HELZ (helicase with zinc finger) - Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Gene: HELZ (helicase with zinc finger) Homo sapiens
Analyze
Symbol: HELZ
Name: helicase with zinc finger
RGD ID: 1316013
HGNC Page HGNC:16878
Description: Enables RNA binding activity. Predicted to be involved in regulatory ncRNA-mediated post-transcriptional gene silencing. Located in membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: DHRC; DKFZp586G1924; down-regulated in human cancers protein; DRHC; helicase with zinc finger domain; HUMORF5; KIAA0054; MGC163454; probable helicase with zinc finger domain
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
GRCh381767,070,444 - 67,245,989 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1767,070,444 - 67,245,989 (-)EnsemblGRCh38hg38GRCh38
GRCh371765,066,560 - 65,241,312 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361762,497,016 - 62,671,781 (-)NCBINCBI36Build 36hg18NCBI36
Build 341762,504,527 - 62,671,774NCBI
Celera1761,639,217 - 61,813,834 (-)NCBICelera
Cytogenetic Map17q24.2NCBI
HuRef1760,455,149 - 60,628,698 (-)NCBIHuRef
CHM1_11765,130,487 - 65,305,305 (-)NCBICHM1_1
T2T-CHM13v2.01767,946,238 - 68,123,293 (-)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

Biological Process

Cellular Component
cytosol  (IBA,IEA)
membrane  (HDA,IEA)
nucleus  (IEA)
P granule  (IBA,IEA)

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:7584044   PMID:10471385   PMID:12477932   PMID:12615363   PMID:12691822   PMID:15235609   PMID:15302935   PMID:15342556   PMID:19322201   PMID:19946888   PMID:20020773   PMID:20378664  
PMID:20936779   PMID:21150319   PMID:21765940   PMID:21873635   PMID:21988832   PMID:22586326   PMID:22658674   PMID:22681889   PMID:23443559   PMID:24255178   PMID:24457600   PMID:24606901  
PMID:25515538   PMID:25665578   PMID:25940091   PMID:26186194   PMID:26460568   PMID:26496610   PMID:26777405   PMID:26972000   PMID:27173435   PMID:27432908   PMID:27609421   PMID:27880917  
PMID:28514442   PMID:28675297   PMID:29395067   PMID:29507755   PMID:30209976   PMID:30463901   PMID:30995489   PMID:30997501   PMID:31091453   PMID:31240132   PMID:31527615   PMID:31586073  
PMID:31640799   PMID:31753913   PMID:32344865   PMID:32460013   PMID:32694731   PMID:33536335   PMID:33660365   PMID:33853758   PMID:33916271   PMID:33961781   PMID:34079125   PMID:34672954  
PMID:34702444   PMID:34709727   PMID:34732716   PMID:35140242   PMID:35271311   PMID:35509820   PMID:35654790   PMID:35803934   PMID:35819319   PMID:36114006   PMID:36232890   PMID:36282215  
PMID:36339263   PMID:36931259   PMID:37689310   PMID:37827155  


Genomics

Comparative Map Data
HELZ
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381767,070,444 - 67,245,989 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1767,070,444 - 67,245,989 (-)EnsemblGRCh38hg38GRCh38
GRCh371765,066,560 - 65,241,312 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361762,497,016 - 62,671,781 (-)NCBINCBI36Build 36hg18NCBI36
Build 341762,504,527 - 62,671,774NCBI
Celera1761,639,217 - 61,813,834 (-)NCBICelera
Cytogenetic Map17q24.2NCBI
HuRef1760,455,149 - 60,628,698 (-)NCBIHuRef
CHM1_11765,130,487 - 65,305,305 (-)NCBICHM1_1
T2T-CHM13v2.01767,946,238 - 68,123,293 (-)NCBIT2T-CHM13v2.0
Helz
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3911107,437,789 - 107,584,652 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl11107,438,756 - 107,584,652 (+)EnsemblGRCm39 Ensembl
GRCm3811107,546,963 - 107,693,826 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl11107,547,930 - 107,693,826 (+)EnsemblGRCm38mm10GRCm38
MGSCv3711107,409,274 - 107,548,257 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv3611107,364,050 - 107,503,033 (+)NCBIMGSCv36mm8
Celera11119,282,487 - 119,422,267 (+)NCBICelera
Cytogenetic Map11E1NCBI
cM Map1170.29NCBI
Helz
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81092,979,039 - 93,144,868 (+)NCBIGRCr8
mRatBN7.21092,479,403 - 92,645,234 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1092,501,518 - 92,638,383 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1097,559,569 - 97,696,460 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01097,022,598 - 97,159,486 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01092,424,222 - 92,561,141 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01095,767,754 - 95,911,025 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1095,770,154 - 95,906,927 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01095,502,595 - 95,645,422 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41096,952,234 - 97,091,028 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11096,966,600 - 97,105,463 (+)NCBI
Celera1091,166,920 - 91,303,954 (+)NCBICelera
Cytogenetic Map10q32.1NCBI
Helz
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554786,325,632 - 6,475,964 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554786,325,632 - 6,475,144 (-)NCBIChiLan1.0ChiLan1.0
HELZ
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21983,099,365 - 83,273,334 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11787,919,176 - 88,093,066 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01761,006,644 - 61,180,588 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11766,220,707 - 66,385,521 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1766,220,715 - 66,384,814 (-)Ensemblpanpan1.1panPan2
HELZ
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1913,250,374 - 13,414,545 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl913,250,372 - 13,409,647 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha914,143,417 - 14,308,826 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0914,910,848 - 15,077,323 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl914,910,899 - 15,073,606 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1913,859,036 - 14,024,744 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0913,509,351 - 13,675,150 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0913,511,081 - 13,676,705 (-)NCBIUU_Cfam_GSD_1.0
Helz
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440560213,176,634 - 13,347,874 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365415,877,008 - 6,010,674 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365415,846,757 - 6,018,618 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
HELZ
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1213,495,119 - 13,654,931 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11213,488,551 - 13,654,979 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21213,865,101 - 14,024,025 (-)NCBISscrofa10.2Sscrofa10.2susScr3
HELZ
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11654,196,505 - 54,369,015 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1654,222,827 - 54,361,438 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366607725,212,749 - 25,388,199 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Helz
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248701,171,975 - 1,316,437 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248701,151,896 - 1,323,727 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in HELZ
58 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 17q21.33-24.2(chr17:36449220-68170214)x3 copy number gain See cases [RCV000050957] Chr17:36449220..68170214 [GRCh38]
Chr17:48563237..65936105 [GRCh37]
Chr17:45918236..63677950 [NCBI36]
Chr17:17q21.33-24.2
pathogenic
GRCh38/hg38 17q23.2-25.3(chr17:36449220-83086677)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|See cases [RCV000052483] Chr17:36449220..83086677 [GRCh38]
Chr17:58617905..81044553 [GRCh37]
Chr17:55972687..78637842 [NCBI36]
Chr17:17q23.2-25.3
pathogenic
NM_014877.3(HELZ):c.3779C>T (p.Thr1260Ile) single nucleotide variant Malignant melanoma [RCV000071625] Chr17:67120464 [GRCh38]
Chr17:65116580 [GRCh37]
Chr17:62547042 [NCBI36]
Chr17:17q24.2
not provided
GRCh38/hg38 17q23.1-25.1(chr17:36449220-75053130)x3 copy number gain See cases [RCV000137437] Chr17:36449220..75053130 [GRCh38]
Chr17:57595736..73049225 [GRCh37]
Chr17:54950518..70560820 [NCBI36]
Chr17:17q23.1-25.1
pathogenic
GRCh38/hg38 17q24.1-24.2(chr17:64634771-67686888)x1 copy number loss See cases [RCV000140815] Chr17:64634771..67686888 [GRCh38]
Chr17:62649313..65683004 [GRCh37]
Chr17:60061351..63113466 [NCBI36]
Chr17:17q24.1-24.2
pathogenic
NM_014877.4(HELZ):c.3322A>G (p.Ile1108Val) single nucleotide variant Abnormal brain morphology [RCV000454348] Chr17:67128716 [GRCh38]
Chr17:65124832 [GRCh37]
Chr17:17q24.2
likely pathogenic
GRCh37/hg19 17q24.2-25.3(chr17:64241326-81041938)x3 copy number gain See cases [RCV000447577] Chr17:64241326..81041938 [GRCh37]
Chr17:17q24.2-25.3
pathogenic
GRCh37/hg19 17q21.31-25.3(chr17:42580684-81085615)x3 copy number gain See cases [RCV000447823] Chr17:42580684..81085615 [GRCh37]
Chr17:17q21.31-25.3
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938) copy number gain See cases [RCV000511439] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
NM_014877.4(HELZ):c.4186C>A (p.Pro1396Thr) single nucleotide variant Inborn genetic diseases [RCV003248936] Chr17:67109419 [GRCh38]
Chr17:65105535 [GRCh37]
Chr17:17q24.2
uncertain significance
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3 copy number gain See cases [RCV000512441] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17q24.2(chr17:64963389-65726146)x3 copy number gain not provided [RCV000683953] Chr17:64963389..65726146 [GRCh37]
Chr17:17q24.2
uncertain significance
GRCh37/hg19 17q24.1-25.3(chr17:63689671-81041938)x3 copy number gain not provided [RCV000683952] Chr17:63689671..81041938 [GRCh37]
Chr17:17q24.1-25.3
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3 copy number gain not provided [RCV000739324] Chr17:8547..81060040 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3 copy number gain not provided [RCV000739320] Chr17:7214..81058310 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3 copy number gain not provided [RCV000739325] Chr17:12344..81057996 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17q24.1-25.2(chr17:64159738-74891024)x3 copy number gain not provided [RCV000762750] Chr17:64159738..74891024 [GRCh37]
Chr17:17q24.1-25.2
likely pathogenic
NM_014877.4(HELZ):c.4349C>T (p.Pro1450Leu) single nucleotide variant Inborn genetic diseases [RCV003270284] Chr17:67109256 [GRCh38]
Chr17:65105372 [GRCh37]
Chr17:17q24.2
uncertain significance
GRCh37/hg19 17q22-24.2(chr17:57357088-66306668) copy number gain not provided [RCV000767764] Chr17:57357088..66306668 [GRCh37]
Chr17:17q22-24.2
pathogenic
NM_014877.4(HELZ):c.499C>T (p.His167Tyr) single nucleotide variant Inborn genetic diseases [RCV003248926] Chr17:67194025 [GRCh38]
Chr17:65190141 [GRCh37]
Chr17:17q24.2
uncertain significance
GRCh37/hg19 17q23.1-24.2(chr17:57869604-67078443)x3 copy number gain not provided [RCV000845965] Chr17:57869604..67078443 [GRCh37]
Chr17:17q23.1-24.2
pathogenic
GRCh37/hg19 17q24.1-25.3(chr17:62778720-81041938)x3 copy number gain not provided [RCV000849900] Chr17:62778720..81041938 [GRCh37]
Chr17:17q24.1-25.3
pathogenic
NM_014877.4(HELZ):c.4840A>G (p.Ser1614Gly) single nucleotide variant Inborn genetic diseases [RCV003273080] Chr17:67107570 [GRCh38]
Chr17:65103686 [GRCh37]
Chr17:17q24.2
uncertain significance
GRCh37/hg19 17q24.2(chr17:65050304-65440440)x3 copy number gain not provided [RCV001006912] Chr17:65050304..65440440 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.2117A>G (p.Tyr706Cys) single nucleotide variant not provided [RCV001092731] Chr17:67160321 [GRCh38]
Chr17:65156437 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.4775G>A (p.Arg1592Gln) single nucleotide variant Inborn genetic diseases [RCV003261068] Chr17:67107635 [GRCh38]
Chr17:65103751 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.4213C>A (p.Gln1405Lys) single nucleotide variant Inborn genetic diseases [RCV002686644] Chr17:67109392 [GRCh38]
Chr17:65105508 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.4289C>A (p.Ala1430Asp) single nucleotide variant Inborn genetic diseases [RCV002729500] Chr17:67109316 [GRCh38]
Chr17:65105432 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.4342G>A (p.Val1448Ile) single nucleotide variant Inborn genetic diseases [RCV002749979] Chr17:67109263 [GRCh38]
Chr17:65105379 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.4903A>C (p.Asn1635His) single nucleotide variant Inborn genetic diseases [RCV002837315] Chr17:67107507 [GRCh38]
Chr17:65103623 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.4184C>T (p.Pro1395Leu) single nucleotide variant Inborn genetic diseases [RCV002860976] Chr17:67109421 [GRCh38]
Chr17:65105537 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.4085C>T (p.Pro1362Leu) single nucleotide variant Inborn genetic diseases [RCV002905288] Chr17:67109520 [GRCh38]
Chr17:65105636 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.4051G>A (p.Ala1351Thr) single nucleotide variant Inborn genetic diseases [RCV002693485] Chr17:67109554 [GRCh38]
Chr17:65105670 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.5513A>G (p.Lys1838Arg) single nucleotide variant Inborn genetic diseases [RCV002886972] Chr17:67078568 [GRCh38]
Chr17:65074684 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.3475A>G (p.Ile1159Val) single nucleotide variant Inborn genetic diseases [RCV002762587] Chr17:67123125 [GRCh38]
Chr17:65119241 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.4448T>C (p.Ile1483Thr) single nucleotide variant Inborn genetic diseases [RCV002783260] Chr17:67109157 [GRCh38]
Chr17:65105273 [GRCh37]
Chr17:17q24.2
likely benign
NM_014877.4(HELZ):c.3511C>T (p.His1171Tyr) single nucleotide variant Inborn genetic diseases [RCV002759573] Chr17:67123089 [GRCh38]
Chr17:65119205 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.4225A>C (p.Asn1409His) single nucleotide variant Inborn genetic diseases [RCV002823411] Chr17:67109380 [GRCh38]
Chr17:65105496 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.3499C>A (p.Pro1167Thr) single nucleotide variant Inborn genetic diseases [RCV002782147] Chr17:67123101 [GRCh38]
Chr17:65119217 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.4417C>T (p.Pro1473Ser) single nucleotide variant Inborn genetic diseases [RCV002757600] Chr17:67109188 [GRCh38]
Chr17:65105304 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.5149A>G (p.Ile1717Val) single nucleotide variant Inborn genetic diseases [RCV002978017] Chr17:67107261 [GRCh38]
Chr17:65103377 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.2624A>G (p.Tyr875Cys) single nucleotide variant Inborn genetic diseases [RCV002892000] Chr17:67145888 [GRCh38]
Chr17:65142004 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.1615G>C (p.Val539Leu) single nucleotide variant Inborn genetic diseases [RCV002788467] Chr17:67167612 [GRCh38]
Chr17:65163728 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.4493G>A (p.Arg1498His) single nucleotide variant Inborn genetic diseases [RCV002805039] Chr17:67108723 [GRCh38]
Chr17:65104839 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.2297G>A (p.Arg766Gln) single nucleotide variant Inborn genetic diseases [RCV003004123] Chr17:67151105 [GRCh38]
Chr17:65147221 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.4582G>A (p.Gly1528Ser) single nucleotide variant Inborn genetic diseases [RCV002826578] Chr17:67108634 [GRCh38]
Chr17:65104750 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.4864C>G (p.Pro1622Ala) single nucleotide variant Inborn genetic diseases [RCV002767387] Chr17:67107546 [GRCh38]
Chr17:65103662 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.1127T>C (p.Met376Thr) single nucleotide variant Inborn genetic diseases [RCV002744801] Chr17:67188354 [GRCh38]
Chr17:65184470 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.2588G>A (p.Cys863Tyr) single nucleotide variant Inborn genetic diseases [RCV002893734] Chr17:67148602 [GRCh38]
Chr17:65144718 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.5767T>C (p.Phe1923Leu) single nucleotide variant Inborn genetic diseases [RCV002915597] Chr17:67078314 [GRCh38]
Chr17:65074430 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.1213C>T (p.Arg405Cys) single nucleotide variant Inborn genetic diseases [RCV002855256] Chr17:67178876 [GRCh38]
Chr17:65174992 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.2248G>A (p.Ala750Thr) single nucleotide variant Inborn genetic diseases [RCV002670608] Chr17:67151154 [GRCh38]
Chr17:65147270 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.5264G>A (p.Arg1755Gln) single nucleotide variant Inborn genetic diseases [RCV002808022] Chr17:67087059 [GRCh38]
Chr17:65083175 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.5005C>G (p.Leu1669Val) single nucleotide variant Inborn genetic diseases [RCV002896806] Chr17:67107405 [GRCh38]
Chr17:65103521 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.5663C>T (p.Ala1888Val) single nucleotide variant Inborn genetic diseases [RCV002877749] Chr17:67078418 [GRCh38]
Chr17:65074534 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.63C>G (p.Asp21Glu) single nucleotide variant Inborn genetic diseases [RCV002668536] Chr17:67218742 [GRCh38]
Chr17:65214858 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.4366C>T (p.Pro1456Ser) single nucleotide variant Inborn genetic diseases [RCV002672947] Chr17:67109239 [GRCh38]
Chr17:65105355 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.706A>G (p.Met236Val) single nucleotide variant Inborn genetic diseases [RCV002855575] Chr17:67190207 [GRCh38]
Chr17:65186323 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.3788A>G (p.Gln1263Arg) single nucleotide variant Inborn genetic diseases [RCV002940260] Chr17:67120455 [GRCh38]
Chr17:65116571 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.3500C>G (p.Pro1167Arg) single nucleotide variant Inborn genetic diseases [RCV002723846] Chr17:67123100 [GRCh38]
Chr17:65119216 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.4117A>G (p.Ile1373Val) single nucleotide variant Inborn genetic diseases [RCV002680304] Chr17:67109488 [GRCh38]
Chr17:65105604 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.4927G>C (p.Val1643Leu) single nucleotide variant Inborn genetic diseases [RCV003212108] Chr17:67107483 [GRCh38]
Chr17:65103599 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.5321T>C (p.Val1774Ala) single nucleotide variant Inborn genetic diseases [RCV003175518] Chr17:67087002 [GRCh38]
Chr17:65083118 [GRCh37]
Chr17:17q24.2
likely benign
NM_014877.4(HELZ):c.4922T>C (p.Ile1641Thr) single nucleotide variant Inborn genetic diseases [RCV003199718] Chr17:67107488 [GRCh38]
Chr17:65103604 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.1132A>G (p.Arg378Gly) single nucleotide variant Inborn genetic diseases [RCV003195576] Chr17:67188349 [GRCh38]
Chr17:65184465 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.4048C>T (p.His1350Tyr) single nucleotide variant Inborn genetic diseases [RCV003340319] Chr17:67109557 [GRCh38]
Chr17:65105673 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.3464T>C (p.Ile1155Thr) single nucleotide variant Inborn genetic diseases [RCV003344728] Chr17:67123136 [GRCh38]
Chr17:65119252 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.1985C>T (p.Pro662Leu) single nucleotide variant Inborn genetic diseases [RCV003345421] Chr17:67160987 [GRCh38]
Chr17:65157103 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.1744C>T (p.Arg582Trp) single nucleotide variant Inborn genetic diseases [RCV003363275] Chr17:67167483 [GRCh38]
Chr17:65163599 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.448C>T (p.Leu150Phe) single nucleotide variant Inborn genetic diseases [RCV003348415] Chr17:67195452 [GRCh38]
Chr17:65191568 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.5434C>G (p.Pro1812Ala) single nucleotide variant Inborn genetic diseases [RCV003352417] Chr17:67086889 [GRCh38]
Chr17:65083005 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.4244C>T (p.Pro1415Leu) single nucleotide variant Inborn genetic diseases [RCV003362219] Chr17:67109361 [GRCh38]
Chr17:65105477 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.4066C>T (p.Pro1356Ser) single nucleotide variant Inborn genetic diseases [RCV003366007] Chr17:67109539 [GRCh38]
Chr17:65105655 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.4766G>C (p.Ser1589Thr) single nucleotide variant Inborn genetic diseases [RCV003386406] Chr17:67107644 [GRCh38]
Chr17:65103760 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.2418G>A (p.Met806Ile) single nucleotide variant Inborn genetic diseases [RCV003366591] Chr17:67149924 [GRCh38]
Chr17:65146040 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.4955G>A (p.Arg1652His) single nucleotide variant not provided [RCV003428414] Chr17:67107455 [GRCh38]
Chr17:65103571 [GRCh37]
Chr17:17q24.2
uncertain significance
NM_014877.4(HELZ):c.1881A>G (p.Pro627=) single nucleotide variant not provided [RCV003413311] Chr17:67166492 [GRCh38]
Chr17:65162608 [GRCh37]
Chr17:17q24.2
likely benign
miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR30Ehsa-miR-30e-3pOncomiRDBexternal_infoNANA21963845

Predicted Target Of
Summary Value
Count of predictions:5777
Count of miRNA genes:1504
Interacting mature miRNAs:2053
Transcripts:ENST00000358691, ENST00000417253, ENST00000578783, ENST00000578938, ENST00000579861, ENST00000579953, ENST00000580168, ENST00000580662, ENST00000580963, ENST00000581159, ENST00000582864, ENST00000584641
Prediction methods:Miranda, Pita, 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
RH92736  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371765,183,116 - 65,183,241UniSTSGRCh37
Build 361762,613,578 - 62,613,703RGDNCBI36
Celera1761,755,747 - 61,755,872RGD
Cytogenetic Map17q24.2UniSTS
HuRef1760,571,411 - 60,571,536UniSTS
D17S584  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371765,119,869 - 65,119,997UniSTSGRCh37
Build 361762,550,331 - 62,550,459RGDNCBI36
Celera1761,692,514 - 61,692,642RGD
Cytogenetic Map17q24.2UniSTS
HuRef1760,508,328 - 60,508,456UniSTS
D17S1599  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371765,080,032 - 65,080,154UniSTSGRCh37
Build 361762,510,494 - 62,510,616RGDNCBI36
Celera1761,652,681 - 61,652,803RGD
Cytogenetic Map17q24.2UniSTS
HuRef1760,468,450 - 60,468,572UniSTS
RH47023  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371765,066,673 - 65,066,813UniSTSGRCh37
Build 361762,497,135 - 62,497,275RGDNCBI36
Celera1761,639,336 - 61,639,476RGD
Cytogenetic Map17q24.2UniSTS
HuRef1760,455,268 - 60,455,408UniSTS
GeneMap99-GB4 RH Map17422.21UniSTS
HELZ__7570  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371765,073,968 - 65,074,641UniSTSGRCh37
Build 361762,504,430 - 62,505,103RGDNCBI36
Celera1761,646,634 - 61,647,308RGD
HuRef1760,462,568 - 60,463,242UniSTS
STS-D29677  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371765,074,382 - 65,074,518UniSTSGRCh37
Build 361762,504,844 - 62,504,980RGDNCBI36
Celera1761,647,049 - 61,647,185RGD
Cytogenetic Map17q24.2UniSTS
HuRef1760,462,983 - 60,463,119UniSTS
GeneMap99-GB4 RH Map17422.11UniSTS
L18010  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371765,192,626 - 65,192,772UniSTSGRCh37
GRCh371765,192,626 - 65,192,752UniSTSGRCh37
Build 361762,623,088 - 62,623,214RGDNCBI36
Celera1761,765,259 - 61,765,405UniSTS
Celera1761,765,259 - 61,765,385RGD
Cytogenetic Map17q24.2UniSTS
HuRef1760,580,877 - 60,581,003UniSTS
HuRef1760,580,877 - 60,581,023UniSTS
SHGC-10970  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371765,074,071 - 65,074,250UniSTSGRCh37
Build 361762,504,533 - 62,504,712RGDNCBI36
Celera1761,646,737 - 61,646,916RGD
Cytogenetic Map17q24.2UniSTS
HuRef1760,462,671 - 60,462,850UniSTS
Stanford-G3 RH Map172835.0UniSTS
NCBI RH Map17697.6UniSTS
GeneMap99-G3 RH Map173336.0UniSTS
D10S275  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map13q12.13UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map14q22-q24UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map10p11UniSTS
Cytogenetic Map1p13.1UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map6q24UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map3p25UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9q22UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic MapXp22.2-p22.1UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map20pter-q11.23UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map10p12.3UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map3q26.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map1q24-q25.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map12q24.32UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map11p14.3UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map4q13UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map7p14.2UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map6q12-q13UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map2p14UniSTS
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
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map20p11.23-p11.21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map6p25.1-p23UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map13q12.1UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic MapXp21.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map12p13-p12UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map19pUniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8q22UniSTS
Cytogenetic Map4p15.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p16.3UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map6q22.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map3p21-p12UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p22-p21.33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map9q22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map2q31.3UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q32-q33UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map14q23-q24.2UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map2p24-p21UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic MapXq25-q26UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map15q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q26.2-q27UniSTS
Cytogenetic Map1q25.1-q25.2UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map4q32-q34UniSTS
Cytogenetic MapXq25-q26.1UniSTS
Cytogenetic Map2p25-p24UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp22.2-p22.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map20q11.22-q12UniSTS
Cytogenetic Map4q34.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q31.2UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map21q21.2UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map8q21.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map2q36.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map20p12UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9p22UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map22q13.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map11p14UniSTS
Cytogenetic Map1p32.1UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map11q23.2UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3p13UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map8q23UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map4q31.3UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic MapXq13UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map16q12-q13UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q13.1UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map22qUniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic MapXp22.12-p22.11UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map8p22-p21.3UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map1p36.12UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map7q22-qterUniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map5p15.1-p14.3UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic MapXq22.2UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p15.1UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map14q32.13UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map20q13.2-q13.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map6q16.3UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic MapXq27.1UniSTS
Cytogenetic Map8q12.3UniSTS
Cytogenetic Map5q21.2UniSTS
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
MARC_15239-15240:1012593750:1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371765,103,580 - 65,104,765UniSTSGRCh37
Celera1761,676,223 - 61,677,408UniSTS
HuRef1760,492,032 - 60,493,217UniSTS


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 869 554 916 126 879 95 1666 483 1210 146 1076 1348 45 1 686 940 5 2
Low 1570 2428 810 498 1066 370 2691 1711 2524 273 384 265 130 518 1848 1
Below cutoff 9 6 3

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001330447 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_014877 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005257888 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006722214 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006722215 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006722216 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011525544 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017025477 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017025478 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047437224 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047437225 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047437226 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047437227 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054318091 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054318092 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054318093 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054318094 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054318095 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054318096 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054318097 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001752712 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001752713 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001752714 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008484972 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA885317 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC005544 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC007448 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI271466 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK310217 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK310639 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL110161 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL699487 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL832149 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC056895 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC094881 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC130582 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC144083 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP353830 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471099 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  D29677 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000358691   ⟹   ENSP00000351524
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1767,070,444 - 67,245,196 (-)Ensembl
RefSeq Acc Id: ENST00000417253   ⟹   ENSP00000411144
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1767,167,526 - 67,245,187 (-)Ensembl
RefSeq Acc Id: ENST00000578783   ⟹   ENSP00000464354
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1767,167,712 - 67,188,401 (-)Ensembl
RefSeq Acc Id: ENST00000578938
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1767,176,321 - 67,188,361 (-)Ensembl
RefSeq Acc Id: ENST00000579861   ⟹   ENSP00000462320
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1767,218,608 - 67,239,800 (-)Ensembl
RefSeq Acc Id: ENST00000579953   ⟹   ENSP00000463727
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1767,077,929 - 67,239,468 (-)Ensembl
RefSeq Acc Id: ENST00000580168   ⟹   ENSP00000464512
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1767,077,972 - 67,245,183 (-)Ensembl
RefSeq Acc Id: ENST00000580662
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1767,190,189 - 67,245,178 (-)Ensembl
RefSeq Acc Id: ENST00000580963
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1767,215,788 - 67,245,178 (-)Ensembl
RefSeq Acc Id: ENST00000581159   ⟹   ENSP00000462763
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1767,203,380 - 67,245,989 (-)Ensembl
RefSeq Acc Id: ENST00000582864
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1767,188,218 - 67,189,614 (-)Ensembl
RefSeq Acc Id: ENST00000584641
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1767,200,613 - 67,245,172 (-)Ensembl
RefSeq Acc Id: NM_001330447   ⟹   NP_001317376
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381767,070,444 - 67,245,196 (-)NCBI
T2T-CHM13v2.01767,946,238 - 68,120,957 (-)NCBI
Sequence:
RefSeq Acc Id: NM_014877   ⟹   NP_055692
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381767,070,444 - 67,245,196 (-)NCBI
GRCh371765,066,554 - 65,241,349 (-)NCBI
Build 361762,497,016 - 62,671,781 (-)NCBI Archive
Celera1761,639,217 - 61,813,834 (-)RGD
HuRef1760,455,149 - 60,628,698 (-)ENTREZGENE
CHM1_11765,130,487 - 65,305,305 (-)NCBI
T2T-CHM13v2.01767,946,238 - 68,120,957 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005257888   ⟹   XP_005257945
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381767,070,444 - 67,245,196 (-)NCBI
GRCh371765,066,554 - 65,241,349 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006722214   ⟹   XP_006722277
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381767,070,444 - 67,245,196 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011525544   ⟹   XP_011523846
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381767,070,444 - 67,245,989 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047437224   ⟹   XP_047293180
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381767,070,444 - 67,245,989 (-)NCBI
RefSeq Acc Id: XM_047437225   ⟹   XP_047293181
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381767,070,444 - 67,245,989 (-)NCBI
RefSeq Acc Id: XM_047437226   ⟹   XP_047293182
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381767,070,444 - 67,201,181 (-)NCBI
RefSeq Acc Id: XM_047437227   ⟹   XP_047293183
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381767,070,444 - 67,185,035 (-)NCBI
RefSeq Acc Id: XM_054318091   ⟹   XP_054174066
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01767,946,238 - 68,120,957 (-)NCBI
RefSeq Acc Id: XM_054318092   ⟹   XP_054174067
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01767,946,238 - 68,121,750 (-)NCBI
RefSeq Acc Id: XM_054318093   ⟹   XP_054174068
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01767,946,238 - 68,120,957 (-)NCBI
RefSeq Acc Id: XM_054318094   ⟹   XP_054174069
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01767,946,238 - 68,121,779 (-)NCBI
RefSeq Acc Id: XM_054318095   ⟹   XP_054174070
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01767,946,238 - 68,123,293 (-)NCBI
RefSeq Acc Id: XM_054318096   ⟹   XP_054174071
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01767,946,238 - 68,076,962 (-)NCBI
RefSeq Acc Id: XM_054318097   ⟹   XP_054174072
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01767,946,238 - 68,060,814 (-)NCBI
RefSeq Acc Id: XR_001752712
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381767,123,970 - 67,245,196 (-)NCBI
Sequence:
RefSeq Acc Id: XR_008484972
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01767,999,781 - 68,120,957 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001317376 (Get FASTA)   NCBI Sequence Viewer  
  NP_055692 (Get FASTA)   NCBI Sequence Viewer  
  XP_005257945 (Get FASTA)   NCBI Sequence Viewer  
  XP_006722277 (Get FASTA)   NCBI Sequence Viewer  
  XP_011523846 (Get FASTA)   NCBI Sequence Viewer  
  XP_047293180 (Get FASTA)   NCBI Sequence Viewer  
  XP_047293181 (Get FASTA)   NCBI Sequence Viewer  
  XP_047293182 (Get FASTA)   NCBI Sequence Viewer  
  XP_047293183 (Get FASTA)   NCBI Sequence Viewer  
  XP_054174066 (Get FASTA)   NCBI Sequence Viewer  
  XP_054174067 (Get FASTA)   NCBI Sequence Viewer  
  XP_054174068 (Get FASTA)   NCBI Sequence Viewer  
  XP_054174069 (Get FASTA)   NCBI Sequence Viewer  
  XP_054174070 (Get FASTA)   NCBI Sequence Viewer  
  XP_054174071 (Get FASTA)   NCBI Sequence Viewer  
  XP_054174072 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH56895 (Get FASTA)   NCBI Sequence Viewer  
  AAH94881 (Get FASTA)   NCBI Sequence Viewer  
  AAI30583 (Get FASTA)   NCBI Sequence Viewer  
  AAI44084 (Get FASTA)   NCBI Sequence Viewer  
  BAA06147 (Get FASTA)   NCBI Sequence Viewer  
  EAW89023 (Get FASTA)   NCBI Sequence Viewer  
  EAW89024 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000351524
  ENSP00000351524.5
  ENSP00000411144.3
  ENSP00000462320.1
  ENSP00000462763.1
  ENSP00000463727.1
  ENSP00000464354.1
  ENSP00000464512
  ENSP00000464512.1
GenBank Protein P42694 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_055692   ⟸   NM_014877
- Peptide Label: isoform 1
- UniProtKB: P42694 (UniProtKB/Swiss-Prot),   I6L9H4 (UniProtKB/Swiss-Prot),   A0A2P0H7U5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005257945   ⟸   XM_005257888
- Peptide Label: isoform X2
- UniProtKB: A0A2P0H7U5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006722277   ⟸   XM_006722214
- Peptide Label: isoform X1
- UniProtKB: B7ZLW2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011523846   ⟸   XM_011525544
- Peptide Label: isoform X1
- UniProtKB: B7ZLW2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001317376   ⟸   NM_001330447
- Peptide Label: isoform 2
- UniProtKB: J3QS41 (UniProtKB/TrEMBL),   B7ZLW2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000464512   ⟸   ENST00000580168
RefSeq Acc Id: ENSP00000462763   ⟸   ENST00000581159
RefSeq Acc Id: ENSP00000411144   ⟸   ENST00000417253
RefSeq Acc Id: ENSP00000464354   ⟸   ENST00000578783
RefSeq Acc Id: ENSP00000463727   ⟸   ENST00000579953
RefSeq Acc Id: ENSP00000462320   ⟸   ENST00000579861
RefSeq Acc Id: ENSP00000351524   ⟸   ENST00000358691
RefSeq Acc Id: XP_047293181   ⟸   XM_047437225
- Peptide Label: isoform X4
- UniProtKB: P42694 (UniProtKB/Swiss-Prot),   I6L9H4 (UniProtKB/Swiss-Prot),   A0A2P0H7U5 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047293180   ⟸   XM_047437224
- Peptide Label: isoform X3
- UniProtKB: J3QS41 (UniProtKB/TrEMBL),   B7ZLW2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047293182   ⟸   XM_047437226
- Peptide Label: isoform X5
- UniProtKB: B7ZLW2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047293183   ⟸   XM_047437227
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054174070   ⟸   XM_054318095
- Peptide Label: isoform X4
- UniProtKB: A0A2P0H7U5 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054174069   ⟸   XM_054318094
- Peptide Label: isoform X3
- UniProtKB: B7ZLW2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054174067   ⟸   XM_054318092
- Peptide Label: isoform X1
- UniProtKB: B7ZLW2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054174068   ⟸   XM_054318093
- Peptide Label: isoform X2
- UniProtKB: A0A2P0H7U5 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054174066   ⟸   XM_054318091
- Peptide Label: isoform X1
- UniProtKB: B7ZLW2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054174071   ⟸   XM_054318096
- Peptide Label: isoform X5
- UniProtKB: B7ZLW2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054174072   ⟸   XM_054318097
- Peptide Label: isoform X6
Protein Domains
C3H1-type

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P42694-F1-model_v2 AlphaFold P42694 1-1942 view protein structure

Promoters
RGD ID:6794194
Promoter ID:HG_KWN:26909
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_014877,   UC010DES.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361762,671,636 - 62,672,577 (-)MPROMDB
RGD ID:7236079
Promoter ID:EPDNEW_H23786
Type:initiation region
Name:HELZ_1
Description:helicase with zinc finger
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H23787  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381767,245,178 - 67,245,238EPDNEW
RGD ID:7236081
Promoter ID:EPDNEW_H23787
Type:initiation region
Name:HELZ_2
Description:helicase with zinc finger
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H23786  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381767,245,953 - 67,246,013EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:16878 AgrOrtholog
COSMIC HELZ COSMIC
Ensembl Genes ENSG00000198265 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000358691 ENTREZGENE
  ENST00000358691.10 UniProtKB/Swiss-Prot
  ENST00000417253.7 UniProtKB/TrEMBL
  ENST00000578783.1 UniProtKB/TrEMBL
  ENST00000579861.1 UniProtKB/TrEMBL
  ENST00000579953.5 UniProtKB/Swiss-Prot
  ENST00000580168 ENTREZGENE
  ENST00000580168.5 UniProtKB/TrEMBL
  ENST00000581159.5 UniProtKB/TrEMBL
Gene3D-CATH 1.25.40.10 UniProtKB/TrEMBL
  3.40.50.300 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Zinc finger, CCCH-type UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000198265 GTEx
HGNC ID HGNC:16878 ENTREZGENE
Human Proteome Map HELZ Human Proteome Map
InterPro DNA2/NAM7-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DNA2/NAM7-like_AAA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DNA2/NAM7_AAA_11 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Helicase/UvrB_N UniProtKB/TrEMBL
  P-loop_NTPase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SF1_C_Upf1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TPR-like_helical_dom_sf UniProtKB/TrEMBL
  UvrD-like_ATP-bd UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_CCCH UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_CCCH_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:9931 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 9931 ENTREZGENE
OMIM 606699 OMIM
PANTHER HELICASE WITH ZINC FINGER DOMAIN-RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR10887 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam AAA_11 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  AAA_12 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ResIII UniProtKB/TrEMBL
  UvrD-helicase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  zf-CCCH UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA29238 PharmGKB
PROSITE ZF_C3H1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART ZnF_C3H1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF48452 UniProtKB/TrEMBL
  SSF52540 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF90229 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A075B6R3_HUMAN UniProtKB/TrEMBL
  A0A2P0H7U5 ENTREZGENE, UniProtKB/TrEMBL
  B7ZLW2 ENTREZGENE, UniProtKB/TrEMBL
  C1KEM4_HUMAN UniProtKB/TrEMBL
  C1KEM5_HUMAN UniProtKB/TrEMBL
  HELZ_HUMAN UniProtKB/Swiss-Prot
  I6L9H4 ENTREZGENE
  J3KS59_HUMAN UniProtKB/TrEMBL
  J3KT20_HUMAN UniProtKB/TrEMBL
  J3QRR8_HUMAN UniProtKB/TrEMBL
  J3QS41 ENTREZGENE, UniProtKB/TrEMBL
  P42694 ENTREZGENE
  Q6PGP6_HUMAN UniProtKB/TrEMBL
UniProt Secondary I6L9H4 UniProtKB/Swiss-Prot