Genes | GeDiPNet - Gene Disease Pathway & Associations

Dataset:

All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

1301 to 1310 of 12229 Genes

Show

	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1301	109864269	MIR302CHG	MiR-302/367 cluster host gene	-	Microcephalic primordial dwarfism
1302	10987	COPS5	COP9 signalosome subunit 5	CSN5, JAB1, MOV-34, SGN5	Joubert syndrome, Liver carcinoma, Stevens-johnson syndrome
1303	10988	METAP2	Methionyl aminopeptidase 2	MAP2, MNPEP, p67eIF2	Leukemia
1304	10989	IMMT	Inner membrane mitochondrial protein	HMP, MICOS60, MINOS2, Mic60, P87, P87/89, P89, PIG4, PIG52	Arthritis, Osteoarthrosis deformans
1305	10990	LILRB5	Leukocyte immunoglobulin like receptor B5	CD85C, LIR-8, LIR8	Liver carcinoma
1306	10991	SLC38A3	Solute carrier family 38 member 3	DEE102, G17, NAT1, SN1, SNAT3	Anxiety disorder, Conotruncal heart defect
1307	10992	SF3B2	Splicing factor 3b subunit 2	CFM, Cus1, HFM, SAP145, SF3B145, SF3b1, SF3b150	Mammary neoplasms, Lymphocytic leukemia, Leukemia, Liver carcinoma, Medulloblastoma, Melanoma, Myelodysplastic syndrome, Pancreatic adenocarcinoma, Renal carcinoma
1308	10998	SLC27A5	Solute carrier family 27 member 5	ACSB, ACSVL6, BACS, BAL, FACVL3, FATP-5, FATP5, VLACSR, VLCS-H2, VLCSH2	Bile acid coa ligase deficiency and defective amidation
1309	10999	SLC27A4	Solute carrier family 27 member 4	ACSVL4, FATP4, IPS	Congenital alveolar dysplasia, Eosinophilia, Ichthyosis, Ichthyosis prematurity syndrome, Ichthyosis-prematurity syndrome
1310	11001	SLC27A2	Solute carrier family 27 member 2	ACSVL1, FACVL1, FATP2, HsT17226, VLACS, VLCS, hFACVL1	Cirrhosis

«««...129 130131132 133...»»»