ENSG00000180340


Homo sapiens

Features
Gene ID: ENSG00000180340
  
Biological name :FZD2
  
Synonyms : frizzled class receptor 2 / FZD2 / Q14332
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 17
Strand: 1
Band: q21.31
Gene start: 44557459
Gene end: 44559570
  
Corresponding Affymetrix probe sets: 210220_at (Human Genome U133 Plus 2.0 Array)   238129_s_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000323901
NCBI entrez gene - 2535     See in Manteia.
OMIM - 600667
RefSeq - NM_001466
RefSeq Peptide - NP_001457
swissprot - Q14332
Ensembl - ENSG00000180340
  
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
 fzd2ENSDARG00000054438Danio rerio
 FZD2ENSGALG00000030847Gallus gallus
 Fzd2ENSMUSG00000050288Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
FZD1 / Q9UP38 / frizzled class receptor 1ENSG0000015724080
FZD7 / O75084 / frizzled class receptor 7ENSG0000015576079
FZD8 / Q9H461 / frizzled class receptor 8ENSG0000017728350
FZD5 / Q13467 / frizzled class receptor 5ENSG0000016325148
FZD10 / Q9ULW2 / frizzled class receptor 10ENSG0000011143245
FZD9 / O00144 / frizzled class receptor 9ENSG0000018876343
FZD4 / Q9ULV1 / frizzled class receptor 4ENSG0000017480442
FZD3 / Q9NPG1 / frizzled class receptor 3ENSG0000010429041
FZD6 / O60353 / frizzled class receptor 6ENSG0000016493040
SMO / Q99835 / smoothened, frizzled class receptorENSG0000012860225
SFRP4 / Q6FHJ7 / secreted frizzled related protein 4ENSG0000010648315
FRZB / Q92765 / frizzled related proteinENSG0000016299815
SFRP1 / Q8N474 / secreted frizzled related protein 1ENSG0000010433213
SFRP5 / Q5T4F7 / secreted frizzled related protein 5ENSG0000012005713
SFRP2 / Q96HF1 / secreted frizzled related protein 2ENSG0000014542312


Protein motifs (from Interpro)
Interpro ID Name
 IPR000539  Frizzled/Smoothened, transmembrane domain
 IPR015526  Frizzled/secreted frizzled-related protein
 IPR017981  GPCR, family 2-like
 IPR020067  Frizzled domain
 IPR026550  Frizzled-2
 IPR036790  Frizzled cysteine-rich domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0003149 membranous septum morphogenesis IEA
 biological_processGO:0003150 muscular septum morphogenesis IEA
 biological_processGO:0003151 outflow tract morphogenesis IEA
 biological_processGO:0007165 signal transduction IEA
 biological_processGO:0007166 cell surface receptor signaling pathway IEA
 biological_processGO:0007186 G-protein coupled receptor signaling pathway IEA
 biological_processGO:0007223 Wnt signaling pathway, calcium modulating pathway TAS
 biological_processGO:0007267 cell-cell signaling IEA
 biological_processGO:0007275 multicellular organism development IEA
 biological_processGO:0007608 sensory perception of smell IEA
 biological_processGO:0016055 Wnt signaling pathway IEA
 biological_processGO:0030182 neuron differentiation ISS
 biological_processGO:0030825 obsolete positive regulation of cGMP metabolic process IMP
 biological_processGO:0030855 epithelial cell differentiation IEA
 biological_processGO:0035567 non-canonical Wnt signaling pathway IBA
 biological_processGO:0045893 positive regulation of transcription, DNA-templated IDA
 biological_processGO:0051091 positive regulation of DNA-binding transcription factor activity IDA
 biological_processGO:0060022 hard palate development IEA
 biological_processGO:0060070 canonical Wnt signaling pathway IDA
 biological_processGO:0060071 Wnt signaling pathway, planar cell polarity pathway NAS
 biological_processGO:0060119 inner ear receptor cell development IEA
 biological_processGO:0060412 ventricular septum morphogenesis IEA
 biological_processGO:0090103 cochlea morphogenesis IEA
 biological_processGO:0090179 planar cell polarity pathway involved in neural tube closure IEA
 biological_processGO:1904886 beta-catenin destruction complex disassembly TAS
 cellular_componentGO:0005737 cytoplasm IDA
 cellular_componentGO:0005886 plasma membrane IDA
 cellular_componentGO:0005925 focal adhesion HDA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IBA
 cellular_componentGO:0030669 clathrin-coated endocytic vesicle membrane TAS
 molecular_functionGO:0004871 obsolete signal transducer activity IEA
 molecular_functionGO:0004888 transmembrane signaling receptor activity IEA
 molecular_functionGO:0004930 G-protein coupled receptor activity IBA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0017147 Wnt-protein binding IBA
 molecular_functionGO:0030165 PDZ domain binding IPI
 molecular_functionGO:0042813 Wnt-activated receptor activity IDA


Pathways (from Reactome)
Pathway description
TCF dependent signaling in response to WNT
Class B/2 (Secretin family receptors)
Ca2+ pathway
Asymmetric localization of PCP proteins
Disassembly of the destruction complex and recruitment of AXIN to the membrane
WNT5A-dependent internalization of FZD2, FZD5 and ROR2


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000023 Inguinal hernia 
Show

 HP:0000028 Cryptorchidism "Absence of one or both testes from the scrotum owing to failure of the testis or testes to descend through the inguinal canal to the testis." [HPO:curators]
Show

 HP:0000039 Epispadias "Displacement of the urethral opening on the dorsal (superior) surface of the penis." [HPO:curators]
Show

 HP:0000047 Hypospadias "Displacement of the urethral opening on the ventral (inferior) surface of the penis." [HPO:curators]
Show

 HP:0000048 Bifid scrotum "Separation of the two halves of the scrotum, whereby commonly the 2 halves of the scrotum meet above the penis." [HPO:curators]
Show

 HP:0000059 Hypoplastic labia majora 
Show

 HP:0000060 Hypoplastic clitoris 
Show

 HP:0000062 Ambiguous genitalia 
Show

 HP:0000064 Hypoplastic labia minora 
Show

 HP:0000212 Gingival hyperplasia 
Show

 HP:0000256 Macrocephaly "The presence of an abnormally large `skull` (FMA:46565)." [HPO:probinson]
Show

 HP:0000272 Malar hypoplasia "Underdeveloped midface region." [HPO:curators]
Show

 HP:0000278 Retrognathia 
Show

 HP:0000286 Epicanthus "An epicanthal fold is a semilunar fold of skin that extends from the upper eyelid across the medial canthal area to the lower eyelid." [HPO:curators]
Show

 HP:0000316 Hypertelorism 
Show

 HP:0000322 Short philtrum 
Show

 HP:0000343 Long philtrum 
Show

 HP:0000347 Mandibular hypoplasia "Underdevelopment of the mandible." [HPO:curators]
Show

 HP:0000358 Posteriorly rotated ears "A type of `abnormal location of the ears` (HP:0000357) in which the position of the ears is characterized by posterior rotation (the superior part of the ears is rotated towards the back of the head, and the inferior part of the ears towards the front)." [HPO:probinson]
Show

 HP:0000365 Hearing loss 
Show

 HP:0000369 Low-set ears "Low-set ears are defined to be set below an arbitrary line drawn between the lateral canthus of the eye and the occipital protruberance." [HPO:curators]
Show

 HP:0000431 Broad nasal bridge "Increased horizontal dimension of the upper, bony part of the nose." [HPO:curators]
Show

 HP:0000445 Broad nose 
Show

 HP:0000463 Nares, anteverted "Anteriorly-facing nostrils viewed with the head in the Frankfurt horizontal and the eyes of the observer level with the eyes of the subject." [pmid:19152422]
Show

 HP:0000470 Short neck 
Show

 HP:0000486 Strabismus "Strabismus (also known as squint) is a condition in which the eyes are not properly aligned with each other." [HPO:curators]
Show

 HP:0000494 Downward slanting palpebral fissures 
Show

 HP:0000508 Ptosis "Drooping of the eyelid." [HPO:curators]
Show

 HP:0000520 Proptosis 
Show

 HP:0000527 Long eyelashes "Mid upper eyelash length >10 mm or increased length of the eyelashes (subjective)." [pmid:19125427]
Show

 HP:0000582 Upslanting palpebral fissures 
Show

 HP:0000592 Blue sclerae 
Show

 HP:0000637 Wide palpebral fissures 
Show

 HP:0000668 Hypodontia "Hypodontia describes a situation when there are fewer than the normal number of teeth, whereby 6 teeth or fewer teeth are missing (oligodontia refers to the condition of missing more than 6 teeth and the congenital absence of all teeth is called anodontia)." [HPO:curators]
Show

 HP:0000674 Anodontia "The congenital absence of all teeth." [HPO:curators]
Show

 HP:0000677 Oligodontia "The condition of missing over 6 teeth (Missing up to 6 teeth is referred to a hypodontia)." [HPO:curators]
Show

 HP:0000767 Pectus excavatum "A defect of the chest wall characterized by a depression of the sternum, giving the chest ("pectus") a caved-in ("excavatum") appearance." [HPO:curators]
Show

 HP:0000768 Pectus carinatum "A deformity of the chest caused by overgrowth of the ribs and characterized by protrusion of the sternum." [HPO:curators]
Show

 HP:0000960 Sacral dimple "A subtype of `skin dimples` (HP:0010781) presenting as an indentation in the skin of the intergluteal cleft ." [HPO:probinson]
Show

 HP:0001156 Brachydactyly 
Show

 HP:0001249 Mental retardation 
Show

 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]
Show

 HP:0001328 Learning disability 
Show

 HP:0001385 Hip dysplasia 
Show

 HP:0001537 Umbilical hernia "Protrusion of abdominal contents through a defect in the abdominal wall musculature around the umbilicus. Skin and subcutaneous tissue overlie the defect." [HPO:curators]
Show

 HP:0001596 Alopecia "Loss of hair from the head or body." [HPO:curators]
Show

 HP:0002007 Frontal bossing "The presence of an unusually prominent forehead." [HPO:curators]
Show

 HP:0002650 Scoliosis "The presence of an abnormal lateral curvature of the spine." [HPO:curators]
Show

 HP:0002673 Coxa valga "Coxa valga is a deformity of the hip in which the angle between the femoral shaft and the femoral neck is increased compared to age-adjusted values (about 150 degrees in newborns gradually reducing to 120-130 degrees in adults)." [HPO:curators]
Show

 HP:0002705 High, narrow palate "The presence of a high and narrow palate." [HPO:curators]
Show

 HP:0002714 Downturned corners of mouth "A morphological `abnormality of the mouth` (HP:0000153) in which the `angle of the mouth` (FMA:77269) is downturned." [HPO:probinson]
Show

 HP:0002812 Coxa vara 
Show

 HP:0002827 Dislocated hips 
Show

 HP:0002937 Hemivertebrae 
Show

 HP:0002983 Micromelia 
Show

 HP:0002999 Dislocation of patella "The kneecap normally is located within the groove termed trochlea on the distal femur and can slide up and down in it. Patellar dislocation occurs if the patella fully dislocates out of the groove." [HPO:curators]
Show

 HP:0003042 Elbow dislocation "A dislocation affecting the elbow joint, where the radius, ulna, and humerus meet." [HPO:curators]
Show

 HP:0003196 Nasal hypoplasia "Underdevelopment of the `nose` (FMA:46472)." [HPO:probinson]
Show

 HP:0003510 Short stature, severe "A severe degree of short stature." [HPO:curators]
Show

 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]
Show

 HP:0004279 Hypoplastic hand 
Show

 HP:0005280 Depressed nasal root and bridge 
Show

 HP:0005306 Capillary hemangiomas "The presence of a capillary hemangiomas, which are hemangiomas with small endothelial spaces." [HPO:curators]
Show

 HP:0005743 Abnormal femoral head with degenerative changes 
Show

 HP:0005792 Humeral hypoplasia 
Show

 HP:0006101 Finger syndactyly "Webbing or fusion of the fingers, involving soft parts only or including bone structure. Bony fusions are revered to as "bony" Syndactyly if the fusion occurs in a radio-ulnar axis. Fusions of bones of the fingers in a proximo-distal axis are refered to as "Symphalangism"." [HPO:curators]
Show

 HP:0007665 Curly eyelashes "Abnormally curly or curved eyelashes." [HPO:curators]
Show

 HP:0008402 Longitudinally grooved fingernails 
Show

 HP:0008501 Median cleft lip/palate "Cleft lip or palate affecting the midline region of the palate." [HPO:curators]
Show

 HP:0008736 Hypoplasia of penis 
Show

 HP:0008905 Rhizomelic short stature 
Show

 HP:0010034 Hypoplastic/short 1st metacarpal "In contrast to the proximal phalanges of the digits 2-5, the proximal phalanx of the thumb is embryologically equivalent to the middle phalanges of the other digits, whereas the first metacarpal is embryologically of phalangeal origin and as such equivalent to the proximal phalanges of the other digits." [HPO:curators]
Show

 HP:0010297 Bifid tongue "Tongue with a median apical indentation or fork." [pmid:19125428]
Show

 HP:0010733 Naevus flammeus of the eyelid "`Naevus flammeus` (HP:0001052) localised in the skin of the eyelid." [HPO:sdoelken]
Show

 HP:0010807 Open bite "Visible space between the dental arches in occlusion." [pmid:19125428]
Show

 HP:0011069 Increased number of teeth "The presence of a `supernumerary` (PATO:0000470), i.e., extra, `tooth` (FMA:12516) or teeth." [HPO:ibailleulforestier]
Show

 HP:0011220 Prominent forehead "Forward prominence of the entire forehead, due to protrusion of the frontal bone." [pmid:19125436]
Show

 HP:0011800 Midface retrusion "Posterior positions and/or vertical shortening of the infraorbital and perialar regions, or increased concavity of the face and/or reduced nasolabial angle." [DDD:jclayton-smith]
Show

 HP:0012905 Euryblepharon "Euryblepharon is a congenital eyelid anomaly characterized by horizontal enlargement of the palpebral fissure. The eyelid is shortened vertically compared with the horizontal dimension, with associated lateral canthal malpositioning and lateral ectropion abnormally wide lid opening." [HPO:probinson, pmid:15249382, pmid:15530943, pmid:24719364]
Show

 HP:0040036 Onychogryposis of fingernail "Thickened fingernails." []
Show

 HP:0100490 Camptodactyly (hands) "Contractures of one ore more joints of the fingers." [HPO:sdoelken]
Show

 HP:0100541 Femoral hernia "A hernia which occurs just below the inguinal ligament, where abdominal contents pass through a naturally occurring weakness called the femoral canal." [HPO:sdoelken]
Show

 HP:0100798 Fingernail dysplasia "An abnormality of the development of the fingernails." [HPO:probinson]
Show

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000004975 DVL2 / O14641 / dishevelled segment polarity protein 2  / complex / reaction
 ENSG00000082701 GSK3B / P49841 / glycogen synthase kinase 3 beta  / reaction / complex
 ENSG00000114251 WNT5A / P41221 / Wnt family member 5A  / complex / reaction
 ENSG00000070018 LRP6 / O75581 / LDL receptor related protein 6  / complex / reaction
 ENSG00000103126 AXIN1 / O15169  / reaction / complex
 ENSG00000154342 WNT3A / P56704 / Wnt family member 3A  / reaction / complex
 ENSG00000161202 DVL3 / Q92997 / dishevelled segment polarity protein 3  / reaction / complex
 ENSG00000125084 WNT1 / P04628 / Wnt family member 1  / complex / reaction
 ENSG00000075290 WNT8B / Q93098 / Wnt family member 8B  / complex / reaction
 ENSG00000061492 WNT8A / Q9H1J5 / Wnt family member 8A  / complex / reaction
 ENSG00000107404 DVL1 / O14640 / dishevelled segment polarity protein 1  / reaction / complex






 

1 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 2007-2024
contact: otassy@igbmc.fr