SLFN12L - schlafen family member 12 like Gene

Homo sapiens

Gene ID: 100506736 | Gene type: protein coding

About SLFN12L

Cytogenetic location: 17q12 Genomic coordinates (GRCh38): 17:35,464,254-35,537,678 (from NCBI)

This gene has 4 transcripts (splice variants), 100 orthologues and 6 paralogues. Broad expression in spleen (RPKM 1.6), lymph node (RPKM 1.2) and 20 other tissues.

Summary

Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

SLFN12L Products(2)

mRNA	Protein	Name
NM_001195790.3	NP_001182719.2	schlafen family member 12-like isoform 2
NM_001363830.2	NP_001350759.2	schlafen family member 12-like isoform 1

SLFN12L Protein Structure

AlbA_2

0
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588 a.a.

Protein Preferred Names

Protein Names

schlafen family member 12-like

Related Diseases

Diseases

Alias

Bleeding Disorder, Platelet-Type, 20

Platelet-Type Bleeding Disorder 20	BDPLT20
Autosomal Dominant Thrombocytopenia With Platelet Secretion Defect

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-RS13365	SLFN12L Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	SLFN12L	RGD	RGD:1308645

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