TSNARE1 - t-SNARE domain containing 1 Gene

Homo sapiens

Gene ID: 203062 | Gene type: protein coding

About TSNARE1

This gene has 9 transcripts (splice variants), 145 orthologues and 12 paralogues. Ubiquitous expression in skin (RPKM 3.2), ovary (RPKM 2.2) and 25 other tissues.

Summary

Predicted to enable SNAP receptor activity and SNARE binding activity. Predicted to be involved in intracellular protein transport; vesicle docking; and vesicle fusion. Predicted to be located in membrane. Predicted to be part of SNARE complex. Predicted to be active in endomembrane system. Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

TSNARE1 Products(7)

mRNA	Protein	Name
NM_001291931.2	NP_001278860.1	t-SNARE domain-containing protein 1 isoform b
NM_001363740.2	NP_001350669.1	t-SNARE domain-containing protein 1 isoform c
NM_001366901.1	NP_001353830.1	t-SNARE domain-containing protein 1 isoform d
NM_001366902.1	NP_001353831.1	t-SNARE domain-containing protein 1 isoform e
NM_001366903.1	NP_001353832.1	t-SNARE domain-containing protein 1 isoform f
NM_001366904.1	NP_001353833.1	t-SNARE domain-containing protein 1 isoform g
NM_145003.5	NP_659440.2	t-SNARE domain-containing protein 1 isoform a

TSNARE1 Protein Structure

Myb_DNA-bind_5

Syntaxin_2

SNARE

0
100
200
300
400
512 a.a.

Protein Preferred Names

Protein Names

t-SNARE domain-containing protein 1

Related Diseases

Diseases

Alias

Intellectual Developmental Disorder With Cardiac Arrhythmia

Gnb5-Related Intellectual Disability-Cardiac Arrhythmia Syndrome	IDDCA
Intellectual Developmental Disorder, With Cardiac Arrhythmia

Deafness, Autosomal Recessive 28

DFNB28	Autosomal Recessive Nonsyndromic Deafness 28
Autosomal Recessive Deafness 28	Deafness, Autosomal Recessive, 28
Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 28	Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 28
Deafness, Autosomal Recessive, Type 28

Pitt-Hopkins-Like Syndrome 1

Cortical Dysplasia-Focal Epilepsy Syndrome	CDFES
PTHSL1	Cdfe Syndrome
Pitt-Hopkins Like Syndrome 1	Pitt-Hopkins-Like Syndrome-1
Cntnap2-Related Developmental And Epileptic Encephalopathy	Cntnap2-Related Dee
Mesh	D006985
Mesh	D008607

Schizophrenia

SCZD	Schizophrenia With Or Without An Affective Disorder
Schizophrenia 12	Schizophrenia, Susceptibility To
Schizophrenia-1	Dementia Praecox
Schizophrenia 1

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

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS15155	TSNARE1 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Felis catus	TSNARE1	VGNC	VGNC:66622
Rattus norvegicus	TSNARE1	RGD	RGD:9421138
Bos taurus	TSNARE1	VGNC	VGNC:36423
Canis familiaris	TSNARE1	VGNC	VGNC:47908
Macaca mulatta	TSNARE1	VGNC	VGNC:99478

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