Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: NCL ENSBTAG00000016174

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Description

nucleolin [Source:HGNC Symbol;Acc:HGNC:7667]

Location

Primary_assembly 2: 119,226,396-119,236,929 reverse strand.

ARS-UCD2.0:CM008169.2

About this gene

This gene has 2 transcripts (splice variants), 121 orthologues and 47 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000021529.6	NCL-201	2715	710aa	ENSBTAP00000021529.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1B8K6	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,
ENSBTAT00000089561.1	NCL-202	3206	680aa	ENSBTAP00000090510.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9T471	-

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Summary

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