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

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Gene: Sec24b ENSRNOG00000023373

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Description

SEC24 homolog B, COPII coat complex component [Source:RGD Symbol;Acc:1309358]

Gene Synonyms

LOC295461

Location

Primary_assembly 2: 221,236,898-221,306,919 reverse strand.

GRCr8:CM070392.1

About this gene

This gene has 5 transcripts (splice variants), 210 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000124463.1	Sec24b-204	5127	1284aa	ENSRNOP00000103705.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000038509.7	Sec24b-201	5031	1252aa	ENSRNOP00000037163.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZW15	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,
ENSRNOT00000109543.2	Sec24b-203	4926	1217aa	ENSRNOP00000086925.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AF73	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,
ENSRNOT00000168086.1	Sec24b-205	4850	1229aa	ENSRNOP00000110926.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000104158.2	Sec24b-202	4752	1159aa	ENSRNOP00000093683.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GKR9	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,

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Summary

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