YKT6 - YKT6 v-SNARE homolog Gene

Homo sapiens

Gene ID: 10652 | Gene type: protein coding

About YKT6

Cytogenetic location: 7p13 Genomic coordinates (GRCh38): 7:44,200,978-44,214,294 (from NCBI)

This gene has 15 transcripts (splice variants), 232 orthologues and 10 paralogues. Ubiquitous expression in brain (RPKM 24.8), colon (RPKM 21.7) and 25 other tissues.

Summary

This gene product is one of the SNARE recognition molecules implicated in vesicular transport between secretory compartments. It is a membrane associated, isoprenylated protein that functions at the endoplasmic reticulum-Golgi transport step. This protein is highly conserved from yeast to human and can functionally complement the loss of the yeast homolog in the yeast secretory pathway. [provided by RefSeq, Jul 2008]

YKT6 Products(3)

mRNA	Protein	Name
NM_001363678.2	NP_001350607.1	synaptobrevin homolog YKT6 isoform 2
NM_001410874.1	NP_001397803.1	synaptobrevin homolog YKT6 isoform 3
NM_006555.4	NP_006546.1	synaptobrevin homolog YKT6 isoform 1

YKT6 Protein Structure

Longin

Synaptobrevin

0
100
198 a.a.

Protein Preferred Names

Protein Names

synaptobrevin homolog YKT6

R-SNARE

Recombinant YKT6 Proteins

Cat. No.	Product Name	Accession	Purity
HY-P71025	YKT6 Protein, Human (His)	O15498 (M1-M198)	≥95%

Related Diseases

Diseases

Alias

Foodborne Botulism

Botulism	Botulism Poisoning
Intoxication With Clostridium Botulinum Toxin	Wound Botulism
Food Poisoning Due To Clostridium Botulinum	Infection Due To Clostridium Botulinum
Infant Botulism	Intoxication Botulism
Botulism, Infantile	Clostridium Botulinum Poisoning
Botulism Nos

Infant Botulism

Infant Intestinal Botulism	Infant Intestinal Toxemia Botulism
Infant Intestinal Toxin-Mediated Botulism	Infantile Botulism
Botulism, Infantile

Cerebral Dysgenesis, Neuropathy, Ichthyosis, And Palmoplantar Keratoderma Syndrome

Cednik Syndrome	CEDNIK
Cerebral Dysgenesis, Neuropathy, Ichthyosis And Keratoderma Syndrome	Cerebral Dysgenesis, Neuropathy, Ichthyosis, And Palmoplantar Keratoderma Syndro
Cerebral Dysgenesis-Neuropathy-Ichthyosis-Palmoplantar Keratoderma Syndrome	Cerebral Dysgenesis-Neuropathy-Ichthyosis-Keratoderma Syndrome
Cerebral Dysgenesis, Neuropathy, Ichthyosis, And Palmoplantar Keratoderma	Neurocutaneous Syndromes

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

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS15927	YKT6 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Bos taurus	YKT6	VGNC	VGNC:37030
Mus musculus	YKT6	MGD	MGI:1927550
Macaca mulatta	YKT6	VGNC	VGNC:81796
Felis catus	YKT6	VGNC	VGNC:67146
Rattus norvegicus	YKT6	RGD	RGD:70897
Others	YKT6	NCBI