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KLF8

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Protein-coding gene in the species Homo sapiens
KLF8
Identifiers
AliasesKLF8, BKLF3, ZNF741, Kruppel-like factor 8, Kruppel like factor 8
External IDsOMIM: 300286; MGI: 2442430; HomoloGene: 68549; GeneCards: KLF8; OMA:KLF8 - orthologs
Gene location (Human)
X chromosome (human)
Chr.X chromosome (human)
X chromosome (human)Genomic location for KLF8Genomic location for KLF8
BandXp11.21Start56,232,356 bp
End56,291,531 bp
Gene location (Mouse)
X chromosome (mouse)
Chr.X chromosome (mouse)
X chromosome (mouse)Genomic location for KLF8Genomic location for KLF8
BandX|X F3Start152,020,462 bp
End152,179,128 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • skin of abdomen

  • oral cavity

  • skin of leg

  • vagina

  • skin of thigh

  • popliteal artery

  • tibial arteries

  • skin of hip

  • parietal pleura

  • gingival epithelium
Top expressed in
  • placenta

  • morula

  • ganglionic eminence

  • epiblast

  • blastocyst

  • embryo

  • granulocyte

  • yolk sac

  • Mesencephalon

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

11279

245671

Ensembl

ENSG00000102349

ENSMUSG00000041649

UniProt

O95600

Q8BLM0

RefSeq (mRNA)
NM_001159296
NM_007250
NM_001324099
NM_001324100
NM_001324102

NM_001324104
NM_001324105

NM_173780
NM_001357183

RefSeq (protein)
NP_001152768
NP_001311028
NP_001311029
NP_001311031
NP_001311033

NP_001311034
NP_009181

NP_776141
NP_001344112

Location (UCSC)Chr X: 56.23 – 56.29 MbChr X: 152.02 – 152.18 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Krueppel-like factor 8 is a protein that in humans is encoded by the KLF8 gene. KLF8 belongs to the family of KLF protein. KLF8 is activated by KLF1 along with KLF3 while KLF3 represses KLF8.

Interactions

KLF8 has been shown to interact with CTBP2.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000102349Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000041649Ensembl, 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. "Entrez Gene: KLF8 Kruppel-like factor 8".
  6. Alister P. W. Funnell; et al. "Generation of Mice Deficient in both KLF3/BKLF and KLF8 Reveals a Genetic Interaction and a Role for These Factors in Embryonic Globin Gene Silencing". asm.org. Archived from the original on 15 December 2018. Retrieved 12 January 2019.
  7. van Vliet J, Turner J, Crossley M (May 2000). "Human Krüppel-like factor 8: a CACCC-box binding protein that associates with CtBP and represses transcription". Nucleic Acids Research. 28 (9): 1955–62. doi:10.1093/nar/28.9.1955. PMC 103308. PMID 10756197.

Further reading

External links

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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