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KIZ (gene)

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Protein-coding gene in the species Homo sapiens
KIZ
Identifiers
AliasesKIZ, C20orf19, Kizuna, NCRNA00153, PLK1S1, RP69, HT013, kizuna centrosomal protein
External IDsOMIM: 615757; MGI: 2684960; HomoloGene: 10219; GeneCards: KIZ; OMA:KIZ - orthologs
Gene location (Human)
Chromosome 20 (human)
Chr.Chromosome 20 (human)
Chromosome 20 (human)Genomic location for KIZGenomic location for KIZ
Band20p11.23Start21,125,983 bp
End21,246,622 bp
Gene location (Mouse)
Chromosome 2 (mouse)
Chr.Chromosome 2 (mouse)
Chromosome 2 (mouse)Genomic location for KIZGenomic location for KIZ
Band2|2 G1-G2Start146,855,864 bp
End146,970,097 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • sperm

  • germinal epithelium

  • Brodmann area 23

  • parietal pleura

  • tibia

  • lateral nuclear group of thalamus

  • inferior ganglion of vagus nerve

  • mucosa of paranasal sinus

  • spinal ganglia

  • muscle layer of sigmoid colon
Top expressed in
  • interventricular septum

  • seminiferous tubule

  • myocardium of ventricle

  • otolith organ

  • utricle

  • spermatid

  • spermatocyte

  • olfactory epithelium

  • Rostral migratory stream

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

55857

228730

Ensembl

ENSG00000088970

ENSMUSG00000074749

UniProt

Q2M2Z5

Q3UXL4

RefSeq (mRNA)
NM_001163022
NM_001163023
NM_001276389
NM_018474
NM_001352434

NM_001352435
NM_001352436

NM_001033298

RefSeq (protein)
NP_001156494
NP_001156495
NP_001263318
NP_060944
NP_001339363

NP_001339364
NP_001339365

NP_001028470

Location (UCSC)Chr 20: 21.13 – 21.25 MbChr 2: 146.86 – 146.97 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Kizuna centrosomal protein is a protein that in humans is encoded by the KIZ gene.

Function

The protein encoded by this gene localizes to centrosomes, strengthening and stabilizing the pericentriolar region prior to spindle formation. The encoded protein usually remains with the mother centrosome after centrosomal duplication. Several transcript variants encoding different isoforms have been found for this gene. .

Clinical significance

Mutations in KIZ cause Rod-cone dystrophy (RCD).

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000088970Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000074749Ensembl, 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: Kizuna centrosomal protein".
  6. El Shamieh S, Neuillé M, Terray A, Orhan E, Condroyer C, Démontant V, Michiels C, Antonio A, Boyard F, Lancelot ME, Letexier M, Saraiva JP, Léveillard T, Mohand-Saïd S, Goureau O, Sahel JA, Zeitz C, Audo I (2014). "Whole-Exome Sequencing Identifies KIZ as a Ciliary Gene Associated with Autosomal-Recessive Rod-Cone Dystrophy". Am. J. Hum. Genet. 94 (4): 625–33. doi:10.1016/j.ajhg.2014.03.005. PMC 3980423. PMID 24680887.

Further reading

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

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