TMEM256-PLSCR3 (TMEM256-PLSCR3 readthrough (NMD candidate))

Gene
Gene Other IDs Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
100529211
Gene name Gene Name - the full gene name approved by the HGNC.
TMEM256-PLSCR3 readthrough (NMD candidate)
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TMEM256-PLSCR3
Synonyms (NCBI Gene) Gene synonyms aliases
C17orf61-PLSCR3, PLSCR3
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17p13.1
Summary Summary of gene provided in NCBI Entrez Gene.
This locus represents naturally occurring read-through transcription between the neighboring chromosome 17 open reading frame 61 (C17orf61) and phospholipid scramblase 3 (PLSCR3) genes. The read-through transcript is a candidate for nonsense-mediated mRNA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene Other IDs Associated diseases
MIM HGNC e!Ensembl
HGNC 49186 N/A
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Gene Other IDs Associated diseases
Show/Hide Causal Diseases (2)
Causal
Disease term Disease name dbSNP ID References
Asphyxiating thoracic dystrophy Asphyxiating Thoracic Dystrophy 1 rs137853115, rs137853025, rs1565310938, rs137853028, rs137853029, rs137853030, rs137853031, rs137853032, rs431905499, rs137853033, rs137853034, rs137853035, rs431905500, rs483352907, rs387906980
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Brachydactyly Brachydactyly rs121908949, rs28937580, rs121909082, rs104894122, rs863223289, rs863223290, rs104894121, rs1587657302, rs863223292, rs74315386, rs74315387, rs28936397, rs753691079, rs121909348, rs121917852
View all (22 more)