Genomic Map
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Target Gene Details
Entrez Gene ID: | 4781 |
Gene Name: | nuclear factor I B |
Gene Aliases: |
CTF, HMGIC/NFIB, NF-I/B, NF1-B, NFI-B, NFI-RED, NFIB2, NFIB3 |
Location: |
Chr.9:14081843-14398983 on Build GRCh38 |
Assay Gene Location: | Within Exon 16 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NFIB | NM_001190737.1 | 11 | 7696 | NP_001177666.1 |
| NM_001190738.1 | 9 | 7369 | NP_001177667.1 | |
| NM_001282787.1 | 11 | 6832 | NP_001269716.1 | |
| NM_005596.3 | 9 | 7474 | NP_005587.2 | |
| XM_005251467.2 | 12 | 7905 | XP_005251524.1 | |
| XM_005251468.4 | 12 | 7378 | XP_005251525.1 | |
| XM_005251469.2 | 12 | 7878 | XP_005251526.1 | |
| XM_005251470.2 | 10 | 7656 | XP_005251527.1 | |
| XM_005251471.3 | 11 | 8740 | XP_005251528.1 | |
| XM_006716773.2 | 12 | 7902 | XP_006716836.1 | |
| XM_006716774.2 | 11 | 7816 | XP_006716837.1 | |
| XM_006716775.2 | 10 | 7733 | XP_006716838.1 | |
| XM_017014739.1 | 9 | 7564 | XP_016870228.1 | |
| XM_017014740.1 | 9 | 7385 | XP_016870229.1 | |
| XM_017014741.1 | 9 | 7502 | XP_016870230.1 | |
| XM_017014742.1 | 9 | 9017 | XP_016870231.1 | |
| AK094066.1 | 1 | 1623 | ||
| AK129782.1 | 1 | 462 | ||
| AL110126.1 | 1 | 660 | ||
| BX537698.1 | 1 | 4271 | ||
| BX537707.1 | 1 | 3843 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1033764 | Chr.9:13764919 - 14226169 on Build GRCh38 | Loss |
 LINC00583
NFIB
|
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Additional Information:
For this assay, SNP(s) [rs35029845] 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
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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