ENSG00000129696


Homo sapiens

Features
Gene ID: ENSG00000129696
  
Biological name :TTI2
  
Synonyms : Q6NXR4 / TELO2 interacting protein 2 / TTI2
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 8
Strand: -1
Band: p12
Gene start: 33473386
Gene end: 33513601
  
Corresponding Affymetrix probe sets: 219124_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000478396
Ensembl peptide - ENSP00000411169
Ensembl peptide - ENSP00000428401
Ensembl peptide - ENSP00000428569
Ensembl peptide - ENSP00000353971
NCBI entrez gene - 80185     See in Manteia.
OMIM - 614426
RefSeq - XM_011544665
RefSeq - NM_001102401
RefSeq - NM_001265581
RefSeq - NM_025115
RefSeq Peptide - NP_001317434
RefSeq Peptide - NP_001095871
RefSeq Peptide - NP_001252510
RefSeq Peptide - NP_079391
swissprot - E5RIH5
swissprot - Q6NXR4
swissprot - E5RHM7
Ensembl - ENSG00000129696
  
Related genetic diseases (OMIM): 615541 - Mental retardation, autosomal recessive 39, 615541
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 tti2ENSDARG00000073773Danio rerio
 TTI2ENSGALG00000001651Gallus gallus
 Tti2ENSMUSG00000031577Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
No match


Protein motifs (from Interpro)
Interpro ID Name
 IPR011989  Armadillo-like helical
 IPR016024  Armadillo-type fold
 IPR018870  Tti2 family


Gene Ontology (GO)
TypeGO IDTermEv.Code
 cellular_componentGO:0005654 nucleoplasm IDA
 cellular_componentGO:0005813 centrosome IDA
 cellular_componentGO:0005829 cytosol IDA
 molecular_functionGO:0005488 binding IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000007 Autosomal recessive inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators]
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 HP:0000252 Microcephaly "Microcephaly is a neurodevelopmental disorder in which the circumference of the head is more than two standard deviations smaller than the age- and gender-dependent norm." [HPO:curators]
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 HP:0000340 Sloping forehead "A form of the forehead that slopes from top to bottom in an anterior direction." [HPO:curators]
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 HP:0000400 Large ears 
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 HP:0000448 Prominent nose 
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 HP:0000486 Strabismus "Strabismus (also known as squint) is a condition in which the eyes are not properly aligned with each other." [HPO:curators]
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 HP:0000490 Deep set eyes 
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 HP:0000664 Synophrys "Fusion of the left and right `eyebrow` (FMA:54237)." [HPO:probinson]
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 HP:0000718 Aggressive behavior "Aggressive behavior can denote verbal aggression, physical aggression against objects, physical aggression against people, and may also include aggression towards oneself." [HPO:curators]
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 HP:0000733 Stereotyped, repetitive behaviour 
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 HP:0000750 Impaired language development 
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 HP:0000752 Hyperactivity 
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 HP:0001249 Mental retardation 
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 HP:0001263 Developmental retardation "A delay in the achievement of motor or mental milestones manifested prior to age 18 and generally associated with lifelong mental and/or physical impairments." [HPO:curators]
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 HP:0002751 Kyphoscoliosis 
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 HP:0003593 Early onset 
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 HP:0004322 Decreased body height "A height below that which is expected according to age and gender norms. Although there is no universally accepted definition of short stature, many refer to "short stature" as height more than 2 standard deviations below the mean for age and gender (or below the 3rd percentile for age and gender dependent norms)." [HPO:curators]
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 HP:0040080 Anteverted ears 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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