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 58201 - 58225 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0948008 Ischemic stroke SPHK2 56848 sphingosine kinase 2 Q9NRA0
C1332979 Childhood Lymphoma SPHK2 56848 sphingosine kinase 2 Q9NRA0
C0023449 Acute lymphocytic leukemia SPHK2 56848 sphingosine kinase 2 Q9NRA0
C0242379 Malignant neoplasm of lung SPHK2 56848 sphingosine kinase 2 Q9NRA0
C0011847 Diabetes SPHK2 56848 sphingosine kinase 2 Q9NRA0
C0023891 Liver Cirrhosis, Alcoholic SPHK2 56848 sphingosine kinase 2 Q9NRA0
C0004936 Mental disorders SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0020071 Hereditary Sensory Autonomic Neuropathy, Type 1 SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0033975 Psychotic Disorders SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0086405 Hereditary Sensory Radicular Neuropathy SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0006118 Brain Neoplasms SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0007959 Charcot-Marie-Tooth Disease SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0027765 nervous system disorder SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0031117 Peripheral Neuropathy SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0442874 Neuropathy SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C4721453 Peripheral Nervous System Diseases SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0005586 Bipolar Disorder SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0870082 Hyperkeratosis SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0027889 Hereditary Sensory and Autonomic Neuropathies SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0018784 Sensorineural Hearing Loss (disorder) SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C1285162 Degenerative disorder SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0006826 Malignant Neoplasms SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0011265 Presenile dementia SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0151313 Sensory neuropathy SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269
C0699739 Sensory Neuropathy, Hereditary SPTLC1 10558 serine palmitoyltransferase long chain base subunit 1 O15269

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