COLGALT2
Procollagen galactosyltransferase 2
Also known as: C1orf17, GLT25D2, GT252_HUMAN, KIAA0584
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8IYK4
- Gene
- COLGALT2
- Ensembl
- ENSG00000198756
- Chromosome
- 1
- Canonical length
- 626 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Vesicles
- Secretome location
- Intracellular and membrane
OverviewNCBI Gene
Predicted to enable procollagen galactosyltransferase activity. Predicted to be involved in collagen fibril organization. Predicted to be located in endoplasmic reticulum lumen. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
626 residues, UniProt reviewed canonical sequence.
>Q8IYK4|COLGALT2
1 MAARPAATLA WSLLLLSSAL LREGCRARFV AERDSEDDGE EPVVFPESPL QSPTVLVAVL
61 ARNAAHTLPH FLGCLERLDY PKSRMAIWAA TDHNVDNTTE IFREWLKNVQ RLYHYVEWRP
121 MDEPESYPDE IGPKHWPTSR FAHVMKLRQA ALRTAREKWS DYILFIDVDN FLTNPQTLNL
181 LIAENKTIVA PMLESRGLYS NFWCGITPKG FYKRTPDYVQ IREWKRTGCF PVPMVHSTFL
241 IDLRKEASDK LTFYPPHQDY TWTFDDIIVF AFSSRQAGIQ MYLCNREHYG YLPIPLKPHQ
301 TLQEDIENLI HVQIEAMIDR PPMEPSQYVS VVPKYPDKMG FDEIFMINLK RRKDRRDRML
361 RTLYEQEIEV KIVEAVDGKA LNTSQLKALN IEMLPGYRDP YSSRPLTRGE IGCFLSHYSV
421 WKEVIDRELE KTLVIEDDVR FEHQFKKKLM KLMDNIDQAQ LDWELIYIGR KRMQVKEPEK
481 AVPNVANLVE ADYSYWTLGY VISLEGAQKL VGANPFGKML PVDEFLPVMY NKHPVAEYKE
541 YYESRDLKAF SAEPLLIYPT HYTGQPGYLS DTETSTIWDN ETVATDWDRT HAWKSRKQSR
601 IYSNAKNTEA LPPPTSLDTV PSRDELLocalizationUniProt · AlphaFold · HPA
Whether an antibody against COLGALT2 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.27
- Highest tissue expression
- 26 nTPM
Expression across tissuesHPA
Tissue
- spinal cord: 26 nTPM
- cerebral cortex: 26 nTPM
- hippocampal formation: 15 nTPM
- midbrain: 15 nTPM
- cerebellum: 13 nTPM
- basal ganglia: 11 nTPM
Single-cell type
- oligodendrocytes: 415 nCPM
- oligodendrocyte progenitor cells: 178 nCPM
- fibro-adipogenic progenitors: 128 nCPM
- adrenal medulla cells: 117 nCPM
- late spermatids: 106 nCPM
- early spermatids: 71 nCPM
Immune cell
- basophil: 11 nTPM
- gdT-cell: 0.3 nTPM
- NK-cell: 0.3 nTPM
- memory CD8 T-cell: 0.2 nTPM
- memory CD4 T-cell: 0.1 nTPM
- naive CD8 T-cell: 0.1 nTPM
Brain region
- white matter: 114 nTPM
- basal ganglia: 72 nTPM
- pons: 72 nTPM
- medulla oblongata: 71 nTPM
- thalamus: 66 nTPM
- midbrain: 62 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.92
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.81
- DepMap mean gene effect
- -0.09
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads COLGALT2 as an antibody target. Whether an autoantibody or antibody against COLGALT2 could matter depends on whether native COLGALT2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
COLGALT2 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label COLGALT2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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