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Protein Coding Gene : Insig1 insulin induced gene 1

Primary Identifier  MGI:1916289 Organism  mouse, laboratory
Chromosome  5 NCBI Gene Number  231070
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

Predicted to enable oxysterol binding activity and protein sequestering activity. Acts upstream of or within several processes, including ear morphogenesis; negative regulation of fat cell differentiation; and negative regulation of lipid biosynthetic process. Predicted to be located in membrane. Predicted to be part of SREBP-SCAP-Insig complex. Predicted to be active in endoplasmic reticulum membrane. Is expressed in several structures, including alimentary system; eye; ganglia; telencephalon ventricular layer; and vibrissa. Orthologous to human INSIG1 (insulin induced gene 1).
PHENOTYPE: Mice homozygous for a knock-out allele exhibit decreased body body weight, increased gonadal and subcutaneous fat pad, decreased circulating triglyceride level and abnormal adipocity differentiation. [provided by MGI curators]
  • synonyms:
  • 1810013C12Rik,
  • insulin induced gene 1,
  • Insig-1,
  • RIKEN cDNA 1810013C12 gene,
  • Insig1

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Genome

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0 Canonical

0 CDSs

0 Exons

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7 Involved In Mutations

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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

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

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0 Driver For