Genomic Map
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Target Gene Details
Entrez Gene ID: | 11046 |
Gene Name: | solute carrier family 35 member D2 |
Gene Aliases: |
HFRC1, SQV7L, UGTrel8, hfrc |
Location: |
Chr.9:96313437-96383710 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 12 - Exon 12 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC35D2 | NM_001286990.1 | NP_001273919.1 | ||
| NM_007001.2 | NP_008932.2 | |||
| NR_104627.1 | ||||
| XM_005251673.1 | XP_005251730.1 | |||
| XM_005251674.1 | XP_005251731.1 | |||
| XM_005251675.2 | XP_005251732.1 | |||
| XM_005251676.1 | XP_005251733.1 | |||
| XM_005251678.4 | XP_005251735.1 | |||
| XM_006716939.2 | XP_006717002.1 | |||
| XM_011518164.1 | XP_011516466.1 | |||
| AB122077.1 | BAC99016.1 | |||
| AJ005866.1 | CAA06743.1 | |||
| AK024841.1 | ||||
| AK307890.1 | ||||
| BC009413.1 | AAH09413.1 | |||
| BC100278.1 | AAI00279.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3891694 | Chr.9:96278219 - 96369762 on Build GRCh38 | Loss |
 HSD17B3
SLC35D2
|
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Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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