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: STARD10 ENSBTAG00000015182

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Description

StAR related lipid transfer domain containing 10 [Source:VGNC Symbol;Acc:VGNC:35361]

Location

Primary_assembly 15: 52,302,299-52,337,108 reverse strand.

ARS-UCD2.0:CM008182.2

About this gene

This gene has 6 transcripts (splice variants), 198 orthologues and 6 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000125952.1	STARD10-203	1514	378aa	ENSBTAP00000091596.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9T713	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,
ENSBTAT00000100050.1	STARD10-206	1463	361aa	ENSBTAP00000094238.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9T8F0	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,
ENSBTAT00000075030.2	STARD10-204	1412	344aa	ENSBTAP00000072662.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MLT4	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,
ENSBTAT00000071421.2	STARD10-202	1340	320aa	ENSBTAP00000074446.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MRL1	-
ENSBTAT00000120166.1	STARD10-201	1270	334aa	ENSBTAP00000097069.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TFX3	-
ENSBTAT00000020202.5	STARD10-205	1257	291aa	ENSBTAP00000020202.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MXU5	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,

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Summary

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