Human (GRCh38.p14)
Description

collectin subfamily member 11 [Source:HGNC Symbol;Acc:HGNC:17213]

Gene Synonyms

CL-11, CL-K1, MGC3279

Location

Chromosome 2: 3,594,832-3,644,644 forward strand.

GRCh38:CM000664.2

About this gene

This gene has 13 transcripts (splice variants), 198 orthologues, 4 paralogues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000349077.9COLEC11-2021425271aaENSP00000339168.4
 
Protein coding
CCDS1649Q9BWP8-1 NM_024027.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000382062.6COLEC11-2031633247aaENSP00000371494.2
 
Protein coding
CCDS58690Q9BWP8-3 -GENCODE basicTSL:1
ENST00000418971.6COLEC11-2091595285aaENSP00000411770.2
 
Protein coding
CCDS58689Q9BWP8-10 -GENCODE basicTSL:2
ENST00000403096.7COLEC11-2061557245aaENSP00000385130.3
 
Protein coding
CCDS58691Q9BWP8-4 -GENCODE basicTSL:1
ENST00000236693.11COLEC11-2011381268aaENSP00000236693.7
 
Protein coding
CCDS1650Q9BWP8-9 -GENCODE basicTSL:1
ENST00000402794.4COLEC11-2041134221aaENSP00000384882.1
 
Protein coding
CCDS58693Q9BWP8-6 -GENCODE basicTSL:1
ENST00000402922.2COLEC11-2051134221aaENSP00000385653.1
 
Protein coding
CCDS58692Q9BWP8-7 -GENCODE basicTSL:1
ENST00000404205.5COLEC11-2071062197aaENSP00000385827.1
 
Protein coding
CCDS58694Q9BWP8-8 -GENCODE basicTSL:1
ENST00000438814.5COLEC11-211581123aaENSP00000393167.1
 
Protein coding
C9JWT5 -TSL:4CDS 3' incomplete
ENST00000416132.5COLEC11-2081378116aaENSP00000410919.1
 
Nonsense mediated decay
F8WB29 -TSL:5
ENST00000487365.5COLEC11-2131312No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000460971.5COLEC11-2121240No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000419002.6COLEC11-210520No protein-
 
Protein coding CDS not defined
--TSL:3