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Human (GRCh37.p13)
Description

nuclear factor I/B [Source:HGNC Symbol;Acc:7785]

Gene Synonyms

CTF, HMGIC/NFIB, NF-I/B, NF1-B, NFI-B, NFI-RED, NFIB2, NFIB3

Location

Chromosome 9: 14,081,842-14,398,982 reverse strand.

GRCh37:CM000671.1

About this gene

This gene has 11 transcripts (splice variants), 3 paralogues and is associated with 75 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000380959.3NFIB-0018198420aaENSP00000370346.3
 
Protein coding
CCDS6474O00712 Q5VW28 Q5VW31
NM_005596
NP_005587
GENCODE basic
ENST00000380934.4NFIB-2018159446aaENSP00000370321.4
 
Protein coding
CCDS55292Q5VW31 NM_001190738
NP_001177667
GENCODE basic
ENST00000397581.2NFIB-0033318570aaENSP00000380711.2
 
Protein coding
Q5VW26 -GENCODE basic
ENST00000397579.2NFIB-0023129487aaENSP00000380709.2
 
Protein coding
Q5VW27 -GENCODE basic
ENST00000397575.3NFIB-0042869561aaENSP00000380705.3
 
Protein coding
G3V1P1 Q5VW30 -GENCODE basic
ENST00000380953.1NFIB-0052381494aaENSP00000370340.1
 
Protein coding
CCDS55291O00712 NM_001190737
NP_001177666
GENCODE basic
ENST00000543693.1NFIB-2021855309aaENSP00000442888.1
 
Protein coding
CCDS65007G3V1P1 NM_001282787
NP_001269716
GENCODE basic
ENST00000380921.3NFIB-0061274200aaENSP00000370308.3
 
Protein coding
Q5W0Y9 -GENCODE basic
ENST00000380924.1NFIB-008840168aaENSP00000370311.1
 
Protein coding
Q5VW31 -GENCODE basic
ENST00000493697.1NFIB-007591166aaENSP00000475362.1
 
Protein coding
U3KPY9 -CDS 3' incomplete
ENST00000606230.1NFIB-00955759aaENSP00000475813.1
 
Protein coding
U3KQE8 -CDS 3' incomplete

Gene-based displays