Syntaxin 16 [Homo sapiens]

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Intrafamilial phenotypic heterogeneity in siblings with pseudohypoparathyroidism 1B due to maternal STX16 deletion. [J Pediatr Endocrinol Metab. 2024]
Intrafamilial phenotypic heterogeneity in siblings with pseudohypoparathyroidism 1B due to maternal STX16 deletion.
Odom J, Bacino CA, Karaviti LP, Bi W, Hoyos-Martinez A. J Pediatr Endocrinol Metab. 2024 Jan 29; 37(1):84-89. Epub 2023 Dec 14.
Progression of PTH Resistance in Autosomal Dominant Pseudohypoparathyroidism Type Ib Due to Maternal STX16 Deletions. [J Clin Endocrinol Metab. 2022]
Progression of PTH Resistance in Autosomal Dominant Pseudohypoparathyroidism Type Ib Due to Maternal STX16 Deletions.
Kiuchi Z, Reyes M, Hanna P, Sharma A, DeClue T, Olney RC, Tebben P, Jüppner H. J Clin Endocrinol Metab. 2022 Jan 18; 107(2):e681-e687.
Macrosomia, obesity, and macrocephaly as first clinical presentation of PHP1b caused by STX16 deletion. [Am J Med Genet A. 2016]
Macrosomia, obesity, and macrocephaly as first clinical presentation of PHP1b caused by STX16 deletion.
de Lange IM, Verrijn Stuart AA, van der Luijt RB, Ploos van Amstel HK, van Haelst MM. Am J Med Genet A. 2016 Sep; 170(9):2431-5. Epub 2016 Jun 23.

RefSeq genomic sequence
See the genomic reference sequence for the STX16 gene (NG_011831.3).
RefSeq protein isoforms
See 5 reference sequence protein isoforms for the STX16 gene.

Nucleotide
Nucleotide sequence from coding region
PubMed
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Order cDNA Clone
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Order cDNA clone
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Related Structures (List)
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MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF) [MODBASE, Database of Comparat...]
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF)
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagent reviews [ExactAntigen/Labome]
reagent reviews
ExactAntigen/Labome
reagents [ExactAntigen/Labome]
reagents
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