TUT1 (terminal uridylyl transferase 1, U6 snRNA-specific) - Rat Genome Database

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Gene: TUT1 (terminal uridylyl transferase 1, U6 snRNA-specific) Homo sapiens
Analyze
Symbol: TUT1
Name: terminal uridylyl transferase 1, U6 snRNA-specific
RGD ID: 1345565
HGNC Page HGNC:26184
Description: Enables several functions, including RNA binding activity; enzyme-substrate adaptor activity; and nucleotidyltransferase activity. Involved in U6 snRNA 3'-end processing and co-transcriptional mRNA 3'-end processing, cleavage and polyadenylation pathway. Located in cytosol and nucleus. Is active in nucleoplasm.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: FLJ21850; FLJ22267; FLJ22347; MGC131987; MGC149809; nuclear speckle targeted phosphatidylinositol 4-phosphate 5-kinase type I-alpha regulated-poly(A) polymerase; nuclear speckle-targeted PIPK1A-regulated-poly(A) polymerase; PAP-associated domain-containing 2; PAPD2; poly(A) polymerase associated domain containing 2; RBM21; RNA binding motif protein 21; RNA uridylyltransferase; RNA-binding motif protein 21; RNA-binding protein 21; speckle targeted PIP5K1A-regulated poly(A) polymerase; star-PAP; STARPAP; TENT1; terminal uridylyl transferase 1 U6 snRNA-specific; TUTase; TUTase 6; U6 snRNA-specific terminal uridylyltransferase 1; U6 TUTase; U6-TUTase; up-regulated in lung cancer 6; URLC6
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381162,575,052 - 62,591,523 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1162,575,045 - 62,591,637 (-)EnsemblGRCh38hg38GRCh38
GRCh371162,342,524 - 62,358,995 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361162,099,096 - 62,115,592 (-)NCBINCBI36Build 36hg18NCBI36
Build 341162,099,096 - 62,115,592NCBI
Celera1159,671,911 - 59,688,674 (-)NCBICelera
Cytogenetic Map11q12.3NCBI
HuRef1158,671,464 - 58,688,025 (-)NCBIHuRef
CHM1_11162,225,562 - 62,242,155 (-)NCBICHM1_1
T2T-CHM13v2.01162,564,505 - 62,580,971 (-)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

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
2. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, etal., Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. Epub 2002 Dec 11.
Additional References at PubMed
PMID:9628908   PMID:12603330   PMID:14702039   PMID:15489334   PMID:16055720   PMID:16751776   PMID:16790842   PMID:17643375   PMID:17872511   PMID:18172165   PMID:18288197   PMID:18305108  
PMID:19615732   PMID:20618440   PMID:21102410   PMID:21873635   PMID:22244330   PMID:22268729   PMID:22863883   PMID:23166591   PMID:23306079   PMID:23416977   PMID:23667531   PMID:23874977  
PMID:25142229   PMID:25147182   PMID:25178676   PMID:26186194   PMID:26496610   PMID:26496945   PMID:26725010   PMID:26871637   PMID:28151486   PMID:28276505   PMID:28514442   PMID:28589955  
PMID:28911096   PMID:29032201   PMID:29229926   PMID:29845934   PMID:32296183   PMID:32839293   PMID:33226137   PMID:33845483   PMID:33961781   PMID:34373451   PMID:34576144   PMID:35271311  
PMID:36215168   PMID:36543142   PMID:37563152   PMID:38364942  


Genomics

Comparative Map Data
TUT1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381162,575,052 - 62,591,523 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1162,575,045 - 62,591,637 (-)EnsemblGRCh38hg38GRCh38
GRCh371162,342,524 - 62,358,995 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361162,099,096 - 62,115,592 (-)NCBINCBI36Build 36hg18NCBI36
Build 341162,099,096 - 62,115,592NCBI
Celera1159,671,911 - 59,688,674 (-)NCBICelera
Cytogenetic Map11q12.3NCBI
HuRef1158,671,464 - 58,688,025 (-)NCBIHuRef
CHM1_11162,225,562 - 62,242,155 (-)NCBICHM1_1
T2T-CHM13v2.01162,564,505 - 62,580,971 (-)NCBIT2T-CHM13v2.0
Tut1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39198,931,199 - 8,943,572 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl198,931,211 - 8,943,574 (+)EnsemblGRCm39 Ensembl
GRCm38198,953,832 - 8,966,210 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl198,953,847 - 8,966,210 (+)EnsemblGRCm38mm10GRCm38
MGSCv37199,028,340 - 9,040,700 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36199,020,892 - 9,033,255 (+)NCBIMGSCv36mm8
Celera198,714,449 - 8,726,831 (+)NCBICelera
Cytogenetic Map19ANCBI
cM Map196.04NCBI
Tut1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81215,277,802 - 215,288,869 (+)NCBIGRCr8
mRatBN7.21205,848,691 - 205,859,767 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1205,848,772 - 205,859,764 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1214,257,244 - 214,268,332 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01221,292,151 - 221,303,134 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01213,985,008 - 213,995,991 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01225,151,462 - 225,162,445 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1225,151,404 - 225,162,595 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01232,088,997 - 232,100,065 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41211,629,025 - 211,640,008 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera1203,361,578 - 203,372,574 (+)NCBICelera
Cytogenetic Map1q43NCBI
Tut1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955599596,650 - 606,486 (+)EnsemblChiLan1.0
ChiLan1.0NW_004955599596,565 - 606,498 (+)NCBIChiLan1.0ChiLan1.0
TUT1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2963,801,920 - 63,819,095 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11164,844,628 - 64,861,803 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01157,932,582 - 57,949,473 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11161,287,375 - 61,303,784 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1161,287,375 - 61,303,784 (-)Ensemblpanpan1.1panPan2
TUT1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11854,048,519 - 54,061,431 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1854,048,563 - 54,061,415 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1852,653,541 - 52,666,455 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01855,100,852 - 55,112,992 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1855,100,856 - 55,126,764 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11854,197,090 - 54,210,000 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01853,771,809 - 53,783,676 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01854,567,401 - 54,580,143 (+)NCBIUU_Cfam_GSD_1.0
Tut1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494710,551,934 - 10,565,414 (+)NCBIHiC_Itri_2
TUT1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl29,148,560 - 9,161,905 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.129,148,563 - 9,161,918 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.228,494,206 - 8,506,620 (+)NCBISscrofa10.2Sscrofa10.2susScr3
TUT1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1111,313,208 - 11,325,912 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl111,312,843 - 11,326,777 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666038108,648,848 - 108,664,259 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Tut1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046249261,112,309 - 1,123,959 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046249261,113,331 - 1,123,930 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in TUT1
68 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
Single allele deletion Intellectual disability [RCV001293382] Chr11:118359328..118372573 [GRCh37]
Chr11:11p15.3-q23.3		 pathogenic
GRCh38/hg38 11q12.3(chr11:62433886-63096003)x3 copy number gain See cases [RCV000053620] Chr11:62433886..63096003 [GRCh38]
Chr11:62201358..62863475 [GRCh37]
Chr11:61957934..62620051 [NCBI36]
Chr11:11q12.3		 pathogenic
GRCh38/hg38 11q12.3(chr11:62452571-62862781)x3 copy number gain See cases [RCV000053621] Chr11:62452571..62862781 [GRCh38]
Chr11:62220043..62630253 [GRCh37]
Chr11:61976619..62386829 [NCBI36]
Chr11:11q12.3		 pathogenic
GRCh38/hg38 11q12.3(chr11:62562836-62840570)x3 copy number gain See cases [RCV000134807] Chr11:62562836..62840570 [GRCh38]
Chr11:62330308..62608042 [GRCh37]
Chr11:62086884..62364618 [NCBI36]
Chr11:11q12.3		 uncertain significance
GRCh38/hg38 11q12.3(chr11:62249520-62946093)x3 copy number gain See cases [RCV000138411] Chr11:62249520..62946093 [GRCh38]
Chr11:62016992..62713565 [GRCh37]
Chr11:61773568..62470141 [NCBI36]
Chr11:11q12.3		 pathogenic
GRCh37/hg19 11p13-q25(chr11:32799481-134938470)x3 copy number gain MISSED ABORTION [RCV002282973] Chr11:32799481..134938470 [GRCh37]
Chr11:11p13-q25		 pathogenic
NM_022830.3(TUT1):c.1297G>A (p.Ala433Thr) single nucleotide variant Abnormal brain morphology [RCV000454332] Chr11:62576991 [GRCh38]
Chr11:62344463 [GRCh37]
Chr11:11q12.3		 likely pathogenic
GRCh37/hg19 11q12.3(chr11:61840997-62987330)x1 copy number loss See cases [RCV000448355] Chr11:61840997..62987330 [GRCh37]
Chr11:11q12.3		 likely pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470) copy number gain See cases [RCV000511729] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3 copy number gain See cases [RCV000510881] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
NM_022830.3(TUT1):c.2405G>T (p.Gly802Val) single nucleotide variant not specified [RCV004328695] Chr11:62575314 [GRCh38]
Chr11:62342786 [GRCh37]
Chr11:11q12.3		 uncertain significance
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3 copy number gain not provided [RCV000737348] Chr11:198510..134934063 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3 copy number gain not provided [RCV000749874] Chr11:70864..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11q12.3(chr11:62157418-62362465)x3 copy number gain not provided [RCV000750070] Chr11:62157418..62362465 [GRCh37]
Chr11:11q12.3		 benign
NM_022830.2(TUT1):c.63G>C (p.Gly21=) single nucleotide variant not provided [RCV000941114] Chr11:62591537 [GRCh38]
Chr11:62359009 [GRCh37]
Chr11:11q12.3		 likely benign
NM_022830.3(TUT1):c.1823C>T (p.Pro608Leu) single nucleotide variant not specified [RCV004304107] Chr11:62575896 [GRCh38]
Chr11:62343368 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.2061C>G (p.Asp687Glu) single nucleotide variant not provided [RCV000881509] Chr11:62575658 [GRCh38]
Chr11:62343130 [GRCh37]
Chr11:11q12.3		 benign
NM_022830.3(TUT1):c.2560C>T (p.Leu854=) single nucleotide variant not provided [RCV000879851] Chr11:62575159 [GRCh38]
Chr11:62342631 [GRCh37]
Chr11:11q12.3		 benign
NM_022830.3(TUT1):c.1181G>A (p.Arg394His) single nucleotide variant not provided [RCV000971785] Chr11:62577271 [GRCh38]
Chr11:62344743 [GRCh37]
Chr11:11q12.3		 benign
NM_022830.2(TUT1):c.10delC (p.Pro4Leufs) deletion not provided [RCV000963277] Chr11:62591589 [GRCh38]
Chr11:62359061 [GRCh37]
Chr11:11q12.3		 benign
GRCh37/hg19 11q12.3(chr11:62314663-62788240)x3 copy number gain not provided [RCV000849841] Chr11:62314663..62788240 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1214G>A (p.Arg405Gln) single nucleotide variant not provided [RCV001091622] Chr11:62577238 [GRCh38]
Chr11:62344710 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.2285C>A (p.Ser762Tyr) single nucleotide variant not specified [RCV004282572] Chr11:62575434 [GRCh38]
Chr11:62342906 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1474+7T>C single nucleotide variant not provided [RCV000887975] Chr11:62576650 [GRCh38]
Chr11:62344122 [GRCh37]
Chr11:11q12.3		 benign
NM_022830.3(TUT1):c.2373G>A (p.Glu791=) single nucleotide variant not provided [RCV000885551] Chr11:62575346 [GRCh38]
Chr11:62342818 [GRCh37]
Chr11:11q12.3		 benign
NM_022830.3(TUT1):c.691-8G>A single nucleotide variant not provided [RCV000885552] Chr11:62579038 [GRCh38]
Chr11:62579038..62579039 [GRCh38]
Chr11:62346510 [GRCh37]
Chr11:62346510..62346511 [GRCh37]
Chr11:11q12.3		 benign
NM_022830.3(TUT1):c.691-8G>T single nucleotide variant not provided [RCV000938824] Chr11:62579038 [GRCh38]
Chr11:62346510 [GRCh37]
Chr11:11q12.3		 likely benign
NM_022830.3(TUT1):c.2238C>T (p.Ala746=) single nucleotide variant not provided [RCV000911679] Chr11:62575481 [GRCh38]
Chr11:62342953 [GRCh37]
Chr11:11q12.3		 likely benign
GRCh37/hg19 11q12.2-12.3(chr11:60385382-62456278)x3 copy number gain not provided [RCV001006412] Chr11:60385382..62456278 [GRCh37]
Chr11:11q12.2-12.3		 uncertain significance
NM_022830.3(TUT1):c.1672C>T (p.Arg558Trp) single nucleotide variant not provided [RCV001091621]|not specified [RCV004031975] Chr11:62576047 [GRCh38]
Chr11:62343519 [GRCh37]
Chr11:11q12.3		 uncertain significance
NC_000011.9:g.(?_59596957)_(68707199_?)dup duplication Familial temporal lobe epilepsy 8 [RCV001372442] Chr11:59596957..68707199 [GRCh37]
Chr11:11q12.1-13.3		 uncertain significance
NM_022830.3(TUT1):c.2362del (p.Gln788fs) deletion not provided [RCV001364622] Chr11:62575357 [GRCh38]
Chr11:62342829 [GRCh37]
Chr11:11q12.3		 uncertain significance
NC_000011.9:g.(?_58916346)_(64972349_?)dup duplication Leukocyte adhesion deficiency 3 [RCV003113394]|not provided [RCV003113393] Chr11:58916346..64972349 [GRCh37]
Chr11:11q12.1-13.1		 uncertain significance|no classifications from unflagged records
NM_022830.2(TUT1):c.67C>T (p.Arg23Trp) single nucleotide variant not specified [RCV004194989] Chr11:62591533 [GRCh38]
Chr11:62359005 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1745G>A (p.Arg582His) single nucleotide variant not specified [RCV004169392] Chr11:62575974 [GRCh38]
Chr11:62343446 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1724G>A (p.Arg575Gln) single nucleotide variant not specified [RCV004206455] Chr11:62575995 [GRCh38]
Chr11:62343467 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.539G>A (p.Arg180His) single nucleotide variant not specified [RCV004146229] Chr11:62581436 [GRCh38]
Chr11:62348908 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1823C>G (p.Pro608Arg) single nucleotide variant not specified [RCV004215311] Chr11:62575896 [GRCh38]
Chr11:62343368 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1671C>G (p.Ser557Arg) single nucleotide variant not specified [RCV004153999] Chr11:62576048 [GRCh38]
Chr11:62343520 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1063G>A (p.Val355Met) single nucleotide variant not specified [RCV004161566] Chr11:62578658 [GRCh38]
Chr11:62346130 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1258C>T (p.Arg420Trp) single nucleotide variant not specified [RCV004117446] Chr11:62577194 [GRCh38]
Chr11:62344666 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.728C>T (p.Ser243Leu) single nucleotide variant not specified [RCV004086755] Chr11:62578993 [GRCh38]
Chr11:62346465 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.797C>T (p.Pro266Leu) single nucleotide variant not specified [RCV004119448] Chr11:62578924 [GRCh38]
Chr11:62346396 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.27A>T (p.Glu9Asp) single nucleotide variant not specified [RCV004240685] Chr11:62591459 [GRCh38]
Chr11:62358931 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.2(TUT1):c.66C>G (p.Phe22Leu) single nucleotide variant not specified [RCV004108357] Chr11:62591534 [GRCh38]
Chr11:62359006 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.2140C>G (p.Leu714Val) single nucleotide variant not specified [RCV004107696] Chr11:62575579 [GRCh38]
Chr11:62343051 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1319A>G (p.Tyr440Cys) single nucleotide variant not specified [RCV004069922] Chr11:62576969 [GRCh38]
Chr11:62344441 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1310T>G (p.Leu437Arg) single nucleotide variant not specified [RCV004080083] Chr11:62576978 [GRCh38]
Chr11:62344450 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1018A>G (p.Met340Val) single nucleotide variant not specified [RCV004191896] Chr11:62578703 [GRCh38]
Chr11:62346175 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1673G>A (p.Arg558Gln) single nucleotide variant not specified [RCV004096973] Chr11:62576046 [GRCh38]
Chr11:62343518 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1865C>T (p.Ala622Val) single nucleotide variant not specified [RCV004214907] Chr11:62575854 [GRCh38]
Chr11:62343326 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1386G>T (p.Glu462Asp) single nucleotide variant not specified [RCV004100538] Chr11:62576745 [GRCh38]
Chr11:62344217 [GRCh37]
Chr11:11q12.3		 likely benign
NM_022830.3(TUT1):c.-12A>G single nucleotide variant not specified [RCV004219778] Chr11:62591497 [GRCh38]
Chr11:62358969 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1928G>A (p.Arg643Gln) single nucleotide variant not specified [RCV004102745] Chr11:62575791 [GRCh38]
Chr11:62343263 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.703G>C (p.Ala235Pro) single nucleotide variant not specified [RCV004169162] Chr11:62579018 [GRCh38]
Chr11:62346490 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1009G>A (p.Gly337Arg) single nucleotide variant not specified [RCV004075415] Chr11:62578712 [GRCh38]
Chr11:62346184 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.997G>A (p.Glu333Lys) single nucleotide variant not specified [RCV004180881] Chr11:62578724 [GRCh38]
Chr11:62346196 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.425C>T (p.Ala142Val) single nucleotide variant not specified [RCV004085701] Chr11:62581550 [GRCh38]
Chr11:62349022 [GRCh37]
Chr11:11q12.3		 likely benign
NM_022830.3(TUT1):c.1994G>C (p.Gly665Ala) single nucleotide variant not specified [RCV004278037] Chr11:62575725 [GRCh38]
Chr11:62343197 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1711G>T (p.Ala571Ser) single nucleotide variant not specified [RCV004256986] Chr11:62576008 [GRCh38]
Chr11:62343480 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1904T>A (p.Ile635Lys) single nucleotide variant not specified [RCV004257247] Chr11:62575815 [GRCh38]
Chr11:62343287 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.38G>C (p.Arg13Pro) single nucleotide variant not specified [RCV004249866] Chr11:62591448 [GRCh38]
Chr11:62358920 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.944G>C (p.Arg315Thr) single nucleotide variant not specified [RCV004258830] Chr11:62578777 [GRCh38]
Chr11:62346249 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1159C>T (p.Arg387Trp) single nucleotide variant not specified [RCV004256669] Chr11:62578562 [GRCh38]
Chr11:62346034 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.2413G>C (p.Ala805Pro) single nucleotide variant not specified [RCV004337481] Chr11:62575306 [GRCh38]
Chr11:62342778 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.2501C>T (p.Ala834Val) single nucleotide variant not specified [RCV004360653] Chr11:62575218 [GRCh38]
Chr11:62342690 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.2522G>A (p.Arg841Gln) single nucleotide variant not specified [RCV004355953] Chr11:62575197 [GRCh38]
Chr11:62342669 [GRCh37]
Chr11:11q12.3		 likely benign
NM_022830.3(TUT1):c.1712C>T (p.Ala571Val) single nucleotide variant not specified [RCV004339650] Chr11:62576007 [GRCh38]
Chr11:62343479 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1312G>A (p.Val438Met) single nucleotide variant not specified [RCV004341676] Chr11:62576976 [GRCh38]
Chr11:62344448 [GRCh37]
Chr11:11q12.3		 uncertain significance
GRCh37/hg19 11q12.2-13.5(chr11:59923608-76272324)x3 copy number gain not provided [RCV003484842] Chr11:59923608..76272324 [GRCh37]
Chr11:11q12.2-13.5		 pathogenic
NM_022830.3(TUT1):c.2514G>T (p.Pro838=) single nucleotide variant not provided [RCV003395870] Chr11:62575205 [GRCh38]
Chr11:62342677 [GRCh37]
Chr11:11q12.3		 likely benign
GRCh37/hg19 11q12.1-13.3(chr11:56895955-69295402)x3 copy number gain not specified [RCV003986944] Chr11:56895955..69295402 [GRCh37]
Chr11:11q12.1-13.3		 likely pathogenic
GRCh37/hg19 11p11.12-q13.1(chr11:50398499-63924462)x3 copy number gain not specified [RCV003986918] Chr11:50398499..63924462 [GRCh37]
Chr11:11p11.12-q13.1		 likely pathogenic
NM_022830.3(TUT1):c.2339G>A (p.Arg780Gln) single nucleotide variant not specified [RCV004481824] Chr11:62575380 [GRCh38]
Chr11:62342852 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.2510C>G (p.Ser837Cys) single nucleotide variant not specified [RCV004481826] Chr11:62575209 [GRCh38]
Chr11:62342681 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.2608A>G (p.Ile870Val) single nucleotide variant not specified [RCV004481827] Chr11:62575111 [GRCh38]
Chr11:62342583 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.2(TUT1):c.35C>T (p.Ser12Phe) single nucleotide variant not specified [RCV004481828] Chr11:62591565 [GRCh38]
Chr11:62359037 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.376C>T (p.Arg126Trp) single nucleotide variant not specified [RCV004481829] Chr11:62581599 [GRCh38]
Chr11:62349071 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.530G>A (p.Arg177Gln) single nucleotide variant not specified [RCV004481830] Chr11:62581445 [GRCh38]
Chr11:62348917 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.617C>T (p.Ser206Phe) single nucleotide variant not specified [RCV004481832] Chr11:62581179 [GRCh38]
Chr11:62348651 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.2(TUT1):c.7C>T (p.Leu3Phe) single nucleotide variant not specified [RCV004481833] Chr11:62591593 [GRCh38]
Chr11:62359065 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.718T>C (p.Ser240Pro) single nucleotide variant not specified [RCV004481834] Chr11:62579003 [GRCh38]
Chr11:62346475 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.10G>T (p.Val4Leu) single nucleotide variant not specified [RCV004481816] Chr11:62591476 [GRCh38]
Chr11:62358948 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1178C>G (p.Ser393Cys) single nucleotide variant not specified [RCV004481817] Chr11:62577274 [GRCh38]
Chr11:62344746 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1228G>A (p.Val410Met) single nucleotide variant not specified [RCV004481818] Chr11:62577224 [GRCh38]
Chr11:62344696 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1463T>C (p.Val488Ala) single nucleotide variant not specified [RCV004481819] Chr11:62576668 [GRCh38]
Chr11:62344140 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1529C>T (p.Ser510Phe) single nucleotide variant not specified [RCV004481820] Chr11:62576190 [GRCh38]
Chr11:62343662 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1574G>T (p.Gly525Val) single nucleotide variant not specified [RCV004481821] Chr11:62576145 [GRCh38]
Chr11:62343617 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1744C>T (p.Arg582Cys) single nucleotide variant not specified [RCV004481822] Chr11:62575975 [GRCh38]
Chr11:62343447 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1762G>C (p.Asp588His) single nucleotide variant not specified [RCV004481823] Chr11:62575957 [GRCh38]
Chr11:62343429 [GRCh37]
Chr11:11q12.3		 uncertain significance
NC_000011.9:g.(?_62105450)_(62414071_?)dup duplication not provided [RCV004580325] Chr11:62105450..62414071 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.80A>G (p.Asn27Ser) single nucleotide variant not specified [RCV004683050] Chr11:62591406 [GRCh38]
Chr11:62358878 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.2168C>G (p.Ala723Gly) single nucleotide variant not specified [RCV004683051] Chr11:62575551 [GRCh38]
Chr11:62343023 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.2213G>A (p.Arg738Gln) single nucleotide variant not specified [RCV004683043] Chr11:62575506 [GRCh38]
Chr11:62342978 [GRCh37]
Chr11:11q12.3		 likely benign
NM_022830.3(TUT1):c.1370C>T (p.Thr457Ile) single nucleotide variant not specified [RCV004683044] Chr11:62576918 [GRCh38]
Chr11:62344390 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1462G>C (p.Val488Leu) single nucleotide variant not specified [RCV004683046] Chr11:62576669 [GRCh38]
Chr11:62344141 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.1764C>A (p.Asp588Glu) single nucleotide variant not specified [RCV004683047] Chr11:62575955 [GRCh38]
Chr11:62343427 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.2525T>A (p.Met842Lys) single nucleotide variant not specified [RCV004683048] Chr11:62575194 [GRCh38]
Chr11:62342666 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_022830.3(TUT1):c.608T>C (p.Phe203Ser) single nucleotide variant not specified [RCV004683049] Chr11:62581188 [GRCh38]
Chr11:62348660 [GRCh37]
Chr11:11q12.3		 uncertain significance
miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR129-2hsa-miR-129-2-3pMirtarbaseexternal_infoCLASHFunctional MTI (Weak)23622248

Predicted Target Of
Summary Value
Count of predictions:2075
Count of miRNA genes:799
Interacting mature miRNAs:967
Transcripts:ENST00000278279, ENST00000308436, ENST00000463241, ENST00000469480, ENST00000476907, ENST00000478537, ENST00000494385
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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
1357380BW64_HBody weight QTL 64 (human)2.2Body weightpercent fat after exercise training116097893786978937Human
407179797GWAS828773_HFEV/FVC ratio QTL GWAS828773 (human)2e-08FEV/FVC ratioforced expiratory volume to forced vital capacity ratio (CMO:0000241)116258106262581063Human
407156790GWAS805766_Hcerebrospinal fluid biomarker measurement QTL GWAS805766 (human)5e-08cerebrospinal fluid biomarker measurementcerebrospinal fluid chemistry measurement (CMO:0001241)116257828962578290Human
407134448GWAS783424_Hforced expiratory volume, response to bronchodilator QTL GWAS783424 (human)0.000001forced expiratory volume, response to bronchodilatorforced expiratory volume (CMO:0000254)116257955962579560Human
407187133GWAS836109_Hphosphatidylcholine measurement QTL GWAS836109 (human)2e-08phosphatidylcholine measurement116258612962586130Human
407159549GWAS808525_Hforced expiratory volume, response to bronchodilator QTL GWAS808525 (human)0.000003forced expiratory volume, response to bronchodilatorforced expiratory volume (CMO:0000254)116258421962584220Human
407159550GWAS808526_Hforced expiratory volume, response to bronchodilator QTL GWAS808526 (human)0.000002forced expiratory volume, response to bronchodilatorforced expiratory volume (CMO:0000254)116257903862579039Human
407039976GWAS688952_Hchronic obstructive pulmonary disease QTL GWAS688952 (human)2e-18chronic obstructive pulmonary disease116258372662583727Human
407163851GWAS812827_HFEV/FVC ratio, response to bronchodilator QTL GWAS812827 (human)0.000005FEV/FVC ratio, response to bronchodilatorforced expiratory volume to forced vital capacity ratio (CMO:0000241)116257955962579560Human
407271049GWAS920025_HBMI-adjusted waist-hip ratio QTL GWAS920025 (human)2e-11BMI-adjusted waist-hip ratio116258106262581063Human

Markers in Region
RH66302  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371162,342,606 - 62,342,773UniSTSGRCh37
Build 361162,099,182 - 62,099,349RGDNCBI36
Celera1159,672,000 - 59,672,167RGD
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map11q12.2UniSTS
HuRef1158,671,553 - 58,671,720UniSTS
GeneMap99-GB4 RH Map11229.09UniSTS
NCBI RH Map11558.0UniSTS
SHGC-2363  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371162,342,572 - 62,342,729UniSTSGRCh37
Build 361162,099,148 - 62,099,305RGDNCBI36
Celera1159,671,966 - 59,672,123RGD
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map11q12.2UniSTS
HuRef1158,671,519 - 58,671,676UniSTS
SHGC-105031  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371162,359,821 - 62,360,092UniSTSGRCh37
Build 361162,116,397 - 62,116,668RGDNCBI36
Celera1159,689,386 - 59,689,657RGD
Cytogenetic Map11q12.2UniSTS
HuRef1158,688,737 - 58,689,008UniSTS
TNG Radiation Hybrid Map1127073.0UniSTS
SHGC-57995  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371162,342,367 - 62,342,515UniSTSGRCh37
Build 361162,098,943 - 62,099,091RGDNCBI36
Celera1159,671,761 - 59,671,909RGD
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map11q12.2UniSTS
HuRef1158,671,314 - 58,671,462UniSTS
TNG Radiation Hybrid Map1127055.0UniSTS


Expression

RNA-SEQ Expression

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 2658 2790 2305 5440 2030 2994 12 859 2715 702 2569 8815 7332 106 3910 2 1192 2091 1998 184 1

Sequence


Ensembl Acc Id: ENST00000278279   ⟹   ENSP00000278279
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1162,578,809 - 62,591,523 (-)Ensembl
Ensembl Acc Id: ENST00000308436   ⟹   ENSP00000308000
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1162,575,045 - 62,591,637 (-)Ensembl
Ensembl Acc Id: ENST00000463241
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1162,576,244 - 62,577,316 (-)Ensembl
Ensembl Acc Id: ENST00000469480
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1162,575,058 - 62,577,257 (-)Ensembl
Ensembl Acc Id: ENST00000476907   ⟹   ENSP00000419607
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1162,575,052 - 62,591,523 (-)Ensembl
Ensembl Acc Id: ENST00000478537   ⟹   ENSP00000419792
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1162,581,492 - 62,591,523 (-)Ensembl
Ensembl Acc Id: ENST00000494385   ⟹   ENSP00000420739
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1162,581,108 - 62,591,612 (-)Ensembl
Ensembl Acc Id: ENST00000496634   ⟹   ENSP00000456163
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1162,559,603 - 62,591,531 (-)Ensembl
Ensembl Acc Id: ENST00000526409
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1162,559,603 - 62,577,321 (-)Ensembl
Ensembl Acc Id: ENST00000534745
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1162,573,886 - 62,576,852 (-)Ensembl
RefSeq Acc Id: NM_001367906   ⟹   NP_001354835
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381162,575,052 - 62,591,523 (-)NCBI
T2T-CHM13v2.01162,564,505 - 62,580,971 (-)NCBI
Sequence:
RefSeq Acc Id: NM_022830   ⟹   NP_073741
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381162,575,052 - 62,591,523 (-)NCBI
GRCh371162,341,431 - 62,359,109 (-)NCBI
Build 361162,099,096 - 62,115,592 (-)NCBI Archive
HuRef1158,671,464 - 58,688,025 (-)ENTREZGENE
CHM1_11162,225,562 - 62,242,155 (-)NCBI
T2T-CHM13v2.01162,564,505 - 62,580,971 (-)NCBI
Sequence:
RefSeq Acc Id: NP_073741   ⟸   NM_022830
- Peptide Label: isoform 1
- UniProtKB: Q9H6E5 (UniProtKB/Swiss-Prot),   Q7L583 (UniProtKB/Swiss-Prot),   Q2NL65 (UniProtKB/Swiss-Prot),   A8K995 (UniProtKB/Swiss-Prot),   A1A527 (UniProtKB/Swiss-Prot),   Q9H6H7 (UniProtKB/Swiss-Prot),   A0A0A8K9B1 (UniProtKB/TrEMBL),   F5H0R1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001354835   ⟸   NM_001367906
- Peptide Label: isoform 2
- UniProtKB: H3BRB1 (UniProtKB/TrEMBL)
Ensembl Acc Id: ENSP00000419792   ⟸   ENST00000478537
Ensembl Acc Id: ENSP00000308000   ⟸   ENST00000308436
Ensembl Acc Id: ENSP00000420739   ⟸   ENST00000494385
Ensembl Acc Id: ENSP00000456163   ⟸   ENST00000496634
Ensembl Acc Id: ENSP00000278279   ⟸   ENST00000278279
Ensembl Acc Id: ENSP00000419607   ⟸   ENST00000476907
Protein Domains
C2H2-type   PAP-associated   RRM

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9H6E5-F1-model_v2 AlphaFold Q9H6E5 1-874 view protein structure

Promoters
RGD ID:6810197
Promoter ID:HG_ACW:12426
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:TUT1ANDEEF1G.QAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 361162,095,056 - 62,095,556 (-)MPROMDB
RGD ID:6789501
Promoter ID:HG_KWN:13105
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:ENST00000308436,   NM_022830
Position:
Human AssemblyChrPosition (strand)Source
Build 361162,115,556 - 62,116,502 (-)MPROMDB
RGD ID:7220647
Promoter ID:EPDNEW_H16069
Type:initiation region
Name:TUT1_2
Description:terminal uridylyl transferase 1, U6 snRNA-specific
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H16070  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381162,575,296 - 62,575,356EPDNEW
RGD ID:7220649
Promoter ID:EPDNEW_H16070
Type:initiation region
Name:TUT1_1
Description:terminal uridylyl transferase 1, U6 snRNA-specific
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H16069  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381162,591,523 - 62,591,583EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:26184 AgrOrtholog
COSMIC TUT1 COSMIC
Ensembl Genes ENSG00000149016 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENSG00000255508 Ensembl, UniProtKB/TrEMBL
Ensembl Transcript ENST00000278279.7 UniProtKB/TrEMBL
  ENST00000308436.11 UniProtKB/TrEMBL
  ENST00000476907 ENTREZGENE
  ENST00000476907.6 UniProtKB/Swiss-Prot
  ENST00000478537.1 UniProtKB/TrEMBL
  ENST00000494385.1 UniProtKB/TrEMBL
  ENST00000496634.2 UniProtKB/TrEMBL
Gene3D-CATH 1.10.1410.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.30.460.10 UniProtKB/TrEMBL
  3.30.70.330 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000149016 GTEx
  ENSG00000255508 GTEx
HGNC ID HGNC:26184 ENTREZGENE
Human Proteome Map TUT1 Human Proteome Map
InterPro NT_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Nucleotide-bd_a/b_plait_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PAP_assoc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RBD_domain_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RRM_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Star-PAP_RRM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_C2H2_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_C2H2_type UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:64852 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 64852 ENTREZGENE
OMIM 610641 OMIM
PANTHER POLY A POLYMERASE CID PAP -RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SPECKLE TARGETED PIP5K1A-REGULATED POLY(A) POLYMERASE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam MTPAP-like_central UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PAP_assoc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RRM_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  zf-met UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA162407405 PharmGKB
PROSITE RRM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART RRM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP PAP/OAS1 substrate-binding domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF54928 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF57667 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF81301 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A0A8K9B1 ENTREZGENE, UniProtKB/TrEMBL
  A0A0S2Z5L2_HUMAN UniProtKB/TrEMBL
  A0A0S2Z5Y5_HUMAN UniProtKB/TrEMBL
  A1A527 ENTREZGENE
  A8K995 ENTREZGENE
  C9JBX0_HUMAN UniProtKB/TrEMBL
  F5H0R1 ENTREZGENE, UniProtKB/TrEMBL
  F8WA97_HUMAN UniProtKB/TrEMBL
  H3BRB1 ENTREZGENE, UniProtKB/TrEMBL
  J3KN81_HUMAN UniProtKB/TrEMBL
  Q2NL65 ENTREZGENE
  Q7L583 ENTREZGENE
  Q9H6E5 ENTREZGENE
  Q9H6H7 ENTREZGENE
  STPAP_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary A1A527 UniProtKB/Swiss-Prot
  A8K995 UniProtKB/Swiss-Prot
  Q2NL65 UniProtKB/Swiss-Prot
  Q7L583 UniProtKB/Swiss-Prot
  Q9H6H7 UniProtKB/Swiss-Prot