Human (GRCh38.p14)
Description

MFSD2 lysolipid transporter B, sphingolipid [Source:HGNC Symbol;Acc:HGNC:37207]

Gene Synonyms

SLC59A2

Location
About this transcript

This transcript has 6 exons, is associated with 2747 variant alleles and maps to 219 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000338315.6MFSD2B-2012846504aaENSP00000342501.4
 
Protein coding
CCDS86824A6NFX1 NM_001346880.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P2TSL:5
ENST00000669179.1MFSD2B-2062934532aaENSP00000499689.1
 
Protein coding
A0A590UK14 -GENCODE basicAPPRIS ALT2
ENST00000406420.7MFSD2B-2021528497aaENSP00000385527.3
 
Protein coding
A0A2I3JL00 -GENCODE basicAPPRIS ALT2TSL:5
ENST00000453731.1MFSD2B-20367444aaENSP00000390490.1
 
Nonsense mediated decay
H7BZN4 -TSL:3CDS 5' incomplete
ENST00000469562.1MFSD2B-2042613No protein-
 
Retained intron
--TSL:1
ENST00000495018.1MFSD2B-2051156No protein-
 
Retained intron
--TSL:1
Statistics

Exons: 6, Coding exons: 0, Transcript length: 1,156 bps,

Transcript Support Level (TSL)

TSL:1

Version

ENST00000495018.1

Type

Retained intron

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.