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Gene: Mia MGI:109615

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Not currently registered for phenotyping at IMPC

Phenotyping is currently not planned for a knockout strain of this gene.

Gene Summary

Name:
MIA SH3 domain containing
Synonyms:
Cdrap,  Mia1

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IMPC Data Collections

  • No Body Weight Data
  • No Embryo Imaging Data
  • No Viability Data

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.

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.

Phenotype associated images not available

Human diseases caused by Mia 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 Mia by phenotypic similarity.

Disease Similarity of
phenotypes		 Matching phenotypes Source
Legg-Calvé-Perthes Disease
Cartilage destruction ORPHA:2380
Ollier Disease
Multiple enchondromatosis, Abnormal cartilage morphology ORPHA:296
Larsen-Like Syndrome, Lethal Type
Abnormal cartilage matrix OMIM:245650
Lethal Kniest-Like Dysplasia
Abnormal cartilage morphology, Abnormal cartilage matrix ORPHA:2347
Adult-Onset Still Disease
Cartilage destruction ORPHA:829
Kniest Dysplasia
Abnormal cartilage collagen OMIM:156550
Lissencephaly Type 3-Metacarpal Bone Dysplasia Syndrome
Abnormal cartilage matrix ORPHA:86822
Spondyloepiphyseal Dysplasia Tarda
Abnormal cartilage morphology ORPHA:93284
Moderate Hemophilia A
Cartilage destruction ORPHA:169805
Kniest Dysplasia
Abnormal cartilage collagen ORPHA:485
Alkaptonuria
Cartilage destruction, Calcification of cartilage ORPHA:56
Encephalocraniocutaneous Lipomatosis
Abnormal cartilage morphology ORPHA:2396
Reactive Arthritis
Cartilage destruction ORPHA:29207
Multiple Osteochondromas
Abnormal cartilage morphology ORPHA:321

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 Mia

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 Mia.

No publications found that use IMPC mice or data for Mia.

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
Miatm1(KOMP)Vlcg Reporter-tagged deletion allele (with selection cassette) ES Cells
Miatm1(KOMP)Wtsi Reporter-tagged deletion allele (with selection cassette) Targeting vectors, ES Cells

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