Nuclear Hormone Receptor family [Source:NCBI gene;Acc:41656994]
Chromosome X: 12,705,563-12,808,318 reverse strand.
WBcel235:BX284606.5
This gene has 3 transcripts (splice variants), 345 orthologues and 189 paralogues.
Due to scheduled maintenance work, Ensembl Genomes BLAST will be temporarily unavailable on Tuesday 7th May 2024. Click here for more details
.
.
Nuclear Hormone Receptor family [Source:NCBI gene;Acc:41656994]
Chromosome X: 12,705,563-12,808,318 reverse strand.
WBcel235:BX284606.5
This gene has 3 transcripts (splice variants), 345 orthologues and 189 paralogues.
Name | Transcript ID | bp | Protein | Translation ID | Biotype | UniProt | RefSeq | Flags |
---|---|---|---|---|---|---|---|---|
- | F16H9.2a.2 | 1200 | 334aa | F16H9.2a.2 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | G5EGN8 | - | APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS ALT2, |
- | F16H9.2a.1 | 1131 | 334aa | F16H9.2a.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | G5EGN8 | - | APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS ALT2, |
- | F16H9.2b.1 | 1062 | 353aa | F16H9.2b.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | G5EGN8 | - | APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P2, |
.
Ensembl Metazoa release 58 - January 2024 © EMBL-EBI EMBL-EBI
.
.