ZNF433-AS1 (ZNF433 and ZNF878 antisense RNA 1) - Rat Genome Database

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Gene: ZNF433-AS1 (ZNF433 and ZNF878 antisense RNA 1) Homo sapiens
Analyze
Symbol: ZNF433-AS1
Name: ZNF433 and ZNF878 antisense RNA 1
RGD ID: 13451046
HGNC Page HGNC:53776
Description: INTERACTS WITH aristolochic acid A; benzo[e]pyrene; methapyrilene
Type: ncrna (Ensembl: lncRNA)
RefSeq Status: VALIDATED
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381911,987,617 - 12,046,275 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1911,987,617 - 12,046,275 (+)EnsemblGRCh38hg38GRCh38
GRCh371912,098,432 - 12,157,090 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map19p13.2NCBI
HuRef1911,672,616 - 11,712,384 (+)NCBIHuRef
CHM1_11912,098,277 - 12,157,000 (+)NCBICHM1_1
T2T-CHM13v2.01912,115,811 - 12,174,482 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
References
Additional References at PubMed
PMID:8889548   PMID:12477932   PMID:12951057   PMID:16341674   PMID:20598377   PMID:32513696  


Genomics

Variants

.
Variants in ZNF433-AS1
49 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19p13.2-13.12(chr19:11525163-14155021)x1 copy number loss See cases [RCV000136909] Chr19:11525163..14155021 [GRCh38]
Chr19:11635978..14265833 [GRCh37]
Chr19:11496978..14126833 [NCBI36]
Chr19:19p13.2-13.12		 pathogenic
GRCh38/hg38 19p13.2-13.12(chr19:10315258-14048994)x3 copy number gain See cases [RCV000052909] Chr19:10315258..14048994 [GRCh38]
Chr19:10425934..14159806 [GRCh37]
Chr19:10286934..14020806 [NCBI36]
Chr19:19p13.2-13.12		 pathogenic
NM_001308348.2(ZNF433):c.1058A>T (p.His353Leu) single nucleotide variant not specified [RCV004299056] Chr19:12015800 [GRCh38]
Chr19:12126615 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001080404.3(ZNF878):c.200T>C (p.Ile67Thr) single nucleotide variant not specified [RCV004331913] Chr19:12045201 [GRCh38]
Chr19:12156016 [GRCh37]
Chr19:19p13.2		 uncertain significance
GRCh38/hg38 19p13.2-13.13(chr19:10319474-13777860)x1 copy number loss See cases [RCV000141568] Chr19:10319474..13777860 [GRCh38]
Chr19:10430150..13888674 [GRCh37]
Chr19:10291150..13749674 [NCBI36]
Chr19:19p13.2-13.13		 pathogenic
GRCh38/hg38 19p13.2-13.13(chr19:11517825-13225287)x1 copy number loss See cases [RCV000053945] Chr19:11517825..13225287 [GRCh38]
Chr19:11628640..13336101 [GRCh37]
Chr19:11489640..13197101 [NCBI36]
Chr19:19p13.2-13.13		 pathogenic
GRCh38/hg38 19p13.2-13.13(chr19:8831147-13331227)x3 copy number gain See cases [RCV000052908] Chr19:8831147..13331227 [GRCh38]
Chr19:8941823..13442041 [GRCh37]
Chr19:8802823..13303041 [NCBI36]
Chr19:19p13.2-13.13		 likely pathogenic
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
NM_001308348.2(ZNF433):c.886A>G (p.Ile296Val) single nucleotide variant not specified [RCV004286055] Chr19:12015972 [GRCh38]
Chr19:12126787 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.698G>A (p.Ser233Asn) single nucleotide variant not specified [RCV004287838] Chr19:12016160 [GRCh38]
Chr19:12126975 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.835T>C (p.Tyr279His) single nucleotide variant not specified [RCV004293535] Chr19:12016023 [GRCh38]
Chr19:12126838 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.1477C>A (p.His493Asn) single nucleotide variant not specified [RCV004301004] Chr19:12015381 [GRCh38]
Chr19:12126196 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001080404.3(ZNF878):c.334A>G (p.Ile112Val) single nucleotide variant not specified [RCV004304498] Chr19:12045067 [GRCh38]
Chr19:12155882 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.1562A>C (p.His521Pro) single nucleotide variant not specified [RCV004208539] Chr19:12015296 [GRCh38]
Chr19:12126111 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.1421C>T (p.Pro474Leu) single nucleotide variant not specified [RCV004090206] Chr19:12015437 [GRCh38]
Chr19:12126252 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.1799C>T (p.Ser600Leu) single nucleotide variant not specified [RCV004205102] Chr19:12015059 [GRCh38]
Chr19:12125874 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.1475G>T (p.Arg492Ile) single nucleotide variant not specified [RCV004215131] Chr19:12015383 [GRCh38]
Chr19:12126198 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.938G>T (p.Gly313Val) single nucleotide variant not specified [RCV004220323] Chr19:12015920 [GRCh38]
Chr19:12126735 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.782A>G (p.His261Arg) single nucleotide variant not specified [RCV004242281] Chr19:12016076 [GRCh38]
Chr19:12126891 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.1700C>G (p.Ala567Gly) single nucleotide variant not specified [RCV004114674] Chr19:12015158 [GRCh38]
Chr19:12125973 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001080404.3(ZNF878):c.1247C>A (p.Thr416Asn) single nucleotide variant not specified [RCV004103639] Chr19:12044154 [GRCh38]
Chr19:12154969 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001080404.3(ZNF878):c.793A>C (p.Asn265His) single nucleotide variant not specified [RCV004195434] Chr19:12044608 [GRCh38]
Chr19:12155423 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.1934G>A (p.Cys645Tyr) single nucleotide variant not specified [RCV004149234] Chr19:12014924 [GRCh38]
Chr19:12125739 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.1260G>T (p.Glu420Asp) single nucleotide variant not specified [RCV004237381] Chr19:12015598 [GRCh38]
Chr19:12126413 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.1550C>G (p.Ser517Cys) single nucleotide variant not specified [RCV004218101] Chr19:12015308 [GRCh38]
Chr19:12126123 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.449G>C (p.Cys150Ser) single nucleotide variant not specified [RCV004093275] Chr19:12016409 [GRCh38]
Chr19:12127224 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.725A>G (p.Glu242Gly) single nucleotide variant not specified [RCV004160735] Chr19:12016133 [GRCh38]
Chr19:12126948 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.43C>A (p.Gln15Lys) single nucleotide variant not specified [RCV004085240] Chr19:12018253 [GRCh38]
Chr19:12129068 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001080404.3(ZNF878):c.979C>T (p.Arg327Cys) single nucleotide variant not specified [RCV004194577] Chr19:12044422 [GRCh38]
Chr19:12155237 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.1539C>A (p.Asn513Lys) single nucleotide variant not specified [RCV004174688] Chr19:12015319 [GRCh38]
Chr19:12126134 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001080404.3(ZNF878):c.1396A>G (p.Ile466Val) single nucleotide variant not specified [RCV004155535] Chr19:12044005 [GRCh38]
Chr19:12154820 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.1330G>C (p.Glu444Gln) single nucleotide variant not specified [RCV004223985] Chr19:12015528 [GRCh38]
Chr19:12126343 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.818A>T (p.His273Leu) single nucleotide variant not specified [RCV004143766] Chr19:12016040 [GRCh38]
Chr19:12126855 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.449G>A (p.Cys150Tyr) single nucleotide variant not specified [RCV004245333] Chr19:12016409 [GRCh38]
Chr19:12127224 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.1925C>G (p.Pro642Arg) single nucleotide variant not specified [RCV004239649] Chr19:12014933 [GRCh38]
Chr19:12125748 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.905C>T (p.Thr302Met) single nucleotide variant not specified [RCV004187822] Chr19:12015953 [GRCh38]
Chr19:12126768 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.790A>G (p.Thr264Ala) single nucleotide variant not specified [RCV004072728] Chr19:12016068 [GRCh38]
Chr19:12126883 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001080404.3(ZNF878):c.761G>A (p.Arg254His) single nucleotide variant not specified [RCV004219285] Chr19:12044640 [GRCh38]
Chr19:12155455 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.584A>G (p.Tyr195Cys) single nucleotide variant not specified [RCV004095389] Chr19:12016274 [GRCh38]
Chr19:12127089 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001080404.3(ZNF878):c.1426G>C (p.Glu476Gln) single nucleotide variant not specified [RCV004151293] Chr19:12043975 [GRCh38]
Chr19:12154790 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.819C>A (p.His273Gln) single nucleotide variant not specified [RCV004237934] Chr19:12016039 [GRCh38]
Chr19:12126854 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.1699G>A (p.Ala567Thr) single nucleotide variant not specified [RCV004151466] Chr19:12015159 [GRCh38]
Chr19:12125974 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001080404.3(ZNF878):c.736G>A (p.Glu246Lys) single nucleotide variant not specified [RCV004283102] Chr19:12044665 [GRCh38]
Chr19:12155480 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.569G>A (p.Arg190His) single nucleotide variant not specified [RCV004250822] Chr19:12016289 [GRCh38]
Chr19:12127104 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.1909C>T (p.His637Tyr) single nucleotide variant not specified [RCV004282760] Chr19:12014949 [GRCh38]
Chr19:12125764 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001080404.3(ZNF878):c.413C>G (p.Thr138Ser) single nucleotide variant not specified [RCV004297857] Chr19:12044988 [GRCh38]
Chr19:12155803 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001080404.3(ZNF878):c.475C>T (p.Arg159Cys) single nucleotide variant not specified [RCV004348556] Chr19:12044926 [GRCh38]
Chr19:12155741 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.1879C>T (p.Pro627Ser) single nucleotide variant not specified [RCV004349479] Chr19:12014979 [GRCh38]
Chr19:12125794 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001080404.3(ZNF878):c.476G>A (p.Arg159His) single nucleotide variant not specified [RCV004334525] Chr19:12044925 [GRCh38]
Chr19:12155740 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.848A>T (p.Gln283Leu) single nucleotide variant not specified [RCV004357348] Chr19:12016010 [GRCh38]
Chr19:12126825 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001080404.3(ZNF878):c.692T>A (p.Ile231Lys) single nucleotide variant not specified [RCV004363363] Chr19:12044709 [GRCh38]
Chr19:12155524 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001080404.3(ZNF878):c.961A>G (p.Ile321Val) single nucleotide variant not specified [RCV004341613] Chr19:12044440 [GRCh38]
Chr19:12155255 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.1904G>A (p.Arg635Lys) single nucleotide variant not specified [RCV004489540] Chr19:12014954 [GRCh38]
Chr19:12125769 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.1313G>T (p.Gly438Val) single nucleotide variant not specified [RCV004489536] Chr19:12015545 [GRCh38]
Chr19:12126360 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.934T>C (p.Cys312Arg) single nucleotide variant not specified [RCV004489546] Chr19:12015924 [GRCh38]
Chr19:12126739 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.1460C>T (p.Pro487Leu) single nucleotide variant not specified [RCV004489538] Chr19:12015398 [GRCh38]
Chr19:12126213 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.628T>G (p.Tyr210Asp) single nucleotide variant not specified [RCV004489542] Chr19:12016230 [GRCh38]
Chr19:12127045 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.1246G>C (p.Glu416Gln) single nucleotide variant not specified [RCV004489535] Chr19:12015612 [GRCh38]
Chr19:12126427 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.304G>A (p.Glu102Lys) single nucleotide variant not specified [RCV004489541] Chr19:12016554 [GRCh38]
Chr19:12127369 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.1394A>G (p.His465Arg) single nucleotide variant not specified [RCV004489537] Chr19:12015464 [GRCh38]
Chr19:12126279 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.692C>G (p.Ala231Gly) single nucleotide variant not specified [RCV004489544] Chr19:12016166 [GRCh38]
Chr19:12126981 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.778T>C (p.Phe260Leu) single nucleotide variant not specified [RCV004489545] Chr19:12016080 [GRCh38]
Chr19:12126895 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.1721T>C (p.Leu574Pro) single nucleotide variant not specified [RCV004489539] Chr19:12015137 [GRCh38]
Chr19:12125952 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.635T>G (p.Ile212Ser) single nucleotide variant not specified [RCV004489543] Chr19:12016223 [GRCh38]
Chr19:12127038 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001308348.2(ZNF433):c.977A>G (p.Glu326Gly) single nucleotide variant not specified [RCV004489547] Chr19:12015881 [GRCh38]
Chr19:12126696 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001080404.3(ZNF878):c.590A>C (p.Lys197Thr) single nucleotide variant not specified [RCV004495309] Chr19:12044811 [GRCh38]
Chr19:12155626 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001080404.3(ZNF878):c.968C>G (p.Ser323Cys) single nucleotide variant not specified [RCV004495312] Chr19:12044433 [GRCh38]
Chr19:12155248 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001080404.3(ZNF878):c.1561A>G (p.Ile521Val) single nucleotide variant not specified [RCV004495305] Chr19:12043840 [GRCh38]
Chr19:12154655 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001080404.3(ZNF878):c.493C>T (p.His165Tyr) single nucleotide variant not specified [RCV004495308] Chr19:12044908 [GRCh38]
Chr19:12155723 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001080404.3(ZNF878):c.738G>T (p.Glu246Asp) single nucleotide variant not specified [RCV004495310] Chr19:12044663 [GRCh38]
Chr19:12155478 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001080404.3(ZNF878):c.389T>G (p.Leu130Arg) single nucleotide variant not specified [RCV004495306] Chr19:12045012 [GRCh38]
Chr19:12155827 [GRCh37]
Chr19:19p13.2		 uncertain significance
NM_001080404.3(ZNF878):c.962T>A (p.Ile321Asn) single nucleotide variant not specified [RCV004495311] Chr19:12044439 [GRCh38]
Chr19:12155254 [GRCh37]
Chr19:19p13.2		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:973
Count of miRNA genes:550
Interacting mature miRNAs:592
Transcripts:ENST00000406892, ENST00000476474, ENST00000489336, ENST00000495324, ENST00000588047, ENST00000589551, ENST00000591838, ENST00000591898, ENST00000592187
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.


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 16 8 8 2 79 2 39 6 1 1 53 6 1
Low 2415 2905 1537 443 1843 284 4295 2124 3296 398 1388 1593 173 1 1203 2772 5 2
Below cutoff 8 78 181 179 29 179 22 66 436 20 19 11 1 1 15

Sequence

Nucleotide Sequences
RefSeq Transcripts NR_134927 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_134928 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_134929 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_134930 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA431306 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC008770 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC022415 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC042379 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC048140 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG059081 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM717321 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM854799 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP428722 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KC877701 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA986965 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA986966 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000406892
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1911,987,617 - 12,027,194 (+)Ensembl
RefSeq Acc Id: ENST00000476474
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1911,987,679 - 12,046,275 (+)Ensembl
RefSeq Acc Id: ENST00000489336
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1911,987,671 - 12,003,811 (+)Ensembl
RefSeq Acc Id: ENST00000495324
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1911,987,656 - 12,018,470 (+)Ensembl
RefSeq Acc Id: ENST00000588047
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1911,987,656 - 12,035,914 (+)Ensembl
RefSeq Acc Id: ENST00000589551
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1911,987,767 - 12,003,595 (+)Ensembl
RefSeq Acc Id: ENST00000591838
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1912,034,576 - 12,046,275 (+)Ensembl
RefSeq Acc Id: ENST00000591898
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1912,035,823 - 12,046,275 (+)Ensembl
RefSeq Acc Id: ENST00000592187
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1912,023,195 - 12,027,194 (+)Ensembl
RefSeq Acc Id: NR_134927
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381911,987,617 - 12,027,194 (+)NCBI
CHM1_11912,098,265 - 12,137,808 (+)NCBI
T2T-CHM13v2.01912,115,811 - 12,155,401 (+)NCBI
Sequence:
RefSeq Acc Id: NR_134928
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381911,987,617 - 12,046,275 (+)NCBI
CHM1_11912,098,265 - 12,156,901 (+)NCBI
T2T-CHM13v2.01912,115,811 - 12,174,482 (+)NCBI
Sequence:
RefSeq Acc Id: NR_134929
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381911,987,617 - 12,046,275 (+)NCBI
CHM1_11912,098,265 - 12,156,901 (+)NCBI
T2T-CHM13v2.01912,115,811 - 12,174,482 (+)NCBI
Sequence:
RefSeq Acc Id: NR_134930
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381911,987,617 - 12,003,811 (+)NCBI
CHM1_11912,098,265 - 12,114,425 (+)NCBI
T2T-CHM13v2.01912,115,811 - 12,132,019 (+)NCBI
Sequence:

Additional Information

Database Acc Id Source(s)
COSMIC ZNF433-AS1 COSMIC
Ensembl Genes ENSG00000219665 Ensembl, ENTREZGENE
Ensembl Transcript ENST00000406892 ENTREZGENE
  ENST00000476474 ENTREZGENE
  ENST00000489336 ENTREZGENE
GTEx ENSG00000219665 GTEx
HGNC ID HGNC:53776 ENTREZGENE
Human Proteome Map ZNF433-AS1 Human Proteome Map
NCBI Gene ZNF433-AS1 ENTREZGENE
RNAcentral URS0000A7653D RNACentral
  URS0000A76B44 RNACentral
  URS0000A76F75 RNACentral
  URS0000A77097 RNACentral