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Protein Coding Gene : Tmem237 transmembrane protein 237
Primary Identifier  MGI:2138365 Organism  mouse, laboratory
Chromosome  1 NCBI Gene Number  381259
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Involved in cilium assembly and regulation of Wnt signaling pathway. Located in cone photoreceptor outer segment; photoreceptor connecting cilium; and rod photoreceptor outer segment. Is expressed in alimentary system; diaphragm; gallbladder; lower urinary tract; and reproductive system. Human ortholog(s) of this gene implicated in Joubert syndrome and Joubert syndrome 14. Orthologous to human TMEM237 (transmembrane protein 237).
  • synonyms:
  • LOC381259,
  • transmembrane protein 237,
  • gene model 972, (NCBI),
  • expressed sequence AI853305,
  • Tmem237,
  • AI853305,
  • amyotrophic lateral sclerosis 2 (juvenile) chromosome region, candidate 4,
  • Als2cr4,
  • Gm972,
  • MGI:2685818
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Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

2 Involved In Mutations

Trail: ProteinCodingGene

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

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

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