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.

TRNI

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

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

Label: TRNI

Synonyms: TRNI, MTTI, tRNA, MT-TI, mitochondrially encoded tRNA isoleucine

Alternative IDs: 4565

API: GO

SPARQL: GO

Similar Entities

TRNI

http://www.ncbi.nlm.nih.gov/gene/4565
TRNL2

http://www.ncbi.nlm.nih.gov/gene/4568
TRI-AAT9-1

http://www.ncbi.nlm.nih.gov/gene/7202
TRNY

http://www.ncbi.nlm.nih.gov/gene/4579
RNASEH1P1

http://www.ncbi.nlm.nih.gov/gene/284203
chronic progressive external ophthalmoplegia

DOID:12558
TRNA

http://www.ncbi.nlm.nih.gov/gene/4553
Kearns-Sayre syndrome

DOID:12934
MERRF syndrome

DOID:310
RNR2

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

http://www.ncbi.nlm.nih.gov/gene/4569
TRS-AGA2-3

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

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

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

DOID:890
Progressive external ophthalmoplegia

HP:0000590
mitochondrial myopathy

DOID:699
MELAS syndrome

DOID:3687
Ru360

http://aber-owl.net/drug/CID116760639
Ru360

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

http://www.ncbi.nlm.nih.gov/gene/7407
OPA1

http://www.ncbi.nlm.nih.gov/gene/4976
mitochondrial disease

DOID:0080013
PERM1

http://www.ncbi.nlm.nih.gov/gene/84808
Leigh disease

DOID:3652
infantile onset spinocerebellar ataxia

DOID:0050556
ATP6

http://www.ncbi.nlm.nih.gov/gene/4508
GLC3B

http://www.ncbi.nlm.nih.gov/gene/2728
Pearson syndrome

DOID:0060067
no_name

DOID:10868
Alpers syndrome

DOID:1442
AC1L9MEY

http://aber-owl.net/drug/CID000448846
VARS2

http://www.ncbi.nlm.nih.gov/gene/57176
STK19B

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

http://www.ncbi.nlm.nih.gov/gene/8422
obsolete Rod-cone dystrophy

HP:0008036
oculomotor nerve paralysis

DOID:11550
glossopharyngeal nerve disease

DOID:3418
ATP8

http://www.ncbi.nlm.nih.gov/gene/4509
MAPKAP1

http://www.ncbi.nlm.nih.gov/gene/79109
alternating esotropia

DOID:9888
SOD2

http://www.ncbi.nlm.nih.gov/gene/6648
crotonyl coenzyme A

http://aber-owl.net/drug/CID005280381
Mitochondrial myopathy

HP:0003737
cyclotropia

DOID:9838
Ophthalmoparesis

HP:0000597
Ophthalmoplegia

HP:0000602
ophthalmoplegia

DOID:539
OAS1

http://www.ncbi.nlm.nih.gov/gene/4938
olivopontocerebellar atrophy

DOID:14784
Wernicke-Korsakoff syndrome

DOID:10915
Mitochondrial encephalopathy

HP:0006789
Stroke-like episode

HP:0002401
ATP2B3

http://www.ncbi.nlm.nih.gov/gene/492
Ragged-red muscle fibers

HP:0003200
Tay-Sachs disease AB variant

DOID:4795
4-(N,N-dimethylamino)cinnamoyl-CoA

http://aber-owl.net/drug/CID000445461
Danon disease

DOID:0050437
SGCG

http://www.ncbi.nlm.nih.gov/gene/6445
guanidine hydrochloride

http://aber-owl.net/drug/CID100005742
anterior horn cell disease

DOID:4873
tick paralysis

DOID:0050265
ACTN3

http://www.ncbi.nlm.nih.gov/gene/89
LAPAO

http://aber-owl.net/drug/CID000094599
Leber hereditary optic neuropathy

DOID:705
TRNK

http://www.ncbi.nlm.nih.gov/gene/4566
UBR4

http://www.ncbi.nlm.nih.gov/gene/23352
TRNG

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

http://www.ncbi.nlm.nih.gov/gene/4570
Machado-Joseph disease

DOID:1440
COX1

http://www.ncbi.nlm.nih.gov/gene/4512
PRPF6

http://www.ncbi.nlm.nih.gov/gene/24148
Progressive encephalopathy

HP:0002448
multiple cranial nerve palsy

DOID:13866
MTO1

http://www.ncbi.nlm.nih.gov/gene/25821
COX2

http://www.ncbi.nlm.nih.gov/gene/4513
guanidine hydrochloride

http://aber-owl.net/drug/CID000005742
striatonigral degeneration

DOID:4751
DHX16

http://www.ncbi.nlm.nih.gov/gene/8449
abnormal threshold of rods

DOID:11874
APTX

http://www.ncbi.nlm.nih.gov/gene/54840
Azelaoyl PAF

http://aber-owl.net/drug/CID011445168
PCAT2

http://www.ncbi.nlm.nih.gov/gene/103164619
DPYD

http://www.ncbi.nlm.nih.gov/gene/1806
HSPB1

http://www.ncbi.nlm.nih.gov/gene/3315
Internal ophthalmoplegia

HP:0007942
TRNP

http://www.ncbi.nlm.nih.gov/gene/4571
External ophthalmoplegia

HP:0000544
TRNV

http://www.ncbi.nlm.nih.gov/gene/4577
olfactory nerve disease

DOID:367
survival motor neuron spinal muscular atrophy

DOID:0060160
vestibular nystagmus

DOID:14070
Multiple mitochondrial DNA deletions

HP:0003689
IVNS1ABP

http://www.ncbi.nlm.nih.gov/gene/10625
Congenital lactic acidosis

HP:0004902
3-HB

http://aber-owl.net/drug/CID000007420
ataxia with oculomotor apraxia type 1

DOID:0050754
ATXN8

http://www.ncbi.nlm.nih.gov/gene/724066
SPG36

http://www.ncbi.nlm.nih.gov/gene/791228
obsolete Peripheral retinal pigmentation abnormalities

HP:0200099

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