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Protein Coding Gene : Scfd1 Sec1 family domain containing 1

Primary Identifier  MGI:1924233 Organism  mouse, laboratory
Chromosome  12 NCBI Gene Number  76983
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable syntaxin binding activity. Predicted to be involved in several processes, including Golgi vesicle transport; negative regulation of autophagosome assembly; and regulation of ER to Golgi vesicle-mediated transport. Predicted to be located in Golgi-associated vesicle and cis-Golgi network. Predicted to be active in Golgi membrane. Is expressed in vertebral axis musculature. Orthologous to human SCFD1 (sec1 family domain containing 1).
PHENOTYPE: Mice homozygous for a knock-out allele show complete embryonic lethality prior to organogenesis. In vitro, some blastocysts fail to hatch from the zona pellucida and do not form outgrowths while others do hatch but form outgrowths with no inner cell mass and dispersed trophectoderm. [provided by MGI curators]
  • synonyms:
  • RIKEN cDNA 3110021P21 gene,
  • Scfd1,
  • Sec1 family domain containing 1,
  • STXBP1L2,
  • RA410,
  • 3110021P21Rik

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

1 Involved In Mutations

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

13 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For