PANTR1 POU3F3 adjacent non-coding transcript 1

Information
Symbol
PANTR1
Type
ncRNA
Description
POU3F3 adjacent non-coding transcript 1
Entrez Gene ID
100506421
Genome
hg19
Position
chr2:105,424,043-105,467,917
Genome
hg38
Position
chr2:104,807,585-104,851,459
MIM
618169 OMIM
HGNC
HGNC:49513 HGNC
Ensembl
ENSG00000233639 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
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Variant name Gene AA change CDS Japanese
frequency
TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence
Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM LINC01158
SYNONYM linc-Brn1a
SYNONYM linc-POU3F3
MIM 618169 OMIM
HGNC HGNC:49513 HGNC
Ensembl ENSG00000233639 Ensembl
AllianceGenome HGNC:49513
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000661120.1 hg38 chr2 104,807,585 104,851,459 43,875
ENST00000686195.1 hg38 chr2 104,807,572 104,851,453 43,882
ENST00000659645.1 hg38 chr2 104,794,848 104,843,672 48,825
ENST00000702977.1 hg38 chr2 104,807,570 104,851,456 43,887
ENST00000443988.7 hg38 chr2 104,805,003 104,851,484 46,482
ENST00000659645.1 hg19 chr2 105,411,306 105,460,130 48,825
ENST00000443988.7 hg19 chr2 105,421,461 105,467,942 46,482
ENST00000661120.1 hg19 chr2 105,424,043 105,467,917 43,875
ENST00000686195.1 hg19 chr2 105,424,030 105,467,911 43,882
ENST00000702977.1 hg19 chr2 105,424,028 105,467,914 43,887
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