MPPED2 - metallophosphoesterase domain containing 2 Gene

Also Known as 239FB; C11orf8

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 744

About MPPED2

Cytogenetic location: 11p14.1 Genomic coordinates (GRCh38): 11:30,384,079-30,586,993 (from NCBI)

This gene has 8 transcripts (splice variants), 135 orthologues and 1 paralogue. Biased expression in thyroid (RPKM 4.7), prostate (RPKM 2.5) and 11 other tissues.

Summary

This gene likely encodes a metallophosphoesterase. The encoded protein may play a role a brain development. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2009]

MPPED2 Products (7)

mRNA Protein Name
NM_001145399.3 NP_001138871.1 metallophosphoesterase MPPED2 isoform 2
NM_001377952.1 NP_001364881.1 metallophosphoesterase MPPED2 isoform 1
NM_001377953.1 NP_001364882.1 metallophosphoesterase MPPED2 isoform 1
NM_001377954.1 NP_001364883.1 metallophosphoesterase MPPED2 isoform 1
NM_001377955.1 NP_001364884.1 metallophosphoesterase MPPED2 isoform 1
NM_001377956.1 NP_001364885.1 metallophosphoesterase MPPED2 isoform 2
NM_001584.3 NP_001575.1 metallophosphoesterase MPPED2 isoform 1
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
19060904 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

MPPED2 Protein Structure

Metallophos

Metallophos: Calcineurin-like phosphoesterase (74 - 255)

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

metallophosphoesterase MPPED2

  • fetal brain protein 239

MPPED2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
MPPED2 Q15777 CAGE1 Homo sapiens Q8TC20 25416956
Intra
MPPED2 Q15777 CAGE1 Homo sapiens Q8TC20 25416956
Intra
MPPED2 Q15777 FAM72A Homo sapiens Q5TYM5 25416956
Intra
MPPED2 Q15777 RIBC1 Homo sapiens Q8N443 32296183
Intra
MPPED2 Q15777 RIBC1 Homo sapiens Q8N443 32296183
Intra
MPPED2 Q15777 RIBC1 Homo sapiens Q8N443 32296183
Intra
MPPED2 Q15777 NUP93 Homo sapiens Q8N1F7 32296183
Intra
MPPED2 Q15777 NUP93 Homo sapiens Q8N1F7 32296183
Intra
MPPED2 Q15777 NUP93 Homo sapiens Q8N1F7 32296183
Intra
MPPED2 Q15777 HOOK2 Homo sapiens Q96ED9-2 32296183
Intra
MPPED2 Q15777 HOOK2 Homo sapiens Q96ED9-2 32296183
Intra
MPPED2 Q15777 HOOK2 Homo sapiens Q96ED9-2 32296183
Intra
MPPED2 Q15777 CAGE1 Homo sapiens Q8TC20-4 32296183
Intra
MPPED2 Q15777 CAGE1 Homo sapiens Q8TC20-4 32296183
Intra
MPPED2 Q15777 CAGE1 Homo sapiens Q8TC20-4 32296183
Intra
MPPED2 Q15777 MBD3L1 Homo sapiens Q8WWY6 32296183
Intra
MPPED2 Q15777 MBD3L1 Homo sapiens Q8WWY6 32296183
Intra
MPPED2 Q15777 MBD3L1 Homo sapiens Q8WWY6 32296183
Intra
MPPED2 Q15777 BEX4 Homo sapiens Q9NWD9 32296183
Intra
MPPED2 Q15777 BEX4 Homo sapiens Q9NWD9 32296183
Intra
MPPED2 Q15777 BEX4 Homo sapiens Q9NWD9 32296183
Intra
MPPED2 Q15777 VAC14 Homo sapiens Q08AM6 32296183
Intra
MPPED2 Q15777 VAC14 Homo sapiens Q08AM6 32296183
Intra
MPPED2 Q15777 TRIP13 Homo sapiens Q15645 19060904
Intra
MPPED2 Q15777 TRIP13 Homo sapiens Q15645 32296183
Intra
MPPED2 Q15777 TRIP13 Homo sapiens Q15645 25416956
Intra
MPPED2 Q15777 TRIP13 Homo sapiens Q15645 25416956
Intra
MPPED2 Q15777 TRIP13 Homo sapiens Q15645 32296183
Intra
MPPED2 Q15777 TRIP13 Homo sapiens Q15645 19060904
Intra
MPPED2 Q15777 POMP Homo sapiens Q9Y244 32296183
Intra
MPPED2 Q15777 POMP Homo sapiens Q9Y244 32296183
Intra
MPPED2 Q15777 POMP Homo sapiens Q9Y244 32296183
Intra
MPPED2 Q15777 RXRG Homo sapiens P48443 32296183
Intra
MPPED2 Q15777 RXRG Homo sapiens P48443 32296183
Intra
MPPED2 Q15777 RXRG Homo sapiens P48443 25416956
Intra
MPPED2 Q15777 RXRG Homo sapiens P48443 25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Wilms Tumor, Aniridia, Genitourinary Anomalies, And Mental Retardation Syndrome
  • Wagr Syndrome

  • 11p Partial Monosomy Syndrome

  • Chromosome 11p13 Deletion Syndrome

  • Wilms Tumor, Aniridia, Genitourinary Anomalies And Mental Retardation Syndrome

  • 11p Deletion Syndrome

  • Chromosome 11p Deletion Syndrome

  • Wagr Complex

  • Wilms Tumor-Aniridia-Genitourinary Anomalies-Intellectual Disability Syndrome

  • Deletion 11p13

  • WAGR

  • Wilms Tumor-Aniridia-Genitourinary Anomalies-Mental Retardation Syndrome

  • Chromosome 11p Deletion

  • 11p Deletion

  • 11p Monosomy

  • Deletion 11p

  • Monosomy 11p

  • Partial Monosomy 11p

  • Agr Triad

  • Wilms Tumor-Aniridia-Gonadoblastoma-Mental Retardation Syndrome

  • Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation Syndrome

  • Wagr Contiguous Gene Syndrome

  • Wilms Tumor-Aniridia-Genital Anomalies-Retardation Syndrome

  • Wilms Tumor-Aniridia-Genitourinary Anomalies-Mr Syndrome

  • Del(11)(P13)

  • Monosomy 11p13

  • Chromosome 11, Deletion 11p

Aniridia 1
  • Aniridia

  • Congenital Aniridia

  • AN1

  • An

  • Cataract With Late-Onset Corneal Dystrophy

  • Aplasia Of Iris

  • Absent Iris

  • Irideremia

  • Aniridia Ii, Formerly

  • An2, Formerly

  • An2

  • Aniridia Type Ii

  • Aniridia, Type 1

  • An-1

  • Absence Of Iris

  • Agenesis Of Iris

  • Congenital Absence Of Iris

  • Hereditary Aniridia

  • Sporadic Aniridia

Urofacial Syndrome 1
  • Urofacial Syndrome

  • Ochoa Syndrome

  • Hydronephrosis With Peculiar Facial Expression

  • Ufs

  • Inverted Smile And Occult Neuropathic Bladder

  • Partial Facial Palsy With Urinary Abnormalities

  • UFS1

  • Urofacial Ochoa'S Syndrome

  • Urofacial Syndrome Type 1

  • Facial Palsy, Partial, With Urinary Abnormalities

  • Hydronephrosis-Inverted Smile

  • Inverted Smile-Neurogenic Bladder

  • Hydronephrosis-Inverted Smile Syndrome

  • Inverted Smile-Neurogenic Bladder Syndrome

  • Partial Facial Palsy Partial With Urinary Abnormalities

  • Urologic Diseases

Iris Disease
  • Iris Diseases

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 MPPED2 VGNC VGNC:43350
Macaca mulatta MPPED2 VGNC VGNC:74727
Rattus norvegicus MPPED2 RGD RGD:735060
Felis catus MPPED2 VGNC VGNC:63575
Bos taurus MPPED2 VGNC VGNC:31588
Mus musculus MPPED2 MGD MGI:1924265
Others MPPED2 NCBI