Genomic Map
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Target Gene Details
Entrez Gene ID: | 9987 |
Gene Name: | heterogeneous nuclear ribonucleoprotein D like |
Gene Aliases: |
HNRNP, HNRPDL, JKTBP, JKTBP2, LGMD1G, laAUF1 |
Location: |
Chr.4:82422564-82430225 on Build GRCh38 |
Assay Gene Location: | Within Exon 5 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| HNRNPDL | NM_001207000.1 | 5 | 1505 | NP_001193929.1 |
| NM_031372.3 | 5 | 1505 | NP_112740.1 | |
| NR_003249.2 | 5 | 1505 | ||
| AB017019.1 | 5 | 1505 | BAA75241.1 | |
| AB066484.1 | 5 | 613 | BAB62188.1 | |
| AK294683.1 | 3 | 374 | ||
| AK300122.1 | 5 | 591 | ||
| AY453824.1 | 5 | 604 | AAR17782.1 | |
| BC007392.2 | 5 | 957 | AAH07392.2 | |
| BC011714.2 | 5 | 1146 | AAH11714.1 | |
| BC071944.1 | 5 | 1086 | AAH71944.1 | |
| CR407623.1 | 5 | 970 | CAG28551.1 | |
| D89092.1 | 5 | 721 | BAA24361.1 | |
| D89678.1 | 5 | 580 | BAA22860.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2727893 | Chr.4:82426649 - 82427407 on Build GRCh38 | Deletion |
 HNRNPDL
|
| nsv829988 | Chr.4:82316984 - 82489338 on Build GRCh38 | Loss |
ENOPH1
TMEM150C
LOC105377310
HNRNPDL
HNRNPD
|
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Set Membership: |
Intragenic
Exonic
DGV Variation
|
Gene Ontology Categories:
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