About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Kctd1
potassium channel tetramerisation domain containing 1
MGI:1918269
46 phenotypes from multigenic genotypes
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Kctd1tm1c(EUCOMM)Wtsi/Kctd1+
Kctd15tm1c(EUCOMM)Wtsi/Kctd15+
E2f1Tg(Wnt1-cre)2Sor/E2f1+
involves: 129S4/SvJae * C57BL/6J * C57BL/6N
normal craniofacial phenotype J:344153
normal integument phenotype J:344153
normal pigmentation phenotype J:344153
Kctd1tm1c(EUCOMM)Wtsi/Kctd1+
Kctd15tm1c(EUCOMM)Wtsi/Kctd15tm1c(EUCOMM)Wtsi
E2f1Tg(Wnt1-cre)2Sor/E2f1+
involves: 129S4/SvJae * C57BL/6J * C57BL/6N
belly spot J:344153
Kctd1tm1c(EUCOMM)Wtsi/Kctd1tm1c(EUCOMM)Wtsi
Kctd15tm1c(EUCOMM)Wtsi/Kctd15+
E2f1Tg(Wnt1-cre)2Sor/E2f1+
involves: 129S4/SvJae * C57BL/6J * C57BL/6N
belly spot J:344153
Kctd1tm1c(EUCOMM)Wtsi/Kctd1tm1c(EUCOMM)Wtsi
Kctd15tm1c(EUCOMM)Wtsi/Kctd15tm1c(EUCOMM)Wtsi
E2f1Tg(Wnt1-cre)2Sor/E2f1+
involves: 129S4/SvJae * C57BL/6J * C57BL/6N
abnormal cranial suture morphology J:344153
abnormal craniofacial development J:344153
abnormal eyelid development J:344153
abnormal heart morphology J:344153
abnormal intramembranous bone ossification J:344153
abnormal nasal cartilage morphology J:344153
abnormal nose morphology J:344153
abnormal scalp morphology J:344153
absent incisors J:344153
absent lower incisors J:344153
absent nasal bone J:344153
absent upper incisors J:344153
bicuspid aortic valve J:344153
delayed cranial suture closure J:344153
delayed intramembranous bone ossification J:344153
ectopic neuron J:344153
eyelids open at birth J:344153
overriding aortic valve J:344153
perimembraneous ventricular septal defect J:344153
short frontal bone J:344153
skin lesions J:344153
small nasal bone J:344153
thin epidermis J:344153
wide metopic suture J:344153
Kctd1tm1c(EUCOMM)Wtsi/Kctd1tm1c(EUCOMM)Wtsi
Kctd15tm1c(EUCOMM)Wtsi/Kctd15tm1c(EUCOMM)Wtsi
Tg(Aqp2-cre)1Dek/0
involves: C57BL/6 * C57BL/6N * SJL
renal/urinary system phenotype J:344153
Kctd1tm1c(EUCOMM)Wtsi/Kctd1tm1c(EUCOMM)Wtsi
Kctd15tm1c(EUCOMM)Wtsi/Kctd15tm1c(EUCOMM)Wtsi
Tg(KRT14-cre)1Amc/0
involves: C57BL/6N * C57BL/6NJ
abnormal coat/ hair morphology J:344153
abnormal hair follicle morphology J:344153
abnormal hair shaft morphology J:344153
abnormal skin development J:344153
abnormal vibrissa follicle morphology J:344153
anhidrosis J:344153
normal craniofacial phenotype J:344153
curly vibrissae J:344153
decreased body size J:344153
decreased eccrine gland number J:344153
delayed eyelid opening J:344153
delayed hair appearance J:344153
interdigital webbing J:344153
postnatal growth retardation J:344153
small hair follicles J:344153
small sebaceous gland J:344153
sparse hair J:344153
thin skin J:344153

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
12/10/2024
MGI 6.24
The Jackson Laboratory