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: SEH1L ENSSSCG00000003673

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Description

centrosomal protein 192 [Source:VGNC Symbol;Acc:VGNC:96946]

Location

Primary_assembly 6: 96,710,701-96,733,795 reverse strand.

Sscrofa11.1:CM000817.5

About this gene

This gene has 4 transcripts (splice variants), 218 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000023051.4	SEH1L-201	2051	456aa	ENSSSCP00000026572.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	I3LR40	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,
ENSSSCT00000096174.1	SEH1L-204	4882	398aa	ENSSSCP00000076729.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8W4FBM9	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,
ENSSSCT00000055764.3	SEH1L-203	4618	310aa	ENSSSCP00000045495.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287ANM0 A0A8D1BAC4	-
ENSSSCT00000058504.3	SEH1L-202	3625	383aa	ENSSSCP00000038312.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287A3I8	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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Breeds

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Genomic alignments

Gene tree

Orthologues

Paralogues

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data