Tmem127 (transmembrane protein 127) - Rat Genome Database

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Gene: Tmem127 (transmembrane protein 127) Rattus norvegicus
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Symbol: Tmem127
Name: transmembrane protein 127
RGD ID: 1309744
Description: Predicted to enable small GTPase binding activity. Predicted to be involved in negative regulation of TOR signaling and negative regulation of cell population proliferation. Predicted to act upstream of or within endosome organization. Predicted to be located in early endosome and plasma membrane. Predicted to be active in membrane. Human ortholog(s) of this gene implicated in pheochromocytoma. Orthologous to human TMEM127 (transmembrane protein 127); INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine; 6-propyl-2-thiouracil; acrylamide.
Type: protein-coding
RefSeq Status: PROVISIONAL
Previously known as: LOC311405; MGC156781; RGD1309744; similar to hypothetical protein FLJ20507
RGD Orthologs
Human
Mouse
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Latest Assembly: GRCr8 - GRCr8 Assembly
Position:
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr83134,919,416 - 134,932,210 (+)NCBIGRCr8
mRatBN7.23114,466,095 - 114,478,894 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl3114,466,171 - 114,477,519 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx3118,357,660 - 118,370,450 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.03126,953,204 - 126,965,994 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.03124,613,584 - 124,626,374 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.03119,677,575 - 119,690,371 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl3119,677,575 - 119,690,366 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.03126,202,774 - 126,215,589 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.43114,746,454 - 114,759,251 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.13114,652,049 - 114,664,824 (+)NCBI
Celera3113,306,634 - 113,319,570 (+)NCBICelera
Cytogenetic Map3q36NCBI
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)
Tmem127Ratacute myeloid leukemia  ISORGD:16019918554872ClinVar Annotator: match by term: Acute myeloid leukemia, adultClinVarPMID:20923864|PMID:25741868|PMID:28492532
Tmem127Ratacute promyelocytic leukemia  ISORGD:16019918554872ClinVar Annotator: match by term: Acute promyelocytic leukemiaClinVarPMID:25741868|PMID:28492532|PMID:32575117
Tmem127RatHereditary Neoplastic Syndromes  ISORGD:16019918554872ClinVar Annotator: match by term: Hereditary Cancer Syndrome | ClinVar Annotator: match by term: Hereditary more ...ClinVarPMID:17576681|PMID:20154675|PMID:20923864|PMID:21156949|PMID:21613359|PMID:22136840|PMID:22419703|PMID:22517554|PMID:22541004|PMID:23551308|PMID:23666964|PMID:24033266|PMID:24334765|PMID:24694336|PMID:25389632|PMID:25637381|PMID:25741868|PMID:26267327|PMID:26269449|PMID:26467025|PMID:26960314|PMID:27153395|PMID:28384794|PMID:28458909|PMID:28492532|PMID:28567294|PMID:28646318|PMID:28855235|PMID:29282712|PMID:29625052|PMID:29909963|PMID:30113886|PMID:30877234|PMID:31666924|PMID:32575117|PMID:32877928|PMID:32994724|PMID:33051659|PMID:33219105|PMID:34308366|PMID:34439168|PMID:34870338|PMID:9536098
Tmem127RatHereditary Neoplastic Syndromes  ISORGD:16019918554872ClinVar Annotator: match by term: Hereditary Cancer Syndrome | ClinVar Annotator: match by term: Hereditary more ...ClinVarPMID:17576681|PMID:20154675|PMID:20923864|PMID:21156949|PMID:21613359|PMID:22136840|PMID:22419703|PMID:22517554|PMID:22541004|PMID:23551308|PMID:23666964|PMID:24033266|PMID:24334765|PMID:24694336|PMID:25389632|PMID:25637381|PMID:25741868|PMID:26267327|PMID:26269449|PMID:26467025|PMID:26960314|PMID:27153395|PMID:28384794|PMID:28458909|PMID:28492532|PMID:28567294|PMID:28646318|PMID:28717660|PMID:28855235|PMID:29282712|PMID:29625052|PMID:29909963|PMID:30113886|PMID:30246500|PMID:30877234|PMID:31666924|PMID:32575117|PMID:32877928|PMID:32994724|PMID:33051659|PMID:33219105|PMID:34308366|PMID:34439168|PMID:34870338|PMID:35189708|PMID:36451132|PMID:36655350|PMID:9536098
Tmem127RatHereditary Neoplastic Syndromes  ISORGD:16019918554872ClinVar Annotator: match by term: Hereditary Cancer Syndrome | ClinVar Annotator: match by term: Hereditary more ...ClinVarPMID:16199547|PMID:17576681|PMID:20154675|PMID:20923864|PMID:21156949|PMID:21613359|PMID:22136840|PMID:22419703|PMID:22517554|PMID:22541004|PMID:23551308|PMID:23666964|PMID:24033266|PMID:24334765|PMID:24694336|PMID:25389632|PMID:25637381|PMID:25741868|PMID:26267327|PMID:26269449|PMID:26467025|PMID:26960314|PMID:27153395|PMID:28384794|PMID:28458909|PMID:28492532|PMID:28567294|PMID:28646318|PMID:28855235|PMID:29282712|PMID:29625052|PMID:29909963|PMID:30113886|PMID:30877234|PMID:31666924|PMID:32575117|PMID:32877928|PMID:32994724|PMID:33051659|PMID:33219105|PMID:34439168|PMID:34870338|PMID:9536098
Tmem127RatHereditary Neoplastic Syndromes  ISORGD:16019918554872ClinVar Annotator: match by term: Hereditary Cancer Syndrome | ClinVar Annotator: match by term: Hereditary more ...ClinVarPMID:16199547|PMID:17576681|PMID:20154675|PMID:20923864|PMID:21156949|PMID:21613359|PMID:22136840|PMID:22419703|PMID:22517554|PMID:22541004|PMID:23666964|PMID:24033266|PMID:24334765|PMID:24694336|PMID:25389632|PMID:25637381|PMID:25741868|PMID:26267327|PMID:26269449|PMID:26467025|PMID:26960314|PMID:28384794|PMID:28492532|PMID:28567294|PMID:28855235|PMID:29282712|PMID:29625052|PMID:29909963|PMID:30113886|PMID:30877234|PMID:31666924|PMID:32575117|PMID:32877928|PMID:33051659|PMID:33219105|PMID:34439168|PMID:34870338|PMID:9536098
Tmem127RatHereditary Neoplastic Syndromes  ISORGD:16019918554872ClinVar Annotator: match by term: Hereditary Cancer Syndrome | ClinVar Annotator: match by term: Hereditary more ...ClinVarPMID:16199547|PMID:20154675|PMID:20923864|PMID:21156949|PMID:21613359|PMID:22136840|PMID:22419703|PMID:22541004|PMID:23666964|PMID:24033266|PMID:24334765|PMID:24694336|PMID:25389632|PMID:25637381|PMID:25741868|PMID:26267327|PMID:26269449|PMID:26467025|PMID:26960314|PMID:28384794|PMID:28492532|PMID:29282712|PMID:29625052|PMID:29909963|PMID:30113886|PMID:30877234|PMID:31666924|PMID:32575117|PMID:32877928|PMID:33051659|PMID:33219105|PMID:34439168|PMID:34870338
Tmem127RatHereditary Neoplastic Syndromes  ISORGD:16019918554872ClinVar Annotator: match by term: Hereditary Cancer Syndrome | ClinVar Annotator: match by term: Hereditary more ...ClinVarPMID:16199547|PMID:20154675|PMID:20923864|PMID:21156949|PMID:21613359|PMID:22136840|PMID:22419703|PMID:22541004|PMID:23666964|PMID:24033266|PMID:24334765|PMID:24694336|PMID:25389632|PMID:25637381|PMID:25741868|PMID:26267327|PMID:26269449|PMID:26467025|PMID:26960314|PMID:28384794|PMID:28492532|PMID:29282712|PMID:29625052|PMID:29909963|PMID:30877234|PMID:31666924|PMID:32575117|PMID:33051659
Tmem127RatHereditary Paraganglioma-Pheochromocytoma Syndromes  ISORGD:16019918554872ClinVar Annotator: match by term: Hereditary Paraganglioma-Pheochromocytoma SyndromesClinVarPMID:16199547|PMID:16266984|PMID:17576681|PMID:20154675|PMID:20923864|PMID:21156949|PMID:21613359|PMID:22136840|PMID:22419703|PMID:22517554|PMID:22541004|PMID:23666964|PMID:24033266|PMID:24334765|PMID:24694336|PMID:25389632|PMID:25637381|PMID:25741868|PMID:25800244|PMID:26267327|PMID:26269449|PMID:26467025|PMID:26960314|PMID:27153395|PMID:28384794|PMID:28458909|PMID:28492532|PMID:28567294|PMID:28646318|PMID:28717660|PMID:28855235|PMID:29282712|PMID:29625052|PMID:29909963|PMID:30113886|PMID:30246500|PMID:30877234|PMID:31666924|PMID:32575117|PMID:32877928|PMID:32994724|PMID:33051659|PMID:33219105|PMID:34308366|PMID:34439168|PMID:34870338|PMID:35189708|PMID:36451132|PMID:36655350|PMID:9536098
Tmem127Ratintellectual disability  ISORGD:16019918554872ClinVar Annotator: match by term: Intellectual disabilityClinVar 
Tmem127RatIslet Cell Tumor Syndrome  ISORGD:16019918554872ClinVar Annotator: match by term: ChromaffinomaClinVarPMID:16266984|PMID:17576681|PMID:20154675|PMID:20923864|PMID:21156949|PMID:21613359|PMID:22136840|PMID:22419703|PMID:22541004|PMID:23666964|PMID:24033266|PMID:24334765|PMID:24694336|PMID:25389632|PMID:25637381|PMID:25741868|PMID:26267327|PMID:26269449|PMID:26467025|PMID:26960314|PMID:27153395|PMID:28384794|PMID:28492532|PMID:28717660|PMID:28855235|PMID:29282712|PMID:29625052|PMID:29909963|PMID:30113886|PMID:30246500|PMID:30877234|PMID:31666924|PMID:32575117|PMID:32877928|PMID:32994724|PMID:33051659|PMID:33219105|PMID:34439168|PMID:34870338|PMID:35189708|PMID:36451132|PMID:36655350|PMID:9536098
Tmem127RatMultiple mitochondrial dysfunctions syndrome 10  ISORGD:16019918554872ClinVar Annotator: match by term: Multiple mitochondrial dysfunctions syndrome 10ClinVarPMID:25741868|PMID:26267327|PMID:26467025|PMID:28492532|PMID:33051659|PMID:33219105
Tmem127Ratocular melanoma  ISORGD:16019918554872ClinVar Annotator: match by term: Intraocular melanomaClinVarPMID:25741868|PMID:28492532
Tmem127Ratovarian cancer  ISORGD:16019918554872ClinVar Annotator: match by term: Ovarian cancerClinVarPMID:25741868|PMID:28492532
Tmem127Ratparaganglioma  ISORGD:16019918554872ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas | ClinVar Annotator: match by term: more ...ClinVarPMID:16199547|PMID:17576681|PMID:20154675|PMID:20923864|PMID:21156949|PMID:21613359|PMID:22136840|PMID:22419703|PMID:22517554|PMID:22541004|PMID:23666964|PMID:24033266|PMID:24334765|PMID:24694336|PMID:25389632|PMID:25637381|PMID:25741868|PMID:25800244|PMID:26267327|PMID:26269449|PMID:26467025|PMID:26960314|PMID:28384794|PMID:28458909|PMID:28492532|PMID:28567294|PMID:28855235|PMID:29282712|PMID:29909963|PMID:30877234|PMID:31666924|PMID:32877928|PMID:33051659|PMID:9536098
Tmem127Ratparaganglioma  ISORGD:16019918554872ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas | ClinVar Annotator: match by term: more ...ClinVarPMID:16199547|PMID:16266984|PMID:17576681|PMID:20154675|PMID:20923864|PMID:21156949|PMID:21613359|PMID:22136840|PMID:22419703|PMID:22517554|PMID:22541004|PMID:23666964|PMID:24033266|PMID:24334765|PMID:24694336|PMID:25389632|PMID:25637381|PMID:25741868|PMID:25800244|PMID:26267327|PMID:26269449|PMID:26467025|PMID:26960314|PMID:27153395|PMID:28384794|PMID:28458909|PMID:28492532|PMID:28567294|PMID:28646318|PMID:28717660|PMID:28855235|PMID:29282712|PMID:29625052|PMID:29909963|PMID:30113886|PMID:30246500|PMID:30877234|PMID:31666924|PMID:32575117|PMID:32877928|PMID:32994724|PMID:33051659|PMID:33219105|PMID:34308366|PMID:34439168|PMID:34870338|PMID:35189708|PMID:36451132|PMID:36655350|PMID:9536098
Tmem127Ratparaganglioma  ISORGD:16019918554872ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas | ClinVar Annotator: match by term: more ...ClinVarPMID:16199547|PMID:16266984|PMID:17576681|PMID:20154675|PMID:20923864|PMID:21156949|PMID:21613359|PMID:22136840|PMID:22419703|PMID:22517554|PMID:22541004|PMID:23666964|PMID:24033266|PMID:24334765|PMID:24694336|PMID:25389632|PMID:25637381|PMID:25741868|PMID:25800244|PMID:26267327|PMID:26269449|PMID:26467025|PMID:26960314|PMID:27153395|PMID:28384794|PMID:28458909|PMID:28492532|PMID:28567294|PMID:28646318|PMID:28855235|PMID:29282712|PMID:29625052|PMID:29909963|PMID:30113886|PMID:30877234|PMID:31666924|PMID:32575117|PMID:32877928|PMID:32994724|PMID:33051659|PMID:33219105|PMID:34308366|PMID:34439168|PMID:34870338|PMID:9536098
Tmem127Ratparaganglioma  ISORGD:16019918554872ClinVar Annotator: match by term: Hereditary Paragangliomas and PheochromocytomasClinVarPMID:16199547|PMID:16266984|PMID:17576681|PMID:20154675|PMID:20923864|PMID:21156949|PMID:21613359|PMID:22136840|PMID:22419703|PMID:22517554|PMID:22541004|PMID:23666964|PMID:24033266|PMID:24334765|PMID:24694336|PMID:25389632|PMID:25637381|PMID:25741868|PMID:25800244|PMID:26267327|PMID:26269449|PMID:26467025|PMID:26960314|PMID:27153395|PMID:28384794|PMID:28458909|PMID:28492532|PMID:28567294|PMID:28855235|PMID:29282712|PMID:29625052|PMID:29909963|PMID:30113886|PMID:30877234|PMID:31666924|PMID:32575117|PMID:32877928|PMID:32994724|PMID:33051659|PMID:33219105|PMID:34308366|PMID:34439168|PMID:34870338|PMID:9536098
Tmem127Ratparaganglioma  ISORGD:16019918554872ClinVar Annotator: match by term: Hereditary Paragangliomas and PheochromocytomasClinVarPMID:16199547|PMID:16266984|PMID:17576681|PMID:20154675|PMID:20923864|PMID:21156949|PMID:21613359|PMID:22136840|PMID:22419703|PMID:22517554|PMID:22541004|PMID:23666964|PMID:24033266|PMID:24334765|PMID:24694336|PMID:25389632|PMID:25637381|PMID:25741868|PMID:25800244|PMID:26267327|PMID:26269449|PMID:26467025|PMID:26960314|PMID:27153395|PMID:28384794|PMID:28458909|PMID:28492532|PMID:28567294|PMID:28855235|PMID:29282712|PMID:29625052|PMID:29909963|PMID:30113886|PMID:30877234|PMID:31666924|PMID:32575117|PMID:32877928|PMID:33051659|PMID:33219105|PMID:34308366|PMID:34439168|PMID:34870338|PMID:9536098
Tmem127Ratparaganglioma  ISORGD:16019918554872ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas | ClinVar Annotator: match by term: more ...ClinVarPMID:16199547|PMID:16266984|PMID:17576681|PMID:20154675|PMID:20923864|PMID:21156949|PMID:21613359|PMID:22136840|PMID:22419703|PMID:22517554|PMID:22541004|PMID:23666964|PMID:24033266|PMID:24334765|PMID:24694336|PMID:25389632|PMID:25637381|PMID:25741868|PMID:25800244|PMID:26267327|PMID:26269449|PMID:26467025|PMID:26960314|PMID:28384794|PMID:28458909|PMID:28492532|PMID:28567294|PMID:28855235|PMID:29282712|PMID:29625052|PMID:29909963|PMID:30113886|PMID:30877234|PMID:31666924|PMID:32575117|PMID:32877928|PMID:33051659|PMID:33219105|PMID:34439168|PMID:34870338|PMID:9536098
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Original Reference(s)
Tmem127Ratpheochromocytoma  ISORGD:160199111554173CTD Direct Evidence: marker/mechanismCTDPMID:20154675
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Original Reference(s)
Tmem127Ratpheochromocytoma susceptibilityISORGD:16019917240710 OMIM 

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Original Reference(s)
Tmem127Rat(1->4)-beta-D-glucan multiple interactionsISORGD:13318606480464[perfluorooctane sulfonic acid co-treated with Cellulose] results in decreased expression of TMEM127 mRNACTDPMID:36331819
Tmem127Rat1,2-dimethylhydrazine affects expressionISORGD:133186064804641,2-Dimethylhydrazine affects the expression of TMEM127 mRNACTDPMID:22206623
Tmem127Rat17alpha-ethynylestradiol affects expressionISORGD:13318606480464Ethinyl Estradiol affects the expression of TMEM127 mRNACTDPMID:17555576
Tmem127Rat2,3,7,8-tetrachlorodibenzodioxine affects expressionISORGD:13318606480464Tetrachlorodibenzodioxin affects the expression of TMEM127 mRNACTDPMID:21570461
Tmem127Rat2,3,7,8-tetrachlorodibenzodioxine decreases expressionEXP 6480464Tetrachlorodibenzodioxin results in decreased expression of TMEM127 mRNACTDPMID:33387578
Tmem127Rat4,4'-sulfonyldiphenol decreases expressionISORGD:13318606480464bisphenol S results in decreased expression of TMEM127 mRNACTDPMID:39298647
Tmem127Rat6-propyl-2-thiouracil decreases expressionEXP 6480464Propylthiouracil results in decreased expression of TMEM127 mRNACTDPMID:24780913
Tmem127Ratacrylamide increases expressionEXP 6480464Acrylamide results in increased expression of TMEM127 mRNACTDPMID:28959563
Tmem127Ratall-trans-retinoic acid increases expressionISORGD:16019916480464Tretinoin results in increased expression of TMEM127 mRNACTDPMID:33167477
Tmem127Ratantirheumatic drug decreases expressionISORGD:16019916480464Antirheumatic Agents results in decreased expression of TMEM127 mRNACTDPMID:24449571
Tmem127Ratbenzene increases expressionISORGD:16019916480464Benzene results in increased expression of TMEM127 mRNACTDPMID:19162166
Tmem127Ratbenzo[a]pyrene decreases methylationISORGD:16019916480464Benzo(a)pyrene results in decreased methylation of TMEM127 3' UTRCTDPMID:27901495
Tmem127Ratbis(2-ethylhexyl) phthalate increases expressionISORGD:13318606480464Diethylhexyl Phthalate results in increased expression of TMEM127 mRNACTDPMID:34319233
Tmem127Ratbisphenol A increases expressionEXP 6480464bisphenol A results in increased expression of TMEM127 mRNACTDPMID:25181051|PMID:30816183
Tmem127Ratbisphenol A affects expressionEXP 6480464bisphenol A affects the expression of TMEM127 mRNACTDPMID:34947998
Tmem127Ratbisphenol A decreases expressionISORGD:13318606480464bisphenol A results in decreased expression of TMEM127 mRNACTDPMID:33221593
Tmem127Ratcarbamazepine affects expressionISORGD:16019916480464Carbamazepine affects the expression of TMEM127 mRNACTDPMID:25979313
Tmem127RatCGP 52608 multiple interactionsISORGD:16019916480464CGP 52608 promotes the reaction [RORA protein binds to TMEM127 gene]CTDPMID:28238834
Tmem127Ratcholine multiple interactionsISORGD:13318606480464[Methionine deficiency co-treated with Choline deficiency co-treated with Folic Acid deficiency] results in increased methylation more ...CTDPMID:20938992
Tmem127Ratcisplatin increases expressionISORGD:16019916480464Cisplatin results in increased expression of TMEM127 mRNACTDPMID:27392435

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Biological Process
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Original Reference(s)
Tmem127Ratbiological_process  ND 159840701/2009: no relevant rat dataRGD 
Tmem127Ratendosome organization acts_upstream_of_or_withinISORGD:13318601624291MGI:5581337 PMID:24334765RGDPMID:24334765
Tmem127Ratendosome organization acts_upstream_of_or_withinIEAUniProtKB:Q8BGP5|ensembl:ENSMUSP000000354341600115GO_REF:0000107EnsemblGO_REF:0000107
Tmem127Ratnegative regulation of cell population proliferation involved_inISORGD:16019911624291 PMID:20154675RGDPMID:20154675
Tmem127Ratnegative regulation of cell population proliferation involved_inIEAUniProtKB:O75204|ensembl:ENSP000002584391600115GO_REF:0000107EnsemblGO_REF:0000107
Tmem127Ratnegative regulation of cell population proliferation involved_inIEAInterPro:IPR0333311600115GO_REF:0000002InterProGO_REF:0000002
Tmem127Ratnegative regulation of TOR signaling involved_inISORGD:16019911624291 PMID:20154675RGDPMID:20154675
Tmem127Ratnegative regulation of TOR signaling involved_inIEAUniProtKB:O75204|ensembl:ENSP000002584391600115GO_REF:0000107EnsemblGO_REF:0000107
Tmem127Ratnegative regulation of TOR signaling involved_inIEAInterPro:IPR0333311600115GO_REF:0000002InterProGO_REF:0000002
Tmem127Ratregulation of TOR signaling involved_inIBAMGI:1916720|PANTHER:PTN002002006|UniProtKB:O752041600115GO_REF:0000033GO_CentralGO_REF:0000033
Tmem127Ratregulation of TOR signaling acts_upstream_of_or_withinIEAUniProtKB:Q8BGP5|ensembl:ENSMUSP000000354341600115GO_REF:0000107EnsemblGO_REF:0000107
Tmem127Ratregulation of TOR signaling acts_upstream_of_or_withinISORGD:13318601624291MGI:5581337 PMID:24334765RGDPMID:24334765
1 to 12 of 12 rows

Cellular Component

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
Tmem127Ratcytoplasm located_inISORGD:16019911624291 PMID:20154675RGDPMID:20154675
Tmem127Ratcytoplasm located_inIEAUniProtKB:O75204|ensembl:ENSP000002584391600115GO_REF:0000107EnsemblGO_REF:0000107
Tmem127Ratearly endosome located_inISORGD:16019911624291 PMID:24334765RGDPMID:24334765
Tmem127Ratearly endosome located_inIEAUniProtKB:O75204|ensembl:ENSP000002584391600115GO_REF:0000107EnsemblGO_REF:0000107
Tmem127Ratmembrane located_inIEAUniProtKB-KW:KW-04721600115GO_REF:0000043UniProtGO_REF:0000043
Tmem127Ratmembrane is_active_inIBAPANTHER:PTN002002006|UniProtKB:O752041600115GO_REF:0000033GO_CentralGO_REF:0000033
Tmem127Ratplasma membrane located_inISORGD:16019911624291 PMID:20154675RGDPMID:20154675
Tmem127Ratplasma membrane located_inIEAUniProtKB:O75204|ensembl:ENSP000002584391600115GO_REF:0000107EnsemblGO_REF:0000107

Molecular Function

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
Tmem127Ratsmall GTPase binding enablesISORGD:16019911624291 PMID:24334765RGDPMID:24334765
Tmem127Ratsmall GTPase binding enablesIEAUniProtKB:O75204|ensembl:ENSP000002584391600115GO_REF:0000107EnsemblGO_REF:0000107


#
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. Rat ISS GO annotations from MGI mouse gene data--August 2006 MGD data from the GO Consortium
3. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
4. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
5. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
6. Comprehensive gene review and curation RGD comprehensive gene curation
PMID:12477932   PMID:20154675   PMID:22871113   PMID:24334765  



Tmem127
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr83134,919,416 - 134,932,210 (+)NCBIGRCr8
mRatBN7.23114,466,095 - 114,478,894 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl3114,466,171 - 114,477,519 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx3118,357,660 - 118,370,450 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.03126,953,204 - 126,965,994 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.03124,613,584 - 124,626,374 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.03119,677,575 - 119,690,371 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl3119,677,575 - 119,690,366 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.03126,202,774 - 126,215,589 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.43114,746,454 - 114,759,251 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.13114,652,049 - 114,664,824 (+)NCBI
Celera3113,306,634 - 113,319,570 (+)NCBICelera
Cytogenetic Map3q36NCBI
TMEM127
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38296,248,514 - 96,265,997 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl296,248,500 - 96,266,047 (-)EnsemblGRCh38hg38GRCh38
GRCh37296,914,252 - 96,931,735 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36296,280,039 - 96,295,459 (-)NCBINCBI36Build 36hg18NCBI36
Celera291,357,500 - 91,372,939 (-)NCBICelera
Cytogenetic Map2q11.2NCBI
HuRef290,877,443 - 90,893,248 (-)NCBIHuRef
CHM1_1296,920,300 - 96,936,106 (-)NCBICHM1_1
T2T-CHM13v2.0296,755,122 - 96,772,605 (-)NCBIT2T-CHM13v2.0
Tmem127
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm392127,089,868 - 127,103,028 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl2127,089,828 - 127,103,027 (+)EnsemblGRCm39 Ensembl
GRCm382127,247,904 - 127,261,108 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl2127,247,908 - 127,261,107 (+)EnsemblGRCm38mm10GRCm38
MGSCv372127,073,711 - 127,086,500 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv362126,939,416 - 126,952,205 (+)NCBIMGSCv36mm8
Celera2128,487,347 - 128,500,147 (+)NCBICelera
Cytogenetic Map2F1NCBI
cM Map261.87NCBI
Tmem127
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554703,808,455 - 3,822,497 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554703,809,835 - 3,822,442 (-)NCBIChiLan1.0ChiLan1.0
TMEM127
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21232,042,817 - 32,057,217 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12A32,045,577 - 32,059,977 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02A103,049,655 - 103,065,116 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12A97,174,322 - 97,189,177 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2A97,174,322 - 97,189,171 (-)Ensemblpanpan1.1panPan2
TMEM127
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11734,512,753 - 34,527,208 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1734,512,792 - 34,523,692 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1734,282,678 - 34,295,473 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01735,283,964 - 35,296,760 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1735,283,938 - 35,296,757 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11734,413,107 - 34,426,110 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01734,481,752 - 34,494,521 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01734,688,570 - 34,701,364 (+)NCBIUU_Cfam_GSD_1.0
Tmem127
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440629283,091,414 - 83,106,154 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936744344,356 - 359,044 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_004936744344,356 - 359,086 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
TMEM127
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl346,966,892 - 46,978,810 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1346,966,858 - 47,017,659 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2349,108,738 - 49,121,833 (+)NCBISscrofa10.2Sscrofa10.2susScr3
TMEM127
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.114671,259 - 685,217 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl14673,375 - 685,228 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666041168,096,788 - 168,111,829 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Tmem127
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247492,333,472 - 2,344,674 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247492,333,472 - 2,344,652 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

.

.
Variants in Tmem127
62 total Variants

Predicted Target Of
Summary Value
Count of predictions:402
Count of miRNA genes:231
Interacting mature miRNAs:276
Transcripts:ENSRNOT00000031577
Prediction methods:Miranda, 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 40 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
2312673Scl63Serum cholesterol level QTL 630.001blood cholesterol amount (VT:0000180)serum total cholesterol level (CMO:0000363)398535255168026850Rat
2301414Kidm37Kidney mass QTL 370.001kidney mass (VT:0002707)both kidneys wet weight to body weight ratio (CMO:0000340)370653097121056321Rat
1582238Bw68Body weight QTL 683.20.0064body mass (VT:0001259)body weight (CMO:0000012)353184593115665732Rat
2302373Gluco39Glucose level QTL 395.01blood glucose amount (VT:0000188)blood glucose level area under curve (AUC) (CMO:0000350)398535386161695835Rat
1582239Epfw1Epididymal fat weight QTL 14.50.0006epididymal fat pad mass (VT:0010421)epididymal fat pad weight to body weight ratio (CMO:0000658)353184593115665732Rat
70216Cm14Cardiac mass QTL 142.1heart mass (VT:0007028)heart wet weight (CMO:0000069)331172320163586636Rat
2292591Esta4Estrogen-induced thymic atrophy QTL 4thymus mass (VT:0004954)thymus wet weight (CMO:0000855)347233211147415807Rat
1358362Srcrt2Stress Responsive Cort QTL 22.78blood corticosterone amount (VT:0005345)plasma corticosterone level (CMO:0001173)338192233133483320Rat
1582216Bw65Body weight QTL 656.3body mass (VT:0001259)body weight (CMO:0000012)3102200529115665732Rat
737818Hcar12Hepatocarcinoma resistance QTL 122.6liver integrity trait (VT:0010547)volume of individual liver tumorous lesion (CMO:0001078)329463235118376539Rat

1 to 10 of 40 rows
RH131467  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.23114,478,542 - 114,478,723 (+)MAPPERmRatBN7.2
Rnor_6.03119,690,020 - 119,690,200NCBIRnor6.0
Rnor_5.03126,215,238 - 126,215,418UniSTSRnor5.0
RGSC_v3.43114,758,900 - 114,759,080UniSTSRGSC3.4
Celera3113,319,219 - 113,319,399UniSTS
RH 3.4 Map3998.6UniSTS
Cytogenetic Map3q36UniSTS
RH134539  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.21137,678,069 - 37,678,260 (+)MAPPERmRatBN7.2
mRatBN7.23114,477,209 - 114,477,400 (-)MAPPERmRatBN7.2
mRatBN7.23114,477,209 - 114,477,400 (+)MAPPERmRatBN7.2
Rnor_6.03119,688,687 - 119,688,877NCBIRnor6.0
Rnor_6.01139,764,643 - 39,764,833NCBIRnor6.0
Rnor_5.03126,213,905 - 126,214,095UniSTSRnor5.0
Rnor_5.01142,970,012 - 42,970,202UniSTSRnor5.0
RGSC_v3.43114,757,567 - 114,757,757UniSTSRGSC3.4
RGSC_v3.41138,545,442 - 38,545,632UniSTSRGSC3.4
Celera1137,556,695 - 37,556,885UniSTS
Celera3113,317,886 - 113,318,076UniSTS
Cytogenetic Map3q36UniSTS
AI317350  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.23114,478,364 - 114,478,451 (+)MAPPERmRatBN7.2
Rnor_6.03119,689,842 - 119,689,928NCBIRnor6.0
Rnor_5.03126,215,060 - 126,215,146UniSTSRnor5.0
RGSC_v3.43114,758,722 - 114,758,808UniSTSRGSC3.4
Celera3113,319,041 - 113,319,127UniSTS
Cytogenetic Map3q36UniSTS




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: ENSRNOT00000031577   ⟹   ENSRNOP00000030631
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
Rnor_6.0 Ensembl3119,677,575 - 119,690,366 (+)Ensembl
Ensembl Acc Id: ENSRNOT00000117496   ⟹   ENSRNOP00000097003
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl3114,466,171 - 114,477,519 (+)Ensembl
RefSeq Acc Id: NM_001100978   ⟹   NP_001094448
RefSeq Status: PROVISIONAL
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr83134,919,417 - 134,932,210 (+)NCBI
mRatBN7.23114,466,101 - 114,478,894 (+)NCBI
Rnor_6.03119,677,575 - 119,690,371 (+)NCBI
Rnor_5.03126,202,774 - 126,215,589 (+)NCBI
RGSC_v3.43114,746,454 - 114,759,251 (+)RGD
Celera3113,306,634 - 113,319,570 (+)RGD
Sequence:
RefSeq Acc Id: XM_039104991   ⟹   XP_038960919
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr83134,919,416 - 134,932,210 (+)NCBI
mRatBN7.23114,466,095 - 114,478,894 (+)NCBI
Protein RefSeqs NP_001094448 (Get FASTA)   NCBI Sequence Viewer  
  XP_038960919 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAI31851 (Get FASTA)   NCBI Sequence Viewer  
  EDL80110 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSRNOP00000097003.1
  ENSRNOP00000102251
RefSeq Acc Id: NP_001094448   ⟸   NM_001100978
- UniProtKB: A2RRU2 (UniProtKB/TrEMBL),   A0A8I6AS31 (UniProtKB/TrEMBL),   A6HQ09 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSRNOP00000030631   ⟸   ENSRNOT00000031577
RefSeq Acc Id: XP_038960919   ⟸   XM_039104991
- Peptide Label: isoform X1
Ensembl Acc Id: ENSRNOP00000097003   ⟸   ENSRNOT00000117496
Name Modeler Protein Id AA Range Protein Structure
AF-A2RRU2-F1-model_v2 AlphaFold A2RRU2 1-238 view protein structure


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

RGD ID:13692400
Promoter ID:EPDNEW_R2925
Type:initiation region
Name:Tmem127_1
Description:transmembrane protein 127
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_6.03119,677,596 - 119,677,656EPDNEW


1 to 22 of 22 rows
Database
Acc Id
Source(s)
BioCyc Gene G2FUF-47999 BioCyc
Ensembl Genes ENSRNOG00000022727 Ensembl
  ENSRNOG00000071101 Ensembl, UniProtKB/TrEMBL
  ENSRNOG00000088819 ENTREZGENE
Ensembl Transcript ENSRNOT00000117496.1 UniProtKB/TrEMBL
  ENSRNOT00000150685 ENTREZGENE
IMAGE_CLONE IMAGE:7125680 IMAGE-MGC_LOAD
InterPro TMEM127 UniProtKB/TrEMBL
  TMEM127_TM UniProtKB/TrEMBL
KEGG Report rno:311405 UniProtKB/TrEMBL
MGC_CLONE MGC:156781 IMAGE-MGC_LOAD
NCBI Gene 311405 ENTREZGENE
PANTHER PTHR28358 UniProtKB/TrEMBL
  TRANSMEMBRANE PROTEIN 127 UniProtKB/TrEMBL
Pfam TMEM127 UniProtKB/TrEMBL
PhenoGen Tmem127 PhenoGen
RatGTEx ENSRNOG00000022727 RatGTEx
  ENSRNOG00000071101 RatGTEx
  ENSRNOG00000088819 RatGTEx
UniProt A0A8I6AS31 ENTREZGENE, UniProtKB/TrEMBL
  A2RRU2 ENTREZGENE, UniProtKB/TrEMBL
  A6HQ09 ENTREZGENE, UniProtKB/TrEMBL
1 to 22 of 22 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2009-01-14 Tmem127  transmembrane protein 127  RGD1309744  similar to hypothetical protein FLJ20507   Nomenclature updated to reflect human and mouse nomenclature 1299863 APPROVED
2008-04-30 RGD1309744  similar to hypothetical protein FLJ20507   RGD1309744_predicted  similar to hypothetical protein FLJ20507 (predicted)  'predicted' is removed 2292626 APPROVED
2005-01-20 RGD1309744_predicted  similar to hypothetical protein FLJ20507 (predicted)  LOC311405_predicted    Symbol and Name status set to approved 1331353 APPROVED
2005-01-12 LOC311405_predicted  similar to hypothetical protein FLJ20507 (predicted)      Symbol and Name status set to provisional 70820 PROVISIONAL