Property Summary

NCBI Gene PubMed Count 20
PubMed Score 14.75
PubTator Score 11.31

Knowledge Summary


No data available


  Disease Sources (5)

Disease Target Count
Autistic Disorder 320
Schizophrenia 503
Disease Target Count P-value
Breast cancer 3099 1.7617631797391E-10
psoriasis 6685 2.25540414365874E-9
tuberculosis 1563 1.01923848479037E-5
acute myeloid leukemia 785 0.00600548052388381
Disease Target Count Z-score Confidence
Attention deficit hyperactivity disorder 156 0.0 1.0
Disease Target Count Z-score Confidence
Atypical autism 25 3.187 1.6
Specific language impairment 31 3.037 1.5
Disease Target Count
Gilles de la Tourette syndrome 47


  Differential Expression (4)

Disease log2 FC p
tuberculosis 1.200 0.000
psoriasis -1.300 0.000
Breast cancer -1.300 0.000
acute myeloid leukemia -1.100 0.006


Accession Q96T52 Q75MF1 Q75MN9 Q75MP0 Q75MS5 Q75MS8 Q96HJ2
Symbols IMP2


PANTHER Protein Class (3)

  Ortholog (7)

Species Source
Chimp OMA EggNOG
Macaque OMA EggNOG Inparanoid
Mouse OMA EggNOG Inparanoid
Cow OMA EggNOG Inparanoid
Opossum OMA EggNOG Inparanoid
C. elegans OMA Inparanoid
S.cerevisiae OMA EggNOG Inparanoid

Pathway (1)

Gene RIF (10)

24549057 genomic rearrangements affecting IMMP2L may be one of the predisposing factors involved in Tourette syndrome and overlapping neurodevelopmental disorders.
22948383 Five genes have been directly disrupted in Tourette Syndrome by independent genomic rearrangements and copy number variations with unique breakpoints.
20877624 Observational study of gene-disease association. (HuGE Navigator)
20398908 Observational study of gene-disease association. (HuGE Navigator)
20379614 Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator)
19546859 Observational study of gene-disease association. (HuGE Navigator)
19401682 AUTS1/AUTS5 linkage to immp2l-dock4 may be involved in autism susceptibility
19401682 Observational study of gene-disease association. (HuGE Navigator)
19240061 Observational study of gene-disease association. (HuGE Navigator)
19058789 Observational study of gene-disease association. (HuGE Navigator)

AA Sequence

LLHAHATHILWPPERWQKLESVLPPERLPVQREEE                                       141 - 175

Text Mined References (20)

PMID Year Title
25056061 2014 Biological insights from 108 schizophrenia-associated genetic loci.
24549057 2014 Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome.
24324551 2013 Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects.
22948383 2012 Pathogenetic model for Tourette syndrome delineates overlap with related neurodevelopmental disorders including Autism.
20877624 2010 Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression.
20398908 2010 Comprehensive copy number variant (CNV) analysis of neuronal pathways genes in psychiatric disorders identifies rare variants within patients.
20379614 Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.
19734545 2009 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.
19546859 2010 Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes.
19401682 2010 High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.