TMEM161B-DT (TMEM161B divergent transcript) - Rat Genome Database

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Gene: TMEM161B-DT (TMEM161B divergent transcript) Homo sapiens
Analyze
Symbol: TMEM161B-DT
Name: TMEM161B divergent transcript
RGD ID: 6480801
HGNC Page HGNC:43839
Description: Predicted to be a structural constituent of ribosome. Predicted to be located in ribosome; INTERACTS WITH 2-hydroxypropanoic acid; bisphenol A; cisplatin.
Type: ncrna (Ensembl: lncRNA)
RefSeq Status: VALIDATED
Previously known as: linc-POLR3G-8; TMEM161B antisense RNA 1; TMEM161B-AS1
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38588,268,882 - 88,436,674 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl588,268,843 - 88,439,337 (+)EnsemblGRCh38hg38GRCh38
GRCh37587,564,699 - 87,732,491 (+)ENTREZGENEGRCh37GRCh37hg19GRCh37
Celera583,456,511 - 83,625,438 (+)NCBICelera
Cytogenetic Map5q14.3NCBI
HuRef582,768,519 - 82,936,849 (+)ENTREZGENEHuRef
CHM1_1586,997,405 - 87,165,234 (+)NCBICHM1_1
T2T-CHM13v2.0588,749,932 - 88,917,732 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


1 to 17 of 17 rows

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
TMEM161B-DTHuman2-hydroxypropanoic acid decreases expressionEXP 6480464Lactic Acid results in decreased expression of TMEM161B-DT mRNACTDPMID:30851411
TMEM161B-DTHumanbisphenol A multiple interactionsEXP 6480464[bisphenol A co-treated with Fulvestrant] results in increased methylation of TMEM161B-DT geneCTDPMID:31601247
TMEM161B-DTHumancisplatin decreases expressionEXP 6480464Cisplatin results in decreased expression of TMEM161B-DT mRNACTDPMID:27594783
TMEM161B-DTHumandorsomorphin multiple interactionsEXP 6480464[NOG protein co-treated with entinostat co-treated with dorsomorphin co-treated with 4-(5-benzo(1 more ...CTDPMID:27188386
TMEM161B-DTHumanentinostat decreases expressionEXP 6480464entinostat results in decreased expression of TMEM161B-DT mRNACTDPMID:26272509
TMEM161B-DTHumanentinostat multiple interactionsEXP 6480464[NOG protein co-treated with entinostat co-treated with dorsomorphin co-treated with 4-(5-benzo(1 and 3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in decreased expression of TMEM161B-DT mRNACTDPMID:27188386
TMEM161B-DTHumanfulvestrant multiple interactionsEXP 6480464[bisphenol A co-treated with Fulvestrant] results in increased methylation of TMEM161B-DT geneCTDPMID:31601247
TMEM161B-DTHumannickel atom decreases expressionEXP 6480464Nickel results in decreased expression of TMEM161B-DT mRNACTDPMID:24768652
TMEM161B-DTHumanphenylmercury acetate decreases expressionEXP 6480464Phenylmercuric Acetate results in decreased expression of TMEM161B-DT mRNACTDPMID:26272509
TMEM161B-DTHumanphenylmercury acetate multiple interactionsEXP 6480464[NOG protein co-treated with Phenylmercuric Acetate co-treated with dorsomorphin co-treated with 4-(5-benzo(1 and 3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in decreased expression of TMEM161B-DT mRNACTDPMID:27188386
TMEM161B-DTHumanrac-lactic acid decreases expressionEXP 6480464Lactic Acid results in decreased expression of TMEM161B-DT mRNACTDPMID:30851411
TMEM161B-DTHumanrotenone increases expressionEXP 6480464Rotenone results in increased expression of TMEM161B-DT mRNACTDPMID:29955902
TMEM161B-DTHumanSB 431542 multiple interactionsEXP 6480464[NOG protein co-treated with entinostat co-treated with dorsomorphin co-treated with 4-(5-benzo(1 more ...CTDPMID:27188386
TMEM161B-DTHumansunitinib increases expressionEXP 6480464Sunitinib results in increased expression of TMEM161B-DT mRNACTDPMID:31533062
TMEM161B-DTHumanvalproic acid affects expressionEXP 6480464Valproic Acid affects the expression of TMEM161B-DT mRNACTDPMID:25979313
TMEM161B-DTHumanvalproic acid decreases expressionEXP 6480464Valproic Acid results in decreased expression of TMEM161B-DT mRNACTDPMID:24383497 more ...
TMEM161B-DTHumanvalproic acid multiple interactionsEXP 6480464[NOG protein co-treated with Valproic Acid co-treated with dorsomorphin co-treated with 4-(5-benzo(1 and 3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide] results in decreased expression of TMEM161B-DT mRNACTDPMID:27188386

1 to 17 of 17 rows

Cellular Component

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
TMEM161B-DTHumanribosome located_inIEARfam:RF00001150520179 RNAcentralGO_REF:0000115

Molecular Function

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
TMEM161B-DTHumanstructural constituent of ribosome enablesIEARfam:RF00001150520179 RNAcentralGO_REF:0000115


#
Reference Title
Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
PMID:8889548   PMID:12477932   PMID:15146197   PMID:16344560   PMID:21890647   PMID:34046994  



.

.
Variants in TMEM161B-DT
31 total Variants

1 to 10 of 15 rows
Name
Type
Condition(s)
Position(s)
Clinical significance
NR_039993.1(TMEM161B-AS1):n.206+34322A>G single nucleotide variant Lung cancer [RCV000096265] Chr5:88304907 [GRCh38]
Chr5:87600724 [GRCh37]
Chr5:5q14.3
uncertain significance
GRCh38/hg38 5q14.3-21.1(chr5:85966055-101335711)x1 copy number loss See cases [RCV000135748] Chr5:85966055..101335711 [GRCh38]
Chr5:85261873..100671415 [GRCh37]
Chr5:85297629..100699314 [NCBI36]
Chr5:5q14.3-21.1
pathogenic
GRCh38/hg38 5q14.3(chr5:87191898-89957449)x1 copy number loss See cases [RCV000135596] Chr5:87191898..89957449 [GRCh38]
Chr5:86487715..89253266 [GRCh37]
Chr5:86523471..89289022 [NCBI36]
Chr5:5q14.3
pathogenic
GRCh38/hg38 5q13.3-22.1(chr5:74163186-110809453)x3 copy number gain See cases [RCV000051839] Chr5:74163186..110809453 [GRCh38]
Chr5:73459011..110145153 [GRCh37]
Chr5:73494767..110173052 [NCBI36]
Chr5:5q13.3-22.1
pathogenic
GRCh38/hg38 5q14.3-15(chr5:88197732-93193163)x3 copy number gain See cases [RCV000136732] Chr5:88197732..93193163 [GRCh38]
Chr5:87493549..92528869 [GRCh37]
Chr5:87529305..92554625 [NCBI36]
Chr5:5q14.3-15
pathogenic
GRCh38/hg38 5q14.3-22.1(chr5:84603580-111435081)x1 copy number loss See cases [RCV000139656] Chr5:84603580..111435081 [GRCh38]
Chr5:83899398..110770779 [GRCh37]
Chr5:83935154..110798678 [NCBI36]
Chr5:5q14.3-22.1
pathogenic
GRCh38/hg38 5q14.3(chr5:86766959-92148845)x1 copy number loss See cases [RCV000141419] Chr5:86766959..92148845 [GRCh38]
Chr5:86062776..91444662 [GRCh37]
Chr5:86098532..91480418 [NCBI36]
Chr5:5q14.3
pathogenic
GRCh38/hg38 5q14.3(chr5:88368289-92363231)x1 copy number loss See cases [RCV000140963] Chr5:88368289..92363231 [GRCh38]
Chr5:87664106..91698938 [GRCh37]
Chr5:87699862..91724694 [NCBI36]
Chr5:5q14.3
pathogenic
GRCh38/hg38 5q14.3(chr5:85876480-88958682)x1 copy number loss See cases [RCV000051010] Chr5:85876480..88958682 [GRCh38]
Chr5:85172298..88254499 [GRCh37]
Chr5:85208054..88290255 [NCBI36]
Chr5:5q14.3
pathogenic
GRCh38/hg38 5q14.3-21.1(chr5:87376883-101524443)x1 copy number loss See cases [RCV000050945] Chr5:87376883..101524443 [GRCh38]
Chr5:86672700..100860147 [GRCh37]
Chr5:86708456..100888046 [NCBI36]
Chr5:5q14.3-21.1
pathogenic
1 to 10 of 15 rows

Predicted Target Of
Summary Value
Count of predictions:1186
Count of miRNA genes:696
Interacting mature miRNAs:782
Transcripts:ENST00000496733, ENST00000501715, ENST00000501869, ENST00000504636, ENST00000504769, ENST00000504922, ENST00000506584, ENST00000507736, ENST00000508015, ENST00000510087, ENST00000512724, ENST00000513011, ENST00000513694
Prediction methods:Microtar, Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


1 to 10 of 102 rows
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD ID
Symbol
Name
LOD
P Value
Trait
Sub Trait
Chr
Start
Stop
Species
597346715GWAS1442789_Hbody mass index QTL GWAS1442789 (human)0.0000004body mass indexbody mass index (BMI) (CMO:0000105)58840171688401717Human
407062862GWAS711838_Hobsessive-compulsive disorder, attention deficit hyperactivity disorder, Tourette syndrome, unipolar depression, bipolar disorder, autism spectrum disorder, schizophrenia, anorexia nervosa QTL GWAS711838 (human)3e-09unipolar depression58833495288334953Human
597434257GWAS1530331_Hdepressive symptom measurement QTL GWAS1530331 (human)6e-11depressive symptom measurement58833794188337942Human
597472659GWAS1568733_Hchronotype measurement QTL GWAS1568733 (human)6e-20sleep behavior trait (VT:0001501)58840540688405407Human
597470094GWAS1566168_Hchronotype measurement QTL GWAS1566168 (human)6e-08sleep behavior trait (VT:0001501)58836577688365777Human
597462152GWAS1558226_Hbody mass index QTL GWAS1558226 (human)5e-18body mass indexbody mass index (BMI) (CMO:0000105)58843421088434211Human
596972675GWAS1092194_Hobsessive-compulsive disorder, attention deficit hyperactivity disorder, Tourette syndrome, bipolar disorder, autism spectrum disorder, schizophrenia, anorexia nervosa, major depressive disorder QTL GWAS1092194 (human)3e-09major depressive disorder58833495288334953Human
597460615GWAS1556689_Hsmoking initiation QTL GWAS1556689 (human)5e-10smoking initiation58843389488433895Human
597618049GWAS1674909_Hbody weight QTL GWAS1674909 (human)9e-20body mass (VT:0001259)body weight (CMO:0000012)58840945188409452Human
597518003GWAS1614077_Hlean body mass QTL GWAS1614077 (human)1e-14lean body mass58838706088387061Human

1 to 10 of 102 rows
RH103517  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37587,732,137 - 87,732,272UniSTSGRCh37
Build 36587,767,893 - 87,768,028RGDNCBI36
Celera583,625,084 - 83,625,219RGD
HuRef582,936,495 - 82,936,630UniSTS
G42183  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37587,581,586 - 87,581,717UniSTSGRCh37
Build 36587,617,342 - 87,617,473RGDNCBI36
Celera583,473,398 - 83,473,529RGD
HuRef582,785,451 - 82,785,582UniSTS
D5S2566  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37587,579,721 - 87,579,813UniSTSGRCh37
Build 36587,615,477 - 87,615,569RGDNCBI36
Celera583,471,533 - 83,471,625RGD
HuRef582,783,586 - 82,783,678UniSTS
TNG Radiation Hybrid Map539944.0UniSTS
Stanford-G3 RH Map53334.0UniSTS
NCBI RH Map5565.3UniSTS
G29279  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37587,625,564 - 87,625,677UniSTSGRCh37
Build 36587,661,320 - 87,661,433RGDNCBI36
Celera583,517,411 - 83,517,524RGD
HuRef582,829,453 - 82,829,566UniSTS
D5S2855  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37587,583,936 - 87,584,172UniSTSGRCh37
Build 36587,619,692 - 87,619,928RGDNCBI36
Celera583,475,748 - 83,475,988RGD
HuRef582,787,802 - 82,788,034UniSTS
Marshfield Genetic Map597.82UniSTS
deCODE Assembly Map5103.14UniSTS
SGC34350  
Human AssemblyChrPosition (strand)SourceJBrowse
GeneMap99-GB4 RH Map5401.13UniSTS
Whitehead-RH Map5295.8UniSTS




adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2439 2788 2253 4974 1726 2351 6 624 1950 465 2270 7305 6471 53 3734 1 852 1744 1617 174 1


1 to 23 of 23 rows
RefSeq Transcripts NR_039993 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_039994 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_039995 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_105019 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_105020 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC010243 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC016555 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC091826 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC114978 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC030122 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC047059 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BF056341 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BF672668 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM719684 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CN260565 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA317999 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA782199 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY089208 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA988404 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA988405 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA988406 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA988407 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
1 to 23 of 23 rows

Ensembl Acc Id: ENST00000496733
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,039 - 88,276,222 (+)Ensembl
Ensembl Acc Id: ENST00000501715
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,024 - 88,436,674 (+)Ensembl
Ensembl Acc Id: ENST00000501869
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,891 - 88,436,672 (+)Ensembl
Ensembl Acc Id: ENST00000504636
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,996 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000504769
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,024 - 88,286,067 (+)Ensembl
Ensembl Acc Id: ENST00000504922
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,843 - 88,438,050 (+)Ensembl
Ensembl Acc Id: ENST00000506584
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,047 - 88,287,656 (+)Ensembl
Ensembl Acc Id: ENST00000507736
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,038 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000508015
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,392,195 - 88,418,049 (+)Ensembl
Ensembl Acc Id: ENST00000510087
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,042 - 88,436,672 (+)Ensembl
Ensembl Acc Id: ENST00000512724
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,050 - 88,292,755 (+)Ensembl
Ensembl Acc Id: ENST00000513011
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,895 - 88,271,225 (+)Ensembl
Ensembl Acc Id: ENST00000513694
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,039 - 88,436,672 (+)Ensembl
Ensembl Acc Id: ENST00000653183
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,282,720 - 88,347,574 (+)Ensembl
Ensembl Acc Id: ENST00000653898
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,028 - 88,293,232 (+)Ensembl
Ensembl Acc Id: ENST00000653918
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,977 - 88,296,332 (+)Ensembl
Ensembl Acc Id: ENST00000654762
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,899 - 88,436,922 (+)Ensembl
Ensembl Acc Id: ENST00000655966
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,015 - 88,273,135 (+)Ensembl
Ensembl Acc Id: ENST00000656152
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,034 - 88,292,275 (+)Ensembl
Ensembl Acc Id: ENST00000656195
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,408,981 - 88,436,665 (+)Ensembl
Ensembl Acc Id: ENST00000656903
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,929 - 88,272,990 (+)Ensembl
Ensembl Acc Id: ENST00000657491
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,281,851 - 88,283,586 (+)Ensembl
Ensembl Acc Id: ENST00000657617
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,073 - 88,427,376 (+)Ensembl
Ensembl Acc Id: ENST00000657972
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,000 - 88,437,089 (+)Ensembl
Ensembl Acc Id: ENST00000658094
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,915 - 88,294,850 (+)Ensembl
Ensembl Acc Id: ENST00000658478
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,868 - 88,439,332 (+)Ensembl
Ensembl Acc Id: ENST00000658611
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,024 - 88,293,238 (+)Ensembl
Ensembl Acc Id: ENST00000659005
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,996 - 88,285,330 (+)Ensembl
Ensembl Acc Id: ENST00000659093
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,995 - 88,292,672 (+)Ensembl
Ensembl Acc Id: ENST00000659215
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,036 - 88,294,547 (+)Ensembl
Ensembl Acc Id: ENST00000659938
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,036 - 88,286,977 (+)Ensembl
Ensembl Acc Id: ENST00000660783
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,015 - 88,287,016 (+)Ensembl
Ensembl Acc Id: ENST00000661351
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,015 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000661377
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,871 - 88,285,345 (+)Ensembl
Ensembl Acc Id: ENST00000661627
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,917 - 88,323,471 (+)Ensembl
Ensembl Acc Id: ENST00000662970
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,007 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000663476
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,917 - 88,292,960 (+)Ensembl
Ensembl Acc Id: ENST00000663490
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,929 - 88,293,209 (+)Ensembl
Ensembl Acc Id: ENST00000664347
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,899 - 88,274,314 (+)Ensembl
Ensembl Acc Id: ENST00000664462
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,015 - 88,286,771 (+)Ensembl
Ensembl Acc Id: ENST00000664546
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,923 - 88,294,980 (+)Ensembl
Ensembl Acc Id: ENST00000665319
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,392,073 - 88,439,337 (+)Ensembl
Ensembl Acc Id: ENST00000665517
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,409,292 - 88,436,672 (+)Ensembl
Ensembl Acc Id: ENST00000665926
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,038 - 88,283,049 (+)Ensembl
Ensembl Acc Id: ENST00000666577
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,899 - 88,293,224 (+)Ensembl
Ensembl Acc Id: ENST00000666808
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,010 - 88,287,092 (+)Ensembl
Ensembl Acc Id: ENST00000667127
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,078 - 88,290,200 (+)Ensembl
Ensembl Acc Id: ENST00000667139
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,033 - 88,293,230 (+)Ensembl
Ensembl Acc Id: ENST00000667511
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,038 - 88,285,622 (+)Ensembl
Ensembl Acc Id: ENST00000668037
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,015 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000668128
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,281,073 - 88,287,616 (+)Ensembl
Ensembl Acc Id: ENST00000668471
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,987 - 88,348,601 (+)Ensembl
Ensembl Acc Id: ENST00000669353
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,871 - 88,287,627 (+)Ensembl
Ensembl Acc Id: ENST00000669465
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,036 - 88,293,230 (+)Ensembl
Ensembl Acc Id: ENST00000669796
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,047 - 88,284,693 (+)Ensembl
Ensembl Acc Id: ENST00000670030
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,015 - 88,286,802 (+)Ensembl
Ensembl Acc Id: ENST00000670451
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,016 - 88,293,988 (+)Ensembl
Ensembl Acc Id: ENST00000670873
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,019 - 88,293,988 (+)Ensembl
Ensembl Acc Id: ENST00000671394
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,996 - 88,439,300 (+)Ensembl
Ensembl Acc Id: ENST00000684909
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,023 - 88,436,672 (+)Ensembl
Ensembl Acc Id: ENST00000685962
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,270,500 - 88,287,650 (+)Ensembl
Ensembl Acc Id: ENST00000686847
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,392,092 - 88,437,262 (+)Ensembl
Ensembl Acc Id: ENST00000686930
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,024 - 88,436,674 (+)Ensembl
Ensembl Acc Id: ENST00000688087
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,891 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000688118
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,905 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000688398
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,996 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000688523
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,913 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000689901
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,891 - 88,436,674 (+)Ensembl
Ensembl Acc Id: ENST00000692797
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,020 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000693402
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,024 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000702628
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,891 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000787430
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,913 - 88,437,091 (+)Ensembl
Ensembl Acc Id: ENST00000787431
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,871 - 88,436,674 (+)Ensembl
Ensembl Acc Id: ENST00000787432
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,871 - 88,436,672 (+)Ensembl
Ensembl Acc Id: ENST00000787433
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,913 - 88,436,675 (+)Ensembl
Ensembl Acc Id: ENST00000787434
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,913 - 88,436,669 (+)Ensembl
Ensembl Acc Id: ENST00000787435
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,973 - 88,436,672 (+)Ensembl
Ensembl Acc Id: ENST00000787436
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,024 - 88,436,674 (+)Ensembl
Ensembl Acc Id: ENST00000787437
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,024 - 88,436,674 (+)Ensembl
Ensembl Acc Id: ENST00000787438
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,083 - 88,436,672 (+)Ensembl
Ensembl Acc Id: ENST00000787439
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,179 - 88,436,672 (+)Ensembl
Ensembl Acc Id: ENST00000787440
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,194 - 88,436,672 (+)Ensembl
Ensembl Acc Id: ENST00000787441
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,917 - 88,347,317 (+)Ensembl
Ensembl Acc Id: ENST00000787442
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,957 - 88,347,317 (+)Ensembl
Ensembl Acc Id: ENST00000787443
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,021 - 88,326,081 (+)Ensembl
Ensembl Acc Id: ENST00000787444
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,390,322 - 88,436,672 (+)Ensembl
Ensembl Acc Id: ENST00000787445
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,390,370 - 88,436,672 (+)Ensembl
Ensembl Acc Id: ENST00000787446
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,392,180 - 88,436,672 (+)Ensembl
Ensembl Acc Id: ENST00000787447
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,392,201 - 88,436,672 (+)Ensembl
Ensembl Acc Id: ENST00000787448
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,392,275 - 88,436,672 (+)Ensembl
Ensembl Acc Id: ENST00000787449
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,392,275 - 88,436,672 (+)Ensembl
Ensembl Acc Id: ENST00000787450
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,392,275 - 88,436,672 (+)Ensembl
Ensembl Acc Id: ENST00000787451
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,392,275 - 88,436,669 (+)Ensembl
Ensembl Acc Id: ENST00000787452
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,879 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000787453
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,913 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000787454
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,924 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000787455
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,928 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000787456
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,953 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000787457
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,971 - 88,287,650 (+)Ensembl
Ensembl Acc Id: ENST00000787458
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,978 - 88,287,655 (+)Ensembl
Ensembl Acc Id: ENST00000787459
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,996 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000787460
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,268,998 - 88,287,650 (+)Ensembl
Ensembl Acc Id: ENST00000787461
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,024 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000787462
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,026 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000787463
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,026 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000787464
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,027 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000787465
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,028 - 88,287,655 (+)Ensembl
Ensembl Acc Id: ENST00000787466
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,024 - 88,287,650 (+)Ensembl
Ensembl Acc Id: ENST00000787467
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,024 - 88,287,650 (+)Ensembl
Ensembl Acc Id: ENST00000787468
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,037 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000787469
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,038 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000787470
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,035 - 88,287,651 (+)Ensembl
Ensembl Acc Id: ENST00000787471
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,034 - 88,287,650 (+)Ensembl
Ensembl Acc Id: ENST00000787472
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,042 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000787473
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,078 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000787474
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,270,526 - 88,287,657 (+)Ensembl
Ensembl Acc Id: ENST00000787475
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl588,269,026 - 88,282,140 (+)Ensembl
RefSeq Acc Id: NR_039993
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38588,268,882 - 88,436,674 (+)NCBI
GRCh37587,564,699 - 87,732,491 (+)ENTREZGENE
HuRef582,768,519 - 82,936,849 (+)ENTREZGENE
CHM1_1586,997,405 - 87,165,234 (+)NCBI
T2T-CHM13v2.0588,749,932 - 88,917,732 (+)NCBI
Sequence:
RefSeq Acc Id: NR_039994
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38588,269,016 - 88,436,674 (+)NCBI
GRCh37587,564,699 - 87,732,491 (+)ENTREZGENE
HuRef582,768,519 - 82,936,849 (+)ENTREZGENE
CHM1_1586,997,539 - 87,165,234 (+)NCBI
T2T-CHM13v2.0588,750,066 - 88,917,732 (+)NCBI
Sequence:
RefSeq Acc Id: NR_039995
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38588,268,882 - 88,436,674 (+)NCBI
GRCh37587,564,699 - 87,732,491 (+)ENTREZGENE
HuRef582,768,519 - 82,936,849 (+)ENTREZGENE
CHM1_1586,997,405 - 87,165,234 (+)NCBI
T2T-CHM13v2.0588,749,932 - 88,917,732 (+)NCBI
Sequence:
RefSeq Acc Id: NR_105019
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38588,269,016 - 88,436,674 (+)NCBI
HuRef582,768,519 - 82,936,849 (+)NCBI
CHM1_1586,997,539 - 87,165,234 (+)NCBI
T2T-CHM13v2.0588,750,066 - 88,917,732 (+)NCBI
Sequence:
RefSeq Acc Id: NR_105020
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38588,392,195 - 88,436,674 (+)NCBI
HuRef582,768,519 - 82,936,849 (+)NCBI
CHM1_1587,120,756 - 87,165,234 (+)NCBI
T2T-CHM13v2.0588,873,261 - 88,917,732 (+)NCBI
Sequence:
RGD ID:15095899
Promoter ID:EPDNEWNC_H741
Type:initiation region
Name:TMEM161B-AS1_1
Description:TMEM161B antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:43839]
SO ACC ID:SO:0000170
Source:EPDNEWNC (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38588,269,026 - 88,269,086EPDNEWNC


1 to 40 of 87 rows
Database
Acc Id
Source(s)
COSMIC TMEM161B-DT COSMIC
Ensembl Genes ENSG00000247828 Ensembl, ENTREZGENE
Ensembl Transcript ENST00000501715 ENTREZGENE
  ENST00000689901 ENTREZGENE
  ENST00000787431 ENTREZGENE
  ENST00000787437 ENTREZGENE
  ENST00000787447 ENTREZGENE
GTEx ENSG00000247828 GTEx
HGNC ID HGNC:43839 ENTREZGENE
Human Proteome Map TMEM161B-DT Human Proteome Map
NCBI Gene TMEM161B-AS1 ENTREZGENE
RNAcentral URS0000037591 RNACentral
  URS00000DBF00 RNACentral
  URS00000FC9F5 RNACentral
  URS000017DA40 RNACentral
  URS000024F414 RNACentral
  URS00002AE53A RNACentral
  URS0000303729 RNACentral
  URS000075A99B RNACentral
  URS000075B297 RNACentral
  URS000075C0F2 RNACentral
  URS000075D38C RNACentral
  URS000075EED9 RNACentral
  URS0000EEB14A RNACentral
  URS0000EEB17A RNACentral
  URS0000EEB56E RNACentral
  URS0000EEBA6A RNACentral
  URS0000EEC249 RNACentral
  URS0000EEC3B3 RNACentral
  URS0000EECB72 RNACentral
  URS0000EED957 RNACentral
  URS0000EEE208 RNACentral
  URS0000EEEBA2 RNACentral
  URS0000EEEC68 RNACentral
  URS0000EEEF31 RNACentral
  URS0000EEEF9A RNACentral
  URS0000EEF058 RNACentral
  URS0000EEF0CE RNACentral
  URS0000EEF68B RNACentral
  URS0000EEFB2C RNACentral
1 to 40 of 87 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2021-05-03 TMEM161B-DT  TMEM161B divergent transcript  TMEM161B-AS1  TMEM161B antisense RNA 1  Symbol and/or name change 19259463 PROVISIONAL
2012-08-21 TMEM161B-AS1  TMEM161B antisense RNA 1  TMEM161B-AS1  TMEM161B antisense RNA 1 (non-protein coding)  Symbol and/or name change 5135510 APPROVED