ENSG00000118162


Homo sapiens

Features
Gene ID: ENSG00000118162
  
Biological name :KPTN
  
Synonyms : kaptin, actin binding protein / KPTN / Q9Y664
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 19
Strand: -1
Band: q13.32
Gene start: 47475144
Gene end: 47484268
  
Corresponding Affymetrix probe sets: 220160_s_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000337850
Ensembl peptide - ENSP00000469446
Ensembl peptide - ENSP00000470364
Ensembl peptide - ENSP00000472291
NCBI entrez gene - 11133     See in Manteia.
OMIM - 615620
RefSeq - XM_017026228
RefSeq - NM_001291296
RefSeq - NM_007059
RefSeq - XM_011526399
RefSeq - XM_017026226
RefSeq - XM_017026227
RefSeq Peptide - NP_008990
RefSeq Peptide - NP_001278225
swissprot - M0QZ83
swissprot - M0R238
swissprot - Q9Y664
swissprot - M0QXX4
Ensembl - ENSG00000118162
  
Related genetic diseases (OMIM): 615637 - Mental retardation, autosomal recessive 41, 615637
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
 kptnENSDARG00000015937Danio rerio
 KptnENSMUSG00000006021Mus musculus


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


Protein motifs (from Interpro)
Interpro ID Name
 IPR029982  Kaptin


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0007015 actin filament organization IEA
 biological_processGO:0034198 cellular response to amino acid starvation IMP
 biological_processGO:0042149 cellular response to glucose starvation IMP
 biological_processGO:0061462 protein localization to lysosome IMP
 biological_processGO:1904262 negative regulation of TORC1 signaling IMP
 cellular_componentGO:0005764 lysosome IEA
 cellular_componentGO:0005765 lysosomal membrane IEA
 cellular_componentGO:0015629 actin cytoskeleton IEA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0030027 lamellipodium IEA
 cellular_componentGO:0031941 filamentous actin IDA
 cellular_componentGO:0032420 stereocilium ISS
 cellular_componentGO:0042995 cell projection IEA
 cellular_componentGO:0098871 postsynaptic actin cytoskeleton IDA
 cellular_componentGO:0140007 KICSTOR complex IDA
 molecular_functionGO:0003779 actin binding IEA
 molecular_functionGO:0051015 actin filament binding IDA


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:0000256 Macrocephaly "The presence of an abnormally large `skull` (FMA:46565)." [HPO:probinson]
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 HP:0000303 Mandibular prognathia "Abnormal prominence of the chin related to an abnormally long mandible." [HPO:curators]
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 HP:0000455 Broad nasal tip 
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 HP:0000494 Downward slanting palpebral fissures 
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 HP:0000733 Stereotyped, repetitive behaviour 
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 HP:0000739 Anxiety 
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 HP:0001249 Mental retardation 
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 HP:0001250 Seizures "Seizures are an intermittent `abnormality of the central nervous system` (FMA:HP:0002011) due to a sudden, excessive, disorderly discharge of cerebral neurons and characterized clinically by some combination of disturbance of sensation, loss of consciousness, impairment of psychic function, or convulsive movements." [HPO:probinson]
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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:0001290 Generalized hypotonia "Generalized muscular hypotonia (abnormally low muscle tone)." [HPO:curators]
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 HP:0002007 Frontal bossing "The presence of an unusually prominent forehead." [HPO:curators]
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 HP:0003577 Onset at birth 
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 HP:0004209 Clinodactyly of the 5th finger "Clinodactyly refers to a bending or curvature of the `fifth finger` (FMA:24949) in the radial direction (i.e., towards the 4th finger)." [HPO:curators]
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 HP:0030799 Scaphocephaly "Scaphocephaly is a subtype of dolichocephaly where the anterior and posterior aspects of the cranial vault are pointed (boat-shaped). Scaphocephaly is caused by a precocious fusion of sagittal suture without other associated synostosis." [HPO:probinson, PMID:16156241, PMID:23960302]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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