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SLX4IP - SLX4 interacting protein Gene

Also Known as C20orf94; bA204H22.1; bA254M13.1; dJ1099D15.3

Species: Homo sapiens

Gene Type: protein coding

Gene ID: 128710

About SLX4IP

Cytogenetic location: 20p12.2 Genomic coordinates (GRCh38): 20:10,435,305-10,628,030 (from NCBI)

This gene has 2 transcripts (splice variants) and 145 orthologues. Ubiquitous expression in skin (RPKM 1.0), testis (RPKM 0.9) and 25 other tissues.

SLX4IP Products (1)

mRNA	Protein	Name
NM_001009608.3	NP_001009608.1	protein SLX4IP

Protein Preferred Names	Protein Names
protein SLX4IP

SLX4IP Protein-protein interaction Information

Type	Protein Name	Protein ID	Interactor	Interactor Species	Interactor ID	Detection Method	References
Intra	SLX4IP	Q5VYV7	SLX4	Homo sapiens	Q8IY92	Y2H	19596235
Intra	SLX4IP	Q5VYV7	SLX4	Homo sapiens	Q8IY92	Anti Tag CoIP	19596235

Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases	Alias
Myasthenic Syndrome, Congenital, 18	Congenital Myasthenic Syndrome 18 CMS18 Myasthenic Syndrome, Congenital, 18, With Intellectual Disability And Ataxia Myasthenic Syndrome, Congenital, 18 With Intellectual Disability And Ataxia Myasthenic Syndrome, Congenital, Type 18
Huntington Disease-Like 1	HDL1 Huntington-Like Neurodegenerative Disorder 1 Hln1 Huntington'S Disease-Like 1 Early-Onset Prion Disease With Prominent Psychiatric Features Huntington-Like Neurodegenerative Disorder, Autosomal Dominant Prion Disease, Early-Onset, With Prominent Psychiatric Features Autosomal Dominant Huntington-Like Neurodegenerative Disorder Huntington Disease-Like, Type 1
Congenital Ptosis	Congenital Blepharoptosis Congenital Eyelid Ptosis
Gerstmann-Straussler Disease	Gerstmann-Straussler-Scheinker Disease Gerstmann-Straussler-Scheinker Syndrome Prion Dementia Cerebral Amyloid Angiopathy, Prnp-Related GSD Gss Cerebellar Ataxia, Progressive Dementia, And Amyloid Deposits In Cns Amyloidosis, Cerebral, With Spongiform Encephalopathy Subacute Spongiform Encephalopathy, Gerstmann-Straussler Type Encephalopathy, Subacute Spongiform, Gerstmann-Straussler Type Amyloidosis Cerebral With Spongiform Encephalopathy Cerebellar Ataxia, Progressive Dementia, And Amyloid Deposits In The Central Nervous System Encephalopathy Subacute Spongiform Gerstmann-Straussler Type Gssd Gerstmann Straussler Scheinker Syndrome Cerebral Amyloidosis With Spongiform Encephalopathy Subacute Spongiform Encephalopathy Gerstmann-Straussler Type Gluthathione Synthetase Deficiency Gerstmann Straussler Syndrome

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

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS13390	SLX4IP Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	SLX4IP	MGD	MGI:1921493
Macaca mulatta	SLX4IP	VGNC	VGNC:77718
Canis familiaris	SLX4IP	VGNC	VGNC:54731
Felis catus	SLX4IP	VGNC	VGNC:65459
Bos taurus	SLX4IP	VGNC	VGNC:57024
Rattus norvegicus	SLX4IP	RGD	RGD:1563120
Others	SLX4IP	NCBI