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Protein Coding Gene : Tlcd3b TLC domain containing 3B
Primary Identifier  MGI:1916202 Organism  mouse, laboratory
Chromosome  7 NCBI Gene Number  68952
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables sphingosine N-acyltransferase activity. Acts upstream of or within ceramide biosynthetic process and negative regulation of fat cell differentiation. Predicted to be located in membrane. Predicted to be active in endoplasmic reticulum. Is expressed in nervous system and neural retina. Used to study cone-rod dystrophy. Human ortholog(s) of this gene implicated in cone-rod dystrophy. Orthologous to human TLCD3B (TLC domain containing 3B).
  • synonyms:
  • A330104J06Rik,
  • RIKEN cDNA A330104J06 gene,
  • MGI:2141927,
  • expressed sequence AW060769,
  • TLC domain containing 3B,
  • AW060769,
  • RIKEN cDNA 1500016O10 gene,
  • family with sequence similarity 57, member B,
  • expressed sequence AI413816,
  • Fam57b,
  • AI413816,
  • MGI:2142201,
  • Tlcd3b,
  • 1500016O10Rik,
  • MGI:1925035
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Features --> Cross References

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Sequence Feature Displayer

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5 Involved In Mutations

Trail: ProteinCodingGene

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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

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Mouse features --> Functions (GO terms)

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Expression

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Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

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