Homo sapiens caspase recruitment domain family member 14 (CARD14), tra - Nucleotide

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A novel mutation in a CARD14-associated papulosquamous eruption. [Pediatr Dermatol. 2023]
A novel mutation in a CARD14-associated papulosquamous eruption.
Li N, Tao J, Zhang J, Liu Z, Yu P. Pediatr Dermatol. 2023 Jul-Aug; 40(4):706-709. Epub 2023 Feb 1.
Correlation of IL36RN and CARD14 mutations with clinical manifestations and laboratory findings in patients with generalised pustular psoriasis. [Indian J Dermatol Venereol Lep...]
Correlation of IL36RN and CARD14 mutations with clinical manifestations and laboratory findings in patients with generalised pustular psoriasis.
Trai NN, Van Em D, Van BT, My LH, Van Tro C, Hao NT, Vu HA, Tram DB, Van Thuong N, Doanh LH. Indian J Dermatol Venereol Leprol. 2023 May-Jun; 89(3):378-384.
Association between CARD14 gene polymorphisms and psoriasis vulgaris in Hainan Han population based on exon sequencing: A case-control study. [Medicine (Baltimore). 2022]
Association between CARD14 gene polymorphisms and psoriasis vulgaris in Hainan Han population based on exon sequencing: A case-control study.
Msafiri Makene A, Liu JL. Medicine (Baltimore). 2022 Oct 7; 101(40):e30890.

RefSeq alternative splicing
See 46 reference mRNA sequence splice variants for the CARD14 gene.
RefSeq protein product
See the reference protein sequence for caspase recruitment domain-containing protein 14 isoform 1 (NP_077015.2).

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Homo sapiens caspase recruitment domain family member 14 (CARD14), transcript va...
Homo sapiens caspase recruitment domain family member 14 (CARD14), transcript variant 1, mRNA
gi|384229056|ref|NM_024110.4|

Nucleotide
Homo sapiens golgi associated PDZ and coiled-coil motif containing (GOPC), trans...
Homo sapiens golgi associated PDZ and coiled-coil motif containing (GOPC), transcript variant 1, mRNA
gi|1519245413|ref|NM_020399.4|

Nucleotide
Oryza rhizomatis isolate RWG-483 granule-bound starch synthase II (gbss2) gene, ...
Oryza rhizomatis isolate RWG-483 granule-bound starch synthase II (gbss2) gene, complete cds
gi|2098698750|gb|MZ749446.1|

Nucleotide
Lysosomal Storage Diseases
Lysosomal Storage Diseases
Inborn errors of metabolism characterized by defects in specific lysosomal hydrolases and resulting in intracellular accumulation of unmetabolized substrates....<br/>Year introduced: 1992

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Nucleotide