ENSG00000155256


Homo sapiens

Features
Gene ID: ENSG00000155256
  
Biological name :ZFYVE27
  
Synonyms : Q5T4F4 / ZFYVE27 / zinc finger FYVE-type containing 27
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 10
Strand: 1
Band: q24.2
Gene start: 97737121
Gene end: 97760907
  
Corresponding Affymetrix probe sets: 225218_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000409594
Ensembl peptide - ENSP00000337993
Ensembl peptide - ENSP00000350148
Ensembl peptide - ENSP00000353069
Ensembl peptide - ENSP00000359642
Ensembl peptide - ENSP00000359646
Ensembl peptide - ENSP00000377282
NCBI entrez gene - 118813     See in Manteia.
OMIM - 610243
RefSeq - XM_017015655
RefSeq - NM_001002261
RefSeq - NM_001002262
RefSeq - NM_001174119
RefSeq - NM_001174120
RefSeq - NM_001174121
RefSeq - NM_001174122
RefSeq - NM_144588
RefSeq - XM_017015647
RefSeq - XM_017015648
RefSeq - XM_017015649
RefSeq - XM_017015650
RefSeq - XM_017015651
RefSeq - XM_017015652
RefSeq - XM_017015653
RefSeq - XM_017015654
RefSeq - XM_005269502
RefSeq - XM_005269503
RefSeq - XM_005269504
RefSeq - XM_005269505
RefSeq - XM_005269506
RefSeq - XM_005269508
RefSeq - XM_005269509
RefSeq - XM_005269510
RefSeq - XM_005269511
RefSeq - XM_011539252
RefSeq - XM_011539253
RefSeq - XM_011539254
RefSeq - XM_011539255
RefSeq - XM_017015644
RefSeq - XM_017015645
RefSeq - XM_017015646
RefSeq Peptide - NP_001002261
RefSeq Peptide - NP_001167590
RefSeq Peptide - NP_001167591
RefSeq Peptide - NP_001167592
RefSeq Peptide - NP_001167593
RefSeq Peptide - NP_653189
RefSeq Peptide - NP_001002262
swissprot - Q5T4F4
Ensembl - ENSG00000155256
  
Related genetic diseases (OMIM): 610244 - Spastic paraplegia 33, autosomal dominant, 610244
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
 zfyve27ENSDARG00000059835Danio rerio
 ZFYVE27ENSGALG00000007531Gallus gallus
 Q3TXX3ENSMUSG00000018820Mus musculus


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


Protein motifs (from Interpro)
Interpro ID Name
 IPR000306  FYVE zinc finger
 IPR011011  Zinc finger, FYVE/PHD-type
 IPR013083  Zinc finger, RING/FYVE/PHD-type
 IPR017455  Zinc finger, FYVE-related


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0016192 vesicle-mediated transport IDA
 biological_processGO:0031175 neuron projection development IDA
 biological_processGO:0045773 positive regulation of axon extension ISS
 biological_processGO:0048011 neurotrophin TRK receptor signaling pathway ISS
 biological_processGO:0071787 endoplasmic reticulum tubular network formation IMP
 biological_processGO:0072659 protein localization to plasma membrane ISS
 cellular_componentGO:0005654 nucleoplasm IDA
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005768 endosome IEA
 cellular_componentGO:0005783 endoplasmic reticulum IEA
 cellular_componentGO:0005789 endoplasmic reticulum membrane IEA
 cellular_componentGO:0005829 cytosol IDA
 cellular_componentGO:0005886 plasma membrane IEA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 cellular_componentGO:0030176 integral component of endoplasmic reticulum membrane IDA
 cellular_componentGO:0030424 axon ISS
 cellular_componentGO:0030425 dendrite ISS
 cellular_componentGO:0032584 growth cone membrane ISS
 cellular_componentGO:0042995 cell projection IEA
 cellular_componentGO:0055038 recycling endosome membrane ISS
 cellular_componentGO:0071782 endoplasmic reticulum tubular network IDA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0043621 protein self-association IDA
 molecular_functionGO:0046872 metal ion binding IEA


Pathways (from Reactome)
Pathway description
No match


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]
Show

 HP:0001258 Spastic paraplegia 
Show

 HP:0001762 Talipes equinovarus "Also called clubfoot typically has 4 main components: inversion and adduction of the forefoot; inversion of the heel and hindfoot; equinus (limitation of extension) of the ankle and subtalar joint; and internal rotation of the leg. Clubfoot is a complex, multifactorial deformity with genetic and intrauterine factors. One popular theory postulates that a clubfoot is a result of intrauterine maldevelopment of the talus that leads to adduction and plantarflexion of the foot. On radiographic projection a clubfoot can be noted as parallel axes of talus and calcaneus." [HPO:curators]
Show

 HP:0002061 Lower limb spasticity 
Show

 HP:0002064 Spastic gait 
Show

 HP:0003487 Babinski sign "Upturning of the big toe (and sometimes fanning of the other toes) in response to stimulation of the sole of the foot. If the Babinski sign is present it can indicate damage to the corticospinal tract." [HPO:curators]
Show

 HP:0007340 Lower limb muscle weakness "Weakness of the muscles of the legs." [HPO:curators]
Show

 HP:0011448 Ankle clonus "Clonus is an involuntary tendon reflex that causes repeated flexion and extension of the foot. Ankle clonus is tested by rapidly flexing the foot upward." [HPO:probinson]
Show

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

0 s.

 
External programs and data are copyrighted by and are the property of their respective authors.
The Manteia system, data and analyses are provided "as is" with no warranties, expressed or implied as to capabilities or accuracy. User assumes the entire risk as to the results and performance of the software, data and documentation


                   


© Olivier Tassy / Olivier Pourquie 2007-2025
contact: otassy@igbmc.fr