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

Configure this page

Share this page

Bookmark this page

.

Gene: SNRPD1 ENSPTRG00000009909

.

Description

small nuclear ribonucleoprotein D1 polypeptide [Source:VGNC Symbol;Acc:VGNC:13289]

Location

Chromosome 18: 18,612,200-18,630,208 forward strand.

Pan_tro_3.0:CM000332.3

About this gene

This gene has 2 transcripts (splice variants), 185 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000079342.1	SNRPD1-202	384	127aa	ENSPTRP00000091530.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3TRF2	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,
ENSPTRT00000018197.3	SNRPD1-201	1603	119aa	ENSPTRP00000016853.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XL67 H2QEB7	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,

.

Summary

.

.