Homo sapiens fatty acid 2-hydroxylase (FA2H), RefSeqGene on chromosome - Nucleotide

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A Novel Homozygous Deletion Including Exon 1 of FA2H Gene Causes Spastic Paraplegia-35: Genetic and Lipidomics Analysis of the Patients. [Pediatr Neurol. 2024]
A Novel Homozygous Deletion Including Exon 1 of FA2H Gene Causes Spastic Paraplegia-35: Genetic and Lipidomics Analysis of the Patients.
Mo L, Tie X, Che F, Zhang L, Li B, Wang G, Yang Y. Pediatr Neurol. 2024 Mar; 152:200-208. Epub 2024 Jan 5.
The first reports of FA2H-associated neurodegeneration from two unrelated Iranian families. [Neurol Sci. 2023]
The first reports of FA2H-associated neurodegeneration from two unrelated Iranian families.
Hashemi N, Abadi RNS, Alavi A, Rohani M, Ghasemi A, Tavasoli AR. Neurol Sci. 2023 Dec; 44(12):4359-4362. Epub 2023 Jul 6.
Assessment of community efforts to advance network-based prediction of protein-protein interactions. [Nat Commun. 2023]
Assessment of community efforts to advance network-based prediction of protein-protein interactions.
Wang XW, Madeddu L, Spirohn K, Martini L, Fazzone A, Becchetti L, Wytock TP, Kovács IA, Balogh OM, Benczik B, et al. Nat Commun. 2023 Mar 22; 14(1):1582. Epub 2023 Mar 22.

Protein
Protein sequence from Nucleotide coding region
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RNA
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SNP
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Homo sapiens heterogeneous nuclear ribonucleoprotein U (HNRNPU), transcript vari...
Homo sapiens heterogeneous nuclear ribonucleoprotein U (HNRNPU), transcript variant 2, mRNA
gi|74229006|ref|NM_004501.3|

Nucleotide
essv6831125 (3)
dbVar
esv1009207 (1)
dbVar

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Nucleotide