Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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- Structural variants
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Gene: Nhlrc3 ENSRNOG00000010843

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Description

NHL repeat containing 3 [Source:RGD Symbol;Acc:1565414]

Gene Synonyms

LOC310416, RGD1565414

Location

Primary_assembly 2: 139,679,866-139,692,691 reverse strand.

GRCr8:CM070392.1

About this gene

This gene has 1 transcript (splice variant) and 196 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000014562.7	Nhlrc3-201	2394	397aa	ENSRNOP00000014562.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZKD4 D4A2F6	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,

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Summary

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