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

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Gene: Siglech ENSRNOG00000021499

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Description

sialic acid binding Ig-like lectin H [Source:RGD Symbol;Acc:1310401]

Gene Synonyms

LOC361584, RGD1310401

Location

Primary_assembly 1: 115,729,491-115,739,959 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 3 transcripts (splice variants), 195 orthologues and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000032254.8	Siglech-201	3037	313aa	ENSRNOP00000036397.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZAH6	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 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,
ENSRNOT00000100820.2	Siglech-202	2989	297aa	ENSRNOP00000085120.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GCH5	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,
ENSRNOT00000114742.2	Siglech-203	2739	220aa	ENSRNOP00000083791.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZXZ3	-

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Summary

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