ENSG00000104093


Homo sapiens

Features
Gene ID: ENSG00000104093
  
Biological name :DMXL2
  
Synonyms : DMXL2 / Dmx like 2 / Q8TDJ6
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 15
Strand: -1
Band: q21.2
Gene start: 51447711
Gene end: 51622833
  
Corresponding Affymetrix probe sets: 212820_at (Human Genome U133 Plus 2.0 Array)   215761_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000453454
Ensembl peptide - ENSP00000453267
Ensembl peptide - ENSP00000453570
Ensembl peptide - ENSP00000251076
Ensembl peptide - ENSP00000400855
Ensembl peptide - ENSP00000441858
NCBI entrez gene - 23312     See in Manteia.
OMIM - 612186
RefSeq - XM_017022034
RefSeq - NM_001174116
RefSeq - NM_001174117
RefSeq - NM_015263
RefSeq - XM_005254255
RefSeq - XM_005254256
RefSeq Peptide - NP_001167587
RefSeq Peptide - NP_056078
RefSeq Peptide - NP_001167588
swissprot - H0YME1
swissprot - A0A024R5V2
swissprot - Q8TDJ6
swissprot - H0YLM8
swissprot - H0YM41
Ensembl - ENSG00000104093
  
Related genetic diseases (OMIM): 616113 - ?Polyendocrine-polyneuropathy syndrome, 616113
  617605 - ?Deafness, autosomal dominant 71, 617605
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
 dmxl2ENSDARG00000091293Danio rerio
 DMXL2ENSGALG00000039924Gallus gallus
 Dmxl2ENSMUSG00000041268Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
DMXL1 / Q9Y485 / Dmx like 1ENSG0000017286956


Protein motifs (from Interpro)
Interpro ID Name
 IPR001680  WD40 repeat
 IPR015943  WD40/YVTN repeat-like-containing domain superfamily
 IPR017986  WD40-repeat-containing domain
 IPR022033  RAVE complex protein Rav1 C-terminal
 IPR036322  WD40-repeat-containing domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0007035 vacuolar acidification IBA
 biological_processGO:0070072 vacuolar proton-transporting V-type ATPase complex assembly IBA
 cellular_componentGO:0005615 extracellular space HDA
 cellular_componentGO:0008021 synaptic vesicle IDA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0030054 cell junction IEA
 cellular_componentGO:0030672 synaptic vesicle membrane IEA
 cellular_componentGO:0031410 cytoplasmic vesicle IEA
 cellular_componentGO:0043291 RAVE complex IBA
 cellular_componentGO:0045202 synapse IEA
 molecular_functionGO:0005515 protein binding IEA
 molecular_functionGO:0017137 Rab GTPase 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:0001251 Ataxia "Ataxia is a nonspecific neurological sign and symptom consisting of gross lack of coordination of muscle movements. Ataxia is caused by dysfunction of one or more parts of the nervous system including the cerebellum, the sensory nervous system, the vestibular system, or the cerebral cortex." [HPO:curators]
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 HP:0001260 Dysarthria "Dysarthric speech is a general description referring to a neurological speech disorder characterized by poor articulation. Depending on the involved neurological structures, dysarthria may be further classified as spastic, flaccid, ataxic, hyperkinetic and hypokinetic, or mixed." [HPO:curators]
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 HP:0001270 Motor retardation 
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 HP:0001321 Cerebellar hypoplasia 
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 HP:0001332 Dystonia "An abnormally increased muscular tone that causes fixed abnormal postures. There is a slow, intermittent twisting motion that leads to exaggerated turning and posture of the extremities and trunk." [HPO:curators]
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 HP:0001730 Progressive hearing loss 
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 HP:0002342 Mental retardation, moderate "Moderate mental retardation is defined as an intelligence quotient (IQ) in the range of 35-49." [HPO:curators]
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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:0008897 Growth retardation, progressive 
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 HP:0011787 Central hypothyroidism "A type of hypothyroidism due to an insufficient stimulation of an otherwise normal thyroid gland. Central hypothyroidism is caused by either pituitary (secondary hypothyroidism) or hypothalamic (tertiary hypothyroidism) defects." [DDD:spark, pmid:18415684]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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