Homo sapiens contactin 6 (CNTN6), transcript variant 5, mRNA

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Contactin 6, A Novel Causative Gene for Congenital Hypothyroidism, Mediates Thyroid Hormone Biosynthesis Through Notch Signaling. [Thyroid. 2024]
Contactin 6, A Novel Causative Gene for Congenital Hypothyroidism, Mediates Thyroid Hormone Biosynthesis Through Notch Signaling.
Zhang HY, Wu FY, Zhang CX, Wu CY, Cui RJ, Liu XY, Yang L, Zhang Y, Sun F, Cheng F, et al. Thyroid. 2024 Mar; 34(3):324-335. Epub 2024 Feb 12.
CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders. [Eur J Med Genet. 2020]
CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders.
Repnikova EA, Lyalin DA, McDonald K, Astbury C, Hansen-Kiss E, Cooley LD, Pfau R, Herman GE, Pyatt RE, Hickey SE. Eur J Med Genet. 2020 Jan; 63(1):103636. Epub 2019 Mar 2.
Case Report: Whole Exome Sequencing Unveils an Inherited Truncating Variant in CNTN6 (p.Ser189Ter) in a Mexican Child with Autism Spectrum Disorder. [J Autism Dev Disord. 2020]
Case Report: Whole Exome Sequencing Unveils an Inherited Truncating Variant in CNTN6 (p.Ser189Ter) in a Mexican Child with Autism Spectrum Disorder.
García-Ortiz JE, Zarazúa-Niño AI, Hernández-Orozco AA, Reyes-Oliva EA, Pérez-Ávila CE, Becerra-Solano LE, Galán-Huerta KA, Rivas-Estilla AM, Córdova-Fletes C. J Autism Dev Disord. 2020 Jun; 50(6):2247-2251.

RefSeq alternative splicing
See 31 reference mRNA sequence splice variants for the CNTN6 gene.

Protein
Protein sequence from Nucleotide coding region
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Taxonomy
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Annotated Genomic
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OMIM
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Nucleotide