FAM111B gene homepage

General information
Gene symbol FAM111B
Gene name family with sequence similarity 111, member B
Chromosome 11
Chromosomal band q12.1
Imprinted Unknown
Genomic reference NC_000011.9
Transcript reference NM_198947.3
Exon/intron information NM_198947.3 exon/intron table
Associated with diseases POIKTMP
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Sébastien Küry
Total number of public variants reported 4
Unique public DNA variants reported 4
Individuals with public variants 1
Hidden variants 0
Download all this gene's data Download all data
Date created May 03, 2013
Date last updated January 27, 2015
Version FAM111B:150127

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_198947.3.
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 http://www.LOVD.nl/FAM111B
HGNC 24200
Entrez Gene 374393
PubMed articles FAM111B
OMIM - Gene 615584
OMIM - Diseases POIKTMP (poikiloderma, hereditary fibrosing, tendon contractures, myopathy, pulmonary fibrosis (POIKTMP))
HGMD FAM111B
GeneCards FAM111B
GeneTests FAM111B


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00007545 11 transcript variant 1 NM_198947.3 NP_945185.1 4


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