The SEMA6B gene homepage

General information
Gene symbol SEMA6B
Gene name semaphorin 6B
Chromosome 19
Chromosomal band p13.3
Imprinted Unknown
Genomic reference NC_000019.10
Transcript reference NM_032108.4
Associated with diseases EPM11
Citation reference(s) -
Curators (1) MyHVP
Total number of public variants reported 1
Unique public DNA variants reported 1
Individuals with public variants 1
Hidden variants -
Date created July 14, 2021
Date last updated July 27, 2021
Version SEMA6B:210727

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
HGNC 10739
Entrez Gene 10501
PubMed articles SEMA6B
OMIM - Gene 608873
OMIM - Diseases EPM11 (Progressive Myoclonic Epilepsy 11)
HGMD SEMA6B
GeneCards SEMA6B
GeneTests SEMA6B
Orphanet SEMA6B


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000773 19 semaphorin 6B NM_032108.4 NP_115484.2 1


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