Details of KRT1 gene in Homo sapiens
IDs |
|---|
| Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
|
| KRT1 | KRTA | P04264 | K2C1_HUMAN | 3848
| Q6GSJ0
| Q9H298 | type II cytoskeleta |
Phenotypes
Abnormal appendicular skeleton morphology, Abnormal immunoglobulin level, Abnormality of blood and blood-forming tissues, Abnormality of B cell physiology, Abnormality of B cells, Abnormality of cellular immune system, Abnormality of humoral immunity, Abnormality of immune system physiology, Abnormality of leukocytes, Abnormality of limb bone morphology, Abnormality of lymphocytes, Abnormality of metabolism/homeostasis, Abnormality of skeletal morphology, Abnormality of skin adnexa, Abnormality of skin morphology, Abnormality of skin physiology, Abnormality of the hair, Abnormality of the hand, Abnormality of the immune system, Abnormality of the integument, Abnormality of the nail, Abnormality of the palm, Abnormality of the plantar skin of foot, Abnormality of the skeletal system, Abnormality of the skin, Abnormality of the upper limb, All, Autosomal dominant inheritance, Congenital bullous ichthyosiform erythroderma, Congenital ichthyosiform erythroderma, Epidermal thickening, Erythema, Erythroderma, Generalized abnormality of skin, Hypergammaglobulinemia, Hyperkeratosis, Ichthyosiform abnormality of the skin, Increased IgE level, Inflammatory abnormality of the skin, Localized epidermolytic hyperkeratosis, Mode of inheritance, Nonepidermolytic palmoplantar keratoderma, Palmar hyperkeratosis, Palmoplantar hyperkeratosis, Palmoplantar keratoderma, Phenotypic abnormality, Plantar hyperkeratosis, Regional abnormality of skin, Thickened skin, Vascular skin abnormality.
Orthologs in other species |
|---|
| M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
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