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
8811 to 8820 of 15380 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

8811
Nuclear pore complex interacting protein family member A5
NPIP
Mobius syndrome

8812
Nuclear pore complex interacting protein family member B2
-
Gastric cancer

8813
Nuclear pore complex interacting protein family member B6
NPIPB
Ankylosing spondylitis, Attention deficit hyperactivity disorder, Autism, Autoimmune disease, Autoimmune thyroid disease, Celiac disease, Common variable immunodeficiency, Crohn disease, Hypogonadism, Inflammatory bowel disease, Juvenile idiopathic arthritis, Psoriasis, Systemic lupus erythematosus, Diabetes mellitus type 1, Ulcerative colitis

8814
Nuclear pore complex interacting protein family member B8
-
Insomnia

8815
N-acetylneuraminate pyruvate lyase
C112, C1orf13, NAL, NPL1
Bone fracture, Cholelithiasis, Color vision deficiency

8816
NPL4 homolog, ubiquitin recognition factor
NPL4
Amblyopia, Atrophic macular degeneration, Eye neoplasms, Cataract, Corneal astigmatism, Hearing loss, Non-melanoma skin carcinoma, Age-related macular degeneration

8817
Nucleophosmin 1
B23, NPM
Bone marrow failure syndromes, Dyskeratosis congenita, Myeloid leukemia, Promyelocytic leukemia, Primary cutaneous anaplastic large cell lymphoma, Stomach neoplasms

8818
Nucleophosmin/nucleoplasmin 2
-
Bile duct disorder, Cholelithiasis, Obesity

8819
Nucleophosmin/nucleoplasmin 3
PORMIN, TMEM123
Attention deficit hyperactivity disorder, Autism

8820
Nephronectin
EGFL6L, POEM
Asthma, Atrial fibrillation, Cardiovascular disease, Obstructive pulmonary disease, Renal agenesis, Gastroesophageal reflux disease, Hypertension, Major depressive disorder, Respiratory system disease, Scoliosis