PARD3B

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Partitioning defective 3 homolog B is a protein that in humans is encoded by the PARD3B gene.[5][6][7]

AliasesPARD3B, ALS2CR19, PAR3B, PAR3L, PAR3LC, PAR3beta, Par3Lb, par-3 family cell polarity regulator beta
End205,620,162 bp[1]
Quick facts Identifiers, Aliases ...
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
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
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[3][4]
Wikidata
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