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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Zfp273l-ps1 ENSRNOG00000046353

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Description

zinc finger protein 273 like, pseudogene 1 [Source:RGD Symbol;Acc:1587241]

Gene Synonyms

LOC501406

Location

Primary_assembly 1: 37,050,465-37,081,353 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 4 transcripts (splice variants), 231 orthologues and 162 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000070999.5	Zfp273l-ps1-201	2702	565aa	ENSRNOP00000065760.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0R8G4	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 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,
ENSRNOT00000098911.2	Zfp273l-ps1-203	2685	501aa	ENSRNOP00000094506.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ARR4	-
ENSRNOT00000071758.3	Zfp273l-ps1-202	2665	509aa	ENSRNOP00000067386.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0RCQ9	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,
ENSRNOT00000144104.1	Zfp273l-ps1-204	1875	510aa	ENSRNOP00000111383.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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