1. Gene
  2. STX12 - syntaxin 12 Gene

STX12 - syntaxin 12 Gene

Homo sapiens

Also known as STX13; STX14

Gene ID: 23673 | Gene type: protein coding

About STX12

Cytogenetic location: 1p35.3 Genomic coordinates (GRCh38): 1:27,773,219-27,824,443 (from NCBI)

This gene has 5 transcripts (splice variants), 248 orthologues and 12 paralogues. Ubiquitous expression in thyroid (RPKM 63.8), fat (RPKM 35.7) and 25 other tissues.

Summary

Predicted to enable SNAP receptor activity and SNARE binding activity. Involved in autophagosome assembly; Cholesterol efflux; and protein stabilization. Located in several cellular components, including membrane raft; phagocytic vesicle; and phagophore assembly site. Part of SNARE complex. Colocalizes with BLOC-1 complex. [provided by Alliance of Genome Resources, Apr 2022]

STX12 Products(1)

mRNA Protein Name
NM_177424.3 NP_803173.1 syntaxin-12

STX12 Protein Structure

Syntaxin_2

Syntaxin_2: Syntaxin-like protein (30 - 131)

SNARE

SNARE: SNARE domain (183 - 245)

  • 0
  • 100
  • 200
  • 276 a.a.
Protein Preferred Names Protein Names

syntaxin-12

STX12 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
STX12 Q86Y82 SNAP47 Homo sapiens Q5SQN1 33961781
Intra
STX12 Q86Y82 SNAP47 Homo sapiens Q5SQN1 28514442
Intra
STX12 Q86Y82 SNAP47 Homo sapiens Q5SQN1 26359495
Intra
STX12 Q86Y82 CISD2 Homo sapiens Q8N5K1 32296183
Intra
STX12 Q86Y82 CISD2 Homo sapiens Q8N5K1 32296183
Intra
STX12 Q86Y82 CISD2 Homo sapiens Q8N5K1 32296183
Intra
STX12 Q86Y82 NEMP1 Homo sapiens O14524-2 32296183
Intra
STX12 Q86Y82 NEMP1 Homo sapiens O14524-2 32296183
Intra
STX12 Q86Y82 STXBP5L Homo sapiens Q9Y2K9 32296183
Intra
STX12 Q86Y82 STXBP5L Homo sapiens Q9Y2K9 32296183
Intra
STX12 Q86Y82 STXBP5L Homo sapiens Q9Y2K9 32296183
Intra
STX12 Q86Y82 STX2 Homo sapiens P32856-2 32296183
Intra
STX12 Q86Y82 STX2 Homo sapiens P32856-2 32296183
Intra
STX12 Q86Y82 RIC3 Homo sapiens Q7Z5B4-5 32296183
Intra
STX12 Q86Y82 RIC3 Homo sapiens Q7Z5B4-5 32296183
Intra
STX12 Q86Y82 TLCD4 Homo sapiens Q96MV1 32296183
Intra
STX12 Q86Y82 TLCD4 Homo sapiens Q96MV1 32296183
Intra
STX12 Q86Y82 TLCD4 Homo sapiens Q96MV1 32296183
Intra
STX12 Q86Y82 PLPPR2 Homo sapiens Q96GM1 32296183
Intra
STX12 Q86Y82 PLPPR2 Homo sapiens Q96GM1 32296183
Intra
STX12 Q86Y82 PLPPR2 Homo sapiens Q96GM1 32296183
Intra
STX12 Q86Y82 AQP6 Homo sapiens Q13520 32296183
Intra
STX12 Q86Y82 AQP6 Homo sapiens Q13520 32296183
Intra
STX12 Q86Y82 TMEM167B Homo sapiens Q9NRX6 32296183
Intra
STX12 Q86Y82 TMEM167B Homo sapiens Q9NRX6 32296183
Intra
STX12 Q86Y82 TMEM167B Homo sapiens Q9NRX6 32296183
Intra
STX12 Q86Y82 SLC10A6 Homo sapiens Q3KNW5 32296183
Intra
STX12 Q86Y82 SLC10A6 Homo sapiens Q3KNW5 32296183
Intra
STX12 Q86Y82 AQP8 Homo sapiens O94778 32296183
Intra
STX12 Q86Y82 AQP8 Homo sapiens O94778 32296183
Intra
STX12 Q86Y82 TMEM86B Homo sapiens Q8N661 32296183
Intra
STX12 Q86Y82 TMEM86B Homo sapiens Q8N661 32296183
Intra
STX12 Q86Y82 TMEM86B Homo sapiens Q8N661 32296183
Intra
STX12 Q86Y82 SEC11C Homo sapiens Q9BY50 32296183
Intra
STX12 Q86Y82 SEC11C Homo sapiens Q9BY50 32296183
Intra
STX12 Q86Y82 SEC11C Homo sapiens Q9BY50 32296183
Intra
STX12 Q86Y82 MFSD6 Homo sapiens Q6ZSS7 32296183
Intra
STX12 Q86Y82 MFSD6 Homo sapiens Q6ZSS7 32296183
Intra
STX12 Q86Y82 SLC66A2 Homo sapiens Q8N2U9 32296183
Intra
STX12 Q86Y82 SLC66A2 Homo sapiens Q8N2U9 32296183
Intra
STX12 Q86Y82 SLC66A2 Homo sapiens Q8N2U9 32296183
Intra
STX12 Q86Y82 EBP Homo sapiens Q15125 32296183
Intra
STX12 Q86Y82 EBP Homo sapiens Q15125 32296183
Intra
STX12 Q86Y82 GORAB Homo sapiens Q5T7V8 32296183
Intra
STX12 Q86Y82 GORAB Homo sapiens Q5T7V8 32296183
Intra
STX12 Q86Y82 SNAP29 Homo sapiens O95721 25416956
Intra
STX12 Q86Y82 SNAP29 Homo sapiens O95721 33961781
Intra
STX12 Q86Y82 SNAP29 Homo sapiens O95721 28514442
Intra
STX12 Q86Y82 SNAP29 Homo sapiens O95721 25416956
Intra
STX12 Q86Y82 SNAP29 Homo sapiens O95721 25416956
Intra
STX12 Q86Y82 SNAP29 Homo sapiens O95721 35271311
Intra
STX12 Q86Y82 MMGT1 Homo sapiens Q8N4V1 32296183
Intra
STX12 Q86Y82 MMGT1 Homo sapiens Q8N4V1 32296183
Intra
STX12 Q86Y82 MMGT1 Homo sapiens Q8N4V1 32296183
Intra
STX12 Q86Y82 TIMMDC1 Homo sapiens Q9NPL8 32296183
Intra
STX12 Q86Y82 TIMMDC1 Homo sapiens Q9NPL8 32296183
Intra
STX12 Q86Y82 TIMMDC1 Homo sapiens Q9NPL8 32296183
Intra
STX12 Q86Y82 TMX2 Homo sapiens Q9Y320 32296183
Intra
STX12 Q86Y82 TMX2 Homo sapiens Q9Y320 32296183
Intra
STX12 Q86Y82 TMX2 Homo sapiens Q9Y320 32296183
Intra
STX12 Q86Y82 STX1A Homo sapiens Q16623 32296183
Intra
STX12 Q86Y82 STX1A Homo sapiens Q16623 32296183
Intra
STX12 Q86Y82 PDZK1IP1 Homo sapiens Q13113 32296183
Intra
STX12 Q86Y82 PDZK1IP1 Homo sapiens Q13113 32296183
Intra
STX12 Q86Y82 DTX2 Homo sapiens Q86UW9 25416956
Intra
STX12 Q86Y82 DTX2 Homo sapiens Q86UW9 32296183
Intra
STX12 Q86Y82 DTX2 Homo sapiens Q86UW9 32296183
Intra
STX12 Q86Y82 STX4 Homo sapiens Q12846 28514442
Intra
STX12 Q86Y82 STX4 Homo sapiens Q12846 25416956
Intra
STX12 Q86Y82 STX4 Homo sapiens Q12846 32296183
Intra
STX12 Q86Y82 STX4 Homo sapiens Q12846 32296183
Intra
STX12 Q86Y82 STX4 Homo sapiens Q12846 33961781
Intra
STX12 Q86Y82 BCL2L13 Homo sapiens Q9BXK5 32296183
Intra
STX12 Q86Y82 BCL2L13 Homo sapiens Q9BXK5 32296183
Intra
STX12 Q86Y82 BCL2L13 Homo sapiens Q9BXK5 32296183
Intra
STX12 Q86Y82 KASH5 Homo sapiens Q8N6L0 32296183
Intra
STX12 Q86Y82 KASH5 Homo sapiens Q8N6L0 32296183
Intra
STX12 Q86Y82 KASH5 Homo sapiens Q8N6L0 32296183
Intra
STX12 Q86Y82 LEPROTL1 Homo sapiens O95214 32296183
Intra
STX12 Q86Y82 LEPROTL1 Homo sapiens O95214 32296183
Intra
STX12 Q86Y82 CD79A Homo sapiens P11912 32296183
Intra
STX12 Q86Y82 CD79A Homo sapiens P11912 32296183
Intra
STX12 Q86Y82 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
STX12 Q86Y82 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
STX12 Q86Y82 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
STX12 Q86Y82 ABCA1 Homo sapiens O95477
IF
15469992
Intra
STX12 Q86Y82 ABCA1 Homo sapiens O95477 15469992
Intra
STX12 Q86Y82 TMEM14B Homo sapiens Q9NUH8 32296183
Intra
STX12 Q86Y82 TMEM14B Homo sapiens Q9NUH8 32296183
Intra
STX12 Q86Y82 TMEM14B Homo sapiens Q9NUH8 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Xia-Gibbs Syndrome

Ahdc1-Related Intellectual Disability-Obstructive Sleep Apnea-Mild Dysmorphism Syndrome

XIGIS

Mrd25

Ahdc1-Related Intellectual Disability - Obstructive Sleep Apnea - Mild Dysmorphism Syndrome

Mental Retardation, Autosomal Dominant 25, Formerly

Mrd25, Formerly

Autosomal Dominant Mental Retardation 25

Autosomal Dominant Intellectual Disability 25

Xgs

Frontotemporal Dementia

Pallidopontonigral Degeneration

Frontotemporal Lobar Degeneration

Semantic Dementia

FTD

Frontotemporal Lobe Dementia

Multiple System Tauopathy With Presenile Dementia

Dementia, Frontotemporal

Frontotemporal Dementia With Parkinsonism

Mstd

Frontotemporal Lobar Degeneration With Tau Inclusions

Ftld With Tau Inclusions

Dementia, Frontotemporal, With Parkinsonism

Fldem

Ftdp17

Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex

Ddpac

Wilhelmsen-Lynch Disease

Wld

Ppnd

Dementia, Frontotemporal, With Or Without Parkinsonism

Semantic Primary Progressive Aphasia

Semantic Variant Ppa

Wilhemsen-Lynch Disease

Frontotemporal Dementia-Amyotrophic Lateral Sclerosis

Frontotemporal Dementia And Parkinsonism Linked To Chromosome 17

Ftd-Als

Ftld

Pick Complex

Pick Disease Of The Brain

Frontotemporal Dementia With Parkinsonism-17

Grn-Related Frontotemporal Dementia

Frontotemporal Dementia With Motor Neuron Disease

Dementia In Fronto-Temporal Lobar Degeneration

Ftd - [Frontotemporal Dementia]

Temple Dementia

Frontal Lobe Dementia

Hermansky-Pudlak Syndrome

Hps

Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial Cells

Hermanski-Pudlak Syndrome

Hermansky Pudlak Syndrome

Platelet Storage Pool Deficiency

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
Felis catus STX12 VGNC VGNC:65807
Canis familiaris STX12 VGNC VGNC:84434
Rattus norvegicus STX12 RGD RGD:620977
Bos taurus STX12 VGNC VGNC:35432
Mus musculus STX12 MGD MGI:1931027