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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: SMARCAD1 ENSPTRG00000023126

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Description

SNF2 related chromatin remodeling ATPase with DExD box 1 [Source:UniProtKB Gene Name;Acc:H2QZE1]

Location

Chromosome 4: 96,692,103-96,775,326 forward strand.

Pan_tro_3.0:CM000318.3

About this gene

This gene has 2 transcripts (splice variants), 225 orthologues and 32 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000050553.4	SMARCAD1-201	5139	1026aa	ENSPTRP00000038869.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2W1Q5 H2QZE1	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,
ENSPTRT00000107207.1	SMARCAD1-202	4203	596aa	ENSPTRP00000071956.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3S5V8 A0A6D2VW83	-

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Summary

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