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Gene: 1600014C10Rik MGI:1919494

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Gene Summary

Name:
RIKEN cDNA 1600014C10 gene
Synonyms:
N/A

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IMPC Data Collections

IMPC Phenotype Summary

Significant
Not Significant
Not tested

View all our phenotype data below

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.

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.

Eye Morphology

Images Slit Lamp

1 Images

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PDF thumbnail PDF
Auditory Brain Stem Response

Click-evoked + 6 to 30kHz tone waveforms (pdf format)

8 Images

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Human diseases caused by 1600014C10Rik 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.

The table below shows human diseases associated to 1600014C10Rik by orthology or direct annotation.

Disease Similarity of
phenotypes		 Matching phenotypes Source
Neurodegeneration With Brain Iron Accumulation 4
OMIM:614298
Autosomal Recessive Spastic Paraplegia Type 43
ORPHA:320370
Mitochondrial Membrane Protein-Associated Neurodegeneration
ORPHA:289560
Spastic Paraplegia 43, Autosomal Recessive
OMIM:615043

The table below shows human diseases predicted to be associated to 1600014C10Rik by phenotypic similarity.

Disease Similarity of
phenotypes		 Matching phenotypes Source
Neurodegeneration With Brain Iron Accumulation 4
OMIM:614298
Autosomal Recessive Spastic Paraplegia Type 43
ORPHA:320370
Mitochondrial Membrane Protein-Associated Neurodegeneration
ORPHA:289560
Spastic Paraplegia 43, Autosomal Recessive
OMIM:615043

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 1600014C10Rik

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 1600014C10Rik.

No publications found that use IMPC mice or data for 1600014C10Rik.

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
1600014C10Rikem1(IMPC)J Exon Deletion Mice
1600014C10Riktm1a(EUCOMM)Hmgu KO first allele (reporter-tagged insertion with conditional potential) Targeting vectors, ES Cells

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