RPPH1 - ribonuclease P RNA component H1 Gene

ADC Targets in Oncology

2026-04-10

Also Known as H1RNA; RPPH1-1

Species: Homo sapiens

Gene Type: ncRNA

Gene ID: 85495

About RPPH1

Cytogenetic location: 14q11.2 Genomic coordinates (GRCh38): 14:20,343,071-20,343,411 (from NCBI)

This gene has 1 transcript (splice variant).

Summary

H1RNA is the RNA component of the RNase P ribonucleoprotein, an endoribonuclease that cleaves tRNA precursor molecules to form the mature 5-prime termini of their tRNA sequences (Baer et al., 1989 [PubMed 2308839]).[supplied by OMIM, Mar 2008]

Diseases	Alias
Visual Epilepsy	Seizures Epilepsy, Visual Visual Seizure Acute Symptomatic Seizure Provoked Seizure Nonepileptic Seizure Disorder Uncontrolled Seizures Seizure Nos Fits Nos Onset Seizure Nos Seizure Disturbance
Hereditary Spastic Paraplegia 51	Autosomal Dominant Spastic Paraplegia 51 Cpsq4 Spastic Quadriplegic Cerebral Palsy 4 Spg51 Spastic Paraplegia 51, Autosomal Recessive
Anauxetic Dysplasia 1	Anauxetic Dysplasia Spondylometaepiphyseal Dysplasia, Menger Type Spondylometaepiphyseal Dysplasia, Anauxetic Type Spondyloepimetaphyseal Dysplasia, Anauxetic Type ANXD1 Anxd Spondylometaepiphyseal Dysplasia Anauxetic Type Spondylometaepiphyseal Dysplasia Menger Type Ad Spondyloepimetaphyseal Dysplasia, Menger Type Dysplasia, Anauxetic, Type 1

Diseases

Alias

Visual Epilepsy

Seizures
Epilepsy, Visual
Visual Seizure
Acute Symptomatic Seizure
Provoked Seizure
Nonepileptic Seizure Disorder
Uncontrolled Seizures
Seizure Nos
Fits Nos
Onset Seizure Nos
Seizure Disturbance

Hereditary Spastic Paraplegia 51

Autosomal Dominant Spastic Paraplegia 51
Cpsq4
Spastic Quadriplegic Cerebral Palsy 4
Spg51
Spastic Paraplegia 51, Autosomal Recessive

Anauxetic Dysplasia 1

Anauxetic Dysplasia
Spondylometaepiphyseal Dysplasia, Menger Type
Spondylometaepiphyseal Dysplasia, Anauxetic Type
Spondyloepimetaphyseal Dysplasia, Anauxetic Type
ANXD1
Anxd
Spondylometaepiphyseal Dysplasia Anauxetic Type
Spondylometaepiphyseal Dysplasia Menger Type
Ad
Spondyloepimetaphyseal Dysplasia, Menger Type
Dysplasia, Anauxetic, Type 1

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

Diseases

Alias

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Pre-clinical Phase

Bioactive Molecules (3)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS11667	RAPH1 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown
HY-RS12213	RPP21 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown
HY-RS12302	RSPH1 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown