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Protein Coding Gene : Galnt11 polypeptide N-acetylgalactosaminyltransferase 11

Primary Identifier  MGI:2444392 Organism  mouse, laboratory
Chromosome  5 NCBI Gene Number  231050
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable Notch binding activity and polypeptide N-acetylgalactosaminyltransferase activity. Predicted to be involved in protein O-linked glycosylation via threonine and regulation of Notch signaling pathway. Predicted to act upstream of or within Notch signaling pathway. Predicted to be located in membrane. Predicted to be active in Golgi apparatus. Is expressed in skeleton; submandibular gland; and submandibular gland primordium. Orthologous to human GALNT11 (polypeptide N-acetylgalactosaminyltransferase 11).
PHENOTYPE: Mice homozygous for a null allele exhibit reduced viability over time, smaller size, low-molecular-weight proteinuria and increased blood urea nitrogen level. [provided by MGI curators]
  • synonyms:
  • AI648252,
  • MGI:2443736,
  • E430002F06Rik,
  • RIKEN cDNA E430002F06 gene,
  • RIKEN cDNA A430075I06 gene,
  • A430075I06Rik,
  • expressed sequence AI648252,
  • MGI:2140948,
  • polypeptide N-acetylgalactosaminyltransferase 11,
  • Galnt11

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

5 Involved In Mutations

0 Strain

0 Transcripts

0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

4 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For