TUT7 (terminal uridylyl transferase 7) - Rat Genome Database

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Gene: TUT7 (terminal uridylyl transferase 7) Homo sapiens
Analyze
Symbol: TUT7
Name: terminal uridylyl transferase 7
RGD ID: 1344359
HGNC Page HGNC:25817
Description: Enables RNA uridylyltransferase activity and miRNA binding activity. Involved in RNA metabolic process and negative regulation of transposition, RNA-mediated. Located in cytosol and nucleoplasm.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: DKFZp666B142; DKFZp686C11112; DKFZp686F119; DKFZp686I1269; PAP associated domain containing 6; PAPD6; TENT3B; terminal uridylyltransferase 7; TUTase 7; ZCCHC6; zinc finger CCHC domain-containing protein 6; zinc finger CCHC-type containing 6; zinc finger, CCHC domain containing 6
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38986,287,733 - 86,354,410 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl986,287,733 - 86,354,454 (-)EnsemblGRCh38hg38GRCh38
GRCh37988,902,648 - 88,969,325 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36988,092,468 - 88,159,189 (-)NCBINCBI36Build 36hg18NCBI36
Build 34986,132,203 - 86,198,923NCBI
Celera959,472,766 - 59,539,516 (-)NCBICelera
Cytogenetic Map9q21.33NCBI
HuRef958,725,479 - 58,792,201 (-)NCBIHuRef
CHM1_1989,049,089 - 89,115,852 (-)NCBICHM1_1
T2T-CHM13v2.0998,438,962 - 98,505,656 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# 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
3. 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.
4. The long and short of microRNA. Yates LA, etal., Cell. 2013 Apr 25;153(3):516-9. doi: 10.1016/j.cell.2013.04.003.
Additional References at PubMed
PMID:8889548   PMID:11076863   PMID:11214970   PMID:11230166   PMID:14702039   PMID:15146197   PMID:15164053   PMID:15489334   PMID:15489336   PMID:16344560   PMID:16381901   PMID:17353264  
PMID:18172165   PMID:20881960   PMID:21832049   PMID:21873635   PMID:22586326   PMID:22658674   PMID:22681889   PMID:22898984   PMID:22939629   PMID:23063654   PMID:24705354   PMID:25480299  
PMID:25979828   PMID:26288249   PMID:26496610   PMID:27609902   PMID:27773672   PMID:28431233   PMID:28514442   PMID:28665939   PMID:28671666   PMID:28718761   PMID:29395067   PMID:29467282  
PMID:29507755   PMID:30122351   PMID:30196744   PMID:30258100   PMID:30302948   PMID:31073040   PMID:31091453   PMID:31178353   PMID:31343991   PMID:31536960   PMID:31586073   PMID:32526260  
PMID:32877691   PMID:33005030   PMID:33060197   PMID:33961781   PMID:34079125   PMID:34244565   PMID:34732716   PMID:34949722   PMID:35013218  


Genomics

Comparative Map Data
TUT7
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38986,287,733 - 86,354,410 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl986,287,733 - 86,354,454 (-)EnsemblGRCh38hg38GRCh38
GRCh37988,902,648 - 88,969,325 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36988,092,468 - 88,159,189 (-)NCBINCBI36Build 36hg18NCBI36
Build 34986,132,203 - 86,198,923NCBI
Celera959,472,766 - 59,539,516 (-)NCBICelera
Cytogenetic Map9q21.33NCBI
HuRef958,725,479 - 58,792,201 (-)NCBIHuRef
CHM1_1989,049,089 - 89,115,852 (-)NCBICHM1_1
T2T-CHM13v2.0998,438,962 - 98,505,656 (-)NCBIT2T-CHM13v2.0
Tut7
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391359,919,690 - 59,971,060 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1359,919,375 - 59,970,961 (-)EnsemblGRCm39 Ensembl
GRCm381359,771,876 - 59,823,169 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1359,771,561 - 59,823,147 (-)EnsemblGRCm38mm10GRCm38
MGSCv371359,873,240 - 59,924,508 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361359,781,502 - 59,832,724 (-)NCBIMGSCv36mm8
Celera1360,831,422 - 60,882,680 (-)NCBICelera
Cytogenetic Map13B2NCBI
Tut7
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.2174,849,287 - 4,903,542 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl174,849,283 - 4,903,169 (+)EnsemblmRatBN7.2 Ensembl
Rnor_6.0175,225,854 - 5,279,674 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl175,225,835 - 5,271,794 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0177,451,199 - 7,505,016 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41710,752,875 - 10,806,477 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera174,970,855 - 5,024,770 (+)NCBICelera
Cytogenetic Map17p14NCBI
Tut7
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554321,268,103 - 1,329,436 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554321,268,217 - 1,330,385 (+)NCBIChiLan1.0ChiLan1.0
TUT7
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1985,489,974 - 85,554,745 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl985,486,521 - 85,554,745 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v0957,433,583 - 57,498,675 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
TUT7
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1173,400,648 - 73,464,935 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl173,401,421 - 73,475,493 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha174,162,268 - 74,226,563 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0173,707,237 - 73,771,495 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl173,707,227 - 73,771,495 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1173,515,084 - 73,579,269 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0173,281,944 - 73,345,972 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0173,987,748 - 74,051,975 (+)NCBIUU_Cfam_GSD_1.0
Tut7
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024404947119,984,394 - 120,043,816 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366801,705,691 - 1,752,423 (-)EnsemblSpeTri2.0
SpeTri2.0NW_0049366801,693,815 - 1,753,641 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
TUT7
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1028,995,565 - 29,061,176 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11028,995,564 - 29,061,179 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21033,038,194 - 33,103,962 (+)NCBISscrofa10.2Sscrofa10.2susScr3
TUT7
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11296,920,632 - 96,987,114 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1296,920,021 - 96,986,165 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366603885,271,931 - 85,337,399 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Tut7
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462480911,031,693 - 11,084,723 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462480911,030,422 - 11,094,754 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in TUT7
11 total Variants
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1983
Count of miRNA genes:523
Interacting mature miRNAs:585
Transcripts:ENST00000277141, ENST00000375947, ENST00000375948, ENST00000375957, ENST00000375960, ENST00000375961, ENST00000375963, ENST00000469004
Prediction methods: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
STS-F09563  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37988,937,434 - 88,937,651UniSTSGRCh37
Build 36988,127,254 - 88,127,471RGDNCBI36
Celera959,507,550 - 59,507,767RGD
Cytogenetic Map9q21UniSTS
HuRef958,760,277 - 58,760,494UniSTS
GeneMap99-GB4 RH Map9278.81UniSTS
NCBI RH Map9748.3UniSTS
RH102753  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37988,910,921 - 88,911,041UniSTSGRCh37
Build 36988,100,741 - 88,100,861RGDNCBI36
Celera959,481,039 - 59,481,159RGD
Cytogenetic Map9q21UniSTS
HuRef958,733,752 - 58,733,872UniSTS
GeneMap99-GB4 RH Map9278.81UniSTS
RH118983  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37988,967,273 - 88,967,566UniSTSGRCh37
Build 36988,157,093 - 88,157,386RGDNCBI36
Celera959,537,387 - 59,537,680RGD
Cytogenetic Map9q21UniSTS
HuRef958,790,072 - 58,790,365UniSTS
TNG Radiation Hybrid Map931328.0UniSTS
STS-D20387  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37988,902,701 - 88,902,821UniSTSGRCh37
Build 36988,092,521 - 88,092,641RGDNCBI36
Celera959,472,819 - 59,472,939RGD
Cytogenetic Map9q21UniSTS
HuRef958,725,532 - 58,725,652UniSTS
GeneMap99-GB4 RH Map9278.81UniSTS
NCBI RH Map9748.3UniSTS
RH41959  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37988,902,809 - 88,903,012UniSTSGRCh37
Build 36988,092,629 - 88,092,832RGDNCBI36
Celera959,472,927 - 59,473,130RGD
Cytogenetic Map9q21UniSTS
HuRef958,725,640 - 58,725,843UniSTS
GeneMap99-GB4 RH Map9278.81UniSTS
NCBI RH Map9748.3UniSTS
A009W34  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37988,938,469 - 88,938,594UniSTSGRCh37
Build 36988,128,289 - 88,128,414RGDNCBI36
Celera959,508,585 - 59,508,710RGD
Cytogenetic Map9q21UniSTS
HuRef958,761,309 - 58,761,434UniSTS
GeneMap99-GB4 RH Map9278.81UniSTS
G32922  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37988,938,469 - 88,938,594UniSTSGRCh37
Celera959,508,585 - 59,508,710UniSTS
Cytogenetic Map9q21UniSTS
HuRef958,761,309 - 58,761,434UniSTS


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 932 1158 795 365 1684 253 2998 448 705 171 1169 1273 125 793 1654 4
Low 1504 1823 930 257 267 211 1358 1743 3006 247 285 337 48 1 411 1134 1
Below cutoff 1 8 1 2 1 6 20 1 5 3 2 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001185059 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001185074 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001330718 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_024617 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005252207 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005252208 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006717283 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011519011 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011519012 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011519013 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011519014 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011519015 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011519016 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017015130 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017015131 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024447671 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024447672 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423867 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423868 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423869 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423870 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001746379 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001746380 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB051498 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK023471 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK055546 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK055948 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK058021 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK094169 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK308352 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL137849 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL353678 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL832026 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL832193 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL832965 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL832988 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC015897 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC016387 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC032456 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC111003 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC144523 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU734789 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX641077 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA773862 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471089 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CN419677 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR933643 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR933644 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR936608 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB156789 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC377509 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HI574282 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000277141   ⟹   ENSP00000277141
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl986,287,733 - 86,354,410 (-)Ensembl
RefSeq Acc Id: ENST00000375947   ⟹   ENSP00000365114
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl986,344,870 - 86,352,706 (-)Ensembl
RefSeq Acc Id: ENST00000375948   ⟹   ENSP00000365115
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl986,336,879 - 86,343,123 (-)Ensembl
RefSeq Acc Id: ENST00000375957   ⟹   ENSP00000365124
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl986,287,735 - 86,319,644 (-)Ensembl
RefSeq Acc Id: ENST00000375960   ⟹   ENSP00000365127
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl986,287,733 - 86,354,454 (-)Ensembl
RefSeq Acc Id: ENST00000375963   ⟹   ENSP00000365130
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl986,287,733 - 86,354,410 (-)Ensembl
RefSeq Acc Id: ENST00000469004
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl986,323,628 - 86,324,653 (-)Ensembl
RefSeq Acc Id: NM_001185059   ⟹   NP_001171988
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38986,287,733 - 86,354,410 (-)NCBI
GRCh37988,902,648 - 88,969,402 (-)RGD
Celera959,472,766 - 59,539,516 (-)RGD
HuRef958,725,479 - 58,792,201 (-)RGD
CHM1_1989,049,089 - 89,115,852 (-)NCBI
T2T-CHM13v2.0998,438,962 - 98,505,656 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001185074   ⟹   NP_001172003
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38986,287,733 - 86,354,410 (-)NCBI
GRCh37988,902,648 - 88,969,402 (-)RGD
Celera959,472,766 - 59,539,516 (-)RGD
HuRef958,725,479 - 58,792,201 (-)RGD
CHM1_1989,049,089 - 89,115,852 (-)NCBI
T2T-CHM13v2.0998,438,962 - 98,505,656 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001330718   ⟹   NP_001317647
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38986,287,733 - 86,354,410 (-)NCBI
T2T-CHM13v2.0998,438,962 - 98,505,656 (-)NCBI
Sequence:
RefSeq Acc Id: NM_024617   ⟹   NP_078893
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38986,287,733 - 86,354,410 (-)NCBI
GRCh37988,902,648 - 88,969,402 (-)RGD
Build 36988,092,468 - 88,159,189 (-)NCBI Archive
Celera959,472,766 - 59,539,516 (-)RGD
HuRef958,725,479 - 58,792,201 (-)RGD
CHM1_1989,049,089 - 89,115,852 (-)NCBI
T2T-CHM13v2.0998,438,962 - 98,505,656 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005252207   ⟹   XP_005252264
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38986,287,733 - 86,354,410 (-)NCBI
GRCh37988,902,648 - 88,969,402 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005252208   ⟹   XP_005252265
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38986,301,544 - 86,354,410 (-)NCBI
GRCh37988,902,648 - 88,969,402 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006717283   ⟹   XP_006717346
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38986,287,733 - 86,354,410 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011519011   ⟹   XP_011517313
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38986,295,298 - 86,354,410 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011519012   ⟹   XP_011517314
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38986,295,298 - 86,354,410 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011519013   ⟹   XP_011517315
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38986,295,298 - 86,354,119 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011519014   ⟹   XP_011517316
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38986,295,298 - 86,354,410 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011519015   ⟹   XP_011517317
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38986,295,298 - 86,354,410 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011519016   ⟹   XP_011517318
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38986,295,298 - 86,354,410 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017015130   ⟹   XP_016870619
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38986,287,733 - 86,354,119 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017015131   ⟹   XP_016870620
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38986,287,733 - 86,354,410 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047423867   ⟹   XP_047279823
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38986,287,733 - 86,354,119 (-)NCBI
RefSeq Acc Id: XM_047423868   ⟹   XP_047279824
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38986,295,298 - 86,354,410 (-)NCBI
RefSeq Acc Id: XM_047423869   ⟹   XP_047279825
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38986,295,298 - 86,354,410 (-)NCBI
RefSeq Acc Id: XM_047423870   ⟹   XP_047279826
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38986,310,768 - 86,354,410 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001171988 (Get FASTA)   NCBI Sequence Viewer  
  NP_001172003 (Get FASTA)   NCBI Sequence Viewer  
  NP_001317647 (Get FASTA)   NCBI Sequence Viewer  
  NP_078893 (Get FASTA)   NCBI Sequence Viewer  
  XP_005252264 (Get FASTA)   NCBI Sequence Viewer  
  XP_005252265 (Get FASTA)   NCBI Sequence Viewer  
  XP_006717346 (Get FASTA)   NCBI Sequence Viewer  
  XP_011517313 (Get FASTA)   NCBI Sequence Viewer  
  XP_011517314 (Get FASTA)   NCBI Sequence Viewer  
  XP_011517315 (Get FASTA)   NCBI Sequence Viewer  
  XP_011517316 (Get FASTA)   NCBI Sequence Viewer  
  XP_011517317 (Get FASTA)   NCBI Sequence Viewer  
  XP_011517318 (Get FASTA)   NCBI Sequence Viewer  
  XP_016870619 (Get FASTA)   NCBI Sequence Viewer  
  XP_016870620 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279823 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279824 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279825 (Get FASTA)   NCBI Sequence Viewer  
  XP_047279826 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH16387 (Get FASTA)   NCBI Sequence Viewer  
  AAH32456 (Get FASTA)   NCBI Sequence Viewer  
  BAB14584 (Get FASTA)   NCBI Sequence Viewer  
  BAB21802 (Get FASTA)   NCBI Sequence Viewer  
  BAB70951 (Get FASTA)   NCBI Sequence Viewer  
  BAB71052 (Get FASTA)   NCBI Sequence Viewer  
  CAE46038 (Get FASTA)   NCBI Sequence Viewer  
  CAH56214 (Get FASTA)   NCBI Sequence Viewer  
  CAH56219 (Get FASTA)   NCBI Sequence Viewer  
  CAI45944 (Get FASTA)   NCBI Sequence Viewer  
  CAI45945 (Get FASTA)   NCBI Sequence Viewer  
  CAI56753 (Get FASTA)   NCBI Sequence Viewer  
  CBX47630 (Get FASTA)   NCBI Sequence Viewer  
  EAW62714 (Get FASTA)   NCBI Sequence Viewer  
  EAW62715 (Get FASTA)   NCBI Sequence Viewer  
  EAW62716 (Get FASTA)   NCBI Sequence Viewer  
  EAW62717 (Get FASTA)   NCBI Sequence Viewer  
  EAW62718 (Get FASTA)   NCBI Sequence Viewer  
  Q5VYS8 (Get FASTA)   NCBI Sequence Viewer  
Reference Sequences
RefSeq Acc Id: NP_001171988   ⟸   NM_001185059
- Peptide Label: isoform 1
- UniProtKB: Q9H8M6 (UniProtKB/Swiss-Prot),   Q5VYS8 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_078893   ⟸   NM_024617
- Peptide Label: isoform 1
- UniProtKB: Q9H8M6 (UniProtKB/Swiss-Prot),   Q5VYS8 (UniProtKB/Swiss-Prot),   Q96KX5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001172003   ⟸   NM_001185074
- Peptide Label: isoform 2
- UniProtKB: Q5VYS8 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005252264   ⟸   XM_005252207
- Peptide Label: isoform X6
- Sequence:
RefSeq Acc Id: XP_005252265   ⟸   XM_005252208
- Peptide Label: isoform X7
- Sequence:
RefSeq Acc Id: XP_006717346   ⟸   XM_006717283
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_011517318   ⟸   XM_011519016
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_011517317   ⟸   XM_011519015
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_011517314   ⟸   XM_011519012
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011517313   ⟸   XM_011519011
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011517316   ⟸   XM_011519014
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011517315   ⟸   XM_011519013
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_016870620   ⟸   XM_017015131
- Peptide Label: isoform X4
- UniProtKB: Q9H8M6 (UniProtKB/Swiss-Prot),   Q5VYS8 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016870619   ⟸   XM_017015130
- Peptide Label: isoform X4
- UniProtKB: Q9H8M6 (UniProtKB/Swiss-Prot),   Q5VYS8 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001317647   ⟸   NM_001330718
- Peptide Label: isoform 3
- UniProtKB: Q5VYS8 (UniProtKB/Swiss-Prot),   X6R3Q3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000365115   ⟸   ENST00000375948
RefSeq Acc Id: ENSP00000365114   ⟸   ENST00000375947
RefSeq Acc Id: ENSP00000365124   ⟸   ENST00000375957
RefSeq Acc Id: ENSP00000365130   ⟸   ENST00000375963
RefSeq Acc Id: ENSP00000365127   ⟸   ENST00000375960
RefSeq Acc Id: ENSP00000277141   ⟸   ENST00000277141
RefSeq Acc Id: XP_047279823   ⟸   XM_047423867
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047279825   ⟸   XM_047423869
- Peptide Label: isoform X6
RefSeq Acc Id: XP_047279824   ⟸   XM_047423868
- Peptide Label: isoform X6
RefSeq Acc Id: XP_047279826   ⟸   XM_047423870
- Peptide Label: isoform X8
Protein Domains
CCHC-type   PAP-associated   TUTase   U1-type

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q5VYS8-F1-model_v2 AlphaFold Q5VYS8 1-1495 view protein structure

Promoters
RGD ID:7215379
Promoter ID:EPDNEW_H13436
Type:initiation region
Name:ZCCHC6_1
Description:zinc finger CCHC-type containing 6
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H13437  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38986,354,410 - 86,354,470EPDNEW
RGD ID:7215389
Promoter ID:EPDNEW_H13437
Type:multiple initiation site
Name:ZCCHC6_2
Description:zinc finger CCHC-type containing 6
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H13436  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38986,354,891 - 86,354,951EPDNEW
RGD ID:6807481
Promoter ID:HG_KWN:63888
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   Lymphoblastoid
Transcripts:ENST00000375947
Position:
Human AssemblyChrPosition (strand)Source
Build 36988,157,219 - 88,157,719 (-)MPROMDB
RGD ID:6807433
Promoter ID:HG_KWN:63889
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:ENST00000375960,   ENST00000375961,   ENST00000375963,   UC004AOR.1,   UC004AOS.1,   UC004AOU.1,   UC004AOV.1,   UC004AOW.2,   UC010MQF.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36988,158,929 - 88,159,429 (-)MPROMDB

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 copy number gain See cases [RCV000050348] Chr9:193412..138179445 [GRCh38]
Chr9:204193..141073897 [GRCh37]
Chr9:194193..140193718 [NCBI36]
Chr9:9p24.3-q34.3
pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138114463)x3 copy number gain See cases [RCV000053746] Chr9:193412..138114463 [GRCh38]
Chr9:214367..141008915 [GRCh37]
Chr9:204367..140128736 [NCBI36]
Chr9:9p24.3-q34.3
pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053748]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053748]|See cases [RCV000053748] Chr9:193412..138179445 [GRCh38]
Chr9:266045..141073897 [GRCh37]
Chr9:256045..140193718 [NCBI36]
Chr9:9p24.3-q34.3
pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124532)x3 copy number gain See cases [RCV000053745] Chr9:193412..138124532 [GRCh38]
Chr9:204193..141018984 [GRCh37]
Chr9:194193..140138805 [NCBI36]
Chr9:9p24.3-q34.3
pathogenic
NM_001185059.1(ZCCHC6):c.3365T>A (p.Leu1122Ter) single nucleotide variant Malignant melanoma [RCV000068728] Chr9:86310719 [GRCh38]
Chr9:88925634 [GRCh37]
Chr9:88115454 [NCBI36]
Chr9:9q21.33
not provided
GRCh38/hg38 9p24.3-q34.3(chr9:204193-138179445) copy number gain See cases [RCV000133791] Chr9:204193..138179445 [GRCh38]
Chr9:204193..141073897 [GRCh37]
Chr9:194193..140193718 [NCBI36]
Chr9:9p24.3-q34.3
pathogenic
GRCh38/hg38 9q21.11-31.2(chr9:68420430-106579493)x3 copy number gain See cases [RCV000136788] Chr9:68420430..106579493 [GRCh38]
Chr9:71130848..109341774 [GRCh37]
Chr9:70225166..108381595 [NCBI36]
Chr9:9q21.11-31.2
pathogenic
GRCh38/hg38 9q21.33-22.31(chr9:86079851-91827221)x1 copy number loss See cases [RCV000137602] Chr9:86079851..91827221 [GRCh38]
Chr9:88694766..94589503 [GRCh37]
Chr9:87884586..93629324 [NCBI36]
Chr9:9q21.33-22.31
pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124524)x3 copy number gain See cases [RCV000138783] Chr9:193412..138124524 [GRCh38]
Chr9:204090..141018976 [GRCh37]
Chr9:194090..140138797 [NCBI36]
Chr9:9p24.3-q34.3
pathogenic
GRCh38/hg38 9p11.2-q34.3(chr9:193412-138159073)x3 copy number gain See cases [RCV000139207] Chr9:193412..138159073 [GRCh38]
Chr9:68420641..141053525 [GRCh37]
Chr9:67910461..140173346 [NCBI36]
Chr9:9p11.2-q34.3
pathogenic
GRCh38/hg38 9q21.33(chr9:84861055-86784049)x1 copy number loss See cases [RCV000139131] Chr9:84861055..86784049 [GRCh38]
Chr9:87475970..89398964 [GRCh37]
Chr9:86665790..88588784 [NCBI36]
Chr9:9q21.33
uncertain significance
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138159073)x3 copy number gain See cases [RCV000138962] Chr9:193412..138159073 [GRCh38]
Chr9:204104..141053525 [GRCh37]
Chr9:194104..140173346 [NCBI36]
Chr9:9p24.3-q34.3
pathogenic|conflicting data from submitters
GRCh38/hg38 9q21.12-31.3(chr9:69627642-111454304)x3 copy number gain See cases [RCV000139789] Chr9:69627642..111454304 [GRCh38]
Chr9:72242558..114216584 [GRCh37]
Chr9:71432378..113256405 [NCBI36]
Chr9:9q21.12-31.3
pathogenic
GRCh38/hg38 9p24.3-q22.1(chr9:203861-88130444)x4 copy number gain See cases [RCV000141904] Chr9:203861..88130444 [GRCh38]
Chr9:203861..90745359 [GRCh37]
Chr9:193861..89935179 [NCBI36]
Chr9:9p24.3-q22.1
pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:203861-138125937)x3 copy number gain See cases [RCV000141876] Chr9:203861..138125937 [GRCh38]
Chr9:203861..141020389 [GRCh37]
Chr9:193861..140140210 [NCBI36]
Chr9:9p24.3-q34.3
pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:203862-138125937)x3 copy number gain See cases [RCV000143476] Chr9:203862..138125937 [GRCh38]
Chr9:203862..141020389 [GRCh37]
Chr9:193862..140140210 [NCBI36]
Chr9:9p24.3-q34.3
pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 copy number gain See cases [RCV000148113] Chr9:193412..138179445 [GRCh38]
Chr9:204193..141073897 [GRCh37]
Chr9:194193..140193718 [NCBI36]
Chr9:9p24.3-q34.3
pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:163131-141122114)x3 copy number gain See cases [RCV000240081] Chr9:163131..141122114 [GRCh37]
Chr9:9p24.3-q34.3
pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:62525-141006407) copy number gain See cases [RCV000449375] Chr9:62525..141006407 [GRCh37]
Chr9:9p24.3-q34.3
pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3 copy number gain See cases [RCV000447207] Chr9:203861..141020389 [GRCh37]
Chr9:9p24.3-q34.3
pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203864-141020389)x3 copy number gain See cases [RCV000448978] Chr9:203864..141020389 [GRCh37]
Chr9:9p24.3-q34.3
pathogenic
GRCh37/hg19 9q21.11-34.3(chr9:71069743-140999928) copy number gain Global developmental delay [RCV000626548] Chr9:71069743..140999928 [GRCh37]
Chr9:9q21.11-34.3
likely pathogenic
GRCh37/hg19 9q21.11-22.1(chr9:70966262-90761254)x4 copy number gain See cases [RCV000512280] Chr9:70966262..90761254 [GRCh37]
Chr9:9q21.11-22.1
pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203862-141020389) copy number gain See cases [RCV000512392] Chr9:203862..141020389 [GRCh37]
Chr9:9p24.3-q34.3
pathogenic
GRCh37/hg19 9q21.33(chr9:88928097-89411190)x3 copy number gain not provided [RCV000683124] Chr9:88928097..89411190 [GRCh37]
Chr9:9q21.33
likely benign
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141114095)x2 copy number gain not provided [RCV000748054] Chr9:10590..141114095 [GRCh37]
Chr9:9p24.3-q34.3
pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141122247)x3 copy number gain not provided [RCV000748055] Chr9:10590..141122247 [GRCh37]
Chr9:9p24.3-q34.3
pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141107672)x3 copy number gain not provided [RCV000748053] Chr9:10590..141107672 [GRCh37]
Chr9:9p24.3-q34.3
pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:46587-141066491)x3 copy number gain not provided [RCV000748063] Chr9:46587..141066491 [GRCh37]
Chr9:9p24.3-q34.3
pathogenic
NM_024617.4(TUT7):c.2551G>A (p.Asp851Asn) single nucleotide variant not provided [RCV000901250] Chr9:86323199 [GRCh38]
Chr9:88938114 [GRCh37]
Chr9:9q21.33
benign
NM_024617.4(TUT7):c.563C>T (p.Thr188Ile) single nucleotide variant not provided [RCV000965109] Chr9:86346438 [GRCh38]
Chr9:88961353 [GRCh37]
Chr9:9q21.33
benign
GRCh37/hg19 9q21.2-22.32(chr9:79520825-97201274) copy number gain not provided [RCV000767645] Chr9:79520825..97201274 [GRCh37]
Chr9:9q21.2-22.32
pathogenic
GRCh37/hg19 9q21.11-34.3(chr9:71416475-141020389)x3 copy number gain not provided [RCV000847808] Chr9:71416475..141020389 [GRCh37]
Chr9:9q21.11-34.3
pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020388)x3 copy number gain not provided [RCV000845900] Chr9:203861..141020388 [GRCh37]
Chr9:9p24.3-q34.3
pathogenic
GRCh37/hg19 9q21.33(chr9:88622823-88951838)x3 copy number gain not provided [RCV001006242] Chr9:88622823..88951838 [GRCh37]
Chr9:9q21.33
uncertain significance
NC_000009.11:g.12246100_101559378inv inversion Recurrent spontaneous abortion [RCV000999471] Chr9:12246100..101559378 [GRCh37]
Chr9:9p23-q22.33
likely pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:353349-141020389) copy number gain not specified [RCV002053823] Chr9:353349..141020389 [GRCh37]
Chr9:9p24.3-q34.3
pathogenic
GRCh37/hg19 9q21.11-33.2(chr9:71349994-122603410) copy number gain not specified [RCV002053853] Chr9:71349994..122603410 [GRCh37]
Chr9:9q21.11-33.2
likely pathogenic
GRCh37/hg19 9p22.1-q33.1(chr9:19356861-119513311) copy number loss Distal tetrasomy 15q [RCV002280776] Chr9:19356861..119513311 [GRCh37]
Chr9:9p22.1-q33.1
uncertain significance
GRCh37/hg19 9p24.3-q34.11(chr9:203861-131603223)x3 copy number gain See cases [RCV002292402] Chr9:203861..131603223 [GRCh37]
Chr9:9p24.3-q34.11
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:25817 AgrOrtholog
COSMIC TUT7 COSMIC
Ensembl Genes ENSG00000083223 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000277141 ENTREZGENE
  ENSP00000277141.6 UniProtKB/TrEMBL
  ENSP00000365114.1 UniProtKB/TrEMBL
  ENSP00000365115.1 UniProtKB/TrEMBL
  ENSP00000365124.1 UniProtKB/TrEMBL
  ENSP00000365127 ENTREZGENE
  ENSP00000365127.2 UniProtKB/Swiss-Prot
  ENSP00000365130 ENTREZGENE
  ENSP00000365130.3 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000277141 ENTREZGENE
  ENST00000277141.10 UniProtKB/TrEMBL
  ENST00000375947.1 UniProtKB/TrEMBL
  ENST00000375948.2 UniProtKB/TrEMBL
  ENST00000375957.5 UniProtKB/TrEMBL
  ENST00000375960 ENTREZGENE
  ENST00000375960.6 UniProtKB/Swiss-Prot
  ENST00000375963 ENTREZGENE
  ENST00000375963.8 UniProtKB/Swiss-Prot
Gene3D-CATH 3.30.460.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000083223 GTEx
HGNC ID HGNC:25817 ENTREZGENE
Human Proteome Map TUT7 Human Proteome Map
InterPro Matrin/U1-like-C_Znf_C2H2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  NT_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PAP_assoc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TUTase_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_C2H2_sf UniProtKB/TrEMBL
  Znf_CCHC UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_CCHC_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:79670 UniProtKB/Swiss-Prot
NCBI Gene 79670 ENTREZGENE
OMIM 613467 OMIM
Pfam PAP_assoc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TUTase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  zf-CCHC UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134971144 PharmGKB
PROSITE ZF_CCHC UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZINC_FINGER_C2H2_1 UniProtKB/Swiss-Prot
SMART ZnF_C2HC UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZnF_U1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF57667 UniProtKB/TrEMBL
  SSF57756 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF81301 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A0C4DFW3_HUMAN UniProtKB/TrEMBL
  Q5VYS8 ENTREZGENE
  Q5VYS9_HUMAN UniProtKB/TrEMBL
  Q5VYT0_HUMAN UniProtKB/TrEMBL
  Q96KX5 ENTREZGENE, UniProtKB/TrEMBL
  Q9H8M6 ENTREZGENE
  TUT7_HUMAN UniProtKB/Swiss-Prot
  X6R3Q3 ENTREZGENE, UniProtKB/TrEMBL
UniProt Secondary Q5H9T0 UniProtKB/Swiss-Prot
  Q5VYS5 UniProtKB/Swiss-Prot
  Q5VYS7 UniProtKB/Swiss-Prot
  Q658Z9 UniProtKB/Swiss-Prot
  Q659A2 UniProtKB/Swiss-Prot
  Q6MZJ3 UniProtKB/Swiss-Prot
  Q8N5F0 UniProtKB/Swiss-Prot
  Q96N57 UniProtKB/Swiss-Prot
  Q96NE8 UniProtKB/Swiss-Prot
  Q9C0F2 UniProtKB/Swiss-Prot
  Q9H8M6 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2018-04-24 TUT7  terminal uridylyl transferase 7  ZCCHC6  zinc finger CCHC-type containing 6  Symbol and/or name change 5135510 APPROVED
2016-02-16 ZCCHC6  zinc finger CCHC-type containing 6    zinc finger, CCHC domain containing 6  Symbol and/or name change 5135510 APPROVED