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Protein Coding Gene : Gpc4 glypican 4

Primary Identifier  MGI:104902 Organism  mouse, laboratory
Chromosome  X NCBI Gene Number  14735
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Involved in synaptic membrane adhesion. Located in collagen-containing extracellular matrix and extracellular space. Is active in glutamatergic synapse. Is expressed in several structures, including alimentary system; central nervous system; embryo ectoderm; limb; and sensory organ. Human ortholog(s) of this gene implicated in Keipert syndrome. Orthologous to human GPC4 (glypican 4).
PHENOTYPE: Male mice hemizygous for a null allele exhibit signs of anemia. [provided by MGI curators]
  • synonyms:
  • MGI:2147905,
  • expressed sequence AI385680,
  • Gpc4,
  • expressed sequence AI661372,
  • AI661372,
  • MGI:2147881,
  • AI385680,
  • glypican 4,
  • MGI:2152785,
  • expressed sequence AF311610,
  • MGD-MRK-29056,
  • RIKEN cDNA 9530073D23 gene,
  • 9530073D23Rik,
  • MGI:1925872,
  • AF311610,
  • K-glypican

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

0 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

13 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