1. Gene
  2. SYTL3 - synaptotagmin like 3 Gene

SYTL3 - synaptotagmin like 3 Gene

Homo sapiens

Also known as SLP3

Gene ID: 94120 | Gene type: protein coding

About SYTL3

This gene has 4 transcripts (splice variants), 157 orthologues and 31 paralogues. Ubiquitous expression in thyroid (RPKM 15.0), small intestine (RPKM 10.0) and 25 other tissues.

Summary

The protein encoded by this gene belongs to a family of peripheral membrane proteins that play a role in vesicular trafficking. This protein binds Phospholipids in the presence of calcium ions. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]

SYTL3 Products(5)

mRNA Protein Name
NM_001009991.4 NP_001009991.2 synaptotagmin-like protein 3 isoform 2
NM_001242384.2 NP_001229313.1 synaptotagmin-like protein 3 isoform 1
NM_001242394.2 NP_001229323.1 synaptotagmin-like protein 3 isoform 1
NM_001242395.2 NP_001229324.1 synaptotagmin-like protein 3 isoform 2
NM_001318745.2 NP_001305674.1 synaptotagmin-like protein 3 isoform 3
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

SYTL3 Protein Structure

FYVE_2

FYVE_2: FYVE-type zinc finger (9 - 123)

C2

C2: C2 domain (323 - 411)

C2

C2: C2 domain (483 - 568)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 610 a.a.
Protein Preferred Names Protein Names

synaptotagmin-like protein 3

exophilin-6

Related Diseases

Diseases Alias
Griscelli Syndrome

Chediak-Higashi-Like Syndrome

Griscelli-Prunieras Syndrome

Partial Albinism-Immunodeficiency Syndrome

Griscelli Disease

Gs

Hypopigmentation Immunodeficiency Disease

Partial Albinism With Immunodeficiency

Immunodeficiency Syndrome With Hypopigmentation

Hypopigmentation-Immunodeficiency Disease

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Canis familiaris SYTL3 VGNC VGNC:47052
Bos taurus SYTL3 VGNC VGNC:35547
Mus musculus SYTL3 MGD MGI:1933367
Felis catus SYTL3 VGNC VGNC:65906
Rattus norvegicus SYTL3 RGD RGD:1561992
Macaca mulatta SYTL3 VGNC VGNC:104431