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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID 		Kctd1tm1d(EUCOMM)Wtsi
targeted mutation 1d, Wellcome Trust Sanger Institute
MGI:6502870
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
 		Kctd1tm1d(EUCOMM)Wtsi/Kctd1tm1d(EUCOMM)Wtsi involves: C57BL/6N MGI:7657815


Genotype
MGI:7657815
hm1
Allelic
Composition		 Kctd1tm1d(EUCOMM)Wtsi/Kctd1tm1d(EUCOMM)Wtsi
Genetic
Background		 involves: C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kctd1tm1d(EUCOMM)Wtsi mutation (0 available); any Kctd1 mutation (39 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
renal/urinary system
renal interstitial fibrosis ( J:344153 )
• mice exhibit severe interstitial renal fibrosis at 7 months of age

pigmentation
pigmentation phenotype ( J:344153 )
N
• mice do not exhibit a pigmentation defect

cardiovascular system
cardiovascular system phenotype ( J:344153 )
N
• mice do not exhibit any cardiac abnormalities at PO




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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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory