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Protein Coding Gene : Midn midnolin

Primary Identifier  MGI:1890222 Organism  mouse, laboratory
Chromosome  10 NCBI Gene Number  59090
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable kinase binding activity and molecular adaptor activity. Predicted to be involved in proteasomal ubiquitin-independent protein catabolic process. Predicted to act upstream of or within negative regulation of glucokinase activity and negative regulation of insulin secretion. Located in cytosol and nucleolus. Is expressed in several structures, including brain; genitourinary system; liver; lung; and spleen. Orthologous to human MIDN (midnolin).
PHENOTYPE: Mice homozygous for a transgenic gene disruption exhibit cleft palate and small ovary. [provided by MGI curators]
  • synonyms:
  • 3000003C15Rik,
  • MGI:1917443,
  • midnolin,
  • RIKEN cDNA 3000003C15 gene,
  • Midn

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

1 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