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Protein Coding Gene : Srms src-related kinase lacking C-terminal regulatory tyrosine and N-terminal myristylation sites

Primary Identifier  MGI:101865 Organism  mouse, laboratory
Chromosome  2 NCBI Gene Number  20811
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

Predicted to enable non-membrane spanning protein tyrosine kinase activity and signaling receptor binding activity. Predicted to be involved in several processes, including innate immune response; positive regulation of TORC1 signaling; and transmembrane receptor protein tyrosine kinase signaling pathway. Predicted to act upstream of or within phosphorylation. Predicted to be located in cytoplasm. Is expressed in several structures, including brain; gut; integumental system; liver and biliary system; and reproductive system. Orthologous to human SRMS (src-related kinase lacking C-terminal regulatory tyrosine and N-terminal myristylation sites).
PHENOTYPE: Homozygous mice exhibit no detectable abnormalities. [provided by MGI curators]
  • synonyms:
  • MGI:2444916,
  • Srms,
  • A230069J08Rik,
  • srm,
  • src-related kinase lacking C-terminal regulatory tyrosine and N-terminal myristylation sites,
  • RIKEN cDNA A230069J08 gene,
  • MGD-MRK-18690

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Genome

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0 CDSs

0 Exons

0 Genomic Clusters

0 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

Interactions

4 Pathways

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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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