IL2Rgbase

Description

More detailed information about this field from each metasource.

X-linked severe combined immunodeficiency mutations

metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657

Lowe Syndrome Mutation Database

Mutations in the OCRL1 gene encoding phosphatidylinositol-4,5-bisphosphate 5-phosphatase

ALPSbase

Autoimmune lymphoproliferative syndrome database

G2Cdb

Genes to Cognition

PubAngioGen

Public angiogenesis research portal

PGDB

Prostate and prostatic diseases gene database

SZGR

SchiZophrenia Gene Resource

HemBase

Genes transcribed in differentiating human erythroid cells

EpilepsyGene

Genes and mutations related to epilepsy

DDMGD

Associations between genes methylated in diseases

PCOSKB

Genes, diseases, and pathways associated with PolyCystic Ovary Syndrome

HbVar

Human haemoglobin variants and thalassemias

GEneSTATION

Evolutionary genomics of pregnancy-related tissues and phenotypes

KERIS

Kaleidoscope of gEne Responses to Inflammation among Species

EyeSite

Families of proteins functioning in the eye

MDPD

Mutation Database for Parkinson's Disease

Digital Ageing Atlas

Human ageing-related data

CRISPRz

CRISPR single guide RNAs to zebrafish genes

DNAreplication.net

Database for the eukaryotic DNA replication community

HOX-PRO

Clustering of homeobox genes

KBERG

KBERG is a database to decipher the functional association of Estrogen Responsive Genes, espcially the transcriptional regulation and functional classification of ERG.

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