The RBBP8 gene homepage

General information
Gene symbol RBBP8
Gene name retinoblastoma binding protein 8
Chromosome 18
Chromosomal band q11.2
Imprinted Unknown
Genomic reference NG_012121.1
Transcript reference NM_002894.2, NM_203291.1, NM_203292.1, XM_005258325.1, XM_005258326.1
Associated with diseases ID, JWDS, SCKL, SCKL-2, cancer, pancreatic
Citation reference(s) -
Curators (1) Johan T. den Dunnen
Total number of public variants reported 92
Unique public DNA variants reported 12
Individuals with public variants 35
Hidden variants 28
Date created October 30, 2013
Date last updated September 28, 2016
Version RBBP8:160928

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
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
External URL List of LSDBs for this gene
The reference LOVD for this gene, if available
HGNC HGNC:9891
Entrez Gene 5932
PubMed articles RBBP8
OMIM - Gene 604124
OMIM - Diseases JWDS (Jawad syndrome (JWDS))
SCKL (Seckel syndrome (SCKL))
SCKL-2 (Seckel syndrome, type 2 (SCKL-2))
cancer, pancreatic
HGMD RBBP8
GeneCards RBBP8
GeneTests RBBP8


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00006517 18 transcript variant 1 NM_002894.2 NP_002885.1 92
00019224 18 Manually created transcript. NM_203291.1 - 92
00019225 18 Manually created transcript. (removed from reference sequence) NM_203292.1 - 92
00039144 18 transcript variant X1 XM_005258325.1 XP_005258382.1 -
00039145 18 transcript variant X2 XM_005258326.1 XP_005258383.1 -


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