Bio2Vec

BIO-KNOWLEDGE-GRAPH

A knowledge graph of biological entities such as genes, gene functions, diseases, phenotypes and chemicals. Embeddings are generated with Walking RDF and OWL method.

VARS

ID: http://www.ncbi.nlm.nih.gov/gene/7407

Type: http://bio2vec.net/ontology/gene

Label: VARS

Synonyms: VARS, G7A, VARS1, VARS2, valyl-tRNA synthetase, valine--tRNA ligase, protein G7a, valRS, valine tRNA ligase 1, cytoplasmic, valyl-tRNA synthetase 2

Alternative IDs: 7407

API: GO

SPARQL: GO

Similar Entities

VARS

http://www.ncbi.nlm.nih.gov/gene/7407
RNR2

http://www.ncbi.nlm.nih.gov/gene/4550
RNASEH1P1

http://www.ncbi.nlm.nih.gov/gene/284203
TRNA

http://www.ncbi.nlm.nih.gov/gene/4553
TRNL2

http://www.ncbi.nlm.nih.gov/gene/4568
TRNR

http://www.ncbi.nlm.nih.gov/gene/4573
mitochondrial encephalomyopathy

DOID:890
TRNC

http://www.ncbi.nlm.nih.gov/gene/4511
VARS2

http://www.ncbi.nlm.nih.gov/gene/57176
TRNM

http://www.ncbi.nlm.nih.gov/gene/4569
TRNI

http://www.ncbi.nlm.nih.gov/gene/4565
MEHMO

http://www.ncbi.nlm.nih.gov/gene/8422
MELAS syndrome

DOID:3687
MAPKAP1

http://www.ncbi.nlm.nih.gov/gene/79109
TRI-AAT9-1

http://www.ncbi.nlm.nih.gov/gene/7202
TRS-AGA2-3

http://www.ncbi.nlm.nih.gov/gene/23437
TRNN

http://www.ncbi.nlm.nih.gov/gene/4570
mitochondrial myopathy

DOID:699
cytochrome-c oxidase deficiency disease

DOID:3762
TRNY

http://www.ncbi.nlm.nih.gov/gene/4579
ATP6V1G2

http://www.ncbi.nlm.nih.gov/gene/534
chronic progressive external ophthalmoplegia

DOID:12558
MERRF syndrome

DOID:310
Congenital lactic acidosis

HP:0004902
Kearns-Sayre syndrome

DOID:12934
SUN1

http://www.ncbi.nlm.nih.gov/gene/23353
SOD2

http://www.ncbi.nlm.nih.gov/gene/6648
Enlarged hippocampus

HP:0100961
Ru360

http://aber-owl.net/drug/CID116760639
mitochondrial complex I deficiency

DOID:0060536
HIST1H3D

http://www.ncbi.nlm.nih.gov/gene/8351
TRE-TTC3-1

http://www.ncbi.nlm.nih.gov/gene/7193
CHEBI:300670

http://aber-owl.net/drug/CID044347267
GGTLC4P

http://www.ncbi.nlm.nih.gov/gene/729838
CHD8

http://www.ncbi.nlm.nih.gov/gene/57680
TRIM10

http://www.ncbi.nlm.nih.gov/gene/10107
biotin-responsive basal ganglia disease

DOID:0050659
multiple mitochondrial dysfunctions syndrome 2

DOID:0080134
Leber hereditary optic neuropathy

DOID:705
RNF20

http://www.ncbi.nlm.nih.gov/gene/56254
ATP6

http://www.ncbi.nlm.nih.gov/gene/4508
STK19B

http://www.ncbi.nlm.nih.gov/gene/373159
PPT2

http://www.ncbi.nlm.nih.gov/gene/9374
BTN2A1

http://www.ncbi.nlm.nih.gov/gene/11120
lactic acidosis

DOID:3650
Mitochondrial myopathy

HP:0003737
EPRS

http://www.ncbi.nlm.nih.gov/gene/2058
SLEB12

http://www.ncbi.nlm.nih.gov/gene/100190928
Tay-Sachs disease AB variant

DOID:4795
no_name

http://www.ncbi.nlm.nih.gov/gene/101927736
mitochondrial disease

DOID:0080013
DXO

http://www.ncbi.nlm.nih.gov/gene/1797
MTO1

http://www.ncbi.nlm.nih.gov/gene/25821
HIST1H3A

http://www.ncbi.nlm.nih.gov/gene/8350
Progressive external ophthalmoplegia

HP:0000590
ITPA

http://www.ncbi.nlm.nih.gov/gene/3704
HSP90B2P

http://www.ncbi.nlm.nih.gov/gene/7190
CLN9

http://www.ncbi.nlm.nih.gov/gene/497231
Lactic acidosis

HP:0003128
Alpers syndrome

DOID:1442
alcohol-related neurodevelopmental disorder

DOID:0050667
RREB1

http://www.ncbi.nlm.nih.gov/gene/6239
LY6G6E

http://www.ncbi.nlm.nih.gov/gene/79136
CDSN

http://www.ncbi.nlm.nih.gov/gene/1041
C6orf47

http://www.ncbi.nlm.nih.gov/gene/57827
AAVS1

http://www.ncbi.nlm.nih.gov/gene/17
Pearson syndrome

DOID:0060067
CHEMBL91882

http://aber-owl.net/drug/CID122096266
sphingolipidosis

DOID:1927
SS18L1

http://www.ncbi.nlm.nih.gov/gene/26039
CHEBI:356715

http://aber-owl.net/drug/CID011826682
DCDC2C

http://www.ncbi.nlm.nih.gov/gene/728597
Leigh disease

DOID:3652
C16orf82

http://www.ncbi.nlm.nih.gov/gene/162083
CCDC190

http://www.ncbi.nlm.nih.gov/gene/339512
cerotoyl-CoA

http://aber-owl.net/drug/CID025202335
CD8B

http://www.ncbi.nlm.nih.gov/gene/926
HLA-DRB5

http://www.ncbi.nlm.nih.gov/gene/3127
SAPCD1

http://www.ncbi.nlm.nih.gov/gene/401251
PERM1

http://www.ncbi.nlm.nih.gov/gene/84808
HIST1H3G

http://www.ncbi.nlm.nih.gov/gene/8355
pyruvate decarboxylase deficiency

DOID:3649
LOC100129940

http://www.ncbi.nlm.nih.gov/gene/100129940
DAB1

http://www.ncbi.nlm.nih.gov/gene/1600
USP17L26

http://www.ncbi.nlm.nih.gov/gene/728379
Ru360

http://aber-owl.net/drug/CID016760639
HLA-DRB4

http://www.ncbi.nlm.nih.gov/gene/3126
PPR2

http://www.ncbi.nlm.nih.gov/gene/780910
TRNK

http://www.ncbi.nlm.nih.gov/gene/4566
PD-172939

http://aber-owl.net/drug/CID009928335
COL13A1

http://www.ncbi.nlm.nih.gov/gene/1305
SureCN55723

http://aber-owl.net/drug/CID046227614
ZDHHC8P1

http://www.ncbi.nlm.nih.gov/gene/150244
mitochondrial complex III deficiency nuclear type 2

DOID:0060351
LST1

http://www.ncbi.nlm.nih.gov/gene/7940
MTMR1

http://www.ncbi.nlm.nih.gov/gene/8776
RNASE1

http://www.ncbi.nlm.nih.gov/gene/6035
SERPINA2

http://www.ncbi.nlm.nih.gov/gene/390502
DPH6

http://www.ncbi.nlm.nih.gov/gene/89978
mitochondrial complex III deficiency nuclear type 6

DOID:0080115

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