CLPP - caseinolytic mitochondrial matrix peptidase proteolytic subunit Gene

Also Known as DFNB81; PRLTS3

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 8192

About CLPP

Cytogenetic location: 19p13.3 Genomic coordinates (GRCh38): 19:6,361,531-6,370,242 (from NCBI)

This gene has 7 transcripts (splice variants), 196 orthologues and is associated with 3 phenotypes. Ubiquitous expression in kidney (RPKM 19.9), fat (RPKM 18.0) and 25 other tissues.

Summary

The protein encoded by this gene belongs to the peptidase family S14 and hydrolyzes proteins into small peptides in the presence of ATP and magnesium. The protein is transported into mitochondrial matrix and is associated with the inner mitochondrial membrane. [provided by RefSeq, Jul 2008]

CLPP Products (1)

mRNA Protein Name
NM_006012.4 NP_006003.1 ATP-dependent Clp protease proteolytic subunit, mitochondrial precursor
Molecular Function GO Annotation Evidence References Source
enables endopeptidase activity IDA
IDA: Inferred from direct assay
22354088 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
11923310 GOA
enables serine-type endopeptidase activity IDA
IDA: Inferred from direct assay
11923310 GOA
Biological Process GO Annotation Evidence References Source
involved in membrane protein proteolysis IDA
IDA: Inferred from direct assay
22354088 GOA
involved in proteolysis IDA
IDA: Inferred from direct assay
15522782 GOA
involved in proteolysis involved in protein catabolic process IDA
IDA: Inferred from direct assay
11923310 GOA
Cellular Component GO Annotation Evidence References Source
part of endopeptidase Clp complex IDA
IDA: Inferred from direct assay
11923310 GOA
part of endopeptidase Clp complex IPI
IPI: Inferred from physical interaction
15522782 GOA
located in mitochondrial matrix IDA
IDA: Inferred from direct assay
10525407 GOA
located in mitochondrion IDA
IDA: Inferred from direct assay
22354088 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

CLPP Protein Structure

CLP_protease

CLP_protease: Clp protease (68 - 246)

  • 0
  • 100
  • 200
  • 277 a.a.
Protein Preferred Names Protein Names

ATP-dependent Clp protease proteolytic subunit, mitochondrial

  • ATP-dependent protease ClpAP, proteolytic subunit, human

CLPP Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
CLPP Q16740 P4HA3 Homo sapiens Q7Z4N8 32296183
Intra
CLPP Q16740 TNPO3 Homo sapiens Q9Y5L0 32296183
Intra
CLPP Q16740 ABI2 Homo sapiens Q9NYB9-2 32296183
Intra
CLPP Q16740 C14orf119 Homo sapiens Q9NWQ9 32296183
Intra
CLPP Q16740 RBPMS Homo sapiens Q93062-3 32296183
Intra
CLPP Q16740 DTX2 Homo sapiens Q86UW9 32296183
Intra
CLPP Q16740 PLSCR4 Homo sapiens Q9NRQ2 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

CLPP Antibodies

Cat. No. Product Name Application Reactivity
HY-P81930 CLPP Antibody (YA1675) WB, IHC-P, IP Human, Mouse, Rat

Related Diseases

Diseases Alias
Perrault Syndrome 3
  • PRLTS3

  • Deafness, Autosomal Recessive 81, Formerly

  • Dfnb81, Formerly

  • Perrault Syndrome, Type 3

Perrault Syndrome
  • Gonadal Dysgenesis, Xx Type, With Deafness

  • Ovarian Dysgenesis With Sensorineural Deafness

  • Gonadal Dysgenesis, Xx Type

  • Gonadal Dysgenesis With Auditory Dysfunction, Autosomal Recessive Inheritance

  • Gonadal Dysgenesis With Sensorineural Deafness, Autosomal Recessive Inheritance

  • Xx Gonodal Dysgenesis-Deafness Syndrome

  • Xx Gonodal Dysgenesis-Hearing Loss Syndrome

  • Gonadal Dysgenesis Xx Type Deafness

Codas Syndrome
  • Cerebral, Ocular, Dental, Auricular, And Skeletal Anomalies Syndrome

  • Cerebral, Ocular, Dental, Auricular, And Skeletal Syndrome

  • Cerebro-Oculo-Dento-Auriculo-Skeletal Syndrome

  • Cerebrooculodentoauriculoskeletal Syndrome

  • CODASS

  • Cerebral, Ocular, Dental, Auricular, Skeletal Syndrome

Acute Laryngopharyngitis
  • Pharyngolaryngitis

  • Laryngopharyngitis

  • Hypopharyngitis

Learning Disability
  • Learning Disabilities

  • Learning Disorders

  • Academic Skill Disorder

  • Learning Disorder

Retinitis Pigmentosa 36
  • RP36

  • Retinitis Pigmentosa-36

  • Retinitis Pigmentosa, Type 36

Hereditary Spastic Paraplegia
  • Familial Spastic Paraplegia

  • Hereditary Spastic Paraparesis

  • Strumpell-Lorrain Disease

  • Familial Spastic Paraparesis

  • Hsp

  • Spg

  • Strümpell-Lorrain Disease

  • Spastic Paraplegia, Hereditary

  • French Settlement Disease

  • Strumpell-Lorrain Syndrome

  • Fsp

  • Spastic Paraplegia, Familial

  • Spastic Paraplegia Hereditary

  • Spastic Paraplegia 3, Autosomal Dominant

  • Spastic Paraparesis

  • Hereditary Spastic Paralysis

  • Familial Spastic Paralysis

  • Hereditary Spastic Ataxia

Pyosalpinx
  • Pyosalpingitis

Multiple Synostoses Syndrome
  • Symphalangism-Brachydactyly Syndrome

  • Deafness-Hermann Type Symphalangism Syndrome

  • Facio-Audio-Symphalangism

  • Hearing Loss-Hermann Type Symphalangism Syndrome

  • Wl Syndrome

  • Multiple Synostosis Syndrome

Myasthenic Syndrome, Congenital, 12
  • Congenital Myasthenic Syndrome 12

  • CMS12

  • Myasthenic Syndrome, Congenital, With Tubular Aggregates 1

  • Cmsta1

  • Myasthenia, Congenital, 12, With Tubular Aggregates

  • Congenital Myasthenia 12 With Tubular Aggregates

  • Limb-Girdle Myasthenia With Tubular Aggregates

  • Myasthenia, Congenital, With Tubular Aggregates 1

  • Myasthenic Syndrome, Congenital, With Tubular Aggregates, 1

46 Xx Gonadal Dysgenesis
  • Ovarian Dysgenesis

  • Gonadal Dysgenesis, 46,Xx

  • Dysgenesis, Ovarian

Intellectual Developmental Disorder, Autosomal Dominant 30, With Speech Delay And Behavioral Abnormalities
  • MRD30

  • Mental Retardation, Autosomal Dominant 30

  • Intellectual Developmental Disorder, Autosomal Dominant 30

  • Autosomal Dominant Non-Syndromic Intellectual Disability 30

  • Autosomal Dominant Intellectual Developmental Disorder 30

  • Autosomal Dominant Mental Retardation 30

  • Mental Retardation, Autosomal Dominant, Type 30

Premature Menopause
  • Primary Ovarian Insufficiency

  • Premature Ovarian Failure

  • Hypergonadotropic Hypogonadism

  • Premature Ovarian Insufficiency

  • Menopause - Premature

  • Menopause Praecox

  • Menopause Premature

  • Menopause, Premature

  • Female Hypergonadotropic Hypogonadism

  • Hypergonadotrophic Ovarian Failure

  • Primary Female Hypogonadism

  • Pof - [Premature Ovarian Failure]

  • Ovarian Failure

  • Ovarian Secretion Suppression

  • Ovary Hyposecretion

  • Ovary Secretion Deficiency

  • Premature Menopause Nos

Mitochondrial Dna Depletion Syndrome 7
  • Ohaha Syndrome

  • Infantile Onset Spinocerebellar Ataxia

  • Iosca

  • Infantile-Onset Spinocerebellar Ataxia

  • Spinocerebellar Ataxia 8

  • MTDPS7

  • Ophthalmoplegia, Hypotonia, Ataxia, Hypacusis, And Athetosis

  • Ophthalmoplegia-Hypotonia-Ataxia-Hypoacusis-Athetosis Syndrome

  • Sca8

  • Spinocerebellar Ataxia Infantile With Sensory Neuropathy

  • Spinocerebellar Ataxia, Infantile-Onset

  • Ophthalmoplegia, Hypotonia, Ataxia, Hypoacusis, And Athetosis

  • Spinocerebellar Ataxia, Infantile, With Sensory Neuropathy

  • Spinocerebellar Ataxia 8, Formerly

  • Sca8, Formerly

  • Iosca, Mitochondrial Dna Depletion Syndrome 7

  • Ophthalmoplegia - Hypotonia - Ataxia - Hypoacusis - Athetosis

  • Mitochondrial Dna Depletion Syndrome, Hepatocerebrorenal Form

  • Mtdna Depletion Syndrome, Hepatocerebrorenal Form

  • Mitochondrial Dna Depletion Syndrome 7 Hepatocerebral Type

  • Ophthalmoplegia Hypotonia Ataxia Hypoacusis And Athetosis

  • Pure Spinocerebellar Ataxia Japanese Type

  • Sca4 Pure Japanese Type

  • Spinocerebellar Ataxia Infantile-Onset

  • Mitochondrial Dna Depletion Syndrome , Type 7

Sensorineural Hearing Loss
  • Sensory Hearing Loss

  • Sensorineural Deafness

  • Sensorineural Hearing Loss Disorder

  • Hearing Loss, Sensorineural

  • Central Hearing Loss

  • High Frequency Deafness

  • High Frequency Hearing Loss

  • High-Frequency Hearing Loss

  • Perceptive Deafness

  • Perceptive Hearing Loss

  • Perceptive Hearing Loss Or Deafness

  • Hearing Loss Sensorineural

  • Deafness Sensorineural

  • Hearing Loss High-Frequency

  • Hearing Loss, Central

  • Hearing Loss, High-Frequency

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

Orthologs Information

Species Symbol Source ID
Canis familiaris CLPP VGNC VGNC:39356
Felis catus CLPP VGNC VGNC:60973
Bos taurus CLPP VGNC VGNC:27459
Macaca mulatta CLPP VGNC VGNC:71263
Mus musculus CLPP MGD MGI:1858213
Rattus norvegicus CLPP RGD RGD:1588583
Others CLPP NCBI