CTU2 (cytosolic thiouridylase subunit 2) - Rat Genome Database

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Gene: CTU2 (cytosolic thiouridylase subunit 2) Homo sapiens
Analyze
Symbol: CTU2
Name: cytosolic thiouridylase subunit 2
RGD ID: 1604165
HGNC Page HGNC
Description: Predicted to have sulfurtransferase activity. Predicted to be involved in tRNA wobble position uridine thiolation. Localizes to protein-containing complex.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: C16orf84; cytoplasmic tRNA 2-thiolation protein 2; cytosolic thiouridylase subunit 2 homolog; cytosolic thiouridylase subunit 2 homolog (S. pombe); MFRG; MGC131681; MGC148063; MGC148064; NCS2; UPF0432
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
GRCh38.p13 Ensembl1688,706,483 - 88,715,396 (+)EnsemblGRCh38hg38GRCh38
GRCh381688,706,481 - 88,715,396 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371688,772,911 - 88,781,804 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361687,300,392 - 87,309,295 (+)NCBINCBI36hg18NCBI36
Celera1673,276,731 - 73,278,805 (-)NCBI
Cytogenetic Map16q24.3NCBI
HuRef1674,467,287 - 74,477,681 (+)NCBIHuRef
CHM1_11690,184,233 - 90,193,064 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

References

Additional References at PubMed
PMID:12477932   PMID:18029348   PMID:19017811   PMID:20881960   PMID:21873635   PMID:22678362   PMID:23891004   PMID:25534755   PMID:26186194   PMID:28514442   PMID:31091453   PMID:31301155  


Genomics

Comparative Map Data
CTU2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1688,706,483 - 88,715,396 (+)EnsemblGRCh38hg38GRCh38
GRCh381688,706,481 - 88,715,396 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371688,772,911 - 88,781,804 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361687,300,392 - 87,309,295 (+)NCBINCBI36hg18NCBI36
Celera1673,276,731 - 73,278,805 (-)NCBI
Cytogenetic Map16q24.3NCBI
HuRef1674,467,287 - 74,477,681 (+)NCBIHuRef
CHM1_11690,184,233 - 90,193,064 (+)NCBICHM1_1
Ctu2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm398123,202,882 - 123,209,831 (+)NCBIGRCm39mm39
GRCm39 Ensembl8123,202,882 - 123,210,877 (+)Ensembl
GRCm388122,476,068 - 122,483,092 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl8122,476,143 - 122,484,138 (+)EnsemblGRCm38mm10GRCm38
MGSCv378125,000,043 - 125,006,992 (+)NCBIGRCm37mm9NCBIm37
MGSCv368125,362,280 - 125,367,837 (+)NCBImm8
MGSCv368122,545,627 - 122,551,185 (+)NCBImm8
Celera8126,705,199 - 126,712,124 (+)NCBICelera
Cytogenetic Map8E1NCBI
Ctu2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21950,539,184 - 50,544,629 (+)NCBI
Rnor_6.0 Ensembl1955,300,395 - 55,305,702 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.01955,300,531 - 55,305,543 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.01966,009,931 - 66,014,988 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41952,765,786 - 52,771,016 (+)NCBIRGSC3.4rn4RGSC3.4
Celera1949,778,881 - 49,784,108 (+)NCBICelera
Cytogenetic Map19q12NCBI
Ctu2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_0049555412,610,021 - 2,618,197 (+)NCBIChiLan1.0ChiLan1.0
CTU2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11689,080,476 - 89,088,363 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1689,079,132 - 89,088,231 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v01669,419,811 - 69,428,500 (+)NCBIMhudiblu_PPA_v0panPan3
CTU2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1564,640,389 - 64,647,298 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl564,640,389 - 64,647,215 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha564,651,709 - 64,658,603 (-)NCBI
ROS_Cfam_1.0564,860,459 - 64,867,333 (-)NCBI
UMICH_Zoey_3.1564,886,634 - 64,893,522 (-)NCBI
UNSW_CanFamBas_1.0564,718,200 - 64,725,080 (-)NCBI
UU_Cfam_GSD_1.0565,124,376 - 65,131,248 (-)NCBI
Ctu2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440934925,225,667 - 25,232,488 (-)NCBI
SpeTri2.0NW_004936641980,493 - 986,015 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CTU2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl6964,566 - 976,832 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.16964,551 - 976,881 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
CTU2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1574,091,156 - 74,100,941 (+)NCBI
ChlSab1.1 Ensembl574,091,258 - 74,100,573 (+)Ensembl
Vero_WHO_p1.0NW_0236660471,579,212 - 1,589,006 (-)NCBI
Ctu2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_004624746871,707 - 878,047 (-)NCBI

Position Markers
RH94123  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371688,781,625 - 88,781,752UniSTSGRCh37
Build 361687,309,126 - 87,309,253RGDNCBI36
Celera1673,852,837 - 73,852,964UniSTS
Celera1673,276,773 - 73,276,900RGD
Cytogenetic Map16q24.3UniSTS
HuRef1674,477,512 - 74,477,639UniSTS
GeneMap99-GB4 RH Map16488.68UniSTS
D16S2592E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371688,781,856 - 88,782,039UniSTSGRCh37
Build 361687,309,357 - 87,309,540RGDNCBI36
Celera1673,853,068 - 73,853,251RGD
Cytogenetic Map16q24.3UniSTS
HuRef1674,477,743 - 74,477,926UniSTS
SHGC-61047  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371688,782,050 - 88,782,234UniSTSGRCh37
Build 361687,309,551 - 87,309,735RGDNCBI36
Celera1673,853,262 - 73,853,446RGD
Cytogenetic Map16q24.3UniSTS
HuRef1674,477,937 - 74,478,121UniSTS
GeneMap99-GB4 RH Map16488.68UniSTS
NCBI RH Map16681.0UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3766
Count of miRNA genes:936
Interacting mature miRNAs:1165
Transcripts:ENST00000312060, ENST00000378384, ENST00000453996, ENST00000562011, ENST00000564105, ENST00000564584, ENST00000564921, ENST00000565071, ENST00000566637, ENST00000567316, ENST00000567949
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.


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 1506 1295 1069 111 874 62 2974 1128 2258 143 1252 1317 60 742 1953 3 1
Low 933 1688 657 513 1066 403 1382 1068 1476 276 207 296 114 1 462 835 3 1
Below cutoff 8 9 1 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001012759 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001012762 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001318507 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001318513 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017023210 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA448486 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC138028 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK299521 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC021056 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC021829 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC044951 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC063512 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC080540 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC108659 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC121805 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC125269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC157881 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BI520274 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM554780 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ430809 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471184 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000312060   ⟹   ENSP00000308617
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1688,706,483 - 88,715,386 (+)Ensembl
RefSeq Acc Id: ENST00000453996   ⟹   ENSP00000388320
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1688,706,503 - 88,715,396 (+)Ensembl
RefSeq Acc Id: ENST00000562011
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1688,714,985 - 88,715,383 (+)Ensembl
RefSeq Acc Id: ENST00000564105   ⟹   ENSP00000454923
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1688,706,483 - 88,715,320 (+)Ensembl
RefSeq Acc Id: ENST00000564584
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1688,713,480 - 88,715,364 (+)Ensembl
RefSeq Acc Id: ENST00000564921   ⟹   ENSP00000455010
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1688,706,589 - 88,712,382 (+)Ensembl
RefSeq Acc Id: ENST00000565071
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1688,706,545 - 88,710,908 (+)Ensembl
RefSeq Acc Id: ENST00000566637
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1688,709,959 - 88,715,386 (+)Ensembl
RefSeq Acc Id: ENST00000567316   ⟹   ENSP00000455305
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1688,714,682 - 88,715,376 (+)Ensembl
RefSeq Acc Id: ENST00000567949   ⟹   ENSP00000456908
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1688,706,522 - 88,715,386 (+)Ensembl
RefSeq Acc Id: NM_001012759   ⟹   NP_001012777
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381688,706,503 - 88,715,396 (+)NCBI
GRCh371688,772,891 - 88,781,794 (+)RGD
Build 361687,300,392 - 87,309,295 (+)NCBI Archive
Celera1673,276,731 - 73,278,805 (-)RGD
HuRef1674,467,287 - 74,477,681 (+)RGD
CHM1_11690,184,213 - 90,193,064 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001012762   ⟹   NP_001012780
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381688,706,503 - 88,715,396 (+)NCBI
GRCh371688,772,891 - 88,781,794 (+)RGD
Build 361687,300,392 - 87,309,295 (+)NCBI Archive
Celera1673,276,731 - 73,278,805 (-)RGD
HuRef1674,467,287 - 74,477,681 (+)RGD
CHM1_11690,184,213 - 90,193,064 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001318507   ⟹   NP_001305436
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381688,706,503 - 88,715,396 (+)NCBI
CHM1_11690,184,213 - 90,193,064 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001318513   ⟹   NP_001305442
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381688,706,503 - 88,715,396 (+)NCBI
CHM1_11690,184,213 - 90,193,064 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017023210   ⟹   XP_016878699
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381688,706,481 - 88,715,386 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_001012780   ⟸   NM_001012762
- Peptide Label: isoform 2
- UniProtKB: Q2VPK5 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001012777   ⟸   NM_001012759
- Peptide Label: isoform 1
- UniProtKB: Q2VPK5 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001305436   ⟸   NM_001318507
- Peptide Label: isoform 3
- UniProtKB: Q2VPK5 (UniProtKB/Swiss-Prot),   H3BSW6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001305442   ⟸   NM_001318513
- Peptide Label: isoform 4
- UniProtKB: Q2VPK5 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016878699   ⟸   XM_017023210
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: ENSP00000388320   ⟸   ENST00000453996
RefSeq Acc Id: ENSP00000308617   ⟸   ENST00000312060
RefSeq Acc Id: ENSP00000454923   ⟸   ENST00000564105
RefSeq Acc Id: ENSP00000455010   ⟸   ENST00000564921
RefSeq Acc Id: ENSP00000456908   ⟸   ENST00000567949
RefSeq Acc Id: ENSP00000455305   ⟸   ENST00000567316

Promoters
RGD ID:6793428
Promoter ID:HG_KWN:24466
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_001012759,   NM_001012762,   NM_001171815,   OTTHUMT00000269544,   UC002FLL.1,   UC010CHZ.1,   UC010CIA.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361687,299,266 - 87,300,472 (-)MPROMDB
RGD ID:7233119
Promoter ID:EPDNEW_H22305
Type:initiation region
Name:CTU2_1
Description:cytosolic thiouridylase subunit 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381688,706,503 - 88,706,563EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 16q23.1-24.3(chr16:78816291-90081985)x3 copy number gain See cases [RCV000050840] Chr16:78816291..90081985 [GRCh38]
Chr16:78850188..90148393 [GRCh37]
Chr16:77407689..88675894 [NCBI36]
Chr16:16q23.1-24.3
pathogenic
GRCh38/hg38 16q21-24.3(chr16:65313395-90081985)x3 copy number gain See cases [RCV000052421] Chr16:65313395..90081985 [GRCh38]
Chr16:65347298..90148393 [GRCh37]
Chr16:63904799..88675894 [NCBI36]
Chr16:16q21-24.3
pathogenic
GRCh38/hg38 16q22.1-24.3(chr16:70514631-90081985)x3 copy number gain See cases [RCV000052422] Chr16:70514631..90081985 [GRCh38]
Chr16:70548534..90148393 [GRCh37]
Chr16:69106035..88675894 [NCBI36]
Chr16:16q22.1-24.3
pathogenic
GRCh38/hg38 16q23.1-24.3(chr16:76873569-90081985)x3 copy number gain See cases [RCV000052423] Chr16:76873569..90081985 [GRCh38]
Chr16:76907466..90148393 [GRCh37]
Chr16:75464967..88675894 [NCBI36]
Chr16:16q23.1-24.3
pathogenic
GRCh38/hg38 16q23.3-24.3(chr16:82173150-90081985)x3 copy number gain See cases [RCV000052424] Chr16:82173150..90081985 [GRCh38]
Chr16:82206755..90148393 [GRCh37]
Chr16:80764256..88675894 [NCBI36]
Chr16:16q23.3-24.3
pathogenic
GRCh38/hg38 16q24.1-24.3(chr16:84707538-90081985)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052425]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052425]|See cases [RCV000052425] Chr16:84707538..90081985 [GRCh38]
Chr16:84741144..90148393 [GRCh37]
Chr16:83298645..88675894 [NCBI36]
Chr16:16q24.1-24.3
pathogenic
GRCh38/hg38 16q24.2-24.3(chr16:87853401-90081985)x3 copy number gain See cases [RCV000052428] Chr16:87853401..90081985 [GRCh38]
Chr16:87887007..90148393 [GRCh37]
Chr16:86444508..88675894 [NCBI36]
Chr16:16q24.2-24.3
pathogenic
GRCh38/hg38 16q24.2-24.3(chr16:88640116-89530475)x1 copy number loss See cases [RCV000053380] Chr16:88640116..89530475 [GRCh38]
Chr16:88706524..89596883 [GRCh37]
Chr16:87234025..88124384 [NCBI36]
Chr16:16q24.2-24.3
pathogenic
GRCh38/hg38 16q24.2-24.3(chr16:88662702-89454555)x1 copy number loss See cases [RCV000053381] Chr16:88662702..89454555 [GRCh38]
Chr16:88729110..89520963 [GRCh37]
Chr16:87256611..88048464 [NCBI36]
Chr16:16q24.2-24.3
pathogenic
GRCh38/hg38 16q24.2-24.3(chr16:87306529-89269079)x1 copy number loss See cases [RCV000053362] Chr16:87306529..89269079 [GRCh38]
Chr16:87340135..89335487 [GRCh37]
Chr16:85897636..87862988 [NCBI36]
Chr16:16q24.2-24.3
pathogenic
GRCh38/hg38 16q24.2-24.3(chr16:88159660-89506042)x1 copy number loss See cases [RCV000053363] Chr16:88159660..89506042 [GRCh38]
Chr16:88193266..89572450 [GRCh37]
Chr16:86750767..88099951 [NCBI36]
Chr16:16q24.2-24.3
pathogenic
NM_001012759.1(CTU2):c.804C>T (p.Cys268=) single nucleotide variant Malignant melanoma [RCV000071268] Chr16:88713378 [GRCh38]
Chr16:88779786 [GRCh37]
Chr16:87307287 [NCBI36]
Chr16:16q24.3
not provided
GRCh38/hg38 16q23.3-24.3(chr16:83988570-90081985)x3 copy number gain See cases [RCV000135659] Chr16:83988570..90081985 [GRCh38]
Chr16:84022175..90148393 [GRCh37]
Chr16:82579676..88675894 [NCBI36]
Chr16:16q23.3-24.3
likely pathogenic
GRCh38/hg38 16q23.2-24.3(chr16:80946659-90081985)x3 copy number gain See cases [RCV000136898] Chr16:80946659..90081985 [GRCh38]
Chr16:80980556..90148393 [GRCh37]
Chr16:79538057..88675894 [NCBI36]
Chr16:16q23.2-24.3
pathogenic|likely pathogenic
GRCh38/hg38 16q22.1-24.3(chr16:70749398-90096995)x3 copy number gain See cases [RCV000137495] Chr16:70749398..90096995 [GRCh38]
Chr16:70783301..90163403 [GRCh37]
Chr16:69340802..88690904 [NCBI36]
Chr16:16q22.1-24.3
pathogenic
GRCh38/hg38 16q24.2-24.3(chr16:87848216-90096995)x3 copy number gain See cases [RCV000138161] Chr16:87848216..90096995 [GRCh38]
Chr16:87881822..90163403 [GRCh37]
Chr16:86439323..88690904 [NCBI36]
Chr16:16q24.2-24.3
likely pathogenic
GRCh38/hg38 16q23.3-24.3(chr16:83478453-89932910)x3 copy number gain See cases [RCV000137980] Chr16:83478453..89932910 [GRCh38]
Chr16:83512058..89999318 [GRCh37]
Chr16:82069559..88526819 [NCBI36]
Chr16:16q23.3-24.3
likely pathogenic
GRCh38/hg38 16q21-24.3(chr16:65511483-90096995)x3 copy number gain See cases [RCV000139426] Chr16:65511483..90096995 [GRCh38]
Chr16:65545386..90163403 [GRCh37]
Chr16:64102887..88690904 [NCBI36]
Chr16:16q21-24.3
pathogenic
GRCh38/hg38 16q23.1-24.3(chr16:75377981-90081992)x3 copy number gain See cases [RCV000139302] Chr16:75377981..90081992 [GRCh38]
Chr16:75411879..90148400 [GRCh37]
Chr16:73969380..88675901 [NCBI36]
Chr16:16q23.1-24.3
pathogenic
GRCh38/hg38 16q24.2-24.3(chr16:88662702-88719577)x1 copy number loss See cases [RCV000140351] Chr16:88662702..88719577 [GRCh38]
Chr16:88729110..88785985 [GRCh37]
Chr16:87256611..87313486 [NCBI36]
Chr16:16q24.2-24.3
benign
GRCh38/hg38 16q24.1-24.3(chr16:85552976-90096995)x3 copy number gain See cases [RCV000139658] Chr16:85552976..90096995 [GRCh38]
Chr16:85586582..90163403 [GRCh37]
Chr16:84144083..88690904 [NCBI36]
Chr16:16q24.1-24.3
pathogenic
GRCh38/hg38 16q23.2-24.3(chr16:80717291-90096662)x3 copy number gain See cases [RCV000141128] Chr16:80717291..90096662 [GRCh38]
Chr16:80751188..90163070 [GRCh37]
Chr16:79308689..88690571 [NCBI36]
Chr16:16q23.2-24.3
pathogenic
GRCh38/hg38 16q23.1-24.3(chr16:76336203-90088654)x3 copy number gain See cases [RCV000141700] Chr16:76336203..90088654 [GRCh38]
Chr16:76370100..90155062 [GRCh37]
Chr16:74927601..88682563 [NCBI36]
Chr16:16q23.1-24.3
pathogenic
GRCh38/hg38 16q23.2-24.3(chr16:80067315-90057871)x3 copy number gain See cases [RCV000142698] Chr16:80067315..90057871 [GRCh38]
Chr16:80101212..90124279 [GRCh37]
Chr16:78658713..88651780 [NCBI36]
Chr16:16q23.2-24.3
pathogenic
GRCh38/hg38 16q21-24.3(chr16:64389378-90081985)x3 copy number gain See cases [RCV000142578] Chr16:64389378..90081985 [GRCh38]
Chr16:64423281..90148393 [GRCh37]
Chr16:62980782..88675894 [NCBI36]
Chr16:16q21-24.3
pathogenic|likely pathogenic
GRCh38/hg38 16q12.2-24.3(chr16:52899183-90088654)x3 copy number gain See cases [RCV000143425] Chr16:52899183..90088654 [GRCh38]
Chr16:52933095..90155062 [GRCh37]
Chr16:51490596..88682563 [NCBI36]
Chr16:16q12.2-24.3
pathogenic
GRCh38/hg38 16q24.1-24.3(chr16:86950106-89335814)x1 copy number loss See cases [RCV000143624] Chr16:86950106..89335814 [GRCh38]
Chr16:86983712..89402222 [GRCh37]
Chr16:85541213..87929723 [NCBI36]
Chr16:16q24.1-24.3
pathogenic
GRCh37/hg19 16q23.1-24.3(chr16:74872514-90274440)x3 copy number gain See cases [RCV000240108] Chr16:74872514..90274440 [GRCh37]
Chr16:16q23.1-24.3
pathogenic
t(5;16)(p15.31;q23.1) translocation not provided [RCV000203391] Chr5:1..8180513 [GRCh37]
Chr16:76935310..90354753 [GRCh37]
Chr5:5p15.33-15.31
Chr16:16q23.1-24.3
likely pathogenic
Single allele deletion 16q24.3 microdeletion syndrome [RCV000258442] Chr16:88556191..89557911 [GRCh37]
Chr16:16q24.2-24.3
pathogenic
Single allele deletion 16q24.3 microdeletion syndrome [RCV000258457] Chr16:88630607..89607742 [GRCh37]
Chr16:16q24.2-24.3
pathogenic
Single allele deletion 16q24.3 microdeletion syndrome [RCV000258180] Chr16:88230961..89363602 [GRCh37]
Chr16:16q24.2-24.3
pathogenic
Single allele deletion 16q24.3 microdeletion syndrome [RCV000258201] Chr16:88666177..89472627 [GRCh37]
Chr16:16q24.2-24.3
pathogenic
Single allele deletion 16q24.3 microdeletion syndrome [RCV000258213] Chr16:88165980..88914268 [GRCh37]
Chr16:16q24.2-24.3
pathogenic
Single allele deletion 16q24.3 microdeletion syndrome [RCV000258230] Chr16:87183661..89520803 [GRCh37]
Chr16:16q24.2-24.3
pathogenic
Single allele deletion 16q24.3 microdeletion syndrome [RCV000258283] Chr16:88643461..89611494 [GRCh37]
Chr16:16q24.2-24.3
pathogenic
Single allele deletion 16q24.3 microdeletion syndrome [RCV000258300] Chr16:88755312..89584412 [GRCh37]
Chr16:16q24.3
pathogenic
Single allele deletion 16q24.3 microdeletion syndrome [RCV000258311] Chr16:88230760..89363742 [GRCh37]
Chr16:16q24.2-24.3
pathogenic
Single allele deletion 16q24.3 microdeletion syndrome [RCV000258380] Chr16:87340135..89335428 [GRCh37]
Chr16:16q24.2-24.3
pathogenic
GRCh37/hg19 16q11.2-24.3(chr16:46615804-90142285)x1 copy number loss Ductal breast carcinoma [RCV000207138] Chr16:46615804..90142285 [GRCh37]
Chr16:16q11.2-24.3
uncertain significance
GRCh37/hg19 16q22.2-24.3(chr16:72107834-90142285)x1 copy number loss Ductal breast carcinoma [RCV000207182] Chr16:72107834..90142285 [GRCh37]
Chr16:16q22.2-24.3
uncertain significance
Single allele complex Ductal breast carcinoma [RCV000207314] Chr16:56368689..90141355 [GRCh37]
Chr16:16q12.2-24.3
uncertain significance
GRCh37/hg19 16q24.2-24.3(chr16:87687199-89304429)x3 copy number gain See cases [RCV000240062] Chr16:87687199..89304429 [GRCh37]
Chr16:16q24.2-24.3
uncertain significance
GRCh37/hg19 16q24.2-24.3(chr16:88601532-89713753)x3 copy number gain See cases [RCV000240352] Chr16:88601532..89713753 [GRCh37]
Chr16:16q24.2-24.3
uncertain significance
GRCh37/hg19 16q11.2-24.3(chr16:46464488-90155062)x3 copy number gain See cases [RCV000446110] Chr16:46464488..90155062 [GRCh37]
Chr16:16q11.2-24.3
pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:69193-90274381)x3 copy number gain See cases [RCV000446684] Chr16:69193..90274381 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
NM_001012759.3(CTU2):c.1097+1GT[4] microsatellite not provided [RCV000948442]|not specified [RCV000455022] Chr16:88714227..88714228 [GRCh38]
Chr16:88780635..88780636 [GRCh37]
Chr16:16q24.3
benign
GRCh37/hg19 16q24.2-24.3(chr16:87219866-89561087)x1 copy number loss not provided [RCV000509325] Chr16:87219866..89561087 [GRCh37]
Chr16:16q24.2-24.3
not provided
GRCh37/hg19 16q24.2-24.3(chr16:88104077-88958038)x3 copy number gain See cases [RCV000510568] Chr16:88104077..88958038 [GRCh37]
Chr16:16q24.2-24.3
likely benign
GRCh37/hg19 16p13.2-q24.3(chr16:9273328-89548493)x3 copy number gain See cases [RCV000511622] Chr16:9273328..89548493 [GRCh37]
Chr16:16p13.2-q24.3
uncertain significance
GRCh37/hg19 16q24.2-24.3(chr16:88116155-89524926)x1 copy number loss See cases [RCV000511455] Chr16:88116155..89524926 [GRCh37]
Chr16:16q24.2-24.3
pathogenic
GRCh37/hg19 16q24.2-24.3(chr16:88445490-89319419)x3 copy number gain See cases [RCV000511531] Chr16:88445490..89319419 [GRCh37]
Chr16:16q24.2-24.3
uncertain significance
GRCh37/hg19 16q24.1-24.3(chr16:84937273-89836905)x4 copy number gain See cases [RCV000511606] Chr16:84937273..89836905 [GRCh37]
Chr16:16q24.1-24.3
likely pathogenic
GRCh37/hg19 16q23.3-24.3(chr16:82761333-90055381) copy number gain not provided [RCV000767619] Chr16:82761333..90055381 [GRCh37]
Chr16:16q23.3-24.3
pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)x3 copy number gain See cases [RCV000512138] Chr16:85881..90155062 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16q11.2-24.3(chr16:46497599-90354753)x1 copy number loss PARP Inhibitor response [RCV000626429] Chr16:46497599..90354753 [GRCh37]
Chr16:16q11.2-24.3
drug response
GRCh37/hg19 16q11.2-24.3(chr16:46455960-90354753)x1 copy number loss PARP Inhibitor response [RCV000626435] Chr16:46455960..90354753 [GRCh37]
Chr16:16q11.2-24.3
drug response
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062) copy number gain See cases [RCV000511296] Chr16:85881..90155062 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16q13-24.3(chr16:57051473-89797669)x3 copy number gain See cases [RCV000512511] Chr16:57051473..89797669 [GRCh37]
Chr16:16q13-24.3
pathogenic
GRCh37/hg19 16q24.1-24.3(chr16:85838574-90155062)x3 copy number gain See cases [RCV000512440] Chr16:85838574..90155062 [GRCh37]
Chr16:16q24.1-24.3
pathogenic
GRCh37/hg19 16q23.3-24.3(chr16:83001540-90155062)x3 copy number gain See cases [RCV000512468] Chr16:83001540..90155062 [GRCh37]
Chr16:16q23.3-24.3
likely pathogenic
Single allele deletion not provided [RCV000677910] Chr16:86890893..89398630 [GRCh37]
Chr16:16q24.1-24.3
pathogenic
GRCh37/hg19 16q22.2-24.3(chr16:72515938-90155062)x3 copy number gain not provided [RCV000683831] Chr16:72515938..90155062 [GRCh37]
Chr16:16q22.2-24.3
pathogenic
GRCh37/hg19 16q23.2-24.3(chr16:79400436-90155062)x3 copy number gain not provided [RCV000683845] Chr16:79400436..90155062 [GRCh37]
Chr16:16q23.2-24.3
pathogenic
NM_001012759.3(CTU2):c.873G>A (p.Thr291=) single nucleotide variant Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome [RCV000709622] Chr16:88713447 [GRCh38]
Chr16:88779855 [GRCh37]
Chr16:16q24.3
pathogenic
GRCh37/hg19 16q24.2-24.3(chr16:88317240-89079407)x3 copy number gain not provided [RCV000709990] Chr16:88317240..89079407 [GRCh37]
Chr16:16q24.2-24.3
not provided
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90274695)x3 copy number gain not provided [RCV000738918] Chr16:88165..90274695 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:61451-90294632)x3 copy number gain not provided [RCV000738915] Chr16:61451..90294632 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90163275)x3 copy number gain not provided [RCV000738917] Chr16:88165..90163275 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
NM_001012759.3(CTU2):c.1289C>T (p.Pro430Leu) single nucleotide variant not provided [RCV000891633] Chr16:88714674 [GRCh38]
Chr16:88781082 [GRCh37]
Chr16:16q24.3
benign
NM_001012759.3(CTU2):c.1120G>T (p.Gly374Cys) single nucleotide variant not provided [RCV000961366] Chr16:88714405 [GRCh38]
Chr16:88780813 [GRCh37]
Chr16:16q24.3
benign
GRCh37/hg19 16q24.3(chr16:88713533-88799238)x1 copy number loss not provided [RCV000751821] Chr16:88713533..88799238 [GRCh37]
Chr16:16q24.3
benign
GRCh37/hg19 16q24.3(chr16:88770621-88812250)x3 copy number gain not provided [RCV000751822] Chr16:88770621..88812250 [GRCh37]
Chr16:16q24.3
benign
GRCh37/hg19 16q24.3(chr16:88773893-88812250)x1 copy number loss not provided [RCV000751823] Chr16:88773893..88812250 [GRCh37]
Chr16:16q24.3
benign
NM_001012759.3(CTU2):c.1206dup (p.Ala403fs) duplication Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome [RCV000984614] Chr16:88714590..88714591 [GRCh38]
Chr16:88780998..88780999 [GRCh37]
Chr16:16q24.3
pathogenic
NM_001012759.3(CTU2):c.188T>C (p.Leu63Pro) single nucleotide variant Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome [RCV000984615] Chr16:88709982 [GRCh38]
Chr16:88776390 [GRCh37]
Chr16:16q24.3
pathogenic
NM_001012759.3(CTU2):c.1514_1517del (p.Ile505fs) deletion Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome [RCV000984616] Chr16:88715214..88715217 [GRCh38]
Chr16:88781622..88781625 [GRCh37]
Chr16:16q24.3
pathogenic
NM_001012759.3(CTU2):c.282+5G>A single nucleotide variant Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome [RCV000984617] Chr16:88710287 [GRCh38]
Chr16:88776695 [GRCh37]
Chr16:16q24.3
pathogenic
NM_001012759.3(CTU2):c.522C>T (p.Tyr174=) single nucleotide variant not provided [RCV000949817] Chr16:88712690 [GRCh38]
Chr16:88779098 [GRCh37]
Chr16:16q24.3
benign
NM_001012759.3(CTU2):c.737+9_737+10insTGAGAG insertion not provided [RCV000948441] Chr16:88712914..88712915 [GRCh38]
Chr16:88779322..88779323 [GRCh37]
Chr16:16q24.3
likely benign
NM_001012759.3(CTU2):c.1221G>A (p.Gly407=) single nucleotide variant not provided [RCV000949818] Chr16:88714606 [GRCh38]
Chr16:88781014 [GRCh37]
Chr16:16q24.3
benign
NM_001012759.3(CTU2):c.612C>G (p.Pro204=) single nucleotide variant not provided [RCV000907164] Chr16:88712780 [GRCh38]
Chr16:88779188 [GRCh37]
Chr16:16q24.3
likely benign
NM_001012759.3(CTU2):c.737+9_737+10insTGAGAGCCCCCTTCCCCGGGCCCTGACCCCCACTCATACCCCTGAGAGCCCCCTTCCCCGGGCCCTGACCCCCACTCATACCCC insertion not provided [RCV000982679] Chr16:88712911..88712912 [GRCh38]
Chr16:88779319..88779320 [GRCh37]
Chr16:16q24.3
likely benign
NM_001012759.3(CTU2):c.737+10_737+52del deletion not provided [RCV000947733] Chr16:88712912..88712954 [GRCh38]
Chr16:88779320..88779362 [GRCh37]
Chr16:16q24.3
benign
NM_001012759.3(CTU2):c.969C>T (p.Ser323=) single nucleotide variant not provided [RCV000969095] Chr16:88713742 [GRCh38]
Chr16:88780150 [GRCh37]
Chr16:16q24.3
benign
NM_001012759.3(CTU2):c.1127G>A (p.Arg376Gln) single nucleotide variant not provided [RCV000961198] Chr16:88714412 [GRCh38]
Chr16:88780820 [GRCh37]
Chr16:16q24.3
benign
NM_001012759.3(CTU2):c.322G>C (p.Ala108Pro) single nucleotide variant not provided [RCV000968731] Chr16:88711674 [GRCh38]
Chr16:88778082 [GRCh37]
Chr16:16q24.3
benign
NM_001012759.3(CTU2):c.1269G>A (p.Leu423=) single nucleotide variant not provided [RCV000895427] Chr16:88714654 [GRCh38]
Chr16:88781062 [GRCh37]
Chr16:16q24.3
benign
GRCh37/hg19 16q24.2-24.3(chr16:88453448-89569215)x1 copy number loss not provided [RCV000847422] Chr16:88453448..89569215 [GRCh37]
Chr16:16q24.2-24.3
pathogenic
GRCh37/hg19 16q24.2-24.3(chr16:87848902-88809407)x3 copy number gain not provided [RCV000849210] Chr16:87848902..88809407 [GRCh37]
Chr16:16q24.2-24.3
uncertain significance
GRCh37/hg19 16q24.2-24.3(chr16:88697092-88791148)x1 copy number loss not provided [RCV000846887] Chr16:88697092..88791148 [GRCh37]
Chr16:16q24.2-24.3
uncertain significance
GRCh37/hg19 16q21-24.3(chr16:61524229-90155062)x3 copy number gain not provided [RCV001249359] Chr16:61524229..90155062 [GRCh37]
Chr16:16q21-24.3
not provided
NM_001012759.3(CTU2):c.737+10C>T single nucleotide variant not provided [RCV000955516] Chr16:88712915 [GRCh38]
Chr16:88779323 [GRCh37]
Chr16:16q24.3
benign
NM_001012759.3(CTU2):c.1298G>C (p.Cys433Ser) single nucleotide variant not provided [RCV000974587] Chr16:88714683 [GRCh38]
Chr16:88781091 [GRCh37]
Chr16:16q24.3
likely benign
NM_001012759.3(CTU2):c.501G>A (p.Leu167=) single nucleotide variant not provided [RCV000969094] Chr16:88712669 [GRCh38]
Chr16:88779077 [GRCh37]
Chr16:16q24.3
benign
NM_001012759.3(CTU2):c.1347C>T (p.Cys449=) single nucleotide variant not provided [RCV000969096] Chr16:88714732 [GRCh38]
Chr16:88781140 [GRCh37]
Chr16:16q24.3
benign
NM_001012759.3(CTU2):c.767C>T (p.Ala256Val) single nucleotide variant not provided [RCV000979410] Chr16:88713341 [GRCh38]
Chr16:88779749 [GRCh37]
Chr16:16q24.3
likely benign
NM_001012759.3(CTU2):c.1357G>A (p.Asp453Asn) single nucleotide variant not provided [RCV000885775] Chr16:88714864 [GRCh38]
Chr16:88781272 [GRCh37]
Chr16:16q24.3
benign
NM_001012759.3(CTU2):c.353C>T (p.Ala118Val) single nucleotide variant not provided [RCV000961365] Chr16:88712283 [GRCh38]
Chr16:88778691 [GRCh37]
Chr16:16q24.3
benign
NM_001012759.3(CTU2):c.771C>G (p.His257Gln) single nucleotide variant not provided [RCV000891163] Chr16:88713345 [GRCh38]
Chr16:88779753 [GRCh37]
Chr16:16q24.3
likely benign
NM_001012759.3(CTU2):c.1188C>T (p.Asp396=) single nucleotide variant not provided [RCV000912021] Chr16:88714473 [GRCh38]
Chr16:88780881 [GRCh37]
Chr16:16q24.3
likely benign
NM_001012759.3(CTU2):c.873+5G>A single nucleotide variant Microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome [RCV000984929] Chr16:88713452 [GRCh38]
Chr16:88779860 [GRCh37]
Chr16:16q24.3
uncertain significance
NM_001012759.3(CTU2):c.404C>G (p.Pro135Arg) single nucleotide variant not provided [RCV000911937] Chr16:88712334 [GRCh38]
Chr16:88778742 [GRCh37]
Chr16:16q24.3
likely benign
NM_001012759.3(CTU2):c.1149C>T (p.Asp383=) single nucleotide variant not provided [RCV001093040] Chr16:88714434 [GRCh38]
Chr16:88780842 [GRCh37]
Chr16:16q24.3
likely benign
GRCh37/hg19 16q24.2-24.3(chr16:88222732-90155062)x3 copy number gain not provided [RCV001258663] Chr16:88222732..90155062 [GRCh37]
Chr16:16q24.2-24.3
uncertain significance
NM_001012759.3(CTU2):c.377G>C (p.Arg126Thr) single nucleotide variant not provided [RCV001357110] Chr16:88712307 [GRCh38]
Chr16:88778715 [GRCh37]
Chr16:16q24.3
uncertain significance
NC_000016.9:g.(?_88709737)_(89220635_?)del deletion Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative [RCV001388209] Chr16:88709737..89220635 [GRCh37]
Chr16:16q24.3
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:28005 AgrOrtholog
COSMIC CTU2 COSMIC
Ensembl Genes ENSG00000174177 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000308617 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000388320 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000454923 UniProtKB/TrEMBL
  ENSP00000455010 UniProtKB/TrEMBL
  ENSP00000455305 UniProtKB/TrEMBL
  ENSP00000456908 ENTREZGENE, UniProtKB/TrEMBL
Ensembl Transcript ENST00000312060 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000453996 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000564105 UniProtKB/TrEMBL
  ENST00000564921 UniProtKB/TrEMBL
  ENST00000567316 UniProtKB/TrEMBL
  ENST00000567949 ENTREZGENE, UniProtKB/TrEMBL
Gene3D-CATH 3.40.50.620 UniProtKB/TrEMBL
GTEx ENSG00000174177 GTEx
HGNC ID HGNC:28005 ENTREZGENE
Human Proteome Map CTU2 Human Proteome Map
InterPro CTU2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Rossmann-like_a/b/a_fold UniProtKB/TrEMBL
KEGG Report hsa:348180 UniProtKB/Swiss-Prot
NCBI Gene 348180 ENTREZGENE
OMIM 617057 OMIM
  618142 OMIM
PANTHER PTHR20882 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam CTU2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA165449882 PharmGKB
UniProt CTU2_HUMAN UniProtKB/Swiss-Prot
  H3BNM3_HUMAN UniProtKB/TrEMBL
  H3BNU5_HUMAN UniProtKB/TrEMBL
  H3BPG4_HUMAN UniProtKB/TrEMBL
  H3BSW6 ENTREZGENE, UniProtKB/TrEMBL
  Q2VPK5 ENTREZGENE
UniProt Secondary B2RXK0 UniProtKB/Swiss-Prot
  Q0P511 UniProtKB/Swiss-Prot
  Q66K78 UniProtKB/Swiss-Prot
  Q6P4C8 UniProtKB/Swiss-Prot
  Q86SV4 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-03-28 CTU2  cytosolic thiouridylase subunit 2    cytosolic thiouridylase subunit 2 homolog (S. pombe)  Symbol and/or name change 5135510 APPROVED