ZRANB2-DT (ZRANB2 divergent transcript) - Rat Genome Database

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Gene: ZRANB2-DT (ZRANB2 divergent transcript) Homo sapiens
Analyze
Symbol: ZRANB2-DT
Name: ZRANB2 divergent transcript
RGD ID: 5683643
HGNC Page HGNC:43595
Description: ASSOCIATED WITH intellectual disability; Intellectual disability, severe; INTERACTS WITH aflatoxin B1; aristolochic acid A; cisplatin
Type: ncrna (Ensembl: lncRNA)
RefSeq Status: VALIDATED
Previously known as: ZRANB2 antisense RNA 2 (head to head); ZRANB2-AS2
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38171,081,324 - 71,237,723 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl171,081,324 - 71,489,976 (+)EnsemblGRCh38hg38GRCh38
GRCh37171,547,007 - 71,703,406 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map1p31.1NCBI
HuRef169,657,281 - 69,813,515 (+)NCBIHuRef
CHM1_1171,662,362 - 71,818,756 (+)NCBICHM1_1
T2T-CHM13v2.0170,959,331 - 71,115,774 (+)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
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References
Additional References at PubMed
PMID:12477932   PMID:16341674  


Genomics

Variants

.
Variants in ZRANB2-DT
3 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 1p32.3-31.1(chr1:52595352-76767765)x3 copy number gain See cases [RCV000051822] Chr1:52595352..76767765 [GRCh38]
Chr1:53061024..77233450 [GRCh37]
Chr1:52833612..77006038 [NCBI36]
Chr1:1p32.3-31.1		 pathogenic
GRCh38/hg38 1p32.2-31.1(chr1:57350574-71325924)x1 copy number loss See cases [RCV000053841] Chr1:57350574..71325924 [GRCh38]
Chr1:57816246..71791607 [GRCh37]
Chr1:57588834..71564195 [NCBI36]
Chr1:1p32.2-31.1		 pathogenic
GRCh38/hg38 1p32.1-31.1(chr1:59632500-76730877)x1 copy number loss See cases [RCV000053842] Chr1:59632500..76730877 [GRCh38]
Chr1:60098172..77196562 [GRCh37]
Chr1:59870760..76969150 [NCBI36]
Chr1:1p32.1-31.1		 pathogenic
GRCh38/hg38 1p31.3-31.1(chr1:67239704-71924806)x1 copy number loss See cases [RCV000053843] Chr1:67239704..71924806 [GRCh38]
Chr1:67705387..72390489 [GRCh37]
Chr1:67477975..72163077 [NCBI36]
Chr1:1p31.3-31.1		 pathogenic
GRCh38/hg38 1p32.1-31.1(chr1:59760856-71578052)x1 copy number loss See cases [RCV000133710] Chr1:59760856..71578052 [GRCh38]
Chr1:60226528..72043735 [GRCh37]
Chr1:59999116..71816323 [NCBI36]
Chr1:1p32.1-31.1		 pathogenic
GRCh38/hg38 1p32.1-22.3(chr1:58819605-86098611)x1 copy number loss See cases [RCV000136913] Chr1:58819605..86098611 [GRCh38]
Chr1:59285277..86564294 [GRCh37]
Chr1:59057865..86336882 [NCBI36]
Chr1:1p32.1-22.3		 pathogenic
GRCh38/hg38 1p31.3-31.1(chr1:64072618-75518432)x3 copy number gain See cases [RCV000142452] Chr1:64072618..75518432 [GRCh38]
Chr1:64538290..75984117 [GRCh37]
Chr1:64310878..75756705 [NCBI36]
Chr1:1p31.3-31.1		 pathogenic
GRCh38/hg38 1p31.3-31.1(chr1:66865125-77123381)x1 copy number loss See cases [RCV000143129] Chr1:66865125..77123381 [GRCh38]
Chr1:67330808..77589066 [GRCh37]
Chr1:67103396..77361654 [NCBI36]
Chr1:1p31.3-31.1		 pathogenic
GRCh38/hg38 1p31.1(chr1:70716347-71407975)x3 copy number gain See cases [RCV000143773] Chr1:70716347..71407975 [GRCh38]
Chr1:71182030..71873658 [GRCh37]
Chr1:70954618..71646246 [NCBI36]
Chr1:1p31.1		 likely benign
GRCh38/hg38 1p31.1(chr1:71112628-71339459)x1 copy number loss See cases [RCV000143600] Chr1:71112628..71339459 [GRCh38]
Chr1:71578311..71805142 [GRCh37]
Chr1:71350899..71577730 [NCBI36]
Chr1:1p31.1		 likely benign|uncertain significance
GRCh37/hg19 1p31.1(chr1:71419650-72398325)x1 copy number loss not provided [RCV001005107] Chr1:71419650..72398325 [GRCh37]
Chr1:1p31.1		 uncertain significance
GRCh37/hg19 1p36.12-12(chr1:20608823-120546301)x3 copy number loss not provided [RCV000762767] Chr1:20608823..120546301 [GRCh37]
Chr1:1p36.12-12		 likely benign
GRCh37/hg19 1p31.3-31.1(chr1:63252828-77402595)x1 copy number loss See cases [RCV000446378] Chr1:63252828..77402595 [GRCh37]
Chr1:1p31.3-31.1		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p31.1(chr1:71650258-72268332)x3 copy number gain See cases [RCV000511372] Chr1:71650258..72268332 [GRCh37]
Chr1:1p31.1		 likely benign
GRCh37/hg19 1p31.3-22.3(chr1:64321264-88153669)x1 copy number loss See cases [RCV000511392] Chr1:64321264..88153669 [GRCh37]
Chr1:1p31.3-22.3		 pathogenic|uncertain significance
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p31.3-31.1(chr1:61351024-79583933)x1 copy number loss See cases [RCV000512152] Chr1:61351024..79583933 [GRCh37]
Chr1:1p31.3-31.1		 pathogenic
GRCh37/hg19 1p31.3-31.1(chr1:62434799-71656180)x3 copy number gain not provided [RCV000684577] Chr1:62434799..71656180 [GRCh37]
Chr1:1p31.3-31.1		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p31.1(chr1:71410579-78131158) copy number gain not provided [RCV000767771] Chr1:71410579..78131158 [GRCh37]
Chr1:1p31.1		 pathogenic
Single allele deletion Intellectual disability, severe [RCV000824954] Chr1:59922631..72058653 [GRCh37]
Chr1:1p32.1-31.1		 pathogenic
GRCh37/hg19 1p31.3-22.3(chr1:67851233-86101340)x1 copy number loss not provided [RCV000846441] Chr1:67851233..86101340 [GRCh37]
Chr1:1p31.3-22.3		 pathogenic
GRCh37/hg19 1p36.22-21.1(chr1:103343285-103455144)x3 copy number gain Global developmental delay [RCV000787285] Chr1:103343285..103455144 [GRCh37]
Chr1:1p36.22-21.1		 uncertain significance
Single allele deletion not provided [RCV000844927] Chr1:66085524..88429789 [GRCh37]
Chr1:1p31.3-22.2		 not provided
GRCh37/hg19 1p31.3-31.1(chr1:66868168-77106425)x1 copy number loss not provided [RCV000847457] Chr1:66868168..77106425 [GRCh37]
Chr1:1p31.3-31.1		 pathogenic
GRCh37/hg19 1p31.1(chr1:71582394-71942586)x1 copy number loss not provided [RCV000848046] Chr1:71582394..71942586 [GRCh37]
Chr1:1p31.1		 uncertain significance
GRCh37/hg19 1p31.3-22.1(chr1:68180293-92731957) copy number loss not specified [RCV002053392] Chr1:68180293..92731957 [GRCh37]
Chr1:1p31.3-22.1		 pathogenic
Single allele duplication not specified [RCV002286371] Chr1:66885559..77949895 [GRCh38]
Chr1:1p31.3-31.1		 uncertain significance
GRCh37/hg19 1p31.1(chr1:69989275-72180606)x1 copy number loss not provided [RCV002475801] Chr1:69989275..72180606 [GRCh37]
Chr1:1p31.1		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1706
Count of miRNA genes:786
Interacting mature miRNAs:909
Transcripts:ENST00000413421, ENST00000415780, ENST00000430605, ENST00000455406, ENST00000583678, ENST00000585415, ENST00000585499, ENST00000586006, ENST00000587066, ENST00000587306, ENST00000590186, ENST00000591654, ENST00000594152, ENST00000596952, ENST00000599146, ENST00000600103, ENST00000608360, ENST00000608579
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
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 1 2
Low 11 6 89 4 73 2 60 11 115 69 469 131 5 1 1 45 2 2
Below cutoff 2369 2393 1518 506 1280 349 4168 2099 3606 330 956 1453 168 1195 2667 4

Sequence

Nucleotide Sequences
RefSeq Transcripts NR_046217 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AL360297 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL512443 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC054887 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM766420 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985395 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985396 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985397 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985398 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985399 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985400 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985401 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985402 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985403 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985404 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985405 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985406 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985407 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985408 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985409 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985410 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985411 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985412 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985413 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985414 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985415 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985416 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985417 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985418 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985419 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985420 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985421 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985422 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985423 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985424 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985425 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985426 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985427 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985428 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985429 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985430 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985431 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA985432 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000411721
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,250,999 - 71,252,119 (+)Ensembl
RefSeq Acc Id: ENST00000413421
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,361 - 71,268,230 (+)Ensembl
RefSeq Acc Id: ENST00000415780
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,093,130 - 71,237,198 (+)Ensembl
RefSeq Acc Id: ENST00000430605
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,401,847 - 71,407,724 (+)Ensembl
RefSeq Acc Id: ENST00000455406
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,324 - 71,241,548 (+)Ensembl
RefSeq Acc Id: ENST00000583678
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,367 - 71,468,896 (+)Ensembl
RefSeq Acc Id: ENST00000585415
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,407,644 - 71,489,976 (+)Ensembl
RefSeq Acc Id: ENST00000585499
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,407,644 - 71,422,975 (+)Ensembl
RefSeq Acc Id: ENST00000586006
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,407,633 - 71,422,975 (+)Ensembl
RefSeq Acc Id: ENST00000587066
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,407,640 - 71,463,380 (+)Ensembl
RefSeq Acc Id: ENST00000587306
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,407,633 - 71,468,510 (+)Ensembl
RefSeq Acc Id: ENST00000590186
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,408,939 - 71,486,447 (+)Ensembl
RefSeq Acc Id: ENST00000591654
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,463,409 - 71,489,903 (+)Ensembl
RefSeq Acc Id: ENST00000594152
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,367 - 71,407,684 (+)Ensembl
RefSeq Acc Id: ENST00000596952
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,353 - 71,202,422 (+)Ensembl
RefSeq Acc Id: ENST00000599146
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,350 - 71,407,684 (+)Ensembl
RefSeq Acc Id: ENST00000600103
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,202,088 - 71,407,679 (+)Ensembl
RefSeq Acc Id: ENST00000608360
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,484,786 - 71,487,068 (+)Ensembl
RefSeq Acc Id: ENST00000608579
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,401,722 - 71,407,658 (+)Ensembl
RefSeq Acc Id: ENST00000623721
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,408,704 - 71,489,976 (+)Ensembl
RefSeq Acc Id: ENST00000624050
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,463,449 - 71,489,919 (+)Ensembl
RefSeq Acc Id: ENST00000625045
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,461,559 - 71,468,843 (+)Ensembl
RefSeq Acc Id: ENST00000625896
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,353 - 71,407,658 (+)Ensembl
RefSeq Acc Id: ENST00000626344
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,351 - 71,237,160 (+)Ensembl
RefSeq Acc Id: ENST00000626510
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,364 - 71,407,658 (+)Ensembl
RefSeq Acc Id: ENST00000627516
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,351 - 71,407,658 (+)Ensembl
RefSeq Acc Id: ENST00000627548
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,350 - 71,407,658 (+)Ensembl
RefSeq Acc Id: ENST00000627902
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,351 - 71,407,658 (+)Ensembl
RefSeq Acc Id: ENST00000628450
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,364 - 71,407,682 (+)Ensembl
RefSeq Acc Id: ENST00000628635
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,364 - 71,407,636 (+)Ensembl
RefSeq Acc Id: ENST00000628670
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,373 - 71,407,658 (+)Ensembl
RefSeq Acc Id: ENST00000628683
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,364 - 71,407,658 (+)Ensembl
RefSeq Acc Id: ENST00000628797
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,364 - 71,407,658 (+)Ensembl
RefSeq Acc Id: ENST00000630350
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,394 - 71,407,658 (+)Ensembl
RefSeq Acc Id: ENST00000630885
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,370 - 71,407,658 (+)Ensembl
RefSeq Acc Id: ENST00000630926
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,351 - 71,407,658 (+)Ensembl
RefSeq Acc Id: ENST00000630994
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,351 - 71,407,656 (+)Ensembl
RefSeq Acc Id: ENST00000634641
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,349 - 71,251,624 (+)Ensembl
RefSeq Acc Id: ENST00000653422
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,367 - 71,408,633 (+)Ensembl
RefSeq Acc Id: ENST00000654734
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,324 - 71,474,007 (+)Ensembl
RefSeq Acc Id: ENST00000663294
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,353 - 71,487,723 (+)Ensembl
RefSeq Acc Id: ENST00000670550
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,368 - 71,409,362 (+)Ensembl
RefSeq Acc Id: ENST00000671179
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl171,081,344 - 71,402,925 (+)Ensembl
RefSeq Acc Id: NR_046217
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38171,081,324 - 71,237,723 (+)NCBI
GRCh37171,547,007 - 71,703,406 (+)NCBI
HuRef169,657,281 - 69,813,515 (+)NCBI
CHM1_1171,662,362 - 71,818,756 (+)NCBI
T2T-CHM13v2.0170,959,331 - 71,115,774 (+)NCBI
Sequence:

Additional Information

Database Acc Id Source(s)
COSMIC ZRANB2-DT COSMIC
Ensembl Genes ENSG00000229956 Ensembl
GTEx ENSG00000229956 GTEx
HGNC ID HGNC:43595 ENTREZGENE
Human Proteome Map ZRANB2-DT Human Proteome Map
NCBI Gene ZRANB2-AS2 ENTREZGENE
RNAcentral URS000075D397 RNACentral


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2021-08-02 ZRANB2-DT  ZRANB2 divergent transcript  ZRANB2-AS2  ZRANB2 antisense RNA 2 (head to head)  Symbol and/or name change 19259463 PROVISIONAL
2012-10-09 ZRANB2-AS2  ZRANB2 antisense RNA 2 (head to head)    ZRANB2 antisense RNA 2  Symbol and/or name change 5135510 APPROVED
2012-08-21 ZRANB2-AS2  ZRANB2 antisense RNA 2  ZRANB2-AS2  ZRANB2 antisense RNA 2 (non-protein coding)  Symbol and/or name change 5135510 APPROVED