ZNF613 (zinc finger protein 613) - Rat Genome Database

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Gene: ZNF613 (zinc finger protein 613) Homo sapiens
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Symbol: ZNF613
Name: zinc finger protein 613
RGD ID: 1346771
HGNC Page HGNC:25827
Description: Predicted to enable DNA-binding transcription factor activity 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 located in nucleus.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: FLJ13590
RGD Orthologs
Bonobo
Dog
Squirrel
Pig
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
GRCh381951,927,472 - 51,946,621 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1951,927,147 - 51,948,759 (+)EnsemblGRCh38.p14 Ensemblhg38GRCh38
GRCh371952,430,725 - 52,449,874 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361957,122,500 - 57,140,817 (+)NCBIBuild 36Build 36hg18NCBI36
Build 341957,122,499 - 57,140,817NCBI
Celera1949,480,254 - 49,498,577 (+)NCBICelera
Cytogenetic Map19q13.41NCBI
HuRef1948,761,338 - 48,779,662 (+)NCBIHuRef
CHM1_11952,432,545 - 52,450,868 (+)NCBICHM1_1
T2T-CHM13v2.01955,014,667 - 55,033,819 (+)NCBIT2T-CHM13v2.0
JBrowse:




Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
nucleus  (IEA)

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
2. 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:15489334   PMID:21873635   PMID:31749838   PMID:32296183   PMID:35563538   PMID:37314216  


Genomics

Comparative Map Data
ZNF613
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381951,927,472 - 51,946,621 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1951,927,147 - 51,948,759 (+)EnsemblGRCh38.p14 Ensemblhg38GRCh38
GRCh371952,430,725 - 52,449,874 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361957,122,500 - 57,140,817 (+)NCBIBuild 36Build 36hg18NCBI36
Build 341957,122,499 - 57,140,817NCBI
Celera1949,480,254 - 49,498,577 (+)NCBICelera
Cytogenetic Map19q13.41NCBI
HuRef1948,761,338 - 48,779,662 (+)NCBIHuRef
CHM1_11952,432,545 - 52,450,868 (+)NCBICHM1_1
T2T-CHM13v2.01955,014,667 - 55,033,819 (+)NCBIT2T-CHM13v2.0
ZNF613
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22057,964,697 - 58,023,932 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11959,888,946 - 59,948,251 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01948,867,586 - 48,889,317 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11957,748,724 - 57,767,160 (+)NCBIPanPan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1957,757,415 - 57,767,160 (+)EnsemblPanPan1.1 EnsemblpanPan2panpan1.1
ZNF613
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11105,197,543 - 105,227,476 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1105,210,569 - 105,219,870 (-)EnsemblCanFam3.1 EnsemblcanFam3CanFam3.1
Dog10K_Boxer_Tasha1104,771,134 - 104,837,189 (-)NCBIDog10K_Boxer_TashaDog10K_Boxer_Tasha
ROS_Cfam_1.01105,707,167 - 105,773,492 (-)NCBIROS_Cfam_1.0ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1105,630,424 - 105,737,074 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11105,379,820 - 105,445,927 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01105,028,188 - 105,084,782 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01105,815,452 - 105,881,718 (-)NCBIUU_Cfam_GSD_1.0UU_Cfam_GSD_1.0
Znf613
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mIctTri1.hap1154,919,880 - 4,938,057 (-)NCBImIctTri1.hap1
HiC_Itri_2NW_0244093494,674,921 - 4,692,926 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004937026216,683 - 226,126 (+)EnsemblSpeTri2.0 Ensembl
SpeTri2.0NW_004937026214,378 - 225,794 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ZNF613
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl658,166,101 - 58,183,504 (-)EnsemblSscrofa11.1 EnsemblsusScr11Sscrofa11.1
Sscrofa11.1658,166,640 - 58,189,111 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2651,973,256 - 52,023,948 (+)NCBISscrofa10.2Sscrofa10.2susScr3
ZNF613
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mChlSab1.0.hap166,361,170 - 6,376,326 (-)NCBImChlSab1.0.hap1
Vero_WHO_p1.0NW_02366607324,800,824 - 24,817,202 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
ChlSab1.1644,746,087 - 44,761,223 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl644,754,982 - 44,762,648 (+)EnsemblChlSab1.1 EnsemblchlSab2Vervet-AGM

Variants

.
Variants in ZNF613
52 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 Developmental delay AND/OR other significant developmental or morphological phenotypes [RCV000050883] Chr19:19q13.33-13.43 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:49907832-58557889)x3 copy number gain Developmental delay AND/OR other significant developmental or morphological phenotypes [RCV000052925] Chr19:19q13.33-13.43 pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:51141518-58539965)x3 copy number gain See cases [RCV000052926] Chr19:19q13.41-13.43 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3 copy number gain Developmental delay AND/OR other significant developmental or morphological phenotypes [RCV000052914] Chr19:19q13.33-13.43 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3 copy number gain Failure to thrive [RCV000052915] Chr19:19q13.33-13.43 pathogenic
GRCh38/hg38 19q13.41(chr19:51824349-52113443)x3 copy number gain Developmental delay AND/OR other significant developmental or morphological phenotypes [RCV000052592] Chr19:19q13.41 uncertain significance
GRCh38/hg38 19q13.33-13.43(chr19:50152520-58581203)x3 copy number gain Abnormal facial shape [RCV000135843] Chr19:19q13.33-13.43 pathogenic
GRCh38/hg38 19q13.41(chr19:51865544-52113443)x3 copy number gain Developmental delay AND/OR other significant developmental or morphological phenotypes [RCV000136779] Chr19:19q13.41 benign
GRCh38/hg38 19q13.41(chr19:51681235-51936423)x3 copy number gain See cases [RCV000138486] Chr19:19q13.41 likely benign
GRCh38/hg38 19q13.41(chr19:51785545-52075049)x3 copy number gain Autistic behavior [RCV000142949] Chr19:19q13.41 likely benign
GRCh38/hg38 19q13.41(chr19:51202361-51993020)x3 copy number gain See cases [RCV000143450] Chr19:19q13.41 uncertain significance
NC_000019.10:g.51770004_52114045dup 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 19q13.33-13.43(chr19:50489390-59095359)x3 copy number gain See cases [RCV000445925] Chr19:19q13.33-13.43 pathogenic
NM_001031721.4(ZNF613):c.321T>G (p.Asn107Lys) single nucleotide variant not specified [RCV004326425] Chr19:51944204 [GRCh38]
Chr19:52447457 [GRCh37]
Chr19:19q13.41		 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
GRCh38/hg38 19q13.41(chr19:51769103-52124150)x3 copy number gain Short stature [RCV000142704] 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 19q13.41(chr19:52287452-52612066)x3 copy number gain not provided [RCV000752752] Chr19:52287452..52612066 [GRCh37]
Chr19:19q13.41		 benign
NM_001031721.4(ZNF613):c.127A>G (p.Asn43Asp) single nucleotide variant not specified [RCV004309506] Chr19:51940320 [GRCh38]
Chr19:52443573 [GRCh37]
Chr19:19q13.41		 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_001031721.4(ZNF613):c.1078A>G (p.Asn360Asp) single nucleotide variant not specified [RCV004302748] Chr19:51944961 [GRCh38]
Chr19:52448214 [GRCh37]
Chr19:19q13.41		 uncertain significance
GRCh37/hg19 19q13.41(chr19:52273226-52631600)x3 copy number gain not provided [RCV000752750] Chr19:52273226..52631600 [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 19q13.32-13.42(chr19:47939842-54626871) copy number gain Generalized hypotonia [RCV001249294] Chr19:19q13.32-13.42 not provided
GRCh37/hg19 19q13.41(chr19:52273226-52617298)x3 copy number gain not provided [RCV000752749] Chr19:52273226..52617298 [GRCh37]
Chr19:19q13.41		 benign
GRCh37/hg19 19q13.31-13.42(chr19:44738088-53621561)x3 copy number gain not provided [RCV001007050] Chr19:19q13.31-13.42 pathogenic
NM_001031721.4(ZNF613):c.284G>C (p.Arg95Thr) single nucleotide variant not specified [RCV005526347] Chr19:51944167 [GRCh38]
Chr19:52447420 [GRCh37]
Chr19:19q13.41		 uncertain significance
GRCh37/hg19 19q13.33-13.41(chr19:49911081-53127438) copy number gain not specified [RCV002052689] Chr19:19q13.33-13.41 likely pathogenic
NM_001031721.4(ZNF613):c.673G>A (p.Val225Ile) single nucleotide variant not specified [RCV004217264] Chr19:51944556 [GRCh38]
Chr19:52447809 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.823C>T (p.Leu275Phe) single nucleotide variant not specified [RCV004195871] Chr19:51944706 [GRCh38]
Chr19:52447959 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1508G>A (p.Arg503Gln) single nucleotide variant not specified [RCV004125827] Chr19:51945391 [GRCh38]
Chr19:52448644 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1303A>G (p.Lys435Glu) single nucleotide variant not specified [RCV004182226] Chr19:51945186 [GRCh38]
Chr19:52448439 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1765G>A (p.Ala589Thr) single nucleotide variant not specified [RCV004128175] Chr19:51945648 [GRCh38]
Chr19:52448901 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.643A>G (p.Lys215Glu) single nucleotide variant not specified [RCV004150945] Chr19:51944526 [GRCh38]
Chr19:52447779 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1728G>C (p.Met576Ile) single nucleotide variant not specified [RCV004154626] Chr19:51945611 [GRCh38]
Chr19:52448864 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.808C>T (p.Arg270Cys) single nucleotide variant not specified [RCV004227833] Chr19:51944691 [GRCh38]
Chr19:52447944 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1344A>T (p.Arg448Ser) single nucleotide variant not specified [RCV004229647] Chr19:51945227 [GRCh38]
Chr19:52448480 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1103G>T (p.Gly368Val) single nucleotide variant not specified [RCV004137289] Chr19:51944986 [GRCh38]
Chr19:52448239 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.538G>A (p.Glu180Lys) single nucleotide variant not specified [RCV004185486] Chr19:51944421 [GRCh38]
Chr19:52447674 [GRCh37]
Chr19:19q13.41		 likely benign
NM_001031721.4(ZNF613):c.1687A>C (p.Ile563Leu) single nucleotide variant not specified [RCV004075393] Chr19:51945570 [GRCh38]
Chr19:52448823 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1039A>C (p.Thr347Pro) single nucleotide variant not specified [RCV004226295] Chr19:51944922 [GRCh38]
Chr19:52448175 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.871A>C (p.Ser291Arg) single nucleotide variant not specified [RCV005526340] Chr19:51944754 [GRCh38]
Chr19:52448007 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1436C>T (p.Thr479Ile) single nucleotide variant not specified [RCV004262737] Chr19:51945319 [GRCh38]
Chr19:52448572 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1567C>T (p.His523Tyr) single nucleotide variant not specified [RCV005526338] Chr19:51945450 [GRCh38]
Chr19:52448703 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1532C>T (p.Pro511Leu) single nucleotide variant not specified [RCV005526341] Chr19:51945415 [GRCh38]
Chr19:52448668 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1096C>G (p.His366Asp) single nucleotide variant not specified [RCV005526342] Chr19:51944979 [GRCh38]
Chr19:52448232 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1391C>T (p.Ser464Phe) single nucleotide variant not specified [RCV005526334] Chr19:51945274 [GRCh38]
Chr19:52448527 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.16-1G>A single nucleotide variant Malignant tumor of urinary bladder [RCV006149365] Chr19:51940208 [GRCh38]
Chr19:52443461 [GRCh37]
Chr19:19q13.41		 evidence_only
NM_001031721.4(ZNF613):c.587G>A (p.Arg196Gln) single nucleotide variant not specified [RCV006350572] Chr19:51944470 [GRCh38]
Chr19:52447723 [GRCh37]
Chr19:19q13.41		 likely benign
NM_001031721.4(ZNF613):c.924A>C (p.Arg308Ser) single nucleotide variant not specified [RCV004357086] Chr19:51944807 [GRCh38]
Chr19:52448060 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.-15C>A single nucleotide variant Melanoma [RCV006149363] Chr19:51936206 [GRCh38]
Chr19:52439459 [GRCh37]
Chr19:19q13.41		 evidence_only
NM_001031721.4(ZNF613):c.235+149G>A single nucleotide variant Sarcoma [RCV006149366] Chr19:51940858 [GRCh38]
Chr19:52444111 [GRCh37]
Chr19:19q13.41		 evidence_only
NM_001031721.4(ZNF613):c.948T>A (p.His316Gln) single nucleotide variant not specified [RCV004345896] Chr19:51944831 [GRCh38]
Chr19:52448084 [GRCh37]
Chr19:19q13.41		 uncertain significance
GRCh37/hg19 19q13.33-13.43(chr19:49625130-57647352)x3 copy number gain not provided [RCV003485200] Chr19:19q13.33-13.43 pathogenic|likely pathogenic
NM_001031721.4(ZNF613):c.904C>T (p.Arg302Trp) single nucleotide variant not specified [RCV004487045] Chr19:51944787 [GRCh38]
Chr19:52448040 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.862T>C (p.Tyr288His) single nucleotide variant not specified [RCV004487044] Chr19:51944745 [GRCh38]
Chr19:52447998 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1068A>C (p.Lys356Asn) single nucleotide variant not specified [RCV004487040] Chr19:51944951 [GRCh38]
Chr19:52448204 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1448C>T (p.Pro483Leu) single nucleotide variant not specified [RCV004487041] Chr19:51945331 [GRCh38]
Chr19:52448584 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.242A>C (p.Lys81Thr) single nucleotide variant not specified [RCV004487043] Chr19:51944125 [GRCh38]
Chr19:52447378 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1679G>A (p.Arg560His) single nucleotide variant not specified [RCV004487042] Chr19:51945562 [GRCh38]
Chr19:52448815 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.311A>G (p.His104Arg) single nucleotide variant not specified [RCV004614681] Chr19:51944194 [GRCh38]
Chr19:52447447 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1698A>C (p.Lys566Asn) single nucleotide variant not specified [RCV006350575] Chr19:51945581 [GRCh38]
Chr19:52448834 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.136T>G (p.Ser46Ala) single nucleotide variant not specified [RCV006350578] Chr19:51940329 [GRCh38]
Chr19:52443582 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.736G>A (p.Gly246Arg) single nucleotide variant not specified [RCV004893766] Chr19:51944619 [GRCh38]
Chr19:52447872 [GRCh37]
Chr19:19q13.41		 likely benign
NM_001031721.4(ZNF613):c.1535A>G (p.Tyr512Cys) single nucleotide variant not specified [RCV004893767] Chr19:51945418 [GRCh38]
Chr19:52448671 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1694A>C (p.Asp565Ala) single nucleotide variant not specified [RCV004893768] Chr19:51945577 [GRCh38]
Chr19:52448830 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.55T>C (p.Trp19Arg) single nucleotide variant not specified [RCV004893769] Chr19:51940248 [GRCh38]
Chr19:52443501 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1307G>C (p.Gly436Ala) single nucleotide variant not specified [RCV004893770] Chr19:51945190 [GRCh38]
Chr19:52448443 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.344A>C (p.Gln115Pro) single nucleotide variant not specified [RCV004893771] Chr19:51944227 [GRCh38]
Chr19:52447480 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1156A>G (p.Asn386Asp) single nucleotide variant not specified [RCV004893772] Chr19:51945039 [GRCh38]
Chr19:52448292 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1000C>G (p.His334Asp) single nucleotide variant not specified [RCV005311541] Chr19:51944883 [GRCh38]
Chr19:52448136 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.779A>G (p.Tyr260Cys) single nucleotide variant not specified [RCV005300559] Chr19:51944662 [GRCh38]
Chr19:52447915 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1259G>A (p.Arg420His) single nucleotide variant not specified [RCV005526337] Chr19:51945142 [GRCh38]
Chr19:52448395 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1203A>G (p.Ile401Met) single nucleotide variant not specified [RCV005526346] Chr19:51945086 [GRCh38]
Chr19:52448339 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.350A>C (p.Lys117Thr) single nucleotide variant not specified [RCV005526335] Chr19:51944233 [GRCh38]
Chr19:52447486 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1040C>T (p.Thr347Ile) single nucleotide variant not specified [RCV005526344] Chr19:51944923 [GRCh38]
Chr19:52448176 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.236-165A>C single nucleotide variant Acute myeloid leukemia [RCV006149367] Chr19:51943954 [GRCh38]
Chr19:52447207 [GRCh37]
Chr19:19q13.41		 evidence_only
NM_001031721.4(ZNF613):c.1634A>G (p.Lys545Arg) single nucleotide variant not specified [RCV005526343] Chr19:51945517 [GRCh38]
Chr19:52448770 [GRCh37]
Chr19:19q13.41		 uncertain significance
GRCh37/hg19 19q13.33-13.43(chr19:48463931-57095254)x3 copy number gain not provided [RCV001259944] Chr19:19q13.33-13.43 pathogenic
NM_001031721.4(ZNF613):c.1258C>T (p.Arg420Cys) single nucleotide variant not specified [RCV004246781] Chr19:51945141 [GRCh38]
Chr19:52448394 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.541G>T (p.Gly181Cys) single nucleotide variant not specified [RCV004245866] Chr19:51944424 [GRCh38]
Chr19:52447677 [GRCh37]
Chr19:19q13.41		 likely benign
NM_001031721.4(ZNF613):c.248T>C (p.Val83Ala) single nucleotide variant not specified [RCV004147877] Chr19:51944131 [GRCh38]
Chr19:52447384 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1208A>G (p.Asn403Ser) single nucleotide variant not specified [RCV004098765] Chr19:51945091 [GRCh38]
Chr19:52448344 [GRCh37]
Chr19:19q13.41		 likely benign
NM_001031721.4(ZNF613):c.308G>T (p.Cys103Phe) single nucleotide variant not specified [RCV004221911] Chr19:51944191 [GRCh38]
Chr19:52447444 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1766C>T (p.Ala589Val) single nucleotide variant not specified [RCV004221229] Chr19:51945649 [GRCh38]
Chr19:52448902 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.106G>A (p.Val36Met) single nucleotide variant not specified [RCV005526336] Chr19:51940299 [GRCh38]
Chr19:52443552 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1375A>T (p.Thr459Ser) single nucleotide variant not specified [RCV005526345] Chr19:51945258 [GRCh38]
Chr19:52448511 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.905G>A (p.Arg302Gln) single nucleotide variant not specified [RCV004262351] Chr19:51944788 [GRCh38]
Chr19:52448041 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1846A>G (p.Thr616Ala) single nucleotide variant not specified [RCV005797094] Chr19:51945729 [GRCh38]
Chr19:52448982 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.133G>A (p.Val45Met) single nucleotide variant not specified [RCV005797084] Chr19:51940326 [GRCh38]
Chr19:52443579 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1561T>G (p.Phe521Val) single nucleotide variant not specified [RCV005797088] Chr19:51945444 [GRCh38]
Chr19:52448697 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1840A>G (p.Ile614Val) single nucleotide variant not specified [RCV005797093] Chr19:51945723 [GRCh38]
Chr19:52448976 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.809G>T (p.Arg270Leu) single nucleotide variant not specified [RCV006350573] Chr19:51944692 [GRCh38]
Chr19:52447945 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1811C>T (p.Ala604Val) single nucleotide variant not specified [RCV006350576] Chr19:51945694 [GRCh38]
Chr19:52448947 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.190G>C (p.Glu64Gln) single nucleotide variant not specified [RCV006350577] Chr19:51940664 [GRCh38]
Chr19:52443917 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.650C>T (p.Ser217Phe) single nucleotide variant not specified [RCV006350574] Chr19:51944533 [GRCh38]
Chr19:52447786 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1693G>T (p.Asp565Tyr) single nucleotide variant not specified [RCV006350579] Chr19:51945576 [GRCh38]
Chr19:52448829 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1766C>A (p.Ala589Glu) single nucleotide variant not specified [RCV006350580] Chr19:51945649 [GRCh38]
Chr19:52448902 [GRCh37]
Chr19:19q13.41		 likely benign
NM_001031721.4(ZNF613):c.809G>A (p.Arg270His) single nucleotide variant not specified [RCV005797083] Chr19:51944692 [GRCh38]
Chr19:52447945 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1396T>C (p.Ser466Pro) single nucleotide variant not specified [RCV005797086] Chr19:51945279 [GRCh38]
Chr19:52448532 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1646C>T (p.Pro549Leu) single nucleotide variant not specified [RCV005797081] Chr19:51945529 [GRCh38]
Chr19:52448782 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.745G>C (p.Glu249Gln) single nucleotide variant not specified [RCV005797082] Chr19:51944628 [GRCh38]
Chr19:52447881 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1283A>G (p.Tyr428Cys) single nucleotide variant not specified [RCV005797085] Chr19:51945166 [GRCh38]
Chr19:52448419 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1580T>G (p.Leu527Arg) single nucleotide variant not specified [RCV005797090] Chr19:51945463 [GRCh38]
Chr19:52448716 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.164A>G (p.Asp55Gly) single nucleotide variant not specified [RCV005797091] Chr19:51940638 [GRCh38]
Chr19:52443891 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.455A>C (p.Lys152Thr) single nucleotide variant not specified [RCV005797092] Chr19:51944338 [GRCh38]
Chr19:52447591 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1093G>A (p.Ala365Thr) single nucleotide variant not specified [RCV005797095] Chr19:51944976 [GRCh38]
Chr19:52448229 [GRCh37]
Chr19:19q13.41		 likely benign
NM_001031721.4(ZNF613):c.808C>G (p.Arg270Gly) single nucleotide variant not specified [RCV004356771] Chr19:51944691 [GRCh38]
Chr19:52447944 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1325G>A (p.Cys442Tyr) single nucleotide variant not specified [RCV005797087] Chr19:51945208 [GRCh38]
Chr19:52448461 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.443G>C (p.Arg148Thr) single nucleotide variant not specified [RCV005797089] Chr19:51944326 [GRCh38]
Chr19:52447579 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1530A>C (p.Arg510Ser) single nucleotide variant not specified [RCV004599988] Chr19:51945413 [GRCh38]
Chr19:52448666 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.76G>A (p.Gly26Ser) single nucleotide variant not specified [RCV004599989] Chr19:51940269 [GRCh38]
Chr19:52443522 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.1790C>A (p.Ala597Asp) single nucleotide variant not specified [RCV005300560] Chr19:51945673 [GRCh38]
Chr19:52448926 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.290T>C (p.Leu97Pro) single nucleotide variant not specified [RCV005300561] Chr19:51944173 [GRCh38]
Chr19:52447426 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.652C>T (p.Arg218Cys) single nucleotide variant not specified [RCV005300562] Chr19:51944535 [GRCh38]
Chr19:52447788 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001031721.4(ZNF613):c.502A>G (p.Lys168Glu) single nucleotide variant not specified [RCV005300564] Chr19:51944385 [GRCh38]
Chr19:52447638 [GRCh37]
Chr19:19q13.41		 uncertain significance
miRNA Target Status (No longer updated)

Predicted Target Of
Summary Value
Count of predictions:717
Count of miRNA genes:519
Interacting mature miRNAs:567
Transcripts:ENST00000293471, ENST00000391794, ENST00000593379, ENST00000593395, ENST00000599683, ENST00000600853, ENST00000601794
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
1559110SCL22_HSerum cholesterol level QTL 22 (human)3.590.000241Lipid levelLDL cholesterol193190759457907594Human
628868778GWAS2777007_Herucate (22:1n9) measurement QTL GWAS2777007 (human)2e-08erucate (22:1n9) measurement195194241851942419Human
645181678GWAS3080158_Hestrogen-receptor positive breast cancer, survival time, breast carcinoma, response to endocrine therapy QTL GWAS3080158 (human)0.0000006estrogen-receptor positive breast cancer, survival time, breast carcinoma, response to endocrine therapy195194213351942134Human
628523261GWAS2431490_Hexecutive function measurement, cognitive function measurement QTL GWAS2431490 (human)0.000007cognitive behavior trait (VT:0010450)195194658751946588Human
1331657COPD9_HChronic obstructive pulmonary disease QTL 9 (human)1.94Chronic airflow obstructionpost-bronchodilator FEV1193102176057021760Human
628559609GWAS2467838_Hlevel of SPARC-related modular calcium-binding protein 2 in blood serum QTL GWAS2467838 (human)8e-14level of SPARC-related modular calcium-binding protein 2 in blood serum195193786551937866Human
628522169GWAS2430398_Hexecutive function measurement, cognitive function measurement, major depressive disorder QTL GWAS2430398 (human)9e-10cognitive behavior trait (VT:0010450)195194658751946588Human

Markers in Region
RH92372  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371952,448,737 - 52,448,913UniSTSGRCh37
Build 361957,140,549 - 57,140,725RGDNCBI36
Celera1949,498,303 - 49,498,479RGD
Cytogenetic Map19q13.41UniSTS
HuRef1948,779,388 - 48,779,564UniSTS
GeneMap99-GB4 RH Map19278.55UniSTS
RH118883  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371952,438,937 - 52,439,219UniSTSGRCh37
Build 361957,130,749 - 57,131,031RGDNCBI36
Celera1949,488,503 - 49,488,785RGD
Cytogenetic Map19q13.41UniSTS
HuRef1948,769,588 - 48,769,870UniSTS
TNG Radiation Hybrid Map1921794.0UniSTS
ZNF613__4711  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371952,448,454 - 52,448,992UniSTSGRCh37
Build 361957,140,266 - 57,140,804RGDNCBI36
Celera1949,498,020 - 49,498,558RGD
HuRef1948,779,105 - 48,779,643UniSTS
D11S2921  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map10q24.33UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map13q12UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic MapXp11.4-p11.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map1q24.1UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map18pter-p11.3UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map4q34.1UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map7q21.12UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map16p13.13UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map8p23-p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map17q21-q22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map11p13-p12UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map5q12-q13UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map15q15-q21.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map21p11.1UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic MapXq25-q26.3UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map12q24.31-q24.32UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map18p11.32UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map20q13.1UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map9p24.1-p23UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map20q12-q13.12UniSTS
Cytogenetic Map1q24-q25.3UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map6q25.1-q26UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic Map12p11.22UniSTS
Cytogenetic Map17q23.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map9p11UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map11p11.11UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map15q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map15q22-qterUniSTS
Cytogenetic Map10q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map5p15.1UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map19p13.2-cenUniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map9q33UniSTS
Cytogenetic Map1p36-p35UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map4q25-q27UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic MapXq26.2UniSTS
Cytogenetic Map8q13.2UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic MapXq21.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map5p13.1-p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map6q14.3-q16.1UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map6q14.3UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map10p11.21UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map17q21.1-q21.3UniSTS
Cytogenetic Map6q11.1UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map12p13.2-p12.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map10q24-q25UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map14q11.2-q21UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map5p14.3UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map9p13.1UniSTS
Cytogenetic Map9q34.13UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2429 2788 2250 4969 1726 2346 6 624 1942 465 2267 7288 6464 53 3732 1 849 1739 1612 174 1

Sequence


Ensembl Acc Id: ENST00000293471   ⟹   ENSP00000293471
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,472 - 51,946,621 (+)Ensembl
Ensembl Acc Id: ENST00000391794   ⟹   ENSP00000375671
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,435 - 51,948,046 (+)Ensembl
Ensembl Acc Id: ENST00000593379
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,484 - 51,942,820 (+)Ensembl
Ensembl Acc Id: ENST00000593395
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,147 - 51,936,125 (+)Ensembl
Ensembl Acc Id: ENST00000599683   ⟹   ENSP00000472455
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,448 - 51,944,246 (+)Ensembl
Ensembl Acc Id: ENST00000600853   ⟹   ENSP00000468850
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,474 - 51,944,165 (+)Ensembl
Ensembl Acc Id: ENST00000601794   ⟹   ENSP00000490115
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,944,885 - 51,948,759 (+)Ensembl
Ensembl Acc Id: ENST00000866494   ⟹   ENSP00000536553
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,374 - 51,948,046 (+)Ensembl
Ensembl Acc Id: ENST00000866495   ⟹   ENSP00000536554
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,375 - 51,948,046 (+)Ensembl
Ensembl Acc Id: ENST00000866496   ⟹   ENSP00000536555
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,375 - 51,948,046 (+)Ensembl
Ensembl Acc Id: ENST00000866497   ⟹   ENSP00000536556
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,375 - 51,948,046 (+)Ensembl
Ensembl Acc Id: ENST00000866498   ⟹   ENSP00000536557
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,374 - 51,948,046 (+)Ensembl
Ensembl Acc Id: ENST00000866499   ⟹   ENSP00000536558
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,375 - 51,948,046 (+)Ensembl
Ensembl Acc Id: ENST00000911548   ⟹   ENSP00000581607
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,374 - 51,948,046 (+)Ensembl
Ensembl Acc Id: ENST00000911549   ⟹   ENSP00000581608
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,487 - 51,948,046 (+)Ensembl
Ensembl Acc Id: ENST00000911550   ⟹   ENSP00000581609
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,375 - 51,948,046 (+)Ensembl
Ensembl Acc Id: ENST00000911551   ⟹   ENSP00000581610
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,375 - 51,948,046 (+)Ensembl
Ensembl Acc Id: ENST00000911552   ⟹   ENSP00000581611
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,374 - 51,948,046 (+)Ensembl
Ensembl Acc Id: ENST00000911553   ⟹   ENSP00000581612
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,375 - 51,948,046 (+)Ensembl
Ensembl Acc Id: ENST00000911554   ⟹   ENSP00000581613
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,375 - 51,948,046 (+)Ensembl
Ensembl Acc Id: ENST00000911555   ⟹   ENSP00000581614
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,374 - 51,948,046 (+)Ensembl
Ensembl Acc Id: ENST00000911556   ⟹   ENSP00000581615
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,487 - 51,948,046 (+)Ensembl
Ensembl Acc Id: ENST00000911557   ⟹   ENSP00000581616
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,487 - 51,948,046 (+)Ensembl
Ensembl Acc Id: ENST00000946116   ⟹   ENSP00000616175
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,374 - 51,948,046 (+)Ensembl
Ensembl Acc Id: ENST00000946117   ⟹   ENSP00000616176
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,375 - 51,948,046 (+)Ensembl
Ensembl Acc Id: ENST00000946118   ⟹   ENSP00000616177
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,375 - 51,948,046 (+)Ensembl
Ensembl Acc Id: ENST00000946119   ⟹   ENSP00000616178
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,375 - 51,948,046 (+)Ensembl
Ensembl Acc Id: ENST00001114316   ⟹   ENSP00000784121
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,375 - 51,938,955 (+)Ensembl
Ensembl Acc Id: ENST00001135778   ⟹   ENSP00000804905
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1951,927,375 - 51,948,046 (+)Ensembl
RefSeq Acc Id: NM_001031721   ⟹   NP_001026891
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381951,927,472 - 51,946,621 (+)NCBI
GRCh371952,430,688 - 52,449,011 (+)RGD
Build 361957,122,541 - 57,140,817 (+)NCBI Archive
Celera1949,480,254 - 49,498,577 (+)RGD
HuRef1948,761,338 - 48,779,662 (+)ENTREZGENE
CHM1_11952,432,545 - 52,450,868 (+)NCBI
T2T-CHM13v2.01955,014,667 - 55,033,819 (+)NCBI
Sequence:
RefSeq Acc Id: NM_024840   ⟹   NP_079116
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381951,927,472 - 51,946,621 (+)NCBI
GRCh371952,430,688 - 52,449,011 (+)RGD
Build 361957,122,500 - 57,140,817 (+)NCBI Archive
Celera1949,480,254 - 49,498,577 (+)RGD
HuRef1948,761,338 - 48,779,662 (+)ENTREZGENE
CHM1_11952,432,545 - 52,450,868 (+)NCBI
T2T-CHM13v2.01955,014,667 - 55,033,819 (+)NCBI
Sequence:
RefSeq Acc Id: NP_001026891   ⟸   NM_001031721
- Peptide Label: isoform 1
- UniProtKB: Q96SS9 (UniProtKB/Swiss-Prot),   Q6PF04 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_079116   ⟸   NM_024840
- Peptide Label: isoform 2
- UniProtKB: Q6PF04 (UniProtKB/Swiss-Prot)
- Sequence:
Ensembl Acc Id: ENSP00000293471   ⟸   ENST00000293471
Ensembl Acc Id: ENSP00000472455   ⟸   ENST00000599683
Ensembl Acc Id: ENSP00000468850   ⟸   ENST00000600853
Ensembl Acc Id: ENSP00000490115   ⟸   ENST00000601794
Ensembl Acc Id: ENSP00000375671   ⟸   ENST00000391794
Ensembl Acc Id: ENSP00000581612   ⟸   ENST00000911553
Ensembl Acc Id: ENSP00000536558   ⟸   ENST00000866499
Ensembl Acc Id: ENSP00000536556   ⟸   ENST00000866497
Ensembl Acc Id: ENSP00000536555   ⟸   ENST00000866496
Ensembl Acc Id: ENSP00000536554   ⟸   ENST00000866495
Ensembl Acc Id: ENSP00000616175   ⟸   ENST00000946116
Ensembl Acc Id: ENSP00000581611   ⟸   ENST00000911552
Ensembl Acc Id: ENSP00000581616   ⟸   ENST00000911557
Ensembl Acc Id: ENSP00000616178   ⟸   ENST00000946119
Ensembl Acc Id: ENSP00000581613   ⟸   ENST00000911554
Ensembl Acc Id: ENSP00000616177   ⟸   ENST00000946118
Ensembl Acc Id: ENSP00000581608   ⟸   ENST00000911549
Ensembl Acc Id: ENSP00000581614   ⟸   ENST00000911555
Ensembl Acc Id: ENSP00000581607   ⟸   ENST00000911548
Ensembl Acc Id: ENSP00000536557   ⟸   ENST00000866498
Ensembl Acc Id: ENSP00000616176   ⟸   ENST00000946117
Ensembl Acc Id: ENSP00000536553   ⟸   ENST00000866494
Ensembl Acc Id: ENSP00000581615   ⟸   ENST00000911556
Ensembl Acc Id: ENSP00000581609   ⟸   ENST00000911550
Ensembl Acc Id: ENSP00000581610   ⟸   ENST00000911551
Ensembl Acc Id: ENSP00000784121   ⟸   ENST00001114316
Ensembl Acc Id: ENSP00000804905   ⟸   ENST00001135778
Protein Domains
C2H2-type   KRAB

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q6PF04-F1-model_v2 AlphaFold Q6PF04 1-617 view protein structure

Promoters
RGD ID:13205427
Promoter ID:EPDNEW_H26294
Type:multiple initiation site
Name:ZNF613_1
Description:zinc finger protein 613
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26295  EPDNEW_H26296  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381951,926,810 - 51,926,870EPDNEW
RGD ID:13205429
Promoter ID:EPDNEW_H26295
Type:initiation region
Name:ZNF613_3
Description:zinc finger protein 613
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26294  EPDNEW_H26296  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381951,927,188 - 51,927,248EPDNEW
RGD ID:13205431
Promoter ID:EPDNEW_H26296
Type:initiation region
Name:ZNF613_2
Description:zinc finger protein 613
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26294  EPDNEW_H26295  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381951,927,476 - 51,927,536EPDNEW
RGD ID:6796394
Promoter ID:HG_KWN:30727
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_001031721,   NM_024840
Position:
Human AssemblyChrPosition (strand)Source
Build 361957,122,036 - 57,122,612 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
COSMIC ZNF613 COSMIC
Ensembl Genes ENSG00000176024 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000293471 ENTREZGENE
  ENST00000293471.11 UniProtKB/Swiss-Prot
  ENST00000391794 ENTREZGENE
  ENST00000391794.8 UniProtKB/Swiss-Prot
  ENST00000866494.1 UniProtKB/Swiss-Prot
  ENST00000866495.1 UniProtKB/Swiss-Prot
  ENST00000866496.1 UniProtKB/Swiss-Prot
  ENST00000866497.1 UniProtKB/Swiss-Prot
  ENST00000866498.1 UniProtKB/Swiss-Prot
  ENST00000866499.1 UniProtKB/Swiss-Prot
  ENST00000911548.1 UniProtKB/Swiss-Prot
  ENST00000911549.1 UniProtKB/Swiss-Prot
  ENST00000911550.1 UniProtKB/Swiss-Prot
  ENST00000911551.1 UniProtKB/Swiss-Prot
  ENST00000911552.1 UniProtKB/Swiss-Prot
  ENST00000911553.1 UniProtKB/Swiss-Prot
  ENST00000911554.1 UniProtKB/Swiss-Prot
  ENST00000911555.1 UniProtKB/Swiss-Prot
  ENST00000911556.1 UniProtKB/Swiss-Prot
  ENST00000911557.1 UniProtKB/Swiss-Prot
  ENST00000946116.1 UniProtKB/Swiss-Prot
  ENST00000946117.1 UniProtKB/Swiss-Prot
  ENST00000946118.1 UniProtKB/Swiss-Prot
  ENST00000946119.1 UniProtKB/Swiss-Prot
Gene3D-CATH 6.10.140.140 UniProtKB/Swiss-Prot
  Classic Zinc Finger UniProtKB/Swiss-Prot
GTEx ENSG00000176024 GTEx
HGNC ID HGNC:25827 ENTREZGENE
Human Proteome Map ZNF613 Human Proteome Map
InterPro KRAB UniProtKB/Swiss-Prot
  KRAB_dom_sf UniProtKB/Swiss-Prot
  Znf_C2H2_sf UniProtKB/Swiss-Prot
  Znf_C2H2_type UniProtKB/Swiss-Prot
KEGG Report hsa:79898 UniProtKB/Swiss-Prot
NCBI Gene 79898 ENTREZGENE
PANTHER ZINC FINGER PROTEIN UniProtKB/Swiss-Prot
  ZINC FINGER WITH KRAB AND SCAN DOMAINS 7 UniProtKB/Swiss-Prot
Pfam KRAB UniProtKB/Swiss-Prot
  zf-C2H2 UniProtKB/Swiss-Prot
PharmGKB PA134937067 PharmGKB
PROSITE KRAB UniProtKB/Swiss-Prot
  ZINC_FINGER_C2H2_1 UniProtKB/Swiss-Prot
  ZINC_FINGER_C2H2_2 UniProtKB/Swiss-Prot
SMART KRAB UniProtKB/Swiss-Prot
  ZnF_C2H2 UniProtKB/Swiss-Prot
Superfamily-SCOP SSF109640 UniProtKB/Swiss-Prot
  SSF57667 UniProtKB/Swiss-Prot
UniProt A0A1B0GUH8_HUMAN UniProtKB/TrEMBL
  M0QX19_HUMAN UniProtKB/TrEMBL
  M0R2C1_HUMAN UniProtKB/TrEMBL
  Q6PF04 ENTREZGENE
  Q96SS9 ENTREZGENE
  ZN613_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary Q96SS9 UniProtKB/Swiss-Prot