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

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Gene: Igh-6-ps1 ENSRNOG00000029776

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Description

immunoglobulin heavy chain 6, pseudogene 1 [Source:RGD Symbol;Acc:2323067]

Gene Synonyms

AABR07065823.1, LOC100359884, LOC100359978

Location

Primary_assembly 6: 136,187,348-136,187,728 reverse strand.

mRatBN7.2:CM026979.1

About this gene

This gene has 1 transcript (splice variant), 274 orthologues and 113 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000044381.4	Igh-6-ps1-201	381	126aa	ENSRNOP00000048583.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LWD1	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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