ZNF214 (zinc finger protein 214) - Rat Genome Database

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Gene: ZNF214 (zinc finger protein 214) Homo sapiens
Analyze
Symbol: ZNF214
Name: zinc finger protein 214
RGD ID: 1349128
HGNC Page HGNC:13006
Description: Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; and metal ion binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: BAZ 1; BAZ-1; BAZ1; BWSCR2-associated zinc finger protein 1
RGD Orthologs
Chinchilla
Bonobo
Dog
Squirrel
Green Monkey
Naked Mole-Rat
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
GRCh38116,997,085 - 7,020,346 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl116,997,085 - 7,020,346 (-)EnsemblGRCh38hg38GRCh38
GRCh37117,018,316 - 7,041,577 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36116,977,125 - 6,998,162 (-)NCBINCBI36Build 36hg18NCBI36
Celera117,139,602 - 7,160,626 (-)NCBICelera
Cytogenetic Map11p15.4NCBI
HuRef116,679,041 - 6,700,081 (-)NCBIHuRef
CHM1_1117,019,496 - 7,040,513 (-)NCBICHM1_1
T2T-CHM13v2.0117,055,490 - 7,078,724 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


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)

References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:7959730   PMID:8889548   PMID:10762538   PMID:12477932   PMID:12970396   PMID:16344560   PMID:20980787   PMID:21448237   PMID:21873635   PMID:22052655   PMID:28514442   PMID:29987050  
PMID:33961781   PMID:34673265   PMID:35914814  


Genomics

Comparative Map Data
ZNF214
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38116,997,085 - 7,020,346 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl116,997,085 - 7,020,346 (-)EnsemblGRCh38hg38GRCh38
GRCh37117,018,316 - 7,041,577 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36116,977,125 - 6,998,162 (-)NCBINCBI36Build 36hg18NCBI36
Celera117,139,602 - 7,160,626 (-)NCBICelera
Cytogenetic Map11p15.4NCBI
HuRef116,679,041 - 6,700,081 (-)NCBIHuRef
CHM1_1117,019,496 - 7,040,513 (-)NCBICHM1_1
T2T-CHM13v2.0117,055,490 - 7,078,724 (-)NCBIT2T-CHM13v2.0
Znf214
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_00495541422,853,386 - 22,857,387 (-)NCBIChiLan1.0ChiLan1.0
ZNF214
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v299,402,963 - 9,426,294 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1119,370,906 - 9,391,703 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0117,099,995 - 7,122,820 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1116,781,948 - 6,805,230 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl116,784,450 - 6,805,207 (-)Ensemblpanpan1.1panPan2
ZNF214
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12130,683,883 - 30,707,172 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2130,692,268 - 30,707,011 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2130,255,080 - 30,278,353 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02131,492,561 - 31,515,834 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2131,499,696 - 31,515,847 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12130,816,264 - 30,839,536 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02130,985,950 - 31,009,297 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02131,281,162 - 31,304,518 (-)NCBIUU_Cfam_GSD_1.0
Znf214
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494754,761,082 - 54,774,210 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936841313,330 - 325,625 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_004936841313,164 - 326,236 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ZNF214
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1157,802,536 - 57,889,074 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl157,822,351 - 57,825,360 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666038155,556,290 - 155,585,815 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Znf214
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046248178,786,072 - 8,796,272 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ZNF214
20 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 11p15.4(chr11:3745061-7846057)x3 copy number gain See cases [RCV000053616] Chr11:3745061..7846057 [GRCh38]
Chr11:3766291..7867604 [GRCh37]
Chr11:3722867..7824180 [NCBI36]
Chr11:11p15.4		 pathogenic
GRCh38/hg38 11p15.5-13(chr11:202758-31726224)x3 copy number gain See cases [RCV000053613] Chr11:202758..31726224 [GRCh38]
Chr11:202758..31747772 [GRCh37]
Chr11:192758..31704348 [NCBI36]
Chr11:11p15.5-13		 pathogenic
NM_013249.2(ZNF214):c.1164T>G (p.Cys388Trp) single nucleotide variant Malignant melanoma [RCV000062341] Chr11:7000519 [GRCh38]
Chr11:7021750 [GRCh37]
Chr11:6978326 [NCBI36]
Chr11:11p15.4		 not provided
GRCh38/hg38 11p15.5-15.1(chr11:446754-18904742)x3 copy number gain See cases [RCV000133997] Chr11:446754..18904742 [GRCh38]
Chr11:446754..18926289 [GRCh37]
Chr11:436754..18882865 [NCBI36]
Chr11:11p15.5-15.1		 pathogenic
GRCh38/hg38 11p15.5-15.4(chr11:61793-10727969)x3 copy number gain See cases [RCV000139987] Chr11:61793..10727969 [GRCh38]
Chr11:61793..10749516 [GRCh37]
Chr11:51793..10706092 [NCBI36]
Chr11:11p15.5-15.4		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470) copy number gain See cases [RCV000511729] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-12(chr11:230615-37698540)x3 copy number gain See cases [RCV000511561] Chr11:230615..37698540 [GRCh37]
Chr11:11p15.5-12		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3 copy number gain See cases [RCV000510881] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
NM_013249.4(ZNF214):c.1463A>G (p.His488Arg) single nucleotide variant not specified [RCV004310906] Chr11:7000220 [GRCh38]
Chr11:7021451 [GRCh37]
Chr11:11p15.4		 uncertain significance
GRCh37/hg19 11p15.5-14.3(chr11:230615-25584362)x3 copy number gain See cases [RCV000512225] Chr11:230615..25584362 [GRCh37]
Chr11:11p15.5-14.3		 pathogenic
GRCh37/hg19 11p15.5-13(chr11:230615-31995219)x3 copy number gain See cases [RCV000512477] Chr11:230615..31995219 [GRCh37]
Chr11:11p15.5-13		 pathogenic
GRCh37/hg19 11p15.5-15.1(chr11:230615-17099213)x3 copy number gain not provided [RCV000683372] Chr11:230615..17099213 [GRCh37]
Chr11:11p15.5-15.1		 pathogenic
GRCh37/hg19 11p15.4(chr11:6905914-7062692)x1 copy number loss not provided [RCV000683310] Chr11:6905914..7062692 [GRCh37]
Chr11:11p15.4		 uncertain significance
GRCh37/hg19 11p15.4(chr11:6969013-9257231)x3 copy number gain not provided [RCV000683360] Chr11:6969013..9257231 [GRCh37]
Chr11:11p15.4		 pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:230615-9704511)x3 copy number gain not provided [RCV000683369] Chr11:230615..9704511 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3 copy number gain not provided [RCV000737348] Chr11:198510..134934063 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3 copy number gain not provided [RCV000749874] Chr11:70864..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-15.3(chr11:193146-12643136) copy number gain Silver-Russell syndrome 1 [RCV000767567] Chr11:193146..12643136 [GRCh37]
Chr11:11p15.5-15.3		 pathogenic
GRCh37/hg19 11p15.4(chr11:6908898-7058885)x1 copy number loss not provided [RCV000847040] Chr11:6908898..7058885 [GRCh37]
Chr11:11p15.4		 uncertain significance
GRCh37/hg19 11p15.5-15.4(chr11:230616-8250724)x3 copy number gain not provided [RCV002472435] Chr11:230616..8250724 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
GRCh37/hg19 11p15.5-13(chr11:235934-33826995)x3 copy number gain not provided [RCV001006372] Chr11:235934..33826995 [GRCh37]
Chr11:11p15.5-13		 pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:210300-8664358)x3 copy number gain Silver-Russell syndrome 1 [RCV001263222] Chr11:210300..8664358 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
GRCh37/hg19 11p15.4(chr11:6502523-7248333)x3 copy number gain not provided [RCV001836564] Chr11:6502523..7248333 [GRCh37]
Chr11:11p15.4		 uncertain significance
GRCh37/hg19 11p15.5-14.2(chr11:230615-26881146)x3 copy number gain See cases [RCV002286351] Chr11:230615..26881146 [GRCh37]
Chr11:11p15.5-14.2		 pathogenic
NM_013249.4(ZNF214):c.686A>G (p.Tyr229Cys) single nucleotide variant not specified [RCV004312782] Chr11:7000997 [GRCh38]
Chr11:7022228 [GRCh37]
Chr11:11p15.4		 likely benign
GRCh37/hg19 11p15.4(chr11:6943254-7051084)x3 copy number gain not provided [RCV002474648] Chr11:6943254..7051084 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_013249.4(ZNF214):c.1802A>T (p.His601Leu) single nucleotide variant not specified [RCV004179369] Chr11:6999881 [GRCh38]
Chr11:7021112 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_013249.4(ZNF214):c.697C>T (p.Arg233Trp) single nucleotide variant not specified [RCV004141694] Chr11:7000986 [GRCh38]
Chr11:7022217 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_013249.4(ZNF214):c.1754G>A (p.Arg585His) single nucleotide variant not specified [RCV004230744] Chr11:6999929 [GRCh38]
Chr11:7021160 [GRCh37]
Chr11:11p15.4		 likely benign
NM_013249.4(ZNF214):c.1294C>A (p.His432Asn) single nucleotide variant not specified [RCV004157070] Chr11:7000389 [GRCh38]
Chr11:7021620 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_013249.4(ZNF214):c.1739A>T (p.Lys580Ile) single nucleotide variant not specified [RCV004237278] Chr11:6999944 [GRCh38]
Chr11:7021175 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_013249.4(ZNF214):c.100G>C (p.Glu34Gln) single nucleotide variant not specified [RCV004205763] Chr11:7002736 [GRCh38]
Chr11:7023967 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_013249.4(ZNF214):c.1418C>T (p.Pro473Leu) single nucleotide variant not specified [RCV004117030] Chr11:7000265 [GRCh38]
Chr11:7021496 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_013249.4(ZNF214):c.1559A>G (p.His520Arg) single nucleotide variant not specified [RCV004187234] Chr11:7000124 [GRCh38]
Chr11:7021355 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_013249.4(ZNF214):c.400A>G (p.Lys134Glu) single nucleotide variant not specified [RCV004199737] Chr11:7001283 [GRCh38]
Chr11:7022514 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_013249.4(ZNF214):c.223G>A (p.Ala75Thr) single nucleotide variant not specified [RCV004208153] Chr11:7001460 [GRCh38]
Chr11:7022691 [GRCh37]
Chr11:11p15.4		 likely benign
NM_013249.4(ZNF214):c.1691G>C (p.Ser564Thr) single nucleotide variant not specified [RCV004211323] Chr11:6999992 [GRCh38]
Chr11:7021223 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_013249.4(ZNF214):c.1061G>T (p.Gly354Val) single nucleotide variant not specified [RCV004169322] Chr11:7000622 [GRCh38]
Chr11:7021853 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_013249.4(ZNF214):c.11C>T (p.Thr4Ile) single nucleotide variant not specified [RCV004285150] Chr11:7002825 [GRCh38]
Chr11:7024056 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_013249.4(ZNF214):c.1373G>A (p.Arg458His) single nucleotide variant not specified [RCV004346753] Chr11:7000310 [GRCh38]
Chr11:7021541 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_013249.4(ZNF214):c.484T>C (p.Phe162Leu) single nucleotide variant not specified [RCV004338153] Chr11:7001199 [GRCh38]
Chr11:7022430 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_013249.4(ZNF214):c.1711A>C (p.Ile571Leu) single nucleotide variant not specified [RCV004338614] Chr11:6999972 [GRCh38]
Chr11:7021203 [GRCh37]
Chr11:11p15.4		 uncertain significance
GRCh37/hg19 11p15.4(chr11:6801941-7136661)x3 copy number gain not provided [RCV003484831] Chr11:6801941..7136661 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_013249.4(ZNF214):c.594A>G (p.Pro198=) single nucleotide variant not provided [RCV003397905] Chr11:7001089 [GRCh38]
Chr11:7022320 [GRCh37]
Chr11:11p15.4		 likely benign
GRCh37/hg19 11p15.5-15.4(chr11:230615-8821443)x3 copy number gain Russell-Silver syndrome [RCV003444025] Chr11:230615..8821443 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
NM_013249.4(ZNF214):c.102G>C (p.Glu34Asp) single nucleotide variant not specified [RCV004491757] Chr11:7002734 [GRCh38]
Chr11:7023965 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_013249.4(ZNF214):c.1551G>T (p.Gln517His) single nucleotide variant not specified [RCV004491760] Chr11:7000132 [GRCh38]
Chr11:7021363 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_013249.4(ZNF214):c.247T>C (p.Tyr83His) single nucleotide variant not specified [RCV004491761] Chr11:7001436 [GRCh38]
Chr11:7022667 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_013249.4(ZNF214):c.451G>A (p.Gly151Ser) single nucleotide variant not specified [RCV004491763] Chr11:7001232 [GRCh38]
Chr11:7022463 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_013249.4(ZNF214):c.856C>A (p.Gln286Lys) single nucleotide variant not specified [RCV004491764] Chr11:7000827 [GRCh38]
Chr11:7022058 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_013249.4(ZNF214):c.262C>G (p.Gln88Glu) single nucleotide variant not specified [RCV004491762] Chr11:7001421 [GRCh38]
Chr11:7022652 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_013249.4(ZNF214):c.1105C>T (p.Arg369Trp) single nucleotide variant not specified [RCV004491758] Chr11:7000578 [GRCh38]
Chr11:7021809 [GRCh37]
Chr11:11p15.4		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:547
Count of miRNA genes:334
Interacting mature miRNAs:344
Transcripts:ENST00000278314, ENST00000525017, ENST00000531083, ENST00000536068
Prediction methods:Microtar, Miranda, Rnahybrid
Result types:miRGate_prediction

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

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

Markers in Region
D11S1098  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37117,035,556 - 7,035,800UniSTSGRCh37
Build 36116,992,132 - 6,992,376RGDNCBI36
Celera117,154,601 - 7,154,845RGD
Cytogenetic Map11p15.4UniSTS
HuRef116,694,051 - 6,694,295UniSTS
D11S4723  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37117,022,394 - 7,022,700UniSTSGRCh37
Build 36116,978,970 - 6,979,276RGDNCBI36
Celera117,141,447 - 7,141,753RGD
Cytogenetic Map11p15.4UniSTS
HuRef116,680,887 - 6,681,193UniSTS


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 2 4 1 3 13 33 11
Low 2159 1547 1538 477 465 334 2683 1035 3165 374 1379 1449 153 1 858 1630 4 2
Below cutoff 269 847 173 139 682 122 1644 1131 552 25 25 111 17 343 1144 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001354830 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001354831 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001354832 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001354833 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_013249 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_148988 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006718309 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011520357 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017018269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047427565 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054369899 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054369900 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054369901 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054369902 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA678604 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC100875 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF056617 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK313462 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC136772 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC144405 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX096368 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA313222 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471064 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA299430 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB262997 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KT585021 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000278314   ⟹   ENSP00000278314
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl116,997,085 - 7,020,346 (-)Ensembl
RefSeq Acc Id: ENST00000525017
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl117,015,820 - 7,020,342 (-)Ensembl
RefSeq Acc Id: ENST00000531083
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl117,001,448 - 7,020,314 (-)Ensembl
RefSeq Acc Id: ENST00000536068   ⟹   ENSP00000445373
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl116,999,363 - 7,020,235 (-)Ensembl
RefSeq Acc Id: NM_001354830   ⟹   NP_001341759
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38116,997,085 - 7,020,346 (-)NCBI
T2T-CHM13v2.0117,055,490 - 7,078,724 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001354831   ⟹   NP_001341760
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38116,997,085 - 7,020,346 (-)NCBI
T2T-CHM13v2.0117,055,490 - 7,078,724 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001354832   ⟹   NP_001341761
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38116,997,085 - 7,020,346 (-)NCBI
T2T-CHM13v2.0117,055,490 - 7,078,724 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001354833   ⟹   NP_001341762
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38116,997,085 - 7,020,346 (-)NCBI
T2T-CHM13v2.0117,055,490 - 7,078,724 (-)NCBI
Sequence:
RefSeq Acc Id: NM_013249   ⟹   NP_037381
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38116,997,085 - 7,020,346 (-)NCBI
GRCh37117,020,549 - 7,041,586 (-)RGD
Build 36116,977,125 - 6,998,162 (-)NCBI Archive
Celera117,139,602 - 7,160,626 (-)RGD
HuRef116,679,041 - 6,700,081 (-)RGD
CHM1_1117,019,496 - 7,040,513 (-)NCBI
T2T-CHM13v2.0117,055,490 - 7,078,724 (-)NCBI
Sequence:
RefSeq Acc Id: NR_148988
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38117,015,820 - 7,020,346 (-)NCBI
T2T-CHM13v2.0117,074,199 - 7,078,724 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006718309   ⟹   XP_006718372
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38116,997,085 - 7,020,346 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011520357   ⟹   XP_011518659
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38116,997,085 - 7,019,735 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017018269   ⟹   XP_016873758
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38116,997,085 - 7,019,745 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047427565   ⟹   XP_047283521
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38116,997,085 - 7,019,750 (-)NCBI
RefSeq Acc Id: XM_054369899   ⟹   XP_054225874
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0117,055,490 - 7,078,128 (-)NCBI
RefSeq Acc Id: XM_054369900   ⟹   XP_054225875
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0117,055,490 - 7,078,123 (-)NCBI
RefSeq Acc Id: XM_054369901   ⟹   XP_054225876
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0117,055,490 - 7,078,724 (-)NCBI
RefSeq Acc Id: XM_054369902   ⟹   XP_054225877
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0117,055,490 - 7,078,113 (-)NCBI
Reference Protein Sequences
RefSeq Acc Id: NP_037381   ⟸   NM_013249
- Peptide Label: isoform 2
- UniProtKB: B2R8Q1 (UniProtKB/Swiss-Prot),   Q9UL59 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_006718372   ⟸   XM_006718309
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_011518659   ⟸   XM_011520357
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_016873758   ⟸   XM_017018269
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: NP_001341761   ⟸   NM_001354832
- Peptide Label: isoform 2
- UniProtKB: Q9UL59 (UniProtKB/Swiss-Prot),   B2R8Q1 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001341762   ⟸   NM_001354833
- Peptide Label: isoform 3
- Sequence:
RefSeq Acc Id: NP_001341759   ⟸   NM_001354830
- Peptide Label: isoform 1
- Sequence:
RefSeq Acc Id: NP_001341760   ⟸   NM_001354831
- Peptide Label: isoform 2
- UniProtKB: Q9UL59 (UniProtKB/Swiss-Prot),   B2R8Q1 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000445373   ⟸   ENST00000536068
RefSeq Acc Id: ENSP00000278314   ⟸   ENST00000278314
RefSeq Acc Id: XP_047283521   ⟸   XM_047427565
- Peptide Label: isoform X1
- UniProtKB: Q9UL59 (UniProtKB/Swiss-Prot),   B2R8Q1 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054225876   ⟸   XM_054369901
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054225874   ⟸   XM_054369899
- Peptide Label: isoform X1
- UniProtKB: B7ZMB1 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054225875   ⟸   XM_054369900
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054225877   ⟸   XM_054369902
- Peptide Label: isoform X2
Protein Domains
C2H2-type   KRAB

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9UL59-F1-model_v2 AlphaFold Q9UL59 1-606 view protein structure

Promoters
RGD ID:6789609
Promoter ID:HG_KWN:12234
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:NM_013249,   NM_176822,   UC009YFH.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36116,997,894 - 6,998,394 (-)MPROMDB
RGD ID:7219543
Promoter ID:EPDNEW_H15516
Type:initiation region
Name:ZNF214_1
Description:zinc finger protein 214
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
GRCh38117,020,346 - 7,020,406EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:13006 AgrOrtholog
COSMIC ZNF214 COSMIC
Ensembl Genes ENSG00000149050 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000278314 ENTREZGENE
  ENST00000278314.5 UniProtKB/Swiss-Prot
  ENST00000525017 ENTREZGENE
  ENST00000536068 ENTREZGENE
  ENST00000536068.5 UniProtKB/Swiss-Prot
Gene3D-CATH 6.10.140.140 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Classic Zinc Finger UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000149050 GTEx
HGNC ID HGNC:13006 ENTREZGENE
Human Proteome Map ZNF214 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:7761 UniProtKB/Swiss-Prot
NCBI Gene 7761 ENTREZGENE
OMIM 605015 OMIM
PANTHER IP01015P-RELATED UniProtKB/TrEMBL
  ZINC FINGER AND SCAN DOMAIN-CONTAINING UniProtKB/Swiss-Prot
  ZINC FINGER PROTEIN 239 UniProtKB/Swiss-Prot
  ZINC FINGER PROTEIN 45 UniProtKB/TrEMBL
Pfam KRAB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  zf-C2H2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA37585 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 B2R8Q1 ENTREZGENE
  B7ZMB1 ENTREZGENE, UniProtKB/TrEMBL
  Q9UL59 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary B2R8Q1 UniProtKB/Swiss-Prot