The B9D1 gene homepage

General information
Gene symbol B9D1
Gene name B9 protein domain 1
Chromosome 17
Chromosomal band p11.2
Imprinted Unknown
Genomic reference NG_031885.1
Transcript reference NM_001243473.1, NM_001243475.1, NM_015681.3, NM_139032.2, XM_005256605.1, XM_005256606.1, XM_005256607.1, XM_005256608.1, XM_005256609.1, XM_005256610.1
Associated with diseases ID, MKS-9
Citation reference(s) -
Curators (1) Johan T. den Dunnen
Total number of public variants reported 85
Unique public DNA variants reported 14
Individuals with public variants 35
Hidden variants 31
Date created October 29, 2013
Date last updated September 28, 2016
Version B9D1:160928

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:24123
Entrez Gene 27077
PubMed articles B9D1
OMIM - Gene 614144
OMIM - Diseases MKS-9 (Meckel syndrome, type 9 (MKS-9))
HGMD B9D1
GeneCards B9D1
GeneTests B9D1


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000785 17 transcript variant 3 NM_001243475.1 NP_001230404.1 73
00015855 17 Manually created transcript. NM_015681.3 - 61
00000786 17 transcript variant 1 NM_001243473.1 NP_001230402.1 45
00031597 17 Manually created transcript (removed from reference sequence) NM_139032.2 - 12
00038295 17 transcript variant X1 XM_005256605.1 XP_005256662.1 -
00038296 17 transcript variant X2 XM_005256606.1 XP_005256663.1 -
00038297 17 transcript variant X4 XM_005256608.1 XP_005256665.1 -
00038298 17 transcript variant X6 XM_005256610.1 XP_005256667.1 -
00038299 17 transcript variant X5 XM_005256609.1 XP_005256666.1 -
00038300 17 transcript variant X3 XM_005256607.1 XP_005256664.1 -


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