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Kmt2bGena263
Chemically induced Allele Detail
Summary
Symbol: Kmt2bGena263
Name: lysine (K)-specific methyltransferase 2B; Gena263, Harwell
MGI ID: MGI:5532297
Synonyms: Mll2M2628K
Gene: Kmt2b  Location: Chr7:30268283-30288151 bp, - strand  Genetic Position: Chr7, 18.63 cM, cytoband A3
Alliance: Kmt2bGena263 page
Mutation
origin
Strain of Origin:  BALB/c
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced a T to A point mutation (c.7883T>A ENSMUST00000108154, NCBIM37) that results in the amino acid substitution of methionine with lysine at position 2628 (p.M2628K). (J:203736)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 10 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Kmt2b Mutation:  65 strains or lines available
References
Original:  J:79719 Hough TA, et al., Novel phenotypes identified by plasma biochemical screening in the mouse. Mamm Genome. 2002 Oct;13(10):595-602
All:  2 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory