Mus musculus megalencephalic leukoencephalopathy with subcortical cyst - Nucleotide

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Genetic determinants of micronucleus formation in vivo. [Nature. 2024]
Genetic determinants of micronucleus formation in vivo.
Adams DJ, Barlas B, McIntyre RE, Salguero I, van der Weyden L, Barros A, Vicente JR, Karimpour N, Haider A, Ranzani M, et al. Nature. 2024 Mar; 627(8002):130-136. Epub 2024 Feb 14.
Dynamic local mRNA localization and translation occurs during the postnatal molecular maturation of perivascular astrocytic processes. [Glia. 2024]
Dynamic local mRNA localization and translation occurs during the postnatal molecular maturation of perivascular astrocytic processes.
Avila-Gutierrez K, Slaoui L, Alvear-Perez R, Kozlowski E, Oudart M, Augustin E, Claveau C, Mailly P, Monnet H, Mignon V, et al. Glia. 2024 Apr; 72(4):777-793. Epub 2024 Jan 8.
Identification of new ciliary signaling pathways in the brain and insights into neurological disorders. [bioRxiv. 2023]
Identification of new ciliary signaling pathways in the brain and insights into neurological disorders.
Loukil A, Ebright E, Uezu A, Gao Y, Soderling SH, Goetz SC. bioRxiv. 2023 Dec 21; . Epub 2023 Dec 21.

RefSeq alternative splicing
See the other reference mRNA sequence splice variant for the Mlc1 gene (NM_133241.2).
RefSeq protein product
See the reference protein sequence for membrane protein MLC1 isoform 2 (NP_001351784.1).

Protein
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Mus musculus megalencephalic leukoencephalopathy with subcortical cysts 1 homolo...
Mus musculus megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) (Mlc1), transcript variant 2, mRNA
gi|1423310405|ref|NM_001364855.1|

Nucleotide
Fibrosis
Fibrosis
Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury.<br/>Year introduced: 1987

MeSH
Aspartylglucosaminuria
Aspartylglucosaminuria
A recessively inherited, progressive lysosomal storage disease caused by a deficiency of GLYCOSYLASPARAGINASE activity. The lack of this enzyme activity results in the accumul...<br/>Year introduced: 2009

MeSH
Fucosidosis
Fucosidosis
An autosomal recessive lysosomal storage disease caused by a deficiency of ALPHA-L-FUCOSIDASE activity resulting in an accumulation of fucose containing SPHINGOLIPIDS; GLYCOPR...<br/>Year introduced: 1985

MeSH
Mucolipidoses
Mucolipidoses
A group of inherited metabolic diseases characterized by the accumulation of excessive amounts of acid mucopolysaccharides, sphingolipids, and/or glycolipids in visceral and m...<br/>Year introduced: 2000(1977)

MeSH

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Nucleotide