Basic Information

RORA

Full name: RAR related orphan receptor A

Gene type: protein coding

HGNC ID: HGNC:10258

Gene location: 15q22.2

Gene resources

NCBI: https://www.ncbi.nlm.nih.gov/gene/6095

Alliance of genome: https://www.alliancegenome.org/gene/HGNC:10258

MANE select: https://www.ncbi.nlm.nih.gov/gene/?term=NM_134261.3

Protein resources

UniProt/Swiss-Prot: https://www.uniprot.org/uniprot/P35398

AlphaFold: https://alphafold.ebi.ac.uk/entry/P35398

MEME motif:

Clinical resources

OMIM: https://www.omim.org/entry/600825

dbVar: https://www.ncbi.nlm.nih.gov/dbvar?LinkName=gene_dbvar&from_uid=6095

Pathway resources

KEGG pathway: https://www.genome.jp/pathway/hsa04659+6095

Variant resources

Gene Disease type Variant type NCBI dbSNP Alleles Variant location
RORA nAMD Intron Variant rs12916023 A>G chr15:61163854 (GRCh38.p13)
RORA nAMD Intron Variant rs4583176 A>G chr15:61160912 (GRCh38.p13)
RORA nAMD Intron Variant rs730754 C>T chr15:61159137 (GRCh38.p13)
RORA nAMD Intron Variant rs8034864 T>C / T>G chr15:61154154 (GRCh38.p13)
RORA nAMD Intron Variant rs975501 C>A / C>G / C>T chr15:61149222 (GRCh38.p13)
RORA nAMD Intron Variant rs12900948 C>A / C>T chr15:61148472 (GRCh38.p13)
RORA nAMD Intron Variant rs782925 C>T chr15:61111225 (GRCh38.p13)
RORA nAMD Intron Variant rs7177611 G>A / G>C chr15:61080560 (GRCh38.p13)
RORA nAMD Intron Variant rs12591914 C>A / C>G / C>T chr15:60994458 (GRCh38.p13)
RORA nAMD Intron Variant rs16943429 T>C / T>G chr15:60987054 (GRCh38.p13)
RORA nAMD Intron Variant rs7495128 C>T chr15:60982031 (GRCh38.p13)
RORA nAMD Intron Variant rs2414687 C>A / C>T chr15:60977046 (GRCh38.p13)
RORA nAMD Intron Variant rs17237514 T>A / T>C / T>G chr15:60954476 (GRCh38.p13)
RORA nAMD Intron Variant rs4335725 T>A / T>C / T>G chr15:60948405 (GRCh38.p13)
RORA nAMD Intron Variant rs17270640 C>G chr15:60926104 (GRCh38.p13)
RORA nAMD Intron Variant rs11071570 G>A / G>C / G>T chr15:60923492 (GRCh38.p13)
RORA nAMD Intron Variant rs6494231 T>C / T>G chr15:60913793 (GRCh38.p13)
RORA AMD-additive model Intron Variant rs1403737 G>A chr15:61024003 (GRCh38.p13)