Summary
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- GO: Molecular function
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Gene: ammecr1 ENSXETG00000035215

Description

Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region 1 [Source:Xenbase;Acc:XB-GENE-992102]

Location

UCB_Xtro_10.0:CM004450.2

About this gene

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSXETT00000102558.2	ammecr1-201	2969	307aa	ENSXETP00000069257.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B1WAT7	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,

Summary