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

Configure this page

Share this page

Bookmark this page

.

Gene: Zfp51l1 ENSRNOG00000043341

.

Description

zinc finger protein 51 like 1 [Source:RGD Symbol;Acc:1560046]

Gene Synonyms

LOC499056, RGD1560046, Zfp51, Znf761

Location

Primary_assembly 1: 70,134,841-70,149,185 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 4 transcripts (splice variants), 955 orthologues and 10 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000029111.7	Zfp51l1-201	3086	796aa	ENSRNOP00000030498.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A813	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,
ENSRNOT00000134942.1	Zfp51l1-204	3129	746aa	ENSRNOP00000098819.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000094650.2	Zfp51l1-202	2926	724aa	ENSRNOP00000091945.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AEL4	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,
ENSRNOT00000132377.1	Zfp51l1-203	2799	731aa	ENSRNOP00000109936.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

.

Summary

.

.