MAPRE3 - microtubule associated protein RP/EB family member 3 Gene

Also Known as EB3; RP3; EBF3; EBF3-S

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 22924

About MAPRE3

Cytogenetic location: 2p23.3 Genomic coordinates (GRCh38): 2:26,970,637-27,027,219 (from NCBI)

This gene has 10 transcripts (splice variants), 279 orthologues and 2 paralogues. Broad expression in brain (RPKM 45.3), testis (RPKM 13.7) and 20 other tissues.

Summary

The protein encoded by this gene is a member of the RP/EB family of genes. The protein localizes to the cytoplasmic microtubule network and binds APCL, a homolog of the adenomatous polyposis coli tumor suppressor gene. [provided by RefSeq, Jul 2008]

MAPRE3 Products (3)

mRNA Protein Name
NM_001303050.2 NP_001289979.1 microtubule-associated protein RP/EB family member 3 isoform 1
NM_001410716.1 NP_001397645.1 microtubule-associated protein RP/EB family member 3 isoform 2
NM_012326.4 NP_036458.2 microtubule-associated protein RP/EB family member 3 isoform 1
Molecular Function GO Annotation Evidence References Source
enables identical protein binding IPI
IPI: Inferred from physical interaction
27107012 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
10644998 GOA
enables protein kinase binding IPI
IPI: Inferred from physical interaction
26323690 GOA
Biological Process GO Annotation Evidence References Source
involved in positive regulation of protein kinase activity IDA
IDA: Inferred from direct assay
26323690 GOA
involved in regulation of microtubule polymerization IMP
IMP: Inferred from mutant phenotype
23159740 GOA
Cellular Component GO Annotation Evidence References Source
colocalizes with cytoplasmic microtubule IDA
IDA: Inferred from direct assay
10644998 GOA
located in microtubule cytoskeleton IDA
IDA: Inferred from direct assay
10644998 GOA
located in mitotic spindle astral microtubule end IDA
IDA: Inferred from direct assay
23509069 GOA
located in perinuclear region of cytoplasm IDA
IDA: Inferred from direct assay
10644998 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

MAPRE3 Protein Structure

CH

CH: Calponin homology (CH) domain (18 - 115)

EB1

EB1: EB1-like C-terminal motif (218 - 257)

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

microtubule-associated protein RP/EB family member 3

  • APC binding protein

MAPRE3 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
MAPRE3 Q9UPY8 MAPRE1 Homo sapiens Q15691
SLC
27107012
Intra
MAPRE3 Q9UPY8 MAPRE1 Homo sapiens Q15691 31515488
Intra
MAPRE3 Q9UPY8 MAPRE1 Homo sapiens Q15691 25416956
Intra
MAPRE3 Q9UPY8 MAPRE1 Homo sapiens Q15691 32296183
Intra
MAPRE3 Q9UPY8 MAPRE1 Homo sapiens Q15691 25416956
Intra
MAPRE3 Q9UPY8 MAPRE1 Homo sapiens Q15691
Y2H
27107012
Intra
MAPRE3 Q9UPY8 MAPRE1 Homo sapiens Q15691 27107012
Intra
MAPRE3 Q9UPY8 MAPRE1 Homo sapiens Q15691 32296183
Intra
MAPRE3 Q9UPY8 CRTAC1 Homo sapiens Q9NQ79 32296183
Intra
MAPRE3 Q9UPY8 CRTAC1 Homo sapiens Q9NQ79 32296183
Intra
MAPRE3 Q9UPY8 GTF2F2 Homo sapiens P13984 32296183
Intra
MAPRE3 Q9UPY8 GTF2F2 Homo sapiens P13984 32296183
Intra
MAPRE3 Q9UPY8 APC2 Homo sapiens O95996 10644998
Intra
MAPRE3 Q9UPY8 APC2 Homo sapiens O95996 10644998
Intra
MAPRE3 Q9UPY8 REL Homo sapiens Q04864-2 32296183
Intra
MAPRE3 Q9UPY8 REL Homo sapiens Q04864-2 32296183
Intra
MAPRE3 Q9UPY8 ZNF526 Homo sapiens Q8TF50 32296183
Intra
MAPRE3 Q9UPY8 ZNF526 Homo sapiens Q8TF50 32296183
Intra
MAPRE3 Q9UPY8 HROB Homo sapiens Q8N3J3-3 32296183
Intra
MAPRE3 Q9UPY8 HROB Homo sapiens Q8N3J3-3 32296183
Intra
MAPRE3 Q9UPY8 FOXD4L1 Homo sapiens Q9NU39 32296183
Intra
MAPRE3 Q9UPY8 FOXD4L1 Homo sapiens Q9NU39 32296183
Intra
MAPRE3 Q9UPY8 IKZF1 Homo sapiens Q13422-7 32296183
Intra
MAPRE3 Q9UPY8 IKZF1 Homo sapiens Q13422-7 32296183
Intra
MAPRE3 Q9UPY8 SIAH1 Homo sapiens Q8IUQ4-2 32296183
Intra
MAPRE3 Q9UPY8 SIAH1 Homo sapiens Q8IUQ4-2 32296183
Intra
MAPRE3 Q9UPY8 TLE5 Homo sapiens Q08117-2 32296183
Intra
MAPRE3 Q9UPY8 TLE5 Homo sapiens Q08117-2 32296183
Intra
MAPRE3 Q9UPY8 LMO2 Homo sapiens P25791-3 32296183
Intra
MAPRE3 Q9UPY8 LMO2 Homo sapiens P25791-3 32296183
Intra
MAPRE3 Q9UPY8 SPMIP2 Homo sapiens Q96LM5 32296183
Intra
MAPRE3 Q9UPY8 SPMIP2 Homo sapiens Q96LM5 32296183
Intra
MAPRE3 Q9UPY8 YAF2 Homo sapiens Q8IY57-5 32296183
Intra
MAPRE3 Q9UPY8 YAF2 Homo sapiens Q8IY57-5 32296183
Intra
MAPRE3 Q9UPY8 CHRDL2 Homo sapiens Q6WN34-2 32296183
Intra
MAPRE3 Q9UPY8 CHRDL2 Homo sapiens Q6WN34-2 32296183
Intra
MAPRE3 Q9UPY8 ZNF547 Homo sapiens Q8IVP9 32296183
Intra
MAPRE3 Q9UPY8 ZNF547 Homo sapiens Q8IVP9 32296183
Intra
MAPRE3 Q9UPY8 FOXD4L4 Homo sapiens Q8WXT5 32296183
Intra
MAPRE3 Q9UPY8 FOXD4L4 Homo sapiens Q8WXT5 32296183
Intra
MAPRE3 Q9UPY8 ZC2HC1C Homo sapiens Q53FD0-2 32296183
Intra
MAPRE3 Q9UPY8 ZC2HC1C Homo sapiens Q53FD0-2 32296183
Intra
MAPRE3 Q9UPY8 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
MAPRE3 Q9UPY8 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
MAPRE3 Q9UPY8 POU4F1 Homo sapiens Q01851 32296183
Intra
MAPRE3 Q9UPY8 POU4F1 Homo sapiens Q01851 32296183
Intra
MAPRE3 Q9UPY8 TRAIP Homo sapiens Q9BWF2 32296183
Intra
MAPRE3 Q9UPY8 TRAIP Homo sapiens Q9BWF2 32296183
Intra
MAPRE3 Q9UPY8 CCSER1 Homo sapiens Q9C0I3-2 32296183
Intra
MAPRE3 Q9UPY8 CCSER1 Homo sapiens Q9C0I3-2 32296183
Intra
MAPRE3 Q9UPY8 SPMIP10 Homo sapiens Q6ZNM6 32296183
Intra
MAPRE3 Q9UPY8 SPMIP10 Homo sapiens Q6ZNM6 32296183
Intra
MAPRE3 Q9UPY8 C20orf202 Homo sapiens A1L168 32296183
Intra
MAPRE3 Q9UPY8 C20orf202 Homo sapiens A1L168 32296183
Intra
MAPRE3 Q9UPY8 LAP3 Homo sapiens P28838 32296183
Intra
MAPRE3 Q9UPY8 LAP3 Homo sapiens P28838 32296183
Intra
MAPRE3 Q9UPY8 TRIM14 Homo sapiens Q14142 32296183
Intra
MAPRE3 Q9UPY8 TRIM14 Homo sapiens Q14142 32296183
Intra
MAPRE3 Q9UPY8 LHX4 Homo sapiens Q969G2 32296183
Intra
MAPRE3 Q9UPY8 LHX4 Homo sapiens Q969G2 32296183
Intra
MAPRE3 Q9UPY8 TXN2 Homo sapiens Q99757 25416956
Intra
MAPRE3 Q9UPY8 TXN2 Homo sapiens Q99757 25416956
Intra
MAPRE3 Q9UPY8 MRPL12 Homo sapiens P52815 32296183
Intra
MAPRE3 Q9UPY8 MRPL12 Homo sapiens P52815 32296183
Intra
MAPRE3 Q9UPY8 PSMA1 Homo sapiens P25786 25416956
Intra
MAPRE3 Q9UPY8 MAPT Homo sapiens P10636 30668577
Intra
MAPRE3 Q9UPY8 PSMB1 Homo sapiens P20618 25416956
Intra
MAPRE3 Q9UPY8 KNSTRN Homo sapiens Q9Y448 32296183
Intra
MAPRE3 Q9UPY8 KNSTRN Homo sapiens Q9Y448 32296183
Intra
MAPRE3 Q9UPY8 KNSTRN Homo sapiens Q9Y448 32296183
Intra
MAPRE3 Q9UPY8 EIF4E2 Homo sapiens O60573 25416956
Intra
MAPRE3 Q9UPY8 EIF4E2 Homo sapiens O60573 25416956
Intra
MAPRE3 Q9UPY8 ZC2HC1A Homo sapiens Q96GY0 32296183
Intra
MAPRE3 Q9UPY8 ZC2HC1A Homo sapiens Q96GY0 32296183
Intra
MAPRE3 Q9UPY8 ANKRD1 Homo sapiens Q15327 32296183
Intra
MAPRE3 Q9UPY8 ANKRD1 Homo sapiens Q15327 32296183
Intra
MAPRE3 Q9UPY8 FAM161B Homo sapiens Q96MY7 32296183
Intra
MAPRE3 Q9UPY8 FAM161B Homo sapiens Q96MY7 32296183
Intra
MAPRE3 Q9UPY8 SDCBP Homo sapiens O00560 32296183
Intra
MAPRE3 Q9UPY8 SDCBP Homo sapiens O00560 25416956
Intra
MAPRE3 Q9UPY8 SDCBP Homo sapiens O00560 32296183
Intra
MAPRE3 Q9UPY8 SDCBP Homo sapiens O00560 25416956
Intra
MAPRE3 Q9UPY8 PSRC1 Homo sapiens Q6PGN9 32296183
Intra
MAPRE3 Q9UPY8 PSRC1 Homo sapiens Q6PGN9 32296183
Intra
MAPRE3 Q9UPY8 LMO2 Homo sapiens P25791 25416956
Intra
MAPRE3 Q9UPY8 LMO2 Homo sapiens P25791 25416956
Intra
MAPRE3 Q9UPY8 MAPRE2 Homo sapiens Q15555 32296183
Intra
MAPRE3 Q9UPY8 MAPRE2 Homo sapiens Q15555 31515488
Intra
MAPRE3 Q9UPY8 MAPRE2 Homo sapiens Q15555 32296183
Intra
MAPRE3 Q9UPY8 APPL2 Homo sapiens Q8NEU8 25814554
Intra
MAPRE3 Q9UPY8 DDIT4L Homo sapiens Q96D03 32296183
Intra
MAPRE3 Q9UPY8 DDIT4L Homo sapiens Q96D03 32296183
Cross
MAPRE3 Q9UPY8 Map1b Mus musculus P14873 23572079
Cross
MAPRE3 Q9UPY8 Map1b Mus musculus P14873 23572079
Cross
MAPRE3 Q9UPY8 Map1b Mus musculus P14873 23572079
Cross
MAPRE3 Q9UPY8 Srcin1 Mus musculus Q9QWI6-2 19146815
Cross
MAPRE3 Q9UPY8 Srcin1 Mus musculus Q9QWI6-2 19146815
Cross
MAPRE3 Q9UPY8 Srcin1 Mus musculus Q9QWI6-2
IF
19146815
Intra
MAPRE3 Q9UPY8 PICK1 Homo sapiens Q9NRD5 32296183
Intra
MAPRE3 Q9UPY8 PICK1 Homo sapiens Q9NRD5 32296183
Intra
MAPRE3 Q9UPY8 GAS2L2 Homo sapiens Q8NHY3 32296183
Intra
MAPRE3 Q9UPY8 GAS2L2 Homo sapiens Q8NHY3 32296183
Intra
MAPRE3 Q9UPY8 JUN Homo sapiens P05412 20195357
Intra
MAPRE3 Q9UPY8 JUN Homo sapiens P05412
TAP
20195357
Intra
MAPRE3 Q9UPY8 KLHDC7B Homo sapiens Q96G42 32296183
Intra
MAPRE3 Q9UPY8 KLHDC7B Homo sapiens Q96G42 32296183
Intra
MAPRE3 Q9UPY8 MARCHF7 Homo sapiens Q9H992 32296183
Intra
MAPRE3 Q9UPY8 MARCHF7 Homo sapiens Q9H992 32296183
Intra
MAPRE3 Q9UPY8 PDE4DIP Homo sapiens Q5VU43-2 32296183
Intra
MAPRE3 Q9UPY8 PDE4DIP Homo sapiens Q5VU43-2 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant MAPRE3 Proteins

Cat. No. Product Name Accession Purity
HY-P75275 EB3/MAPRE3 Protein, Human (His) Q9UPY8-1 (M1-Y281) ≥ 95%, as determined by reducing SDS-PAGE.

MAPRE3 Antibodies

Cat. No. Product Name Application Reactivity
HY-P82030 EB3 Antibody (YA1775) WB, IHC-P, ICC/IF, FC Human, Mouse, Rat

Related Diseases

Diseases Alias
Distal Hereditary Motor Neuronopathy Type 7
  • Dhmn7

  • Dhmnvpy

  • Distal Spinal Muscular Atrophy With Vocal Cord Paralysis

Neuronopathy, Distal Hereditary Motor, Type Viib
  • HMN7B

  • Hmn Viib

  • Dhmn7b

  • Neuropathy, Distal Hereditary Motor, Type Viib

  • Distal Hereditary Motor Neuronopathy Type 7b

  • Distal Hereditary Motor Neuropathy Type Viib

  • Neuronopathy, Distal Hereditary Motor, Type 7b

  • Neuropathy, Distal Hereditary Motor, With Vocal Cord Paralysis, Type Viib

  • Lower Motor Neuron Disease, Dynactin Type

  • Distal Spinal Muscular Atrophy With Vocal Cord Paralysis Type 7b

  • Harper-Young Myopathy

  • Neuronopathy, Distal Hereditary Motor, 7b

  • Distal Hereditary Motor Neuropathy With Vocal Cord Paralysis Type Viib

  • Lower Motor Neuron Disease Dynactin Type

  • Plmnd

  • Progressive Lower Motor Neuron Disease

  • Neuropathy, Motor, Distal, Hereditary, Type Viib

Marburg Hemorrhagic Fever
  • Marburg Virus Disease

  • Marburg Disease

  • Green Monkey Disease

  • Mhf

  • Vervet Monkey Disease

  • Mard - [Marburg Disease]

  • Mvd - [Marburg Virus Disease]

  • Marburg Haemorrhagic Fever

  • Mhf - [Marburg Haemorrhagic Fever]

Ebola Hemorrhagic Fever
  • Ebola Virus Disease

  • Viral Hemorrhagic Fever

  • Hemorrhagic Fever, Ebola

  • Ebola

  • Ehf

  • Ebola Fever

  • Hemorrhagic Fevers, Viral

  • Ebola Haemorrhagic Fever

  • Ebod - [Ebola Disease]

  • Evd - [Ebola Virus Disease]

  • Ebola Virus Haemorrhagic Fever

  • Vhf - [Viral Haemorrhagic Fever] Nos

  • Viral Haemorrhagic Fever, Not Otherwise Specified

Arthrogryposis, Distal, Type 4
  • Distal Arthrogryposis Type 4

  • DA4

  • Daiid

  • Arthrogryposis-Severe Scoliosis Syndrome

  • Distal Arthrogryposis Type Iid

  • Arthrogryposis With Severe Scoliosis

  • Arthrogryposis, Distal, Type Iid

Bolivian Hemorrhagic Fever
  • Machupo Hemorrhagic Fever

  • Hemorrhagic Fever, Bolivian

  • Bhf - [Bolivian Haemorrhagic Fever]

  • Machupo Haemorrhagic Fever

Omsk Hemorrhagic Fever
  • Ohf

  • Hemorrhagic Fever, Omsk

  • Ohf - [Omsk Haemorrhagic Fever]

  • Spring-Fall Haemorrhagic Fever

Nipah Virus Encephalitis
  • Equine Morbillivirus

Perry Syndrome
  • Parkinsonism With Alveolar Hypoventilation And Mental Depression

  • PERRYS

Helsmoortel-Van Der Aa Syndrome
  • HVDAS

  • Mrd28

  • Adnp Syndrome

  • Adnp-Related Syndromic Intellectual Disability-Autism Spectrum Disorder

  • Mental Retardation, Autosomal Dominant 28

  • Adnp-Related Multiple Congenital Anomalies - Intellectual Disability - Autism Spectrum Disorder

  • Mental Retardation, Autosomal Dominant 28, Formerly

  • Mrd28, Formerly

  • Autosomal Dominant Mental Retardation 28

  • Adnp-Related Intellectual Disability And Autism Spectrum Disorder

  • Adnp-Related Multiple Congenital Anomalies-Intellectual Disability-Autism Spectrum Disorder

Congenital Fibrosis Of The Extraocular Muscles
  • Congenital Fibrosis Of Extraocular Muscles

  • Cfeom

  • Feom

  • Congenital External Ophthalmoplegia

  • Congenital Fibrosis Syndrome

  • General Fibrosis Syndrome

Congenital Nervous System Abnormality
  • Congenital Neurologic Anomaly

  • Congenital Nervous System Disorder

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
Bos taurus MAPRE3 VGNC VGNC:31234
Macaca mulatta MAPRE3 VGNC VGNC:74657
Felis catus MAPRE3 VGNC VGNC:68181
Mus musculus MAPRE3 MGD MGI:2140967
Rattus norvegicus MAPRE3 RGD RGD:1359297
Canis familiaris MAPRE3 VGNC VGNC:43011
Others MAPRE3 NCBI