TNKS (tankyrase) - Rat Genome Database

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Gene: TNKS (tankyrase) Homo sapiens
Analyze
Symbol: TNKS
Name: tankyrase
RGD ID: 1343497
HGNC Page HGNC:11941
Description: Enables histone binding activity; pentosyltransferase activity; and zinc ion binding activity. Involved in several processes, including positive regulation of canonical Wnt signaling pathway; post-translational protein modification; and regulation of chromosome organization. Located in several cellular components, including chromosome, telomeric region; mitotic spindle pole; and nucleus.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: ADP-ribosyltransferase diphtheria toxin-like 5; ARTD5; PARP-5a; PARP5A; PARPL; pART5; poly [ADP-ribose] polymerase 5A; poly [ADP-ribose] polymerase tankyrase-1; TANK1; tankyrase I; tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase; tankyrase-1; TIN1; TINF1; TNKS-1; TNKS1; TRF1-interacting ankyrin-related ADP-ribose polymerase; TRF1-interacting ankyrin-related ADP-ribose polymerase 1
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
GRCh3889,555,912 - 9,782,346 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl89,555,912 - 9,782,346 (+)EnsemblGRCh38hg38GRCh38
GRCh3789,413,422 - 9,639,856 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 3689,450,855 - 9,677,266 (+)NCBINCBI36Build 36hg18NCBI36
Build 3489,450,854 - 9,671,801NCBI
Celera88,541,508 - 8,765,562 (+)NCBICelera
Cytogenetic Map8p23.1NCBI
HuRef88,339,612 - 8,568,337 (+)NCBIHuRef
CHM1_189,478,677 - 9,705,116 (+)NCBICHM1_1
T2T-CHM13v2.089,959,097 - 10,187,973 (-)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

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. Structures and Mechanisms of Enzymes Employed in the Synthesis and Degradation of PARP-Dependent Protein ADP-Ribosylation. Barkauskaite E, etal., Mol Cell. 2015 Jun 18;58(6):935-46. doi: 10.1016/j.molcel.2015.05.007.
2. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8619474   PMID:9110174   PMID:9822378   PMID:10198177   PMID:10523501   PMID:10988299   PMID:11278563   PMID:11382755   PMID:11454873   PMID:11739745   PMID:11802774   PMID:11854288  
PMID:12080061   PMID:12381316   PMID:12475993   PMID:12477932   PMID:12768206   PMID:12782650   PMID:14596906   PMID:14966275   PMID:15064417   PMID:15133513   PMID:15795250   PMID:16076287  
PMID:16132700   PMID:16884355   PMID:17003112   PMID:17026964   PMID:17043677   PMID:17561506   PMID:18026951   PMID:18221737   PMID:18436240   PMID:18470924   PMID:18676680   PMID:19170196  
PMID:19245366   PMID:19615732   PMID:19625176   PMID:19692168   PMID:19759176   PMID:19759537   PMID:19766477   PMID:19773453   PMID:19996280   PMID:20056641   PMID:20237496   PMID:20379614  
PMID:20421936   PMID:20508983   PMID:20696165   PMID:20811636   PMID:20811689   PMID:20937264   PMID:21037379   PMID:21251231   PMID:21270334   PMID:21314979   PMID:21455637   PMID:21478859  
PMID:21531765   PMID:21799911   PMID:21818122   PMID:21873635   PMID:22013039   PMID:22153076   PMID:22154485   PMID:22438990   PMID:22645305   PMID:22699936   PMID:22864114   PMID:22916037  
PMID:23277359   PMID:23414517   PMID:23502783   PMID:23583392   PMID:23800953   PMID:23933993   PMID:24116873   PMID:24291818   PMID:24403055   PMID:24419084   PMID:24747911   PMID:24792382  
PMID:24927181   PMID:25043379   PMID:25327252   PMID:25332235   PMID:25547115   PMID:25876076   PMID:25880085   PMID:25939383   PMID:26027929   PMID:26186194   PMID:26246473   PMID:26373281  
PMID:26496610   PMID:26513298   PMID:26617760   PMID:26673895   PMID:26729153   PMID:26820603   PMID:26845027   PMID:26972000   PMID:27068743   PMID:27129302   PMID:27328430   PMID:27494558  
PMID:27499439   PMID:27521426   PMID:27594684   PMID:27993934   PMID:28030839   PMID:28514442   PMID:28619731   PMID:28675297   PMID:28723574   PMID:29117863   PMID:29180619   PMID:29263426  
PMID:29420262   PMID:29507755   PMID:29604130   PMID:30021884   PMID:30055800   PMID:30472184   PMID:30571846   PMID:30915350   PMID:30926223   PMID:31134845   PMID:31375564   PMID:31554794  
PMID:31806370   PMID:31849489   PMID:32203420   PMID:32296183   PMID:32393760   PMID:32698014   PMID:32916703   PMID:33361107   PMID:33811251   PMID:33923443   PMID:33961781   PMID:34079125  
PMID:34128958   PMID:34298950   PMID:34383978   PMID:34876695   PMID:35044719   PMID:35450028   PMID:35733260   PMID:35914814   PMID:36383218   PMID:36603485   PMID:37741944   PMID:38216082  


Genomics

Comparative Map Data
TNKS
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3889,555,912 - 9,782,346 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl89,555,912 - 9,782,346 (+)EnsemblGRCh38hg38GRCh38
GRCh3789,413,422 - 9,639,856 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 3689,450,855 - 9,677,266 (+)NCBINCBI36Build 36hg18NCBI36
Build 3489,450,854 - 9,671,801NCBI
Celera88,541,508 - 8,765,562 (+)NCBICelera
Cytogenetic Map8p23.1NCBI
HuRef88,339,612 - 8,568,337 (+)NCBIHuRef
CHM1_189,478,677 - 9,705,116 (+)NCBICHM1_1
T2T-CHM13v2.089,959,097 - 10,187,973 (-)NCBIT2T-CHM13v2.0
Tnks
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39835,296,333 - 35,432,844 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl835,293,614 - 35,432,844 (-)EnsemblGRCm39 Ensembl
GRCm38834,829,179 - 34,965,690 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl834,826,460 - 34,965,690 (-)EnsemblGRCm38mm10GRCm38
MGSCv37835,892,233 - 36,028,744 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36836,297,696 - 36,434,207 (-)NCBIMGSCv36mm8
Celera837,445,126 - 37,580,726 (-)NCBICelera
Cytogenetic Map8A4NCBI
cM Map821.16NCBI
Tnks
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81663,922,969 - 64,073,972 (+)NCBIGRCr8
mRatBN7.21657,223,174 - 57,370,740 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1657,225,094 - 57,366,260 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1662,551,555 - 62,698,125 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01665,965,468 - 66,112,037 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01661,185,515 - 61,332,088 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01660,925,093 - 61,067,192 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1660,925,093 - 61,067,192 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01660,595,492 - 60,747,261 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41660,953,917 - 61,095,523 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11660,954,529 - 61,095,505 (+)NCBI
Celera1655,274,422 - 55,414,315 (+)NCBICelera
Cytogenetic Map16q12.2NCBI
Tnks
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554635,588,423 - 5,764,581 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554635,589,194 - 5,770,141 (+)NCBIChiLan1.0ChiLan1.0
TNKS
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2726,008,707 - 26,228,344 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan182,040,716 - 2,260,823 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v089,435,412 - 9,654,810 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
TNKS
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11634,826,248 - 35,040,004 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1634,831,662 - 35,039,946 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1635,288,261 - 35,501,954 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01636,853,307 - 37,067,471 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1636,857,336 - 37,067,463 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11634,954,332 - 35,174,394 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01635,524,234 - 35,737,885 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01635,643,380 - 35,857,095 (-)NCBIUU_Cfam_GSD_1.0
Tnks
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494344,149,106 - 44,353,527 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936573794,184 - 994,247 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_004936573788,909 - 993,453 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
TNKS
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1555,514,248 - 55,681,505 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11555,513,874 - 55,681,544 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21562,930,160 - 63,096,784 (-)NCBISscrofa10.2Sscrofa10.2susScr3
TNKS
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.189,300,234 - 9,524,350 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl89,305,872 - 9,524,104 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605232,885,368 - 33,110,014 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Tnks
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248395,675,656 - 5,856,787 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248395,675,581 - 5,860,736 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in TNKS
73 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 8p23.3-21.1(chr8:2475295-27504279)x1 copy number loss See cases [RCV000050297] Chr8:2475295..27504279 [GRCh38]
Chr8:2292235..27361796 [GRCh37]
Chr8:2121457..27417713 [NCBI36]
Chr8:8p23.3-21.1		 pathogenic
GRCh38/hg38 8p23.1(chr8:8222339-12383643)x1 copy number loss See cases [RCV000050658] Chr8:8222339..12383643 [GRCh38]
Chr8:8079861..12241152 [GRCh37]
Chr8:8117271..12285523 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.1(chr8:7411297-12182465)x3 copy number gain See cases [RCV000051192] Chr8:7411297..12182465 [GRCh38]
Chr8:7268819..12039974 [GRCh37]
Chr8:7256229..12077383 [NCBI36]
Chr8:8p23.1		 pathogenic|uncertain significance
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145049449)x3 copy number gain See cases [RCV000051206] Chr8:241530..145049449 [GRCh38]
Chr8:191530..146274835 [GRCh37]
Chr8:181530..146245639 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p23.1(chr8:9239988-10057038)x3 copy number gain See cases [RCV000052153] Chr8:9239988..10057038 [GRCh38]
Chr8:9097498..9914548 [GRCh37]
Chr8:9134908..9951958 [NCBI36]
Chr8:8p23.1		 likely pathogenic|uncertain significance
GRCh38/hg38 8p23.1(chr8:7195664-12383643)x1 copy number loss See cases [RCV000053154] Chr8:7195664..12383643 [GRCh38]
Chr8:7053186..12241152 [GRCh37]
Chr8:7040596..12285523 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.1(chr8:7234837-12514815)x1 copy number loss See cases [RCV000053165] Chr8:7234837..12514815 [GRCh38]
Chr8:7092359..12372324 [GRCh37]
Chr8:7079769..12416695 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.1(chr8:7411097-12610175)x1 copy number loss See cases [RCV000053166] Chr8:7411097..12610175 [GRCh38]
Chr8:7268619..12467684 [GRCh37]
Chr8:7256029..12512055 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.1(chr8:7411297-11961807)x1 copy number loss See cases [RCV000053167] Chr8:7411297..11961807 [GRCh38]
Chr8:7268819..11819316 [GRCh37]
Chr8:7256229..11856725 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.1(chr8:7411297-12546553)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053168]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053168]|See cases [RCV000053168] Chr8:7411297..12546553 [GRCh38]
Chr8:7268819..12404062 [GRCh37]
Chr8:7256229..12448433 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:8079861-12039974)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053169]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053169] Chr8:8079861..12039974 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.1(chr8:8222139-12383784)x3 copy number gain See cases [RCV000053482] Chr8:8222139..12383784 [GRCh38]
Chr8:8079661..12241293 [GRCh37]
Chr8:8117071..12285664 [NCBI36]
Chr8:8p23.1		 pathogenic|uncertain significance
GRCh38/hg38 8p23.1(chr8:8272908-12182621)x3 copy number gain See cases [RCV000053483] Chr8:8272908..12182621 [GRCh38]
Chr8:8130430..12040130 [GRCh37]
Chr8:8167840..12077539 [NCBI36]
Chr8:8p23.1		 pathogenic|uncertain significance
GRCh38/hg38 8p23.1(chr8:8273108-11948451)x3 copy number gain Abnormality of the heart [RCV000053484]|See cases [RCV000053484] Chr8:8273108..11948451 [GRCh38]
Chr8:8130630..11805960 [GRCh37]
Chr8:8p23.1		 pathogenic|uncertain significance
GRCh38/hg38 8p23.1(chr8:8336212-11984392)x3 copy number gain See cases [RCV000053485] Chr8:8336212..11984392 [GRCh38]
Chr8:8193728..11841901 [GRCh37]
Chr8:8231138..11879310 [NCBI36]
Chr8:8p23.1		 pathogenic|uncertain significance
GRCh38/hg38 8p23.1(chr8:8336212-11984392)x1 copy number loss See cases [RCV000053486] Chr8:8336212..11984392 [GRCh38]
Chr8:8193728..11841901 [GRCh37]
Chr8:8231138..11879310 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.1(chr8:8336212-12021806)x3 copy number gain See cases [RCV000053489] Chr8:8336212..12021806 [GRCh38]
Chr8:8193728..11879315 [GRCh37]
Chr8:8231138..11916724 [NCBI36]
Chr8:8p23.1		 pathogenic|uncertain significance
GRCh38/hg38 8p23.3-q24.3(chr8:244417-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|See cases [RCV000053604] Chr8:244417..145054775 [GRCh38]
Chr8:194417..146280161 [GRCh37]
Chr8:184417..146250965 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p23.3-22(chr8:241530-17678697)x3 copy number gain See cases [RCV000053603] Chr8:241530..17678697 [GRCh38]
Chr8:191530..17536206 [GRCh37]
Chr8:181530..17580486 [NCBI36]
Chr8:8p23.3-22		 pathogenic
GRCh38/hg38 8p23.3-12(chr8:96310-30614703)x3 copy number gain See cases [RCV000053599] Chr8:96310..30614703 [GRCh38]
Chr8:46310..30472220 [GRCh37]
Chr8:36310..30591762 [NCBI36]
Chr8:8p23.3-12		 pathogenic
GRCh38/hg38 8p23.3-23.1(chr8:96310-12021806)x3 copy number gain See cases [RCV000053600] Chr8:96310..12021806 [GRCh38]
Chr8:46310..11879315 [GRCh37]
Chr8:36310..11916724 [NCBI36]
Chr8:8p23.3-23.1		 pathogenic
GRCh38/hg38 8p23.3-23.1(chr8:219853-10165486)x3 copy number gain See cases [RCV000053601] Chr8:219853..10165486 [GRCh38]
Chr8:169853..10022996 [GRCh37]
Chr8:159853..10060406 [NCBI36]
Chr8:8p23.3-23.1		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000053602] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p23.1(chr8:8336212-9953226)x1 copy number loss See cases [RCV000054225] Chr8:8336212..9953226 [GRCh38]
Chr8:8193728..9810736 [GRCh37]
Chr8:8231138..9848146 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.3-11.1(chr8:176814-43396776) copy number gain Abnormal fetal cardiovascular morphology [RCV001291977] Chr8:176814..43396776 [GRCh37]
Chr8:8p23.3-11.1		 pathogenic
GRCh38/hg38 8p23.1(chr8:8222339-12182465)x1 copy number loss See cases [RCV000053169] Chr8:8222339..12182465 [GRCh38]
Chr8:8079861..12039974 [GRCh37]
Chr8:8117271..12077383 [NCBI36]
Chr8:8p23.1		 pathogenic|likely pathogenic|conflicting data from submitters
GRCh38/hg38 8p23.1(chr8:8273108-11948451)x3 copy number gain See cases [RCV000053484] Chr8:8273108..11948451 [GRCh38]
Chr8:8130630..11805960 [GRCh37]
Chr8:8168040..11843369 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.1(chr8:7834379-12182465)x3 copy number gain See cases [RCV000134177] Chr8:7834379..12182465 [GRCh38]
Chr8:7691901..12039974 [GRCh37]
Chr8:7729311..12077383 [NCBI36]
Chr8:8p23.1		 pathogenic|likely pathogenic
GRCh38/hg38 8p23.1(chr8:8545843-11814470)x1 copy number loss See cases [RCV000134092] Chr8:8545843..11814470 [GRCh38]
Chr8:8403353..11671979 [GRCh37]
Chr8:8440763..11709388 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.3-23.1(chr8:241530-10191595)x1 copy number loss See cases [RCV000134879] Chr8:241530..10191595 [GRCh38]
Chr8:191530..10049105 [GRCh37]
Chr8:181530..10086515 [NCBI36]
Chr8:8p23.3-23.1		 pathogenic
GRCh38/hg38 8p23.1(chr8:9240101-9687009)x3 copy number gain See cases [RCV000134829] Chr8:9240101..9687009 [GRCh38]
Chr8:9097611..9544519 [GRCh37]
Chr8:9135021..9581929 [NCBI36]
Chr8:8p23.1		 likely benign
GRCh38/hg38 8p23.1(chr8:9543912-9567334)x1 copy number loss See cases [RCV000135164] Chr8:9543912..9567334 [GRCh38]
Chr8:9401422..9424844 [GRCh37]
Chr8:9438832..9462254 [NCBI36]
Chr8:8p23.1		 likely benign
GRCh38/hg38 8p23.1(chr8:8273108-12546553)x3 copy number gain See cases [RCV000134923] Chr8:8273108..12546553 [GRCh38]
Chr8:8130630..12404062 [GRCh37]
Chr8:8168040..12448433 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.1(chr8:8273108-11948451)x1 copy number loss See cases [RCV000135749] Chr8:8273108..11948451 [GRCh38]
Chr8:8130630..11805960 [GRCh37]
Chr8:8168040..11843369 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.1(chr8:8273108-12383643)x1 copy number loss See cases [RCV000135775] Chr8:8273108..12383643 [GRCh38]
Chr8:8130630..12241152 [GRCh37]
Chr8:8168040..12285523 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.3-23.1(chr8:241530-10867132)x1 copy number loss See cases [RCV000135534] Chr8:241530..10867132 [GRCh38]
Chr8:191530..10724642 [GRCh37]
Chr8:181530..10762052 [NCBI36]
Chr8:8p23.3-23.1		 pathogenic
GRCh38/hg38 8p23.1(chr8:7311968-12546553)x3 copy number gain See cases [RCV000136522] Chr8:7311968..12546553 [GRCh38]
Chr8:7169490..12404062 [GRCh37]
Chr8:7156900..12448433 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.1(chr8:7311968-12546553)x1 copy number loss See cases [RCV000136523] Chr8:7311968..12546553 [GRCh38]
Chr8:7169490..12404062 [GRCh37]
Chr8:7156900..12448433 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.3-21.2(chr8:241605-24656971)x3 copy number gain See cases [RCV000136026] Chr8:241605..24656971 [GRCh38]
Chr8:191605..24514484 [GRCh37]
Chr8:181605..24570374 [NCBI36]
Chr8:8p23.3-21.2		 pathogenic
GRCh38/hg38 8p23.3-21.3(chr8:241530-23198398)x3 copy number gain See cases [RCV000135967] Chr8:241530..23198398 [GRCh38]
Chr8:191530..23055911 [GRCh37]
Chr8:181530..23111856 [NCBI36]
Chr8:8p23.3-21.3		 pathogenic
GRCh38/hg38 8p23.1(chr8:8253505-12610034)x1 copy number loss See cases [RCV000137505] Chr8:8253505..12610034 [GRCh38]
Chr8:8111027..12467543 [GRCh37]
Chr8:8148437..12511914 [NCBI36]
Chr8:8p23.1		 pathogenic|likely benign
GRCh38/hg38 8p23.3-23.1(chr8:226452-12712987)x3 copy number gain See cases [RCV000137984] Chr8:226452..12712987 [GRCh38]
Chr8:176452..12570496 [GRCh37]
Chr8:166452..12614867 [NCBI36]
Chr8:8p23.3-23.1		 pathogenic
GRCh38/hg38 8p23.1(chr8:8222339-12050329)x3 copy number gain See cases [RCV000137864] Chr8:8222339..12050329 [GRCh38]
Chr8:8079861..11907838 [GRCh37]
Chr8:8117271..11945247 [NCBI36]
Chr8:8p23.1		 likely pathogenic
GRCh38/hg38 8p23.3-11.23(chr8:226452-38021728)x3 copy number gain See cases [RCV000137807] Chr8:226452..38021728 [GRCh38]
Chr8:176452..37879246 [GRCh37]
Chr8:166452..37998403 [NCBI36]
Chr8:8p23.3-11.23		 pathogenic|likely pathogenic
GRCh38/hg38 8p23.3-12(chr8:241605-31091074)x3 copy number gain See cases [RCV000138831] Chr8:241605..31091074 [GRCh38]
Chr8:191605..30948590 [GRCh37]
Chr8:181605..31068132 [NCBI36]
Chr8:8p23.3-12		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241605-145054781)x3 copy number gain See cases [RCV000138643] Chr8:241605..145054781 [GRCh38]
Chr8:191605..146280167 [GRCh37]
Chr8:181605..146250971 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p23.1(chr8:7103661-12299882)x3 copy number gain See cases [RCV000138529] Chr8:7103661..12299882 [GRCh38]
Chr8:6961183..12157391 [GRCh37]
Chr8:6948593..12201760 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.1(chr8:8253505-12003060)x1 copy number loss See cases [RCV000138559] Chr8:8253505..12003060 [GRCh38]
Chr8:8111027..11860569 [GRCh37]
Chr8:8148437..11897978 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.2-23.1(chr8:3934205-11526939)x1 copy number loss See cases [RCV000138943] Chr8:3934205..11526939 [GRCh38]
Chr8:3791727..11384448 [GRCh37]
Chr8:3779135..11421857 [NCBI36]
Chr8:8p23.2-23.1		 pathogenic
GRCh38/hg38 8p23.1-11.22(chr8:7141697-38695546)x3 copy number gain See cases [RCV000139891] Chr8:7141697..38695546 [GRCh38]
Chr8:6999219..38553064 [GRCh37]
Chr8:6986629..38672221 [NCBI36]
Chr8:8p23.1-11.22		 pathogenic
GRCh38/hg38 8p23.1(chr8:8253505-9758024)x1 copy number loss See cases [RCV000139792] Chr8:8253505..9758024 [GRCh38]
Chr8:8111027..9615534 [GRCh37]
Chr8:8148437..9652944 [NCBI36]
Chr8:8p23.1		 uncertain significance
GRCh38/hg38 8p23.3-12(chr8:226452-34491890)x3 copy number gain See cases [RCV000141410] Chr8:226452..34491890 [GRCh38]
Chr8:176452..34349408 [GRCh37]
Chr8:166452..34468950 [NCBI36]
Chr8:8p23.3-12		 pathogenic
GRCh38/hg38 8p23.3-22(chr8:226452-16280146)x3 copy number gain See cases [RCV000141418] Chr8:226452..16280146 [GRCh38]
Chr8:176452..16137655 [GRCh37]
Chr8:166452..16182026 [NCBI36]
Chr8:8p23.3-22		 pathogenic
GRCh38/hg38 8p23.1(chr8:8253505-11422633)x1 copy number loss See cases [RCV000141377] Chr8:8253505..11422633 [GRCh38]
Chr8:8111027..11280142 [GRCh37]
Chr8:8148437..11317552 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.1(chr8:8222339-11984333)x1 copy number loss See cases [RCV000140886] Chr8:8222339..11984333 [GRCh38]
Chr8:8079861..11841842 [GRCh37]
Chr8:8117271..11879251 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.1(chr8:8235647-12037723)x1 copy number loss See cases [RCV000141976] Chr8:8235647..12037723 [GRCh38]
Chr8:8093169..11895232 [GRCh37]
Chr8:8130579..11932641 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.1(chr8:8764178-11063564)x3 copy number gain See cases [RCV000141557] Chr8:8764178..11063564 [GRCh38]
Chr8:8621688..10921074 [GRCh37]
Chr8:8659098..10958484 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:208048-145070385)x3 copy number gain See cases [RCV000141808] Chr8:208048..145070385 [GRCh38]
Chr8:158048..146295771 [GRCh37]
Chr8:148048..146266575 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p23.1(chr8:9456230-11013618)x1 copy number loss See cases [RCV000141459] Chr8:9456230..11013618 [GRCh38]
Chr8:9313740..10871128 [GRCh37]
Chr8:9351150..10908538 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.1(chr8:8273108-9687019)x1 copy number loss See cases [RCV000142515] Chr8:8273108..9687019 [GRCh38]
Chr8:8130630..9544529 [GRCh37]
Chr8:8168040..9581939 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:226452-145068712)x3 copy number gain See cases [RCV000142858] Chr8:226452..145068712 [GRCh38]
Chr8:176452..146294098 [GRCh37]
Chr8:166452..146264902 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p23.1(chr8:8273108-12610034)x1 copy number loss See cases [RCV000142710] Chr8:8273108..12610034 [GRCh38]
Chr8:8130630..12467543 [GRCh37]
Chr8:8168040..12511914 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.3-23.1(chr8:241530-10458484)x1 copy number loss See cases [RCV000142596] Chr8:241530..10458484 [GRCh38]
Chr8:191530..10315994 [GRCh37]
Chr8:181530..10353404 [NCBI36]
Chr8:8p23.3-23.1		 pathogenic|likely pathogenic
GRCh38/hg38 8p23.1(chr8:8235647-12077956)x1 copy number loss See cases [RCV000143356] Chr8:8235647..12077956 [GRCh38]
Chr8:8093169..11935465 [GRCh37]
Chr8:8130579..11972874 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.1(chr8:8235544-12088347)x3 copy number gain See cases [RCV000143280] Chr8:8235544..12088347 [GRCh38]
Chr8:8093066..11945856 [GRCh37]
Chr8:8130476..11983265 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.3-23.1(chr8:226452-12698554)x3 copy number gain See cases [RCV000143248] Chr8:226452..12698554 [GRCh38]
Chr8:176452..12556063 [GRCh37]
Chr8:166452..12600434 [NCBI36]
Chr8:8p23.3-23.1		 pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000148092] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3		 pathogenic
GRCh38/hg38 8p23.1(chr8:9009853-10496260)x3 copy number gain See cases [RCV000143514] Chr8:9009853..10496260 [GRCh38]
Chr8:8867363..10353770 [GRCh37]
Chr8:8904773..10391180 [NCBI36]
Chr8:8p23.1		 likely benign|uncertain significance
GRCh38/hg38 8p23.1(chr8:8222339-12182465)x1 copy number loss See cases [RCV000148286] Chr8:8222339..12182465 [GRCh38]
Chr8:8079861..12039974 [GRCh37]
Chr8:8117271..12077383 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.2-21.1(chr8:2475295-27504279)x1 copy number loss See cases [RCV000148252] Chr8:2475295..27504279 [GRCh38]
Chr8:2292235..27361796 [GRCh37]
Chr8:2121457..27417713 [NCBI36]
Chr8:8p23.2-21.1		 pathogenic
GRCh37/hg19 8p23.3-22(chr8:158991-13304906)x3 copy number gain See cases [RCV000240124] Chr8:158991..13304906 [GRCh37]
Chr8:8p23.3-22		 pathogenic
GRCh37/hg19 8p23.1(chr8:8127723-11858461)x1 copy number loss See cases [RCV000203433] Chr8:8127723..11858461 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:8131816-12249050)x1 copy number loss Premature ovarian failure [RCV000225350] Chr8:8131816..12249050 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.3-23.1(chr8:164984-11860845)x3 copy number gain See cases [RCV000239409] Chr8:164984..11860845 [GRCh37]
Chr8:8p23.3-23.1		 pathogenic
Single allele complex 8p inverted duplication/deletion syndrome [RCV002280753] Chr8:158048..43019304 [GRCh37]
Chr8:8p23.3-11.21		 pathogenic
NM_003747.3(TNKS):c.103C>G (p.Leu35Val) single nucleotide variant Inborn genetic diseases [RCV003244902] Chr8:9556042 [GRCh38]
Chr8:9413552 [GRCh37]
Chr8:8p23.1		 uncertain significance
GRCh37/hg19 8p23.3-12(chr8:158048-30262760)x3 copy number gain See cases [RCV000449225] Chr8:158048..30262760 [GRCh37]
Chr8:8p23.3-12		 pathogenic
GRCh37/hg19 8p23.1(chr8:8093169-11888779)x1 copy number loss See cases [RCV000446839] Chr8:8093169..11888779 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:8747488-9958927)x3 copy number gain See cases [RCV000447479] Chr8:8747488..9958927 [GRCh37]
Chr8:8p23.1		 uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:158991-146280828)x3 copy number gain See cases [RCV000447507] Chr8:158991..146280828 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p23.1(chr8:8093169-11845219)x3 copy number gain See cases [RCV000446314] Chr8:8093169..11845219 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.3-23.1(chr8:1166068-12570914)x3 copy number gain See cases [RCV000448692] Chr8:1166068..12570914 [GRCh37]
Chr8:8p23.3-23.1		 pathogenic
GRCh37/hg19 8p23.3-22(chr8:158991-17536147)x4 copy number gain See cases [RCV000448695] Chr8:158991..17536147 [GRCh37]
Chr8:8p23.3-22		 pathogenic
GRCh37/hg19 8p23.1(chr8:9144943-11945856)x3 copy number gain See cases [RCV000448829] Chr8:9144943..11945856 [GRCh37]
Chr8:8p23.1		 likely pathogenic
GRCh37/hg19 8p23.3-11.1(chr8:158048-43786723)x3 copy number gain See cases [RCV000447909] Chr8:158048..43786723 [GRCh37]
Chr8:8p23.3-11.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:9046102-9628541)x3 copy number gain See cases [RCV000448369] Chr8:9046102..9628541 [GRCh37]
Chr8:8p23.1		 uncertain significance
GRCh37/hg19 8p23.3-22(chr8:158048-13309069)x1 copy number loss See cases [RCV000510201] Chr8:158048..13309069 [GRCh37]
Chr8:8p23.3-22		 likely pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771) copy number gain See cases [RCV000510234] Chr8:158049..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p23.3-23.1(chr8:158048-9749574)x1 copy number loss See cases [RCV000510827] Chr8:158048..9749574 [GRCh37]
Chr8:8p23.3-23.1		 pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)x3 copy number gain See cases [RCV000511095] Chr8:158049..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
NM_003747.3(TNKS):c.31C>T (p.His11Tyr) single nucleotide variant Inborn genetic diseases [RCV003252373] Chr8:9555970 [GRCh38]
Chr8:9413480 [GRCh37]
Chr8:8p23.1		 uncertain significance
GRCh37/hg19 8p23.1(chr8:7053186-11805960)x3 copy number gain See cases [RCV000512636] Chr8:7053186..11805960 [GRCh37]
Chr8:7040596..11843369 [NCBI36]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:8093169-11881742)x1 copy number loss See cases [RCV000512227] Chr8:8093169..11881742 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:9556061-9852711)x1 copy number loss not provided [RCV000682966] Chr8:9556061..9852711 [GRCh37]
Chr8:8p23.1		 uncertain significance
GRCh37/hg19 8p23.3-22(chr8:158048-13974319)x3 copy number gain not provided [RCV000683039] Chr8:158048..13974319 [GRCh37]
Chr8:8p23.3-22		 pathogenic
GRCh37/hg19 8p23.1-21.2(chr8:8770948-27079636)x3 copy number gain not provided [RCV000683041] Chr8:8770948..27079636 [GRCh37]
Chr8:8p23.1-21.2		 pathogenic
GRCh37/hg19 8p23.3-21.2(chr8:1825200-24533193)x3 copy number gain not provided [RCV000683042] Chr8:1825200..24533193 [GRCh37]
Chr8:8p23.3-21.2		 pathogenic
GRCh37/hg19 8p23.3-23.1(chr8:158048-9750676)x3 copy number gain not provided [RCV000683034] Chr8:158048..9750676 [GRCh37]
Chr8:8p23.3-23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:8093169-11935465)x1 copy number loss not provided [RCV000683027] Chr8:8093169..11935465 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:8093065-11945855)x3 copy number gain not provided [RCV000683028] Chr8:8093065..11945855 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:6999219-11898980)x3 copy number gain not provided [RCV000683030] Chr8:6999219..11898980 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.3-22(chr8:158048-15423270)x3 copy number gain not provided [RCV000683040] Chr8:158048..15423270 [GRCh37]
Chr8:8p23.3-22		 pathogenic
GRCh37/hg19 8p23.1(chr8:9551476-9803102)x3 copy number gain not provided [RCV000682957] Chr8:9551476..9803102 [GRCh37]
Chr8:8p23.1		 uncertain significance
GRCh37/hg19 8p23.3-23.1(chr8:158048-10939681)x1 copy number loss not provided [RCV000683036] Chr8:158048..10939681 [GRCh37]
Chr8:8p23.3-23.1		 pathogenic
GRCh37/hg19 8p23.3-22(chr8:168483-13147575)x1,2 copy number gain not provided [RCV000683037] Chr8:168483..13147575 [GRCh37]
Chr8:8p23.3-22		 pathogenic
GRCh37/hg19 8p23.1(chr8:8902423-9628541)x3 copy number gain not provided [RCV000682999] Chr8:8902423..9628541 [GRCh37]
Chr8:8p23.1		 uncertain significance
GRCh37/hg19 8p23.1(chr8:8093169-11898980)x1 copy number loss not provided [RCV000683026] Chr8:8093169..11898980 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:8119295-11765719)x3 copy number gain not provided [RCV000683025] Chr8:8119295..11765719 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3 copy number gain not provided [RCV000848478] Chr8:158048..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:10213-146293414)x3 copy number gain not provided [RCV000747248] Chr8:10213..146293414 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:164984-146293414)x3 copy number gain not provided [RCV000747254] Chr8:164984..146293414 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p23.3-23.1(chr8:10213-10197718)x1 copy number loss not provided [RCV000747247] Chr8:10213..10197718 [GRCh37]
Chr8:8p23.3-23.1		 pathogenic
GRCh37/hg19 8p23.3-23.1(chr8:164984-10007227)x1 copy number loss not provided [RCV000747253] Chr8:164984..10007227 [GRCh37]
Chr8:8p23.3-23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:8105359-11859851)x3 copy number gain not provided [RCV000747347] Chr8:8105359..11859851 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:8111659-11898209)x3 copy number gain not provided [RCV000747348] Chr8:8111659..11898209 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:9471265-9500595)x3 copy number gain not provided [RCV000747377] Chr8:9471265..9500595 [GRCh37]
Chr8:8p23.1		 benign
GRCh37/hg19 8p23.1(chr8:9471265-9500692)x3 copy number gain not provided [RCV000747378] Chr8:9471265..9500692 [GRCh37]
Chr8:8p23.1		 benign
GRCh37/hg19 8p23.1(chr8:9479127-9500595)x3 copy number gain not provided [RCV000747379] Chr8:9479127..9500595 [GRCh37]
Chr8:8p23.1		 benign
GRCh37/hg19 8p23.1(chr8:9479127-9500692)x3 copy number gain not provided [RCV000747380] Chr8:9479127..9500692 [GRCh37]
Chr8:8p23.1		 benign
GRCh37/hg19 8p23.1(chr8:9479127-9500692)x0 copy number loss not provided [RCV000747381] Chr8:9479127..9500692 [GRCh37]
Chr8:8p23.1		 benign
GRCh37/hg19 8p23.1(chr8:9479127-9500876)x1 copy number loss not provided [RCV000747382] Chr8:9479127..9500876 [GRCh37]
Chr8:8p23.1		 benign
GRCh37/hg19 8p23.1(chr8:9498014-9500876)x1 copy number loss not provided [RCV000747383] Chr8:9498014..9500876 [GRCh37]
Chr8:8p23.1		 benign
GRCh37/hg19 8p23.1(chr8:9572088-10302429)x3 copy number gain not provided [RCV000762702] Chr8:9572088..10302429 [GRCh37]
Chr8:8p23.1		 likely benign
NM_003747.3(TNKS):c.285A>T (p.Thr95=) single nucleotide variant not provided [RCV000972443] Chr8:9556224 [GRCh38]
Chr8:9413734 [GRCh37]
Chr8:8p23.1		 benign
NM_003747.3(TNKS):c.444G>A (p.Ser148=) single nucleotide variant not provided [RCV000969539] Chr8:9556383 [GRCh38]
Chr8:9413893 [GRCh37]
Chr8:8p23.1		 benign
NM_003747.3(TNKS):c.2949C>T (p.Pro983=) single nucleotide variant not provided [RCV000880640] Chr8:9751725 [GRCh38]
Chr8:9609235 [GRCh37]
Chr8:8p23.1		 benign
GRCh37/hg19 8p23.1(chr8:8093169-11272546)x1 copy number loss not provided [RCV001006064] Chr8:8093169..11272546 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:8403375-11805960) copy number loss Tetralogy of Fallot [RCV000767642] Chr8:8403375..11805960 [GRCh37]
Chr8:8p23.1		 pathogenic
Single allele duplication Neurodevelopmental disorder [RCV000787445] Chr8:8112589..11967869 [GRCh37]
Chr8:8p23.1		 likely pathogenic
GRCh37/hg19 8p23.3-22(chr8:194617-13947374) copy number gain not provided [RCV000767676] Chr8:194617..13947374 [GRCh37]
Chr8:8p23.3-22		 pathogenic
GRCh37/hg19 8p23.1(chr8:8093169-11936001)x1 copy number loss not provided [RCV001006063] Chr8:8093169..11936001 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:8093065-11882913)x3 copy number gain not provided [RCV000848343] Chr8:8093065..11882913 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:8093065-11945856)x3 copy number gain not provided [RCV000847864] Chr8:8093065..11945856 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:8093169-11898980)x1 copy number loss not provided [RCV000849225] Chr8:8093169..11898980 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.3-22(chr8:158048-14214722)x1 copy number loss not provided [RCV000847768] Chr8:158048..14214722 [GRCh37]
Chr8:8p23.3-22		 pathogenic
GRCh37/hg19 8p23.1(chr8:7881478-11860845)x1 copy number loss See cases [RCV001195073] Chr8:7881478..11860845 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:8093169-11888779)x3 copy number gain not provided [RCV000848227] Chr8:8093169..11888779 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:9635218-9819173)x3 copy number gain not provided [RCV001006071] Chr8:9635218..9819173 [GRCh37]
Chr8:8p23.1		 uncertain significance
GRCh37/hg19 8p23.1(chr8:6999219-11895232)x3 copy number gain not provided [RCV001006060] Chr8:6999219..11895232 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:8093065-11945856)x3 copy number gain not provided [RCV000846764] Chr8:8093065..11945856 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:8102723-11936107)x3 copy number gain not provided [RCV000847249] Chr8:8102723..11936107 [GRCh37]
Chr8:8p23.1		 pathogenic
NM_003747.3(TNKS):c.274A>G (p.Thr92Ala) single nucleotide variant Inborn genetic diseases [RCV003273436] Chr8:9556213 [GRCh38]
Chr8:9413723 [GRCh37]
Chr8:8p23.1		 uncertain significance
GRCh37/hg19 8p23.1(chr8:9613875-9742841)x3 copy number gain not provided [RCV001006070] Chr8:9613875..9742841 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.271A>G (p.Ser91Gly) single nucleotide variant Inborn genetic diseases [RCV003250195] Chr8:9556210 [GRCh38]
Chr8:9413720 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.1456+4C>T single nucleotide variant not provided [RCV000888236] Chr8:9707001 [GRCh38]
Chr8:9564511 [GRCh37]
Chr8:8p23.1		 benign
NM_003747.3(TNKS):c.2331T>C (p.Thr777=) single nucleotide variant not provided [RCV000885490] Chr8:9734882 [GRCh38]
Chr8:9592392 [GRCh37]
Chr8:8p23.1		 benign|likely benign
NM_003747.3(TNKS):c.1047A>G (p.Glu349=) single nucleotide variant not provided [RCV000948799] Chr8:9680740 [GRCh38]
Chr8:9538250 [GRCh37]
Chr8:8p23.1		 benign
NM_003747.3(TNKS):c.674-5T>C single nucleotide variant not provided [RCV000954171] Chr8:9580154 [GRCh38]
Chr8:9437664 [GRCh37]
Chr8:8p23.1		 benign
GRCh37/hg19 8p23.1(chr8:8093066-12548732)x1 copy number loss not provided [RCV002472610] Chr8:8093066..12548732 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:9257738-9874909)x3 copy number gain not provided [RCV001006069] Chr8:9257738..9874909 [GRCh37]
Chr8:8p23.1		 uncertain significance
GRCh37/hg19 8p23.1(chr8:8093065-11881742)x3 copy number gain not provided [RCV001006062] Chr8:8093065..11881742 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:9171734-9608096)x1 copy number loss not provided [RCV001006068] Chr8:9171734..9608096 [GRCh37]
Chr8:8p23.1		 uncertain significance
GRCh37/hg19 8p23.3-23.1(chr8:176814-11472913)x1 copy number loss Cerebellar ataxia [RCV001251057] Chr8:176814..11472913 [GRCh37]
Chr8:8p23.3-23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:9598226-10803255)x1 copy number loss Intellectual disability [RCV001250263] Chr8:9598226..10803255 [GRCh37]
Chr8:8p23.1		 uncertain significance
GRCh37/hg19 8p23.1(chr8:9010028-9567941)x3 copy number gain not provided [RCV001260028] Chr8:9010028..9567941 [GRCh37]
Chr8:8p23.1		 uncertain significance
GRCh37/hg19 8p23.1(chr8:9511554-9647023)x3 copy number gain not provided [RCV001260029] Chr8:9511554..9647023 [GRCh37]
Chr8:8p23.1		 uncertain significance
GRCh37/hg19 8p23.1(chr8:9447087-9687874)x3 copy number gain not provided [RCV001827922] Chr8:9447087..9687874 [GRCh37]
Chr8:8p23.1		 uncertain significance
GRCh37/hg19 8p23.3-23.1(chr8:158048-11936107)x3 copy number gain not provided [RCV001827598] Chr8:158048..11936107 [GRCh37]
Chr8:8p23.3-23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:8851466-9623653)x3 copy number gain not provided [RCV001829054] Chr8:8851466..9623653 [GRCh37]
Chr8:8p23.1		 uncertain significance
GRCh37/hg19 8p23.1(chr8:9556847-10268805)x3 copy number gain not provided [RCV001832944] Chr8:9556847..10268805 [GRCh37]
Chr8:8p23.1		 uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771) copy number gain Polydactyly [RCV002280629] Chr8:158048..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p23.3-23.1(chr8:158048-10348413) copy number gain Neurodevelopmental delay [RCV002280754] Chr8:158048..10348413 [GRCh37]
Chr8:8p23.3-23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:8093168-11898980) copy number gain Neurodevelopmental delay [RCV002280755] Chr8:8093168..11898980 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh37/hg19 8p23.3-12(chr8:158048-30187456)x1 copy number loss See cases [RCV002286343] Chr8:158048..30187456 [GRCh37]
Chr8:8p23.3-12		 pathogenic
Single allele complex See cases [RCV002292428] Chr8:6999114..11935023 [GRCh37]
Chr8:8p23.3-11.21		 pathogenic
GRCh37/hg19 8p23.3-23.1(chr8:158048-11281408)x1 copy number loss See cases [RCV002287568] Chr8:158048..11281408 [GRCh37]
Chr8:8p23.3-23.1		 pathogenic
NM_003747.3(TNKS):c.3468G>C (p.Lys1156Asn) single nucleotide variant Inborn genetic diseases [RCV003299290] Chr8:9765712 [GRCh38]
Chr8:9623222 [GRCh37]
Chr8:8p23.1		 uncertain significance
GRCh37/hg19 8p23.1(chr8:8999456-9440325)x3 copy number gain not provided [RCV002473553] Chr8:8999456..9440325 [GRCh37]
Chr8:8p23.1		 uncertain significance
GRCh37/hg19 8p23.3-23.1(chr8:158049-10965627)x1 copy number loss not provided [RCV002474566] Chr8:158049..10965627 [GRCh37]
Chr8:8p23.3-23.1		 pathogenic
GRCh37/hg19 8p23.3-22(chr8:158049-18936715)x1 copy number loss not provided [RCV002472557] Chr8:158049..18936715 [GRCh37]
Chr8:8p23.3-22		 pathogenic
NM_003747.3(TNKS):c.239C>T (p.Ser80Phe) single nucleotide variant Inborn genetic diseases [RCV002990968] Chr8:9556178 [GRCh38]
Chr8:9413688 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.58C>G (p.Pro20Ala) single nucleotide variant Inborn genetic diseases [RCV002682120] Chr8:9555997 [GRCh38]
Chr8:9413507 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.853C>T (p.Pro285Ser) single nucleotide variant Inborn genetic diseases [RCV002901103] Chr8:9580338 [GRCh38]
Chr8:9437848 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.2302C>A (p.Leu768Ile) single nucleotide variant Inborn genetic diseases [RCV002818623] Chr8:9733433 [GRCh38]
Chr8:9590943 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.358C>G (p.Pro120Ala) single nucleotide variant Inborn genetic diseases [RCV002990052] Chr8:9556297 [GRCh38]
Chr8:9413807 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.3797T>C (p.Met1266Thr) single nucleotide variant Inborn genetic diseases [RCV002821909] Chr8:9770162 [GRCh38]
Chr8:9627672 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.733C>T (p.Arg245Cys) single nucleotide variant Inborn genetic diseases [RCV002705023] Chr8:9580218 [GRCh38]
Chr8:9437728 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.3470A>G (p.Lys1157Arg) single nucleotide variant Inborn genetic diseases [RCV002704384] Chr8:9765714 [GRCh38]
Chr8:9623224 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.124G>C (p.Gly42Arg) single nucleotide variant Inborn genetic diseases [RCV002704037] Chr8:9556063 [GRCh38]
Chr8:9413573 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.587C>G (p.Ser196Cys) single nucleotide variant Inborn genetic diseases [RCV002783351] Chr8:9556526 [GRCh38]
Chr8:9414036 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.796A>C (p.Ser266Arg) single nucleotide variant Inborn genetic diseases [RCV002911780] Chr8:9580281 [GRCh38]
Chr8:9437791 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.122C>T (p.Pro41Leu) single nucleotide variant Inborn genetic diseases [RCV002925995] Chr8:9556061 [GRCh38]
Chr8:9413571 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.2547C>G (p.Asn849Lys) single nucleotide variant Inborn genetic diseases [RCV002930692] Chr8:9735390 [GRCh38]
Chr8:9592900 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.3958G>A (p.Ala1320Thr) single nucleotide variant Inborn genetic diseases [RCV002826686] Chr8:9776710 [GRCh38]
Chr8:9634220 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.2872C>T (p.Pro958Ser) single nucleotide variant Inborn genetic diseases [RCV002826117] Chr8:9751648 [GRCh38]
Chr8:9609158 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.230G>A (p.Arg77Lys) single nucleotide variant Inborn genetic diseases [RCV002743135] Chr8:9556169 [GRCh38]
Chr8:9413679 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.1058C>A (p.Ala353Asp) single nucleotide variant Inborn genetic diseases [RCV002892844] Chr8:9680751 [GRCh38]
Chr8:9538261 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.3293C>G (p.Thr1098Ser) single nucleotide variant Inborn genetic diseases [RCV002767302] Chr8:9763165 [GRCh38]
Chr8:9620675 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.427C>G (p.Pro143Ala) single nucleotide variant Inborn genetic diseases [RCV002763100] Chr8:9556366 [GRCh38]
Chr8:9413876 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.2429C>T (p.Ala810Val) single nucleotide variant Inborn genetic diseases [RCV002718083] Chr8:9734980 [GRCh38]
Chr8:9592490 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.166T>G (p.Phe56Val) single nucleotide variant Inborn genetic diseases [RCV002835678] Chr8:9556105 [GRCh38]
Chr8:9413615 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.711G>T (p.Gln237His) single nucleotide variant Inborn genetic diseases [RCV002812933] Chr8:9580196 [GRCh38]
Chr8:9437706 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.206A>G (p.Asp69Gly) single nucleotide variant Inborn genetic diseases [RCV002793008] Chr8:9556145 [GRCh38]
Chr8:9413655 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.1639A>G (p.Lys547Glu) single nucleotide variant Inborn genetic diseases [RCV002939999] Chr8:9710015 [GRCh38]
Chr8:9567525 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.424T>C (p.Ser142Pro) single nucleotide variant Inborn genetic diseases [RCV002921426] Chr8:9556363 [GRCh38]
Chr8:9413873 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.2948C>G (p.Pro983Arg) single nucleotide variant Inborn genetic diseases [RCV002674152] Chr8:9751724 [GRCh38]
Chr8:9609234 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.3059A>G (p.Lys1020Arg) single nucleotide variant Inborn genetic diseases [RCV002809353] Chr8:9751835 [GRCh38]
Chr8:9609345 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.1895A>G (p.Asn632Ser) single nucleotide variant Inborn genetic diseases [RCV002674829] Chr8:9720519 [GRCh38]
Chr8:9578029 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.3488G>A (p.Cys1163Tyr) single nucleotide variant Inborn genetic diseases [RCV002809537] Chr8:9765732 [GRCh38]
Chr8:9623242 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.2948C>T (p.Pro983Leu) single nucleotide variant Inborn genetic diseases [RCV002856063] Chr8:9751724 [GRCh38]
Chr8:9609234 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.8C>A (p.Ala3Glu) single nucleotide variant Inborn genetic diseases [RCV003200428] Chr8:9555947 [GRCh38]
Chr8:9413457 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.2132A>G (p.His711Arg) single nucleotide variant Inborn genetic diseases [RCV003201518] Chr8:9731020 [GRCh38]
Chr8:9588530 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.2998G>A (p.Ala1000Thr) single nucleotide variant Inborn genetic diseases [RCV003214761] Chr8:9751774 [GRCh38]
Chr8:9609284 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.3263G>A (p.Gly1088Asp) single nucleotide variant Inborn genetic diseases [RCV003286208] Chr8:9761625 [GRCh38]
Chr8:9619135 [GRCh37]
Chr8:8p23.1		 uncertain significance
GRCh37/hg19 8p23.3-23.1(chr8:10501-11142629)x1 copy number loss See cases [RCV003329533] Chr8:10501..11142629 [GRCh37]
Chr8:8p23.3-23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:7080281-12045269)x3 copy number gain 8p23.1 duplication syndrome [RCV003329529] Chr8:7080281..12045269 [GRCh37]
Chr8:8p23.1		 pathogenic
GRCh38/hg38 8p23.3-21.2(chr8:449893-23854904)x1 copy number loss Neurodevelopmental disorder [RCV003327729] Chr8:449893..23854904 [GRCh38]
Chr8:8p23.3-21.2		 pathogenic
NM_003747.3(TNKS):c.458G>A (p.Ser153Asn) single nucleotide variant Inborn genetic diseases [RCV003376608] Chr8:9556397 [GRCh38]
Chr8:9413907 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.1037G>A (p.Gly346Asp) single nucleotide variant Inborn genetic diseases [RCV003371026] Chr8:9680730 [GRCh38]
Chr8:9538240 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.2558C>G (p.Ala853Gly) single nucleotide variant Inborn genetic diseases [RCV003364911] Chr8:9735401 [GRCh38]
Chr8:9592911 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.866C>G (p.Ala289Gly) single nucleotide variant Inborn genetic diseases [RCV003347224] Chr8:9580351 [GRCh38]
Chr8:9437861 [GRCh37]
Chr8:8p23.1		 uncertain significance
NM_003747.3(TNKS):c.1709A>G (p.His570Arg) single nucleotide variant Inborn genetic diseases [RCV003369988] Chr8:9710180 [GRCh38]
Chr8:9567690 [GRCh37]
Chr8:8p23.1		 uncertain significance
GRCh37/hg19 8p23.1-22(chr8:8093169-14526969)x3 copy number gain not provided [RCV003484718] Chr8:8093169..14526969 [GRCh37]
Chr8:8p23.1-22		 pathogenic
GRCh37/hg19 8p23.2-11.21(chr8:2201405-41723095)x3 copy number gain not provided [RCV003484713] Chr8:2201405..41723095 [GRCh37]
Chr8:8p23.2-11.21		 pathogenic
GRCh37/hg19 8p23.3-23.1(chr8:158049-10007143)x1 copy number loss not provided [RCV003482998] Chr8:158049..10007143 [GRCh37]
Chr8:8p23.3-23.1		 pathogenic
GRCh37/hg19 8p23.1(chr8:9208205-10501320)x1 copy number loss not provided [RCV003483015] Chr8:9208205..10501320 [GRCh37]
Chr8:8p23.1		 uncertain significance
GRCh37/hg19 8p23.3-23.1(chr8:158049-11898696)x1 copy number loss not provided [RCV003482999] Chr8:158049..11898696 [GRCh37]
Chr8:8p23.3-23.1		 pathogenic
NM_003747.3(TNKS):c.71C>T (p.Ala24Val) single nucleotide variant not provided [RCV003491676] Chr8:9556010 [GRCh38]
Chr8:9413520 [GRCh37]
Chr8:8p23.1		 uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3 copy number gain not specified [RCV003986742] Chr8:158048..146295771 [GRCh37]
Chr8:8p23.3-q24.3		 pathogenic
GRCh37/hg19 8p23.3-11.21(chr8:158048-41600696)x3 copy number gain not specified [RCV003986756] Chr8:158048..41600696 [GRCh37]
Chr8:8p23.3-11.21		 pathogenic
miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR324hsa-miR-324-5pMirtarbaseexternal_infoCLASHFunctional MTI (Weak)23622248

Predicted Target Of
Summary Value
Count of predictions:3953
Count of miRNA genes:1409
Interacting mature miRNAs:1830
Transcripts:ENST00000310430, ENST00000517652, ENST00000517770, ENST00000517989, ENST00000518027, ENST00000518281, ENST00000518635, ENST00000519191, ENST00000519392, ENST00000519930, ENST00000520408, ENST00000521039, ENST00000522110
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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

Markers in Region
G20573  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3789,639,630 - 9,639,818UniSTSGRCh37
Build 3689,677,040 - 9,677,228RGDNCBI36
Celera88,765,336 - 8,765,524RGD
Cytogenetic Map8p23.1UniSTS
HuRef88,568,111 - 8,568,299UniSTS
A005X23  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3789,639,630 - 9,639,818UniSTSGRCh37
Build 3689,677,040 - 9,677,228RGDNCBI36
Celera88,765,336 - 8,765,524RGD
Cytogenetic Map8p23.1UniSTS
HuRef88,568,111 - 8,568,299UniSTS
GeneMap99-GB4 RH Map839.77UniSTS
SHGC-24414  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3789,636,206 - 9,636,314UniSTSGRCh37
Build 3689,673,616 - 9,673,724RGDNCBI36
Celera88,761,912 - 8,762,020RGD
Cytogenetic Map8p23.1UniSTS
HuRef88,564,687 - 8,564,795UniSTS
Stanford-G3 RH Map8387.0UniSTS
NCBI RH Map878.0UniSTS
GeneMap99-G3 RH Map8474.0UniSTS
SHGC-63000  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3789,557,808 - 9,558,039UniSTSGRCh37
Build 3689,595,218 - 9,595,449RGDNCBI36
Celera88,682,010 - 8,682,241RGD
Cytogenetic Map8p23.1UniSTS
HuRef88,483,450 - 8,483,681UniSTS
RH103385  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3789,636,137 - 9,636,302UniSTSGRCh37
Build 3689,673,547 - 9,673,712RGDNCBI36
Celera88,761,843 - 8,762,008RGD
Cytogenetic Map8p23.1UniSTS
HuRef88,564,618 - 8,564,783UniSTS
GeneMap99-GB4 RH Map851.33UniSTS
RH104269  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3789,628,002 - 9,628,122UniSTSGRCh37
Build 3689,665,412 - 9,665,532RGDNCBI36
Celera88,752,237 - 8,752,357RGD
Cytogenetic Map8p23.1UniSTS
HuRef88,553,635 - 8,553,755UniSTS
GeneMap99-GB4 RH Map839.67UniSTS
RH120367  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3789,429,874 - 9,430,205UniSTSGRCh37
Build 3689,467,284 - 9,467,615RGDNCBI36
Celera88,557,956 - 8,558,287RGD
Cytogenetic Map8p23.1UniSTS
HuRef88,356,042 - 8,356,373UniSTS
TNG Radiation Hybrid Map88318.0UniSTS
HSC2QE062  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3789,639,592 - 9,639,796UniSTSGRCh37
Build 3689,677,002 - 9,677,206RGDNCBI36
Celera88,765,298 - 8,765,502RGD
Cytogenetic Map8p23.1UniSTS
HuRef88,568,073 - 8,568,277UniSTS
GeneMap99-GB4 RH Map851.33UniSTS
Whitehead-RH Map843.8UniSTS
NCBI RH Map892.4UniSTS
SHGC-132382  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3789,636,193 - 9,636,386UniSTSGRCh37
Build 3689,673,603 - 9,673,796RGDNCBI36
Celera88,761,899 - 8,762,092RGD
Cytogenetic Map8p23.1UniSTS
HuRef88,564,674 - 8,564,867UniSTS
TNG Radiation Hybrid Map860610.0UniSTS
RH11883  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3789,635,425 - 9,635,554UniSTSGRCh37
Build 3689,672,835 - 9,672,964RGDNCBI36
Celera88,761,132 - 8,761,261RGD
Cytogenetic Map8p23.1UniSTS
HuRef88,563,907 - 8,564,036UniSTS
GeneMap99-GB4 RH Map831.44UniSTS
RH18302  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3789,637,936 - 9,638,089UniSTSGRCh37
Build 3689,675,346 - 9,675,499RGDNCBI36
Celera88,763,642 - 8,763,795RGD
Cytogenetic Map8p23.1UniSTS
HuRef88,566,417 - 8,566,570UniSTS
GeneMap99-GB4 RH Map839.77UniSTS
NCBI RH Map885.6UniSTS
UniSTS:45338  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3789,534,156 - 9,534,392UniSTSGRCh37
Build 3689,571,566 - 9,571,802RGDNCBI36
Celera88,658,494 - 8,658,736RGD
HuRef88,459,759 - 8,460,001UniSTS
RH44938  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3789,530,003 - 9,530,103UniSTSGRCh37
Build 3689,567,413 - 9,567,513RGDNCBI36
Celera88,654,339 - 8,654,439RGD
Cytogenetic Map8p23.1UniSTS
HuRef88,455,603 - 8,455,703UniSTS
GeneMap99-GB4 RH Map851.33UniSTS
NCBI RH Map892.4UniSTS
D8S2278  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map3p25.3-p24.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map10q11UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map12q21.31UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic MapXp22.1UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map4q34.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map2p23.1UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map12p12.3UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map14q22UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map4q31UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map15q15-q21.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map12q14.3-q15UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map21q21.1UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1p13-p12UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map10q21.1UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map14q31UniSTS
G59681  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map8p23.1UniSTS
HuRef88,437,706 - 8,437,898UniSTS
TNG Radiation Hybrid Map88252.0UniSTS
TNG Radiation Hybrid Map88199.0UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
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Cytogenetic Map5q15UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map18p11.3UniSTS
Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS


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
High
Medium 785 844 899 56 764 37 2861 723 2237 139 1128 1012 28 337 1964 2
Low 1648 2118 826 566 1165 427 1494 1467 1493 278 320 596 144 867 824 2
Below cutoff 2 23 19 1 3 3 1 2 1 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_003747 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006716263 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011543845 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011543846 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054332269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054332270 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054332271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054332272 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054332273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054361430 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054361431 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054361432 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054361433 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054361434 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB209339 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC021242 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC103834 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC103877 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC104052 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC270292 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC275369 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC275566 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC275567 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF070613 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF082556 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF082557 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF082558 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF082559 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK301798 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302031 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302534 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL706619 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC023578 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC098394 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471157 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068270 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000310430   ⟹   ENSP00000311579
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl89,555,912 - 9,782,346 (+)Ensembl
RefSeq Acc Id: ENST00000517652
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl89,566,260 - 9,566,526 (+)Ensembl
RefSeq Acc Id: ENST00000517770   ⟹   ENSP00000428185
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl89,555,940 - 9,777,036 (+)Ensembl
RefSeq Acc Id: ENST00000517989
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl89,679,846 - 9,708,406 (+)Ensembl
RefSeq Acc Id: ENST00000518027
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl89,615,290 - 9,707,008 (+)Ensembl
RefSeq Acc Id: ENST00000518281   ⟹   ENSP00000429890
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl89,575,007 - 9,776,929 (+)Ensembl
RefSeq Acc Id: ENST00000518635   ⟹   ENSP00000431098
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl89,734,991 - 9,748,212 (+)Ensembl
RefSeq Acc Id: ENST00000519191
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl89,740,914 - 9,751,713 (+)Ensembl
RefSeq Acc Id: ENST00000519392
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl89,679,754 - 9,707,008 (+)Ensembl
RefSeq Acc Id: ENST00000519930
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl89,720,456 - 9,730,973 (+)Ensembl
RefSeq Acc Id: ENST00000520408   ⟹   ENSP00000428299
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl89,555,914 - 9,710,409 (+)Ensembl
RefSeq Acc Id: ENST00000521039
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl89,670,119 - 9,681,156 (+)Ensembl
RefSeq Acc Id: ENST00000522110   ⟹   ENSP00000430920
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl89,555,932 - 9,558,831 (+)Ensembl
RefSeq Acc Id: NM_003747   ⟹   NP_003738
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3889,555,912 - 9,782,346 (+)NCBI
GRCh3789,412,756 - 9,639,856 (+)NCBI
Build 3689,450,855 - 9,677,266 (+)NCBI Archive
HuRef88,339,612 - 8,568,337 (+)ENTREZGENE
CHM1_189,478,677 - 9,705,116 (+)NCBI
T2T-CHM13v2.089,959,097 - 10,187,973 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011543845   ⟹   XP_011542147
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3889,555,912 - 9,773,062 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011543846   ⟹   XP_011542148
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3889,555,912 - 9,773,062 (+)NCBI
Sequence:
RefSeq Acc Id: XM_054361430   ⟹   XP_054217405
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.089,965,520 - 10,187,973 (-)NCBI
RefSeq Acc Id: XM_054361431   ⟹   XP_054217406
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.089,965,520 - 10,187,973 (-)NCBI
RefSeq Acc Id: XM_054361432   ⟹   XP_054217407
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.089,959,097 - 10,187,973 (-)NCBI
RefSeq Acc Id: XM_054361433   ⟹   XP_054217408
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.089,965,520 - 10,187,973 (-)NCBI
RefSeq Acc Id: XM_054361434   ⟹   XP_054217409
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.089,965,520 - 10,187,973 (-)NCBI
Protein Sequences
Protein RefSeqs NP_003738 (Get FASTA)   NCBI Sequence Viewer  
  XP_011542147 (Get FASTA)   NCBI Sequence Viewer  
  XP_011542148 (Get FASTA)   NCBI Sequence Viewer  
  XP_054188244 (Get FASTA)   NCBI Sequence Viewer  
  XP_054188245 (Get FASTA)   NCBI Sequence Viewer  
  XP_054188246 (Get FASTA)   NCBI Sequence Viewer  
  XP_054188247 (Get FASTA)   NCBI Sequence Viewer  
  XP_054188248 (Get FASTA)   NCBI Sequence Viewer  
  XP_054217405 (Get FASTA)   NCBI Sequence Viewer  
  XP_054217406 (Get FASTA)   NCBI Sequence Viewer  
  XP_054217407 (Get FASTA)   NCBI Sequence Viewer  
  XP_054217408 (Get FASTA)   NCBI Sequence Viewer  
  XP_054217409 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAC79841 (Get FASTA)   NCBI Sequence Viewer  
  AAC79842 (Get FASTA)   NCBI Sequence Viewer  
  AAC79843 (Get FASTA)   NCBI Sequence Viewer  
  AAC79844 (Get FASTA)   NCBI Sequence Viewer  
  AAH98394 (Get FASTA)   NCBI Sequence Viewer  
  BAD92576 (Get FASTA)   NCBI Sequence Viewer  
  BAG63250 (Get FASTA)   NCBI Sequence Viewer  
  BAG63428 (Get FASTA)   NCBI Sequence Viewer  
  BAG63806 (Get FASTA)   NCBI Sequence Viewer  
  EAW65579 (Get FASTA)   NCBI Sequence Viewer  
  EAW65580 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000311579
  ENSP00000311579.6
  ENSP00000428185
  ENSP00000428185.2
  ENSP00000428299.1
  ENSP00000429890.1
  ENSP00000430920.1
  ENSP00000431098.1
  ENSP00000493602.2
  ENSP00000518575.1
GenBank Protein O95271 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_003738   ⟸   NM_003747
- UniProtKB: Q4G0F2 (UniProtKB/Swiss-Prot),   O95272 (UniProtKB/Swiss-Prot),   Q59FX0 (UniProtKB/Swiss-Prot),   O95271 (UniProtKB/Swiss-Prot),   E7EQ52 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011542147   ⟸   XM_011543845
- Peptide Label: isoform X1
- UniProtKB: H0YAW5 (UniProtKB/TrEMBL),   E7EQ52 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011542148   ⟸   XM_011543846
- Peptide Label: isoform X2
- UniProtKB: E7EQ52 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000428185   ⟸   ENST00000517770
RefSeq Acc Id: ENSP00000431098   ⟸   ENST00000518635
RefSeq Acc Id: ENSP00000429890   ⟸   ENST00000518281
RefSeq Acc Id: ENSP00000428299   ⟸   ENST00000520408
RefSeq Acc Id: ENSP00000311579   ⟸   ENST00000310430
RefSeq Acc Id: ENSP00000430920   ⟸   ENST00000522110
RefSeq Acc Id: XP_054217407   ⟸   XM_054361432
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054217409   ⟸   XM_054361434
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054217408   ⟸   XM_054361433
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054217406   ⟸   XM_054361431
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054217405   ⟸   XM_054361430
- Peptide Label: isoform X1
- UniProtKB: H0YAW5 (UniProtKB/TrEMBL)
Protein Domains
PARP catalytic   SAM

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-O95271-F1-model_v2 AlphaFold O95271 1-1327 view protein structure

Promoters
RGD ID:6807074
Promoter ID:HG_KWN:60676
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   K562,   Lymphoblastoid
Transcripts:OTTHUMT00000206935
Position:
Human AssemblyChrPosition (strand)Source
Build 3689,449,846 - 9,451,497 (+)MPROMDB
RGD ID:7212603
Promoter ID:EPDNEW_H12048
Type:initiation region
Name:TNKS_1
Description:tankyrase
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh3889,555,914 - 9,555,974EPDNEW
RGD ID:6807075
Promoter ID:HG_KWN:60677
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid
Transcripts:UC010LRS.1
Position:
Human AssemblyChrPosition (strand)Source
Build 3689,614,596 - 9,615,447 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:11941 AgrOrtholog
COSMIC TNKS COSMIC
Ensembl Genes ENSG00000173273 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENSG00000285372 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000310430 ENTREZGENE
  ENST00000310430.11 UniProtKB/Swiss-Prot
  ENST00000517770 ENTREZGENE
  ENST00000517770.2 UniProtKB/TrEMBL
  ENST00000518281.5 UniProtKB/TrEMBL
  ENST00000518635.2 UniProtKB/TrEMBL
  ENST00000519930.2 UniProtKB/TrEMBL
  ENST00000520408.5 UniProtKB/TrEMBL
  ENST00000522110.1 UniProtKB/TrEMBL
  ENST00000646522.2 UniProtKB/Swiss-Prot
Gene3D-CATH 1.10.150.50 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  1.25.40.20 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.90.228.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  6.20.320.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000173273 GTEx
  ENSG00000285372 GTEx
HGNC ID HGNC:11941 ENTREZGENE
Human Proteome Map TNKS Human Proteome Map
InterPro Ankyrin_rpt UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ankyrin_rpt-contain_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Poly(ADP-ribose)pol_cat_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SAM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SAM/pointed_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:8658 UniProtKB/Swiss-Prot
NCBI Gene 8658 ENTREZGENE
OMIM 603303 OMIM
PANTHER ANK_REP_REGION DOMAIN-CONTAINING PROTEIN UniProtKB/TrEMBL
  CYCLIN-DEPENDENT KINASE INHIBITOR 2C UniProtKB/TrEMBL
  CYCLIN-DEPENDENT KINASE INHIBITOR 2C-RELATED UniProtKB/TrEMBL
  MOLTING PROTEIN MLT-4 UniProtKB/TrEMBL
  MYOTROPHIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  POLY [ADP-RIBOSE] POLYMERASE TANKYRASE-1 UniProtKB/TrEMBL
  SI:CH211-203B8.6 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Ank UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ank_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ank_4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ank_5 UniProtKB/TrEMBL
  PARP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SAM_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA36631 PharmGKB
PRINTS ANKYRIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE ANK_REP_REGION UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ANK_REPEAT UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PARP_CATALYTIC UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SAM_DOMAIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART ANK UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SAM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP ADP-ribosylation UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF47769 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF48403 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A0C4DGE3_HUMAN UniProtKB/TrEMBL
  A0AA34QVM1_HUMAN UniProtKB/TrEMBL
  E5RHD2_HUMAN UniProtKB/TrEMBL
  E7EQ52 ENTREZGENE, UniProtKB/TrEMBL
  E7EWY6_HUMAN UniProtKB/TrEMBL
  H0YAW5 ENTREZGENE, UniProtKB/TrEMBL
  O95271 ENTREZGENE
  O95272 ENTREZGENE
  Q4G0F2 ENTREZGENE
  Q59FX0 ENTREZGENE
  TNKS1_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary O95272 UniProtKB/Swiss-Prot
  Q4G0F2 UniProtKB/Swiss-Prot
  Q59FX0 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-03-07 TNKS  tankyrase    tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase  Symbol and/or name change 5135510 APPROVED