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NR_033824.2 - -
NM_006917.5 - NP_008848.1 (MANE)
NM_001256570.2 - NP_001243499.1
NM_001256571.2 - NP_001243500.1
DNA
Protein
Gene Info.
Genome Build
GRCh38
Chromosome
1
Location
Chr1:165,400,422-165,445,626
LOEUF
0.461
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ClinVar
Pathogenic/ Likely pa...
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VUS
Benign/Likely benign
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GnomAD
Common [>1%]
Rare [<1%]
ToMMo
Common [>1%]
Rare [<1%]
By consequences
Missense
Loss-of-function
Synonymous
Others
Gene region:
CDS
SpliceSite
UTR
Intron
Flanking
External resources
NCBI Gene
6258
Ensembl
ENSG00000143171
GeneCards
RXRG
UniProt
P48443
KEGG
hsa:6258
gnomAD
ENSG00000143171
ICGC
ENSG00000143171
RefDIC
6258
RefEx
6258
DTX
RXRG
AS-ALPS
RXRG
RXRG
retinoid X receptor gamma
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Amino Acid Sequence
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