Human (GRCh38.p14)
Description

retinoic acid induced 2 [Source:HGNC Symbol;Acc:HGNC:9835]

Location

Chromosome X: 17,800,049-17,861,337 reverse strand.

GRCh38:CM000685.2

About this gene

This gene has 6 transcripts (splice variants), 169 orthologues and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000451717.6RAI2-2042187530aaENSP00000401323.1
 
Protein coding
CCDS14183Q9Y5P3-1 NM_021785.6MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000545871.1RAI2-2062421530aaENSP00000444210.1
 
Protein coding
CCDS14183Q9Y5P3-1 -GENCODE basicAPPRIS P1TSL:4
ENST00000360011.5RAI2-2022377530aaENSP00000353106.1
 
Protein coding
CCDS14183Q9Y5P3-1 -GENCODE basicAPPRIS P1TSL:1
ENST00000331511.5RAI2-2012317530aaENSP00000333456.1
 
Protein coding
CCDS14183Q9Y5P3-1 -GENCODE basicAPPRIS P1TSL:2
ENST00000415486.7RAI2-2032037480aaENSP00000392578.2
 
Protein coding
CCDS55374Q9Y5P3-2 -GENCODE basicTSL:2
ENST00000509491.2RAI2-20546381aaENSP00000473562.1
 
Protein coding
R4GNA9 -TSL:3CDS 3' incomplete