Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
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Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Gene: nhr-46 WBGene00003636

Description

Nuclear Hormone Receptor family [Source:NCBI gene;Acc:177350]

Location

WBcel235:BX284604.4

About this gene

This gene has 3 transcripts (splice variants).

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
C45E5.6b.1	-	2154	576aa	C45E5.6b.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q95QR2	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,
C45E5.6a.1	-	1976	528aa	C45E5.6a.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2KZB8	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,
C45E5.6c.1	-	1188	395aa	C45E5.6c.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q95QR3	-

Summary