Human (GRCh38.p14)
Description

intraflagellar transport 56 [Source:HGNC Symbol;Acc:HGNC:21882]

Gene Synonyms

DYF-13, DYF13, FLJ12571, TTC26

Location

Chromosome 7: 139,133,744-139,191,986 forward strand.

GRCh38:CM000669.2

About this gene

This gene has 10 transcripts (splice variants), 226 orthologues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000464848.5IFT56-2034299554aaENSP00000419279.1
 
Protein coding
CCDS5852A0AVF1-1 NM_024926.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000430935.5IFT56-2024198487aaENSP00000410655.1
 
Protein coding
CCDS55172A0AVF1-2 -GENCODE basicTSL:1
ENST00000343187.8IFT56-2012015523aaENSP00000339135.4
 
Protein coding
CCDS55173A0AVF1-3 -GENCODE basicTSL:2
ENST00000478836.6IFT56-2071794447aaENSP00000419178.2
 
Protein coding
B7Z6R6 -GENCODE basicTSL:2
ENST00000495038.5IFT56-2101599423aaENSP00000418788.1
 
Protein coding
CCDS75665B7Z2T3 -GENCODE basicTSL:2
ENST00000474035.6IFT56-2051193271aaENSP00000443253.1
 
Protein coding
CCDS83230Q96CU4 -GENCODE basicTSL:1
ENST00000476296.1IFT56-2062756135aaENSP00000419639.1
 
Nonsense mediated decay
F8WEZ4 -TSL:5
ENST00000481482.5IFT56-2091267No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000479132.5IFT56-208581No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000468866.1IFT56-204553No protein-
 
Protein coding CDS not defined
--TSL:4