Human (GRCh38.p14)
Description

solute carrier family 35 member E1 [Source:HGNC Symbol;Acc:HGNC:20803]

Gene Synonyms

FLJ14251

Location

Chromosome 19: 16,549,831-16,572,415 reverse strand.

GRCh38:CM000681.2

About this gene

This gene has 11 transcripts (splice variants), 199 orthologues and 9 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000595753.6SLC35E1-2085126410aaENSP00000470652.1
 
Protein coding
CCDS12346Q96K37-1 NM_024881.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000436553.6SLC35E1-2031343344aaENSP00000400435.2
 
Protein coding
H7C1I0 -TSL:3CDS 5' incomplete
ENST00000421082.1SLC35E1-202552116aaENSP00000394092.1
 
Protein coding
C9JK45 -TSL:4CDS 3' incomplete
ENST00000409648.8SLC35E1-2013691105aaENSP00000387152.4
 
Nonsense mediated decay
A0A0A0MSG4 -TSL:2CDS 5' incomplete
ENST00000652421.1SLC35E1-2111950No protein-
 
Protein coding CDS not defined
---
ENST00000593812.1SLC35E1-207924No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000600356.1SLC35E1-210869No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000470077.1SLC35E1-205552No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000596387.1SLC35E1-209446No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000488894.1SLC35E1-2061905No protein-
 
Retained intron
--TSL:2
ENST00000469055.1SLC35E1-204511No protein-
 
Retained intron
--TSL:2