TARBP2 (TARBP2 subunit of RISC loading complex) - Rat Genome Database

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Pathways
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Gene: TARBP2 (TARBP2 subunit of RISC loading complex) Homo sapiens
Analyze
Symbol: TARBP2
Name: TARBP2 subunit of RISC loading complex
RGD ID: 1316539
HGNC Page HGNC:11569
Description: Enables several functions, including RNA binding activity; protein homodimerization activity; and protein sequestering activity. Contributes to pre-miRNA binding activity. Involved in several processes, including negative regulation of gene expression; positive regulation of viral genome replication; and regulation of defense response. Located in cytoplasm and nuclear body. Part of RISC complex and RISC-loading complex.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: LOQS; RISC-loading complex subunit TARBP2; TAR (HIV) RNA binding protein 2; TAR (HIV) RNA-binding protein 2; TAR (HIV) RNA-binding protein TRBP1; TAR (HIV-1) RNA binding protein 2; TAR RNA binding protein 2; TAR RNA-binding protein 2; TARBP2, RISC loading complex RNA binding subunit; trans-activation responsive RNA-binding protein; trans-activation-responsive RNA-binding protein; TRBP; TRBP1; TRBP2
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Related Pseudogenes: TARBP2P1  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381253,500,923 - 53,506,431 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1253,500,921 - 53,506,431 (+)EnsemblGRCh38hg38GRCh38
GRCh371253,894,707 - 53,900,215 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361252,180,972 - 52,186,482 (+)NCBINCBI36Build 36hg18NCBI36
Build 341252,180,971 - 52,186,480NCBI
Celera1253,545,063 - 53,550,573 (+)NCBICelera
Cytogenetic Map12q13.13NCBI
HuRef1250,934,287 - 50,939,797 (+)NCBIHuRef
CHM1_11253,861,761 - 53,867,271 (+)NCBICHM1_1
T2T-CHM13v2.01253,466,928 - 53,472,436 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
cytoplasm  (IBA,IDA,IEA)
cytosol  (TAS)
nuclear body  (IDA)
nucleoplasm  (IDA)
nucleus  (IBA,IEA)
perinuclear region of cytoplasm  (IEA)
RISC complex  (IBA,IDA,IEA)
RISC-loading complex  (IBA,IDA,IEA,IPI)

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. The widespread regulation of microRNA biogenesis, function and decay. Krol J, etal., Nat Rev Genet. 2010 Sep;11(9):597-610. Epub 2010 Jul 27.
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:2011739   PMID:7568151   PMID:7774957   PMID:8455607   PMID:8723388   PMID:10330179   PMID:10759868   PMID:11060498   PMID:11228241   PMID:11438532   PMID:11443112   PMID:11641396  
PMID:12023963   PMID:12477932   PMID:12549820   PMID:14585207   PMID:14585331   PMID:15123692   PMID:15973356   PMID:16142218   PMID:16169070   PMID:16271387   PMID:16343534   PMID:16357216  
PMID:16424907   PMID:16629595   PMID:17360756   PMID:17452327   PMID:17507929   PMID:17531811   PMID:17932509   PMID:18029348   PMID:18178619   PMID:18654987   PMID:18936160   PMID:18948111  
PMID:19047128   PMID:19060904   PMID:19138993   PMID:19422693   PMID:19668211   PMID:19716330   PMID:19804757   PMID:19820710   PMID:19836333   PMID:19953087   PMID:20211142   PMID:20211803  
PMID:20585341   PMID:20732906   PMID:20877318   PMID:21080422   PMID:21145461   PMID:21526770   PMID:21832049   PMID:21858095   PMID:21873635   PMID:21900206   PMID:21903422   PMID:22025453  
PMID:22163034   PMID:22658674   PMID:22698405   PMID:22933564   PMID:22999255   PMID:23006623   PMID:23251028   PMID:23361462   PMID:23435228   PMID:23550157   PMID:23622242   PMID:23636329  
PMID:23658827   PMID:23661684   PMID:23671264   PMID:23690119   PMID:24025624   PMID:24141778   PMID:24563327   PMID:24563462   PMID:24778252   PMID:25043050   PMID:25277244   PMID:25416956  
PMID:25437560   PMID:25446899   PMID:25557550   PMID:25608000   PMID:25659891   PMID:25668122   PMID:25814554   PMID:25910212   PMID:26186194   PMID:26486325   PMID:26496610   PMID:26582366  
PMID:26796812   PMID:26972000   PMID:27173435   PMID:27332119   PMID:27407113   PMID:27432908   PMID:27599909   PMID:27743889   PMID:28174252   PMID:28380382   PMID:28514442   PMID:29229926  
PMID:29231267   PMID:29348664   PMID:29373753   PMID:29395067   PMID:29509190   PMID:29939295   PMID:30390472   PMID:30657254   PMID:30927622   PMID:31300274   PMID:31495888   PMID:31527615  
PMID:31753913   PMID:31799626   PMID:32296183   PMID:32305960   PMID:32513696   PMID:32640226   PMID:32989298   PMID:32994395   PMID:33328224   PMID:33459340   PMID:33484209   PMID:33845483  
PMID:33957083   PMID:33961781   PMID:34133714   PMID:34578187   PMID:34732716   PMID:35008634   PMID:35013218   PMID:35271311   PMID:35563538   PMID:35819319   PMID:36217029   PMID:36244648  
PMID:36543142  


Genomics

Comparative Map Data
TARBP2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381253,500,923 - 53,506,431 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1253,500,921 - 53,506,431 (+)EnsemblGRCh38hg38GRCh38
GRCh371253,894,707 - 53,900,215 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361252,180,972 - 52,186,482 (+)NCBINCBI36Build 36hg18NCBI36
Build 341252,180,971 - 52,186,480NCBI
Celera1253,545,063 - 53,550,573 (+)NCBICelera
Cytogenetic Map12q13.13NCBI
HuRef1250,934,287 - 50,939,797 (+)NCBIHuRef
CHM1_11253,861,761 - 53,867,271 (+)NCBICHM1_1
T2T-CHM13v2.01253,466,928 - 53,472,436 (+)NCBIT2T-CHM13v2.0
Tarbp2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3915102,423,327 - 102,432,112 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl15102,426,627 - 102,432,111 (+)EnsemblGRCm39 Ensembl
GRCm3815102,516,077 - 102,523,676 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl15102,518,192 - 102,523,676 (+)EnsemblGRCm38mm10GRCm38
MGSCv3715102,348,677 - 102,354,107 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv3615102,346,493 - 102,351,708 (+)NCBIMGSCv36mm8
Celera15104,676,011 - 104,681,441 (+)NCBICelera
Cytogenetic Map15F3NCBI
cM Map1557.65NCBI
Tarbp2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr87135,527,710 - 135,532,826 (+)NCBIGRCr8
mRatBN7.27133,649,118 - 133,654,306 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl7133,649,090 - 133,654,314 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx7135,404,936 - 135,410,051 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.07137,634,303 - 137,639,418 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.07137,620,556 - 137,625,671 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.07144,121,688 - 144,126,860 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl7144,121,744 - 144,126,857 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.07141,912,728 - 141,918,855 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.47141,272,043 - 141,273,188 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.17141,348,156 - 141,349,625 (+)NCBI
Celera7130,076,808 - 130,081,909 (+)NCBICelera
Cytogenetic Map7q36NCBI
Tarbp2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955458793,759 - 798,806 (+)EnsemblChiLan1.0
ChiLan1.0NW_004955458793,753 - 798,755 (+)NCBIChiLan1.0ChiLan1.0
TARBP2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21040,678,185 - 40,683,408 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11240,674,949 - 40,681,391 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01235,246,937 - 35,253,378 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11236,031,822 - 36,038,080 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1236,031,818 - 36,038,008 (-)Ensemblpanpan1.1panPan2
TARBP2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1271,715,157 - 1,720,050 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl271,715,158 - 1,726,885 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2744,530,279 - 44,535,121 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0271,719,078 - 1,723,920 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl271,719,077 - 1,723,754 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1271,736,610 - 1,741,453 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0271,719,877 - 1,724,720 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02744,931,979 - 44,936,821 (+)NCBIUU_Cfam_GSD_1.0
Tarbp2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494562,384,789 - 62,390,032 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493651210,774,213 - 10,796,268 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493651210,774,793 - 10,780,041 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
TARBP2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl518,718,688 - 18,723,839 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1518,718,588 - 18,723,843 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2519,154,223 - 19,159,472 (+)NCBISscrofa10.2Sscrofa10.2susScr3
TARBP2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11149,601,634 - 49,607,097 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1149,602,113 - 49,606,816 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666037196,446,953 - 196,453,171 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Tarbp2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046249041,597,428 - 1,603,504 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046249041,598,422 - 1,603,494 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in TARBP2
12 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 12q13.13(chr12:53099658-53724525)x1 copy number loss See cases [RCV000052811] Chr12:53099658..53724525 [GRCh38]
Chr12:53493442..54118309 [GRCh37]
Chr12:51779709..52404576 [NCBI36]
Chr12:12q13.13		 pathogenic
GRCh38/hg38 12q13.13(chr12:53224024-54222450)x1 copy number loss See cases [RCV000052812] Chr12:53224024..54222450 [GRCh38]
Chr12:53617808..54616234 [GRCh37]
Chr12:51904075..52902501 [NCBI36]
Chr12:12q13.13		 pathogenic
GRCh38/hg38 12q13.13(chr12:52851850-53558824)x3 copy number gain See cases [RCV000138030] Chr12:52851850..53558824 [GRCh38]
Chr12:53245634..53952608 [GRCh37]
Chr12:51531901..52238875 [NCBI36]
Chr12:12q13.13		 likely pathogenic
GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3 copy number gain See cases [RCV000139555] Chr12:121271..133196807 [GRCh38]
Chr12:282465..133773393 [GRCh37]
Chr12:100698..132283466 [NCBI36]
Chr12:12p13.33-q24.33		 pathogenic
GRCh38/hg38 12q13.13-13.3(chr12:53420606-56202942)x3 copy number gain See cases [RCV000141435] Chr12:53420606..56202942 [GRCh38]
Chr12:53814390..56596726 [GRCh37]
Chr12:52100657..54882993 [NCBI36]
Chr12:12q13.13-13.3		 pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:1-133851895)x3 copy number gain See cases [RCV000258805] Chr12:1..133851895 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic|likely pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)x3 copy number gain See cases [RCV000510482] Chr12:173787..133777902 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902) copy number gain See cases [RCV000511643] Chr12:173787..133777902 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic
NM_134323.2(TARBP2):c.269T>A (p.Val90Glu) single nucleotide variant Inborn genetic diseases [RCV003276395] Chr12:53503072 [GRCh38]
Chr12:53896856 [GRCh37]
Chr12:12q13.13		 uncertain significance
NC_000012.11:g.26370251_54361538inv inversion not specified [RCV000714265] Chr12:26370251..54361538 [GRCh37]
Chr12:12p12.1-q13.13		 uncertain significance
GRCh37/hg19 12p13.33-q24.33(chr12:621220-133779118)x3 copy number gain not provided [RCV000750253] Chr12:621220..133779118 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:191619-133777645)x3 copy number gain not provided [RCV000750246] Chr12:191619..133777645 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic
Single allele deletion Neurodevelopmental disorder [RCV000787381] Chr12:53784698..54741363 [GRCh37]
Chr12:12q13.13		 pathogenic
NM_134323.2(TARBP2):c.423-3C>G single nucleotide variant not provided [RCV000962472] Chr12:53504394 [GRCh38]
Chr12:53898178 [GRCh37]
Chr12:12q13.13		 benign
NM_134323.2(TARBP2):c.942T>C (p.Ile314=) single nucleotide variant not provided [RCV000957070] Chr12:53505849 [GRCh38]
Chr12:53899633 [GRCh37]
Chr12:12q13.13		 benign
GRCh37/hg19 12q13.13(chr12:53614278-53971802)x1 copy number loss not provided [RCV001259613] Chr12:53614278..53971802 [GRCh37]
Chr12:12q13.13		 likely pathogenic
NM_134323.2(TARBP2):c.47T>C (p.Leu16Pro) single nucleotide variant Inborn genetic diseases [RCV002749276] Chr12:53501455 [GRCh38]
Chr12:53895239 [GRCh37]
Chr12:12q13.13		 uncertain significance
NM_134323.2(TARBP2):c.52A>G (p.Ser18Gly) single nucleotide variant Inborn genetic diseases [RCV002693084] Chr12:53501460 [GRCh38]
Chr12:53895244 [GRCh37]
Chr12:12q13.13		 uncertain significance
NM_134323.2(TARBP2):c.977T>C (p.Leu326Pro) single nucleotide variant Inborn genetic diseases [RCV002831523] Chr12:53506024 [GRCh38]
Chr12:53899808 [GRCh37]
Chr12:12q13.13		 uncertain significance
NM_134323.2(TARBP2):c.1050G>C (p.Glu350Asp) single nucleotide variant Inborn genetic diseases [RCV002920933] Chr12:53506097 [GRCh38]
Chr12:53899881 [GRCh37]
Chr12:12q13.13		 uncertain significance
NM_134323.2(TARBP2):c.520C>T (p.Arg174Trp) single nucleotide variant Inborn genetic diseases [RCV003213060] Chr12:53504722 [GRCh38]
Chr12:53898506 [GRCh37]
Chr12:12q13.13		 uncertain significance
NM_134323.2(TARBP2):c.298A>G (p.Met100Val) single nucleotide variant Inborn genetic diseases [RCV003185573] Chr12:53503101 [GRCh38]
Chr12:53896885 [GRCh37]
Chr12:12q13.13		 uncertain significance
NM_134323.2(TARBP2):c.1000G>A (p.Ala334Thr) single nucleotide variant Inborn genetic diseases [RCV003302637] Chr12:53506047 [GRCh38]
Chr12:53899831 [GRCh37]
Chr12:12q13.13		 uncertain significance
NM_134323.2(TARBP2):c.25G>A (p.Gly9Ser) single nucleotide variant Inborn genetic diseases [RCV003356449] Chr12:53501433 [GRCh38]
Chr12:53895217 [GRCh37]
Chr12:12q13.13		 uncertain significance
NM_134323.2(TARBP2):c.983A>T (p.Glu328Val) single nucleotide variant Inborn genetic diseases [RCV003369603] Chr12:53506030 [GRCh38]
Chr12:53899814 [GRCh37]
Chr12:12q13.13		 uncertain significance
GRCh37/hg19 12q13.13(chr12:53583828-53922629)x3 copy number gain not provided [RCV003484869] Chr12:53583828..53922629 [GRCh37]
Chr12:12q13.13		 uncertain significance
GRCh37/hg19 12q13.13(chr12:53502510-54256094)x3 copy number gain not specified [RCV003986989] Chr12:53502510..54256094 [GRCh37]
Chr12:12q13.13		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:7688
Count of miRNA genes:970
Interacting mature miRNAs:1179
Transcripts:ENST00000266987, ENST00000394357, ENST00000456234, ENST00000546763, ENST00000546889, ENST00000547064, ENST00000547388, ENST00000547541, ENST00000548971, ENST00000549028, ENST00000549572, ENST00000549610, ENST00000549679, ENST00000550147, ENST00000550407, ENST00000551157, ENST00000551741, ENST00000552650, ENST00000552817, ENST00000552857
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
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.

Markers in Region
RH39878  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371253,900,059 - 53,900,201UniSTSGRCh37
Build 361252,186,326 - 52,186,468RGDNCBI36
Celera1253,550,417 - 53,550,559RGD
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q13.13UniSTS
HuRef1250,939,641 - 50,939,783UniSTS
RH120510  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371253,893,983 - 53,894,275UniSTSGRCh37
Build 361252,180,250 - 52,180,542RGDNCBI36
Celera1253,544,341 - 53,544,633RGD
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q13UniSTS
HuRef1250,933,564 - 50,933,856UniSTS
TNG Radiation Hybrid Map1225340.0UniSTS
G42930  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371253,899,933 - 53,900,207UniSTSGRCh37
Build 361252,186,200 - 52,186,474RGDNCBI36
Celera1253,550,291 - 53,550,565RGD
Cytogenetic Map12q12-q13UniSTS
HuRef1250,939,515 - 50,939,789UniSTS
STS-M60801  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371253,899,939 - 53,900,134UniSTSGRCh37
Build 361252,186,206 - 52,186,401RGDNCBI36
Celera1253,550,297 - 53,550,492RGD
Cytogenetic Map12q12-q13UniSTS
HuRef1250,939,521 - 50,939,716UniSTS
GeneMap99-GB4 RH Map12230.23UniSTS
NCBI RH Map12423.0UniSTS
TARBP2__5191  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371253,899,834 - 53,900,206UniSTSGRCh37
Build 361252,186,101 - 52,186,473RGDNCBI36
Celera1253,550,192 - 53,550,564RGD
HuRef1250,939,416 - 50,939,788UniSTS
STS-R72841  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371253,899,907 - 53,900,071UniSTSGRCh37
Build 361252,186,174 - 52,186,338RGDNCBI36
Celera1253,550,265 - 53,550,429RGD
Cytogenetic Map12q12-q13UniSTS
HuRef1250,939,489 - 50,939,653UniSTS
GeneMap99-GB4 RH Map12229.2UniSTS
NCBI RH Map12442.2UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 2099 1157 1528 450 1255 296 3278 846 1866 295 1427 1529 168 1086 1757 3
Low 338 1830 197 174 696 169 1078 1351 1861 124 32 82 5 1 118 1031 3 2
Below cutoff 1 7 1 2 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_004178 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_134323 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_134324 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005269114 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005269115 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005269117 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005269120 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005269122 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006719581 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011538712 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019910 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019911 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047429485 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054373102 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054373103 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054373104 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054373105 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001748860 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_944695 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC023509 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF281068 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK290737 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK293728 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK309569 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC002419 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC005860 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC150583 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BI771121 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BT007140 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471054 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068266 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M60801 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U08998 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000266987   ⟹   ENSP00000266987
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1253,501,283 - 53,506,431 (+)Ensembl
RefSeq Acc Id: ENST00000394357   ⟹   ENSP00000377885
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1253,501,619 - 53,506,412 (+)Ensembl
RefSeq Acc Id: ENST00000456234   ⟹   ENSP00000416077
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1253,500,953 - 53,506,424 (+)Ensembl
RefSeq Acc Id: ENST00000546763
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1253,503,714 - 53,504,787 (+)Ensembl
RefSeq Acc Id: ENST00000546889
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1253,501,305 - 53,502,920 (+)Ensembl
RefSeq Acc Id: ENST00000547064   ⟹   ENSP00000448199
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1253,501,366 - 53,505,793 (+)Ensembl
RefSeq Acc Id: ENST00000547388
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1253,501,332 - 53,503,472 (+)Ensembl
RefSeq Acc Id: ENST00000547541
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1253,503,474 - 53,504,719 (+)Ensembl
RefSeq Acc Id: ENST00000548971   ⟹   ENSP00000447993
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1253,501,306 - 53,506,399 (+)Ensembl
RefSeq Acc Id: ENST00000549028
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1253,501,599 - 53,503,549 (+)Ensembl
RefSeq Acc Id: ENST00000549572   ⟹   ENSP00000448948
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1253,501,604 - 53,506,423 (+)Ensembl
RefSeq Acc Id: ENST00000549610
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1253,501,302 - 53,504,395 (+)Ensembl
RefSeq Acc Id: ENST00000549679   ⟹   ENSP00000448943
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1253,501,605 - 53,506,396 (+)Ensembl
RefSeq Acc Id: ENST00000550147   ⟹   ENSP00000450320
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1253,500,921 - 53,506,431 (+)Ensembl
RefSeq Acc Id: ENST00000550407   ⟹   ENSP00000447767
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1253,502,051 - 53,506,396 (+)Ensembl
RefSeq Acc Id: ENST00000551157
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1253,502,603 - 53,505,731 (+)Ensembl
RefSeq Acc Id: ENST00000551741   ⟹   ENSP00000447262
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1253,501,591 - 53,505,851 (+)Ensembl
RefSeq Acc Id: ENST00000552650
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1253,501,350 - 53,503,698 (+)Ensembl
RefSeq Acc Id: ENST00000552817   ⟹   ENSP00000458011
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1253,501,597 - 53,505,686 (+)Ensembl
RefSeq Acc Id: ENST00000552857   ⟹   ENSP00000449537
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1253,501,274 - 53,506,229 (+)Ensembl
RefSeq Acc Id: ENST00000710362   ⟹   ENSP00000518233
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1253,501,283 - 53,506,431 (+)Ensembl
RefSeq Acc Id: NM_004178   ⟹   NP_004169
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381253,500,923 - 53,506,431 (+)NCBI
GRCh371253,893,557 - 53,900,215 (+)NCBI
Build 361252,180,972 - 52,186,482 (+)NCBI Archive
HuRef1250,934,287 - 50,939,797 (+)ENTREZGENE
CHM1_11253,861,761 - 53,867,271 (+)NCBI
T2T-CHM13v2.01253,466,928 - 53,472,436 (+)NCBI
Sequence:
RefSeq Acc Id: NM_134323   ⟹   NP_599150
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381253,501,283 - 53,506,431 (+)NCBI
GRCh371253,893,557 - 53,900,215 (+)NCBI
Build 361252,180,972 - 52,186,482 (+)NCBI Archive
HuRef1250,934,287 - 50,939,797 (+)ENTREZGENE
CHM1_11253,861,761 - 53,867,271 (+)NCBI
T2T-CHM13v2.01253,467,288 - 53,472,436 (+)NCBI
Sequence:
RefSeq Acc Id: NM_134324   ⟹   NP_599151
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381253,501,586 - 53,506,431 (+)NCBI
GRCh371253,893,557 - 53,900,215 (+)NCBI
Build 361252,181,644 - 52,186,482 (+)NCBI Archive
HuRef1250,934,287 - 50,939,797 (+)ENTREZGENE
CHM1_11253,862,433 - 53,867,271 (+)NCBI
T2T-CHM13v2.01253,467,591 - 53,472,436 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005269115   ⟹   XP_005269172
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381253,501,586 - 53,506,431 (+)NCBI
GRCh371253,893,557 - 53,900,215 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011538712   ⟹   XP_011537014
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381253,503,037 - 53,506,431 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017019911   ⟹   XP_016875400
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381253,503,037 - 53,506,431 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047429485   ⟹   XP_047285441
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381253,501,283 - 53,505,845 (+)NCBI
RefSeq Acc Id: XM_054373102   ⟹   XP_054229077
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01253,467,591 - 53,472,436 (+)NCBI
RefSeq Acc Id: XM_054373103   ⟹   XP_054229078
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01253,467,288 - 53,471,850 (+)NCBI
RefSeq Acc Id: XM_054373104   ⟹   XP_054229079
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01253,469,042 - 53,472,436 (+)NCBI
RefSeq Acc Id: XM_054373105   ⟹   XP_054229080
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01253,469,042 - 53,472,436 (+)NCBI
Protein Sequences
Protein RefSeqs NP_004169 (Get FASTA)   NCBI Sequence Viewer  
  NP_599150 (Get FASTA)   NCBI Sequence Viewer  
  NP_599151 (Get FASTA)   NCBI Sequence Viewer  
  XP_005269172 (Get FASTA)   NCBI Sequence Viewer  
  XP_011537014 (Get FASTA)   NCBI Sequence Viewer  
  XP_016875400 (Get FASTA)   NCBI Sequence Viewer  
  XP_047285441 (Get FASTA)   NCBI Sequence Viewer  
  XP_054229077 (Get FASTA)   NCBI Sequence Viewer  
  XP_054229078 (Get FASTA)   NCBI Sequence Viewer  
  XP_054229079 (Get FASTA)   NCBI Sequence Viewer  
  XP_054229080 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAA36765 (Get FASTA)   NCBI Sequence Viewer  
  AAB50581 (Get FASTA)   NCBI Sequence Viewer  
  AAH05860 (Get FASTA)   NCBI Sequence Viewer  
  AAL55730 (Get FASTA)   NCBI Sequence Viewer  
  AAL55731 (Get FASTA)   NCBI Sequence Viewer  
  AAP35804 (Get FASTA)   NCBI Sequence Viewer  
  BAF83426 (Get FASTA)   NCBI Sequence Viewer  
  BAH11581 (Get FASTA)   NCBI Sequence Viewer  
  EAW96717 (Get FASTA)   NCBI Sequence Viewer  
  EAW96718 (Get FASTA)   NCBI Sequence Viewer  
  EAW96719 (Get FASTA)   NCBI Sequence Viewer  
  EAW96720 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000266987
  ENSP00000266987.2
  ENSP00000377885
  ENSP00000377885.2
  ENSP00000416077
  ENSP00000416077.2
  ENSP00000447262.1
  ENSP00000447767
  ENSP00000447767.1
  ENSP00000447993.1
  ENSP00000448199.2
  ENSP00000448943.1
  ENSP00000448948.1
  ENSP00000449537.1
  ENSP00000450320.1
  ENSP00000458011.1
  ENSP00000518233.1
GenBank Protein Q15633 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_599150   ⟸   NM_134323
- Peptide Label: isoform a
- UniProtKB: Q8WY33 (UniProtKB/Swiss-Prot),   Q8WY32 (UniProtKB/Swiss-Prot),   Q12878 (UniProtKB/Swiss-Prot),   Q9BRY2 (UniProtKB/Swiss-Prot),   Q15633 (UniProtKB/Swiss-Prot),   A8K3X2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_004169   ⟸   NM_004178
- Peptide Label: isoform b
- UniProtKB: A8K3X2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_599151   ⟸   NM_134324
- Peptide Label: isoform b
- UniProtKB: A8K3X2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005269172   ⟸   XM_005269115
- Peptide Label: isoform X1
- UniProtKB: A8K3X2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011537014   ⟸   XM_011538712
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_016875400   ⟸   XM_017019911
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: ENSP00000266987   ⟸   ENST00000266987
RefSeq Acc Id: ENSP00000448199   ⟸   ENST00000547064
RefSeq Acc Id: ENSP00000447993   ⟸   ENST00000548971
RefSeq Acc Id: ENSP00000416077   ⟸   ENST00000456234
RefSeq Acc Id: ENSP00000448943   ⟸   ENST00000549679
RefSeq Acc Id: ENSP00000448948   ⟸   ENST00000549572
RefSeq Acc Id: ENSP00000450320   ⟸   ENST00000550147
RefSeq Acc Id: ENSP00000447767   ⟸   ENST00000550407
RefSeq Acc Id: ENSP00000377885   ⟸   ENST00000394357
RefSeq Acc Id: ENSP00000447262   ⟸   ENST00000551741
RefSeq Acc Id: ENSP00000458011   ⟸   ENST00000552817
RefSeq Acc Id: ENSP00000449537   ⟸   ENST00000552857
RefSeq Acc Id: XP_047285441   ⟸   XM_047429485
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054229078   ⟸   XM_054373103
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054229077   ⟸   XM_054373102
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054229079   ⟸   XM_054373104
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054229080   ⟸   XM_054373105
- Peptide Label: isoform X3
RefSeq Acc Id: ENSP00000518233   ⟸   ENST00000710362
Protein Domains
DRBM

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q15633-F1-model_v2 AlphaFold Q15633 1-366 view protein structure

Promoters
RGD ID:6790528
Promoter ID:HG_KWN:15765
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_004178,   NM_134323,   NM_134324,   UC001SDQ.1,   UC001SDR.1,   UC001SDS.1,   UC001SDU.1,   UC001SDV.1,   UC009ZNB.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361252,180,031 - 52,181,722 (+)MPROMDB
RGD ID:7224135
Promoter ID:EPDNEW_H17813
Type:initiation region
Name:TARBP2_3
Description:TARBP2, RISC loading complex RNA binding subunit
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H17814  EPDNEW_H17816  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381253,500,923 - 53,500,983EPDNEW
RGD ID:7224137
Promoter ID:EPDNEW_H17814
Type:initiation region
Name:TARBP2_1
Description:TARBP2, RISC loading complex RNA binding subunit
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H17813  EPDNEW_H17816  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381253,501,283 - 53,501,343EPDNEW
RGD ID:7224141
Promoter ID:EPDNEW_H17816
Type:initiation region
Name:TARBP2_2
Description:TARBP2, RISC loading complex RNA binding subunit
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H17813  EPDNEW_H17814  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381253,501,586 - 53,501,646EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:11569 AgrOrtholog
COSMIC TARBP2 COSMIC
Ensembl Genes ENSG00000139546 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000266987 ENTREZGENE
  ENST00000266987.7 UniProtKB/Swiss-Prot
  ENST00000394357 ENTREZGENE
  ENST00000394357.6 UniProtKB/Swiss-Prot
  ENST00000456234 ENTREZGENE
  ENST00000456234.6 UniProtKB/Swiss-Prot
  ENST00000547064.5 UniProtKB/TrEMBL
  ENST00000548971.5 UniProtKB/TrEMBL
  ENST00000549572.5 UniProtKB/TrEMBL
  ENST00000549679.5 UniProtKB/TrEMBL
  ENST00000550147.5 UniProtKB/TrEMBL
  ENST00000550407 ENTREZGENE
  ENST00000550407.1 UniProtKB/TrEMBL
  ENST00000551741.5 UniProtKB/TrEMBL
  ENST00000552817.5 UniProtKB/TrEMBL
  ENST00000552857.5 UniProtKB/TrEMBL
  ENST00000710362.1 UniProtKB/TrEMBL
Gene3D-CATH 3.30.160.20 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000139546 GTEx
HGNC ID HGNC:11569 ENTREZGENE
Human Proteome Map TARBP2 Human Proteome Map
InterPro dsRBD_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TRBP2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TRBP2_DSRM_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TRBP2_DSRM_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TRBP2_DSRM_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:6895 UniProtKB/Swiss-Prot
NCBI Gene 6895 ENTREZGENE
OMIM 605053 OMIM
PANTHER LOQUACIOUS, ISOFORM B UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR46205:SF1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam dsrm UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA36334 PharmGKB
PROSITE DS_RBD UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART DSRM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP dsRNA-binding domain-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0AA34QVS4_HUMAN UniProtKB/TrEMBL
  A8K3X2 ENTREZGENE, UniProtKB/TrEMBL
  F8VP94_HUMAN UniProtKB/TrEMBL
  F8VSA1_HUMAN UniProtKB/TrEMBL
  F8VTT7_HUMAN UniProtKB/TrEMBL
  F8VW32_HUMAN UniProtKB/TrEMBL
  F8VYK3_HUMAN UniProtKB/TrEMBL
  F8VYK6_HUMAN UniProtKB/TrEMBL
  F8VZ57_HUMAN UniProtKB/TrEMBL
  F8VZZ7_HUMAN UniProtKB/TrEMBL
  H3BV98_HUMAN UniProtKB/TrEMBL
  Q12878 ENTREZGENE
  Q15633 ENTREZGENE
  Q8WY32 ENTREZGENE
  Q8WY33 ENTREZGENE
  Q9BRY2 ENTREZGENE
  TRBP2_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary Q12878 UniProtKB/Swiss-Prot
  Q8WY32 UniProtKB/Swiss-Prot
  Q8WY33 UniProtKB/Swiss-Prot
  Q9BRY2 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2019-02-19 TARBP2  TARBP2 subunit of RISC loading complex  TARBP2  TARBP2, RISC loading complex RNA binding subunit  Symbol and/or name change 5135510 APPROVED
2016-05-19 TARBP2  TARBP2, RISC loading complex RNA binding subunit  TARBP2  TAR (HIV-1) RNA binding protein 2  Symbol and/or name change 5135510 APPROVED