Genomic Map
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Target Gene Details
Entrez Gene ID: | 4782 |
Gene Name: | nuclear factor I C |
Gene Aliases: |
CTF, CTF5, NF-I, NFI |
Location: |
Chr.19:3359563-3469217 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NFIC | NM_001245005.1 | NP_001231934.1 | ||
| NM_205843.2 | NP_995315.1 | |||
| XM_006722759.2 | XP_006722822.2 | |||
| XM_017026836.1 | XP_016882325.1 | |||
| AK289885.1 | ||||
| AK304816.1 | ||||
| BP279194.1 | ||||
| BQ894051.1 | ||||
| X12492.1 | CAA31012.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv509717 | Chr.19:3271020 - 3392050 on Build GRCh38 | Insertion |
 CELF5
NFIC
|
| nsv1058546 | Chr.19:3321667 - 3369170 on Build GRCh38 | Gain |
NFIC
|
| nsv953948 | Chr.19:3171703 - 3700002 on Build GRCh38 | Deletion |
CACTIN-AS1
MFSD12
SMIM24
FZR1
HMG20B
C19orf71
NFIC
CACTIN
DOHH
NCLN
TBXA2R
PIP5K1C
CELF5
GIPC3
S1PR4
|
| nsv833712 | Chr.19:3230782 - 3365290 on Build GRCh38 | Loss |
CELF5
NFIC
|
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Additional Information:
For this assay, SNP(s) [rs73919113] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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