Human (GRCh37.p13)
Description

Fraser syndrome 1 [Source:HGNC Symbol;Acc:19185]

Gene Synonyms

DKFZp686I05113, FLJ14927, FLJ22031, KIAA1500

Location
About this transcript

This transcript has 19 exons, is annotated with 54 domains and features, is associated with 115318 variant alleles and maps to 473 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000264895.6FRAS1-201124794012aaENSP00000264895.6
 
Protein coding
CCDS54771Q4W596 Q69YV4 Q86XX4
NM_025074.6GENCODE basic
ENST00000512123.1FRAS1-00898692241aaENSP00000422834.1
 
Protein coding
Q69YV4 -CDS 5' incomplete
ENST00000325942.6FRAS1-00171421976aaENSP00000326330.6
 
Protein coding
CCDS54772Q4W596 Q86XX4 NM_001166133.1GENCODE basic
ENST00000264899.6FRAS1-2022654737aaENSP00000264899.6
 
Protein coding
Q4W596 Q86XX4 -GENCODE basic
ENST00000502446.1FRAS1-0042217666aaENSP00000423645.1
 
Protein coding
--CDS 5' incomplete
ENST00000508900.1FRAS1-0052169652aaENSP00000423809.1
 
Protein coding
--CDS 5' incomplete
ENST00000510944.1FRAS1-0072125426aaENSP00000422221.1
 
Protein coding
--CDS 5' incomplete
ENST00000508909.1FRAS1-003229739aaENSP00000425583.1
 
Nonsense mediated decay
D6RCP6 --
ENST00000509802.1FRAS1-010564No protein-
 
Retained intron
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Statistics

Exons: 19, Coding exons: 19, Transcript length: 2,654 bps, Translation length: 737 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q86XX4

Version

ENST00000264899.6

Type

Protein coding

Annotation Method

Annotation produced by the Ensembl genebuild.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.