Genomic Map
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Target Gene Details
Entrez Gene ID: | 140459 |
Gene Name: | ankyrin repeat and SOCS box containing 6 |
Gene Aliases: |
- |
Location: |
Chr.9:129634604-129642169 on Build GRCh38 |
Assay Gene Location: | Within Exon 6 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ASB6 | NM_001202403.1 | 5 | 3823 | NP_001189332.1 |
| NM_017873.3 | 6 | 3910 | NP_060343.1 | |
| NM_177999.2 | 5 | 3801 | NP_821066.1 | |
| AK093539.1 | 1 | 1458 | ||
| AL390135.1 | 1 | 2183 | ||
| BX648923.1 | 5 | 4431 | CAH10563.1 | |
| CR627462.1 | 1 | 2183 |
Target Gene Details
Entrez Gene ID: | 28989 |
Gene Name: | N-terminal Xaa-Pro-Lys N-methyltransferase 1 |
Gene Aliases: |
AD-003, C9orf32, HOMT1A, METTL11A, NRMT, NTM1A |
Location: |
Chr.9:129608884-129636742 on Build GRCh38 |
Assay Gene Location: | Within Exon 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NTMT1 | NM_001286796.1 | 4 | 873 | NP_001273725.1 |
| NM_001286797.1 | 4 | 686 | NP_001273726.1 | |
| NM_001286798.1 | 4 | 747 | NP_001273727.1 | |
| NM_001286799.1 | 4 | 676 | NP_001273728.1 | |
| NM_001286800.1 | 4 | 636 | NP_001273729.1 | |
| NM_001286801.1 | 4 | 662 | NP_001273730.1 | |
| NM_001286802.1 | 3 | 531 | NP_001273731.1 | |
| NM_001286803.1 | 3 | 505 | NP_001273732.1 | |
| NM_014064.3 | 4 | 721 | NP_054783.2 | |
| NR_104596.1 | 4 | 572 | ||
| XM_005251939.3 | 4 | 662 | XP_005251996.1 | |
| XM_017014642.1 | 4 | 579 | XP_016870131.1 | |
| AF110776.1 | 4 | 664 | AAF14859.1 | |
| AI802417.1 | 1 | 290 | ||
| AK290957.1 | 4 | 718 | ||
| AK292332.1 | 4 | 723 | ||
| AK298840.1 | 4 | 626 | ||
| AK307056.1 | 4 | 563 | ||
| AK313829.1 | 4 | 711 | ||
| BC001396.2 | 4 | 700 | AAH01396.1 | |
| BC033234.1 | 4 | 675 | AAH33234.1 | |
| BE392289.1 | ||||
| BI083998.1 | ||||
| BM009113.1 | 3 | 458 | ||
| BM554138.1 | 4 | 676 | ||
| BQ923165.1 | 4 | 700 | ||
| HY058177.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv469901 | Chr.9:129597897 - 129681820 on Build GRCh38 | Loss |
 NTMT1
ASB6
C9orf50
PRRX2
|
| nsv1046477 | Chr.9:129608081 - 129997996 on Build GRCh38 | Gain |
MIR6855
NTMT1
FNBP1
ASB6
C9orf78
TOR1B
USP20
C9orf50
PTGES
TOR1A
PRRX2
PRRX2-AS1
|
| nsv951784 | Chr.9:129625222 - 129655421 on Build GRCh38 | Deletion |
NTMT1
ASB6
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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