6981
|
|
|
Keratinocyte differentiation associated protein |
KDAP, UNQ467 |
|
6982
|
|
|
Kinase suppressor of ras 1 |
KSR, RSU2 |
|
6983
|
|
|
Kinase suppressor of ras 2 |
- |
Androgenetic alopecia, Autism, Central nervous system cancer, Cerebral amyloid angiopathy, Obesity, Coronary artery disease, Diabetes mellitus, Diabetes mellitus type 2, Endometriosis, Glioblastoma, Glioma, Hyperlipidemia, Hypertension, Insomnia, Alzheimer disease, Major depressive disorder, Migraine, Neurotic disorder, Psoriasis, Willis-ekbom disease, Systemic lupus erythematosusView all (6 more) |
6984
|
|
|
Kinectin 1 |
CG1, KNT, MU-RMS-40.19 |
|
6985
|
|
|
Kyphoscoliosis peptidase |
MFM7 |
|
6986
|
|
|
Kynurenine aminotransferase 1 |
CCBL1, GTK, KAT1, KATI |
|
6987
|
|
|
- |
- |
|
6988
|
|
|
Kynurenine aminotransferase 3 |
CCBL2, KAT3, KATIII |
|
6989
|
|
|
Kynureninase |
KYNUU, VCRL2 |
Asthma, Catel-manzke syndrome, Congenital vertebral-cardiac-renal anomalies syndrome, Degenerative disorder, Desbuquois syndrome, Hyperopia, Neurodegenerative disorder, Scoliosis, Vertebral, cardiac, renal, and limb defects syndrome |
6990
|
|
|
L1 cell adhesion molecule |
CAML1, CD171, HSAS, HSAS1, HYCX, MASA, MIC5, N-CAM-L1, N-CAML1, NCAM-L1, S10, SPG1 |
Aphasia, Postictal aphasia, Renal cell carcinoma, Cerebellar ataxia, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Commisural aphasia, Congenital hand deformities, Partial corpus callosum agenesis, x-linked, Dejerine-lichtheim phenomenon, Dyslexia, Dysphasia, Global developmental delay, Hydrocephalus, Congenital hydrocephalus, Hydrops fetalis, Intellectual developmental disorder, Masa syndrome, Peripheral neuropathy, Schizophrenia, Spastic paraplegia, Hereditary spastic paraplegia, Syntactic aphasia, X-linked complicated corpus callosum dysgenesis, X-linked complicated spastic paraplegia, X-linked hydrocephalus syndrome, X-linked hydrocephalus with stenosis of the aqueduct of sylviusView all (11 more) |
