Gene: Stat5b ENSRNOG00000019075

Description

signal transducer and activator of transcription 5B [Source:RGD Symbol;Acc:3774]

Location

Primary_assembly 10: 86,207,293-86,275,990 reverse strand.

GRCr8:CM070400.1

About this gene

This gene has 5 transcripts (splice variants), 289 orthologues, 5 paralogues and is associated with 26 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000026354.5	Stat5b-201	2588	795aa	ENSRNOP00000026354.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JSR4	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,
ENSRNOT00000131078.1	Stat5b-205	3440	763aa	ENSRNOP00000098874.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000104227.2	Stat5b-203	2779	780aa	ENSRNOP00000095287.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GLJ7	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,
ENSRNOT00000081247.3	Stat5b-202	2586	758aa	ENSRNOP00000070284.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JXI4	-
ENSRNOT00000107303.2	Stat5b-204	2514	788aa	ENSRNOP00000092900.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GK04	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,