laminin subunit alpha-5 isoform X8 [Homo sapiens]

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View conserved domains detected in this protein sequence using CD-search.
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Opens the Genome Data Viewer, NCBI's genome browser, at the genomic location at which this sequence is annotated. View this sequence in the context of other features annotated at the same location and browse to other genome regions.

Laminin 511 and WNT signalling sustain prolonged expansion of hiPSC-derived hippocampal progenitors. [Development. 2022]
Laminin 511 and WNT signalling sustain prolonged expansion of hiPSC-derived hippocampal progenitors.
Dunville K, Tonelli F, Novelli E, Codino A, Massa V, Frontino AM, Galfrè S, Biondi F, Gustincich S, Caleo M, et al. Development. 2022 Oct 15; 149(20). Epub 2022 Sep 9.
Recessive LAMA5 Variants Associated With Partial Epilepsy and Spasms in Infancy. [Front Mol Neurosci. 2022]
Recessive LAMA5 Variants Associated With Partial Epilepsy and Spasms in Infancy.
Luo S, Liu ZG, Wang J, Luo JX, Ye XG, Li X, Zhai QX, Liu XR, Wang J, Gao LD, et al. Front Mol Neurosci. 2022; 15:825390. Epub 2022 May 19.
Clear Evidence of LAMA5 Gene Biallelic Truncating Variants Causing Infantile Nephrotic Syndrome. [Kidney360. 2021]
Clear Evidence of LAMA5 Gene Biallelic Truncating Variants Causing Infantile Nephrotic Syndrome.
Taniguchi Y, Nagano C, Sekiguchi K, Tashiro A, Sugawara N, Sakaguchi H, Umeda C, Aoto Y, Ishiko S, Rossanti R, et al. Kidney360. 2021 Dec 30; 2(12):1968-1978. Epub 2021 Oct 15.

RefSeq genomic sequence
See the genomic reference sequence for the LAMA5 gene (NG_050626.2).
RefSeq mRNA
See reference mRNA sequence for the LAMA5 gene (XM_054323448.1).
RefSeq protein isoforms
See 16 reference sequence protein isoforms for the LAMA5 gene.

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Protein