SLITRK6

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

SLITRK6

SLIT and NTRK-like protein 6 is a protein that in humans is encoded by the SLITRK6 gene.[5][6]

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SLITRK6
Identifiers
AliasesSLITRK6, DFNMYP, SLIT and NTRK like family member 6
External IDsOMIM: 609681; MGI: 2443198; HomoloGene: 12986; GeneCards: SLITRK6; OMA:SLITRK6 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_032229

NM_175499

RefSeq (protein)

NP_115605

NP_780708

Location (UCSC)Chr 13: 85.79 – 85.81 MbChr 14: 110.99 – 110.99 Mb
PubMed search[3][4]
Wikidata
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Function

Members of the SLITRK family, such as SLITRK6, are integral membrane proteins with 2 N-terminal leucine-rich repeat (LRR) domains similar to those of SLIT proteins (see SLIT1). Most SLITRKs, including SLITRK6, also have C-terminal regions that share homology with neurotrophin receptors (see NTRK1). SLITRKs are expressed predominantly in neural tissues and have neurite-modulating activity.[5][6]

Clinical significance

Mutations in SLITRK6 cause high myopia and deafness in humans and mice.[7]

As a drug target

The protein is the target for the antibody-drug conjugate ASG-15ME which is in phase 1 clinical trials for urothelial cancer.[8]

References

Further reading

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