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: Glt1d1 ENSRNOG00000000961

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Description

glycosyltransferase 1 domain containing 1 [Source:RGD Symbol;Acc:1304896]

Gene Synonyms

LOC304445, RGD1304896

Location

Primary_assembly 12: 34,612,643-34,685,468 reverse strand.

GRCr8:CM070402.1

About this gene

This gene has 2 transcripts (splice variants), 192 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000064526.6	Glt1d1-201	2241	346aa	ENSRNOP00000063482.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZUX2	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,
ENSRNOT00000119832.2	Glt1d1-202	2238	345aa	ENSRNOP00000097536.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GMK0	APPRIS ALT1: 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 is conserved in at least 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 ALT1,

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Summary

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