Nuclear hormone receptor family member nhr-35 [Source:NCBI gene;Acc:180725]
Chromosome X: 4,532,691-4,537,546 forward strand.
WBcel235:BX284606.5
This gene has 2 transcripts (splice variants), 206 orthologues and 27 paralogues.
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Nuclear hormone receptor family member nhr-35 [Source:NCBI gene;Acc:180725]
Chromosome X: 4,532,691-4,537,546 forward strand.
WBcel235:BX284606.5
This gene has 2 transcripts (splice variants), 206 orthologues and 27 paralogues.
Transcript ID | Name | bp | Protein | Translation ID | Biotype | UniProt Match | Flags |
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C07A12.3a.1 | - | 1917 | 542aa | C07A12.3a.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | Q17771 | 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, |
C07A12.3b.1 | - | 1468 | 486aa | C07A12.3b.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | Q17771 | 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, |
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Ensembl release 111 - January 2024 ©
EMBL-EBI
EMBL-EBI
http://useast.ensembl.org
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