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: SAMD11 ENSBTAG00000008739

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Description

sterile alpha motif domain containing 11 [Source:VGNC Symbol;Acc:VGNC:59361]

Location

Primary_assembly 16: 51,524,092-51,545,932 reverse strand.

ARS-UCD2.0:CM008183.2

About this gene

This gene has 4 transcripts (splice variants), 197 orthologues and 17 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000079851.2	SAMD11-202	3768	855aa	ENSBTAP00000073275.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MN31	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,
ENSBTAT00000079990.2	SAMD11-203	3750	849aa	ENSBTAP00000062408.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1N0U3	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,
ENSBTAT00000081353.2	SAMD11-201	3273	812aa	ENSBTAP00000066731.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1N7K9	-
ENSBTAT00000011517.7	SAMD11-204	3124	818aa	ENSBTAP00000011517.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BDR5	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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