Genomic Map
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Target Gene Details
Entrez Gene ID: | 4093 |
Gene Name: | SMAD family member 9 |
Gene Aliases: |
MADH6, MADH9, PPH2, SMAD8, SMAD8/9, SMAD8A, SMAD8B |
Location: |
Chr.13:36844831-36920721 on Build GRCh38 |
Assay Gene Location: | Within Exon 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SMAD9 | NM_001127217.2 | 6 | 1448 | NP_001120689.1 |
| NM_005905.5 | 5 | 1337 | NP_005896.1 | |
| XM_005266401.3 | 4 | 1046 | XP_005266458.1 | |
| XM_005266403.3 | 5 | 1151 | XP_005266460.1 | |
| XM_005266404.3 | 4 | 1040 | XP_005266461.1 | |
| XM_006719827.3 | 6 | 1378 | XP_006719890.1 | |
| AK311686.1 | 4 | 483 | ||
| AK314920.1 | 5 | 1157 | ||
| BC011559.1 | 4 | 1134 | AAH11559.1 | |
| BC104760.1 | 5 | 1200 | AAI04761.1 | |
| BC104762.1 | 5 | 1200 | AAI04763.1 | |
| BC143240.1 | 5 | 1200 | ||
| D83760.1 | 5 | 1160 | BAA21128.1 | |
| D83761.1 | 4 | 1049 | BAA21129.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv522336 | Chr.13:36731504 - 37010701 on Build GRCh38 | Gain |
 ALG5
SUPT20H
EXOSC8
SMAD9
RFXAP
|
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Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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