Genomic Map
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Target Gene Details
Entrez Gene ID: | 3185 |
Gene Name: | heterogeneous nuclear ribonucleoprotein F |
Gene Aliases: |
HNRPF, OK/SW-cl.23, mcs94-1 |
Location: |
Chr.10:43385617-43409248 on Build GRCh38 |
Assay Gene Location: | Within Exon 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| HNRNPF | NM_001098204.1 | 4 | 840 | NP_001091674.1 |
| NM_001098205.1 | 4 | 880 | NP_001091675.1 | |
| NM_001098206.1 | 4 | 857 | NP_001091676.1 | |
| NM_001098207.1 | 4 | 884 | NP_001091677.1 | |
| NM_001098208.1 | 3 | 963 | NP_001091678.1 | |
| NM_004966.3 | 4 | 841 | NP_004957.1 | |
| AK001364.1 | 4 | 878 | ||
| AK296696.1 | 5 | 661 | ||
| AL542769.3 | 4 | 801 | ||
| BC001432.2 | 3 | 635 | AAH01432.1 | |
| BC004254.1 | 4 | 799 | AAH04254.1 | |
| BC015580.2 | 4 | 756 | AAH15580.1 | |
| BC016736.1 | 4 | 829 | AAH16736.1 | |
| BC106008.1 | 4 | 768 | AAI06009.1 | |
| L28010.1 | 1 | 504 | AAC37584.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv831842 | Chr.10:43351093 - 43492053 on Build GRCh38 | Loss |
 FXYD4
HNRNPF
ZNF487
|
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Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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