Phyh (phytanoyl-CoA 2-hydroxylase) - Rat Genome Database

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Gene: Phyh (phytanoyl-CoA 2-hydroxylase) Rattus norvegicus
Analyze
Symbol: Phyh
Name: phytanoyl-CoA 2-hydroxylase
RGD ID: 620317
Description: Enables phytanoyl-CoA dioxygenase activity. Involved in 2-oxobutyrate catabolic process and fatty acid alpha-oxidation. Located in peroxisome. Biomarker of metabolic dysfunction-associated steatotic liver disease. Human ortholog(s) of this gene implicated in Refsum disease; Zellweger syndrome; orofacial cleft; and peroxisomal disease. Orthologous to human PHYH (phytanoyl-CoA 2-hydroxylase); PARTICIPATES IN phytanic acid degradation pathway; Refsum disease pathway; INTERACTS WITH 17alpha-ethynylestradiol; 17beta-estradiol; 2,3,4,7,8-Pentachlorodibenzofuran.
Type: protein-coding
RefSeq Status: PROVISIONAL
Previously known as: phytanic acid oxidase; phytanoyl-CoA alpha-hydroxylase; phytanoyl-CoA dioxygenase, peroxisomal; phytanoyl-CoA hydroxylase; phytanoyl-CoA hydroxylase (Refsum disease)
RGD Orthologs
Human
Mouse
Chinchilla
Bonobo
Dog
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Latest Assembly: GRCr8 - GRCr8 Assembly
Position:
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81778,238,747 - 78,255,645 (-)NCBIGRCr8
mRatBN7.21773,329,461 - 73,346,359 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1773,329,082 - 73,346,409 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1776,834,020 - 76,851,123 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01780,658,833 - 80,675,645 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01774,709,804 - 74,727,044 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01777,287,580 - 77,304,482 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1777,287,188 - 77,304,530 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01778,953,400 - 78,970,299 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41784,418,173 - 84,435,073 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11784,429,005 - 84,445,906 (-)NCBI
Celera1772,770,062 - 72,786,946 (-)NCBICelera
Cytogenetic Map17q12.3NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model



  
Object Symbol
Species
Term
Qualifier
Evidence
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Reference
Notes
Source
Original Reference(s)
PhyhRatmetabolic dysfunction-associated steatotic liver disease treatmentIEP 13831310 RGD 
PhyhRatorofacial cleft  ISOPHYH (Homo sapiens)13831309DNA:insertion and missense mutations: :p.Asn337_Leu338insHis (rs566116760), p.Arg245Gln (rs62619919), p.Arg82Gly (rs145404396) (human)RGD 
PhyhRatperoxisomal disease  ISOPHYH (Homo sapiens)13831311 RGD 
PhyhRatRefsum disease  ISOPHYH (Homo sapiens)13831337 RGD 
PhyhRatRefsum disease  ISOPhyh (Mus musculus)13831313 RGD 
PhyhRatZellweger syndrome  ISOPHYH (Homo sapiens)13831312 RGD 
PhyhRatZellweger syndrome  ISOPHYH (Homo sapiens)13831337 RGD 
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Original Reference(s)
PhyhRatAdult Refsum Disease, 1  ISOPHYH (Homo sapiens)8554872ClinVar Annotator: match by term: REFSUM DISEASE more ...ClinVarPMID:10767344 more ...
PhyhRatFamilial Hypophosphatemic Rickets  ISOPHYH (Homo sapiens)8554872ClinVar Annotator: match by term: RICKETS and HEREDITARY VITAMIN D-RESISTANTClinVarPMID:10767344 more ...
PhyhRatfundus dystrophy  ISOPHYH (Homo sapiens)8554872ClinVar Annotator: match by term: Retinal dystrophyClinVarPMID:10767344 more ...
PhyhRatgenetic disease  ISOPHYH (Homo sapiens)8554872ClinVar Annotator: match by term: Inborn genetic diseasesClinVarPMID:10767344 more ...
PhyhRathypoparathyroidism-deafness-renal disease syndrome  ISOPHYH (Homo sapiens)8554872ClinVar Annotator: match by term: Hypoparathyroidism more ...ClinVarPMID:25741868
PhyhRatHypophosphatemic Rickets  ISOPHYH (Homo sapiens)8554872ClinVar Annotator: match by term: HYPOCALCEMIC VITAMIN D-RESISTANT RICKETSClinVarPMID:10767344 more ...
PhyhRatoptic atrophy  ISOPHYH (Homo sapiens)8554872ClinVar Annotator: match by term: Optic atrophyClinVarPMID:25133751 more ...
PhyhRatorofacial cleft  ISOPHYH (Homo sapiens)8554872ClinVar Annotator: match by term: Nonsyndromic cleft lip palateClinVarPMID:10767344 more ...
PhyhRatRefsum disease  ISOPHYH (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10767344 more ...
PhyhRatretinitis pigmentosa  ISOPHYH (Homo sapiens)8554872ClinVar Annotator: match by term: Retinitis pigmentosaClinVarPMID:10767344 more ...
PhyhRatvitamin D-dependent rickets type 2A  ISOPHYH (Homo sapiens)8554872ClinVar Annotator: match by term: VITAMIN D-RESISTANT RICKETS WITH END-ORGAN UNRESPONSIVENESS TO 1 and 25-DIHYDROXYCHOLECALCIFEROLClinVarPMID:10767344 more ...
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Original Reference(s)
PhyhRatRefsum disease  ISOPHYH (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:12522768
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Original Reference(s)
PhyhRatRefsum disease  ISSPhyh (Mus musculus)13592920OMIM:266500MouseDO 
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Original Reference(s)
PhyhRatRefsum disease  ISOPHYH (Homo sapiens)7240710 OMIM 

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Original Reference(s)
PhyhRat1,2-dimethylhydrazine multiple interactionsISOPhyh (Mus musculus)6480464[1 and 2-Dimethylhydrazine co-treated with Folic Acid] results in decreased expression of PHYH mRNACTDPMID:22206623
PhyhRat1,2-dimethylhydrazine decreases expressionISOPhyh (Mus musculus)64804641 and 2-Dimethylhydrazine results in decreased expression of PHYH mRNACTDPMID:22206623
PhyhRat17alpha-ethynylestradiol multiple interactionsISOPhyh (Mus musculus)6480464[Tetrachlorodibenzodioxin co-treated with Ethinyl Estradiol] results in increased expression of PHYH mRNACTDPMID:17942748
PhyhRat17alpha-ethynylestradiol decreases expressionEXP 6480464Ethinyl Estradiol results in decreased expression of PHYH mRNACTDPMID:15953391 more ...
PhyhRat17beta-estradiol multiple interactionsEXP 6480464[bisphenol A co-treated with Estradiol] results in decreased expression of PHYH mRNACTDPMID:26496021
PhyhRat17beta-estradiol decreases expressionEXP 6480464Estradiol results in decreased expression of PHYH proteinCTDPMID:32145629
PhyhRat2,3,4,7,8-Pentachlorodibenzofuran decreases expressionEXP 64804642 more ...CTDPMID:21724226
PhyhRat2,3,7,8-tetrachlorodibenzodioxine multiple interactionsISOPhyh (Mus musculus)6480464[Tetrachlorodibenzodioxin co-treated with Ethinyl Estradiol] results in increased expression of PHYH mRNACTDPMID:17942748
PhyhRat2,3,7,8-tetrachlorodibenzodioxine affects expressionEXP 6480464Tetrachlorodibenzodioxin affects the expression of PHYH mRNACTDPMID:34747641
PhyhRat2,4-dibromophenyl 2,4,5-tribromophenyl ether affects expressionISOPhyh (Mus musculus)64804642 more ...CTDPMID:38648751
PhyhRat2-acetamidofluorene multiple interactionsEXP 6480464[2-Acetylaminofluorene co-treated with Diethylnitrosamine] results in decreased expression of PHYH mRNA and [Diethylnitrosamine co-treated with 2-Acetylaminofluorene] results in decreased expression of PHYH mRNACTDPMID:14656948 and PMID:16158176
PhyhRat2-methylcholine affects expressionISOPHYH (Homo sapiens)6480464beta-methylcholine affects the expression of PHYH mRNACTDPMID:21179406
PhyhRat3,3',4,4',5-pentachlorobiphenyl decreases expressionEXP 64804643 more ...CTDPMID:23196670
PhyhRat3,3',4,4'-tetrachlorobiphenyl multiple interactionsISOPhyh (Mus musculus)64804643 more ...CTDPMID:19467301
PhyhRat4,4'-sulfonyldiphenol increases expressionISOPhyh (Mus musculus)6480464bisphenol S results in increased expression of PHYH mRNACTDPMID:39298647
PhyhRat5-aza-2'-deoxycytidine affects expressionISOPHYH (Homo sapiens)6480464Decitabine affects the expression of PHYH mRNACTDPMID:23300844
PhyhRat5-fluorouracil affects response to substanceISOPHYH (Homo sapiens)6480464PHYH protein affects the susceptibility to FluorouracilCTDPMID:16217747
PhyhRat5-methoxy-2-\{[(4-methoxy-3,5-dimethylpyridin-2-yl)methyl]sulfinyl\}-1H-benzimidazole affects expressionEXP 6480464Omeprazole affects the expression of PHYH mRNACTDPMID:19483382
PhyhRat6-propyl-2-thiouracil affects expressionEXP 6480464Propylthiouracil affects the expression of PHYH mRNACTDPMID:19483382
PhyhRatacetamide affects expressionEXP 6480464acetamide affects the expression of PHYH mRNACTDPMID:31881176

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Biological Process
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Original Reference(s)
PhyhRat2-oxobutyrate catabolic process  IDA 727286 RGD 
PhyhRat2-oxoglutarate metabolic process involved_inISOPHYH (Homo sapiens)1624291 PMID:16186124RGDPMID:16186124
PhyhRat2-oxoglutarate metabolic process involved_inIEAUniProtKB:O14832 and ensembl:ENSP000002630381600115GO_REF:0000107EnsemblGO_REF:0000107
PhyhRatfatty acid alpha-oxidation  IDA 727286 RGD 
PhyhRatfatty acid alpha-oxidation acts_upstream_of_or_withinIEAUniProtKB:O35386 and ensembl:ENSMUSP000000279751600115GO_REF:0000107EnsemblGO_REF:0000107
PhyhRatfatty acid alpha-oxidation acts_upstream_of_or_withinISOPhyh (Mus musculus)1624291 PMID:12915479 and PMID:9326939RGDPMID:12915479 and PMID:9326939
PhyhRatfatty acid alpha-oxidation involved_inIBAMGI:891978 more ...1600115GO_REF:0000033GO_CentralGO_REF:0000033
PhyhRatfatty acid alpha-oxidation involved_inIEAInterPro:IPR0471281600115GO_REF:0000002InterProGO_REF:0000002
PhyhRatfatty acid alpha-oxidation involved_inIEAUniProtKB:O14832 and ensembl:ENSP000002630381600115GO_REF:0000107EnsemblGO_REF:0000107
PhyhRatfatty acid alpha-oxidation involved_inISOPHYH (Homo sapiens)1624291 PMID:16186124 and PMID:9326939RGDPMID:16186124 and PMID:9326939
PhyhRatfatty acid metabolic process involved_inIEAUniPathway:UPA001991600115GO_REF:0000041UniProtGO_REF:0000041
PhyhRatisoprenoid metabolic process involved_inISOPHYH (Homo sapiens)1624291 PMID:11555634RGDPMID:11555634
PhyhRatisoprenoid metabolic process involved_inIEAUniProtKB:O14832 and ensembl:ENSP000002630381600115GO_REF:0000107EnsemblGO_REF:0000107
PhyhRatmethyl-branched fatty acid metabolic process involved_inISOPHYH (Homo sapiens)1624291 PMID:10744784RGDPMID:10744784
PhyhRatmethyl-branched fatty acid metabolic process involved_inIEAUniProtKB:O14832 and ensembl:ENSP000002630381600115GO_REF:0000107EnsemblGO_REF:0000107
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Cellular Component

  
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Original Reference(s)
PhyhRat9+0 non-motile cilium located_inISOPHYH (Homo sapiens)1624291 PMID:29257953RGDPMID:29257953
PhyhRat9+0 non-motile cilium located_inIEAUniProtKB:O14832 and ensembl:ENSP000002630381600115GO_REF:0000107EnsemblGO_REF:0000107
PhyhRatperoxisome  IDA 727286 RGD 
PhyhRatperoxisome located_inIEAUniProtKB:O14832 and ensembl:ENSP000002630381600115GO_REF:0000107EnsemblGO_REF:0000107
PhyhRatperoxisome located_inIEAUniProtKB-SubCell:SL-02041600115GO_REF:0000044UniProtGO_REF:0000044
PhyhRatperoxisome located_inIEAUniProtKB-KW:KW-05761600115GO_REF:0000043UniProtGO_REF:0000043
PhyhRatperoxisome located_inISOPHYH (Homo sapiens)1624291 PMID:9326939RGDPMID:9326939
PhyhRatperoxisome located_inIDA 1580664PMID:14561759HGNC-UCL 

Molecular Function
1 to 20 of 21 rows

  
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Original Reference(s)
PhyhRatcarboxylic acid binding enablesISOPHYH (Homo sapiens)1624291 PMID:16186124RGDPMID:16186124
PhyhRatcarboxylic acid binding enablesIEAUniProtKB:O14832 and ensembl:ENSP000002630381600115GO_REF:0000107EnsemblGO_REF:0000107
PhyhRatcatalytic activity enablesISOPhyh (Mus musculus)1624291 PMID:9326939RGDPMID:9326939
PhyhRatcatalytic activity enablesIEAUniProtKB:O35386 and ensembl:ENSMUSP000000279751600115GO_REF:0000107EnsemblGO_REF:0000107
PhyhRatdioxygenase activity enablesIEAUniProtKB-KW:KW-02231600115GO_REF:0000043UniProtGO_REF:0000043
PhyhRatferrous iron binding enablesISOPHYH (Homo sapiens)1624291 PMID:10744784 more ...RGDPMID:10744784 more ...
PhyhRatferrous iron binding enablesIEAUniProtKB:O14832 and ensembl:ENSP000002630381600115GO_REF:0000107EnsemblGO_REF:0000107
PhyhRatL-ascorbic acid binding enablesISOPHYH (Homo sapiens)1624291 PMID:10744784RGDPMID:10744784
PhyhRatL-ascorbic acid binding enablesIEAUniProtKB:O14832 and ensembl:ENSP000002630381600115GO_REF:0000107EnsemblGO_REF:0000107
PhyhRatL-ascorbic acid binding enablesIEAUniProtKB-KW:KW-08471600115GO_REF:0000043UniProtGO_REF:0000043
PhyhRatmetal ion binding enablesIEAUniProtKB-KW:KW-04791600115GO_REF:0000043UniProtGO_REF:0000043
PhyhRatoxidoreductase activity enablesIEAUniProtKB-KW:KW-05601600115GO_REF:0000043UniProtGO_REF:0000043
PhyhRatphytanoyl-CoA dioxygenase activity  IDA 727286 RGD 
PhyhRatphytanoyl-CoA dioxygenase activity enablesIEARHEA:160651600115GO_REF:0000116RHEAGO_REF:0000116
PhyhRatphytanoyl-CoA dioxygenase activity enablesIEAInterPro:IPR0471281600115GO_REF:0000002InterProGO_REF:0000002
PhyhRatphytanoyl-CoA dioxygenase activity enablesIEAUniProtKB:O14832 and ensembl:ENSP000002630381600115GO_REF:0000107EnsemblGO_REF:0000107
PhyhRatphytanoyl-CoA dioxygenase activity enablesIBAPANTHER:PTN001084068 more ...1600115GO_REF:0000033GO_CentralGO_REF:0000033
PhyhRatphytanoyl-CoA dioxygenase activity enablesIEAEC:1.14.11.181600115GO_REF:0000003UniProtGO_REF:0000003
PhyhRatphytanoyl-CoA dioxygenase activity enablesISOPHYH (Homo sapiens)1624291 PMID:10744784 more ...RGDPMID:10744784 more ...
PhyhRatprotein binding enablesISOPHYH (Homo sapiens)1624291UniProtKB:A5PKX9 more ...RGDPMID:10051602 more ...
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Imported Annotations - SMPDB

Object Symbol
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Original Reference(s)
PhyhRatphytanic acid degradation pathway  ISOPHYH (Homo sapiens)10402751 SMPDBSMP:00450
PhyhRatRefsum disease pathway  ISOPHYH (Homo sapiens)10402751 SMPDBSMP:00451

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#
Reference Title
Reference Citation
1. Using Whole Exome Sequencing to Identify Candidate Genes With Rare Variants In Nonsyndromic Cleft Lip and Palate. Aylward A, etal., Genet Epidemiol. 2016 Jul;40(5):432-41. doi: 10.1002/gepi.21972. Epub 2016 May 27.
2. Ataxia with loss of Purkinje cells in a mouse model for Refsum disease. Ferdinandusse S, etal., Proc Natl Acad Sci U S A. 2008 Nov 18;105(46):17712-7. doi: 10.1073/pnas.0806066105. Epub 2008 Nov 11.
3. Further studies on the substrate spectrum of phytanoyl-CoA hydroxylase: implications for Refsum disease? Foulon V, etal., J Lipid Res 2003 Dec;44(12):2349-55. Epub 2003 Aug 16.
4. Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Gaudet P, etal., Brief Bioinform. 2011 Sep;12(5):449-62. doi: 10.1093/bib/bbr042. Epub 2011 Aug 27.
5. Rat ISS GO annotations from GOA human gene data--August 2006 GOA data from the GO Consortium
6. Phytanoyl-CoA hydroxylase deficiency. Enzymological and molecular basis of classical Refsum disease. Jansen GA, etal., Adv Exp Med Biol. 1999;466:371-6.
7. Phytanoyl-CoA hydroxylase is present in human liver, located in peroxisomes, and deficient in Zellweger syndrome: direct, unequivocal evidence for the new, revised pathway of phytanic acid alpha-oxidation in humans. Jansen GA, etal., Biochem Biophys Res Commun. 1996 Dec 4;229(1):205-10. doi: 10.1006/bbrc.1996.1781.
8. Phytanoyl-CoA hydroxylase is not only deficient in classical Refsum disease but also in rhizomelic chondrodysplasia punctata. Jansen GA, etal., J Inherit Metab Dis. 1997 Jul;20(3):444-6.
9. Phytanoyl-CoA hydroxylase from rat liver. Protein purification and cDNA cloning with implications for the subcellular localization of phytanic acid alpha-oxidation. Jansen GA, etal., J Lipid Res 1999 Dec;40(12):2244-54.
10. Proteomic analysis of rat liver peroxisome: presence of peroxisome-specific isozyme of Lon protease. Kikuchi M, etal., J Biol Chem. 2004 Jan 2;279(1):421-8. Epub 2003 Oct 15.
11. Rat ISS GO annotations from MGI mouse gene data--August 2006 MGD data from the GO Consortium
12. Electronic Transfer of LocusLink and RefSeq Data NCBI rat LocusLink and RefSeq merged data July 26, 2002
13. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
14. SMPDB Annotation Import Pipeline Pipeline to import SMPDB annotations from SMPDB into RGD
15. GOA pipeline RGD automated data pipeline
16. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
17. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
18. The subcellular localization of phytanic acid oxidase in rat liver. Skjeldal OH and Stokke O, Biochim Biophys Acta. 1987 Sep 4;921(1):38-42.
19. Isobaric tags for relative and absolute quantitation (iTRAQ)-based proteomics for the investigation of the effect of Hugan Qingzhi on non-alcoholic fatty liver disease in rats. Yao X, etal., J Ethnopharmacol. 2018 Feb 15;212:208-215. doi: 10.1016/j.jep.2017.09.016. Epub 2017 Oct 13.
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PMID:9326939   PMID:9326940   PMID:10744784   PMID:11555634   PMID:12477932   PMID:12915479   PMID:15489334   PMID:16186124   PMID:18614015  



Phyh
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81778,238,747 - 78,255,645 (-)NCBIGRCr8
mRatBN7.21773,329,461 - 73,346,359 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1773,329,082 - 73,346,409 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1776,834,020 - 76,851,123 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01780,658,833 - 80,675,645 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01774,709,804 - 74,727,044 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01777,287,580 - 77,304,482 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1777,287,188 - 77,304,530 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01778,953,400 - 78,970,299 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41784,418,173 - 84,435,073 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11784,429,005 - 84,445,906 (-)NCBI
Celera1772,770,062 - 72,786,946 (-)NCBICelera
Cytogenetic Map17q12.3NCBI
PHYH
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381013,277,799 - 13,300,064 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1013,277,796 - 13,302,412 (-)EnsemblGRCh38hg38GRCh38
GRCh371013,319,799 - 13,342,064 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361013,359,802 - 13,382,136 (-)NCBINCBI36Build 36hg18NCBI36
Build 341013,359,805 - 13,382,107NCBI
Celera1013,246,935 - 13,269,237 (-)NCBICelera
Cytogenetic Map10p13NCBI
HuRef1013,232,668 - 13,254,996 (-)NCBIHuRef
CHM1_11013,319,709 - 13,342,691 (-)NCBICHM1_1
T2T-CHM13v2.01013,290,862 - 13,313,116 (-)NCBIT2T-CHM13v2.0
Phyh
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3924,923,807 - 4,943,554 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl24,923,830 - 4,943,541 (+)EnsemblGRCm39 Ensembl
GRCm3824,918,996 - 4,938,743 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl24,919,019 - 4,938,730 (+)EnsemblGRCm38mm10GRCm38
MGSCv3724,840,042 - 4,859,789 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv3624,836,303 - 4,855,996 (+)NCBIMGSCv36mm8
Celera24,874,084 - 4,893,837 (+)NCBICelera
Cytogenetic Map2A1NCBI
cM Map23.06NCBI
Phyh
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554621,238,622 - 1,250,736 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554621,238,622 - 1,250,731 (-)NCBIChiLan1.0ChiLan1.0
PHYH
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2825,798,371 - 25,822,011 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11025,803,696 - 25,826,001 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01013,277,804 - 13,300,115 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11013,250,722 - 13,634,152 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1013,251,223 - 13,636,018 (-)Ensemblpanpan1.1panPan2
LOC478000
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1223,185,901 - 23,206,719 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl223,185,782 - 23,253,497 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha220,243,502 - 20,263,391 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0223,491,323 - 23,512,130 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl223,491,168 - 23,619,903 (+)EnsemblROS_Cfam_1.0 Ensembl
UNSW_CanFamBas_1.0221,525,646 - 21,546,459 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0222,153,837 - 22,174,674 (+)NCBIUU_Cfam_GSD_1.0
PHYH
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1048,404,293 - 48,423,973 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11048,404,298 - 48,423,978 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
PHYH
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1913,309,059 - 13,331,606 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl913,308,951 - 13,331,504 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605118,841,615 - 18,862,691 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Phyh
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046248055,801,392 - 5,813,696 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

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Variants in Phyh
109 total Variants

Predicted Target Of
Summary Value
Count of predictions:34
Count of miRNA genes:29
Interacting mature miRNAs:34
Transcripts:ENSRNOT00000024362
Prediction methods:Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


1 to 10 of 30 rows
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD ID
Symbol
Name
LOD
P Value
Trait
Sub Trait
Chr
Start
Stop
Species
1358295Aocep1Aortic cell protein QTL 16.17e-07thoracic aorta cellular protein amount (VT:0010598)aortic cell percentage174099000585990005Rat
152023626Bp403Blood pressure QTL 4033.86arterial blood pressure trait (VT:2000000)172393042179524188Rat
7411575Bw140Body weight QTL 14030.20.001body mass (VT:0001259)body weight gain (CMO:0000420)174856093586533673Rat
2301412Kidm40Kidney mass QTL 400.001kidney mass (VT:0002707)both kidneys wet weight to body weight ratio (CMO:0000340)173747984782479847Rat
631502Cm26Cardiac mass QTL 263.71heart left ventricle mass (VT:0007031)heart left ventricle wet weight (CMO:0000071)176570358081153923Rat
1354588Bvd4Brain ventricular dilatation QTL 45.310.001brain ventricle morphology trait (VT:0000822)hydrocephalus severity score (CMO:0001881)175349882882479847Rat
7411577Bw141Body weight QTL 1410.001body mass (VT:0001259)body weight gain (CMO:0000420)176261951686533673Rat
9590107Sffal7Serum free fatty acids level QTL 74.810.001blood free fatty acid amount (VT:0001553)plasma free fatty acids level (CMO:0000546)172840914773409147Rat
2317038Ginf3Gastrointestinal inflammation QTL 32.890.005liver integrity trait (VT:0010547)liver granuloma severity score (CMO:0002157)174992015486533673Rat
724549Niddm56Non-insulin dependent diabetes mellitus QTL 560.03blood glucose amount (VT:0000188)blood glucose level area under curve (AUC) (CMO:0000350)173199078476990784Rat

1 to 10 of 30 rows
RH129871  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.21773,329,149 - 73,329,343 (+)MAPPERmRatBN7.2
Rnor_6.01777,287,269 - 77,287,462NCBIRnor6.0
Rnor_5.01778,953,089 - 78,953,282UniSTSRnor5.0
RGSC_v3.41784,417,862 - 84,418,055UniSTSRGSC3.4
Celera1772,769,751 - 72,769,944UniSTS
RH 3.4 Map17725.7UniSTS
Cytogenetic Map17q12.3UniSTS
AI256161  
Rat AssemblyChrPosition (strand)SourceJBrowse
GRCr81778,238,595 - 78,238,675 (+)Marker Load Pipeline
mRatBN7.21773,329,308 - 73,329,389 (+)MAPPERmRatBN7.2
Rnor_6.01777,287,428 - 77,287,508NCBIRnor6.0
Rnor_5.01778,953,248 - 78,953,328UniSTSRnor5.0
RGSC_v3.41784,418,021 - 84,418,101UniSTSRGSC3.4
Celera1772,769,910 - 72,769,990UniSTS
Cytogenetic Map17q12.3UniSTS
BE114499  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.21773,334,356 - 73,334,526 (+)MAPPERmRatBN7.2
Rnor_6.01777,292,480 - 77,292,649NCBIRnor6.0
Rnor_5.01778,958,298 - 78,958,467UniSTSRnor5.0
RGSC_v3.41784,423,071 - 84,423,240UniSTSRGSC3.4
Celera1772,774,928 - 72,775,097UniSTS
RH 3.4 Map17729.8UniSTS
Cytogenetic Map17q12.3UniSTS




alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
nervous system
renal system
reproductive system
respiratory system
9 11 49 113 91 90 59 25 59 6 218 97 93 45 60 31



Ensembl Acc Id: ENSRNOT00000024362   ⟹   ENSRNOP00000024362
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl1773,329,082 - 73,346,409 (-)Ensembl
Rnor_6.0 Ensembl1777,287,188 - 77,304,530 (-)Ensembl
RefSeq Acc Id: NM_053674   ⟹   NP_446126
RefSeq Status: PROVISIONAL
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr81778,238,747 - 78,255,645 (-)NCBI
mRatBN7.21773,329,461 - 73,346,359 (-)NCBI
Rnor_6.01777,287,580 - 77,304,482 (-)NCBI
Rnor_5.01778,953,400 - 78,970,299 (-)NCBI
RGSC_v3.41784,418,173 - 84,435,073 (-)RGD
Celera1772,770,062 - 72,786,946 (-)RGD
Sequence:
1 to 9 of 9 rows
Protein RefSeqs NP_446126 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAF15971 (Get FASTA)   NCBI Sequence Viewer  
  AAH86573 (Get FASTA)   NCBI Sequence Viewer  
  EDL78672 (Get FASTA)   NCBI Sequence Viewer  
  EDL78673 (Get FASTA)   NCBI Sequence Viewer  
  EDL78674 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSRNOP00000024362
  ENSRNOP00000024362.3
GenBank Protein P57093 (Get FASTA)   NCBI Sequence Viewer  
1 to 9 of 9 rows
RefSeq Acc Id: NP_446126   ⟸   NM_053674
- Peptide Label: precursor
- UniProtKB: Q9QY64 (UniProtKB/Swiss-Prot),   P57093 (UniProtKB/Swiss-Prot),   A6JLZ6 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSRNOP00000024362   ⟸   ENSRNOT00000024362

Name Modeler Protein Id AA Range Protein Structure
AF-P57093-F1-model_v2 AlphaFold P57093 1-338 view protein structure


eQTL   View at Phenogen
WGCNA   View at Phenogen
Tissue/Strain Expression   View at Phenogen

RGD ID:13700574
Promoter ID:EPDNEW_R11098
Type:multiple initiation site
Name:Phyh_1
Description:phytanoyl-CoA 2-hydroxylase
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Rat AssemblyChrPosition (strand)Source
Rnor_6.01777,304,489 - 77,304,549EPDNEW


1 to 24 of 24 rows
Database
Acc Id
Source(s)
BioCyc Gene G2FUF-8687 BioCyc
BioCyc Pathway PWY66-387 [3-methyl-branched fatty acid alpha-oxidation] BioCyc
BioCyc Pathway Image PWY66-387 BioCyc
Ensembl Genes ENSRNOG00000018044 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENSRNOT00000024362 ENTREZGENE
  ENSRNOT00000024362.7 UniProtKB/Swiss-Prot
Gene3D-CATH q2cbj1_9rhob like domain UniProtKB/Swiss-Prot
IMAGE_CLONE IMAGE:7306754 IMAGE-MGC_LOAD
InterPro PhyH UniProtKB/Swiss-Prot
  Phytyl_CoA_dOase UniProtKB/Swiss-Prot
KEGG Report rno:114209 UniProtKB/Swiss-Prot
MGC_CLONE MGC:105364 IMAGE-MGC_LOAD
NCBI Gene 114209 ENTREZGENE
PANTHER PHYTANOYL-COA ALPHA-HYDROXYLASE UniProtKB/Swiss-Prot
  PHYTANOYL-COA DIOXYGENASE, PEROXISOMAL UniProtKB/Swiss-Prot
Pfam PhyH UniProtKB/Swiss-Prot
PhenoGen Phyh PhenoGen
RatGTEx ENSRNOG00000018044 RatGTEx
Superfamily-SCOP Clavaminate synthase-like UniProtKB/Swiss-Prot
UniProt A6JLZ6 ENTREZGENE, UniProtKB/TrEMBL
  A6JLZ7_RAT UniProtKB/TrEMBL
  P57093 ENTREZGENE, UniProtKB/Swiss-Prot
  Q9QY64 ENTREZGENE
UniProt Secondary Q9QY64 UniProtKB/Swiss-Prot
1 to 24 of 24 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2008-11-06 Phyh  phytanoyl-CoA 2-hydroxylase  Phyh  phytanoyl-CoA hydroxylase  Nomenclature updated to reflect human and mouse nomenclature 1299863 APPROVED
2005-01-20 Phyh  phytanoyl-CoA hydroxylase    phytanoyl-CoA hydroxylase (Refsum disease)  Name updated 1299863 APPROVED
2002-08-07 Phyh  phytanoyl-CoA hydroxylase (Refsum disease)      Symbol and Name status set to provisional 70820 PROVISIONAL