Homo sapiens solute carrier family 34 member 1 (SLC34A1), transcript v - Nucleotide

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High frequency of heterozygous rare variants of the SLC34A1 and SLC9A3R1 genes in patients with atypical femur fracture. [Eur J Endocrinol. 2023]
High frequency of heterozygous rare variants of the SLC34A1 and SLC9A3R1 genes in patients with atypical femur fracture.
Marini F, Giusti F, Marasco E, Xumerle L, Kwiatkowska KM, Garagnani P, Biver E, Ferrari S, Iolascon G, Iantomasi T, et al. Eur J Endocrinol. 2023 Jan 10; 188(1).
The human pathogenic 91del7 mutation in SLC34A1 has no effect in mineral homeostasis in mice. [Sci Rep. 2022]
The human pathogenic 91del7 mutation in SLC34A1 has no effect in mineral homeostasis in mice.
Bieri C, Daryadel A, Bettoni C, Pastor-Arroyo EM, Schnitzbauer U, Hernando N, Wagner CA. Sci Rep. 2022 Apr 12; 12(1):6102. Epub 2022 Apr 12.
CYP24A1 and SLC34A1 Pathogenic Variants Are Uncommon in a Canadian Cohort of Children with Hypercalcemia or Hypercalciuria. [Horm Res Paediatr. 2021]
CYP24A1 and SLC34A1 Pathogenic Variants Are Uncommon in a Canadian Cohort of Children with Hypercalcemia or Hypercalciuria.
Rousseau-Nepton I, Jones G, Schlingmann K, Kaufmann M, Zuijdwijk CS, Khatchadourian K, Gupta IR, Pacaud D, Pinsk MN, Mokashi A, et al. Horm Res Paediatr. 2021; 94(3-4):124-132. Epub 2021 Jul 28.

RefSeq alternative splicing
See the other reference mRNA sequence splice variant for the SLC34A1 gene (NM_001167579.2).
RefSeq protein product
See the reference protein sequence for sodium-dependent phosphate transport protein 2A isoform 1 (NP_003043.3).

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Protein sequence from Nucleotide coding region
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Homo sapiens solute carrier family 34 member 1 (SLC34A1), transcript variant 1, ...
Homo sapiens solute carrier family 34 member 1 (SLC34A1), transcript variant 1, mRNA
gi|1519311656|ref|NM_003052.5|

Nucleotide

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Nucleotide