SLFN12L - schlafen family member 12 like Gene

生物種: Homo sapiens

遺伝子タイプ: protein coding
遺伝子ID: 100506736

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

AlbA_2: Putative DNA-binding domain (218 - 346)

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  • 588 a.a.
Protein Preferred Names Protein Names

schlafen family member 12-like

関連疾患

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

Pre-clinical Phase

Bioactive Molecules (1)
製品番号 製品名
製品効果
純度
Rare Diseases
HY-RS13365 SLFN12L Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

生物種 Symbol 由来 ID
Rattus norvegicus SLFN12L RGD RGD:1308645
Others SLFN12L NCBI