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

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Gene: ADAM17 ENSSSCG00000008641

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Description

ADAM metallopeptidase domain 17 [Source:VGNC Symbol;Acc:VGNC:85065]

Location

Primary_assembly 3: 126,795,426-126,853,995 forward strand.

Sscrofa11.1:CM000814.5

About this gene

This gene has 4 transcripts (splice variants), 282 orthologues and 33 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000072504.2	ADAM17-202	3905	785aa	ENSSSCP00000065601.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QLA4 A0A8D0RA90	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,
ENSSSCT00000048512.2	ADAM17-203	5445	702aa	ENSSSCP00000054422.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287BEA0 A0A4X1UB62	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,
ENSSSCT00000033196.3	ADAM17-204	3911	752aa	ENSSSCP00000029260.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1UDM2 K7GN11	-
ENSSSCT00000070528.2	ADAM17-201	3893	751aa	ENSSSCP00000060994.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1UB79 A0A5G2Q9K7	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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