ZNF816-ZNF321P (ZNF816-ZNF321P readthrough) - Rat Genome Database

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Gene: ZNF816-ZNF321P (ZNF816-ZNF321P readthrough) Homo sapiens
Analyze
Symbol: ZNF816-ZNF321P
Name: ZNF816-ZNF321P readthrough
RGD ID: 5013859
HGNC Page HGNC:38879
Description: Predicted to be involved in regulation of DNA-templated transcription.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: DKFZp781C2298; FLJ79402; ZNF816-ZNF321; ZNF816-ZNF321 read-through transcript; ZNF816-ZNF321 readthrough
RGD Orthologs
Bonobo
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381952,927,135 - 52,962,881 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1952,928,475 - 52,962,823 (-)EnsemblGRCh38hg38GRCh38
GRCh371953,430,388 - 53,466,134 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map19q13.41NCBI
HuRef1949,756,286 - 49,792,345 (-)NCBIHuRef
CHM1_11953,432,179 - 53,467,969 (-)NCBICHM1_1
T2T-CHM13v2.01956,009,652 - 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
urethane  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:14702039   PMID:15489334   PMID:16344560   PMID:17974005   PMID:20967262  


Genomics

Comparative Map Data
ZNF816-ZNF321P
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381952,927,135 - 52,962,881 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1952,928,475 - 52,962,823 (-)EnsemblGRCh38hg38GRCh38
GRCh371953,430,388 - 53,466,134 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map19q13.41NCBI
HuRef1949,756,286 - 49,792,345 (-)NCBIHuRef
CHM1_11953,432,179 - 53,467,969 (-)NCBICHM1_1
T2T-CHM13v2.01956,009,652 - 56,045,413 (-)NCBIT2T-CHM13v2.0
LOC103786729
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22058,965,485 - 58,987,521 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11960,886,083 - 60,905,532 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01949,866,396 - 49,881,719 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11958,733,837 - 58,753,605 (-)NCBIpanpan1.1PanPan1.1panPan2

Variants

.
Variants in ZNF816-ZNF321P
38 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(chr19:47929575-58572206)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 19q13.33-13.43(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
NM_001202473.1(ZNF816-ZNF321P):c.190+9276C>A single nucleotide variant Lung cancer [RCV000101314] Chr19:52943475 [GRCh38]
Chr19:53446728 [GRCh37]
Chr19:19q13.41		 uncertain significance
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(chr19:52616146-52929716)x3 copy number gain See cases [RCV000134490] Chr19:52616146..52929716 [GRCh38]
Chr19:53119399..53432969 [GRCh37]
Chr19:57811211..58124781 [NCBI36]
Chr19:19q13.41		 uncertain significance
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
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 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
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 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 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
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
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 19q13.31-13.42(chr19:44738088-53621561)x3 copy number gain not provided [RCV001007050] Chr19:44738088..53621561 [GRCh37]
Chr19:19q13.31-13.42		 pathogenic
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 19q13.32-13.42(chr19:47939842-54626871) copy number gain not provided [RCV001249294] Chr19:47939842..54626871 [GRCh37]
Chr19:19q13.32-13.42		 not provided
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_001202473.2(ZNF816-ZNF321P):c.218A>T (p.Glu73Val) single nucleotide variant Inborn genetic diseases [RCV002684905] Chr19:52929387 [GRCh38]
Chr19:53432640 [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.1094G>A (p.Gly365Glu) single nucleotide variant Inborn genetic diseases [RCV002906976] Chr19:52950681 [GRCh38]
Chr19:53453934 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001202473.2(ZNF816-ZNF321P):c.584G>T (p.Arg195Ile) single nucleotide variant Inborn genetic diseases [RCV002974442] Chr19:52929021 [GRCh38]
Chr19:53432274 [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_001202473.2(ZNF816-ZNF321P):c.424C>T (p.His142Tyr) single nucleotide variant Inborn genetic diseases [RCV002693117] Chr19:52929181 [GRCh38]
Chr19:53432434 [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_001202473.2(ZNF816-ZNF321P):c.425A>G (p.His142Arg) single nucleotide variant Inborn genetic diseases [RCV002739433] Chr19:52929180 [GRCh38]
Chr19:53432433 [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_001202473.2(ZNF816-ZNF321P):c.373C>T (p.His125Tyr) single nucleotide variant Inborn genetic diseases [RCV002743436] Chr19:52929232 [GRCh38]
Chr19:53432485 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001202473.2(ZNF816-ZNF321P):c.325G>C (p.Asp109His) single nucleotide variant Inborn genetic diseases [RCV002941517] Chr19:52929280 [GRCh38]
Chr19:53432533 [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_001202473.2(ZNF816-ZNF321P):c.513G>T (p.Gln171His) single nucleotide variant Inborn genetic diseases [RCV002656095] Chr19:52929092 [GRCh38]
Chr19:53432345 [GRCh37]
Chr19:19q13.41		 uncertain significance
NM_001202473.2(ZNF816-ZNF321P):c.670A>G (p.Ser224Gly) single nucleotide variant Inborn genetic diseases [RCV002725059] Chr19:52928935 [GRCh38]
Chr19:53432188 [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_001202473.2(ZNF816-ZNF321P):c.191A>G (p.Asp64Gly) single nucleotide variant Inborn genetic diseases [RCV003183189] Chr19:52929414 [GRCh38]
Chr19:53432667 [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:185
Count of miRNA genes:176
Interacting mature miRNAs:185
Transcripts:ENST00000313956, ENST00000550843
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
D10S2448  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map13q32.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map4p15.31UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map1p31UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic MapXq13-q21UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map4q31.21UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map19qUniSTS
Cytogenetic Map2q32.3UniSTS
D13S116  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map8q24UniSTS
Cytogenetic Map1p35.3-p33UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map19qUniSTS
Cytogenetic Map1q32UniSTS
STS-U09414  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map19qUniSTS
Cytogenetic Map19q13.4UniSTS
GeneMap99-GB4 RH Map19278.07UniSTS
NCBI RH Map19576.1UniSTS
GDB:631813  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map9p13.3-p12UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map11p12UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map5q11.2-q13.1UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map15q24.2UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map1p32UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map16p12.1UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map10q24.2UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map3p21.33UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map2p23.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map19qUniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map19p13.3UniSTS


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 appendage entire extraembryonic component pharyngeal arch
High
Medium
Low 4 4 1 2 8 2 10 2 8 2 13 5 2 1 1 2
Below cutoff 63 5 12 7 119 9 131 29 56 15 45 73 7 1 3

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000391777   ⟹   ENSP00000375656
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1952,928,475 - 52,962,823 (-)Ensembl
RefSeq Acc Id: NM_001202473   ⟹   NP_001189402
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381952,927,135 - 52,962,881 (-)NCBI
GRCh371953,430,388 - 53,466,164 (-)ENTREZGENE
HuRef1949,756,286 - 49,792,345 (-)ENTREZGENE
CHM1_11953,432,179 - 53,467,969 (-)NCBI
T2T-CHM13v2.01956,009,652 - 56,045,413 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001189402 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein BAH14874 (Get FASTA)   NCBI Sequence Viewer  
  CAH18080 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000375656
  ENSP00000375656.3
Reference Protein Sequences
RefSeq Acc Id: NP_001189402   ⟸   NM_001202473
- UniProtKB: A0A0X1KG74 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000375656   ⟸   ENST00000391777
Protein Domains
KRAB

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8N8H1-F1-model_v2 AlphaFold Q8N8H1 1-164 view protein structure


Additional Information

Database Acc Id Source(s)
COSMIC ZNF816-ZNF321P COSMIC
Ensembl Genes ENSG00000221874 Ensembl, ENTREZGENE, UniProtKB/TrEMBL
Ensembl Transcript ENST00000391777 ENTREZGENE
  ENST00000391777.3 UniProtKB/TrEMBL
Gene3D-CATH 6.10.140.140 UniProtKB/TrEMBL
GTEx ENSG00000221874 GTEx
HGNC ID HGNC:38879 ENTREZGENE
Human Proteome Map ZNF816-ZNF321P Human Proteome Map
InterPro KRAB UniProtKB/TrEMBL
  KRAB_dom_sf UniProtKB/TrEMBL
KEGG Report hsa:100529240 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 100529240 ENTREZGENE
PANTHER KRAB DOMAIN C2H2 ZINC FINGER UniProtKB/TrEMBL
  KRAB DOMAIN-CONTAINING PROTEIN 5-RELATED UniProtKB/TrEMBL
Pfam KRAB UniProtKB/TrEMBL
PROSITE KRAB UniProtKB/TrEMBL
SMART KRAB UniProtKB/TrEMBL
Superfamily-SCOP SSF109640 UniProtKB/TrEMBL
UniProt A0A0X1KG74 ENTREZGENE, UniProtKB/TrEMBL
  ZN321_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary B7ZB38 UniProtKB/Swiss-Prot
  Q68DZ0 UniProtKB/Swiss-Prot
  Q86SS5 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2011-09-01 ZNF816-ZNF321P  ZNF816-ZNF321P readthrough  ZNF816-ZNF321P  ZNF816-ZNF321P readthrough  Symbol and/or name change 5135510 APPROVED
2011-07-27 ZNF816-ZNF321P  ZNF816-ZNF321P readthrough  ZNF816-ZNF321  ZNF816-ZNF321 readthrough  Symbol and/or name change 5135510 APPROVED