|
Symbol Name ID |
Kctd1
potassium channel tetramerisation domain containing 1 MGI:1918269 |
| Darker colors indicate more annotations |
| Human Phenotypes | Frontal bossing |
Calvarial skull defect |
Mandibular prognathia |
Clinodactyly of the 5th finger |
Broad thumb |
2-3 toe syndactyly |
3-4 finger cutaneous syndactyly |
Finger syndactyly |
| Disease(s) Associated with KCTD1 | ||||||||
| scalp-ear-nipple syndrome |
| Mouse Phenotypes | decreased bone mineral density |
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| Availability | Mouse Genotype | |
| Kctd1em1(IMPC)J/Kctd1em1(IMPC)J | ||
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 04/30/2024 MGI 6.23 |
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