Loading…

Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Configure this page

Share this page

Bookmark this page

.

Gene: SYNDIG1L ENSG00000183379

.

Description

synapse differentiation inducing 1-like [Source:HGNC Symbol;Acc:32388]

Gene Synonyms

CAPUCIN, DSPC1, IFITMD4, TMEM90A, capucin

Location

Chromosome 14: 74,872,596-74,892,805 reverse strand.

GRCh37:CM000676.1

About this gene

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

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000331628.3	SYNDIG1L-201	2607	238aa	ENSP00000331474.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS41970	A6NDD5 G3V402	NM_001105579.1	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000554823.1	SYNDIG1L-001	2420	238aa	ENSP00000450439.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS41970	A6NDD5 G3V402	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000554953.1	SYNDIG1L-002	488	80aa	ENSP00000451519.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		G3V402	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,

.

Summary

.

.