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

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Gene: STARD13 ENSBTAG00000021815

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Description

StAR related lipid transfer domain containing 13 [Source:VGNC Symbol;Acc:VGNC:35362]

Location

Primary_assembly 12: 27,520,140-28,013,526 forward strand.

ARS-UCD2.0:CM008179.2

About this gene

This gene has 5 transcripts (splice variants), 275 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000029081.8	STARD13-205	5101	1142aa	ENSBTAP00000029081.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MCN4	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 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,
ENSBTAT00000088023.2	STARD13-201	5973	1121aa	ENSBTAP00000084453.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SKL2	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,
ENSBTAT00000132123.2	STARD13-202	5874	1088aa	ENSBTAP00000079928.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9S968	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,
ENSBTAT00000106344.2	STARD13-203	5667	1079aa	ENSBTAP00000079628.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9S3E7	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,
ENSBTAT00000067678.3	STARD13-204	5096	1108aa	ENSBTAP00000066929.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MDL7	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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