Abnormality Of The Spleen Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An abnormality of the spleen. (Human Phenotype Ontology, HP_0001743)
External Link https://www.disgenet.org/browser/0/1/0/C4025749
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Genes

26 genes associated with the disease Abnormality Of The Spleen in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
A2ML1 alpha-2-macroglobulin-like 1
BRAF B-Raf proto-oncogene, serine/threonine kinase
GABRD gamma-aminobutyric acid (GABA) A receptor, delta
GLB1 galactosidase, beta 1
HBB hemoglobin, beta
HMGA2 high mobility group AT-hook 2
KAT6B K(lysine) acetyltransferase 6B
KCNAB2 potassium channel, voltage gated subfamily A regulatory beta subunit 2
KRAS Kirsten rat sarcoma viral oncogene homolog
LEMD3 LEM domain containing 3
LZTR1 leucine-zipper-like transcription regulator 1
MRAS muscle RAS oncogene homolog
MYC v-myc avian myelocytomatosis viral oncogene homolog
NRAS neuroblastoma RAS viral (v-ras) oncogene homolog
POMP proteasome maturation protein
PRDM16 PR domain containing 16
PTPN11 protein tyrosine phosphatase, non-receptor type 11
RAF1 Raf-1 proto-oncogene, serine/threonine kinase
RASA2 RAS p21 protein activator 2
RERE arginine-glutamic acid dipeptide (RE) repeats
RIT1 Ras-like without CAAX 1
RRAS related RAS viral (r-ras) oncogene homolog
SKI SKI proto-oncogene
SOS1 son of sevenless homolog 1 (Drosophila)
SOS2 son of sevenless homolog 2 (Drosophila)
WT1 Wilms tumor 1