protein wntless homolog isoform 1 [Homo sapiens]

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Expanding the phenotypic spectrum and clinical severity associated with WLS gene. [J Hum Genet. 2023]
Expanding the phenotypic spectrum and clinical severity associated with WLS gene.
Abdel-Salam GMH, Afifi HH, Abdel-Hamid MS, Ahmed NEB, Taher MB, El-Kamah G, Thiele H, Nürnberg PN, Bolz HJ. J Hum Genet. 2023 Sep; 68(9):607-613. Epub 2023 Apr 28.
Compound heterozygous variants in WLS gene causes Zaki syndrome. [Clin Genet. 2023]
Compound heterozygous variants in WLS gene causes Zaki syndrome.
Yu C, Wang C, Zhou W, Zhang A, Jia Z, Zheng B, Ding G. Clin Genet. 2023 Aug; 104(2):226-229. Epub 2023 Apr 2.
Mutations in the WLS are associated with dental anomalies, torus palatinus, and torus mandibularis. [Eur J Orthod. 2023]
Mutations in the WLS are associated with dental anomalies, torus palatinus, and torus mandibularis.
Kantaputra P, Tripuwabhrut K, Jatooratthawichot P, Adisornkanj P, Hatsadaloi A, Porntrakoolsaree N, Kaewgaya M, Olsen B, Tongsima S, Ngamphiw C, et al. Eur J Orthod. 2023 May 31; 45(3):317-323.

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NP_079187 [Domain Mapping of Disease Mut...]
NP_079187
Domain Mapping of Disease Mutations
Ensembl [Ensembl]
Ensembl
OncoMX cancer biomarker resource [OncoMX cancer biomarker resou...]
OncoMX cancer biomarker resource
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
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reagent reviews [ExactAntigen/Labome]
reagent reviews
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reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

glycosyltransferase family 69 [Pochonia chlamydosporia 170]
glycosyltransferase family 69 [Pochonia chlamydosporia 170]
gi|1069530674|ref|XP_018143206.1|

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