KIAA1557 protein, partial [Homo sapiens]

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View conserved domains detected in this protein sequence using CD-search.

ARID2 mutations may relay a distinct subset of cutaneous melanoma patients with different outcomes. [Sci Rep. 2024]
ARID2 mutations may relay a distinct subset of cutaneous melanoma patients with different outcomes.
Akinjiyan FA, Nassief G, Phillipps J, Adeyelu T, Elliott A, Abdulla F, Zhou AY, Souroullas G, Kim KB, Vanderwalde A, et al. Sci Rep. 2024 Feb 11; 14(1):3444. Epub 2024 Feb 11.
ARID2, a milder cause of Coffin-Siris Syndrome? Broadening the phenotype with 17 additional individuals. [Am J Med Genet A. 2024]
ARID2, a milder cause of Coffin-Siris Syndrome? Broadening the phenotype with 17 additional individuals.
Schrier Vergano SA. Am J Med Genet A. 2024 Jun; 194(6):e63540. Epub 2024 Jan 19.
Coffin-Siris Syndrome: Case Series of Three Patients and a Novel ARID2 Variant. [Ann Clin Lab Sci. 2023]
Coffin-Siris Syndrome: Case Series of Three Patients and a Novel ARID2 Variant.
Shin D, Lee YJ, Jo YH, Kong J, Lee YJ, Nam SO, Lee BL, Oh SH, Kim YM. Ann Clin Lab Sci. 2023 Nov; 53(6):959-963.

RefSeq genomic sequence
See the genomic reference sequence for the ARID2 gene (NG_052800.1).
RefSeq protein isoforms
See 4 reference sequence protein isoforms for the ARID2 gene.

Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome
reagent reviews [ExactAntigen/Labome]
reagent reviews
ExactAntigen/Labome

PREDICTED: Mus musculus unc-79 homolog (Unc79), transcript variant X18, mRNA
PREDICTED: Mus musculus unc-79 homolog (Unc79), transcript variant X18, mRNA
gi|1907087160|ref|XM_036157360.1|

Nucleotide
Homo sapiens AT-rich interaction domain 2 (ARID2), RefSeqGene on chromosome 12
Homo sapiens AT-rich interaction domain 2 (ARID2), RefSeqGene on chromosome 12
gi|1139349403|ref|NG_052800.1|

Nucleotide

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Protein