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Protein Coding Gene : Exoc6 exocyst complex component 6

Primary Identifier  MGI:1351611 Organism  mouse, laboratory
Chromosome  19 NCBI Gene Number  107371
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Acts upstream of or within erythrocyte differentiation. Predicted to be located in plasma membrane. Predicted to be part of exocyst. Is expressed in central nervous system; dorsal root ganglion; foregut; genitourinary system; and liver lobe. Orthologous to human EXOC6 (exocyst complex component 6).
PHENOTYPE: Homozygotes for a spontaneous mutation exhibit severe microcytic anemia, erythrocyte hyperchromia, and markedly increased levels of red cell protoporphyrin. [provided by MGI curators]
  • synonyms:
  • MGD-MRK-10640,
  • msec15,
  • expressed sequence AW413330,
  • SEC15-like 1 (S. cerevisiae),
  • Exoc6,
  • RIKEN cDNA 4833405E05 gene,
  • MGI:96028,
  • MGI:2147727,
  • sec15 homolog (S.cerevisiae),
  • hbd,
  • hemoglobin deficient,
  • AW413330,
  • SEC15 homolog (S. cerevisiae),
  • Sec15,
  • exocyst complex component 6,
  • 4833405E05Rik,
  • Sec15l1

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

7 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