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Protein Coding Gene : Tmem41b transmembrane protein 41B

Primary Identifier  MGI:1289225 Organism  mouse, laboratory
Chromosome  7 NCBI Gene Number  233724
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

Predicted to enable phospholipid scramblase activity. Predicted to be involved in autophagosome assembly; intracellular lipid transport; and modulation by host of viral RNA genome replication. Predicted to act upstream of or within autophagy; lipid transport; and nervous system development. Located in mitochondria-associated endoplasmic reticulum membrane. Is expressed in embryo. Orthologous to human TMEM41B (transmembrane protein 41B).
PHENOTYPE: Mice homozygous for a gene trapped allele exhibit embryonic growth arrest and complete embryonic lethality between implantation and placentation. Mice heterozygous for a null allele display reduced serum lipid levels, impaired autophagic flux, and resistance to coronavirus infection. [provided by MGI curators]
  • synonyms:
  • AU018901,
  • Tmem41b,
  • expressed sequence AU018901,
  • DNA segment, Chr 7, ERATO Doi 743, expressed,
  • D7Ertd70e,
  • MGI:2143199,
  • RIKEN cDNA 1500031M19 gene,
  • RIKEN cDNA 1500015G02 gene,
  • MGI:1916268,
  • transmembrane protein 41B,
  • DNA segment, Chr 7, ERATO Doi 70, expressed,
  • MGI:1098618,
  • D7Ertd743e,
  • 1500031M19Rik,
  • 1500015G02Rik,
  • MGI:1923591

Features --> Cross References

Genome

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0 CDSs

0 Exons

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2 Involved In Mutations

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0 Transgenic Expressors

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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

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Mouse features --> Functions (GO terms)

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Genes --> Homologs

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Disease

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0 Driver For