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  2. MPPED2 - metallophosphoesterase domain containing 2 Gene

MPPED2 - metallophosphoesterase domain containing 2 Gene

Homo sapiens

Also known as 239FB; C11orf8

Gene ID: 744 | Gene type: protein coding

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

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

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