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Symbol
Name
ID
Kansl1
KAT8 regulatory NSL complex subunit 1
MGI:1923969
Phenotype annotations related to integument
Darker colors indicate more annotations
Human Phenotypes
Prominent fingertip pads
Wide intermamillary distance
Eczema
Abnormality of hair pigmentation
Hypopigmentation of hair
Abnormality of hair texture
Dry skin
Sacral dimple
Ichthyosis
Disease(s) Associated with KANSL1
Koolen de Vries syndrome

Mouse Phenotypes
abnormal coat/hair pigmentation
Availability Mouse Genotype
Kansl1tm1b(EUCOMM)Hmgu/Kansl1+

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
02/11/2020
MGI 6.14
The Jackson Laboratory