Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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6791 to 6800 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6791
Kinesin family binding protein
KBP, KIAA1279, KIF1BP, TTC20
Color vision deficiency, Coronary artery disease, Intellectual developmental disorder, Cortical development malformation, Microcephaly, Peripheral neuropathy, Schizophrenia

6792
Kinesin family member C1
HSET, KNSL2
Autism, Hepatocellular carcinoma, Breast neoplasms

6793
Kinesin family member C2
-
Holoprosencephaly, Noonan syndrome

6794
Kinesin family member C3
-
Alzheimer disease

6795
Killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 1
CD158A, KIR-K64, KIR221, KIR2DL3, NKAT, NKAT-1, NKAT1, p58.1
Keratoconus

6796
Killer cell immunoglobulin like receptor, two Ig domains and long cytoplasmic tail 2
CD158B1, CD158b, NKAT-6, NKAT6, p58.2
Autoimmune hepatitis

6797
Killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1
CD158E1, KIR, KIR2DL5B, KIR3DL1/S1, NKAT-3, NKAT3, NKB1, NKB1B
Hydatidiform mole, Keratoconus

6798
Killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 2
3DL2, CD158K, KIR-3DL2, NKAT-4, NKAT4, NKAT4B, p140
Alzheimer disease, Crohn disease, Inflammatory bowel disease, Ulcerative colitis

6799
Killer cell immunoglobulin like receptor, three Ig domains and short cytoplasmic tail 1
CD158E2, KIR-123FM, KIR-G1, NKAT-10, NKAT10
Fatigue syndrome, Liver cirrhosis, Lymphoproliferative syndrome

6800
Kirre like nephrin family adhesion molecule 1
KIRREL, NEPH1, NPHS23
Color vision deficiency, Multiple myeloma, Nephrotic syndrome, Obesity