ZNF615 (zinc finger protein 615) - Rat Genome Database

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Gene: ZNF615 (zinc finger protein 615) Homo sapiens
Analyze
Symbol: ZNF615
Name: zinc finger protein 615
RGD ID: 1353580
HGNC Page HGNC:24740
Description: Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: DKFZp686O1554; FLJ33710; FLJ39372
RGD Orthologs
Bonobo
Squirrel
Pig
Green Monkey
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
GRCh381951,991,332 - 52,008,211 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1951,991,332 - 52,008,230 (-)EnsemblGRCh38hg38GRCh38
GRCh371952,494,585 - 52,511,464 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361957,186,400 - 57,203,270 (-)NCBINCBI36Build 36hg18NCBI36
Build 341957,186,399 - 57,203,270NCBI
Celera1949,544,146 - 49,561,016 (-)NCBICelera
Cytogenetic Map19q13.41NCBI
HuRef1948,825,231 - 48,842,127 (-)NCBIHuRef
CHM1_11952,496,445 - 52,513,341 (-)NCBICHM1_1
T2T-CHM13v2.01955,078,529 - 55,095,409 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
nucleus  (IBA,IEA)

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
4. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, etal., Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. Epub 2002 Dec 11.
Additional References at PubMed
PMID:14702039   PMID:16344560   PMID:21873635   PMID:29507755   PMID:34079125   PMID:35563538   PMID:36168627  


Genomics

Comparative Map Data
ZNF615
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381951,991,332 - 52,008,211 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1951,991,332 - 52,008,230 (-)EnsemblGRCh38hg38GRCh38
GRCh371952,494,585 - 52,511,464 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361957,186,400 - 57,203,270 (-)NCBINCBI36Build 36hg18NCBI36
Build 341957,186,399 - 57,203,270NCBI
Celera1949,544,146 - 49,561,016 (-)NCBICelera
Cytogenetic Map19q13.41NCBI
HuRef1948,825,231 - 48,842,127 (-)NCBIHuRef
CHM1_11952,496,445 - 52,513,341 (-)NCBICHM1_1
T2T-CHM13v2.01955,078,529 - 55,095,409 (-)NCBIT2T-CHM13v2.0
ZNF615
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22058,033,901 - 58,050,765 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11959,956,419 - 59,975,068 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01948,934,529 - 48,951,400 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11957,813,499 - 57,830,360 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1957,813,499 - 57,830,360 (-)Ensemblpanpan1.1panPan2
Znf615
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244093494,635,408 - 4,637,318 (-)NCBIHiC_Itri_2
SpeTri2.0NW_004937026261,317 - 265,286 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ZNF615
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1658,057,509 - 58,079,057 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2652,111,591 - 52,131,820 (+)NCBISscrofa10.2Sscrofa10.2susScr3
ZNF615
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1644,808,575 - 44,820,020 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl644,809,408 - 44,814,443 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366607324,865,905 - 24,877,241 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in ZNF615
27 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19q13.33-13.43(chr19:50191219-58535818)x3 copy number gain See cases [RCV000050883] Chr19:50191219..58535818 [GRCh38]
Chr19:50694476..59047185 [GRCh37]
Chr19:55386288..63738997 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:49907832-58557889)x3 copy number gain See cases [RCV000052925] Chr19:49907832..58557889 [GRCh38]
Chr19:50411089..59069256 [GRCh37]
Chr19:55102901..63761068 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:51141518-58539965)x3 copy number gain See cases [RCV000052926] Chr19:51141518..58539965 [GRCh38]
Chr19:51644775..59051332 [GRCh37]
Chr19:56336587..63743144 [NCBI36]
Chr19:19q13.41-13.43		 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3 copy number gain See cases [RCV000052914] Chr19:47908540..58539965 [GRCh38]
Chr19:48411797..59051332 [GRCh37]
Chr19:53103609..63743144 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3 copy number gain See cases [RCV000052915] Chr19:47929575..58572206 [GRCh38]
Chr19:48432832..59083573 [GRCh37]
Chr19:53124644..63775385 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.41(chr19:51824349-52113443)x3 copy number gain See cases [RCV000052592] Chr19:51824349..52113443 [GRCh38]
Chr19:52327602..52616696 [GRCh37]
Chr19:57019414..57308508 [NCBI36]
Chr19:19q13.41		 uncertain significance
NM_001199324.1(ZNF615):c.526C>T (p.Leu176Phe) single nucleotide variant Malignant melanoma [RCV000063614] Chr19:51994583 [GRCh38]
Chr19:52497836 [GRCh37]
Chr19:57189648 [NCBI36]
Chr19:19q13.41		 not provided
GRCh38/hg38 19q13.33-13.43(chr19:50152520-58581203)x3 copy number gain See cases [RCV000135843] Chr19:50152520..58581203 [GRCh38]
Chr19:50655777..59092570 [GRCh37]
Chr19:55347589..63784382 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.41(chr19:51865544-52113443)x3 copy number gain See cases [RCV000136779] Chr19:51865544..52113443 [GRCh38]
Chr19:52368797..52616696 [GRCh37]
Chr19:57060609..57308508 [NCBI36]
Chr19:19q13.41		 benign
GRCh38/hg38 19q13.41(chr19:51785545-52075049)x3 copy number gain See cases [RCV000142949] Chr19:51785545..52075049 [GRCh38]
Chr19:52288798..52578302 [GRCh37]
Chr19:56980610..57270114 [NCBI36]
Chr19:19q13.41		 likely benign
GRCh38/hg38 19q13.41(chr19:51769103-52124150)x3 copy number gain See cases [RCV000142704] Chr19:51769103..52124150 [GRCh38]
Chr19:52272356..52627403 [GRCh37]
Chr19:56964168..57319215 [NCBI36]
Chr19:19q13.41		 benign
GRCh38/hg38 19q13.41(chr19:51202361-51993020)x3 copy number gain See cases [RCV000143450] Chr19:51202361..51993020 [GRCh38]
Chr19:51705617..52496273 [GRCh37]
Chr19:56397429..57188085 [NCBI36]
Chr19:19q13.41		 uncertain significance
NM_001005738.1(FPR2):c.*290_*344331dup duplication Gestational diabetes mellitus uncontrolled [RCV000161884] Chr19:51770004..52114045 [GRCh38]
Chr19:52273257..52617298 [GRCh37]
Chr19:19q13.41		 not provided
GRCh37/hg19 19q13.41(chr19:52272131-52588718)x3 copy number gain Premature ovarian failure [RCV000225187] Chr19:52272131..52588718 [GRCh37]
Chr19:19q13.41		 benign
GRCh37/hg19 19q13.41(chr19:52273257-52612066)x3 copy number gain not provided [RCV000752751] Chr19:52273257..52612066 [GRCh37]
Chr19:19q13.41		 benign
GRCh37/hg19 19q13.33-13.43(chr19:50489390-59095359)x3 copy number gain See cases [RCV000445925] Chr19:50489390..59095359 [GRCh37]
Chr19:19q13.33-13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 copy number gain See cases [RCV000511289] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic|uncertain significance
NM_001199324.2(ZNF615):c.1466A>G (p.His489Arg) single nucleotide variant Inborn genetic diseases [RCV003289916] Chr19:51993643 [GRCh38]
Chr19:52496896 [GRCh37]
Chr19:19q13.41		 uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) copy number gain See cases [RCV000512296] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19q13.41(chr19:52273226-52617298)x3 copy number gain not provided [RCV000752749] Chr19:52273226..52617298 [GRCh37]
Chr19:19q13.41		 benign
GRCh37/hg19 19q13.41(chr19:52273226-52631600)x3 copy number gain not provided [RCV000752750] Chr19:52273226..52631600 [GRCh37]
Chr19:19q13.41		 benign
GRCh37/hg19 19q13.41(chr19:52287452-52612066)x3 copy number gain not provided [RCV000752752] Chr19:52287452..52612066 [GRCh37]
Chr19:19q13.41		 benign
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3 copy number gain not provided [RCV000752444] Chr19:260912..59097160 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 copy number gain not provided [RCV000752439] Chr19:68029..59110290 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19q13.33-13.43(chr19:50740074-59097160)x3 copy number gain not provided [RCV000740208] Chr19:50740074..59097160 [GRCh37]
Chr19:19q13.33-13.43		 pathogenic
GRCh37/hg19 19q13.31-13.42(chr19:44738088-53621561)x3 copy number gain not provided [RCV001007050] Chr19:44738088..53621561 [GRCh37]
Chr19:19q13.31-13.42		 pathogenic
GRCh37/hg19 19q13.32-13.42(chr19:47939842-54626871) copy number gain not provided [RCV001249294] Chr19:47939842..54626871 [GRCh37]
Chr19:19q13.32-13.42		 not provided
GRCh37/hg19 19q13.33-13.43(chr19:48463931-57095254)x3 copy number gain not provided [RCV001259944] Chr19:48463931..57095254 [GRCh37]
Chr19:19q13.33-13.43		 pathogenic
GRCh37/hg19 19q13.33-13.41(chr19:49911081-53127438) copy number gain not specified [RCV002052689] Chr19:49911081..53127438 [GRCh37]
Chr19:19q13.33-13.41		 likely pathogenic
NM_001199324.2(ZNF615):c.652A>C (p.Ser218Arg) single nucleotide variant Inborn genetic diseases [RCV003258258] Chr19:51994457 [GRCh38]
Chr19:52497710 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.2188C>T (p.His730Tyr) single nucleotide variant Inborn genetic diseases [RCV002684039] Chr19:51992921 [GRCh38]
Chr19:52496174 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.2013C>A (p.Phe671Leu) single nucleotide variant Inborn genetic diseases [RCV002691794] Chr19:51993096 [GRCh38]
Chr19:52496349 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.920C>G (p.Ala307Gly) single nucleotide variant Inborn genetic diseases [RCV002694067] Chr19:51994189 [GRCh38]
Chr19:52497442 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.1082G>A (p.Gly361Glu) single nucleotide variant Inborn genetic diseases [RCV002694099] Chr19:51994027 [GRCh38]
Chr19:52497280 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.1177A>G (p.Thr393Ala) single nucleotide variant Inborn genetic diseases [RCV002757590] Chr19:51993932 [GRCh38]
Chr19:52497185 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.956G>A (p.Arg319Gln) single nucleotide variant Inborn genetic diseases [RCV002956549] Chr19:51994153 [GRCh38]
Chr19:52497406 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.1376G>A (p.Arg459Gln) single nucleotide variant Inborn genetic diseases [RCV002666141] Chr19:51993733 [GRCh38]
Chr19:52496986 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.623C>T (p.Thr208Ile) single nucleotide variant Inborn genetic diseases [RCV002673892] Chr19:51994486 [GRCh38]
Chr19:52497739 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.1882A>C (p.Thr628Pro) single nucleotide variant Inborn genetic diseases [RCV002648597] Chr19:51993227 [GRCh38]
Chr19:52496480 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.106G>A (p.Val36Met) single nucleotide variant Inborn genetic diseases [RCV002877976] Chr19:52002191 [GRCh38]
Chr19:52505444 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.1408A>C (p.Thr470Pro) single nucleotide variant Inborn genetic diseases [RCV002934943] Chr19:51993701 [GRCh38]
Chr19:52496954 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.2099T>C (p.Phe700Ser) single nucleotide variant Inborn genetic diseases [RCV002878013] Chr19:51993010 [GRCh38]
Chr19:52496263 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.1567T>C (p.Tyr523His) single nucleotide variant Inborn genetic diseases [RCV002747725] Chr19:51993542 [GRCh38]
Chr19:52496795 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.494A>G (p.Asn165Ser) single nucleotide variant Inborn genetic diseases [RCV002808519] Chr19:51994615 [GRCh38]
Chr19:52497868 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.1150A>G (p.Ile384Val) single nucleotide variant Inborn genetic diseases [RCV003256938] Chr19:51993959 [GRCh38]
Chr19:52497212 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.989G>A (p.Ser330Asn) single nucleotide variant Inborn genetic diseases [RCV003197242] Chr19:51994120 [GRCh38]
Chr19:52497373 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.1913A>T (p.Asn638Ile) single nucleotide variant Inborn genetic diseases [RCV003304247] Chr19:51993196 [GRCh38]
Chr19:52496449 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.2135A>G (p.Lys712Arg) single nucleotide variant Inborn genetic diseases [RCV003209033] Chr19:51992974 [GRCh38]
Chr19:52496227 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.305A>T (p.His102Leu) single nucleotide variant Inborn genetic diseases [RCV003200012] Chr19:51994804 [GRCh38]
Chr19:52498057 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.1526G>A (p.Arg509His) single nucleotide variant Inborn genetic diseases [RCV003341304] Chr19:51993583 [GRCh38]
Chr19:52496836 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.1009T>G (p.Ser337Ala) single nucleotide variant Inborn genetic diseases [RCV003351074] Chr19:51994100 [GRCh38]
Chr19:52497353 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.1958A>T (p.His653Leu) single nucleotide variant Inborn genetic diseases [RCV003355111] Chr19:51993151 [GRCh38]
Chr19:52496404 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.807A>C (p.Lys269Asn) single nucleotide variant Inborn genetic diseases [RCV003362357] Chr19:51994302 [GRCh38]
Chr19:52497555 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001199324.2(ZNF615):c.1152A>G (p.Ile384Met) single nucleotide variant Inborn genetic diseases [RCV003356093] Chr19:51993957 [GRCh38]
Chr19:52497210 [GRCh37]
Chr19:19q13.41		 uncertain significance
GRCh37/hg19 19q13.33-13.43(chr19:49625130-57647352)x3 copy number gain not provided [RCV003485200] Chr19:49625130..57647352 [GRCh37]
Chr19:19q13.33-13.43		 likely pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3490
Count of miRNA genes:953
Interacting mature miRNAs:1093
Transcripts:ENST00000376716, ENST00000391795, ENST00000593650, ENST00000594083, ENST00000595114, ENST00000597747, ENST00000597905, ENST00000598071, ENST00000599115, ENST00000599177, ENST00000599631, ENST00000601178, ENST00000602063
Prediction methods: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.

Markers in Region
SHGC-32428  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371952,494,615 - 52,494,710UniSTSGRCh37
Build 361957,186,427 - 57,186,522RGDNCBI36
Celera1949,544,173 - 49,544,268RGD
Cytogenetic Map19q13.41UniSTS
HuRef1948,825,259 - 48,825,354UniSTS
RH65399  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371952,494,736 - 52,494,871UniSTSGRCh37
GRCh37X130,518,826 - 130,518,961UniSTSGRCh37
Build 36X130,346,507 - 130,346,642RGDNCBI36
CeleraX130,905,262 - 130,905,397RGD
Celera1949,544,294 - 49,544,429UniSTS
Cytogenetic Map19q13.41UniSTS
HuRef1948,825,380 - 48,825,515UniSTS
HuRefX119,924,504 - 119,924,639UniSTS
G59887  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371952,494,744 - 52,494,871UniSTSGRCh37
GRCh37X130,518,826 - 130,518,953UniSTSGRCh37
Build 36X130,346,507 - 130,346,634RGDNCBI36
CeleraX130,905,262 - 130,905,389RGD
Celera1949,544,302 - 49,544,429UniSTS
Cytogenetic Map19q13.41UniSTS
HuRef1948,825,388 - 48,825,515UniSTS
HuRefX119,924,504 - 119,924,631UniSTS
TNG Radiation Hybrid Map1921702.0UniSTS


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 97 193 188 8 102 9 342 54 399 66 443 240 2 1 25 252
Low 2319 2596 1531 609 1636 449 4009 2128 3331 347 1007 1367 171 1178 2535 6 2
Below cutoff 14 202 7 7 204 7 5 15 4 4 4 4 1 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001199324 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321317 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321318 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321319 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321320 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321321 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321322 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321323 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_198480 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526829 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526830 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026648 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026649 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026650 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026651 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438644 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438645 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438646 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438647 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438648 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320643 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320644 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320645 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320646 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320647 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320648 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC011460 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC011468 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK091029 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK094071 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK096691 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK128361 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK131494 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK291734 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294977 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC053884 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC105100 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC105102 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC112961 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC143429 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX647556 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX648594 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR936612 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA095942 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA119086 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA236166 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA240372 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA244381 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA322276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA802380 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB235427 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB290987 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KT584722 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000376716   ⟹   ENSP00000365906
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,991,345 - 52,008,230 (-)Ensembl
RefSeq Acc Id: ENST00000391795   ⟹   ENSP00000375672
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,992,453 - 52,008,230 (-)Ensembl
RefSeq Acc Id: ENST00000593650   ⟹   ENSP00000471202
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,994,615 - 52,008,200 (-)Ensembl
RefSeq Acc Id: ENST00000594083   ⟹   ENSP00000471549
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,991,334 - 52,008,196 (-)Ensembl
RefSeq Acc Id: ENST00000595114
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1952,003,849 - 52,008,201 (-)Ensembl
RefSeq Acc Id: ENST00000597747   ⟹   ENSP00000470709
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1952,000,125 - 52,008,163 (-)Ensembl
RefSeq Acc Id: ENST00000597905
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1952,003,782 - 52,008,217 (-)Ensembl
RefSeq Acc Id: ENST00000598071   ⟹   ENSP00000471041
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,991,332 - 52,008,211 (-)Ensembl
RefSeq Acc Id: ENST00000599115   ⟹   ENSP00000470880
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,994,707 - 52,008,201 (-)Ensembl
RefSeq Acc Id: ENST00000599177   ⟹   ENSP00000470475
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,991,338 - 52,008,215 (-)Ensembl
RefSeq Acc Id: ENST00000599631   ⟹   ENSP00000472341
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1952,002,273 - 52,008,201 (-)Ensembl
RefSeq Acc Id: ENST00000601178   ⟹   ENSP00000471608
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,994,808 - 52,008,223 (-)Ensembl
RefSeq Acc Id: ENST00000602063   ⟹   ENSP00000473089
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,991,332 - 52,008,081 (-)Ensembl
RefSeq Acc Id: ENST00000618049   ⟹   ENSP00000484711
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,992,857 - 52,003,749 (-)Ensembl
RefSeq Acc Id: ENST00000618487   ⟹   ENSP00000483676
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,992,880 - 52,003,711 (-)Ensembl
RefSeq Acc Id: NM_001199324   ⟹   NP_001186253
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381951,991,332 - 52,008,211 (-)NCBI
GRCh371952,494,587 - 52,511,494 (-)NCBI
HuRef1948,825,231 - 48,842,127 (-)ENTREZGENE
CHM1_11952,496,445 - 52,513,341 (-)NCBI
T2T-CHM13v2.01955,078,529 - 55,095,409 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321317   ⟹   NP_001308246
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381951,991,332 - 52,008,211 (-)NCBI
CHM1_11952,496,445 - 52,513,341 (-)NCBI
T2T-CHM13v2.01955,078,529 - 55,095,409 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321318   ⟹   NP_001308247
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381951,991,332 - 52,008,211 (-)NCBI
CHM1_11952,496,445 - 52,513,341 (-)NCBI
T2T-CHM13v2.01955,078,529 - 55,095,409 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321319   ⟹   NP_001308248
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381951,991,332 - 52,008,211 (-)NCBI
CHM1_11952,496,445 - 52,513,341 (-)NCBI
T2T-CHM13v2.01955,078,529 - 55,095,409 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321320   ⟹   NP_001308249
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381951,991,332 - 52,008,211 (-)NCBI
CHM1_11952,496,445 - 52,513,341 (-)NCBI
T2T-CHM13v2.01955,078,529 - 55,095,409 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321321   ⟹   NP_001308250
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381951,991,332 - 52,008,211 (-)NCBI
CHM1_11952,496,445 - 52,513,341 (-)NCBI
T2T-CHM13v2.01955,078,529 - 55,095,409 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321322   ⟹   NP_001308251
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381951,991,332 - 52,008,211 (-)NCBI
CHM1_11952,496,445 - 52,513,341 (-)NCBI
T2T-CHM13v2.01955,078,529 - 55,095,409 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001321323   ⟹   NP_001308252
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381951,991,332 - 52,008,211 (-)NCBI
CHM1_11952,496,445 - 52,513,341 (-)NCBI
T2T-CHM13v2.01955,078,529 - 55,095,409 (-)NCBI
Sequence:
RefSeq Acc Id: NM_198480   ⟹   NP_940882
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381951,991,332 - 52,008,211 (-)NCBI
GRCh371952,494,587 - 52,511,494 (-)NCBI
Build 361957,186,400 - 57,203,270 (-)NCBI Archive
Celera1949,544,146 - 49,561,016 (-)RGD
HuRef1948,825,231 - 48,842,127 (-)ENTREZGENE
CHM1_11952,496,445 - 52,513,341 (-)NCBI
T2T-CHM13v2.01955,078,529 - 55,095,409 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017026648   ⟹   XP_016882137
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381951,991,332 - 52,008,211 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047438644   ⟹   XP_047294600
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381951,991,332 - 52,008,211 (-)NCBI
RefSeq Acc Id: XM_047438645   ⟹   XP_047294601
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381951,991,332 - 52,008,211 (-)NCBI
RefSeq Acc Id: XM_047438646   ⟹   XP_047294602
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381951,991,332 - 52,008,211 (-)NCBI
RefSeq Acc Id: XM_047438647   ⟹   XP_047294603
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381951,991,332 - 52,008,211 (-)NCBI
RefSeq Acc Id: XM_047438648   ⟹   XP_047294604
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381951,991,332 - 52,001,879 (-)NCBI
RefSeq Acc Id: XM_054320643   ⟹   XP_054176618
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01955,078,529 - 55,095,409 (-)NCBI
RefSeq Acc Id: XM_054320644   ⟹   XP_054176619
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01955,078,529 - 55,095,409 (-)NCBI
RefSeq Acc Id: XM_054320645   ⟹   XP_054176620
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01955,078,529 - 55,095,409 (-)NCBI
RefSeq Acc Id: XM_054320646   ⟹   XP_054176621
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01955,078,529 - 55,095,409 (-)NCBI
RefSeq Acc Id: XM_054320647   ⟹   XP_054176622
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01955,078,529 - 55,095,409 (-)NCBI
RefSeq Acc Id: XM_054320648   ⟹   XP_054176623
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01955,078,529 - 55,089,077 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001186253 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308246 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308247 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308248 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308249 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308250 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308251 (Get FASTA)   NCBI Sequence Viewer  
  NP_001308252 (Get FASTA)   NCBI Sequence Viewer  
  NP_940882 (Get FASTA)   NCBI Sequence Viewer  
  XP_016882137 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294600 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294601 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294602 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294603 (Get FASTA)   NCBI Sequence Viewer  
  XP_047294604 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176618 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176619 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176620 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176621 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176622 (Get FASTA)   NCBI Sequence Viewer  
  XP_054176623 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAI05101 (Get FASTA)   NCBI Sequence Viewer  
  AAI05103 (Get FASTA)   NCBI Sequence Viewer  
  AAI43430 (Get FASTA)   NCBI Sequence Viewer  
  BAC87399 (Get FASTA)   NCBI Sequence Viewer  
  BAD18638 (Get FASTA)   NCBI Sequence Viewer  
  BAF84423 (Get FASTA)   NCBI Sequence Viewer  
  BAG58048 (Get FASTA)   NCBI Sequence Viewer  
  CAI56755 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000365906
  ENSP00000365906.4
  ENSP00000375672
  ENSP00000375672.3
  ENSP00000470475.1
  ENSP00000470709.1
  ENSP00000470880.1
  ENSP00000471041
  ENSP00000471041.1
  ENSP00000471202.1
  ENSP00000471549
  ENSP00000471549.1
  ENSP00000471608.1
  ENSP00000472341.1
  ENSP00000473089.1
  ENSP00000483676
  ENSP00000483676.1
GenBank Protein Q8N8J6 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_940882   ⟸   NM_198480
- Peptide Label: isoform 2
- UniProtKB: Q6ZMT7 (UniProtKB/Swiss-Prot),   Q5CZB0 (UniProtKB/Swiss-Prot),   Q2M2Y6 (UniProtKB/Swiss-Prot),   B7ZKW9 (UniProtKB/Swiss-Prot),   Q6ZRB3 (UniProtKB/Swiss-Prot),   Q8N8J6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001186253   ⟸   NM_001199324
- Peptide Label: isoform 1
- UniProtKB: Q8N8J6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001308246   ⟸   NM_001321317
- Peptide Label: isoform 3
- UniProtKB: H9KV89 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001308252   ⟸   NM_001321323
- Peptide Label: isoform 5
- Sequence:
RefSeq Acc Id: NP_001308250   ⟸   NM_001321321
- Peptide Label: isoform 1
- UniProtKB: Q8N8J6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001308249   ⟸   NM_001321320
- Peptide Label: isoform 2
- UniProtKB: Q6ZMT7 (UniProtKB/Swiss-Prot),   Q5CZB0 (UniProtKB/Swiss-Prot),   Q2M2Y6 (UniProtKB/Swiss-Prot),   B7ZKW9 (UniProtKB/Swiss-Prot),   Q6ZRB3 (UniProtKB/Swiss-Prot),   Q8N8J6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001308251   ⟸   NM_001321322
- Peptide Label: isoform 6
- Sequence:
RefSeq Acc Id: NP_001308248   ⟸   NM_001321319
- Peptide Label: isoform 1
- UniProtKB: Q8N8J6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001308247   ⟸   NM_001321318
- Peptide Label: isoform 4
- UniProtKB: Q8N8J6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016882137   ⟸   XM_017026648
- Peptide Label: isoform X2
- UniProtKB: Q6ZMT7 (UniProtKB/Swiss-Prot),   Q5CZB0 (UniProtKB/Swiss-Prot),   Q2M2Y6 (UniProtKB/Swiss-Prot),   B7ZKW9 (UniProtKB/Swiss-Prot),   Q6ZRB3 (UniProtKB/Swiss-Prot),   Q8N8J6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000470709   ⟸   ENST00000597747
RefSeq Acc Id: ENSP00000471041   ⟸   ENST00000598071
RefSeq Acc Id: ENSP00000470880   ⟸   ENST00000599115
RefSeq Acc Id: ENSP00000470475   ⟸   ENST00000599177
RefSeq Acc Id: ENSP00000472341   ⟸   ENST00000599631
RefSeq Acc Id: ENSP00000365906   ⟸   ENST00000376716
RefSeq Acc Id: ENSP00000471608   ⟸   ENST00000601178
RefSeq Acc Id: ENSP00000375672   ⟸   ENST00000391795
RefSeq Acc Id: ENSP00000473089   ⟸   ENST00000602063
RefSeq Acc Id: ENSP00000484711   ⟸   ENST00000618049
RefSeq Acc Id: ENSP00000483676   ⟸   ENST00000618487
RefSeq Acc Id: ENSP00000471202   ⟸   ENST00000593650
RefSeq Acc Id: ENSP00000471549   ⟸   ENST00000594083
RefSeq Acc Id: XP_047294603   ⟸   XM_047438647
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047294600   ⟸   XM_047438644
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047294601   ⟸   XM_047438645
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047294602   ⟸   XM_047438646
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047294604   ⟸   XM_047438648
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054176621   ⟸   XM_054320646
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054176622   ⟸   XM_054320647
- Peptide Label: isoform X2
- UniProtKB: Q6ZRB3 (UniProtKB/Swiss-Prot),   Q8N8J6 (UniProtKB/Swiss-Prot),   Q6ZMT7 (UniProtKB/Swiss-Prot),   Q5CZB0 (UniProtKB/Swiss-Prot),   Q2M2Y6 (UniProtKB/Swiss-Prot),   B7ZKW9 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054176618   ⟸   XM_054320643
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054176619   ⟸   XM_054320644
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054176620   ⟸   XM_054320645
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054176623   ⟸   XM_054320648
- Peptide Label: isoform X3
Protein Domains
C2H2-type   KRAB

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8N8J6-F1-model_v2 AlphaFold Q8N8J6 1-731 view protein structure

Promoters
RGD ID:13205437
Promoter ID:EPDNEW_H26299
Type:initiation region
Name:ZNF615_1
Description:zinc finger protein 615
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381952,008,201 - 52,008,261EPDNEW
RGD ID:6795495
Promoter ID:HG_KWN:30732
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000354939,   ENST00000391793,   UC002PYF.1,   UC002PYG.1,   UC002PYH.1,   UC010EPI.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361957,203,084 - 57,203,584 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:24740 AgrOrtholog
COSMIC ZNF615 COSMIC
Ensembl Genes ENSG00000197619 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000376716 ENTREZGENE
  ENST00000376716.9 UniProtKB/Swiss-Prot
  ENST00000391795 ENTREZGENE
  ENST00000391795.7 UniProtKB/TrEMBL
  ENST00000593650.5 UniProtKB/TrEMBL
  ENST00000594083 ENTREZGENE
  ENST00000594083.5 UniProtKB/Swiss-Prot
  ENST00000597747.5 UniProtKB/TrEMBL
  ENST00000598071 ENTREZGENE
  ENST00000598071.6 UniProtKB/Swiss-Prot
  ENST00000599115.5 UniProtKB/TrEMBL
  ENST00000599177.5 UniProtKB/TrEMBL
  ENST00000599631.5 UniProtKB/TrEMBL
  ENST00000601178.5 UniProtKB/TrEMBL
  ENST00000602063.5 UniProtKB/Swiss-Prot
  ENST00000618487 ENTREZGENE
  ENST00000618487.4 UniProtKB/Swiss-Prot
Gene3D-CATH 6.10.140.140 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Classic Zinc Finger UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000197619 GTEx
HGNC ID HGNC:24740 ENTREZGENE
Human Proteome Map ZNF615 Human Proteome Map
InterPro KRAB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  KRAB_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_C2H2_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_C2H2_type UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:284370 UniProtKB/Swiss-Prot
NCBI Gene 284370 ENTREZGENE
PANTHER KRAB DOMAIN C2H2 ZINC FINGER UniProtKB/TrEMBL
  ZINC FINGER AND SCAN DOMAIN-CONTAINING UniProtKB/TrEMBL
  ZINC FINGER PROTEIN UniProtKB/Swiss-Prot
  ZINC FINGER PROTEIN UniProtKB/TrEMBL
  ZINC FINGER PROTEIN 133 UniProtKB/TrEMBL
  ZINC FINGER PROTEIN 281-RELATED UniProtKB/Swiss-Prot
  ZINC FINGER PROTEIN 715 UniProtKB/TrEMBL
  ZINC FINGER PROTEIN 8 UniProtKB/TrEMBL
Pfam KRAB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  zf-C2H2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134872929 PharmGKB
PROSITE KRAB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZINC_FINGER_C2H2_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZINC_FINGER_C2H2_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART KRAB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZnF_C2H2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF109640 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF57667 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A0G2JLJ6_HUMAN UniProtKB/TrEMBL
  B4DH87_HUMAN UniProtKB/TrEMBL
  B7ZKW9 ENTREZGENE
  H9KV89 ENTREZGENE, UniProtKB/TrEMBL
  M0QZR2_HUMAN UniProtKB/TrEMBL
  M0QZZ4_HUMAN UniProtKB/TrEMBL
  M0R0F8_HUMAN UniProtKB/TrEMBL
  M0R130_HUMAN UniProtKB/TrEMBL
  Q2M2Y6 ENTREZGENE
  Q5CZB0 ENTREZGENE
  Q6ZMT7 ENTREZGENE
  Q6ZRB3 ENTREZGENE
  Q8N8J6 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary B7ZKW9 UniProtKB/Swiss-Prot
  Q2M2Y6 UniProtKB/Swiss-Prot
  Q5CZB0 UniProtKB/Swiss-Prot
  Q6ZMT7 UniProtKB/Swiss-Prot
  Q6ZRB3 UniProtKB/Swiss-Prot