Description

amelogenin, Y-linked [Source:HGNC Symbol;Acc:HGNC:462]

Synonyms

AMGL

Location
INSDC coordinates

chromosome:GRCh38:CM000686.2:6865918:6874027:1

About this gene

This gene has 2 transcripts (splice variants), 35 orthologues, 1 paralogue, is a member of 1 Ensembl protein family and is associated with 12 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
AMELY-001ENST00000215479802192aaENSP00000215479
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS14778Q99218 NM_001143
NP_001134
TSL:1

TSL1: All splice junctions of the transcript are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS PI1APPRIS principal isoform
Glossary entry for APPRIS
APPRIS website
AMELY-002ENST00000383036621206aaENSP00000372505
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-Q99218 -TSL:5

TSL5: No single transcript (mRNA or EST) supports this transcript model's structure.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).

Gene-based displays