Summary
- Splice variants
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Sequence
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Comparative Genomics
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Genetic Variation
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Gene: Prmt1l1 ENSRNOG00000004090

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Description

protein arginine methyltransferase 1 like 1 [Source:RGD Symbol;Acc:2320935]

Gene Synonyms

LOC100361025

Location

Primary_assembly 14: 91,764,754-91,765,815 reverse strand.

GRCr8:CM070404.1

About this gene

This gene has 1 transcript (splice variant).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	Flags
ENSRNOT00000005432.7	Prmt1l1-201	957	No protein	-	A gene that has homology to known protein-coding genes but contain a frameshift and/or stop codon(s) which disrupts the ORF. Thought to have arisen through duplication followed by loss of function.Pseudogene	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 P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,

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Summary

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