Gene: Myl7 MGI:107495

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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:
myosin, light polypeptide 7, regulatory
Synonyms:
N/A

IMPC Data Collections

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

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.

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 Myl7 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 Myl7 by phenotypic similarity.

Disease Similarity of
phenotypes
Matching phenotypes Source
Left Ventricular Noncompaction 1
OMIM:604169
Cardiomyopathy, Dilated, 1C, With Or Without Left Ventricular Noncompaction
OMIM:601493
Coenzyme Q10 Deficiency, Primary, 7
OMIM:616276
Cardiomyopathy, Dilated, 1Aa, With Or Without Left Ventricular Noncompaction
OMIM:612158
Left Ventricular Noncompaction 8
OMIM:615373
Cardiomyopathy, Dilated, 1R
OMIM:613424
Atrial Standstill
ORPHA:1344
Long Qt Syndrome 16
OMIM:618782
Congenital Heart Defects, Multiple Types, 3
OMIM:614954
Left Ventricular Noncompaction 10
OMIM:615396
Cardiomyopathy, Dilated, 1D
OMIM:601494
Myopathy, Myofibrillar, 1
OMIM:601419
Cardiomyopathy, Familial Hypertrophic, 10
OMIM:608758
Glycogen Storage Disease With Severe Cardiomyopathy Due To Glycogenin Deficiency
ORPHA:263297
Incessant Infant Ventricular Tachycardia
ORPHA:45453
Peripartum Cardiomyopathy
ORPHA:563
Familial Dilated Cardiomyopathy
ORPHA:217607
Cardiomyopathy, Familial Hypertrophic, 17
OMIM:613873
Timothy Syndrome
OMIM:601005
Atrial Septal Defect, Sinus Venosus Type
ORPHA:99105
Chronic Atrial And Intestinal Dysrhythmia
OMIM:616201
Cardiac Conduction Disease With Or Without Dilated Cardiomyopathy
OMIM:616117
Congenitally Corrected Transposition Of The Great Arteries
ORPHA:216694
Mitochondrial Complex Iv Deficiency, Nuclear Type 13
OMIM:616501
Arrhythmogenic Right Ventricular Dysplasia, Familial, 5
OMIM:604400
Sudden Cardiac Failure, Infantile
OMIM:617222
Hirschsprung Disease, Cardiac Defects, And Autonomic Dysfunction
OMIM:613870
Atrial Septal Defect 6
OMIM:613087
Cardiomyopathy, Dilated, 1G
OMIM:604145
Sick Sinus Syndrome 2
OMIM:163800
Arrhythmogenic Right Ventricular Dysplasia, Familial, 14
OMIM:618920
Naxos Disease
OMIM:601214
Double Outlet Right Ventricle
ORPHA:3426
Tako-Tsubo Cardiomyopathy
ORPHA:66529
Complete Atrioventricular Septal Defect
ORPHA:1329
Glycogen Storage Disease Of Heart, Lethal Congenital
OMIM:261740
Cardiomyopathy, Dilated, 1S
OMIM:613426
Atrial Septal Defect, Ostium Secundum Type
ORPHA:99103
Atrial Standstill 2
OMIM:615745
Brugada Syndrome
ORPHA:130
Truncus Arteriosus
ORPHA:3384
Congenital Total Pulmonary Venous Return Anomaly
ORPHA:99125
Homozygous Familial Hypercholesterolemia
ORPHA:391665
Visceral Steatosis, Congenital
OMIM:228100

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 Myl7

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 Myl7.

No publications found that use IMPC mice or data for Myl7.

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