RIN2 gene homepage

General information
Gene symbol RIN2
Gene name Ras and Rab interactor 2
Chromosome 20
Chromosomal band p11.22
Imprinted Unknown
Genomic reference NG_016310.2
Transcript reference NM_001242581.1
Associated with diseases MACS
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 41
Unique public DNA variants reported 31
Individuals with public variants 47
Hidden variants 7
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was performed by Johan den Dunnen, supported by Global Variome.
Date created May 03, 2013
Date last updated September 15, 2020
Version RIN2:200915

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
Homepage URL https://www.LOVD.nl/RIN2
HGNC 18750
Entrez Gene 54453
PubMed articles RIN2
OMIM - Gene 610222
OMIM - Diseases MACS (MACS syndrome (MACS, macrocephaly, alopecia, cutis laxa, and scoliosis))
GeneCards RIN2
GeneTests RIN2

Active transcripts




NCBI ID     

NCBI Protein ID     

00017783 20 transcript variant 1 NM_001242581.1 NP_001229510.1 41

Copyright & disclaimer
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