DisGeNET

DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.

Source Last Updated
DisGeNET July 29, 2024
Displaying entries 16651 - 16675 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0036341 Schizophrenia CFC1 55997 cripto, FRL-1, cryptic family 1 P0CG37
C0018799 Heart Diseases CFC1 55997 cripto, FRL-1, cryptic family 1 P0CG37
C3553676 HETEROTAXY, VISCERAL, 6, AUTOSOMAL CFC1 55997 cripto, FRL-1, cryptic family 1 P0CG37
C0858252 Breast adenocarcinoma LYNX1 66004 Ly6/neurotoxin 1 P0DP58
C0684249 Carcinoma of lung LYNX1 66004 Ly6/neurotoxin 1 P0DP58
C0699790 Colon Carcinoma LYNX1 66004 Ly6/neurotoxin 1 P0DP58
C0004096 Asthma LYNX1 66004 Ly6/neurotoxin 1 P0DP58
C0033860 Psoriasis LYNX1 66004 Ly6/neurotoxin 1 P0DP58
C0678222 Breast Carcinoma SRGN 5552 serglycin P10124
C0010054 Coronary Arteriosclerosis SRGN 5552 serglycin P10124
C0006826 Malignant Neoplasms SRGN 5552 serglycin P10124
C0023467 Leukemia, Myelocytic, Acute SRGN 5552 serglycin P10124
C0271650 Impaired glucose tolerance SRGN 5552 serglycin P10124
C0017636 Glioblastoma SRGN 5552 serglycin P10124
C0085110 Severe Combined Immunodeficiency SRGN 5552 serglycin P10124
C0684249 Carcinoma of lung SRGN 5552 serglycin P10124
C0029408 Degenerative polyarthritis SRGN 5552 serglycin P10124
C0158266 Intervertebral Disc Degeneration SRGN 5552 serglycin P10124
C0021364 Male infertility SRGN 5552 serglycin P10124
C0027651 Neoplasms SRGN 5552 serglycin P10124
C0003864 Arthritis SRGN 5552 serglycin P10124
C0019270 Hernia SRGN 5552 serglycin P10124
C0011334 Dental caries SRGN 5552 serglycin P10124
C0028960 Oligospermia SRGN 5552 serglycin P10124
C0024138 Lupus Erythematosus, Discoid SRGN 5552 serglycin P10124

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Last updated: August 19, 2024