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CNTRL

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(Redirected from CEP110) Protein-coding gene in the species Homo sapiens For other uses, see CNTRL (disambiguation).
CNTRL
Identifiers
AliasesCNTRL, CEP1, CEP110, FAN, bA165P4.1, centriolin
External IDsOMIM: 605496; MGI: 1889576; HomoloGene: 38260; GeneCards: CNTRL; OMA:CNTRL - orthologs
Gene location (Human)
Chromosome 9 (human)
Chr.Chromosome 9 (human)
Chromosome 9 (human)Genomic location for CNTRLGenomic location for CNTRL
Band9q33.2Start121,074,660 bp
End121,177,729 bp
Gene location (Mouse)
Chromosome 2 (mouse)
Chr.Chromosome 2 (mouse)
Chromosome 2 (mouse)Genomic location for CNTRLGenomic location for CNTRL
Band2|2 BStart35,109,492 bp
End35,178,822 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • Achilles tendon

  • secondary oocyte

  • ventricular zone

  • bronchial epithelial cell

  • testicle

  • left testis

  • right testis

  • sural nerve

  • sperm

  • monocyte
Top expressed in
  • genital tubercle

  • ventricular zone

  • granulocyte

  • spermatocyte

  • tail of embryo

  • thymus

  • mesenteric lymph nodes

  • spermatid

  • spleen

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

11064

26920

Ensembl

ENSG00000119397

ENSMUSG00000057110

UniProt

Q7Z7A1

A2AL36

RefSeq (mRNA)
NM_007018
NM_001330762
NM_001369892
NM_001369893
NM_001369894

NM_001369895
NM_001369896

NM_001290635
NM_012018
NM_030000
NM_001379274
NM_001379275

RefSeq (protein)
NP_001317691
NP_008949
NP_001356821
NP_001356822
NP_001356823

NP_001356824
NP_001356825

NP_001277564
NP_036148
NP_001366203
NP_001366204

Location (UCSC)Chr 9: 121.07 – 121.18 MbChr 2: 35.11 – 35.18 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Centriolin is a protein that in humans is encoded by the CNTRL gene. It was previously known as CEP110.

This gene encodes a centrosomal protein required for the centrosome to function as a microtubule organizing center. The gene product is also associated with centrosome maturation. One version of stem cell myeloproliferative disorder is the result of a reciprocal translocation between chromosomes 8 and 9, with the breakpoint associated with fibroblast growth factor receptor 1 and centriolin.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000119397Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000057110Ensembl, 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. Guasch G, Mack GJ, Popovici C, Dastugue N, Birnbaum D, Rattner JB, Pebusque MJ (Mar 2000). "FGFR1 is fused to the centrosome-associated protein CEP110 in the 8p12 stem cell myeloproliferative disorder with t(8;9)(p12;q33)". Blood. 95 (5): 1788–96. doi:10.1182/blood.V95.5.1788.005k15_1788_1796. PMID 10688839.
  6. ^ "Entrez Gene: CEP110 centrosomal protein 110kDa".

External links

Further reading

The centrosome and its components
Centrioles
Pericentriolar material
other proteins


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