nuclear receptor subfamily 0 group B member 2 [Source:HGNC Symbol;Acc:HGNC:7961]
SHP
Chromosome 1: 26,911,489-26,913,975 reverse strand.
GRCh38:CM000663.2
This gene has 1 transcript (splice variant), 239 orthologues, 1 paralogue and is associated with 1 phenotype.
Transcript ID | Name | bp | Protein | Translation ID | Biotype | CCDS | UniProt Match | RefSeq Match | Flags |
---|---|---|---|---|---|---|---|---|---|
ENST00000254227.4 | NR0B2-201 | 1165 | 257aa | ENSP00000254227.3 | Protein coding | CCDS291 | Q15466 | NM_021969.3 | MANE Select, Ensembl Canonical, GENCODE Primary, GENCODE Basic, APPRIS P1, TSL:1, |