Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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6581 to 6590 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6581
Katanin regulatory subunit B1
KAT, LIS6
Lissencephaly, Microlissencephaly

6582
Katanin interacting protein
JBTS26, KIAA0556
Ciliopathy, Aplasia of the vermis, Joubert syndrome, Scoliosis

6583
Kazrin, periplakin interacting protein
C1orf196, KAZ
Alzheimer disease, Jeune syndrome, Asthma, Brain infarction, Central nervous system cancer, Cerebral amyloid angiopathy, Chagas cardiomyopathy, Obstructive pulmonary disease, Colorectal cancer, Conotruncal cardiac defect, Dementia, Major depressive disorder, Gastroesophageal reflux disease, Glioblastoma, Glioma
View all (12 more)

6584
Kelch repeat and BTB domain containing 11
KLHDC7C
Hepatocellular carcinoma, Cervical cancer, Obesity

6585
Kelch repeat and BTB domain containing 12
KLHDC6
Central nervous system cancer, Glioblastoma, Glioma, Oligodendroglioma

6586
Kelch repeat and BTB domain containing 13
HCG1645727, NEM6
Nemaline myopathy

6587
Kelch repeat and BTB domain containing 4
BKLHD4, HSPC252
Anorexia nervosa, Attention deficit hyperactivity disorder, Diabetes mellitus type 2, Venous thromboembolism

6588
Kelch repeat and BTB domain containing 8
TA-KRP, TAKRP
Alzheimer disease, Atherosclerosis, Color vision deficiency, Tourette syndrome, Migraine, Oligodendroglioma, Open angle glaucoma, Retinal detachment, Diabetes mellitus type 2

6589
Potassium voltage-gated channel subfamily A member 1
AEMK, EA1, HBK1, HUK1, KV1.1, MBK1, MK1, RBK1
Color vision deficiency, Conduct disorder, Hereditary continuous muscle fiber activity, Dementia, Developmental and epileptic encephalopathy, Episodic ataxia, Episodic kinesigenic dyskinesia, Paroxysmal dystonic choreoathetosis, Paroxysmal dyskinesia, Paroxysmal nonkinesigenic dyskinesia, Schizophrenia, Scoliosis

6590
Potassium voltage-gated channel subfamily A member 10
Kcn1, Kv1.8
Long qt syndrome