latent transforming growth factor beta binding protein 2, isoform CRA_ - Protein

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Autosomal Dominant Weill-Marchesani-Like Syndrome in a Chinese Family due to Novel Haplotypic Mutations in LTBP2. [Ophthalmic Res. 2024]
Autosomal Dominant Weill-Marchesani-Like Syndrome in a Chinese Family due to Novel Haplotypic Mutations in LTBP2.
Chen J, Wan J, Jin J, Jin G, Zheng Y, Zheng D, Zhong L. Ophthalmic Res. 2024; 67(1):340-347. Epub 2024 May 21.
Identification and phenotypic analysis of novel LTBP2 mutations in a Chinese cohort with congenital ectopia lentis. [Mol Vis. 2023]
Identification and phenotypic analysis of novel LTBP2 mutations in a Chinese cohort with congenital ectopia lentis.
Liu L, Guo D, Yang F, Qi H, Zhou Y, Zheng D, Jin G. Mol Vis. 2023; 29:169-179. Epub 2023 Oct 10.
Plasma LTBP2 as a potential biomarker in differential diagnosis of connective tissue disease-associated interstitial lung disease and idiopathic pulmonary fibrosis: a pilot study. [Clin Exp Med. 2023]
Plasma LTBP2 as a potential biomarker in differential diagnosis of connective tissue disease-associated interstitial lung disease and idiopathic pulmonary fibrosis: a pilot study.
Zou M, Hu X, Song W, Gao H, Wu C, Zheng W, Cheng Z. Clin Exp Med. 2023 Dec; 23(8):4809-4816. Epub 2023 Oct 21.

RefSeq genomic sequence
See the genomic reference sequence for the LTBP2 gene (NG_021486.2).
RefSeq protein
See the reference protein sequence for latent-transforming growth factor beta-binding protein 2 precursor (NP_000419.1).

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Lacticaseibacillus paracasei strain Lpc10 chromosome, complete genome
Lacticaseibacillus paracasei strain Lpc10 chromosome, complete genome
gi|1397595770|gb|CP029686.1|

Nucleotide
Staphylococcus epidermidis strain JONWP052 NODE_1_length_491215_cov_136.362242, ...
Staphylococcus epidermidis strain JONWP052 NODE_1_length_491215_cov_136.362242, whole genome shotgun sequence
gi|2713187955|ref|NZ_JBBLPT01000000 gnl|WGS:NZ_JBBLPT01|NODE_1_length_491215_cov_136.362242

Nucleotide
Dyskeratosis congenita, autosomal recessive 3
Dyskeratosis congenita, autosomal recessive 3

MedGen
C3151442[conceptid] (1)
MedGen
PREDICTED: Phalacrocorax carbo calpain 3 (CAPN3), transcript variant X5, mRNA
PREDICTED: Phalacrocorax carbo calpain 3 (CAPN3), transcript variant X5, mRNA
gi|2716822129|ref|XM_064462451.1|

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