Genomic Map
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Target Gene Details
Entrez Gene ID: | 4773 |
Gene Name: | nuclear factor of activated T-cells 2 |
Gene Aliases: |
NFAT1, NFATP |
Location: |
Chr.20:51386957-51562857 on Build GRCh38 |
Assay Gene Location: | Within Intron 12 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NFATC2 | NM_001136021.2 | NP_001129493.1 | ||
| NM_001258292.1 | NP_001245221.1 | |||
| NM_001258294.1 | NP_001245223.1 | |||
| NM_001258295.1 | NP_001245224.1 | |||
| NM_001258296.1 | NP_001245225.1 | |||
| NM_001258297.1 | NP_001245226.1 | |||
| NM_012340.4 | NP_036472.2 | |||
| NM_173091.3 | NP_775114.1 | |||
| XM_017027851.1 | XP_016883340.1 | |||
| AK226146.1 | ||||
| AK304147.1 | ||||
| BC136418.1 | ||||
| BC144074.1 | ||||
| BF914609.1 | ||||
| BU429325.1 | ||||
| CF136470.1 | ||||
| EU887573.1 | ||||
| EU887574.1 | ||||
| EU887575.1 | ||||
| EU887576.1 | ||||
| EU887577.1 | ||||
| EU887578.1 | ||||
| EU887579.1 | ||||
| EU887580.1 | ||||
| U43342.1 | AAC50887.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2751917 | Chr.20:51052156 - 51598401 on Build GRCh38 | Gain |
 MIR3194
NFATC2
ATP9A
|
| esv2722510 | Chr.20:51395435 - 51395917 on Build GRCh38 | Deletion |
NFATC2
|
| esv2722509 | Chr.20:51395081 - 51395717 on Build GRCh38 | Deletion |
NFATC2
|
| esv2722511 | Chr.20:51395481 - 51395652 on Build GRCh38 | Deletion |
NFATC2
|
| nsv1055542 | Chr.20:51378130 - 51402077 on Build GRCh38 | Gain |
NFATC2
|
Back To TopMore Information
Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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