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Protein Coding Gene : Amot angiomotin

Primary Identifier  MGI:108440 Organism  mouse, laboratory
Chromosome  X NCBI Gene Number  27494
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable angiostatin binding activity and signaling receptor activity. Acts upstream of or within several processes, including gastrulation; positive regulation of embryonic development; and vasculogenesis. Located in bicellular tight junction; cytoplasmic vesicle; and lamellipodium. Is expressed in several structures, including egg cylinder; embryo endoderm; embryo mesoderm; and mesendoderm. Orthologous to human AMOT (angiomotin).
PHENOTYPE: Homozygotes for a null mutation exhibit impaired migration into proximal extraembryonic regions resulting in furrows of visceral endoderm at the junction of embryonic and extraembryonic regions, vascular insufficiency in the intersomitic region, dilated vessels in the brain and embryonic lethality. [provided by MGI curators]
  • synonyms:
  • Sii6,
  • DNA segment, KIST 1,
  • E230009N18Rik,
  • MGD-MRK-37484,
  • SII6,
  • MGI:2148071,
  • angiomotin,
  • RIKEN cDNA E230009N18 gene,
  • mKIAA1071,
  • MGI:2442022,
  • Amot,
  • D0Kist1,
  • expressed sequence C81439,
  • MGI:2180948,
  • C81439

Features --> Cross References

Genome

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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

10 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

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