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.

LINC01621

ID: http://www.ncbi.nlm.nih.gov/gene/89758

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

Label: LINC01621

Synonyms: LINC01621, C6orf7, long intergenic non-protein coding RNA 1621

Alternative IDs: 89758

API: GO

SPARQL: GO

Similar Entities

LINC01621

http://www.ncbi.nlm.nih.gov/gene/89758
SH3BGRL2

http://www.ncbi.nlm.nih.gov/gene/83699
ETL2

http://www.ncbi.nlm.nih.gov/gene/619399
partial sensory epilepsy

DOID:3330
H2BFWT

http://www.ncbi.nlm.nih.gov/gene/158983
IGLV6-57

http://www.ncbi.nlm.nih.gov/gene/28778
ERVK-24

http://www.ncbi.nlm.nih.gov/gene/100862684
gangliosidosis GM1

DOID:3322
MIRLET7I

http://www.ncbi.nlm.nih.gov/gene/406891
D1S111

http://www.ncbi.nlm.nih.gov/gene/7824
TMC2

http://www.ncbi.nlm.nih.gov/gene/117532
Muenke Syndrome

DOID:0060703
cyclic hematopoiesis

DOID:5339
frontal lobe epilepsy

DOID:3331
GLC1J

http://www.ncbi.nlm.nih.gov/gene/574078
RIMBP3C

http://www.ncbi.nlm.nih.gov/gene/150221
atrophic muscular disease

DOID:913
phlebitis

DOID:864
ENO4

http://www.ncbi.nlm.nih.gov/gene/387712
temporal lobe epilepsy

DOID:3328
TSSK1A

http://www.ncbi.nlm.nih.gov/gene/23752
ANOS2P

http://www.ncbi.nlm.nih.gov/gene/3734
LY6G6F

http://www.ncbi.nlm.nih.gov/gene/259215
B- and T-cell mixed leukemia

DOID:9953
pseudohermaphroditism

DOID:3765
primary angle-closure glaucoma

DOID:1405
CUTA

http://www.ncbi.nlm.nih.gov/gene/51596
porokeratosis

DOID:3805
STK40

http://www.ncbi.nlm.nih.gov/gene/83931
autosomal dominant microcephaly

DOID:14725
ADCP1

http://www.ncbi.nlm.nih.gov/gene/106
primary progressive multiple sclerosis

DOID:0050784
TTTY13

http://www.ncbi.nlm.nih.gov/gene/83868
normal pressure hydrocephalus

DOID:1572
juvenile pilocytic astrocytoma

DOID:6811
MT2P1

http://www.ncbi.nlm.nih.gov/gene/4503
invasive tubular breast carcinoma

DOID:6587
acute closed-angle glaucoma

DOID:13862
sclerosing adenosis of breast

DOID:8310
benign epilepsy with centrotemporal spikes

DOID:3329
arteriovenous malformation

DOID:11294
ethylmalonic encephalopathy

DOID:0060640
CLLS3

http://www.ncbi.nlm.nih.gov/gene/100270642
T-cell adult acute lymphocytic leukemia

DOID:5602
ZNF182

http://www.ncbi.nlm.nih.gov/gene/7569
Noonan syndrome

DOID:3490
intracranial arterial disease

DOID:13089
pulmonary valve stenosis

DOID:6420
background diabetic retinopathy

DOID:13208
FAM227B

http://www.ncbi.nlm.nih.gov/gene/196951
pyridoxine deficiency anemia

DOID:8455
CDC14C

http://www.ncbi.nlm.nih.gov/gene/168448
SLEB7

http://www.ncbi.nlm.nih.gov/gene/100188803
gynecomastia

DOID:12698
adamantinous craniopharyngioma

DOID:3846
COLCA1

http://www.ncbi.nlm.nih.gov/gene/399948
kernicterus

DOID:2382
androgen insensitivity syndrome

DOID:4674
HSCR6

http://www.ncbi.nlm.nih.gov/gene/246321
pituitary hypoplasia

DOID:7378
MIR450B

http://www.ncbi.nlm.nih.gov/gene/100126302
pantothenate kinase-associated neurodegeneration

DOID:3981
Froelich syndrome

DOID:6676
mesenteric vascular occlusion

DOID:13252
lymphedema

DOID:4977
retinal degeneration

DOID:8466
CELIAC11

http://www.ncbi.nlm.nih.gov/gene/100188873
central retinal vein occlusion

DOID:2450
MIRLET7F2

http://www.ncbi.nlm.nih.gov/gene/406889
pyruvate carboxylase deficiency disease

DOID:3651
Coats disease

DOID:7765
SPD3

http://www.ncbi.nlm.nih.gov/gene/780922
AUTS12

http://www.ncbi.nlm.nih.gov/gene/100188314
CHEBI:498624

http://aber-owl.net/drug/CID044433363
photosensitive trichothiodystrophy

DOID:2960
gum cancer

DOID:8602
SLEB5

http://www.ncbi.nlm.nih.gov/gene/100188798
megacystis-microcolon-intestinal hypoperistalsis syndrome

DOID:0060610
LOAS

http://www.ncbi.nlm.nih.gov/gene/100188775
GLC1H

http://www.ncbi.nlm.nih.gov/gene/399564
RCD1

http://www.ncbi.nlm.nih.gov/gene/5953
KANSL3

http://www.ncbi.nlm.nih.gov/gene/55683
listeriosis

DOID:11573
CHEBI:271581

http://aber-owl.net/drug/CID044335356
MIR711

http://www.ncbi.nlm.nih.gov/gene/100313843
MORN5

http://www.ncbi.nlm.nih.gov/gene/254956
chorea-acanthocytosis

DOID:0050766
SNORD1C

http://www.ncbi.nlm.nih.gov/gene/677850
BVR1

http://www.ncbi.nlm.nih.gov/gene/700
tracheal stenosis

DOID:3227
cerebral atherosclerosis

DOID:12720
sex differentiation disease

DOID:1923
Aicardi syndrome

DOID:8461
Shwachman-Diamond syndrome

DOID:0060479
hypobetalipoproteinemia

DOID:1390
VSPA

http://www.ncbi.nlm.nih.gov/gene/59332
intracranial thrombosis

DOID:4193
precursor B lymphoblastic lymphoma/leukemia

DOID:7061
Leber hereditary optic neuropathy

DOID:705
GLC1B

http://www.ncbi.nlm.nih.gov/gene/2722

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