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NM_005060.4 - NP_005051.2 (MANE)
NM_001001523.2 - NP_001001523.1
DNA
Protein
Gene Info.
Genome Build
GRCh38
Chromosome
1
Location
Chr1:151,805,571-151,832,302
LOEUF
0.161
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ClinVar
Pathogenic/ Likely pa...
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VUS
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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
6097
Ensembl
ENSG00000143365
GeneCards
RORC
UniProt
P51449
KEGG
hsa:6097
gnomAD
ENSG00000143365
ICGC
ENSG00000143365
RefDIC
6097
RefEx
6097
DTX
RORC
AS-ALPS
RORC
RORC
RAR related orphan receptor C
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