Description

Fraser syndrome 1 homolog (human) [Source:MGI Symbol;Acc:MGI:2385368]

Location
INSDC coordinates

chromosome:GRCm38:CM000998.2:96373955:96784728:1

About this gene

This gene has 6 transcripts (splice variants), 64 orthologues, 5 paralogues and is a member of 1 Ensembl protein family.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
Fras1-001ENSMUST00000036019158484010aaENSMUSP00000043250
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS19450Q80T14 NM_175473
NP_780682
TSL:1

Transcript Support Level 1, when transcripts 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 P1

PRINCIPAL1 - APPRIS candidate principal isoform.

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

Fras1-005ENSMUST00000199204553No protein-
 
Processed transcriptTranscripts that don't contain an open reading frame (ORF) and cannot be placed in one of the other categories.
---
Fras1-004ENSMUST00000197126427No protein-
 
Processed transcriptTranscripts that don't contain an open reading frame (ORF) and cannot be placed in one of the other categories.
---
Fras1-006ENSMUST00000198016245No protein-
 
Processed transcriptTranscripts that don't contain an open reading frame (ORF) and cannot be placed in one of the other categories.
---
Fras1-003ENSMUST000001967512017No protein-
 
Retained intronAlternatively spliced transcript that is believed to contain intronic sequence relative to other coding transcripts in a given locus.
---
Fras1-002ENSMUST000001998411273No protein-
 
Retained intronAlternatively spliced transcript that is believed to contain intronic sequence relative to other coding transcripts in a given locus.
---

Gene-based displays