Genomic Map
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Target Gene Details
Entrez Gene ID: | 4784 |
Gene Name: | nuclear factor I X |
Gene Aliases: |
MRSHSS, NF1A, SOTOS2 |
Location: |
Chr.19:12995512-13098796 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NFIX | NM_002501.3 | NP_002492.2 | ||
| XM_005259918.4 | XP_005259975.1 | |||
| XM_017026837.1 | XP_016882326.1 | |||
| BF115883.1 | ||||
| BT019732.1 | AAV38537.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv828444 | Chr.19:13012681 - 13027353 on Build GRCh38 | Loss |
 NFIX
|
| nsv1055900 | Chr.19:12979147 - 13034197 on Build GRCh38 | Gain |
NFIX
|
| nsv953977 | Chr.19:12666887 - 13095486 on Build GRCh38 | Deletion |
RNASEH2A
FARSA
PRDX2
JUNB
DNASE2
GCDH
MIR5684
RTBDN
RAD23A
SYCE2
KLF1
NFIX
CALR
GADD45GIP1
SNORD41
MIR6794
MIR6515
MAST1
DHPS
C19orf43
LOC105372280
WDR83OS
TNPO2
MIR5695
WDR83
ASNA1
BEST2
SNORD135
DAND5
HOOK2
FBXW9
|
| nsv2422 | Chr.19:13000362 - 13032711 on Build GRCh38 | Insertion |
NFIX
|
| nsv833754 | Chr.19:12876208 - 13028186 on Build GRCh38 | Loss |
MIR5695
GADD45GIP1
FARSA
MIR6515
RAD23A
DAND5
DNASE2
SYCE2
GCDH
KLF1
NFIX
CALR
|
| esv275430 | Chr.19:13015145 - 13020565 on Build GRCh38 | Gain+Loss |
NFIX
|
Back To TopMore Information
Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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