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.

TRNY

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

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

Label: TRNY

Synonyms: TRNY, MTTY, tRNA, MT-TY, mitochondrially encoded tRNA tyrosine

Alternative IDs: 4579

API: GO

SPARQL: GO

Similar Entities

TRNY

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

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

http://www.ncbi.nlm.nih.gov/gene/4565
Kearns-Sayre syndrome

DOID:12934
TRNC

http://www.ncbi.nlm.nih.gov/gene/4511
TRI-AAT9-1

http://www.ncbi.nlm.nih.gov/gene/7202
chronic progressive external ophthalmoplegia

DOID:12558
RNR2

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

http://www.ncbi.nlm.nih.gov/gene/4563
Ru360

http://aber-owl.net/drug/CID116760639
TRS-AGA2-3

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

http://www.ncbi.nlm.nih.gov/gene/4570
VWA7

http://www.ncbi.nlm.nih.gov/gene/80737
PCOS1

http://www.ncbi.nlm.nih.gov/gene/5120
RNASEH1P1

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

http://www.ncbi.nlm.nih.gov/gene/11188
mitochondrial myopathy

DOID:699
MIR132

http://www.ncbi.nlm.nih.gov/gene/406921
MELAS syndrome

DOID:3687
TCF19

http://www.ncbi.nlm.nih.gov/gene/6941
mitochondrial encephalomyopathy

DOID:890
FPGT-TNNI3K

http://www.ncbi.nlm.nih.gov/gene/100526835
VARS

http://www.ncbi.nlm.nih.gov/gene/7407
IVNS1ABP

http://www.ncbi.nlm.nih.gov/gene/10625
PART1

http://www.ncbi.nlm.nih.gov/gene/25859
MAGEE1

http://www.ncbi.nlm.nih.gov/gene/57692
VAV2

http://www.ncbi.nlm.nih.gov/gene/7410
FLOT1

http://www.ncbi.nlm.nih.gov/gene/10211
OPA1

http://www.ncbi.nlm.nih.gov/gene/4976
RGSL1

http://www.ncbi.nlm.nih.gov/gene/353299
Ophthalmoparesis

HP:0000597
DHX16

http://www.ncbi.nlm.nih.gov/gene/8449
PPT2

http://www.ncbi.nlm.nih.gov/gene/9374
HLA-F-AS1

http://www.ncbi.nlm.nih.gov/gene/285830
Tay-Sachs disease AB variant

DOID:4795
AC1L9MEY

http://aber-owl.net/drug/CID000448846
CHD8

http://www.ncbi.nlm.nih.gov/gene/57680
CT55

http://www.ncbi.nlm.nih.gov/gene/54967
Ophthalmoplegia

HP:0000602
MIR591

http://www.ncbi.nlm.nih.gov/gene/693176
TTC39B

http://www.ncbi.nlm.nih.gov/gene/158219
MEHMO

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

DOID:1442
CCDC82

http://www.ncbi.nlm.nih.gov/gene/79780
MERRF syndrome

DOID:310
NPCA1

http://www.ncbi.nlm.nih.gov/gene/257641
TRAPPC2L

http://www.ncbi.nlm.nih.gov/gene/51693
Progressive external ophthalmoplegia

HP:0000590
no_name

DOID:10868
Ru360

http://aber-owl.net/drug/CID016760639
APH1A

http://www.ncbi.nlm.nih.gov/gene/51107
no_name

http://www.ncbi.nlm.nih.gov/gene/101669765
MIR3976HG

http://www.ncbi.nlm.nih.gov/gene/645355
diabetic peripheral angiopathy

DOID:10182
BMIQ10

http://www.ncbi.nlm.nih.gov/gene/353126
COL13A1

http://www.ncbi.nlm.nih.gov/gene/1305
MEF2C-AS1

http://www.ncbi.nlm.nih.gov/gene/101929423
ANKLE1

http://www.ncbi.nlm.nih.gov/gene/126549
SYBU

http://www.ncbi.nlm.nih.gov/gene/55638
PSMD1

http://www.ncbi.nlm.nih.gov/gene/5707
COBL

http://www.ncbi.nlm.nih.gov/gene/23242
ND2

http://www.ncbi.nlm.nih.gov/gene/4536
mitochondrial disease

DOID:0080013
IGKV2D-29

http://www.ncbi.nlm.nih.gov/gene/28882
TRNK

http://www.ncbi.nlm.nih.gov/gene/4566
CHEMBL51499

http://aber-owl.net/drug/CID010340034
ST8

http://www.ncbi.nlm.nih.gov/gene/6765
SPON1

http://www.ncbi.nlm.nih.gov/gene/10418
IGHV1-17

http://www.ncbi.nlm.nih.gov/gene/28469
MAPKAP1

http://www.ncbi.nlm.nih.gov/gene/79109
POLG

http://www.ncbi.nlm.nih.gov/gene/5428
PEMT

http://www.ncbi.nlm.nih.gov/gene/10400
SOD2

http://www.ncbi.nlm.nih.gov/gene/6648
SERPINA3

http://www.ncbi.nlm.nih.gov/gene/12
Leber hereditary optic neuropathy

DOID:705
BMIQ8

http://www.ncbi.nlm.nih.gov/gene/56694
DB02426

http://aber-owl.net/drug/CID046936378
IKBKE

http://www.ncbi.nlm.nih.gov/gene/9641
PIAS3

http://www.ncbi.nlm.nih.gov/gene/10401
PERM1

http://www.ncbi.nlm.nih.gov/gene/84808
MIR563

http://www.ncbi.nlm.nih.gov/gene/693148
BCDIN3D-AS1

http://www.ncbi.nlm.nih.gov/gene/100286844
MEST

http://www.ncbi.nlm.nih.gov/gene/4232
FKBP1AP1

http://www.ncbi.nlm.nih.gov/gene/2282
Progressive ophthalmoplegia

HP:0007650
Pearson syndrome

DOID:0060067
SERPINA13P

http://www.ncbi.nlm.nih.gov/gene/388007
ARID4B

http://www.ncbi.nlm.nih.gov/gene/51742
OAS1

http://www.ncbi.nlm.nih.gov/gene/4938
MIR483

http://www.ncbi.nlm.nih.gov/gene/619552
MBL2

http://www.ncbi.nlm.nih.gov/gene/4153
CRYGEP

http://www.ncbi.nlm.nih.gov/gene/200575
ZBTB12

http://www.ncbi.nlm.nih.gov/gene/221527
CNR1

http://www.ncbi.nlm.nih.gov/gene/1268
IDDM3

http://www.ncbi.nlm.nih.gov/gene/3402
Ragged-red muscle fibers

HP:0003200
LINC02135

http://www.ncbi.nlm.nih.gov/gene/146513

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