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PARD3B

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Protein-coding gene in the species Homo sapiens

PARD3B
Identifiers
AliasesPARD3B, ALS2CR19, PAR3B, PAR3L, PAR3LC, PAR3beta, Par3Lb, par-3 family cell polarity regulator beta
External IDsMGI: 1919301; HomoloGene: 35389; GeneCards: PARD3B; OMA:PARD3B - orthologs
Gene location (Human)
Chromosome 2 (human)
Chr.Chromosome 2 (human)
Chromosome 2 (human)Genomic location for PARD3BGenomic location for PARD3B
Band2q33.3Start204,545,475 bp
End205,620,162 bp
Gene location (Mouse)
Chromosome 1 (mouse)
Chr.Chromosome 1 (mouse)
Chromosome 1 (mouse)Genomic location for PARD3BGenomic location for PARD3B
Band1|1 C2Start61,677,983 bp
End62,681,443 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • sural nerve

  • ventricular zone

  • Achilles tendon

  • epithelium of colon

  • saphenous vein

  • tibial arteries

  • mucosa of ileum

  • testicle

  • gonad

  • skin of hip
Top expressed in
  • Rostral migratory stream

  • crypt of lieberkuhn of small intestine

  • internal carotid artery

  • external carotid artery

  • sciatic nerve

  • lumbar spinal ganglion

  • renal corpuscle

  • ciliary body

  • iris

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

117583

72823

Ensembl

ENSG00000116117

ENSMUSG00000052062

UniProt

Q8TEW8

Q9CSB4

RefSeq (mRNA)

NM_001302769
NM_057177
NM_152526
NM_205863

NM_001081050

RefSeq (protein)

NP_001289698
NP_476518
NP_689739
NP_995585

NP_001074519

Location (UCSC)Chr 2: 204.55 – 205.62 MbChr 1: 61.68 – 62.68 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Partitioning defective 3 homolog B is a protein that in humans is encoded by the PARD3B gene.


Interactions

PARD3B has been shown to interact with Mothers against decapentaplegic homolog 3.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000116117Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000052062Ensembl, 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. Hadano S, Hand CK, Osuga H, Yanagisawa Y, Otomo A, Devon RS, Miyamoto N, Showguchi-Miyata J, Okada Y, Singaraja R, Figlewicz DA, Kwiatkowski T, Hosler BA, Sagie T, Skaug J, Nasir J, Brown RH Jr, Scherer SW, Rouleau GA, Hayden MR, Ikeda JE (Oct 2001). "A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2". Nat Genet. 29 (2): 166–73. doi:10.1038/ng1001-166. PMID 11586298. S2CID 52828189.
  6. Kohjima M, Noda Y, Takeya R, Saito N, Takeuchi K, Sumimoto H (Dec 2002). "PAR3beta, a novel homologue of the cell polarity protein PAR3, localizes to tight junctions". Biochem Biophys Res Commun. 299 (4): 641–6. doi:10.1016/S0006-291X(02)02698-0. PMID 12459187.
  7. "Entrez Gene: PARD3B par-3 partitioning defective 3 homolog B (C. elegans)".
  8. Warner DR, Pisano M Michele, Roberts Emily A, Greene Robert M (Mar 2003). "Identification of three novel Smad binding proteins involved in cell polarity". FEBS Lett. 539 (1–3). Netherlands: 167–73. doi:10.1016/S0014-5793(03)00155-8. ISSN 0014-5793. PMID 12650946. S2CID 7429554.

Further reading

PDB gallery
  • 1wg6: Solution structure of PDZ domain in protein XP_110852 1wg6: Solution structure of PDZ domain in protein XP_110852


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