Description

amelogenin, X-linked [Source:HGNC Symbol;Acc:HGNC:461]

Synonyms

AIH1, AMG

Location
INSDC coordinates

chromosome:GRCh38:CM000685.2:11293413:11300761:1

About this gene

This gene has 3 transcripts (splice variants), 41 orthologues, 1 paralogue, is a member of 1 Ensembl protein family and is associated with 2 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
AMELX-002ENST00000380712835205aaENSP00000370088
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS14145Q99217 NM_182680
NP_872621
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).
AMELX-001ENST00000380714793191aaENSP00000370090
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS14144Q99217 NM_001142
NP_001133
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
AMELX-201ENST00000348912737175aaENSP00000335312
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS14146Q99217 NM_182681
NP_872622
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