Genomic Map
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Target Gene Details
Entrez Gene ID: | 4149 |
Gene Name: | MYC associated factor X |
Gene Aliases: |
bHLHd4 |
Location: |
Chr.14:65006101-65102695 on Build GRCh38 |
Assay Gene Location: | Within Exon 9 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| MAX | NM_001271069.1 | NP_001257998.1 | ||
| NM_001320415.1 | 6 | 1996 | NP_001307344.1 | |
| NM_002382.4 | 5 | 1911 | NP_002373.3 | |
| NM_145112.2 | 4 | 1884 | NP_660087.1 | |
| NM_145113.2 | 6 | 2012 | NP_660088.1 | |
| NM_197957.3 | NP_932061.1 | |||
| NR_073137.1 | 4 | 1830 | ||
| XM_017021312.1 | 5 | 1955 | XP_016876801.1 | |
| XM_017021313.1 | 6 | 1875 | XP_016876802.1 | |
| AI652319.1 | ||||
| AI655674.1 | ||||
| AI917842.1 | ||||
| AI954328.1 | 1 | 135 | ||
| AL833643.1 | 6 | 1972 | ||
| AW043562.1 | 1 | 146 | ||
| BC003525.1 | 4 | 1794 | AAH03525.1 | |
| BC025685.1 | 4 | 1831 | AAH25685.1 | |
| BC027924.1 | 4 | 1841 | AAH27924.1 | |
| BC036092.1 | AAH36092.1 | |||
| DB482510.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv832816 | Chr.14:65006526 - 65177927 on Build GRCh38 | Gain |
 LOC100506321
CHURC1-FNTB
MAX
FNTB
MIR4706
|
| esv2748779 | Chr.14:63663324 - 66595809 on Build GRCh38 | Deletion |
TEX21P
FUT8
PLEKHG3
FUT8-AS1
CHURC1
GPHN
ESR2
SGPP1
SPTB
GPX2
MIR625
LOC102723809
CHURC1-FNTB
MIR4708
ZBTB25
LINC00238
AKAP5
MIR548H1
MAX
MIR7855
RAB15
HSPA2
SYNE2
PPP1R36
LOC100506321
ZBTB1
FNTB
MIR4706
MTHFD1
LOC100128233
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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