EuRBPDB

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  • Basic Information
  • Cancer Related Information

  • Description
  • RBDs
  • Expression
  • Transcripts
  • Gene Model
  • Phenotypes
  • GWAS
  • PPI
  • Orthologs
  • Gene Ontology
Description
Ensembl ID
ENSG00000172794 (Gene tree)
Gene ID
326624
Gene Symbol
RAB37
Alias
-
Full Name
RAB37, member RAS oncogene family
Gene Type
protein_coding
Species
Homo_sapiens
Status
putative
Strand
Plus strand
Length
76,758 bases
Position
chr17:74,670,578-74,747,335
Accession
30268
RBP type
canonical RBP
Summary
Rab proteins are low molecular mass GTPases that are critical regulators of vesicle trafficking. For additional background information on Rab proteins, see MIM 179508.[supplied by OMIM, Apr 2006]
RNA binding domains(RBDs)
Protein IDDomain Pfam IDE-value Domain number Total number
ENSP00000341354MMR_HSR1PF01926.230.0004911
Expression
Transcripts
Transcript IDNameLengthRefSeq ID Protein IDLengthRefSeq IDUniportKB ID
ENST00000481224RAB37-2091654-ENSP00000436563223 (aa)-Q96AX2
ENST00000613645RAB37-2161653-ENSP00000483155223 (aa)-Q96AX2
ENST00000531420RAB37-213561--- (aa)--
ENST00000488977RAB37-2102195--- (aa)--
ENST00000533530RAB37-214578--- (aa)--
ENST00000577548RAB37-215950--- (aa)--
ENST00000402449RAB37-2081560-ENSP00000383934216 (aa)-Q96AX2
ENST00000392610RAB37-2022858-ENSP00000376387189 (aa)-A8MTC6
ENST00000528438RAB37-2121494-ENSP00000432086196 (aa)-B7Z3L0
ENST00000527040RAB37-211559--- (aa)--
ENST00000340415RAB37-2013804-ENSP00000341354182 (aa)-A8MSP2
ENST00000392612RAB37-2032528-ENSP00000376388186 (aa)-Q96AX2
ENST00000392613RAB37-2042617-ENSP00000376389223 (aa)-Q96AX2
ENST00000392614RAB37-2052704-ENSP00000376390228 (aa)-Q96AX2
ENST00000392615RAB37-2062655-ENSP00000376391191 (aa)-A8MZI4
ENST00000392617RAB37-2073780--- (aa)--
Gene Model
Click here to download ENSG00000172794's gene model file
Phenotypes
ensgIDTraitpValuePubmed ID
ENSG00000172794Cardiovascular Diseases1.1600000E-005-
ENSG00000172794Fibrinogen2E-828107422
ENSG00000172794Fibrinogen2E-828107422
ENSG00000172794Fibrinogen1E-823969696
ENSG00000172794Fibrinogen8E-1120031577
GWAS
ensgIDSNPChromosomePositionSNP-risk TraitPubmedID95% CIOr or BEAT EFO ID
ENSG00000172794rs10371711774706839AMonocyte count27863252[0.033-0.049] unit increase0.04078738EFO_0005091
ENSG00000172794rs105125971774703694TFibrinogen23969696[0.006-0.01] unit decrease0.008EFO_0004623
ENSG00000172794rs105125971774703694AFibrinogen20031577[NR] mg/dl decrease6.45EFO_0004623
ENSG00000172794rs354899711774704804ACoronary artery disease29212778[0.028-0.06] unit increase0.0438EFO_0000378
ENSG00000172794rs20343101774695789CLymphocyte counts27863252[0.018-0.036] unit increase0.02706763EFO_0004587
ENSG00000172794rs7497801774703245AMyeloid white cell count27863252[0.019-0.035] unit increase0.02737397EFO_0007988
ENSG00000172794rs7497801774703245AWhite blood cell count27863252[0.022-0.038] unit increase0.03030224EFO_0004308
ENSG00000172794rs129423111774714657CLiver fibrosis in pediatric non-alcoholic fatty acid liver disease28918882EFO_0003095|HP_0001395
ENSG00000172794rs7497801774703245ANeutrophil count27863252[0.016-0.032] unit increase0.02374859EFO_0004833
ENSG00000172794rs99063201774694690APlateletcrit27863252[0.017-0.035] unit increase0.02613192EFO_0007985
ENSG00000172794rs779368631774700954TGranulocyte count27863252[0.016-0.032] unit increase0.02419283EFO_0007987
ENSG00000172794rs7497801774703245ASum neutrophil eosinophil counts27863252[0.016-0.032] unit increase0.02407953EFO_0004833|EFO_0004842
ENSG00000172794rs105125971774703694?Fibrinogen levels28107422unit increase0.0078EFO_0004623
ENSG00000172794rs354899711774704804?Fibrinogen levels28107422unit increase0.0077EFO_0004623
ENSG00000172794rs7497801774703245ASum basophil neutrophil counts27863252[0.016-0.032] unit increase0.02390133EFO_0004833|EFO_0005090
ENSG00000172794rs20843121774699072?White blood cell count30595370EFO_0004308
ENSG00000172794rs105125971774703694TC-reactive protein levels30388399[0.027-0.047] unit decrease0.037EFO_0004458
ENSG00000172794rs23849551774699028TC-reactive protein levels30388399[0.029-0.053] unit decrease0.041EFO_0004458
ENSG00000172794rs23849551774699028TC-reactive protein levels30388399[0.026-0.05] unit decrease0.038EFO_0004458
Protein-Protein Interaction (PPI)

Clik here to download ENSG00000172794's network

* RBP PPI network refers to all genes directly bind to RBP
Orthologs
Ensembl IDGene SymbolCoverageIdentiy OrthologGene SymbolCoverageIdentiy Species
ENSG00000172794RAB378982.099ENSACIG00000023222-8677.041Amphilophus_citrinellus
ENSG00000172794RAB3710093.956ENSCPOG00000025645RAB3710091.667Cavia_porcellus
ENSG00000172794RAB3710096.154ENSCLAG00000008913RAB3710094.444Chinchilla_lanigera
ENSG00000172794RAB378789.937ENSCVAG00000014416-9283.420Cyprinodon_variegatus
ENSG00000172794RAB379479.532ENSELUG00000023120-9575.122Esox_lucius
ENSG00000172794RAB3710095.055ENSFDAG00000015285RAB3710093.056Fukomys_damarensis
ENSG00000172794RAB378788.679ENSGAFG00000014730-9682.383Gambusia_affinis
ENSG00000172794RAB3710096.703ENSHGLG00000004384RAB3710094.907Heterocephalus_glaber_female
ENSG00000172794RAB3710096.703ENSHGLG00100012557-10094.907Heterocephalus_glaber_male
ENSG00000172794RAB379881.461ENSLBEG00000027539-9476.887Labrus_bergylta
ENSG00000172794RAB378789.873ENSMAMG00000020286-7689.873Mastacembelus_armatus
ENSG00000172794RAB3710096.154MGP_CAROLIEiJ_G0017386Rab3710095.370Mus_caroli
ENSG00000172794RAB3710096.154ENSMUSG00000020732Rab3710095.370Mus_musculus
ENSG00000172794RAB3710096.154MGP_PahariEiJ_G0018517Rab3710095.370Mus_pahari
ENSG00000172794RAB3710096.154MGP_SPRETEiJ_G0018231Rab3710095.370Mus_spretus
ENSG00000172794RAB379167.857ENSNBRG00000011872-9367.857Neolamprologus_brichardi
ENSG00000172794RAB379385.799ENSORLG00000024558-8380.198Oryzias_latipes
ENSG00000172794RAB379385.799ENSORLG00020015717-8380.198Oryzias_latipes_hni
ENSG00000172794RAB379385.799ENSORLG00015013564-9781.865Oryzias_latipes_hsok
ENSG00000172794RAB379385.207ENSOMEG00000018494-8379.703Oryzias_melastigma
ENSG00000172794RAB3710088.525ENSPCIG00000004450-10086.239Phascolarctos_cinereus
ENSG00000172794RAB379386.391ENSPFOG00000019144-8381.281Poecilia_formosa
ENSG00000172794RAB379386.391ENSPFOG00000006314-8381.281Poecilia_formosa
ENSG00000172794RAB379385.799ENSPMEG00000017161-8380.788Poecilia_mexicana
ENSG00000172794RAB379385.799ENSPMEG00000002564-8380.788Poecilia_mexicana
ENSG00000172794RAB3710085.648ENSPPYG00000008601-10085.648Pongo_abelii
ENSG00000172794RAB379185.542ENSPNAG00000021675-9377.889Pygocentrus_nattereri
ENSG00000172794RAB379385.207ENSXMAG00000021303-8480.296Xiphophorus_maculatus
Gene Ontology
Go IDGo_termPubmedIDEvidenceCategory
GO:0003924GTPase activity21873635.IBAFunction
GO:0005515protein binding25416956.IPIFunction
GO:0005525GTP binding-IEAFunction
GO:0005793endoplasmic reticulum-Golgi intermediate compartment15308636.IDAComponent
GO:0005886plasma membrane-TASComponent
GO:0006886intracellular protein transport21873635.IBAProcess
GO:0032482Rab protein signal transduction21873635.IBAProcess
GO:0035577azurophil granule membrane-TASComponent
GO:0035579specific granule membrane-TASComponent
GO:0043312neutrophil degranulation-TASProcess

Cancer associated literatures
PIDTitleArticle TimeAuthorDoi
28151721Dysregulation of Rab37-Mediated Cross-talk between Cancer Cells and Endothelial Cells via Thrombospondin-1 Promotes Tumor Neovasculature and Metastasis.Clin Cancer Res2017 May 1Tzeng HTdoi: 10.1158/1078-0432.CCR-16-1520
25183545Small GTPase Rab37 targets tissue inhibitor of metalloproteinase 1 for exocytosis and thus suppresses tumour metastasis.Nat Commun2014 Sep 3Tsai CHdoi: 10.1038/ncomms5804.

Differential Expression

Expression in 33 cancers

Mutations
CancerChrPosition Mutation TypedbSNPProtein-change Allele FreqRBD
ACCchr1774744355SilentnovelI138I0.08
ACCchr1774729344Missense_MutationNAA54V0.2MMR_HSR1
BLCAchr1774744873Missense_MutationNAA145S0.34
BLCAchr1774745187Intronnovel0.17
BLCAchr17747454433'UTRnovel0.4
BLCAchr1774743184Missense_Mutationrs527644258R101K0.37MMR_HSR1
BLCAchr1774744352Silentrs765627620V137V0.13
BLCAchr1774742253Splice_SitenovelX69_splice0.33
BLCAchr1774745187Intronnovel0.49
BRCAchr1774743141Missense_Mutationrs772882123A87T0.27MMR_HSR1
BRCAchr1774740767Splice_SiteNAX32_splice0.44
BRCAchr1774743324Missense_MutationNAS117C0.34MMR_HSR1
BRCAchr1774729366Splice_Regionrs759047469T61T0.14
BRCAchr1774744386Intronnovel0.14
BRCAchr1774744767Intronnovel0.18
BRCAchr1774729309Silentrs115636998F42F0.32
CESCchr1774729331Missense_Mutationrs753157903G50S0.37MMR_HSR1
CESCchr1774744892Missense_MutationnovelR151T0.68
COADchr1774744788Intronnovel0.22
COADchr1774744929Missense_MutationnovelR163S0.09
COADchr1774740791SilentNAG39G0.17
COADchr1774745239Intronnovel0.4
COADchr1774744444Intronnovel0.27
COADchr1774744952Intronnovel0.29
COADchr1774745226Intronnovel0.17
COADchr1774743165Missense_Mutationrs143690968V95I0.23MMR_HSR1
ESCAchr17747486233'Flanknovel0.21
GBMchr1774744957Intronnovel0.24
GBMchr1774744739Intronnovel0.42
GBMchr1774743294Missense_MutationnovelL107H0.14MMR_HSR1
GBMchr1774744744Intronnovel0.65
HNSCchr1774743168Missense_MutationnovelT96A0.27MMR_HSR1
HNSCchr1774745151Intronnovel0.46
HNSCchr1774745024Missense_MutationnovelF169S0.08
HNSCchr1774745075Frame_Shift_DelnovelI187Pfs*40.27
HNSCchr1774744868Splice_Regionnovel0.05
KIRCchr1774729338Missense_MutationnovelF52C0.37MMR_HSR1
KIRCchr1774743340Missense_MutationNAR122S0.25MMR_HSR1
KIRCchr1774729363Frame_Shift_InsnovelT61Ffs*70.05MMR_HSR1
KIRCchr17747370595'Flanknovel0.28
KIRPchr1774740792Missense_Mutationrs750256354V40I0.06MMR_HSR1
KIRPchr17747368615'Flanknovel0.27
LGGchr1774729293Missense_MutationnovelS37Y0.39MMR_HSR1
LGGchr1774744796Intronnovel0.36
LIHCchr17747455903'UTRnovel0.75
LUADchr1774740861Missense_MutationNAV63F0.32MMR_HSR1
LUADchr1774744809Intronnovel0.14
LUADchr1774744799Intronnovel0.11
LUADchr1774745040SilentnovelA174A0.09
LUADchr1774743170SilentnovelT96T0.54
LUADchr1774745268Intronnovel0.23
LUADchr1774744851Intronnovel0.09
LUADchr1774745042Missense_MutationNAK175R0.12
LUADchr1774745253Intronnovel0.2
LUADchr1774745013Frame_Shift_DelnovelG166Wfs*90.06
LUSCchr1774743165Missense_Mutationrs143690968V95I0.11MMR_HSR1
LUSCchr1774744790Intronnovel0.23
LUSCchr1774744754Intronnovel0.43
LUSCchr1774742274Missense_MutationnovelD75E0.11MMR_HSR1
LUSCchr1774744344Frame_Shift_InsnovelV136Tfs*30.14
OVchr1774744941Intronnovel0.05
OVchr1774745354Missense_MutationNAQ205H0.38
OVchr1774729346Missense_MutationNAT55S0.15MMR_HSR1
OVchr1774744384Intronnovel0.33
PAADchr17747370355'Flanknovel0.2
PRADchr1774740827Silentrs530556816D51D0.08
PRADchr1774745017Missense_MutationNAV167I0.12
PRADchr1774745144Intronnovel0.35
PRADchr1774740835Missense_MutationNAF54S0.12MMR_HSR1
PRADchr1774740827Silentrs530556816D51D0.44
READchr1774729309Silentrs115636998F42F0.32
READchr17747454493'UTRnovel0.75
SARCchr17747370045'Flanknovel0.35
SKCMchr1774744344Missense_Mutationrs762982946D135N0.17
SKCMchr1774745242Intronnovel0.35
SKCMchr1774744786Intronnovel0.29
SKCMchr1774743158SilentNAF92F0.08
SKCMchr1774745021Missense_MutationNAP168L0.12
SKCMchr1774740815SilentNAI47I0.19
SKCMchr1774743149SilentNAQ89Q0.22
SKCMchr1774743149SilentNAQ89Q0.35
SKCMchr1774745201Intronnovel0.41
SKCMchr1774740809SilentNAF45F0.41
SKCMchr1774742280SilentNAV77V0.13
SKCMchr1774744307Splice_SiteNAX123_splice0.23
SKCMchr1774745097Intronnovel0.25
SKCMchr1774745196Intronnovel0.59
SKCMchr1774744948Intronnovel0.33
SKCMchr1774743314Missense_MutationnovelN114D0.63MMR_HSR1
SKCMchr1774729284Missense_MutationnovelG34E0.21MMR_HSR1
SKCMchr1774743289Splice_RegionnovelA105A0.83
SKCMchr1774743155SilentNAR91R0.4
STADchr1774743153Missense_Mutationrs770507152R91W0.29MMR_HSR1
STADchr1774740870Missense_MutationNAD66Y0.32MMR_HSR1
STADchr1774745294Intronnovel0.22
STADchr1774740795Missense_Mutationrs149746610G41S0.4MMR_HSR1
STADchr1774745240Intronnovel0.22
STADchr1774743305Missense_MutationnovelD111Y0.37MMR_HSR1
THCAchr1774729355Frame_Shift_DelnovelI58Sfs*80.39MMR_HSR1
UCECchr1774743296Missense_MutationNAL108M0.35MMR_HSR1
UCECchr1774744310Splice_RegionnovelA123A0.26
UCECchr1774743193Missense_MutationnovelQ104R0.38MMR_HSR1
UCECchr1774729309Silentrs115636998F42F0.5
UCECchr1774745287Intronnovel0.35
UCECchr1774743159Nonsense_Mutationrs150761775R93*0.13MMR_HSR1
UCECchr17747454173'UTRnovel0.39
UCECchr1774729309Silentrs115636998F42F0.32
UCECchr1774743299SilentnovelL109L0.25
UCECchr17747370525'Flanknovel0.56
UCECchr1774745245Intronrs3747197610.43
UCECchr1774743164Silentrs763968925S94S0.22
UCECchr17747455643'UTRnovel0.45
UCECchr1774745248Intronnovel0.46
UCECchr17747369875'Flankrs7748489060.18
UCECchr1774729310Missense_MutationNAD43N0.11MMR_HSR1
UCECchr1774742287Missense_MutationnovelK80E0.35MMR_HSR1
UCECchr1774729357Silentrs749871961I58I0.83
UCECchr1774744742Intronnovel0.33
UCECchr1774729293Missense_MutationnovelS37Y0.34MMR_HSR1
UCECchr1774740810SilentnovelL46L0.23
UCECchr1774745119Intronnovel0.41
UCECchr1774742267Missense_MutationnovelT73N0.28MMR_HSR1
UCECchr1774744718Intronnovel0.28
UCECchr1774745194Intronnovel0.35
UCSchr1774744794Intronnovel0.25
UCSchr1774729309Silentrs115636998F42F0.41

Copy Number Variations (CNVs)
CancerTypeFreq Q-value
BLCAAMP0.39220.00012456
KIRPAMP0.67010.14801
LGGAMP0.06631.52e-05
LUSCAMP0.35730.001059
SARCAMP0.23740.032181
SKCMAMP0.29437.0388e-08
THCADEL0.0020.221
UVMAMP0.16250.054583

Survival Analysis
CancerP-value Q-value
THYM0.0091

Kaplan-Meier Survival Analysis

KIRC0.0033

Kaplan-Meier Survival Analysis

SARC0.0055

Kaplan-Meier Survival Analysis

MESO0.0013

Kaplan-Meier Survival Analysis

ACC0.0011

Kaplan-Meier Survival Analysis

UCS0.0055

Kaplan-Meier Survival Analysis

HNSC0.0001

Kaplan-Meier Survival Analysis

SKCM0.00011

Kaplan-Meier Survival Analysis

PRAD0.028

Kaplan-Meier Survival Analysis

BRCA0.041

Kaplan-Meier Survival Analysis

PAAD0.038

Kaplan-Meier Survival Analysis

CESC0.0015

Kaplan-Meier Survival Analysis

KICH0.039

Kaplan-Meier Survival Analysis

UCEC0.0018

Kaplan-Meier Survival Analysis

LUAD0.024

Kaplan-Meier Survival Analysis

UVM0.049

Kaplan-Meier Survival Analysis

OV0.028

Kaplan-Meier Survival Analysis


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