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NFIC (gene)

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Protein-coding gene in the species Homo sapiens
NFIC
Identifiers
AliasesNFIC, CTF, CTF5, NF-I, NFI, nuclear factor I C
External IDsOMIM: 600729; MGI: 109591; HomoloGene: 4088; GeneCards: NFIC; OMA:NFIC - orthologs
Gene location (Human)
Chromosome 19 (human)
Chr.Chromosome 19 (human)
Chromosome 19 (human)Genomic location for NFICGenomic location for NFIC
Band19p13.3Start3,314,403 bp
End3,469,217 bp
Gene location (Mouse)
Chromosome 10 (mouse)
Chr.Chromosome 10 (mouse)
Chromosome 10 (mouse)Genomic location for NFICGenomic location for NFIC
Band10 C1|10 39.72 cMStart81,232,020 bp
End81,291,469 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • nipple

  • parotid gland

  • cardia

  • pylorus

  • seminal vesicula

  • renal medulla

  • pericardium

  • urethra

  • trigeminal ganglion

  • body of tongue
Top expressed in
  • ankle

  • lacrimal gland

  • triceps brachii muscle

  • aortic valve

  • extensor digitorum longus muscle

  • muscle of thigh

  • ascending aorta

  • plantaris muscle

  • vestibular membrane of cochlear duct

  • internal carotid artery
More reference expression data
BioGPS


More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

4782

18029

Ensembl

ENSG00000141905

ENSMUSG00000055053

UniProt

P08651

P70255

RefSeq (mRNA)

NM_001245002
NM_001245004
NM_001245005
NM_005597
NM_205843

NM_008688
NM_026756

RefSeq (protein)

NP_001231931
NP_001231933
NP_001231934
NP_005588
NP_995315

NP_032714
NP_081032

Location (UCSC)Chr 19: 3.31 – 3.47 MbChr 10: 81.23 – 81.29 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Nuclear factor 1 C-type is a protein that in humans is encoded by the NFIC gene.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000141905Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000055053Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Santoro C, Mermod N, Andrews PC, Tjian R (Aug 1988). "A family of human CCAAT-box-binding proteins active in transcription and DNA replication: cloning and expression of multiple cDNAs". Nature. 334 (6179): 218–24. Bibcode:1988Natur.334..218S. doi:10.1038/334218a0. PMID 3398920. S2CID 4287831.
  6. Qian F, Kruse U, Lichter P, Sippel AE (Dec 1995). "Chromosomal localization of the four genes (NFIA, B, C, and X) for the human transcription factor nuclear factor I by FISH". Genomics. 28 (1): 66–73. doi:10.1006/geno.1995.1107. PMID 7590749.
  7. "Entrez Gene: NFIC nuclear factor I/C (CCAAT-binding transcription factor)".

Further reading

External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

Transcription factors and intracellular receptors
(1) Basic domains
(1.1) Basic leucine zipper (bZIP)
(1.2) Basic helix-loop-helix (bHLH)
Group A
Group B
Group C
bHLH-PAS
Group D
Group E
Group F
bHLH-COE
(1.3) bHLH-ZIP
(1.4) NF-1
(1.5) RF-X
(1.6) Basic helix-span-helix (bHSH)
(2) Zinc finger DNA-binding domains
(2.1) Nuclear receptor (Cys4)
subfamily 1
subfamily 2
subfamily 3
subfamily 4
subfamily 5
subfamily 6
subfamily 0
(2.2) Other Cys4
(2.3) Cys2His2
(2.4) Cys6
(2.5) Alternating composition
(2.6) WRKY
(3) Helix-turn-helix domains
(3.1) Homeodomain
Antennapedia
ANTP class
protoHOX
Hox-like
metaHOX
NK-like
other
(3.2) Paired box
(3.3) Fork head / winged helix
(3.4) Heat shock factors
(3.5) Tryptophan clusters
(3.6) TEA domain
  • transcriptional enhancer factor
(4) β-Scaffold factors with minor groove contacts
(4.1) Rel homology region
(4.2) STAT
(4.3) p53-like
(4.4) MADS box
(4.6) TATA-binding proteins
(4.7) High-mobility group
(4.9) Grainyhead
(4.10) Cold-shock domain
(4.11) Runt
(0) Other transcription factors
(0.2) HMGI(Y)
(0.3) Pocket domain
(0.5) AP-2/EREBP-related factors
(0.6) Miscellaneous
see also transcription factor/coregulator deficiencies
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