ZNF625 (zinc finger protein 625) - Rat Genome Database

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Gene: ZNF625 (zinc finger protein 625) Homo sapiens
Analyze
Symbol: ZNF625
Name: zinc finger protein 625
RGD ID: 1352371
HGNC Page HGNC:30571
Description: Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription 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
RGD Orthologs
Mouse
Bonobo
Green Monkey
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381912,144,890 - 12,156,734 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1912,142,088 - 12,156,832 (-)EnsemblGRCh38.p14 Ensemblhg38GRCh38
GRCh371912,255,705 - 12,267,549 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361912,116,705 - 12,128,529 (-)NCBIBuild 36Build 36hg18NCBI36
Build 341912,116,710 - 12,128,529NCBI
Celera1912,150,092 - 12,161,917 (-)NCBICelera
Cytogenetic Map19p13.2NCBI
HuRef1911,830,762 - 11,842,604 (-)NCBIHuRef
CHM1_11912,255,515 - 12,267,359 (-)NCBICHM1_1
T2T-CHM13v2.01912,273,146 - 12,284,990 (-)NCBIT2T-CHM13v2.0
JBrowse:




Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

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:15489334   PMID:16344560   PMID:20562864   PMID:21873635   PMID:25416956   PMID:26598620   PMID:30021884   PMID:32296183   PMID:32814053   PMID:33961781   PMID:35509820  


Genomics

Comparative Map Data
ZNF625
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381912,144,890 - 12,156,734 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1912,142,088 - 12,156,832 (-)EnsemblGRCh38.p14 Ensemblhg38GRCh38
GRCh371912,255,705 - 12,267,549 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361912,116,705 - 12,128,529 (-)NCBIBuild 36Build 36hg18NCBI36
Build 341912,116,710 - 12,128,529NCBI
Celera1912,150,092 - 12,161,917 (-)NCBICelera
Cytogenetic Map19p13.2NCBI
HuRef1911,830,762 - 11,842,604 (-)NCBIHuRef
CHM1_11912,255,515 - 12,267,359 (-)NCBICHM1_1
T2T-CHM13v2.01912,273,146 - 12,284,990 (-)NCBIT2T-CHM13v2.0
Zfp931
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm392177,708,239 - 177,721,858 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl2177,693,532 - 177,720,294 (-)EnsemblGRCm39 EnsemblGRCm39
GRCm382178,066,446 - 178,078,425 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl2178,067,695 - 178,078,476 (-)EnsemblGRCm38.p6 Ensemblmm10GRCm38
MGSCv372177,801,583 - 177,813,130 (-)NCBIMGSCv37MGSCv37mm9NCBIm37
MGSCv362177,988,766 - 178,007,833 (-)NCBIMGSCv36mm8
Celera2182,150,049 - 182,161,596 (-)NCBICelera
Cytogenetic Map2H4NCBI
cM Map299.65NCBI
ZNF625
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22017,063,659 - 17,080,934 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11916,063,935 - 16,082,206 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01911,695,318 - 11,715,239 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11912,466,592 - 12,483,466 (-)NCBIPanPan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1912,466,592 - 12,483,466 (-)EnsemblPanPan1.1 EnsemblpanPan2panpan1.1
ZNF625
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mChlSab1.0.hap1650,595,422 - 50,613,078 (+)NCBImChlSab1.0.hap1
Vero_WHO_p1.0NW_0236660748,842,013 - 8,857,359 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
ChlSab1.1610,949,115 - 10,962,152 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl610,949,715 - 10,961,909 (-)EnsemblChlSab1.1 EnsemblchlSab2Vervet-AGM
ChlSab1.1 Ensembl610,963,575 - 10,964,498 (-)EnsemblChlSab1.1 EnsemblchlSab2Vervet-AGM

Variants

.
Variants in ZNF625
20 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19p13.2-13.13(chr19:8831147-13331227)x3 copy number gain Developmental delay AND/OR other significant developmental or morphological phenotypes [RCV000052908] Chr19:19p13.2-13.13 likely pathogenic
GRCh38/hg38 19p13.2-13.12(chr19:10315258-14048994)x3 copy number gain Developmental delay AND/OR other significant developmental or morphological phenotypes [RCV000052909] Chr19:19p13.2-13.12 pathogenic
GRCh38/hg38 19p13.2-13.12(chr19:12132052-14751798)x3 copy number gain See cases [RCV000052910] Chr19:19p13.2-13.12 pathogenic
GRCh38/hg38 19p13.2-13.12(chr19:11227942-14532135)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053944]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053944]|See cases [RCV000053944] Chr19:11227942..14532135 [GRCh38]
Chr19:11338618..14642947 [GRCh37]
Chr19:11199618..14503947 [NCBI36]
Chr19:19p13.2-13.12		 pathogenic
GRCh38/hg38 19p13.2-13.13(chr19:11517825-13225287)x1 copy number loss Episodic vomiting [RCV000053945] Chr19:19p13.2-13.13 pathogenic
NM_145233.3(ZNF625):c.260T>C (p.Val87Ala) single nucleotide variant Malignant melanoma [RCV000071931] Chr19:12146156 [GRCh38]
Chr19:12256971 [GRCh37]
Chr19:12117971 [NCBI36]
Chr19:19p13.2		 not provided
GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3 copy number gain Developmental delay AND/OR other significant developmental or morphological phenotypes [RCV000133888] Chr19:19p13.2-q13.31 pathogenic
GRCh38/hg38 19p13.2-13.12(chr19:11525163-14155021)x1 copy number loss Developmental delay AND/OR other significant developmental or morphological phenotypes [RCV000136909] Chr19:19p13.2-13.12 pathogenic
GRCh38/hg38 19p13.2-13.13(chr19:10319474-13777860)x1 copy number loss Developmental delay AND/OR other significant developmental or morphological phenotypes [RCV000141568] Chr19:19p13.2-13.13 pathogenic
GRCh37/hg19 19p13.2(chr19:12059800-12259323)x3 copy number gain not provided [RCV000752562] Chr19:12059800..12259323 [GRCh37]
Chr19:19p13.2		 benign
GRCh37/hg19 19p13.2(chr19:12204632-13497073)x1 copy number loss See cases [RCV000449161] Chr19:19p13.2 pathogenic
GRCh37/hg19 19p13.2-13.12(chr19:9678768-14853426) copy number gain Developmental delay AND/OR other significant developmental or morphological phenotypes [RCV000446985] Chr19:19p13.2-13.12 pathogenic
GRCh37/hg19 19p13.2-13.12(chr19:11608072-14543046)x3 copy number gain See cases [RCV000511013] Chr19:19p13.2-13.12 uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 copy number gain Ventricular septal defect [RCV000511289] Chr19:19p13.3-q13.43 pathogenic|uncertain significance
NM_145233.4(ZNF625):c.230A>T (p.Asp77Val) single nucleotide variant not specified [RCV004314283] Chr19:12146186 [GRCh38]
Chr19:12257001 [GRCh37]
Chr19:19p13.2		 uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) copy number gain Abnormality of the ear [RCV000512296] Chr19:19p13.3-q13.43 pathogenic
NM_145233.4(ZNF625):c.1072C>A (p.Pro358Thr) single nucleotide variant not specified [RCV004309873] Chr19:12145344 [GRCh38]
Chr19:12256159 [GRCh37]
Chr19:19p13.2		 uncertain significance
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
Single allele deletion Hypertonia [RCV000844961] Chr19:19p13.2 not provided
GRCh37/hg19 19p13.2(chr19:10642984-12810067) copy number loss Depressivity [RCV001249213] Chr19:19p13.2 not provided
NM_145233.4(ZNF625):c.770A>G (p.His257Arg) single nucleotide variant not specified [RCV004326527] Chr19:12145646 [GRCh38]
Chr19:12256461 [GRCh37]
Chr19:19p13.2		 uncertain significance
NC_000019.9:g.(?_11277234)_(13249220_?)dup duplication not provided [RCV003105511] Chr19:19p13.2 uncertain significance
NM_145233.4(ZNF625):c.262C>T (p.Pro88Ser) single nucleotide variant not specified [RCV005788255] Chr19:12146154 [GRCh38]
Chr19:12256969 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.896G>A (p.Gly299Glu) single nucleotide variant not specified [RCV005526436] Chr19:12145520 [GRCh38]
Chr19:12256335 [GRCh37]
Chr19:19p13.2		 uncertain significance
NC_000019.9:g.(?_10828919)_(13482613_?)dup duplication Developmental and epileptic encephalopathy, 42 [RCV003109234] Chr19:19p13.2 uncertain significance
NM_145233.4(ZNF625):c.1006T>C (p.Cys336Arg) single nucleotide variant not specified [RCV005788257] Chr19:12145410 [GRCh38]
Chr19:12256225 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.1063G>A (p.Gly355Arg) single nucleotide variant not specified [RCV005788258] Chr19:12145353 [GRCh38]
Chr19:12256168 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.535C>G (p.Arg179Gly) single nucleotide variant not specified [RCV005788259] Chr19:12145881 [GRCh38]
Chr19:12256696 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.289C>T (p.Pro97Ser) single nucleotide variant not specified [RCV005788256] Chr19:12146127 [GRCh38]
Chr19:12256942 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.1010G>A (p.Gly337Asp) single nucleotide variant not specified [RCV005788254] Chr19:12145406 [GRCh38]
Chr19:12256221 [GRCh37]
Chr19:19p13.2		 uncertain significance
GRCh37/hg19 19p13.2(chr19:11753820-12272905)x1 copy number loss not provided [RCV002474999] Chr19:19p13.2 uncertain significance
NM_145233.4(ZNF625):c.860T>C (p.Phe287Ser) single nucleotide variant not specified [RCV004318384] Chr19:12145556 [GRCh38]
Chr19:12256371 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.956G>A (p.Arg319Gln) single nucleotide variant not specified [RCV004129249] Chr19:12145460 [GRCh38]
Chr19:12256275 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.317G>A (p.Ser106Asn) single nucleotide variant not specified [RCV004116342] Chr19:12146099 [GRCh38]
Chr19:12256914 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.293G>A (p.Arg98Gln) single nucleotide variant not specified [RCV004117408] Chr19:12146123 [GRCh38]
Chr19:12256938 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.442C>T (p.Pro148Ser) single nucleotide variant not specified [RCV004179392] Chr19:12145974 [GRCh38]
Chr19:12256789 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.1105G>C (p.Glu369Gln) single nucleotide variant not specified [RCV004179491] Chr19:12145311 [GRCh38]
Chr19:12256126 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.557G>C (p.Ser186Thr) single nucleotide variant not specified [RCV004114817] Chr19:12145859 [GRCh38]
Chr19:12256674 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.910G>A (p.Glu304Lys) single nucleotide variant not specified [RCV004277752] Chr19:12145506 [GRCh38]
Chr19:12256321 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.407A>G (p.Lys136Arg) single nucleotide variant not specified [RCV005526434] Chr19:12146009 [GRCh38]
Chr19:12256824 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.409T>C (p.Cys137Arg) single nucleotide variant not specified [RCV005526438] Chr19:12146007 [GRCh38]
Chr19:12256822 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.416A>G (p.Tyr139Cys) single nucleotide variant not specified [RCV005526441] Chr19:12146000 [GRCh38]
Chr19:12256815 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.878A>G (p.His293Arg) single nucleotide variant not specified [RCV006350679] Chr19:12145538 [GRCh38]
Chr19:12256353 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.239A>C (p.His80Pro) single nucleotide variant not specified [RCV006350680] Chr19:12146177 [GRCh38]
Chr19:12256992 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.524G>A (p.Arg175His) single nucleotide variant not specified [RCV006350678] Chr19:12145892 [GRCh38]
Chr19:12256707 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.964G>A (p.Gly322Arg) single nucleotide variant not specified [RCV006350681] Chr19:12145452 [GRCh38]
Chr19:12256267 [GRCh37]
Chr19:19p13.2		 uncertain significance
GRCh37/hg19 19p13.2(chr19:10441330-13077352)x1 copy number loss not specified [RCV003986120] Chr19:19p13.2 pathogenic
NM_145233.4(ZNF625):c.995A>G (p.Glu332Gly) single nucleotide variant not specified [RCV004487157] Chr19:12145421 [GRCh38]
Chr19:12256236 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.145G>A (p.Asp49Asn) single nucleotide variant not specified [RCV004487155] Chr19:12147441 [GRCh38]
Chr19:12258256 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.947C>T (p.Ser316Leu) single nucleotide variant not specified [RCV004600039] Chr19:12145469 [GRCh38]
Chr19:12256284 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.700C>A (p.Leu234Ile) single nucleotide variant not specified [RCV004893856] Chr19:12145716 [GRCh38]
Chr19:12256531 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.1105G>A (p.Glu369Lys) single nucleotide variant not specified [RCV004893857] Chr19:12145311 [GRCh38]
Chr19:12256126 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.1031C>T (p.Ser344Leu) single nucleotide variant not specified [RCV004893858] Chr19:12145385 [GRCh38]
Chr19:12256200 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.868G>A (p.Val290Ile) single nucleotide variant not specified [RCV005311570] Chr19:12145548 [GRCh38]
Chr19:12256363 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.282G>T (p.Lys94Asn) single nucleotide variant not specified [RCV005526437] Chr19:12146134 [GRCh38]
Chr19:12256949 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.237G>C (p.Gln79His) single nucleotide variant not specified [RCV005526435] Chr19:12146179 [GRCh38]
Chr19:12256994 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.908A>G (p.Tyr303Cys) single nucleotide variant not specified [RCV005526439] Chr19:12145508 [GRCh38]
Chr19:12256323 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_145233.4(ZNF625):c.1073C>T (p.Pro358Leu) single nucleotide variant not specified [RCV004893855] Chr19:12145343 [GRCh38]
Chr19:12256158 [GRCh37]
Chr19:19p13.2		 uncertain significance
miRNA Target Status (No longer updated)

Predicted Target Of
Summary Value
Count of predictions:1028
Count of miRNA genes:597
Interacting mature miRNAs:656
Transcripts:ENST00000355738, ENST00000414892, ENST00000439556, ENST00000455799, ENST00000542938
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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
1298499UAE1_HUrinary albumin excretion QTL 1 (human)2.730.0009Urinary albumin excretionurine albumin:creatinine ratio (ACR)19116075902Human
1300034BP50_HBlood pressure QTL 50 (human)2.10.00094Blood pressuresystolic191108946337089463Human
1643451SLIPL6_HSerum lipid level QTL 6 (human)2.190.0008Lipid level19116075902Human
1581534BP76_HBlood pressure QTL 76 (human)20.001Blood pressurepulse pressure19116075902Human
1581535BP65_HBlood pressure QTL 65 (human)3.10.001Blood pressurepulse pressure19116075902Human
2314591INSUL4_HInsulin level QTL 4 (human)3.80.000038Insulin levelfasting19116075902Human
1298476BP3_HBlood pressure QTL 3 (human)2.4Blood pressuresystolic19116075902Human


Expression

RNA-SEQ Expression


Sequence


Ensembl Acc Id: ENST00000414892   ⟹   ENSP00000405156
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1912,142,090 - 12,147,802 (-)Ensembl
Ensembl Acc Id: ENST00000439556   ⟹   ENSP00000394380
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1912,144,890 - 12,156,734 (-)Ensembl
Ensembl Acc Id: ENST00000455799   ⟹   ENSP00000398518
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1912,144,890 - 12,156,832 (-)Ensembl
Ensembl Acc Id: ENST00000996953   ⟹   ENSP00000666770
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1912,142,088 - 12,156,832 (-)Ensembl
Ensembl Acc Id: ENST00001138537   ⟹   ENSP00000812658
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1912,144,890 - 12,156,832 (-)Ensembl
RefSeq Acc Id: NM_145233   ⟹   NP_660276
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381912,144,890 - 12,156,734 (-)NCBI
GRCh371912,255,705 - 12,267,546 (-)ENTREZGENE
Build 361912,116,705 - 12,128,529 (-)NCBI Archive
Celera1912,150,092 - 12,161,917 (-)RGD
HuRef1911,830,762 - 11,842,604 (-)ENTREZGENE
CHM1_11912,255,515 - 12,267,359 (-)NCBI
T2T-CHM13v2.01912,273,146 - 12,284,990 (-)NCBI
Sequence:
RefSeq Acc Id: NR_037801
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381912,144,890 - 12,156,734 (-)NCBI
GRCh371912,255,705 - 12,267,546 (-)ENTREZGENE
HuRef1911,830,762 - 11,842,604 (-)ENTREZGENE
CHM1_11912,255,515 - 12,267,359 (-)NCBI
T2T-CHM13v2.01912,273,146 - 12,284,990 (-)NCBI
Sequence:
RefSeq Acc Id: NP_660276   ⟸   NM_145233
- UniProtKB: Q96I27 (UniProtKB/Swiss-Prot)
- Sequence:
Ensembl Acc Id: ENSP00000394380   ⟸   ENST00000439556
Ensembl Acc Id: ENSP00000405156   ⟸   ENST00000414892
Ensembl Acc Id: ENSP00000398518   ⟸   ENST00000455799
Ensembl Acc Id: ENSP00000666770   ⟸   ENST00000996953
Ensembl Acc Id: ENSP00000812658   ⟸   ENST00001138537
Protein Domains
KRAB

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q96I27-F1-model_v2 AlphaFold Q96I27 1-306 view protein structure

Promoters
RGD ID:6796284
Promoter ID:HG_KWN:28978
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid
Transcripts:OTTHUMT00000344093,   UC002MTG.1,   UC010DYN.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361912,128,381 - 12,128,881 (-)MPROMDB
RGD ID:7238665
Promoter ID:EPDNEW_H25076
Type:initiation region
Name:ZNF625_1
Description:zinc finger protein 625
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381912,156,734 - 12,156,794EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:30571 AgrOrtholog
COSMIC ZNF625 COSMIC
Ensembl Genes ENSG00000257591 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000439556 ENTREZGENE
  ENST00000439556.3 UniProtKB/Swiss-Prot
  ENST00000455799 ENTREZGENE
Gene3D-CATH Classic Zinc Finger UniProtKB/Swiss-Prot
GTEx ENSG00000257591 GTEx
HGNC ID HGNC:30571 ENTREZGENE
Human Proteome Map ZNF625 Human Proteome Map
InterPro Znf_C2H2_sf UniProtKB/Swiss-Prot
  Znf_C2H2_type UniProtKB/Swiss-Prot
KEGG Report hsa:90589 UniProtKB/Swiss-Prot
NCBI Gene 90589 ENTREZGENE
PANTHER ZINC FINGER PROTEIN UniProtKB/Swiss-Prot
  ZINC FINGER PROTEIN 491 UniProtKB/Swiss-Prot
Pfam zf-C2H2 UniProtKB/Swiss-Prot
  zf-C2H2_6 UniProtKB/Swiss-Prot
PharmGKB PA134911932 PharmGKB
PROSITE ZINC_FINGER_C2H2_1 UniProtKB/Swiss-Prot
  ZINC_FINGER_C2H2_2 UniProtKB/Swiss-Prot
SMART ZnF_C2H2 UniProtKB/Swiss-Prot
Superfamily-SCOP SSF57667 UniProtKB/Swiss-Prot
UniProt F2Z3I2_HUMAN UniProtKB/TrEMBL
  H7C2C9_HUMAN UniProtKB/TrEMBL
  Q96I27 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary A4FU45 UniProtKB/Swiss-Prot
  I3L0E9 UniProtKB/Swiss-Prot