ZNF707 (zinc finger protein 707) - Rat Genome Database

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Gene: ZNF707 (zinc finger protein 707) Homo sapiens
Analyze
Symbol: ZNF707
Name: zinc finger protein 707
RGD ID: 1603343
Description:
Type: ncrna
RefSeq Status: VALIDATED
RGD Orthologs
Chinchilla
Bonobo
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl8143,684,452 - 143,713,898 (+)EnsemblGRCh38hg38GRCh38
GRCh388143,708,051 - 143,713,898 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh378144,790,221 - 144,796,068 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 368144,838,610 - 144,849,543 (+)NCBINCBI36hg18NCBI36
Celera8141,077,613 - 141,088,543 (+)NCBI
Cytogenetic Map8q24.3NCBI
HuRef8140,042,991 - 140,048,894 (+)NCBIHuRef
CHM1_18144,830,237 - 144,836,112 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


References


Genomics

Comparative Map Data
ZNF707
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl8143,684,452 - 143,713,898 (+)EnsemblGRCh38hg38GRCh38
GRCh388143,708,051 - 143,713,898 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh378144,790,221 - 144,796,068 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 368144,838,610 - 144,849,543 (+)NCBINCBI36hg18NCBI36
Celera8141,077,613 - 141,088,543 (+)NCBI
Cytogenetic Map8q24.3NCBI
HuRef8140,042,991 - 140,048,894 (+)NCBIHuRef
CHM1_18144,830,237 - 144,836,112 (+)NCBICHM1_1
Znf707
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_0049554542,377,306 - 2,387,449 (+)NCBIChiLan1.0ChiLan1.0
ZNF707
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.18143,451,966 - 143,462,051 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl8143,451,994 - 143,462,314 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v08140,437,170 - 140,448,765 (+)NCBIMhudiblu_PPA_v0panPan3
Znf707
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244053031,023,455 - 1,032,237 (-)NCBI
SpeTri2.0NW_0049364708,449,554 - 8,458,330 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
LOC110257542
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.11855,960,637 - 55,967,427 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
ZNF707
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.18137,895,455 - 137,906,765 (+)NCBI
ChlSab1.1 Ensembl8137,901,513 - 137,905,923 (+)Ensembl
Znf707
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462473513,083,303 - 13,094,773 (-)NCBI

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:10419
Count of miRNA genes:1212
Interacting mature miRNAs:1557
Transcripts:ENST00000358656, ENST00000418203, ENST00000442058, ENST00000454097, ENST00000508587, ENST00000525185, ENST00000525538, ENST00000525619, ENST00000525862, ENST00000526315, ENST00000526970, ENST00000527293, ENST00000527561, ENST00000528134, ENST00000528456, ENST00000529833, ENST00000530341, ENST00000530574, ENST00000531254, ENST00000531811, ENST00000531985, ENST00000532003, ENST00000532158, ENST00000532205, ENST00000532486, ENST00000532571, ENST00000533031, ENST00000533254, ENST00000534303, ENST00000534589
Prediction methods:Microtar, Miranda, Rnahybrid
Result types:miRGate_prediction

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

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


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 38 3 80 9 224 10 63 14 48 10 506 163 8 34
Low 2400 2948 1646 615 1701 455 4282 2150 3649 409 952 1450 167 1 1204 2742 6 2
Below cutoff 1 40 25 12 33 37 12

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000358656   ⟹   ENSP00000351482
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,479 - 143,695,385 (+)Ensembl
RefSeq Acc Id: ENST00000418203   ⟹   ENSP00000413215
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,688,659 - 143,695,380 (+)Ensembl
RefSeq Acc Id: ENST00000442058   ⟹   ENSP00000393748
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,481 - 143,691,700 (+)Ensembl
RefSeq Acc Id: ENST00000508587
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,708,051 - 143,713,898 (+)Ensembl
RefSeq Acc Id: ENST00000525185   ⟹   ENSP00000434791
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,452 - 143,693,830 (+)Ensembl
RefSeq Acc Id: ENST00000525538
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,481 - 143,691,914 (+)Ensembl
RefSeq Acc Id: ENST00000525619
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,462 - 143,690,419 (+)Ensembl
RefSeq Acc Id: ENST00000525862   ⟹   ENSP00000436394
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,507 - 143,693,703 (+)Ensembl
RefSeq Acc Id: ENST00000526315   ⟹   ENSP00000435906
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,508 - 143,693,959 (+)Ensembl
RefSeq Acc Id: ENST00000526970   ⟹   ENSP00000436634
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,487 - 143,691,199 (+)Ensembl
RefSeq Acc Id: ENST00000527293   ⟹   ENSP00000434215
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,479 - 143,693,756 (+)Ensembl
RefSeq Acc Id: ENST00000527561   ⟹   ENSP00000495224
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,484 - 143,712,737 (+)Ensembl
RefSeq Acc Id: ENST00000528134
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,505 - 143,691,426 (+)Ensembl
RefSeq Acc Id: ENST00000528456   ⟹   ENSP00000435251
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,462 - 143,693,772 (+)Ensembl
RefSeq Acc Id: ENST00000529833   ⟹   ENSP00000434503
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,473 - 143,691,694 (+)Ensembl
RefSeq Acc Id: ENST00000530341
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,510 - 143,693,711 (+)Ensembl
RefSeq Acc Id: ENST00000530574   ⟹   ENSP00000436362
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,473 - 143,693,827 (+)Ensembl
RefSeq Acc Id: ENST00000531254
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,691,515 - 143,694,029 (+)Ensembl
RefSeq Acc Id: ENST00000531811
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,483 - 143,693,748 (+)Ensembl
RefSeq Acc Id: ENST00000531985   ⟹   ENSP00000435679
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,479 - 143,693,723 (+)Ensembl
RefSeq Acc Id: ENST00000532003
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,452 - 143,691,474 (+)Ensembl
RefSeq Acc Id: ENST00000532158   ⟹   ENSP00000436250
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,492 - 143,695,357 (+)Ensembl
RefSeq Acc Id: ENST00000532205   ⟹   ENSP00000436212
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,508 - 143,695,380 (+)Ensembl
RefSeq Acc Id: ENST00000532486
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,484 - 143,695,384 (+)Ensembl
RefSeq Acc Id: ENST00000532571
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,482 - 143,690,099 (+)Ensembl
RefSeq Acc Id: ENST00000533031   ⟹   ENSP00000434322
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,456 - 143,695,356 (+)Ensembl
RefSeq Acc Id: ENST00000533254
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,481 - 143,691,393 (+)Ensembl
RefSeq Acc Id: ENST00000534303   ⟹   ENSP00000437134
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,453 - 143,693,839 (+)Ensembl
RefSeq Acc Id: ENST00000534589
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8143,684,482 - 143,691,811 (+)Ensembl
RefSeq Acc Id: NR_134306
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388143,708,051 - 143,713,898 (+)NCBI
Sequence:
Promoters
RGD ID:7214393
Promoter ID:EPDNEW_H12936
Type:initiation region
Name:ZNF707_2
Description:zinc finger protein 707
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H12935  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh388143,708,002 - 143,708,062EPDNEW
RGD ID:6807191
Promoter ID:HG_KWN:62276
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_001100598,   NM_001100599,   NM_173831,   UC003YZF.2,   UC003YZG.2,   UC003YZH.2
Position:
Human AssemblyChrPosition (strand)Source
Build 368144,838,434 - 144,838,934 (+)MPROMDB

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 8q24.21-24.3(chr8:128220912-145049449)x3 copy number gain See cases [RCV000050830] Chr8:128220912..145049449 [GRCh38]
Chr8:129233158..146274835 [GRCh37]
Chr8:129302340..146245639 [NCBI36]
Chr8:8q24.21-24.3
pathogenic
GRCh38/hg38 8q23.3-24.3(chr8:113580402-145054634)x3 copy number gain See cases [RCV000050638] Chr8:113580402..145054634 [GRCh38]
Chr8:114592631..146280020 [GRCh37]
Chr8:114661807..146250824 [NCBI36]
Chr8:8q23.3-24.3
pathogenic
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 8q22.1-24.3(chr8:95606052-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053677]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053677]|See cases [RCV000053677] Chr8:95606052..145054775 [GRCh38]
Chr8:96618280..146280161 [GRCh37]
Chr8:96687456..146250965 [NCBI36]
Chr8:8q22.1-24.3
pathogenic
GRCh38/hg38 8q24.13-24.3(chr8:124514090-145054634)x3 copy number gain See cases [RCV000053678] Chr8:124514090..145054634 [GRCh38]
Chr8:125526331..146280020 [GRCh37]
Chr8:125595512..146250824 [NCBI36]
Chr8:8q24.13-24.3
pathogenic
GRCh38/hg38 8q24.3(chr8:139447227-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053701]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053701]|See cases [RCV000053701] Chr8:139447227..145054775 [GRCh38]
Chr8:140459470..146280161 [GRCh37]
Chr8:140528652..146250965 [NCBI36]
Chr8:8q24.3
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 8p23.3-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 8q24.3(chr8:143684819-144287978)x1 copy number loss See cases [RCV000054310] Chr8:143684819..144287978 [GRCh38]
Chr8:144940777..145511679 [GRCh37]
Chr8:144838977..145482487 [NCBI36]
Chr8:8q24.3
pathogenic
NM_001100598.1(ZNF707):c.459C>T (p.Leu153=) single nucleotide variant Malignant melanoma [RCV000068199] Chr8:143693873 [GRCh38]
Chr8:144776043 [GRCh37]
Chr8:144848031 [NCBI36]
Chr8:8q24.3
not provided
GRCh38/hg38 8q22.1-24.3(chr8:94682154-145068656)x3 copy number gain See cases [RCV000134353] Chr8:94682154..145068656 [GRCh38]
Chr8:95694382..146294042 [GRCh37]
Chr8:95763558..146264846 [NCBI36]
Chr8:8q22.1-24.3
pathogenic
GRCh38/hg38 8q24.3(chr8:142201468-144002730)x1 copy number loss See cases [RCV000135981] Chr8:142201468..144002730 [GRCh38]
Chr8:143282829..145076898 [GRCh37]
Chr8:143280736..145148886 [NCBI36]
Chr8:8q24.3
pathogenic
GRCh38/hg38 8q24.22-24.3(chr8:130639182-145068712)x3 copy number gain See cases [RCV000137644] Chr8:130639182..145068712 [GRCh38]
Chr8:131651428..146294098 [GRCh37]
Chr8:131720610..146264902 [NCBI36]
Chr8:8q24.22-24.3
pathogenic|conflicting data from submitters
GRCh38/hg38 8q24.3(chr8:139236824-145068712)x3 copy number gain See cases [RCV000137466] Chr8:139236824..145068712 [GRCh38]
Chr8:140249067..146294098 [GRCh37]
Chr8:140318249..146264902 [NCBI36]
Chr8:8q24.3
likely pathogenic
GRCh38/hg38 8q24.3(chr8:139004218-145049449)x3 copy number gain See cases [RCV000137340] Chr8:139004218..145049449 [GRCh38]
Chr8:140016461..146274835 [GRCh37]
Chr8:140085643..146245639 [NCBI36]
Chr8:8q24.3
likely pathogenic
GRCh38/hg38 8q24.13-24.3(chr8:124498498-145068712)x3 copy number gain See cases [RCV000137346] Chr8:124498498..145068712 [GRCh38]
Chr8:125510739..146294098 [GRCh37]
Chr8:125579920..146264902 [NCBI36]
Chr8:8q24.13-24.3
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 8q21.3-24.3(chr8:87931152-145068712)x3 copy number gain See cases [RCV000138551] Chr8:87931152..145068712 [GRCh38]
Chr8:88943380..146294098 [GRCh37]
Chr8:89012496..146264902 [NCBI36]
Chr8:8q21.3-24.3
pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:77480050-145068712)x3 copy number gain See cases [RCV000139036] Chr8:77480050..145068712 [GRCh38]
Chr8:78392286..146294098 [GRCh37]
Chr8:78554841..146264902 [NCBI36]
Chr8:8q21.13-24.3
pathogenic
GRCh38/hg38 8q22.1-24.3(chr8:97382873-145070385)x3 copy number gain See cases [RCV000140447] Chr8:97382873..145070385 [GRCh38]
Chr8:98395101..146295771 [GRCh37]
Chr8:98464277..146266575 [NCBI36]
Chr8:8q22.1-24.3
pathogenic
GRCh38/hg38 8q24.3(chr8:141738068-144140607)x1 copy number loss See cases [RCV000140913] Chr8:141738068..144140607 [GRCh38]
Chr8:142764538..145195510 [GRCh37]
Chr8:142823655..145267498 [NCBI36]
Chr8:8q24.3
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 8q22.3-24.3(chr8:100867343-145070385)x3 copy number gain See cases [RCV000141694] Chr8:100867343..145070385 [GRCh38]
Chr8:101879571..146295771 [GRCh37]
Chr8:101948747..146266575 [NCBI36]
Chr8:8q22.3-24.3
pathogenic
GRCh38/hg38 8p21.3-q24.3(chr8:21291522-145070385)x3 copy number gain See cases [RCV000142021] Chr8:21291522..145070385 [GRCh38]
Chr8:21149033..146295771 [GRCh37]
Chr8:21193313..146266575 [NCBI36]
Chr8:8p21.3-q24.3
pathogenic
GRCh38/hg38 8q22.3-24.3(chr8:103306336-145068712)x3 copy number gain See cases [RCV000142810] Chr8:103306336..145068712 [GRCh38]
Chr8:104318564..146294098 [GRCh37]
Chr8:104387740..146264902 [NCBI36]
Chr8:8q22.3-24.3
pathogenic|likely 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 8q21.13-24.3(chr8:78614077-145054634)x3 copy number gain See cases [RCV000142597] Chr8:78614077..145054634 [GRCh38]
Chr8:79526312..146280020 [GRCh37]
Chr8:79688867..146250824 [NCBI36]
Chr8:8q21.13-24.3
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 8q21.2-24.3(chr8:85765999-145070385)x3 copy number gain See cases [RCV000143659] Chr8:85765999..145070385 [GRCh38]
Chr8:86778228..146295771 [GRCh37]
Chr8:86863079..146266575 [NCBI36]
Chr8:8q21.2-24.3
pathogenic
GRCh38/hg38 8q24.13-24.3(chr8:124514090-145054634)x3 copy number gain See cases [RCV000148117] Chr8:124514090..145054634 [GRCh38]
Chr8:125526331..146280020 [GRCh37]
Chr8:125595512..146250824 [NCBI36]
Chr8:8q24.13-24.3
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:27815 AgrOrtholog
COSMIC ZNF707 COSMIC
Ensembl Genes ENSG00000181135 Ensembl, ENTREZGENE
Ensembl Transcript ENST00000508587 ENTREZGENE
GTEx ENSG00000181135 GTEx
Human Proteome Map ZNF707 Human Proteome Map
NCBI Gene LOC101928160 ENTREZGENE
RNAcentral URS00008C141A RNACentral