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: Hmgn1l1 ENSRNOG00000047566

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Description

high mobility group nucleosomal binding domain 1 like 1 [Source:RGD Symbol;Acc:1585825]

Gene Synonyms

AABR07059807.1, LOC680964

Location

Primary_assembly 4: 39,571,924-39,572,214 reverse strand.

GRCr8:CM070394.1

About this gene

This gene has 1 transcript (splice variant), 334 orthologues and 9 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000071058.4	Hmgn1l1-201	291	96aa	ENSRNOP00000095686.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6APM2	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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