201
|
|
|
Keratin 19 |
CK19, K19, K1CS |
|
202
|
|
|
Keratin 32 |
HA2, HKA2, KRTHA2, hHa2 |
|
203
|
|
|
Keratin 81 |
HB1, Hb-1, K81, KRTHB1, MLN137, MNLIX2, ghHkb1, hHAKB2-1 |
Alopecia, Asthma, Cataract, Hypotrichosis, Impaired cognition, Keratosis pilaris, Mental retardation, Monilethrix, Nail diseases, Nail dysplasia, Nail dystrophy, Perifollicular hyperkeratosis, Phrynoderma, Schizophrenia |
204
|
|
|
Keratin 83 |
EKVP5, HB3, Hb-3, KRTHB3, MNLIX, MNLIX3 |
Alopecia, Cataract, Erythrokeratodermia variabilis, Hypotrichosis, Impaired cognition, Keratosis pilaris, Leukemia, Mental retardation, Monilethrix, Nail diseases, Nail dysplasia, Nail dystrophy, Palmoplantar keratoderma, Palmoplantar keratosis, Perifollicular hyperkeratosis, Phrynoderma, Progressive symmetric erythrokeratodermia, SchizophreniaView all (3 more) |
205
|
|
|
Keratin 85 |
ECTD4, HB5, Hb-5, K85, KRTHB5, hHb5 |
|
206
|
|
|
Keratin 86 |
HB6, Hb1, K86, KRTHB1, KRTHB6, MNX, NMLIX1 |
Alopecia, Cataract, Hypotrichosis, Impaired cognition, Keratosis pilaris, Mental retardation, Monilethrix, Nail diseases, Nail dysplasia, Nail dystrophy, Perifollicular hyperkeratosis, Phrynoderma, Schizophrenia |
207
|
|
|
Kinectin 1 |
CG1, KNT, MU-RMS-40.19 |
|
208
|
|
|
Keratin 8 pseudogene 26 |
- |
|
209
|
|
|
Kelch repeat and BTB domain containing 13 |
HCG1645727, NEM6 |
Arthrogryposis multiplex congenita, Cardiomyopathy, High palate, Limb muscle atrophy, Micrognathism, Motor delay, Myopathy, Nemaline myopathy, Neuromuscular dysphagia, Pena shokeir syndrome, Ptosis, Scoliosis |
210
|
|
|
Keratin 16 pseudogene 2 |
- |
|