1. Gene
  2. GALNTL6 - polypeptide N-acetylgalactosaminyltransferase like 6 Gene

GALNTL6 - polypeptide N-acetylgalactosaminyltransferase like 6 Gene

Homo sapiens

Also known as GALNT17; GALNACT20; GalNAc-T6L

Gene ID: 442117 | Gene type: protein coding

About GALNTL6

Cytogenetic location: 4q34.1 Genomic coordinates (GRCh38): 4:171,813,404-173,041,559 (from NCBI)

This gene has 7 transcripts (splice variants), 202 orthologues and 19 paralogues. Low expression observed in reference dataset.

Summary

Enables polypeptide N-acetylgalactosaminyltransferase activity. Involved in protein O-linked glycosylation via threonine. Predicted to be located in Golgi membrane. Predicted to be integral component of membrane. Predicted to be active in Golgi apparatus. [provided by Alliance of Genome Resources, Apr 2022]

GALNTL6 Products(1)

mRNA Protein Name
NM_001034845.3 NP_001030017.2 polypeptide N-acetylgalactosaminyltransferase-like 6
Gene Ontology
  • Molecular Function
  • Biological Process
Molecular Function GO Annotation Evidence Reference Source
enables polypeptide N-acetylgalactosaminyltransferase activity IDA
IDA: Inferred from direct assay
22186971 GOA
Biological Process GO Annotation Evidence Reference Source
involved in protein O-linked glycosylation via threonine IDA
IDA: Inferred from direct assay
22186971 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

GALNTL6 Protein Structure

Glycos_transf_2

Glycos_transf_2: Glycosyl transferase family 2 (143 - 327)

Ricin_B_lectin

Ricin_B_lectin: Ricin-type beta-trefoil lectin domain (454 - 582)

  • 0
  • 100
  • 200
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  • 400
  • 500
  • 601 a.a.
Protein Preferred Names Protein Names

polypeptide N-acetylgalactosaminyltransferase-like 6

GaNTase 17

Related Diseases

Diseases Alias
Williams-Beuren Syndrome

Williams Syndrome

WBS

Wms

Deletion 7q11.23

Monosomy 7q11.23

Chromosome 7q11.23 Deletion Syndrome, 1.5- To 1.8-Mb

Fanconi Schlesinger Syndrome

Beuren Syndrome

Elfin Facies Syndrome

Elfin Facies With Hypercalcemia

Hypercalcemia-Supravalvar Aortic Stenosis

Ws

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Mus musculus GALNTL6 MGD MGI:1913581
Rattus norvegicus GALNTL6 RGD RGD:1564773
Canis familiaris GALNTL6 VGNC VGNC:59080
Macaca mulatta GALNTL6 VGNC VGNC:72813
Felis catus GALNTL6 VGNC VGNC:107336
Bos taurus GALNTL6 VGNC VGNC:29238