Ift140 (intraflagellar transport 140) - Rat Genome Database

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Gene: Ift140 (intraflagellar transport 140) Rattus norvegicus
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Symbol: Ift140
Name: intraflagellar transport 140
RGD ID: 2318759
Description: Predicted to be involved in intraciliary retrograde transport and regulation of cilium assembly. Predicted to act upstream of or within several processes, including cilium organization; embryonic organ development; and regionalization. Predicted to be located in several cellular components, including microtubule organizing center; nucleoplasm; and photoreceptor cell cilium. Predicted to be part of intraciliary transport particle A. Predicted to be active in axoneme and ciliary basal body. Human ortholog(s) of this gene implicated in retinitis pigmentosa and short-rib thoracic dysplasia 9 with or without polydactyly. Orthologous to human IFT140 (intraflagellar transport 140); INTERACTS WITH (+)-schisandrin B; 2,3,7,8-tetrachlorodibenzodioxine; endosulfan.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: intraflagellar transport protein 140 homolog; LOC100362124
RGD Orthologs
Human
Mouse
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: Ift140em1Kyo
Genetic Models: W-Ift140em1Kyo
Latest Assembly: GRCr8 - GRCr8 Assembly
Position:
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81014,537,134 - 14,624,926 (+)NCBIGRCr8
mRatBN7.21014,032,665 - 14,121,682 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1014,032,648 - 14,120,433 (+)EnsemblmRatBN7.2 Ensembl
Rnor_6.01014,373,668 - 14,461,509 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1014,373,679 - 14,461,160 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01014,189,328 - 14,276,940 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41014,258,556 - 14,348,468 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera1013,711,169 - 13,793,096 (+)NCBICelera
Cytogenetic Map10q12NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


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Object Symbol
Species
Term
Qualifier
Evidence
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Reference
Notes
Source
Original Reference(s)
Ift140Ratasphyxiating thoracic dystrophy  ISORGD:16054138554872ClinVar Annotator: match by term: Jeune thoracic dystrophyClinVarPMID:16199547|PMID:17576681|PMID:22503633|PMID:23418020|PMID:24009529|PMID:25741868|PMID:26216056|PMID:28288023|PMID:28492532|PMID:28559085|PMID:28724397|PMID:29068549|PMID:29688594|PMID:30773290|PMID:31589614|PMID:31964843|PMID:32483926|PMID:34429528|PMID:34890546|PMID:35140360|PMID:9536098
Ift140Ratasphyxiating thoracic dystrophy 1  ISORGD:16054138554872ClinVar Annotator: match by term: Chondroectodermal dysplasia-like syndrome | ClinVar Annotator: match by term: Short-rib more ...ClinVarPMID:17576681|PMID:22503633|PMID:23418020|PMID:24009529|PMID:25741868|PMID:26216056|PMID:28288023|PMID:28492532|PMID:28559085|PMID:28724397|PMID:29068549|PMID:29688594|PMID:30773290|PMID:9536098
Ift140Ratautosomal dominant polycystic kidney disease  ISORGD:16054138554872ClinVar Annotator: match by term: Autosomal dominant polycystic kidney diseaseClinVarPMID:16199547|PMID:22282595|PMID:22503633|PMID:23418020|PMID:24009529|PMID:25741868|PMID:26216056|PMID:26968735|PMID:28492532|PMID:31589614|PMID:31964843|PMID:31980526|PMID:32037395|PMID:34890546|PMID:35649421
Ift140Ratcystic kidney disease  ISORGD:16054138554872ClinVar Annotator: match by term: Renal cystClinVarPMID:16199547|PMID:22282595|PMID:22503633|PMID:23418020|PMID:24009529|PMID:25741868|PMID:26216056|PMID:26968735|PMID:28492532|PMID:31589614|PMID:31630094|PMID:31736247|PMID:31964843|PMID:31980526|PMID:32037395|PMID:34890546|PMID:34906470|PMID:35649421
Ift140Ratepilepsy  ISORGD:16054138554872ClinVar Annotator: match by term: EpilepsyClinVarPMID:28492532
Ift140Ratfundus dystrophy  ISORGD:16054138554872ClinVar Annotator: match by term: Retinal dystrophyClinVarPMID:16199547|PMID:17576681|PMID:22282595|PMID:22503633|PMID:23418020|PMID:24009529|PMID:25741868|PMID:26216056|PMID:26497376|PMID:26766544|PMID:26968735|PMID:28492532|PMID:29068549|PMID:29688594|PMID:30479745|PMID:30902645|PMID:31213501|PMID:31456290|PMID:31589614|PMID:31630094|PMID:31736247|PMID:3196484|PMID:31964843|PMID:31980526|PMID:32007091|PMID:32037395|PMID:32483926|PMID:32531858|PMID:32901917|PMID:33452237|PMID:33946315|PMID:34217267|PMID:34596737|PMID:34758253|PMID:34890546|PMID:35140360|PMID:35649421|PMID:36460718|PMID:9536098
Ift140Ratgenetic disease  ISORGD:16054138554872ClinVar Annotator: match by term: Inborn genetic diseasesClinVarPMID:25741868|PMID:28492532|PMID:32901917|PMID:34217267
Ift140RatIdiopathic Generalized Epilepsy  ISORGD:16054138554872ClinVar Annotator: match by term: Idiopathic generalized epilepsyClinVarPMID:28492532
Ift140Ratkidney disease  ISORGD:16054138554872ClinVar Annotator: match by term: renal diseaseClinVarPMID:25741868|PMID:32037395
Ift140RatLeber congenital amaurosis  ISORGD:16054138554872ClinVar Annotator: match by term: Leber congenital amaurosisClinVarPMID:25741868
Ift140Ratmicrocephaly  ISORGD:16054138554872ClinVar Annotator: match by term: MicrocephalyClinVarPMID:25741868|PMID:28492532
Ift140Ratmyoepithelioma  ISORGD:16054138554872ClinVar Annotator: match by term: Myoepithelial tumorClinVar 
Ift140Ratnephronophthisis  ISORGD:16054138554872ClinVar Annotator: match by term: NephronophthisisClinVarPMID:17576681|PMID:22503633|PMID:25741868|PMID:28288023|PMID:28492532|PMID:28559085|PMID:28724397|PMID:28844315|PMID:29068549|PMID:29688594|PMID:29706353|PMID:30773290|PMID:9536098
Ift140Ratnephronophthisis 1  ISORGD:16054138554872ClinVar Annotator: match by term: juvenile nephronophthisisClinVarPMID:17576681|PMID:22503633|PMID:25741868|PMID:28288023|PMID:28492532|PMID:28559085|PMID:28724397|PMID:29068549|PMID:29688594|PMID:30773290|PMID:9536098
Ift140Ratoptic atrophy  ISORGD:16054138554872ClinVar Annotator: match by term: Optic atrophyClinVarPMID:25741868|PMID:28492532
Ift140Ratpolycystic kidney disease  ISORGD:16054138554872ClinVar Annotator: match by term: Polycystic kidney diseaseClinVarPMID:16199547|PMID:22282595|PMID:22503633|PMID:23418020|PMID:24009529|PMID:25741868|PMID:26216056|PMID:26968735|PMID:28492532|PMID:31589614|PMID:31964843|PMID:31980526|PMID:32037395|PMID:34890546|PMID:35649421
Ift140Ratretinitis pigmentosa  ISORGD:16054138554872ClinVar Annotator: match by term: Retinitis pigmentosaClinVarPMID:16199547|PMID:22503633|PMID:23418020|PMID:24009529|PMID:25741868|PMID:26216056|PMID:26497376|PMID:26766544|PMID:26968735|PMID:28041643|PMID:28492532|PMID:28559085|PMID:29068549|PMID:29688594|PMID:30479745|PMID:31213501|PMID:31456290|PMID:31589614|PMID:31630094|PMID:31736247|PMID:3196484|PMID:31964843|PMID:31980526|PMID:32007091|PMID:32483926|PMID:32531858|PMID:33452237|PMID:34429528|PMID:34596737|PMID:34758253|PMID:34890546|PMID:34906470|PMID:35140360|PMID:36084042|PMID:38219857
Ift140Ratretinitis pigmentosa 80  ISORGD:16054138554872ClinVar Annotator: match by term: Retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene more ...ClinVarPMID:16199547|PMID:17576681|PMID:22282595|PMID:22503633|PMID:23418020|PMID:24009529|PMID:24698627|PMID:25741868|PMID:26216056|PMID:26359340|PMID:26766544|PMID:26968735|PMID:28288023|PMID:28492532|PMID:28512305|PMID:28559085|PMID:28724397|PMID:29068549|PMID:29111861|PMID:29688594|PMID:30479745|PMID:30773290|PMID:31047384|PMID:31054281|PMID:31130284|PMID:31213501|PMID:31589614|PMID:31630094|PMID:31736247|PMID:31964843|PMID:31980526|PMID:32007091|PMID:32037395|PMID:32531858|PMID:32860008|PMID:33452237|PMID:34429528|PMID:34596737|PMID:34758253|PMID:34890546|PMID:34906470|PMID:35649421|PMID:36084042|PMID:38219857|PMID:9536098
Ift140Ratshort-rib thoracic dysplasia 9 with or without polydactyly  ISORGD:16054138554872ClinVar Annotator: match by term: Saldino-Mainzer syndrome | ClinVar Annotator: match by term: Short-rib thoracic more ...ClinVarPMID:16199547|PMID:17576681|PMID:19370764|PMID:19561590|PMID:20301784|PMID:20354512|PMID:22282595|PMID:22503633|PMID:23418020|PMID:24009529|PMID:24183451|PMID:24698627|PMID:25640679|PMID:25741868|PMID:26216056|PMID:26359340|PMID:26766544|PMID:26968735|PMID:27058611|PMID:27874174|PMID:28041643|PMID:28288023|PMID:28492532|PMID:28512305|PMID:28559085|PMID:28724397|PMID:28844315|PMID:28991257|PMID:29068549|PMID:29111861|PMID:29688594|PMID:29706353|PMID:29758562|PMID:29801666|PMID:30479745|PMID:30773290|PMID:30902645|PMID:31047384|PMID:31054281|PMID:31130284|PMID:31213501|PMID:31456290|PMID:31589614|PMID:31630094|PMID:31736247|PMID:31964843|PMID:31980526|PMID:32007091|PMID:32037395|PMID:32483926|PMID:32531858|PMID:32860008|PMID:32901917|PMID:33452237|PMID:33532864|PMID:33576794|PMID:33946315|PMID:34217267|PMID:34429528|PMID:34596737|PMID:34662339|PMID:34758253|PMID:34890546|PMID:34906470|PMID:35140360|PMID:35649421|PMID:36084042|PMID:36460718|PMID:38219857|PMID:9536098
Ift140Rattuberous sclerosis 2  ISORGD:16054138554872ClinVar Annotator: match by term: Tuberous sclerosis 2ClinVarPMID:16114042|PMID:17287951|PMID:20498439|PMID:28492532|PMID:29932062
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Original Reference(s)
Ift140Ratasphyxiating thoracic dystrophy  ISORGD:160541311554173CTD Direct Evidence: marker/mechanismCTD 
Object Symbol
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Original Reference(s)
Ift140Ratasphyxiating thoracic dystrophy 1  ISSRGD:155366413592920OMIM:208500MouseDO 
Ift140Ratshort-rib thoracic dysplasia 9 with or without polydactyly  ISSRGD:155366413592920OMIM:266920MouseDO 
Object Symbol
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Original Reference(s)
Ift140Ratretinitis pigmentosa 80  ISORGD:16054137240710 OMIM 
Ift140Ratshort-rib thoracic dysplasia 9 with or without polydactyly  ISORGD:16054137240710 OMIM 

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Original Reference(s)
Ift140Rat(+)-schisandrin B multiple interactionsEXP 6480464schizandrin B inhibits the reaction [Carbon Tetrachloride results in decreased expression of IFT140 mRNA]CTDPMID:31150632
Ift140Rat(1->4)-beta-D-glucan multiple interactionsISORGD:15536646480464[perfluorooctane sulfonic acid co-treated with Cellulose] results in decreased expression of IFT140 mRNACTDPMID:36331819
Ift140Rat17beta-estradiol decreases expressionISORGD:16054136480464Estradiol results in decreased expression of IFT140 mRNACTDPMID:31614463
Ift140Rat2,3,7,8-tetrachlorodibenzodioxine decreases expressionISORGD:15536646480464Tetrachlorodibenzodioxin results in decreased expression of IFT140 mRNACTDPMID:19770486
Ift140Rat2,3,7,8-tetrachlorodibenzodioxine decreases expressionEXP 6480464Tetrachlorodibenzodioxin results in decreased expression of IFT140 mRNACTDPMID:33387578
Ift140Rat2,3,7,8-tetrachlorodibenzodioxine affects expressionISORGD:15536646480464Tetrachlorodibenzodioxin affects the expression of IFT140 mRNACTDPMID:21570461
Ift140Rat4,4'-sulfonyldiphenol decreases expressionISORGD:15536646480464bisphenol S results in decreased expression of IFT140 mRNACTDPMID:39298647
Ift140Ratacrylamide decreases expressionISORGD:16054136480464Acrylamide results in decreased expression of IFT140 mRNACTDPMID:32763439
Ift140Rataristolochic acid A decreases expressionISORGD:16054136480464aristolochic acid I results in decreased expression of IFT140 mRNACTDPMID:33212167
Ift140Ratarsane affects methylationISORGD:16054136480464Arsenic affects the methylation of IFT140 geneCTDPMID:25304211
Ift140Ratarsane multiple interactionsISORGD:16054136480464[sodium arsenite results in increased abundance of Arsenic] which results in decreased expression of IFT140 more ...CTDPMID:39836092
Ift140Ratarsenic atom affects methylationISORGD:16054136480464Arsenic affects the methylation of IFT140 geneCTDPMID:25304211
Ift140Ratarsenic atom multiple interactionsISORGD:16054136480464[sodium arsenite results in increased abundance of Arsenic] which results in decreased expression of IFT140 more ...CTDPMID:39836092
Ift140Ratarsenous acid increases expressionISORGD:15536646480464Arsenic Trioxide results in increased expression of IFT140 mRNACTDPMID:35676786
Ift140Ratbenzo[a]pyrene decreases expressionISORGD:15536646480464Benzo(a)pyrene results in decreased expression of IFT140 mRNACTDPMID:22228805
Ift140Ratbenzo[a]pyrene increases methylationISORGD:16054136480464Benzo(a)pyrene results in increased methylation of IFT140 5' UTRCTDPMID:27901495
Ift140Ratbenzo[a]pyrene affects methylationISORGD:16054136480464Benzo(a)pyrene affects the methylation of IFT140 intronCTDPMID:30157460
Ift140Ratbenzo[a]pyrene increases methylationISORGD:15536646480464Benzo(a)pyrene results in increased methylation of IFT140 intronCTDPMID:27901495
Ift140Ratbenzo[e]pyrene increases methylationISORGD:16054136480464benzo(e)pyrene results in increased methylation of IFT140 intronCTDPMID:30157460
Ift140Ratbis(2-ethylhexyl) phthalate decreases expressionISORGD:16054136480464Diethylhexyl Phthalate results in decreased expression of IFT140 mRNACTDPMID:31163220

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Biological Process
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Original Reference(s)
Ift140Ratcilium assembly involved_inISORGD:16054131624291 PMID:28724397RGDPMID:28724397
Ift140Ratcilium assembly acts_upstream_of_or_withinIEAUniProtKB:E9PY46|ensembl:ENSMUSP000000249831600115GO_REF:0000107EnsemblGO_REF:0000107
Ift140Ratcilium assembly acts_upstream_of_or_withinISORGD:15536641624291MGI:5311831 PMID:22282595RGDPMID:22282595
Ift140Ratcilium assembly involved_inIEAUniProtKB:Q96RY7|ensembl:ENSP000004060121600115GO_REF:0000107EnsemblGO_REF:0000107
Ift140Ratcilium organization involved_inIEAARBA:ARBA000275401600115GO_REF:0000117UniProtGO_REF:0000117
Ift140Ratdetermination of left/right symmetry acts_upstream_of_or_withinIEAUniProtKB:E9PY46|ensembl:ENSMUSP000000249831600115GO_REF:0000107EnsemblGO_REF:0000107
Ift140Ratdetermination of left/right symmetry acts_upstream_of_or_withinISORGD:15536641624291 PMID:25807483RGDPMID:25807483
Ift140Ratembryonic brain development acts_upstream_of_or_withinIEAUniProtKB:E9PY46|ensembl:ENSMUSP000000249831600115GO_REF:0000107EnsemblGO_REF:0000107
Ift140Ratembryonic brain development acts_upstream_of_or_withinISORGD:15536641624291MGI:4458412 PMID:23469164RGDPMID:23469164
Ift140Ratembryonic camera-type eye development acts_upstream_of_or_withinISORGD:15536641624291MGI:4458412 PMID:23469164RGDPMID:23469164
Ift140Ratembryonic camera-type eye development acts_upstream_of_or_withinIEAUniProtKB:E9PY46|ensembl:ENSMUSP000000249831600115GO_REF:0000107EnsemblGO_REF:0000107
Ift140Ratembryonic cranial skeleton morphogenesis acts_upstream_of_or_withinIEAUniProtKB:E9PY46|ensembl:ENSMUSP000000249831600115GO_REF:0000107EnsemblGO_REF:0000107
Ift140Ratembryonic cranial skeleton morphogenesis acts_upstream_of_or_withinISORGD:15536641624291MGI:4458412 PMID:23469164RGDPMID:23469164
Ift140Ratembryonic digit morphogenesis acts_upstream_of_or_withinISORGD:15536641624291MGI:4458412 PMID:23469164RGDPMID:23469164
Ift140Ratembryonic digit morphogenesis acts_upstream_of_or_withinIEAUniProtKB:E9PY46|ensembl:ENSMUSP000000249831600115GO_REF:0000107EnsemblGO_REF:0000107
Ift140Ratheart development acts_upstream_of_or_withinISORGD:15536641624291 PMID:25807483RGDPMID:25807483
Ift140Ratheart development acts_upstream_of_or_withinIEAUniProtKB:E9PY46|ensembl:ENSMUSP000000249831600115GO_REF:0000107EnsemblGO_REF:0000107
Ift140Ratintraciliary retrograde transport involved_inISORGD:16054131624291 PMID:22503633RGDPMID:22503633
Ift140Ratintraciliary retrograde transport involved_inIEAUniProtKB:Q96RY7|ensembl:ENSP000004060121600115GO_REF:0000107EnsemblGO_REF:0000107
Ift140Ratintraciliary retrograde transport involved_inIBAFB:FBgn0260933|MGI:2146906|PANTHER:PTN000404361|UniProtKB:Q96RY71600115GO_REF:0000033GO_CentralGO_REF:0000033
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Cellular Component
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Original Reference(s)
Ift140Rataxoneme is_active_inIBAMGI:2146906|PANTHER:PTN000404360|UniProtKB:A0A644F0T7|UniProtKB:A8BAF1|UniProtKB:A8BJ871600115GO_REF:0000033GO_CentralGO_REF:0000033
Ift140Rataxoneme located_inIEAUniProtKB:E9PY46|ensembl:ENSMUSP000000249831600115GO_REF:0000107EnsemblGO_REF:0000107
Ift140Rataxoneme located_inISORGD:15536641624291 PMID:20368623, PMID:23418020RGDPMID:20368623|PMID:23418020
Ift140Ratcell projection located_inIEAUniProtKB-KW:KW-09661600115GO_REF:0000043UniProtGO_REF:0000043
Ift140Ratcentriole located_inISORGD:15536641624291 PMID:29487109RGDPMID:29487109
Ift140Ratcentriole located_inIEAUniProtKB:E9PY46|ensembl:ENSMUSP000000249831600115GO_REF:0000107EnsemblGO_REF:0000107
Ift140Ratcentrosome located_inISORGD:16054131624291 PMID:23418020RGDPMID:23418020
Ift140Ratcentrosome located_inIEAUniProtKB:Q96RY7|ensembl:ENSP000004060121600115GO_REF:0000107EnsemblGO_REF:0000107
Ift140Ratciliary basal body is_active_inIBAMGI:2146906|PANTHER:PTN000404360|UniProtKB:A0A644F0T7|UniProtKB:A8BAF1|UniProtKB:A8BJ87|UniProtKB:Q96RY71600115GO_REF:0000033GO_CentralGO_REF:0000033
Ift140Ratciliary basal body located_inIEAUniProtKB:E9PY46|ensembl:ENSMUSP000000249831600115GO_REF:0000107EnsemblGO_REF:0000107
Ift140Ratciliary basal body located_inISORGD:1605413|UniProtKB:Q96RY7-11624291 RGDGO_REF:0000052
Ift140Ratciliary basal body located_inIEAUniProtKB:Q96RY7|ensembl:ENSP000004060121600115GO_REF:0000107EnsemblGO_REF:0000107
Ift140Ratciliary basal body located_inISORGD:16054131624291 PMID:22503633RGDPMID:22503633
Ift140Ratciliary basal body located_inISORGD:15536641624291 PMID:23418020, PMID:23955340, PMID:24619649RGDPMID:23418020|PMID:23955340|PMID:24619649
Ift140Ratcilium located_inISORGD:16054131624291 PMID:27932497RGDPMID:27932497
Ift140Ratcilium located_inIEAUniProtKB-SubCell:SL-00661600115GO_REF:0000044UniProtGO_REF:0000044
Ift140Ratcilium located_inIEAARBA:ARBA000283531600115GO_REF:0000117UniProtGO_REF:0000117
Ift140Ratcilium located_inIEAUniProtKB-KW:KW-09691600115GO_REF:0000043UniProtGO_REF:0000043
Ift140Ratcilium located_inISORGD:15536641624291 PMID:20368623, PMID:21209331, PMID:29487109RGDPMID:20368623|PMID:21209331|PMID:29487109
Ift140Ratcilium located_inIEAUniProtKB:E9PY46|ensembl:ENSMUSP000000249831600115GO_REF:0000107EnsemblGO_REF:0000107
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Molecular Function

  
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Original Reference(s)
Ift140Ratprotein binding enablesISORGD:16054131624291UniProtKB:Q8NEZ3|UniProtKB:Q9HBG6 PMID:27173435, PMID:27932497, PMID:29220510RGDPMID:27173435|PMID:27932497|PMID:29220510


#
Reference Title
Reference Citation
1. 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.
2. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
3. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
PMID:20368623   PMID:20889716   PMID:21209331   PMID:22282595   PMID:22503633   PMID:23418020   PMID:23469164   PMID:23955340   PMID:24009529   PMID:24619649   PMID:25807483   PMID:27932497  
PMID:28724397   PMID:29487109  



Ift140
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81014,537,134 - 14,624,926 (+)NCBIGRCr8
mRatBN7.21014,032,665 - 14,121,682 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1014,032,648 - 14,120,433 (+)EnsemblmRatBN7.2 Ensembl
Rnor_6.01014,373,668 - 14,461,509 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1014,373,679 - 14,461,160 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01014,189,328 - 14,276,940 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41014,258,556 - 14,348,468 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera1013,711,169 - 13,793,096 (+)NCBICelera
Cytogenetic Map10q12NCBI
IFT140
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38161,510,427 - 1,612,072 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl161,510,427 - 1,612,072 (-)EnsemblGRCh38hg38GRCh38
GRCh37161,560,428 - 1,662,073 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36161,500,431 - 1,597,299 (-)NCBINCBI36Build 36hg18NCBI36
Celera161,772,703 - 1,874,383 (-)NCBICelera
Cytogenetic Map16p13.3NCBI
HuRef161,486,013 - 1,587,550 (-)NCBIHuRef
CHM1_1161,560,388 - 1,662,050 (-)NCBICHM1_1
T2T-CHM13v2.0161,525,455 - 1,627,919 (-)NCBIT2T-CHM13v2.0
Ift140
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391725,235,056 - 25,318,461 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1725,235,059 - 25,318,469 (+)EnsemblGRCm39 Ensembl
GRCm381725,016,083 - 25,099,499 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1725,016,085 - 25,099,495 (+)EnsemblGRCm38mm10GRCm38
MGSCv371725,153,031 - 25,236,444 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361724,744,323 - 24,827,086 (+)NCBIMGSCv36mm8
Celera1725,543,013 - 25,624,378 (+)NCBICelera
Cytogenetic Map17A3.3NCBI
cM Map1712.53NCBI
Ift140
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495544215,630,501 - 15,718,484 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495544215,625,429 - 15,719,006 (+)NCBIChiLan1.0ChiLan1.0
IFT140
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2181,772,348 - 1,877,046 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1165,560,156 - 5,659,086 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v016130,150 - 232,369 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1161,566,309 - 1,662,833 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl161,566,824 - 1,658,884 (-)Ensemblpanpan1.1panPan2
IFT140
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1639,262,887 - 39,308,912 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl639,295,045 - 39,308,758 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha640,497,349 - 40,577,227 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0639,574,931 - 39,655,255 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl639,577,733 - 39,655,241 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1639,252,090 - 39,332,397 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0639,224,274 - 39,304,564 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0639,702,970 - 39,783,289 (+)NCBIUU_Cfam_GSD_1.0
Ift140
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024409344104,290,046 - 104,364,999 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366942,344,283 - 2,423,520 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049366942,344,448 - 2,419,396 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
IFT140
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl340,309,635 - 40,372,135 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1340,309,298 - 40,372,139 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2341,776,363 - 41,835,312 (+)NCBISscrofa10.2Sscrofa10.2susScr3
IFT140
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.151,419,432 - 1,523,342 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl51,415,664 - 1,521,843 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366606829,562,562 - 29,667,409 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Ift140
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_004624913621,203 - 711,493 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_004624913616,283 - 712,040 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

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Variants in Ift140
282 total Variants

Predicted Target Of
Summary Value
Count of predictions:107
Count of miRNA genes:94
Interacting mature miRNAs:99
Transcripts:ENSRNOT00000022063
Prediction methods:Microtar, 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 25 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
9589136Insul27Insulin level QTL 2710.460.001blood insulin amount (VT:0001560)plasma insulin level (CMO:0000342)101147401056474010Rat
8662860Vetf10Vascular elastic tissue fragility QTL 10artery integrity trait (VT:0010639)number of ruptures of the internal elastic lamina of the abdominal aorta and iliac arteries (CMO:0002562)10615418273453136Rat
2313066Bss63Bone structure and strength QTL 631.40.0001tibia strength trait (VT:1000284)bone polar moment of inertia (CMO:0001558)10538701450387014Rat
631554Bp133Blood pressure QTL 1330.005arterial blood pressure trait (VT:2000000)systolic blood pressure (CMO:0000004)1074336463851208Rat
2313064Bmd71Bone mineral density QTL 710.90.0001tibia mineral mass (VT:1000283)compact volumetric bone mineral density (CMO:0001730)10538701450387014Rat
70223Bp57Blood pressure QTL 575arterial blood pressure trait (VT:2000000)systolic blood pressure (CMO:0000004)10180676123Rat
634329Pia15Pristane induced arthritis QTL 153.1joint integrity trait (VT:0010548)joint inflammation composite score (CMO:0000919)10124158324Rat
1578761Stresp21Stress response QTL 213.3thymus mass (VT:0004954)thymus wet weight (CMO:0000855)10637574651375746Rat
2293680Bss40Bone structure and strength QTL 405.660.0001femur strength trait (VT:0010010)femur total energy absorbed before break (CMO:0001677)10135225947Rat
7387235Uae41Urinary albumin excretion QTL 415.260.1874urine albumin amount (VT:0002871)urine albumin excretion rate (CMO:0000757)10129497586Rat

1 to 10 of 25 rows
RH127790  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.21014,076,808 - 14,077,001 (+)MAPPERmRatBN7.2
Rnor_6.01014,417,899 - 14,418,091NCBIRnor6.0
Rnor_5.01014,233,321 - 14,233,513UniSTSRnor5.0
RGSC_v3.41014,304,856 - 14,305,048UniSTSRGSC3.4
Celera1013,749,486 - 13,749,678UniSTS
Cytogenetic Map10q12UniSTS
RH133574  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.21014,056,395 - 14,056,595 (+)MAPPERmRatBN7.2
Rnor_6.01014,397,500 - 14,397,699NCBIRnor6.0
Rnor_5.01014,213,142 - 14,213,341UniSTSRnor5.0
RGSC_v3.41014,284,461 - 14,284,660UniSTSRGSC3.4
Celera1013,729,059 - 13,729,258UniSTS
RH 3.4 Map10168.8UniSTS


This gene Ift140 is modified in the following models/strains:




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: ENSRNOT00000022063   ⟹   ENSRNOP00000022063
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl1014,032,648 - 14,120,433 (+)Ensembl
Rnor_6.0 Ensembl1014,373,679 - 14,461,160 (+)Ensembl
RefSeq Acc Id: NM_001427126   ⟹   NP_001414055
RefSeq Status: VALIDATED
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr81014,537,466 - 14,624,926 (+)NCBI
RefSeq Acc Id: XM_039087092   ⟹   XP_038943020
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr81014,537,134 - 14,624,926 (+)NCBI
mRatBN7.21014,032,668 - 14,121,682 (+)NCBI
RefSeq Acc Id: XM_039087093   ⟹   XP_038943021
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr81014,537,165 - 14,624,926 (+)NCBI
mRatBN7.21014,032,668 - 14,121,682 (+)NCBI
RefSeq Acc Id: XM_039087096   ⟹   XP_038943024
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr81014,571,927 - 14,624,926 (+)NCBI
mRatBN7.21014,067,416 - 14,121,682 (+)NCBI
RefSeq Acc Id: XM_039087097   ⟹   XP_038943025
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr81014,537,134 - 14,606,569 (+)NCBI
mRatBN7.21014,032,665 - 14,092,962 (+)NCBI
RefSeq Acc Id: XM_063268240   ⟹   XP_063124310
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr81014,537,165 - 14,624,926 (+)NCBI
1 to 9 of 9 rows
Protein RefSeqs NP_001414055 (Get FASTA)   NCBI Sequence Viewer  
  XP_038943020 (Get FASTA)   NCBI Sequence Viewer  
  XP_038943021 (Get FASTA)   NCBI Sequence Viewer  
  XP_038943024 (Get FASTA)   NCBI Sequence Viewer  
  XP_038943025 (Get FASTA)   NCBI Sequence Viewer  
  XP_063124310 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSRNOP00000022063
  ENSRNOP00000022063.5
  ENSRNOP00000100739
1 to 9 of 9 rows
Ensembl Acc Id: ENSRNOP00000022063   ⟸   ENSRNOT00000022063
RefSeq Acc Id: XP_038943025   ⟸   XM_039087097
- Peptide Label: isoform X5
RefSeq Acc Id: XP_038943020   ⟸   XM_039087092
- Peptide Label: isoform X1
RefSeq Acc Id: XP_038943021   ⟸   XM_039087093
- Peptide Label: isoform X2
RefSeq Acc Id: XP_038943024   ⟸   XM_039087096
- Peptide Label: isoform X4

Name Modeler Protein Id AA Range Protein Structure
AF-F1LY69-F1-model_v2 AlphaFold F1LY69 1-1463 view protein structure


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

RGD ID:13697040
Promoter ID:EPDNEW_R7563
Type:single initiation site
Name:Ift140_1
Description:intraflagellar transport 140
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_R7564  
Experiment Methods:Single-end sequencing.
Position:
Rat AssemblyChrPosition (strand)Source
Rnor_6.01014,373,691 - 14,373,751EPDNEW
RGD ID:13697044
Promoter ID:EPDNEW_R7564
Type:initiation region
Name:Ift140_2
Description:intraflagellar transport 140
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_R7563  
Experiment Methods:Single-end sequencing.
Position:
Rat AssemblyChrPosition (strand)Source
Rnor_6.01014,373,994 - 14,374,054EPDNEW


1 to 21 of 21 rows
Database
Acc Id
Source(s)
BioCyc Gene G2FUF-25809 BioCyc
Ensembl Genes ENSRNOG00000016545 Ensembl, ENTREZGENE, UniProtKB/TrEMBL
Ensembl Transcript ENSRNOT00000022063 ENTREZGENE
  ENSRNOT00000022063.7 UniProtKB/TrEMBL
  ENSRNOT00000146112 ENTREZGENE
Gene3D-CATH 1.25.40.470 UniProtKB/TrEMBL
  2.130.10.10 UniProtKB/TrEMBL
InterPro TPR-like_helical_dom UniProtKB/TrEMBL
  WD40/YVTN_repeat-like_dom UniProtKB/TrEMBL
  WD40_repeat UniProtKB/TrEMBL
  WD40_repeat_dom_sf UniProtKB/TrEMBL
NCBI Gene 100362124 ENTREZGENE
PANTHER IFT140/172-RELATED UniProtKB/TrEMBL
  INTRAFLAGELLAR TRANSPORT PROTEIN 140 HOMOLOG UniProtKB/TrEMBL
PhenoGen Ift140 PhenoGen
RatGTEx ENSRNOG00000016545 RatGTEx
SMART WD40 UniProtKB/TrEMBL
Superfamily-SCOP NHL repeat UniProtKB/TrEMBL
  SSF48452 UniProtKB/TrEMBL
  WD40_like UniProtKB/TrEMBL
UniProt F1LY69 ENTREZGENE, UniProtKB/TrEMBL
1 to 21 of 21 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2012-08-27 Ift140  intraflagellar transport 140  LOC100362124  intraflagellar transport 140  Nomenclature updated to reflect human and mouse nomenclature 1299863 APPROVED
2010-05-05 LOC100362124  intraflagellar transport 140      Symbol and Name status set to provisional 70820 PROVISIONAL