ENSG00000134313


Homo sapiens

Features
Gene ID: ENSG00000134313
  
Biological name :KIDINS220
  
Synonyms : KIDINS220 / kinase D interacting substrate 220 / Q9ULH0
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 2
Strand: -1
Band: p25.1
Gene start: 8721081
Gene end: 8837630
  
Corresponding Affymetrix probe sets: 1557246_at (Human Genome U133 Plus 2.0 Array)   212162_at (Human Genome U133 Plus 2.0 Array)   212163_at (Human Genome U133 Plus 2.0 Array)   214932_at (Human Genome U133 Plus 2.0 Array)   236166_at (Human Genome U133 Plus 2.0 Array)   242032_at (Human Genome U133 Plus 2.0 Array)   242852_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000419964
Ensembl peptide - ENSP00000319947
Ensembl peptide - ENSP00000256707
Ensembl peptide - ENSP00000419232
Ensembl peptide - ENSP00000420364
Ensembl peptide - ENSP00000491810
Ensembl peptide - ENSP00000491461
Ensembl peptide - ENSP00000417390
Ensembl peptide - ENSP00000418974
NCBI entrez gene - 57498     See in Manteia.
OMIM - 615759
RefSeq - NM_001348745
RefSeq - NM_001348729
RefSeq - NM_001348731
RefSeq - NM_001348732
RefSeq - NM_020738
RefSeq Peptide - NP_001335658
RefSeq Peptide - NP_065789
RefSeq Peptide - NP_001335674
RefSeq Peptide - NP_001335661
RefSeq Peptide - NP_001335660
swissprot - Q9ULH0
swissprot - A0A1W2PPB7
swissprot - A0A1W2PPY4
swissprot - E9PH70
swissprot - F8WAY8
swissprot - H0Y8E4
swissprot - H7C584
Ensembl - ENSG00000134313
  
Related genetic diseases (OMIM): 617296 - Spastic paraplegia, intellectual disability, nystagmus, and obesity, 617296
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
 kidins220aENSDARG00000031240Danio rerio
 kidins220bENSDARG00000017338Danio rerio
 KIDINS220ENSGALG00000016409Gallus gallus
 Kidins220ENSMUSG00000036333Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
ANKHD1 / Q8IWZ3 / ankyrin repeat and KH domain containing 1ENSG0000013150318
ANKHD1-EIF4EBP3 / ANKHD1-EIF4EBP3 readthroughENSG0000025499618
O75179 / ANKRD17 / ankyrin repeat domain 17ENSG0000013246617
TANC2 / Q9HCD6 / tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 2ENSG0000017092113
TANC1 / Q9C0D5 / tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1ENSG0000011518313
Q9ULJ7 / ANKRD50 / ankyrin repeat domain 50ENSG0000015145811
ANKS6 / Q68DC2 / ankyrin repeat and sterile alpha motif domain containing 6ENSG000001651389
Q05823 / RNASEL / ribonuclease LENSG000001358288
Q8N6D5 / ANKRD29 / ankyrin repeat domain 29ENSG000001540655
FANK1 / Q8TC84 / fibronectin type III and ankyrin repeat domains 1ENSG000002037804


Protein motifs (from Interpro)
Interpro ID Name
 IPR002110  Ankyrin repeat
 IPR011646  KAP family P-loop domain
 IPR013761  Sterile alpha motif/pointed domain superfamily
 IPR020683  Ankyrin repeat-containing domain
 IPR036770  Ankyrin repeat-containing domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0000186 activation of MAPKK activity TAS
 biological_processGO:0001701 in utero embryonic development IEA
 biological_processGO:0007399 nervous system development IEA
 biological_processGO:0010976 positive regulation of neuron projection development ISS
 biological_processGO:0038180 nerve growth factor signaling pathway IBA
 biological_processGO:0045859 regulation of protein kinase activity IBA
 biological_processGO:0048813 dendrite morphogenesis IEA
 biological_processGO:1990090 cellular response to nerve growth factor stimulus ISS
 cellular_componentGO:0005768 endosome IEA
 cellular_componentGO:0005770 late endosome ISS
 cellular_componentGO:0005829 cytosol TAS
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 cellular_componentGO:0032991 protein-containing complex ISS
 molecular_functionGO:0005515 protein binding IEA
 molecular_functionGO:0019887 protein kinase regulator activity IBA
 molecular_functionGO:0030165 PDZ domain binding IBA


Pathways (from Reactome)
Pathway description
ARMS-mediated activation


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000006 Autosomal dominant 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 heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele." [HPO:curators]
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 HP:0000293 Full cheeks 
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 HP:0000483 Astigmatism 
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 HP:0000490 Deep set eyes 
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 HP:0000540 Hypermetropia 
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 HP:0000565 Esotropia 
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 HP:0000639 Nystagmus "Rhythmic, involuntary oscillations of one or both eyes related to abnormality in fixation, conjugate gaze, or vestibular mechanisms." [HPO:curators]
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 HP:0000750 Impaired language development 
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 HP:0001249 Mental retardation 
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 HP:0001258 Spastic paraplegia 
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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:0001338 Partial agenesis of the corpus callosum "A partial failure of the development of the corpus callosum." [HPO:curators]
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 HP:0001347 Hyperreflexia "The presence of overactive or overresponsive reflexes." [HPO:curators]
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 HP:0002059 Cerebral atrophy 
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 HP:0002509 Limb hypertonia 
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 HP:0003593 Early onset 
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 HP:0006956 Dilation of lateral ventricles 
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 HP:0007663 Decreased central vision 
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 HP:0008936 Muscular hypotonia of the trunk "Muscular hypotonia (abnormally low muscle tone) affecting the musculature of the trunk." [HPO:curators]
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 HP:0011220 Prominent forehead "Forward prominence of the entire forehead, due to protrusion of the frontal bone." [pmid:19125436]
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 HP:0012448 Delayed myelination "`Delayed` (PATO:0000502) `myelination` (GO:0042552)." [ORCID:0000-0001-5208-3432]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000134259 NGF / P01138 / nerve growth factor  / complex / reaction
 ENSG00000116473 RAP1A / P62834 / RAP1A, member of RAS oncogene family  / reaction / complex
 ENSG00000198400 NTRK1 / P04629 / neurotrophic receptor tyrosine kinase 1  / reaction / complex
 ENSG00000157764 BRAF / P15056 / B-Raf proto-oncogene, serine/threonine kinase  / complex / reaction
 ENSG00000167193 CRK / P46108 / CRK proto-oncogene, adaptor protein  / complex
 ENSG00000166913 YWHAB / P31946 / tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein beta  / reaction / complex






 

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