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 59301 - 59325 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0023492 Leukemia, T-Cell SACM1L 22908 SAC1 like phosphatidylinositide phosphatase Q9NTJ5
C0011847 Diabetes SACM1L 22908 SAC1 like phosphatidylinositide phosphatase Q9NTJ5
C0007282 Carotid Stenosis SACM1L 22908 SAC1 like phosphatidylinositide phosphatase Q9NTJ5
C0006142 Malignant neoplasm of breast SACM1L 22908 SAC1 like phosphatidylinositide phosphatase Q9NTJ5
C1961102 Precursor Cell Lymphoblastic Leukemia Lymphoma SACM1L 22908 SAC1 like phosphatidylinositide phosphatase Q9NTJ5
C0234533 Generalized seizures SACM1L 22908 SAC1 like phosphatidylinositide phosphatase Q9NTJ5
C0003873 Rheumatoid Arthritis SACM1L 22908 SAC1 like phosphatidylinositide phosphatase Q9NTJ5
C0342276 Maturity onset diabetes mellitus in young SACM1L 22908 SAC1 like phosphatidylinositide phosphatase Q9NTJ5
C0011849 Diabetes Mellitus SACM1L 22908 SAC1 like phosphatidylinositide phosphatase Q9NTJ5
C0751955 Brain Infarction SACM1L 22908 SAC1 like phosphatidylinositide phosphatase Q9NTJ5
C0011860 Diabetes Mellitus, Non-Insulin-Dependent SACM1L 22908 SAC1 like phosphatidylinositide phosphatase Q9NTJ5
C0020538 Hypertensive disease SACM1L 22908 SAC1 like phosphatidylinositide phosphatase Q9NTJ5
C1956346 Coronary Artery Disease SACM1L 22908 SAC1 like phosphatidylinositide phosphatase Q9NTJ5
C0029422 Osteochondrodysplasias SLC35D1 23169 solute carrier family 35 member D1 Q9NTN3
C0024236 Lymphedema SLC35D1 23169 solute carrier family 35 member D1 Q9NTN3
C0008925 Cleft Palate SLC35D1 23169 solute carrier family 35 member D1 Q9NTN3
C0020224 Polyhydramnios SLC35D1 23169 solute carrier family 35 member D1 Q9NTN3
C0432194 Schneckenbecken dysplasia SLC35D1 23169 solute carrier family 35 member D1 Q9NTN3
C0010417 Cryptorchidism SLC35D1 23169 solute carrier family 35 member D1 Q9NTN3
C0265282 Fibrochondrogenesis SLC35D1 23169 solute carrier family 35 member D1 Q9NTN3
C0013595 Eczema SLC35D1 23169 solute carrier family 35 member D1 Q9NTN3
C4721610 Carcinoma, Ovarian Epithelial ECHDC1 55862 ethylmalonyl-CoA decarboxylase 1 Q9NTX5
C1140680 Malignant neoplasm of ovary ECHDC1 55862 ethylmalonyl-CoA decarboxylase 1 Q9NTX5
C0699885 Carcinoma of bladder ECHDC1 55862 ethylmalonyl-CoA decarboxylase 1 Q9NTX5
C0005684 Malignant neoplasm of urinary bladder ECHDC1 55862 ethylmalonyl-CoA decarboxylase 1 Q9NTX5

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024