zinc finger protein 335 isoform X4 [Homo sapiens]

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Find regions of similarity between this sequence and other sequences using BLAST.
Identify Conserved Domains
View conserved domains detected in this protein sequence using CD-search.
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Opens the Highlight Feature Bar and highlights feature annotations from the FEATURES table of the record. The Highlight Feature Bar can be used to navigate to and highlight other features and provides links to display the highlighted region separately. Links in the FEATURES table will also highlight the corresponding region of the sequence. More...
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Finds sub-sequences or patterns in the sequence and highlights the matching regions. The tool works with standard single letter nucleotide or protein codes including ambiguities and can match Prosite patterns in protein sequences. More...

Expanding the clinical spectrum of biallelic ZNF335 variants. [Clin Genet. 2018]
Expanding the clinical spectrum of biallelic ZNF335 variants.
Stouffs K, Stergachis AB, Vanderhasselt T, Dica A, Janssens S, Vandervore L, Gheldof A, Bodamer O, Keymolen K, Seneca S, et al. Clin Genet. 2018 Aug; 94(2):246-251. Epub 2018 May 3.
Association Between Invisible Basal Ganglia and ZNF335 Mutations: A Case Report. [Pediatrics. 2016]
Association Between Invisible Basal Ganglia and ZNF335 Mutations: A Case Report.
Sato R, Takanashi J, Tsuyusaki Y, Kato M, Saitsu H, Matsumoto N, Takahashi T. Pediatrics. 2016 Sep; 138(3). Epub 2016 Aug 18.
Anaesthesia and orphan disease: primary autosomal recessive microcephaly-10 caused by a mutation in the ZNF335 gene. [Eur J Anaesthesiol. 2016]
Anaesthesia and orphan disease: primary autosomal recessive microcephaly-10 caused by a mutation in the ZNF335 gene.
Nishida T, Mihara T, Horiki T, Ka K. Eur J Anaesthesiol. 2016 Jul; 33(7):543-5.

RefSeq genomic sequence
See the genomic reference sequence for the ZNF335 gene (NG_029772.1).
RefSeq mRNA
See reference mRNA sequence for the ZNF335 gene (XM_054323818.1).
RefSeq protein isoforms
See 11 reference sequence protein isoforms for the ZNF335 gene.