PANTR1 POU3F3 adjacent non-coding transcript 1
Information
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 | : |
|
Search word | : | |
Filtering | : |
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 |
Type | ID |
---|---|
SYNONYM | LINC01158 |
SYNONYM | linc-Brn1a |
SYNONYM | linc-POU3F3 |
MIM | 618169 OMIM |
HGNC | HGNC:49513 HGNC |
Ensembl | ENSG00000233639 Ensembl |
AllianceGenome | HGNC:49513 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
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 |
Genome browser