SLX4IP - SLX4 interacting protein Gene

Homo sapiens

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

Gene ID: 128710 | Gene type: protein coding

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.

mRNA	Protein	Name
NM_001009608.3	NP_001009608.1	protein SLX4IP

Protein Preferred Names

Protein Names

protein SLX4IP

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

Pre-clinical Phase

Bioactive Molecules (1)

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

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

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