PLEKHH2 - pleckstrin homology, MyTH4 and FERM domain containing H2 Gene

Also Known as PLEKHH1L

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 130271

About PLEKHH2

Cytogenetic location: 2p21 Genomic coordinates (GRCh38): 2:43,637,260-43,767,987 (from NCBI)

This gene has 8 transcripts (splice variants), 195 orthologues and 1 paralogue. Broad expression in lung (RPKM 15.4), endometrium (RPKM 10.8) and 21 other tissues.

Summary

Predicted to enable actin binding activity. Predicted to be involved in negative regulation of actin filament depolymerization. Located in several cellular components, including cytosol; lamellipodium; and nuclear body. [provided by Alliance of Genome Resources, Apr 2022]

PLEKHH2 Products (1)

mRNA Protein Name
NM_172069.4 NP_742066.2 pleckstrin homology domain-containing family H member 2

Gene Ontology

  • Molecular Function
  • Cellular Component
Molecular Function GO Annotation Evidence Références Source
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
Cellular Component GO Annotation Evidence Références Source
located in cytoplasm IDA
IDA: Inferred from direct assay
22832517 GOA
located in lamellipodium IDA
IDA: Inferred from direct assay
22832517 GOA
located in plasma membrane IDA
IDA: Inferred from direct assay
22832517 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

PLEKHH2 Protein Structure

PH

PH: PH domain (705 - 796)

MyTH4

MyTH4: MyTH4 domain (999 - 1109)

FERM_M

FERM_M: FERM central domain (1235 - 1354)

  • 0
  • 300
  • 600
  • 900
  • 1200
  • 1493 a.a.
Protein Preferred Names Protein Names

pleckstrin homology domain-containing family H member 2

  • pleckstrin homology domain containing, family H (with MyTH4 domain) member 2

PLEKHH2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Références
Intra
PLEKHH2 Q8IVE3 LPXN Homo sapiens O60711
Y2H Prey Pooling
25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Focal Segmental Glomerulosclerosis

  • Familial Idiopathic Steroid-Resistant Nephrotic Syndrome

  • Focal Glomerulosclerosis

  • Fsgs

  • Segmental Glomerulosclerosis

  • Glomerulosclerosis, Focal Segmental

  • Fgs

  • Focal Glomerular Sclerosis

  • Familial Idiopathic Nephrotic Syndrome

  • Focal Sclerosis With Hyalinosis

  • Glomerulosclerosis, Focal

  • Glomerulosclerosis Focal

  • Glomerulosclerosis, Segmental, Focal

  • Focal Segmental Glomerulosclerosis, Not Otherwise Specified
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. Nom du produit
Effect
Pureté
Rare Diseases
HY-RS10696 PLEKHH2 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Canis familiaris PLEKHH2 VGNC VGNC:44683
Felis catus PLEKHH2 VGNC VGNC:64234
Bos taurus PLEKHH2 VGNC VGNC:33021
Macaca mulatta PLEKHH2 VGNC VGNC:76146
Mus musculus PLEKHH2 MGD MGI:2146813
Rattus norvegicus PLEKHH2 RGD RGD:1304935
Others PLEKHH2 NCBI