The FAM161A gene homepage

This database is one of the "Eye disease" gene variant databases.
General information
Gene symbol FAM161A
Gene name family with sequence similarity 161, member A
Chromosome 2
Chromosomal band p15
Imprinted Unknown
Genomic reference NG_028125.1
Transcript reference NM_001201543.1
Exon/intron information NM_001201543.1 exon/intron table
Associated with diseases RP28
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 269
Unique public DNA variants reported 101
Individuals with public variants 946
Hidden variants 12
Download all this gene's data Download all data
Notes This database is one of the "Eye disease" gene variant databases.
Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created November 24, 2010
Date last updated February 26, 2024
Version FAM161A:240226

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_001201543.1.
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/FAM161A
HGNC 25808
Entrez Gene 84140
PubMed articles FAM161A
OMIM - Gene 613596
OMIM - Diseases RP28 (retinitis pigmentosa, type 28 (RP28))
HGMD FAM161A
GeneCards FAM161A
GeneTests FAM161A
Orphanet FAM161A


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00024224 2 transcript variant 1 NM_001201543.1 NP_001188472.1 269


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