ZNF155 (zinc finger protein 155) - Rat Genome Database

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Gene: ZNF155 (zinc finger protein 155) Homo sapiens
Analyze
Symbol: ZNF155
Name: zinc finger protein 155
RGD ID: 1352629
HGNC Page HGNC:12940
Description: Predicted to enable 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: VALIDATED
Previously known as: KRAB A domain; MGC161655; pHZ-96
RGD Orthologs
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
GRCh381943,984,188 - 43,998,326 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1943,967,862 - 43,998,326 (+)EnsemblGRCh38hg38GRCh38
GRCh371944,488,340 - 44,502,478 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361949,180,195 - 49,194,317 (+)NCBINCBI36Build 36hg18NCBI36
Build 341949,180,194 - 49,194,317NCBI
Celera1941,291,854 - 41,305,968 (+)NCBICelera
Cytogenetic Map19q13.31NCBI
HuRef1940,920,543 - 40,934,693 (+)NCBIHuRef
CHM1_11944,490,246 - 44,504,394 (+)NCBICHM1_1
T2T-CHM13v2.01946,807,096 - 46,821,233 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


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
Schizophrenia  (IAGP)
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:7557990   PMID:8617494   PMID:12477932   PMID:12743021   PMID:14702039   PMID:15057824   PMID:15489334   PMID:16344560   PMID:17220478   PMID:18029348   PMID:21873635   PMID:25416956  
PMID:32296183   PMID:32393512   PMID:34673265   PMID:36543142  


Genomics

Comparative Map Data
ZNF155
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381943,984,188 - 43,998,326 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1943,967,862 - 43,998,326 (+)EnsemblGRCh38hg38GRCh38
GRCh371944,488,340 - 44,502,478 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361949,180,195 - 49,194,317 (+)NCBINCBI36Build 36hg18NCBI36
Build 341949,180,194 - 49,194,317NCBI
Celera1941,291,854 - 41,305,968 (+)NCBICelera
Cytogenetic Map19q13.31NCBI
HuRef1940,920,543 - 40,934,693 (+)NCBIHuRef
CHM1_11944,490,246 - 44,504,394 (+)NCBICHM1_1
T2T-CHM13v2.01946,807,096 - 46,821,233 (+)NCBIT2T-CHM13v2.0
ZNF155
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22050,147,222 - 50,161,546 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11952,019,581 - 52,035,412 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01940,917,031 - 40,950,552 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11949,543,625 - 49,575,399 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1949,564,348 - 49,575,399 (+)Ensemblpanpan1.1panPan2
ZNF155
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1637,476,605 - 37,603,208 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl637,482,533 - 37,492,376 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366607317,026,797 - 17,041,351 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in ZNF155
30 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3 copy number gain See cases [RCV000133888] Chr19:11227942..44626354 [GRCh38]
Chr19:11338618..45129651 [GRCh37]
Chr19:11199618..49821491 [NCBI36]
Chr19:19p13.2-q13.31		 pathogenic
GRCh37/hg19 19q13.2-13.32(chr19:43013365-47241534)x1 copy number loss See cases [RCV000240182] Chr19:43013365..47241534 [GRCh37]
Chr19:19q13.2-13.32		 pathogenic
GRCh37/hg19 19q13.31(chr19:44466919-45029206)x1 copy number loss Breast ductal adenocarcinoma [RCV000207290] Chr19:44466919..45029206 [GRCh37]
Chr19:19q13.31		 uncertain significance
chr19:44501518-45322744 complex variant complex Breast ductal adenocarcinoma [RCV000207162] Chr19:44501518..45322744 [GRCh37]
Chr19:19q13.31-13.32		 uncertain significance
GRCh37/hg19 19q13.31-13.32(chr19:44300416-45639540)x1 copy number loss See cases [RCV000512107] Chr19:44300416..45639540 [GRCh37]
Chr19:19q13.31-13.32		 uncertain significance
NM_198089.3(ZNF155):c.274G>A (p.Ala92Thr) single nucleotide variant not specified [RCV004300462] Chr19:43996131 [GRCh38]
Chr19:44500283 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.877T>C (p.Cys293Arg) single nucleotide variant not specified [RCV004302617] Chr19:43996734 [GRCh38]
Chr19:44500886 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.842T>A (p.Ile281Asn) single nucleotide variant not specified [RCV004306795] Chr19:43996699 [GRCh38]
Chr19:44500851 [GRCh37]
Chr19:19q13.31		 uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) copy number gain See cases [RCV000512296] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
NM_198089.3(ZNF155):c.5C>T (p.Thr2Ile) single nucleotide variant not specified [RCV004293148] Chr19:43988548 [GRCh38]
Chr19:44492700 [GRCh37]
Chr19:19q13.31		 uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 copy number gain See cases [RCV000511289] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic|uncertain significance
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 duplication Schizophrenia [RCV000754211] Chr19:41608672..44315856 [GRCh38]
Chr19:19q13.2-13.31		 likely pathogenic
GRCh37/hg19 19q13.31(chr19:44470177-44513250)x3 copy number gain not provided [RCV000740181] Chr19:44470177..44513250 [GRCh37]
Chr19:19q13.31		 benign
GRCh37/hg19 19q13.31(chr19:44470331-44513250)x3 copy number gain not provided [RCV000740182] Chr19:44470331..44513250 [GRCh37]
Chr19:19q13.31		 benign
GRCh37/hg19 19q11-13.33(chr19:28271106-49213832)x3 copy number gain not provided [RCV000845733] Chr19:28271106..49213832 [GRCh37]
Chr19:19q11-13.33		 pathogenic
NM_198089.3(ZNF155):c.1381T>G (p.Cys461Gly) single nucleotide variant not specified [RCV004284437] Chr19:43997238 [GRCh38]
Chr19:44501390 [GRCh37]
Chr19:19q13.31		 uncertain significance
NC_000019.9:g.(?_44011002)_(45213778_?)dup duplication Ethylmalonic encephalopathy [RCV003116731] Chr19:44011002..45213778 [GRCh37]
Chr19:19q13.31-13.32		 uncertain significance
NM_198089.3(ZNF155):c.1307G>A (p.Gly436Asp) single nucleotide variant not specified [RCV004301742] Chr19:43997164 [GRCh38]
Chr19:44501316 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.1105G>A (p.Glu369Lys) single nucleotide variant not specified [RCV004304462] Chr19:43996962 [GRCh38]
Chr19:44501114 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.1480G>C (p.Val494Leu) single nucleotide variant not specified [RCV004319948] Chr19:43997337 [GRCh38]
Chr19:44501489 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.677A>G (p.His226Arg) single nucleotide variant not specified [RCV004294706] Chr19:43996534 [GRCh38]
Chr19:44500686 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.1316C>G (p.Thr439Ser) single nucleotide variant not specified [RCV004219927] Chr19:43997173 [GRCh38]
Chr19:44501325 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.1312G>A (p.Val438Ile) single nucleotide variant not specified [RCV004219926] Chr19:43997169 [GRCh38]
Chr19:44501321 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.149A>G (p.Gln50Arg) single nucleotide variant not specified [RCV004115457] Chr19:43991848 [GRCh38]
Chr19:44496000 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.1333T>A (p.Leu445Met) single nucleotide variant not specified [RCV004238069] Chr19:43997190 [GRCh38]
Chr19:44501342 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.634G>A (p.Glu212Lys) single nucleotide variant not specified [RCV004175639] Chr19:43996491 [GRCh38]
Chr19:44500643 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.1495C>G (p.Arg499Gly) single nucleotide variant not specified [RCV004191833] Chr19:43997352 [GRCh38]
Chr19:44501504 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.1036T>A (p.Cys346Ser) single nucleotide variant not specified [RCV004209496] Chr19:43996893 [GRCh38]
Chr19:44501045 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.1457G>A (p.Cys486Tyr) single nucleotide variant not specified [RCV004216261] Chr19:43997314 [GRCh38]
Chr19:44501466 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.943C>T (p.Pro315Ser) single nucleotide variant not specified [RCV004229366] Chr19:43996800 [GRCh38]
Chr19:44500952 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.822G>T (p.Gln274His) single nucleotide variant not specified [RCV004107628] Chr19:43996679 [GRCh38]
Chr19:44500831 [GRCh37]
Chr19:19q13.31		 likely benign
NM_198089.3(ZNF155):c.1196G>A (p.Ser399Asn) single nucleotide variant not specified [RCV004117028] Chr19:43997053 [GRCh38]
Chr19:44501205 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.227G>A (p.Gly76Glu) single nucleotide variant not specified [RCV004169994] Chr19:43991926 [GRCh38]
Chr19:44496078 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.1427G>A (p.Arg476Lys) single nucleotide variant not specified [RCV004283248] Chr19:43997284 [GRCh38]
Chr19:44501436 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.744T>A (p.Asn248Lys) single nucleotide variant not specified [RCV004256252] Chr19:43996601 [GRCh38]
Chr19:44500753 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.1406C>T (p.Ser469Leu) single nucleotide variant not specified [RCV004275789] Chr19:43997263 [GRCh38]
Chr19:44501415 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.401T>C (p.Val134Ala) single nucleotide variant not specified [RCV004254811] Chr19:43996258 [GRCh38]
Chr19:44500410 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.395C>T (p.Ser132Phe) single nucleotide variant not specified [RCV004302921] Chr19:43996252 [GRCh38]
Chr19:44500404 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.1477C>T (p.Leu493Phe) single nucleotide variant not specified [RCV004358302] Chr19:43997334 [GRCh38]
Chr19:44501486 [GRCh37]
Chr19:19q13.31		 likely benign
NM_198089.3(ZNF155):c.850G>T (p.Gly284Trp) single nucleotide variant not specified [RCV004491474] Chr19:43996707 [GRCh38]
Chr19:44500859 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.805T>C (p.Phe269Leu) single nucleotide variant not specified [RCV004491473] Chr19:43996662 [GRCh38]
Chr19:44500814 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.598G>A (p.Gly200Arg) single nucleotide variant not specified [RCV004491471] Chr19:43996455 [GRCh38]
Chr19:44500607 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.1310A>C (p.Tyr437Ser) single nucleotide variant not specified [RCV004491469] Chr19:43997167 [GRCh38]
Chr19:44501319 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.1042C>G (p.Gln348Glu) single nucleotide variant not specified [RCV004491467] Chr19:43996899 [GRCh38]
Chr19:44501051 [GRCh37]
Chr19:19q13.31		 likely benign
NM_198089.3(ZNF155):c.455A>G (p.Lys152Arg) single nucleotide variant not specified [RCV004491470] Chr19:43996312 [GRCh38]
Chr19:44500464 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.998G>T (p.Arg333Met) single nucleotide variant not specified [RCV004491476] Chr19:43996855 [GRCh38]
Chr19:44501007 [GRCh37]
Chr19:19q13.31		 uncertain significance
NM_198089.3(ZNF155):c.728G>A (p.Arg243His) single nucleotide variant not specified [RCV004491472] Chr19:43996585 [GRCh38]
Chr19:44500737 [GRCh37]
Chr19:19q13.31		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1237
Count of miRNA genes:644
Interacting mature miRNAs:713
Transcripts:ENST00000270014, ENST00000407951, ENST00000586454, ENST00000587302, ENST00000588531, ENST00000590411, ENST00000590615, ENST00000591532
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

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

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

Markers in Region
RH101969  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371944,501,162 - 44,501,281UniSTSGRCh37
Build 361949,193,002 - 49,193,121RGDNCBI36
Celera1941,304,653 - 41,304,772RGD
Cytogenetic Map19q13.2-q13.32UniSTS
HuRef1940,933,378 - 40,933,497UniSTS
GeneMap99-GB4 RH Map19247.43UniSTS
STS-U46188  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371944,495,782 - 44,495,996UniSTSGRCh37
Build 361949,187,622 - 49,187,836RGDNCBI36
Celera1941,299,274 - 41,299,488RGD
Cytogenetic Map19q13.2-q13.32UniSTS
HuRef1940,927,999 - 40,928,213UniSTS
GeneMap99-GB4 RH Map19243.84UniSTS
NCBI RH Map19445.7UniSTS
G31036  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371944,501,152 - 44,501,281UniSTSGRCh37
Build 361949,192,992 - 49,193,121RGDNCBI36
Celera1941,304,643 - 41,304,772RGD
Cytogenetic Map19q13.2-q13.32UniSTS
HuRef1940,933,368 - 40,933,497UniSTS


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 4 2 20 5 55 5 7 17 51 4 30 46 2
Low 2408 2764 1678 595 1658 436 4312 2087 3517 400 1416 1557 174 1 1202 2751 6 2
Below cutoff 19 222 27 23 190 23 37 93 166 15 13 10 2 35

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001260486 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001260487 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001260488 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_003445 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_198089 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005259215 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011527278 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011527279 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017027248 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024451694 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047439370 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047439371 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047439372 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047439373 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322018 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322019 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322020 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322021 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322022 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322023 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC006213 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC018725 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF187986 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK022875 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK297360 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK297384 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK314510 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC075050 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC075051 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC126377 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC130381 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ893627 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471126 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA111916 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA164828 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA504192 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC330742 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DN994146 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U09852 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U46188 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U46190 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000270014   ⟹   ENSP00000270014
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1943,984,188 - 43,998,326 (+)Ensembl
RefSeq Acc Id: ENST00000407951   ⟹   ENSP00000385163
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1943,984,194 - 43,997,853 (+)Ensembl
RefSeq Acc Id: ENST00000586454   ⟹   ENSP00000465981
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1943,984,221 - 43,996,203 (+)Ensembl
RefSeq Acc Id: ENST00000587302
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1943,984,219 - 43,988,943 (+)Ensembl
RefSeq Acc Id: ENST00000588531
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1943,984,188 - 43,988,968 (+)Ensembl
RefSeq Acc Id: ENST00000590411   ⟹   ENSP00000465201
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1943,967,862 - 43,996,129 (+)Ensembl
RefSeq Acc Id: ENST00000590615   ⟹   ENSP00000465691
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1943,984,217 - 43,997,554 (+)Ensembl
RefSeq Acc Id: ENST00000591532   ⟹   ENSP00000467110
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1943,984,191 - 43,996,307 (+)Ensembl
RefSeq Acc Id: ENST00000611002   ⟹   ENSP00000481677
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1943,984,170 - 43,998,325 (+)Ensembl
RefSeq Acc Id: NM_001260486   ⟹   NP_001247415
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381943,984,188 - 43,998,326 (+)NCBI
GRCh371944,472,014 - 44,502,477 (+)NCBI
HuRef1940,920,543 - 40,934,693 (+)NCBI
CHM1_11944,490,246 - 44,504,394 (+)NCBI
T2T-CHM13v2.01946,807,096 - 46,821,233 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001260487   ⟹   NP_001247416
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381943,984,188 - 43,998,326 (+)NCBI
GRCh371944,472,014 - 44,502,477 (+)NCBI
HuRef1940,920,543 - 40,934,693 (+)NCBI
CHM1_11944,490,246 - 44,504,394 (+)NCBI
T2T-CHM13v2.01946,807,096 - 46,821,233 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001260488   ⟹   NP_001247417
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381943,984,188 - 43,998,326 (+)NCBI
GRCh371944,472,014 - 44,502,477 (+)NCBI
HuRef1940,920,543 - 40,934,693 (+)NCBI
CHM1_11944,490,246 - 44,504,394 (+)NCBI
T2T-CHM13v2.01946,807,096 - 46,821,233 (+)NCBI
Sequence:
RefSeq Acc Id: NM_003445   ⟹   NP_003436
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381943,984,188 - 43,998,326 (+)NCBI
GRCh371944,472,014 - 44,502,477 (+)NCBI
Build 361949,180,195 - 49,194,317 (+)NCBI Archive
Celera1941,291,854 - 41,305,968 (+)RGD
HuRef1940,920,543 - 40,934,693 (+)NCBI
CHM1_11944,490,246 - 44,504,394 (+)NCBI
T2T-CHM13v2.01946,807,096 - 46,821,233 (+)NCBI
Sequence:
RefSeq Acc Id: NM_198089   ⟹   NP_932355
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381943,984,188 - 43,998,326 (+)NCBI
GRCh371944,472,014 - 44,502,477 (+)NCBI
Build 361949,180,195 - 49,194,317 (+)NCBI Archive
Celera1941,291,854 - 41,305,968 (+)RGD
HuRef1940,920,543 - 40,934,693 (+)NCBI
CHM1_11944,490,246 - 44,504,394 (+)NCBI
T2T-CHM13v2.01946,807,096 - 46,821,233 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011527278   ⟹   XP_011525580
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381943,984,188 - 43,998,326 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024451694   ⟹   XP_024307462
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381943,984,188 - 43,998,326 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047439370   ⟹   XP_047295326
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381943,984,188 - 43,998,326 (+)NCBI
RefSeq Acc Id: XM_047439371   ⟹   XP_047295327
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381943,985,533 - 43,998,326 (+)NCBI
RefSeq Acc Id: XM_047439372   ⟹   XP_047295328
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381943,984,188 - 43,998,326 (+)NCBI
RefSeq Acc Id: XM_047439373   ⟹   XP_047295329
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381943,985,319 - 43,998,326 (+)NCBI
RefSeq Acc Id: XM_054322018   ⟹   XP_054177993
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01946,807,096 - 46,821,233 (+)NCBI
RefSeq Acc Id: XM_054322019   ⟹   XP_054177994
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01946,807,096 - 46,821,233 (+)NCBI
RefSeq Acc Id: XM_054322020   ⟹   XP_054177995
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01946,808,441 - 46,821,233 (+)NCBI
RefSeq Acc Id: XM_054322021   ⟹   XP_054177996
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01946,807,096 - 46,821,233 (+)NCBI
RefSeq Acc Id: XM_054322022   ⟹   XP_054177997
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01946,807,096 - 46,821,233 (+)NCBI
RefSeq Acc Id: XM_054322023   ⟹   XP_054177998
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01946,808,227 - 46,821,233 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001247415 (Get FASTA)   NCBI Sequence Viewer  
  NP_001247416 (Get FASTA)   NCBI Sequence Viewer  
  NP_001247417 (Get FASTA)   NCBI Sequence Viewer  
  NP_003436 (Get FASTA)   NCBI Sequence Viewer  
  NP_932355 (Get FASTA)   NCBI Sequence Viewer  
  XP_011525580 (Get FASTA)   NCBI Sequence Viewer  
  XP_024307462 (Get FASTA)   NCBI Sequence Viewer  
  XP_047295326 (Get FASTA)   NCBI Sequence Viewer  
  XP_047295327 (Get FASTA)   NCBI Sequence Viewer  
  XP_047295328 (Get FASTA)   NCBI Sequence Viewer  
  XP_047295329 (Get FASTA)   NCBI Sequence Viewer  
  XP_054177993 (Get FASTA)   NCBI Sequence Viewer  
  XP_054177994 (Get FASTA)   NCBI Sequence Viewer  
  XP_054177995 (Get FASTA)   NCBI Sequence Viewer  
  XP_054177996 (Get FASTA)   NCBI Sequence Viewer  
  XP_054177997 (Get FASTA)   NCBI Sequence Viewer  
  XP_054177998 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAB03530 (Get FASTA)   NCBI Sequence Viewer  
  AAB03532 (Get FASTA)   NCBI Sequence Viewer  
  AAC50268 (Get FASTA)   NCBI Sequence Viewer  
  AAF04102 (Get FASTA)   NCBI Sequence Viewer  
  AAF18684 (Get FASTA)   NCBI Sequence Viewer  
  AAH75050 (Get FASTA)   NCBI Sequence Viewer  
  AAH75051 (Get FASTA)   NCBI Sequence Viewer  
  AAI26378 (Get FASTA)   NCBI Sequence Viewer  
  AAI30382 (Get FASTA)   NCBI Sequence Viewer  
  BAB14287 (Get FASTA)   NCBI Sequence Viewer  
  BAG37110 (Get FASTA)   NCBI Sequence Viewer  
  BAG59807 (Get FASTA)   NCBI Sequence Viewer  
  BAG59825 (Get FASTA)   NCBI Sequence Viewer  
  EAW57238 (Get FASTA)   NCBI Sequence Viewer  
  EAW57239 (Get FASTA)   NCBI Sequence Viewer  
  EAW57240 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000270014
  ENSP00000270014.1
  ENSP00000385163
  ENSP00000385163.2
  ENSP00000465201.1
  ENSP00000465691
  ENSP00000465691.1
  ENSP00000465981.1
  ENSP00000467110.1
  ENSP00000481677
  ENSP00000481677.1
GenBank Protein Q12901 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_003436   ⟸   NM_003445
- Peptide Label: isoform 1
- UniProtKB: Q9UIE1 (UniProtKB/Swiss-Prot),   Q6AZZ8 (UniProtKB/Swiss-Prot),   Q12901 (UniProtKB/Swiss-Prot),   J3KQ08 (UniProtKB/Swiss-Prot),   B4DM95 (UniProtKB/Swiss-Prot),   B2RB63 (UniProtKB/Swiss-Prot),   A2BDE6 (UniProtKB/Swiss-Prot),   Q9UK14 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_932355   ⟸   NM_198089
- Peptide Label: isoform 1
- UniProtKB: Q9UIE1 (UniProtKB/Swiss-Prot),   Q6AZZ8 (UniProtKB/Swiss-Prot),   Q12901 (UniProtKB/Swiss-Prot),   J3KQ08 (UniProtKB/Swiss-Prot),   B4DM95 (UniProtKB/Swiss-Prot),   B2RB63 (UniProtKB/Swiss-Prot),   A2BDE6 (UniProtKB/Swiss-Prot),   Q9UK14 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001247415   ⟸   NM_001260486
- Peptide Label: isoform 1
- UniProtKB: Q9UIE1 (UniProtKB/Swiss-Prot),   Q6AZZ8 (UniProtKB/Swiss-Prot),   Q12901 (UniProtKB/Swiss-Prot),   J3KQ08 (UniProtKB/Swiss-Prot),   B4DM95 (UniProtKB/Swiss-Prot),   B2RB63 (UniProtKB/Swiss-Prot),   A2BDE6 (UniProtKB/Swiss-Prot),   Q9UK14 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001247417   ⟸   NM_001260488
- Peptide Label: isoform 2
- Sequence:
RefSeq Acc Id: NP_001247416   ⟸   NM_001260487
- Peptide Label: isoform 1
- UniProtKB: Q9UIE1 (UniProtKB/Swiss-Prot),   Q6AZZ8 (UniProtKB/Swiss-Prot),   Q12901 (UniProtKB/Swiss-Prot),   J3KQ08 (UniProtKB/Swiss-Prot),   B4DM95 (UniProtKB/Swiss-Prot),   B2RB63 (UniProtKB/Swiss-Prot),   A2BDE6 (UniProtKB/Swiss-Prot),   Q9UK14 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011525580   ⟸   XM_011527278
- Peptide Label: isoform X1
- UniProtKB: Q12901 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_024307462   ⟸   XM_024451694
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: ENSP00000481677   ⟸   ENST00000611002
RefSeq Acc Id: ENSP00000465981   ⟸   ENST00000586454
RefSeq Acc Id: ENSP00000270014   ⟸   ENST00000270014
RefSeq Acc Id: ENSP00000385163   ⟸   ENST00000407951
RefSeq Acc Id: ENSP00000465691   ⟸   ENST00000590615
RefSeq Acc Id: ENSP00000465201   ⟸   ENST00000590411
RefSeq Acc Id: ENSP00000467110   ⟸   ENST00000591532
RefSeq Acc Id: XP_047295326   ⟸   XM_047439370
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047295328   ⟸   XM_047439372
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047295329   ⟸   XM_047439373
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047295327   ⟸   XM_047439371
- Peptide Label: isoform X2
- UniProtKB: Q9UIE1 (UniProtKB/Swiss-Prot),   Q6AZZ8 (UniProtKB/Swiss-Prot),   Q12901 (UniProtKB/Swiss-Prot),   J3KQ08 (UniProtKB/Swiss-Prot),   B4DM95 (UniProtKB/Swiss-Prot),   B2RB63 (UniProtKB/Swiss-Prot),   A2BDE6 (UniProtKB/Swiss-Prot),   Q9UK14 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054177994   ⟸   XM_054322019
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054177997   ⟸   XM_054322022
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054177996   ⟸   XM_054322021
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054177993   ⟸   XM_054322018
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054177998   ⟸   XM_054322023
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054177995   ⟸   XM_054322020
- Peptide Label: isoform X2
Protein Domains
KRAB

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q12901-F1-model_v2 AlphaFold Q12901 1-538 view protein structure

Promoters
RGD ID:7240285
Promoter ID:EPDNEW_H25888
Type:initiation region
Name:ZNF155_1
Description:zinc finger protein 155
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
GRCh381943,984,188 - 43,984,248EPDNEW
RGD ID:6796261
Promoter ID:HG_KWN:30179
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid
Transcripts:NM_003445,   NM_198089
Position:
Human AssemblyChrPosition (strand)Source
Build 361949,179,956 - 49,180,456 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:12940 AgrOrtholog
COSMIC ZNF155 COSMIC
Ensembl Genes ENSG00000204920 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000270014 ENTREZGENE
  ENST00000270014.7 UniProtKB/Swiss-Prot
  ENST00000407951 ENTREZGENE
  ENST00000407951.6 UniProtKB/Swiss-Prot
  ENST00000586454.1 UniProtKB/TrEMBL
  ENST00000590411.5 UniProtKB/TrEMBL
  ENST00000590615 ENTREZGENE
  ENST00000590615.5 UniProtKB/Swiss-Prot
  ENST00000591532.5 UniProtKB/TrEMBL
  ENST00000611002 ENTREZGENE
  ENST00000611002.4 UniProtKB/Swiss-Prot
Gene3D-CATH 6.10.140.140 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Classic Zinc Finger UniProtKB/Swiss-Prot
GTEx ENSG00000204920 GTEx
HGNC ID HGNC:12940 ENTREZGENE
Human Proteome Map ZNF155 Human Proteome Map
InterPro KRAB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  KRAB_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Znf_C2H2_sf UniProtKB/Swiss-Prot
  Znf_C2H2_type UniProtKB/Swiss-Prot
KEGG Report hsa:7711 UniProtKB/Swiss-Prot
NCBI Gene 7711 ENTREZGENE
OMIM 604086 OMIM
PANTHER IP01201P-RELATED UniProtKB/Swiss-Prot
  KRAB DOMAIN C2H2 ZINC FINGER UniProtKB/TrEMBL
  KRAB DOMAIN-CONTAINING PROTEIN UniProtKB/TrEMBL
  ZINC FINGER PROTEIN UniProtKB/Swiss-Prot
Pfam KRAB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  zf-C2H2 UniProtKB/Swiss-Prot
PharmGKB PA37524 PharmGKB
PROSITE KRAB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZINC_FINGER_C2H2_1 UniProtKB/Swiss-Prot
  ZINC_FINGER_C2H2_2 UniProtKB/Swiss-Prot
SMART KRAB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZnF_C2H2 UniProtKB/Swiss-Prot
Superfamily-SCOP SSF109640 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF57667 UniProtKB/Swiss-Prot
UniProt A2BDE6 ENTREZGENE
  B2RB63 ENTREZGENE
  B4DM95 ENTREZGENE
  J3KQ08 ENTREZGENE
  K7EJJ6_HUMAN UniProtKB/TrEMBL
  K7ELA0_HUMAN UniProtKB/TrEMBL
  K7ENV6_HUMAN UniProtKB/TrEMBL
  Q12901 ENTREZGENE
  Q6AZZ8 ENTREZGENE
  Q9UIE1 ENTREZGENE
  Q9UK14 ENTREZGENE
  ZN155_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary A2BDE6 UniProtKB/Swiss-Prot
  B2RB63 UniProtKB/Swiss-Prot
  B4DM95 UniProtKB/Swiss-Prot
  J3KQ08 UniProtKB/Swiss-Prot
  Q6AZZ8 UniProtKB/Swiss-Prot
  Q9UIE1 UniProtKB/Swiss-Prot
  Q9UK14 UniProtKB/Swiss-Prot