GOLGA6L26
gene geneOn this page
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
| Field | Value |
|---|---|
| HGNC ID | HGNC:56306 |
| Approved symbol | GOLGA6L26 |
| Name | golgin A6 family like 26 |
| Location | 15q11.2 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000273756 |
| Ensembl biotype | protein_coding |
| Entrez | 102723623 |
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
| Exon | Start | End |
|---|---|---|
| ENSE00001772841 | 23334016 | 23334196 |
| ENSE00003719096 | 23326935 | 23328158 |
| ENSE00003719320 | 23329284 | 23329342 |
| ENSE00003732271 | 23331105 | 23331155 |
| ENSE00003736586 | 23330923 | 23331016 |
| ENSE00003739287 | 23330721 | 23330827 |
| ENSE00003752863 | 23328812 | 23328953 |
| ENSE00003754842 | 23332241 | 23332369 |
| ENSE00003935942 | 23324535 | 23326278 |
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):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 82.76 | gold quality |
| left testis | UBERON:0004533 | 72.15 | gold quality |
| testis | UBERON:0000473 | 71.98 | gold quality |
| right testis | UBERON:0004534 | 69.34 | gold quality |
| sural nerve | UBERON:0015488 | 44.34 | silver quality |
| ventricular zone | UBERON:0003053 | 40.11 | gold quality |
| superior frontal gyrus | UBERON:0002661 | 39.47 | gold quality |
| bone marrow cell | CL:0002092 | 39.06 | gold quality |
| colonic epithelium | UBERON:0000397 | 37.20 | gold quality |
| cortical plate | UBERON:0005343 | 36.47 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 36.37 | gold quality |
| ganglionic eminence | UBERON:0004023 | 35.49 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 35.45 | gold quality |
| muscle tissue | UBERON:0002385 | 33.25 | gold quality |
| bone marrow | UBERON:0002371 | 33.22 | gold quality |
| monocyte | CL:0000576 | 31.72 | silver quality |
| leukocyte | CL:0000738 | 31.35 | silver quality |
| tonsil | UBERON:0002372 | 30.57 | gold quality |
| vermiform appendix | UBERON:0001154 | 30.27 | silver quality |
| stromal cell of endometrium | CL:0002255 | 29.87 | gold quality |
| liver | UBERON:0002107 | 28.77 | gold quality |
| lymph node | UBERON:0000029 | 28.76 | gold quality |
| right uterine tube | UBERON:0001302 | 28.19 | gold quality |
| duodenum | UBERON:0002114 | 28.14 | gold quality |
| placenta | UBERON:0001987 | 27.57 | gold quality |
| cortex of kidney | UBERON:0001225 | 27.37 | gold quality |
| muscle of leg | UBERON:0001383 | 27.37 | silver quality |
| primary visual cortex | UBERON:0002436 | 27.25 | gold quality |
| calcaneal tendon | UBERON:0003701 | 27.00 | gold quality |
| islet of Langerhans | UBERON:0000006 | 26.90 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.52 |
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 26 — P0DX02 (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)
| ID | Name | Type |
|---|---|---|
| IPR026737 | GOLGA6L | Family |
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)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-P0DX02-F1 | 76.12 | 0.23 |
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):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 0 |
| Likely benign | 0 |
| Benign | 0 |
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.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.