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
8941 to 8950 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

8941
Neurotrophic receptor tyrosine kinase 2
DEE58, EIEE58, GP145-TrkB, OBHD, TRKB, trk-B
Alzheimer disease, Androgenetic alopecia, Anxiety disorder, Astrocytoma, Autism, Bipolar disorder, Ischemic stroke, Colorectal cancer, Bipolar depression, Major depressive disorder, Developmental and epileptic encephalopathy, Developmental disability, Diabetic retinopathy, Dysthymic disorder, Early-onset obesity-hyperphagia-severe developmental delay syndrome
View all (18 more)

8942
Neurotrophic receptor tyrosine kinase 3
GP145-TrkC, TRKC, gp145(trkC)
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Central nervous system cancer, Congenital heart disease, Congenital mesoblastic nephroma, Dementia, Differentiated thyroid carcinoma, Endometriosis, Gaucher disease, Glioblastoma, Glioma, Hypertrophic cardiomyopathy, Internet addiction disorder
View all (9 more)

8943
Neurotensin
NMN-125, NN, NT, NT/N, NTS1
Astrocytoma, Bradycardia, Catalepsy, Major depressive disorder, Hyperkinesia, Lewy body disease, Mood disorder, Schizophrenia, Small vessel stroke

8944
Neurotensin receptor 1
NTR
Alzheimer disease, Autism, Mood disorder, Schizophrenia

8945
Neurotensin receptor 2
NTR2
Stroke

8946
NUAK family kinase 1
ARK5
Color vision deficiency, Keratoconus, Kidney disease, Multiple myeloma, Rheumatoid arthritis

8947
NUAK family kinase 2
ANPH2, SNARK
Anencephaly, Aprosencephaly

8948
NUBP iron-sulfur cluster assembly factor 1, cytosolic
CIAO5, NBP, NBP1, NBP35
Alzheimer disease, Color vision deficiency

8949
NUBP iron-sulfur cluster assembly factor 2, cytosolic
CFD1, CIAO6, NBP 2, NUBP1
Ocular hypertension

8950
NUBP iron-sulfur cluster assembly factor, mitochondrial
C14orf127, IND1, MC1DN21, huInd1
Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Multiple sclerosis, Obsessive-compulsive disorder, Tourette syndrome