L1TD1 - LINE1 type transposase domain containing 1 Gene

Also Known as ECAT11

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 54596

About L1TD1

This gene has 1 transcript (splice variant) and 1094 orthologues. Biased expression in placenta (RPKM 6.2), testis (RPKM 4.7) and 4 other tissues.

Summary

Predicted to enable single-stranded RNA binding activity. Predicted to be involved in transposition, RNA-mediated. Located in intracellular membrane-bounded organelle. [provided by Alliance of Genome Resources, Apr 2022]

L1TD1 Products (2)

mRNA Protein Name
NM_001164835.2 NP_001158307.1 LINE-1 type transposase domain-containing protein 1
NM_019079.5 NP_061952.3 LINE-1 type transposase domain-containing protein 1

L1TD1 Protein Structure

Transposase_22

Transposase_22: L1 transposable element RBD-like domain (216 - 322)

Transposase_22

Transposase_22: L1 transposable element RBD-like domain (529 - 862)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 865 a.a.
Protein Preferred Names Protein Names

LINE-1 type transposase domain-containing protein 1

  • ES cell-associated protein 11

L1TD1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
L1TD1 Q5T7N2 HNRNPA2B1 Homo sapiens P22626
Crosslink
30021884
Intra
L1TD1 Q5T7N2 HNRNPA2B1 Homo sapiens P22626
Anti Bait CoIP
25702638
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Testis Seminoma

  • Seminoma Of Testis

  • Seminoma Testis

  • Testicular Seminoma Pure

  • Seminoma
Inflammatory Bowel Disease 7

  • IBD7
Spastic Paraplegia 16, X-Linked

  • SPG16

  • Hereditary Spastic Paraplegia 16

  • X-Linked Spastic Paraplegia Type 16

  • Spastic Paraplegia 16, X-Linked, Complicated

  • X-Linked Spastic Paraplegia 16

  • Spastic Paraplegia 16

  • Spastic Paraplegia-16, X-Linked, Complicated
Spastic Paraplegia 12, Autosomal Dominant

  • SPG12

  • Hereditary Spastic Paraplegia 12

  • Autosomal Dominant Spastic Paraplegia Type 12

  • Autosomal Dominant Spastic Paraplegia 12

  • Spastic Paraplegia 12

  • Spastic Paraplegia-12

  • Paraplegia, Spastic, Autosomal Dominant, Type 12
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-RS07482 L1TD1 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Felis catus L1TD1 VGNC VGNC:107571
Mus musculus L1TD1 MGD MGI:3578435
Macaca mulatta L1TD1 VGNC VGNC:74125
Rattus norvegicus L1TD1 RGD RGD:1595093
Others L1TD1 NCBI