Human (GRCh38.p14) ▼ 
Summary
SequenceProtein InformationGenetic VariationVariant tableVariant imageHaplotypesPopulation comparisonComparison imageExternal ReferencesSupporting evidenceID History.
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.
This transcript has 2 exons, is annotated with 37 domains and features, is associated with 1229 variant alleles and maps to 301 oligo probes.
This transcript is a product of gene ENSG00000131910.5 Show transcript tableHide transcript table
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Exons: 2, Coding exons: 2, Transcript length: 1,165 bps, Translation length: 257 residues
This MANE Select transcript contains ENSP00000254227 and matches to NM_021969.3 and NP_068804.1
This transcript corresponds to the following Uniprot identifiers: Q15466
This transcript is a member of the Human CCDS set: CCDS291
TSL:1
ENST00000254227.4
Protein coding
Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.
This transcript is a member of the Gencode basic gene set.
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Ensembl release 111 - January 2024 ©
EMBL-EBI
EMBL-EBI
http://useast.ensembl.org
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