An integrated knowledge database dedicated to ncRNAs, especially lncRNAs.
Detail infomation of NONHSAG010712.2

General info


NONCODE GENE IDNONHSAG010712.2
Chromosomechr12
Start Site25779286
End Site25779569
Strand-
Length283
Assemblyhg38
ClassLinc;
Other Gene VersionsNONHSAG010712.1(old version)

Transcripts in Gene


NONCODE TRANSCRIPT ID
NONHSAT027360.2

Expression Profile (Data Source:Human Body Map)


adiposeadrenalbrainbrain_Rbreastcolon
000000
foreskinheartheart_RHLF_1HLF_2kidney
000000
liverliver_RlunglymphNodeovaryplacenta_R
000000
prostateskeltalMuscletestestestes_RthyroidwhiteBloodCell
000000
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Exosome Expression Profile (Data Source: NCBI GEO)


A431_cellLine
(Squamous Cell Carcinoma Cell Line Exosomes)
BJ_cellLine
(Foreskin Fibroblast Cell Line Exosomes)
HepG2_cellLine
(Hepatocellular Carcinoma Cell Line Exosomes)
HUVEC_cellLine
(Human Umbilical Vein Endothelial Cell Line Exosomes)
invasive_NFPAs
(Invasive Non-functional Pituitary Adenomas Exosomes)
00005.73235
non-invasive_NFPAs
(Non-invasive Non-functional Pituitary Adenomas Exosomes)
MCF7_cellLine
(Human Breast Cancer Cell Line Exosomes)
MDA-MB-231_cellLine
(Human Breast Cancer Cell Line Exosomes)
tuberculosis_patients_serum
(Active Tuberculosis Patients Serum Exosomes)
normal_people_blood
(Normal People Blood Exosomes)
1.81646006.55050
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Expression Profile (Data Source: Single Cell)


Conservation Info


Note: T = There are transcripts in this region.


Disease related


Disease:

NONCODE IDGene SymbolDisease nameSource DatabaseSource PMID
NONHSAG010712.27SKAIDS,cardiac hypertrophy,gastric cancerLncRNAWiki0
NONHSAG010712.27SKAIDSLncRNADisease20471949
NONHSAG010712.27SKAIDSLncRNADisease21098020
NONHSAG010712.27SKAIDSLncRNADisease20976203
NONHSAG010712.27SKAIDSLncRNADisease21087998
NONHSAG010712.27SKAIDSLncRNADisease22377309
NONHSAG010712.27SKcancerLncRNADisease22377309
NONHSAG010712.27SKcardiac hypertrophyLncRNADisease22377309
NONHSAG010712.27SKgastric cancerLncRNADisease22488152
NONHSAG010712.2RN7SKhuman immunodeficiency virus infectious diseaseLncRNADisease21087998

Mutations:

NONCODE IDSNP IDGWAS traitSource PMID