Human (GRCh38.p14)
Description

villin like [Source:HGNC Symbol;Acc:HGNC:30906]

Location

Chromosome 3: 37,988,059-38,007,188 forward strand.

GRCh38:CM000665.2

About this gene

This gene has 10 transcripts (splice variants), 197 orthologues and 7 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000383759.7VILL-2022831856aaENSP00000373266.2
 
Protein coding
CCDS2670O15195-1 NM_015873.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000283713.10VILL-2012970856aaENSP00000283713.6
 
Protein coding
CCDS2670O15195-1 -GENCODE basicAPPRIS P1TSL:1
ENST00000465644.5VILL-2061857574aaENSP00000422096.1
 
Protein coding
D6R9H2 -GENCODE basicTSL:5
ENST00000492491.6VILL-210686187aaENSP00000427355.1
 
Protein coding
E9PFV5 -TSL:5CDS 3' incomplete
ENST00000412008.5VILL-203813101aaENSP00000387659.1
 
Nonsense mediated decay
H7BZ43 -TSL:3CDS 5' incomplete
ENST00000486616.5VILL-2084439No protein-
 
Retained intron
--TSL:2
ENST00000484717.5VILL-2072072No protein-
 
Retained intron
--TSL:1
ENST00000463080.2VILL-205831No protein-
 
Retained intron
--TSL:5
ENST00000488209.1VILL-209543No protein-
 
Retained intron
--TSL:2
ENST00000460040.1VILL-204448No protein-
 
Retained intron
--TSL:3