nuclear receptor subfamily 5, group A, member 2 [Source:HGNC Symbol;Acc:7984]
B1F, B1F2, CPF, FTF, FTZ-F1, FTZ-F1beta, LRH-1, LRH1, hB1F, hB1F-2
Chromosome 1: 199,996,730-200,146,552 forward strand.
GRCh37:CM000663.1
This gene has 6 transcripts (splice variants) and 2 paralogues.
Transcript ID | Name | bp | Protein | Translation ID | Biotype | CCDS | UniProt Match | RefSeq | Flags |
---|---|---|---|---|---|---|---|---|---|
ENST00000367362.3 | NR5A2-001 | 5086 | 541aa | ENSP00000356331.3 | Protein coding | CCDS1401 | B4E2P3 O00482 Q8WY08 | NM_205860.2 | Ensembl Canonical, GENCODE basic, |
ENST00000236914.3 | NR5A2-003 | 3115 | 495aa | ENSP00000236914.3 | Protein coding | CCDS1400 | B4E2P3 F1D8R9 O00482 Q8WY08 | NM_003822.4 | GENCODE basic, |
ENST00000544748.1 | NR5A2-201 | 1852 | 469aa | ENSP00000439116.1 | Protein coding | CCDS60383 | B4E2P3 | NM_001276464.1 | GENCODE basic, |
ENST00000367357.3 | NR5A2-005 | 1793 | 377aa | ENSP00000356326.3 | Protein coding | - | - | CDS 5' incomplete, | |
ENST00000447034.1 | NR5A2-004 | 213 | 71aa | ENSP00000414888.1 | Protein coding | Q9Y5V6 | - | CDS 5' and 3' incomplete, | |
ENST00000474307.1 | NR5A2-002 | 1713 | 113aa | ENSP00000436776.1 | Nonsense mediated decay | E9PQH2 Q8WY08 | - | - |