Not currently registered for phenotyping at IMPC

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

Gene Summary

Name:
RecQ protein-like
Synonyms:
RecQ1

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 Recql 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 Recql by phenotypic similarity.

Disease Similarity of
phenotypes
Matching phenotypes Source
Fraxf Syndrome
Folate-dependent fragile site at Xq28 ORPHA:100974
Nijmegen Breakage Syndrome-Like Disorder
Chromosomal breakage induced by ionizing radiation OMIM:613078
Scleroderma, Familial Progressive
Abnormality of chromosome stability, Chromosome breakage OMIM:181750
Fanconi Anemia, Complementation Group J
Chromosomal breakage induced by crosslinking agents OMIM:609054
Chromosomal Instability With Tissue-Specific Radiosensitivity
Abnormality of chromosome stability OMIM:215510
Radial-Renal Syndrome
Chromosome breakage OMIM:179280
Intrauterine Growth Retardation With Increased Mitomycin C Sensitivity
Abnormality of chromosome stability OMIM:600546
Immunodeficiency 54
Chromosome breakage OMIM:609981
Fanconi Anemia, Complementation Group D1
Chromosomal breakage induced by crosslinking agents OMIM:605724
Mitochondrial Complex Iv Deficiency, Nuclear Type 16
Chromosomal breakage induced by crosslinking agents OMIM:619060
Fragile X Syndrome
Folate-dependent fragile site at Xq28 OMIM:300624
N Syndrome
Abnormality of chromosome stability OMIM:310465
Fanconi Anemia, Complementation Group S
Chromosome breakage OMIM:617883
Fragile X Syndrome
Folate-dependent fragile site at Xq28 ORPHA:908
Bloom Syndrome
Abnormality of chromosome stability, Chromosome breakage, Azoospermia OMIM:210900
Porokeratosis 1, Multiple Types
Abnormality of chromosome stability OMIM:175800
Fanconi Anemia, Complementation Group L
Abnormality of chromosome stability, Chromosome breakage OMIM:614083
Fanconi Anemia, Complementation Group G
Abnormality of chromosome stability OMIM:614082
Fanconi Anemia, Complementation Group Q
Chromosome breakage OMIM:615272
Ataxia-Telangiectasia With Generalized Skin Pigmentation And Early Death
Abnormality of chromosome stability, Chromosome breakage OMIM:208910
Transcobalamin Deficiency
Abnormality of chromosome stability ORPHA:859
Fanconi Anemia, Complementation Group U
Chromosome breakage OMIM:617247
Fanconi Anemia, Complementation Group I
Chromosomal breakage induced by crosslinking agents OMIM:609053
Fanconi Anemia, Complementation Group N
Chromosomal breakage induced by crosslinking agents OMIM:610832
Fanconi Anemia, Complementation Group E
Chromosomal breakage induced by crosslinking agents, Prolonged G2 phase of cell cycle OMIM:600901
Fanconi Anemia, Complementation Group A
Chromosomal breakage induced by crosslinking agents, Prolonged G2 phase of cell cycle OMIM:227650
Fanconi Anemia, Complementation Group C
Chromosomal breakage induced by crosslinking agents, Prolonged G2 phase of cell cycle OMIM:227645
Ataxia-Telangiectasia
Abnormality of chromosome stability ORPHA:100
Fanconi Anemia, Complementation Group D2
Chromosomal breakage induced by crosslinking agents, Prolonged G2 phase of cell cycle OMIM:227646
Fanconi Anemia, Complementation Group F
Chromosomal breakage induced by crosslinking agents OMIM:603467
Riddle Syndrome
Chromosomal breakage induced by ionizing radiation ORPHA:420741
Lig4 Syndrome
Abnormality of chromosome stability ORPHA:99812
Icf Syndrome
Abnormality of chromosome stability ORPHA:2268
Meningioma
Chromosomal breakage induced by ionizing radiation ORPHA:2495
Fanconi Anemia, Complementation Group B
Abnormality of chromosome stability OMIM:300514
Cartilage-Hair Hypoplasia
Abnormality of chromosome stability ORPHA:175
Fanconi Anemia
Abnormality of chromosome stability, Azoospermia ORPHA:84
Nijmegen Breakage Syndrome
Abnormality of chromosome stability ORPHA:647

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 Recql

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 Recql.

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

Order Mouse and ES Cells

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MGI Allele Allele Type Produced
Recqltm2e(EUCOMM)Hmgu Targeted, non-conditional allele ES Cells
Recqltm1e(EUCOMM)Hmgu Targeted, non-conditional allele ES Cells
Recqltm1(KOMP)Vlcg Reporter-tagged deletion allele (with selection cassette) ES Cells
Recqltm1a(EUCOMM)Hmgu KO first allele (reporter-tagged insertion with conditional potential) Targeting vectors, ES Cells

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