ZNF816 (zinc finger protein 816) - Rat Genome Database

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Gene: ZNF816 (zinc finger protein 816) Homo sapiens
Analyze
Symbol: ZNF816
Name: zinc finger protein 816
RGD ID: 1604241
HGNC Page HGNC:26995
Description: Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in membrane. Predicted to be active in nucleus.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: MGC125619; zinc finger protein 816A; ZNF816A
RGD Orthologs
Rat
Bonobo
Pig
Alliance Genes
More Info more info ...
Related Pseudogenes: LOC100128713  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381952,949,385 - 52,962,881 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1952,949,379 - 52,962,911 (-)EnsemblGRCh38hg38GRCh38
GRCh371953,452,638 - 53,466,134 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361958,144,444 - 58,157,926 (-)NCBINCBI36Build 36hg18NCBI36
Celera1950,500,194 - 50,513,676 (-)NCBICelera
Cytogenetic Map19q13.41NCBI
HuRef1949,778,813 - 49,792,345 (-)NCBIHuRef
CHM1_11953,454,437 - 53,467,969 (-)NCBICHM1_1
T2T-CHM13v2.01956,031,917 - 56,045,413 (-)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
membrane  (IEA)
nucleus  (IBA,IEA)

References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12477932   PMID:16344560   PMID:20953187   PMID:21873635   PMID:28514442   PMID:33961781   PMID:35563538  


Genomics

Comparative Map Data
ZNF816
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381952,949,385 - 52,962,881 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1952,949,379 - 52,962,911 (-)EnsemblGRCh38hg38GRCh38
GRCh371953,452,638 - 53,466,134 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361958,144,444 - 58,157,926 (-)NCBINCBI36Build 36hg18NCBI36
Celera1950,500,194 - 50,513,676 (-)NCBICelera
Cytogenetic Map19q13.41NCBI
HuRef1949,778,813 - 49,792,345 (-)NCBIHuRef
CHM1_11953,454,437 - 53,467,969 (-)NCBICHM1_1
T2T-CHM13v2.01956,031,917 - 56,045,413 (-)NCBIT2T-CHM13v2.0
Zfp141
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81102,267,194 - 102,300,911 (+)NCBIGRCr8
mRatBN7.2193,130,574 - 93,164,293 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl193,130,598 - 93,163,404 (+)EnsemblmRatBN7.2 Ensembl
Rnor_6.0198,168,457 - 98,201,189 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.0199,248,701 - 99,286,645 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4193,011,706 - 93,026,296 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera187,429,924 - 87,463,216 (+)NCBICelera
Cytogenetic Map1q22NCBI
LOC100977156
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22058,995,399 - 59,067,558 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11960,911,652 - 60,986,005 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01949,888,155 - 49,960,753 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11958,760,189 - 58,773,655 (-)NCBIpanpan1.1PanPan1.1panPan2
LOC100627241
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1657,008,838 - 57,052,907 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1

Variants

.
Variants in ZNF816
28 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19q13.33-13.43(chr19:50191219-58535818)x3 copy number gain See cases [RCV000050883] Chr19:50191219..58535818 [GRCh38]
Chr19:50694476..59047185 [GRCh37]
Chr19:55386288..63738997 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.41-13.42(chr19:52707235-53192628)x1 copy number loss See cases [RCV000052096] Chr19:52707235..53192628 [GRCh38]
Chr19:53210488..53695881 [GRCh37]
Chr19:57902300..58387693 [NCBI36]
Chr19:19q13.41-13.42		 uncertain significance
GRCh38/hg38 19q13.33-13.43(chr19:49907832-58557889)x3 copy number gain See cases [RCV000052925] Chr19:49907832..58557889 [GRCh38]
Chr19:50411089..59069256 [GRCh37]
Chr19:55102901..63761068 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:51141518-58539965)x3 copy number gain See cases [RCV000052926] Chr19:51141518..58539965 [GRCh38]
Chr19:51644775..59051332 [GRCh37]
Chr19:56336587..63743144 [NCBI36]
Chr19:19q13.41-13.43		 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3 copy number gain See cases [RCV000052914] Chr19:47908540..58539965 [GRCh38]
Chr19:48411797..59051332 [GRCh37]
Chr19:53103609..63743144 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3 copy number gain See cases [RCV000052915] Chr19:47929575..58572206 [GRCh38]
Chr19:48432832..59083573 [GRCh37]
Chr19:53124644..63775385 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:52612432-58581203)x3 copy number gain See cases [RCV000134174] Chr19:52612432..58581203 [GRCh38]
Chr19:53115685..59092570 [GRCh37]
Chr19:57807497..63784382 [NCBI36]
Chr19:19q13.41-13.43		 pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:52955056-58581203)x3 copy number gain See cases [RCV000134139] Chr19:52955056..58581203 [GRCh38]
Chr19:53458309..59092570 [GRCh37]
Chr19:58150121..63784382 [NCBI36]
Chr19:19q13.41-13.43		 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:50152520-58581203)x3 copy number gain See cases [RCV000135843] Chr19:50152520..58581203 [GRCh38]
Chr19:50655777..59092570 [GRCh37]
Chr19:55347589..63784382 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:52143873-58445521)x3 copy number gain See cases [RCV000142008] Chr19:52143873..58445521 [GRCh38]
Chr19:52647126..58956888 [GRCh37]
Chr19:57338938..63648700 [NCBI36]
Chr19:19q13.41-13.43		 pathogenic
GRCh37/hg19 19q13.33-13.43(chr19:50489390-59095359)x3 copy number gain See cases [RCV000445925] Chr19:50489390..59095359 [GRCh37]
Chr19:19q13.33-13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 copy number gain See cases [RCV000511289] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic|uncertain significance
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_001202457.3(ZNF816):c.1028G>A (p.Cys343Tyr) single nucleotide variant Inborn genetic diseases [RCV003268683] Chr19:52950747 [GRCh38]
Chr19:53454000 [GRCh37]
Chr19:19q13.41		 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
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 19q13.41-13.42(chr19:53184204-54346718)x3 copy number gain not provided [RCV000740221] Chr19:53184204..54346718 [GRCh37]
Chr19:19q13.41-13.42		 uncertain significance
GRCh37/hg19 19q13.41(chr19:53463680-53520702)x3 copy number gain not provided [RCV000740231] Chr19:53463680..53520702 [GRCh37]
Chr19:19q13.41		 benign
NM_001202457.3(ZNF816):c.658C>T (p.Gln220Ter) single nucleotide variant not provided [RCV000907209] Chr19:52951117 [GRCh38]
Chr19:53454370 [GRCh37]
Chr19:19q13.41		 likely benign
GRCh37/hg19 19q13.32-13.42(chr19:47939842-54626871) copy number gain not provided [RCV001249294] Chr19:47939842..54626871 [GRCh37]
Chr19:19q13.32-13.42		 not provided
NM_001202457.3(ZNF816):c.1498C>G (p.His500Asp) single nucleotide variant not provided [RCV000953097] Chr19:52950277 [GRCh38]
Chr19:53453530 [GRCh37]
Chr19:19q13.41		 likely benign
NM_001202457.3(ZNF816):c.941A>G (p.Lys314Arg) single nucleotide variant not provided [RCV000953098] Chr19:52950834 [GRCh38]
Chr19:53454087 [GRCh37]
Chr19:19q13.41		 likely benign
GRCh37/hg19 19q13.31-13.42(chr19:44738088-53621561)x3 copy number gain not provided [RCV001007050] Chr19:44738088..53621561 [GRCh37]
Chr19:19q13.31-13.42		 pathogenic
GRCh37/hg19 19q13.33-13.43(chr19:48463931-57095254)x3 copy number gain not provided [RCV001259944] Chr19:48463931..57095254 [GRCh37]
Chr19:19q13.33-13.43		 pathogenic
NM_001202457.3(ZNF816):c.1543G>C (p.Asp515His) single nucleotide variant Inborn genetic diseases [RCV003304427] Chr19:52950232 [GRCh38]
Chr19:53453485 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001202457.3(ZNF816):c.1094G>A (p.Gly365Glu) single nucleotide variant Inborn genetic diseases [RCV002906976] Chr19:52950681 [GRCh38]
Chr19:53453934 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001202457.3(ZNF816):c.1475G>A (p.Arg492Gln) single nucleotide variant Inborn genetic diseases [RCV002861017] Chr19:52950300 [GRCh38]
Chr19:53453553 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001202457.3(ZNF816):c.803A>G (p.Gln268Arg) single nucleotide variant Inborn genetic diseases [RCV002688580] Chr19:52950972 [GRCh38]
Chr19:53454225 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001202457.3(ZNF816):c.994C>T (p.Arg332Cys) single nucleotide variant Inborn genetic diseases [RCV002974407] Chr19:52950781 [GRCh38]
Chr19:53454034 [GRCh37]
Chr19:19q13.41		 likely benign
NM_001202457.3(ZNF816):c.1519A>C (p.Lys507Gln) single nucleotide variant Inborn genetic diseases [RCV002689730] Chr19:52950256 [GRCh38]
Chr19:53453509 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001202457.3(ZNF816):c.1733G>C (p.Gly578Ala) single nucleotide variant Inborn genetic diseases [RCV002845776] Chr19:52950042 [GRCh38]
Chr19:53453295 [GRCh37]
Chr19:19q13.41		 likely benign
NM_001202457.3(ZNF816):c.1937G>A (p.Arg646Lys) single nucleotide variant Inborn genetic diseases [RCV003000993] Chr19:52949838 [GRCh38]
Chr19:53453091 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001202457.3(ZNF816):c.1223G>A (p.Arg408His) single nucleotide variant Inborn genetic diseases [RCV002704134] Chr19:52950552 [GRCh38]
Chr19:53453805 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001202457.3(ZNF816):c.405G>C (p.Leu135Phe) single nucleotide variant Inborn genetic diseases [RCV002924524] Chr19:52951370 [GRCh38]
Chr19:53454623 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001202457.3(ZNF816):c.1537G>A (p.Glu513Lys) single nucleotide variant Inborn genetic diseases [RCV002743215] Chr19:52950238 [GRCh38]
Chr19:53453491 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001202457.3(ZNF816):c.707A>G (p.Lys236Arg) single nucleotide variant Inborn genetic diseases [RCV002709908] Chr19:52951068 [GRCh38]
Chr19:53454321 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001202457.3(ZNF816):c.581G>A (p.Arg194Lys) single nucleotide variant Inborn genetic diseases [RCV002920699] Chr19:52951194 [GRCh38]
Chr19:53454447 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001202457.3(ZNF816):c.1775C>G (p.Pro592Arg) single nucleotide variant Inborn genetic diseases [RCV003203841] Chr19:52950000 [GRCh38]
Chr19:53453253 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001202457.3(ZNF816):c.1919A>C (p.Gln640Pro) single nucleotide variant Inborn genetic diseases [RCV003196253] Chr19:52949856 [GRCh38]
Chr19:53453109 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001202457.3(ZNF816):c.1106A>G (p.Tyr369Cys) single nucleotide variant Inborn genetic diseases [RCV003209874] Chr19:52950669 [GRCh38]
Chr19:53453922 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001202457.3(ZNF816):c.529A>C (p.Ser177Arg) single nucleotide variant Inborn genetic diseases [RCV003266055] Chr19:52951246 [GRCh38]
Chr19:53454499 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001202457.3(ZNF816):c.1036T>C (p.Cys346Arg) single nucleotide variant Inborn genetic diseases [RCV003266184] Chr19:52950739 [GRCh38]
Chr19:53453992 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001202457.3(ZNF816):c.499C>T (p.Leu167Phe) single nucleotide variant Inborn genetic diseases [RCV003385881] Chr19:52951276 [GRCh38]
Chr19:53454529 [GRCh37]
Chr19:19q13.41		 uncertain significance
GRCh37/hg19 19q13.33-13.43(chr19:49625130-57647352)x3 copy number gain not provided [RCV003485200] Chr19:49625130..57647352 [GRCh37]
Chr19:19q13.33-13.43		 likely pathogenic
NM_001202457.3(ZNF816):c.1371A>G (p.Lys457=) single nucleotide variant not provided [RCV003407098] Chr19:52950404 [GRCh38]
Chr19:53453657 [GRCh37]
Chr19:19q13.41		 likely benign
NM_001202457.3(ZNF816):c.1143A>G (p.Lys381=) single nucleotide variant not provided [RCV003415403] Chr19:52950632 [GRCh38]
Chr19:53453885 [GRCh37]
Chr19:19q13.41		 likely benign
NM_001202457.3(ZNF816):c.1383T>C (p.Ser461=) single nucleotide variant not provided [RCV003407097] Chr19:52950392 [GRCh38]
Chr19:53453645 [GRCh37]
Chr19:19q13.41		 likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1779
Count of miRNA genes:879
Interacting mature miRNAs:997
Transcripts:ENST00000270457, ENST00000332302, ENST00000357666, ENST00000391786, ENST00000434371, ENST00000438970, ENST00000444460, ENST00000457013, ENST00000535506, ENST00000549216
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
RH93828  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371953,409,153 - 53,409,325UniSTSGRCh37
Build 361958,100,965 - 58,101,137RGDNCBI36
Celera1950,458,725 - 50,458,897RGD
Cytogenetic Map19q13.41UniSTS
HuRef1949,417,254 - 49,417,427UniSTS
HuRef1949,737,037 - 49,737,209UniSTS
GeneMap99-GB4 RH Map19278.55UniSTS
STS-T63342  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371953,452,656 - 53,452,794UniSTSGRCh37
Build 361958,144,468 - 58,144,606RGDNCBI36
Celera1950,500,218 - 50,500,356RGD
Cytogenetic Map19q13.41UniSTS
HuRef1949,778,837 - 49,778,975UniSTS
GeneMap99-GB4 RH Map19277.0UniSTS
NCBI RH Map19576.1UniSTS


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 79 3 19 10 374 14 136 14 148 55 238 68 1 2
Low 2353 2623 1596 507 1320 344 3784 1658 3330 357 1214 1528 173 1 1196 2360 3 2
Below cutoff 4 363 109 105 245 105 433 525 255 4 7 11 8 427

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000270457   ⟹   ENSP00000472475
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1952,952,519 - 52,962,871 (-)Ensembl
RefSeq Acc Id: ENST00000332302   ⟹   ENSP00000333199
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1952,952,751 - 52,962,825 (-)Ensembl
RefSeq Acc Id: ENST00000357666   ⟹   ENSP00000350295
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1952,949,379 - 52,962,861 (-)Ensembl
RefSeq Acc Id: ENST00000391786   ⟹   ENSP00000471215
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1952,951,336 - 52,962,851 (-)Ensembl
RefSeq Acc Id: ENST00000438970   ⟹   ENSP00000469688
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1952,951,751 - 52,962,871 (-)Ensembl
RefSeq Acc Id: ENST00000444460   ⟹   ENSP00000403266
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1952,949,385 - 52,962,881 (-)Ensembl
RefSeq Acc Id: ENST00000457013   ⟹   ENSP00000408965
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1952,951,432 - 52,962,911 (-)Ensembl
RefSeq Acc Id: ENST00000535506   ⟹   ENSP00000470838
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1952,952,589 - 52,962,878 (-)Ensembl
RefSeq Acc Id: NM_001031665   ⟹   NP_001026835
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381952,949,385 - 52,962,881 (-)NCBI
GRCh371953,452,632 - 53,466,164 (-)ENTREZGENE
Build 361958,144,444 - 58,157,926 (-)NCBI Archive
Celera1950,500,194 - 50,513,676 (-)RGD
HuRef1949,778,813 - 49,792,345 (-)ENTREZGENE
CHM1_11953,454,437 - 53,467,969 (-)NCBI
T2T-CHM13v2.01956,031,917 - 56,045,413 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001202456   ⟹   NP_001189385
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381952,949,385 - 52,962,881 (-)NCBI
GRCh371953,452,632 - 53,466,164 (-)ENTREZGENE
HuRef1949,778,813 - 49,792,345 (-)ENTREZGENE
CHM1_11953,454,437 - 53,467,969 (-)NCBI
T2T-CHM13v2.01956,031,917 - 56,045,413 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001202457   ⟹   NP_001189386
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381952,949,385 - 52,962,881 (-)NCBI
GRCh371953,452,632 - 53,466,164 (-)ENTREZGENE
HuRef1949,778,813 - 49,792,345 (-)ENTREZGENE
CHM1_11953,454,437 - 53,467,969 (-)NCBI
T2T-CHM13v2.01956,031,917 - 56,045,413 (-)NCBI
Sequence:
Reference Protein Sequences
RefSeq Acc Id: NP_001026835   ⟸   NM_001031665
- UniProtKB: Q3KR39 (UniProtKB/Swiss-Prot),   A8K7H5 (UniProtKB/Swiss-Prot),   Q659B3 (UniProtKB/Swiss-Prot),   Q0VGE8 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001189386   ⟸   NM_001202457
- UniProtKB: Q3KR39 (UniProtKB/Swiss-Prot),   A8K7H5 (UniProtKB/Swiss-Prot),   Q659B3 (UniProtKB/Swiss-Prot),   Q0VGE8 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001189385   ⟸   NM_001202456
- UniProtKB: Q3KR39 (UniProtKB/Swiss-Prot),   A8K7H5 (UniProtKB/Swiss-Prot),   Q659B3 (UniProtKB/Swiss-Prot),   Q0VGE8 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000469688   ⟸   ENST00000438970
RefSeq Acc Id: ENSP00000333199   ⟸   ENST00000332302
RefSeq Acc Id: ENSP00000472475   ⟸   ENST00000270457
RefSeq Acc Id: ENSP00000470838   ⟸   ENST00000535506
RefSeq Acc Id: ENSP00000408965   ⟸   ENST00000457013
RefSeq Acc Id: ENSP00000403266   ⟸   ENST00000444460
RefSeq Acc Id: ENSP00000471215   ⟸   ENST00000391786
RefSeq Acc Id: ENSP00000350295   ⟸   ENST00000357666
Protein Domains
KRAB

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q0VGE8-F1-model_v2 AlphaFold Q0VGE8 1-651 view protein structure

Promoters
RGD ID:13205503
Promoter ID:EPDNEW_H26333
Type:initiation region
Name:ZNF816_1
Description:zinc finger protein 816
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381952,962,881 - 52,962,941EPDNEW
RGD ID:6796345
Promoter ID:HG_KWN:30796
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000391781,   NM_001031665,   UC002QAK.1,   UC002QAM.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361958,157,649 - 58,158,149 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:26995 AgrOrtholog
COSMIC ZNF816 COSMIC
Ensembl Genes ENSG00000180257 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000270457.8 UniProtKB/TrEMBL
  ENST00000332302.8 UniProtKB/TrEMBL
  ENST00000357666 ENTREZGENE
  ENST00000357666.8 UniProtKB/Swiss-Prot
  ENST00000391786.6 UniProtKB/TrEMBL
  ENST00000438970.6 UniProtKB/TrEMBL
  ENST00000444460 ENTREZGENE
  ENST00000444460.7 UniProtKB/Swiss-Prot
  ENST00000457013.6 UniProtKB/TrEMBL
  ENST00000535506.5 UniProtKB/TrEMBL
Gene3D-CATH 6.10.140.140 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Classic Zinc Finger UniProtKB/Swiss-Prot
GTEx ENSG00000180257 GTEx
HGNC ID HGNC:26995 ENTREZGENE
Human Proteome Map ZNF816 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:125893 UniProtKB/Swiss-Prot
NCBI Gene 125893 ENTREZGENE
PANTHER KRAB DOMAIN C2H2 ZINC FINGER UniProtKB/TrEMBL
  KRAB DOMAIN-CONTAINING PROTEIN UniProtKB/TrEMBL
  KRAB DOMAIN-CONTAINING PROTEIN 5-RELATED UniProtKB/TrEMBL
  PROTEIN GVQW1-RELATED UniProtKB/TrEMBL
  ZINC FINGER PROTEIN UniProtKB/Swiss-Prot
  ZINC FINGER PROTEIN 487-RELATED UniProtKB/Swiss-Prot
Pfam KRAB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  zf-C2H2 UniProtKB/Swiss-Prot
PharmGKB PA165394953 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 A8K7H5 ENTREZGENE
  F5GXJ3_HUMAN UniProtKB/TrEMBL
  I3L0H5_HUMAN UniProtKB/TrEMBL
  M0QY99_HUMAN UniProtKB/TrEMBL
  M0QZX7_HUMAN UniProtKB/TrEMBL
  M0R0G1_HUMAN UniProtKB/TrEMBL
  Q0VGE8 ENTREZGENE
  Q3KR39 ENTREZGENE
  Q659B3 ENTREZGENE
  ZN816_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary A8K7H5 UniProtKB/Swiss-Prot
  Q3KR39 UniProtKB/Swiss-Prot
  Q659B3 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2011-07-27 ZNF816  zinc finger protein 816  ZNF816A  zinc finger protein 816A  Symbol and/or name change 5135510 APPROVED