Gene Summary

Name:
exocyst complex component 1
Synonyms:
2810407P21Rik,  Sec3l1,  A730011E05Rik,  Sec3p,  SEC3

IMPC Data Collections

IMPC Phenotype Summary

Significant
Not Significant
Not tested

Phenotypes

The IMPC applies a panel of phenotyping screens to characterise single-gene knockout mice by comparison to wild types. Click on the different tabs to visualise significant phenotypes identified by the IMPC, as well as all data that was measured.

Phenotype System Allele Zyg Sex Life Stage P Value
embryonic lethality prior to organogenesis Exoc1em1(IMPC)Mbp HOM   E9.5 0.00
preweaning lethality, complete penetrance Exoc1em1(IMPC)Mbp HOM   Early adult 0.00
increased exploration in new environment Exoc1em1(IMPC)Mbp HET Early adult 8.99×10-05

Download data as:  TSV  XLS

Select physiological systems to view:
Viewing: all phenotypes
Select physiological systems to view:
Viewing: all phenotypes

lacZ Expression

Expression data not available

Associated Images

Images submitted by IMPC centres for a selection of procedures. Each set of images is available to view in our image comparator.

X-ray

XRay Images Whole Body Dorso Ventral

30 Images

Gross Morphology Embryo E9.5

Images

2 Images

X-ray

XRay Images Whole Body Lateral Orientation

10 Images

Human diseases caused by Exoc1 mutations

The analysis uses data from IMPC, along with published data on other mouse mutants, in comparison to human disease reports in OMIM, Orphanet, and DECIPHER.

Phenotype comparisons summarize the similarity of mouse phenotypes with human disease phenotypes.

No human diseases associated to this gene by orthology or annotation.

The table below shows human diseases predicted to be associated to Exoc1 by phenotypic similarity.

Disease Similarity of
phenotypes
Matching phenotypes Source
Monoamine Oxidase A Deficiency
Cognitive impairment ORPHA:3057

Histopathology

Summary table of phenotypes displayed during the Histopathology procedure which are considered significant. Full histopathology data table, including submitted images, can be accessed by clicking any row in this table.

There is no histopathology data for Exoc1

IMPC related publications

The table below lists publications which used either products generated by the IMPC or data produced by the phenotyping efforts of the IMPC. These publications have also been associated to Exoc1.

There are 2 publications which use IMPC produced mice or data.

Title Journal IMPC Allele PubMed ID
EXOC1 plays an integral role in spermatogonia pseudopod elongation and spermatocyte stable syncytium formation in mice. eLife (May 2021) Exoc1tm1a(EUCOMM)Hmgu Exoc1tm1c(EUCOMM)Hmgu PMC8112867
Peri-implantation lethality in mice carrying megabase-scale deletion on 5qc3.3 is caused by Exoc1 null mutation. Scientific reports (September 2015) Exoc1tm1a(EUCOMM)Hmgu PMC4562154

Order Mouse and ES Cells

All available products are supplied via our member's centres or partnerships. When ordering a product from the IMPC you will be redirected to one of their websites or prompted to start an email.

MGI Allele Allele Type Produced
Exoc1tm1e(EUCOMM)Hmgu Targeted, non-conditional allele ES Cells
Exoc1tm1a(EUCOMM)Hmgu KO first allele (reporter-tagged insertion with conditional potential) Targeting vectors, ES Cells
Exoc1em1(IMPC)Mbp Exon Deletion Mice, Tissue

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