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LZTFL1 (NM_001276378) - leucine zipper transcription factor like 1

Leucine Zipper Transcription Factor-Like Protein 1 Isoform 2

Mutations Visualisation

Protein summary

This is an alternative isoform of LZTFL1 protein. View all 3 isoforms
LZTFL1: leucine zipper transcription factor-like protein 1 isoform 2
Description:

This gene encodes a ubiquitously expressed protein that localizes to the cytoplasm. This protein interacts with Bardet-Biedl Syndrome (BBS) proteins and, through its interaction with BBS protein complexes, regulates protein trafficking to the ciliary membrane. Nonsense mutations in this gene cause a form of Bardet-Biedl Syndrome; a ciliopathy characterized in part by polydactyly, obesity, cognitive impairment, hypogonadism, and kidney failure. This gene may also function as a tumor suppressor; possibly by interacting with E-cadherin and the actin cytoskeleton and thereby regulating the transition of epithelial cells to mesenchymal cells. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Feb 2013].

Strand
-
Chromosome
3
Protein
282 residues
All mutations
42
PTM sites
13
CDS
45,867,805 - 45,879,495
Transcription
45,864,809 - 45,957,216
4.61% of sequence is predicted to be disordered

External references

Mappings retrieved from NCBI & UniProt.
RefSeq
Entrez
gene: 54585
UniProt
Ensembl