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NR_110524.2 - -
NM_005126.5 - NP_005117.3 (MANE)
NM_001145425.2 - NP_001138897.1
DNA
Protein
Gene Info.
Genome Build
GRCh38
Chromosome
3
Location
Chr3:23,944,786-23,981,117
LOEUF
0.621
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ClinVar
Pathogenic/ Likely pa...
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Drug response
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VUS
Benign/Likely benign
Others
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
9975
Ensembl
ENSG00000174738
GeneCards
NR1D2
UniProt
Q14995
KEGG
hsa:9975
gnomAD
ENSG00000174738
ICGC
ENSG00000174738
RefDIC
9975
RefEx
9975
DTX
NR1D2
AS-ALPS
NR1D2
NR1D2
nuclear receptor subfamily 1 group D member 2
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