Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

Configure this page

Share this page

Bookmark this page

.

Gene: smarcad1b ENSDARG00000073721

.

Description

SNF2 related chromatin remodeling ATPase with DExD box 1b [Source:NCBI gene (formerly Entrezgene);Acc:563175]

Location

Chromosome 10: 17,552,733-17,587,832 reverse strand.

GRCz11:CM002894.2

About this gene

This gene has 2 transcripts (splice variants), 155 orthologues and 36 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000113101.4	smarcad1b-201	3464	954aa	ENSDARP00000104253.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AB13A787 E7F1C4	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 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,
ENSDART00000139113.2	smarcad1b-202	598	No protein	-	Gene/transcript that doesn't contain an open reading frame (ORF).Processed transcript	-	-

.

Summary

.

.