The ALKBH8 gene homepage

General information
Gene symbol ALKBH8
Gene name alkB, alkylation repair homolog 8 (E. coli)
Chromosome 11
Chromosomal band q22.3
Imprinted Unknown
Genomic reference NC_000011.9
Transcript reference NM_138775.2
Exon/intron information NM_138775.2 exon/intron table
Associated with diseases ID, MRT71
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 19
Unique public DNA variants reported 19
Individuals with public variants 12
Hidden variants 1
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created May 03, 2013
Date last updated November 11, 2025
Version ALKBH8:251111

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_138775.2.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL https://www.LOVD.nl/ALKBH8
HGNC HGNC:25189
Entrez Gene 91801
PubMed articles ALKBH8
OMIM - Gene 613306
OMIM - Diseases MRT71 (Intellectual developmental disorder, autosomal recessive 71)
HGMD ALKBH8
GeneCards ALKBH8
NIH Genetic Testing Registry ALKBH8
Orphanet ALKBH8


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00002390 11 alkB, alkylation repair homolog 8 (E. coli) NM_138775.2 NP_620130.2 19


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