold quality
superior frontal gyrusUBERON:000266139.47gold quality
bone marrow cellCL:000209239.06gold quality
colonic epitheliumUBERON:000039737.20gold quality
cortical plateUBERON:000534336.47gold quality
skeletal muscle tissueUBERON:000113436.37gold quality
ganglionic eminenceUBERON:000402335.49gold quality
hindlimb stylopod muscleUBERON:000425235.45gold quality
muscle tissueUBERON:000238533.25gold quality
bone marrowUBERON:000237133.22gold quality
monocyteCL:000057631.72silver quality
leukocyteCL:000073831.35silver quality
tonsilUBERON:000237230.57gold quality
vermiform appendixUBERON:000115430.27silver quality
stromal cell of endometriumCL:000225529.87gold quality
liverUBERON:000210728.77gold quality
lymph nodeUBERON:000002928.76gold quality
right uterine tubeUBERON:000130228.19gold quality
duodenumUBERON:000211428.14gold quality
placentaUBERON:000198727.57gold quality
cortex of kidneyUBERON:000122527.37gold quality
muscle of legUBERON:000138327.37silver quality
primary visual cortexUBERON:000243627.25gold quality
calcaneal tendonUBERON:000370127.00gold quality
islet of LangerhansUBERON:000000626.90gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.52

Regulation

Is transcription factor: no

Cross-species orthologs

0 orthologs

Paralogs (10): GOLGA6L2 (ENSG00000174450), GOLGA6L4 (ENSG00000184206), GOLGA6L9 (ENSG00000197978), GOLGA6L25 (ENSG00000227717), GOLGA6L24 (ENSG00000237850), GOLGA6L7 (ENSG00000261649), GOLGA6L1 (ENSG00000273976), GOLGA6L6 (ENSG00000277322), GOLGA6L22 (ENSG00000277865), GOLGA6L10 (ENSG00000278662)

Protein

Protein identifiers

Golgin subfamily A member 6-like protein 26P0DX02 (reviewed: P0DX02)

All UniProt accessions (2): P0DX02, A0A8I5KQN6

UniProt curated annotations — full annotation on UniProt →

Similarity. Belongs to the GOLGA6 family.

RefSeq proteins (1): NP_001369375* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR026737GOLGA6LFamily

UniProt features (12 total): region of interest 5, compositionally biased region 5, chain 1, coiled-coil region 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-P0DX02-F176.120.23

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 1 (showing top): chr15q11

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (0):

Protein interactions and networks

STRING

0 interactions, top by confidence (×1000):

IntAct

0 interactions, top by confidence:

ESM2 similar proteins: A0A0J9YWL9, A0A0J9YY54, A0A1B0GV03, A6NEF3, A6NEM1, A6NI86, A8MZA4, B4DH59, D3YVF0, F6QRE9, H0YKK7, H0YM25, P0C6Y7, P0C7A2, P0DX00, P0DX01, P0DX02, P14590, P21263, P22793, P24587, P24710, P48997, P48998, Q07283, Q0II65, Q0P6D6, Q13342, Q3BBV2, Q4R9C9, Q5W0A0, Q6AXX0, Q6NSX1, Q6P5H2, Q6P902, Q86T75, Q8CHD8, Q8N2N9, Q8N660, Q8N7Z2

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

0 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance0
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

0 predictions. Top by Δscore:

AlphaMissense

4444 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1003301556 (15:23330150 C>A,T), RS1005077184 (15:23327182 T>G), RS1011656537 (15:23330271 C>A,G), RS1011708873 (15:23332708 A>C,G), RS1014911059 (15:23327413 T>C), RS1022173092 (15:23330364 A>G), RS1030814771 (15:23334065 A>G), RS1031343487 (15:23331471 C>A,T), RS1036457947 (15:23332165 T>C), RS1036573976 (15:23329976 C>T), RS1043165673 (15:23332733 C>T), RS1049247634 (15:23329824 T>G), RS1055776867 (15:23330159 G>C), RS1056229518 (15:23332539 GA>G,GAA), RS111143840 (15:23327655 C>T)

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)

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.