SP110base: Hepatic veno-occlusive disease with immunodeficiency syndrome (VODI) | Bioinformatics |

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SP110base
Variation registry for Hepatic veno-occlusive disease with immunodeficiency syndrome (VODI)

Bioinformatics
Database entries	IDR fact file

Mutation statistics
Table of mutation types	Aminoacid substitutions	Codon changes	Nucleotide substitutions

Other resources
GeneCards	GDB	GenAtlas	UniGene
Source	Ensembl	GeneLynx	UniProt
EntrezGene	euGenes	UCSC browser
OMIM resources
604457

SP110 Reference Sequences
Sequence type	Accession number	Description
Genomic sequence	IDRefSeq: D0116	The reference sequence was derived from Ensembl Human sequence AC009950.6.1.135506 .
mRNA	IDRefSeq: C0116	Homo sapiens SP110 nuclear body protein (SP110), transcript variant c, mRNA.
Amino Acid Sequence	NP_536349.1	SP110 nuclear body protein isoform c [Homo sapiens].

This site is updated by Gerard Schaafsma
© Protein Structure and Bioinformatics, Lund University, 2017
Last modified 02.03.2025