Gene: Serpind1 ENSRNOG00000001865

Description

serpin family D member 1 [Source:RGD Symbol;Acc:619854]

Gene Synonyms

HC-II, rls2var1

Location

GRCr8:CM070401.1

About this gene

This gene has 2 transcripts (splice variants), 200 orthologues, 48 paralogues and is associated with 6 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000084973.3	Serpind1-202	2107	527aa	ENSRNOP00000074639.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K8K3	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,
ENSRNOT00000031819.7	Serpind1-201	2082	479aa	ENSRNOP00000031829.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6JSM3 Q64268	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,

Upcoming Ensembl Platform Transition