Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
7231 to 7240 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

7231
Leucyl and cystinyl aminopeptidase
CAP, IRAP, P-LAP, PLAP
Birdshot chorioretinopathy, Coronary artery disease, Iga nephropathy, Memory disorders, Oligoarticular juvenile idiopathic arthritis, Oligodendroglioma, Polyarticular juvenile idiopathic arthritis, Juvenile idiopathic arthritis

7232
Lunapark, ER junction formation factor
KIAA1715, LNP, LNP1, NEDEHCC, Ul, ulnaless
Carpal tunnel syndrome, Congenital heart disease, Exostoses, Gestational diabetes, Hypertension, Major depressive disorder, Neurodevelopmental disorder, Neurotic disorder, Obesity, Pelvic organ prolapse, Periodontitis, Schizophrenia

7233
Ligand of numb-protein X 1
LNX, MPDZ, PDZRN2
Alzheimer disease, Androgenetic alopecia, Asthma, Atherosclerosis, Obstructive pulmonary disease, Coronary artery disease, Dementia, Diabetic foot, Neuropathy, Oligodendroglioma, Upper aerodigestive tract neoplasm, Uterine fibroid

7234
Ligand of numb-protein X 2
PDZRN1
Dental caries, Schizophrenia

7235
-
SIK, SIK-1, SIK1, SIK1B, SNF1LK
Rolandic epilepsy

7236
-
ALDA, ALDOA
Glycogen storage disease

7237
-
-
Left ventricular disease

7238
-
-
Bardet-biedl syndrome

7239
-
-
Bardet-biedl syndrome

7240
Lon peptidase 1, mitochondrial
CODASS, LON, LONP, LonHS, PIM1, PRSS15, hLON
Codas syndrome, Congenital cataract, Congenital diaphragmatic hernia, Desbuquois syndrome, Leigh syndrome, Mitochondrial encephalomyopathy, Neurodevelopmental disorder