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: SMAD1 ENSPTRG00000016485

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Description

SMAD family member 1 [Source:VGNC Symbol;Acc:VGNC:737]

Location

Chromosome 4: 149,209,185-149,256,715 forward strand.

Pan_tro_3.0:CM000318.3

About this gene

This gene has 4 transcripts (splice variants), 221 orthologues and 7 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000030641.5	SMAD1-201	1410	469aa	ENSPTRP00000028297.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2QQ88	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,
ENSPTRT00000104349.1	SMAD1-203	5831	466aa	ENSPTRP00000092134.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3TSA6	-
ENSPTRT00000098190.1	SMAD1-202	1293	430aa	ENSPTRP00000090699.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3TN82	-
ENSPTRT00000106209.1	SMAD1-204	705	234aa	ENSPTRP00000080524.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3SU31	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,

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Summary

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