Human (GRCh37.p13)
Description

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

Location

Chromosome 3: 38,029,550-38,048,679 forward strand.

GRCh37:CM000665.1

About this gene

This gene has 11 transcripts (splice variants), 197 orthologues and 7 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000283713.6VILL-0012970856aaENSP00000283713.6
 
Protein coding
CCDS2670C9JUR8 E9PFV5 O15195
-Ensembl CanonicalGENCODE Basic
ENST00000383759.2VILL-2012787856aaENSP00000373266.2
 
Protein coding
CCDS2670C9JUR8 E9PFV5 O15195
NM_015873.3GENCODE Basic
ENST00000465644.1VILL-0021857574aaENSP00000422096.1
 
Protein coding
D6R9H2 -GENCODE Basic
ENST00000492491.2VILL-007686187aaENSP00000427355.1
 
Protein coding
C9JUR8 E9PFV5 -CDS 3' incomplete
ENST00000416303.1VILL-006582130aaENSP00000393661.1
 
Protein coding
C9JUR8 -CDS 3' incomplete
ENST00000412008.1VILL-009813101aaENSP00000387659.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000486616.1VILL-0054439No protein-
 
Retained intron
---
ENST00000484717.1VILL-0042072No protein-
 
Retained intron
---
ENST00000463080.2VILL-010831No protein-
 
Retained intron
---
ENST00000488209.1VILL-011543No protein-
 
Retained intron
---
ENST00000460040.1VILL-008448No protein-
 
Retained intron
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