|  Help  |  About  |  Contact Us

Protein Coding Gene : Gmnc geminin coiled-coil domain containing

Primary Identifier  MGI:2685452 Organism  mouse, laboratory
Chromosome  16 NCBI Gene Number  239789
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Involved in DNA replication. Acts upstream of or within cilium assembly. Predicted to be active in nucleus. Is expressed in brain; bronchus; female reproductive system; olfactory epithelium; and respiratory system epithelium. Orthologous to human GMNC (geminin coiled-coil domain containing).
PHENOTYPE: Homozygotes for a null allele show postnatal growth retardation and lethality and absent respiratory motile cilia. Homozygotes for a different null allele are runted and show hydrocephaly and infertility due to impaired formation of multiciliated cells in the brain, respiratory tract, and germline. [provided by MGI curators]
  • synonyms:
  • LOC239789,
  • Gm606,
  • gene model 1778, (NCBI),
  • Gm1778,
  • gene model 606, (NCBI),
  • MGI:2686624,
  • LOC385639,
  • predicted gene 606,
  • Gmnc,
  • geminin coiled-coil domain containing

Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

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

0 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