Human (GRCh38.p14)
Description

tolloid like 1 [Source:HGNC Symbol;Acc:HGNC:11843]

Location

Chromosome 4: 165,873,237-166,104,457 forward strand.

GRCh38:CM000666.2

About this gene

This gene has 6 transcripts (splice variants), 209 orthologues, 35 paralogues and is associated with 4 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000061240.7TLL1-20172911013aaENSP00000061240.2
 
Protein coding
CCDS3811O43897-1 NM_012464.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000507499.5TLL1-20448181036aaENSP00000426082.1
 
Protein coding
E9PD25 -GENCODE basicTSL:1
ENST00000513213.5TLL1-2061829392aaENSP00000422937.1
 
Protein coding
CCDS56342O43897-2 -GENCODE basicTSL:1
ENST00000506144.1TLL1-203558110aaENSP00000423748.1
 
Protein coding
D6RCE0 -TSL:4CDS 3' incomplete
ENST00000509505.5TLL1-2054787130aaENSP00000422692.1
 
Nonsense mediated decay
D6RBI6 -TSL:1
ENST00000504560.5TLL1-20268657aaENSP00000421732.1
 
Nonsense mediated decay
D6RAK5 -TSL:3