Details for: ITGB6
Gene ID: 3694
Gene Type: Protein-coding - A gene that serves as a template for producing a messenger RNA (mRNA) molecule, which is then translated into a functional protein.
Symbol: ITGB6
Ensembl ID: ENSG00000115221
Description: integrin subunit beta 6
Selected Context(s): Overall
Cell Significance Landscape
Associated with
Significant Cells
Cell Significance Index (CSI) scores for the chosen context(s)
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CSI 9.72rCSI 10.18%PRS 86.09
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CSI 3.85rCSI 4.01%PRS 87.39
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CSI 3.81rCSI 5.81%PRS 87.92
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CSI 3.63rCSI 2.81%PRS 91.38
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CSI 3.48rCSI 3.29%PRS 86.37
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CSI 3.44rCSI 3.56%PRS 90.48
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CSI 3.24rCSI 2.88%PRS 86.06
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CSI 3.15rCSI 8.2%PRS 89.89
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CSI 2.92rCSI 8.67%PRS 94.48
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CSI 2.84rCSI 2.35%PRS 89.51
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CSI 2.66rCSI 3.78%PRS 85.97
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CSI 2.64rCSI 2.81%PRS 90.96
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CSI 2.57rCSI 4.85%PRS 94.19
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CSI 2.42rCSI 2.33%PRS 84.01
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CSI 2.39rCSI 4.25%PRS 92.97
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CSI 2.28rCSI 2.83%PRS 88.46
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CSI 2.26rCSI 4.1%PRS 94.11
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CSI 2.25rCSI 2.88%PRS 90.52
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CSI 2.23rCSI 3.22%PRS 91.82
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CSI 2.2rCSI 2.11%PRS 87.3
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CSI 2.18rCSI 2.89%PRS 91.82
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CSI 2.09rCSI 6.06%PRS 91.72
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CSI 2.09rCSI 3.24%PRS 90.09
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CSI 1.97rCSI 2.28%PRS 82.73
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CSI 1.9rCSI 4.69%PRS 88.91
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CSI 1.88rCSI 4.76%PRS 81.57
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CSI 1.87rCSI 2.5%PRS 85.92
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CSI 1.83rCSI 4.48%PRS 81.55
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CSI 1.62rCSI 4.19%PRS 85.18
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CSI 1.55rCSI 4.03%PRS 88.05
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CSI 1.54rCSI 3.28%PRS 91.29
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CSI 1.32rCSI 2.04%PRS 87.07
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CSI 1.31rCSI 2.55%PRS 90.24
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CSI 1.17rCSI 4.11%PRS 92.95
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CSI 1.02rCSI 5.49%PRS 93.02
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CSI 0.73rCSI 4.19%PRS 85.37
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CSI 0.66rCSI 5.74%PRS 82.97
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CSI 0.45rCSI 11.28%PRS 91.84
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CSI 0.33rCSI 3.44%PRS 84.54
Fold Change: Represents the ratio of the current Cell Significance Index to the Cell Significance Index Threshold, indicating how much the gene expression has changed compared to a baseline.
Cell Significance Index: Reflects how strongly a gene is expressed in this specific cell.
Fold Change: Represents the ratio of the current Cell Significance Index to the Cell Significance Index Threshold, indicating how much the gene expression has changed compared to a baseline.
Cell Significance Index: Reflects how strongly a gene is expressed in this cell type. Calculated using techniques like effect size estimation and bootstrapping for reliability.
Fold Change: Represents the ratio of the current Cell Significance Index to the Cell Significance Index Threshold, indicating how much the gene expression has changed compared to a baseline.
Cell Significance Index: Reflects how strongly a gene is expressed in this cell type. Calculated using techniques like effect size estimation and bootstrapping for reliability.
Network Configuration
Explore relationships of the current gene. Select an Interaction Source: 'ONTOLOGY' for shared pathways (GO/Reactome) or 'STRING' for protein-protein interactions. Further refine by selecting context genes and comparing Cell Significance Index (CSI) scores between baseline and target cell types and their specific contexts.
Legend:
- Query Gene
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Node Color (Target Cell CSI, relative to current network):
- Very High
- High
- Medium
- Low
- Very Low
- CSI N/A
- Node Size: Proportional to Target Cell CSI magnitude
- STRING PPI Edge
- Shared Pathway Edge (ONTOLOGY)
Other Information
This section provides additional information about the gene, including a description generated by an AI language model and details about associated proteins.
Genular Protein ID: 2926514725
Symbol: ITB6_HUMAN
Name: Integrin beta-6
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 2365683
Title: Complete amino acid sequence of a novel integrin beta subunit (beta 6) identified in epithelial cells using the polymerase chain reaction.
PubMed ID: 2365683
PubMed ID: 14702039
Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.
PubMed ID: 14702039
DOI: 10.1038/ng1285
PubMed ID: 15815621
Title: Generation and annotation of the DNA sequences of human chromosomes 2 and 4.
PubMed ID: 15815621
DOI: 10.1038/nature03466
PubMed ID: 15489334
Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
PubMed ID: 15489334
DOI: 10.1101/gr.2596504
PubMed ID: 1382574
Title: The gene organization of the human beta 7 subunit, the common beta subunit of the leukocyte integrins HML-1 and LPAM-1.
PubMed ID: 1382574
PubMed ID: 9426447
Title: Integrin alpha v beta 6 enhances coxsackievirus B1 lytic infection of human colon cancer cells.
PubMed ID: 9426447
PubMed ID: 11807098
Title: Different splice variants of filamin-B affect myogenesis, subcellular distribution, and determine binding to integrin (beta) subunits.
PubMed ID: 11807098
PubMed ID: 15184403
Title: Integrin alphaVbeta6-mediated activation of latent TGF-beta requires the latent TGF-beta binding protein-1.
PubMed ID: 15184403
PubMed ID: 15194773
Title: Integrin alpha v beta 6 is an RGD-dependent receptor for coxsackievirus A9.
PubMed ID: 15194773
PubMed ID: 17545607
Title: HS1-associated protein X-1 regulates carcinoma cell migration and invasion via clathrin-mediated endocytosis of integrin alphavbeta6.
PubMed ID: 17545607
PubMed ID: 17158881
Title: alphaVbeta6 is a novel receptor for human fibrillin-1. Comparative studies of molecular determinants underlying integrin-rgd affinity and specificity.
PubMed ID: 17158881
PubMed ID: 22278742
Title: GARP regulates the bioavailability and activation of TGFbeta.
PubMed ID: 22278742
PubMed ID: 24367260
Title: alphavbeta6- and alphavbeta8-integrins serve as interchangeable receptors for HSV gH/gL to promote endocytosis and activation of membrane fusion.
PubMed ID: 24367260
PubMed ID: 25383667
Title: Structural determinants of integrin beta-subunit specificity for latent TGF-beta.
PubMed ID: 25383667
DOI: 10.1038/nsmb.2905
PubMed ID: 28117447
Title: Force interacts with macromolecular structure in activation of TGF-beta.
PubMed ID: 28117447
DOI: 10.1038/nature21035
PubMed ID: 24319098
Title: A missense mutation in ITGB6 causes pitted hypomineralized amelogenesis imperfecta.
PubMed ID: 24319098
DOI: 10.1093/hmg/ddt616
PubMed ID: 24305999
Title: ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfecta.
PubMed ID: 24305999
DOI: 10.1093/hmg/ddt611
Sequence Information:
- Length: 788
- Mass: 85936
- Checksum: EDB7D533EC4C8C4D
- Sequence:
MGIELLCLFF LFLGRNDHVQ GGCALGGAET CEDCLLIGPQ CAWCAQENFT HPSGVGERCD TPANLLAKGC QLNFIENPVS QVEILKNKPL SVGRQKNSSD IVQIAPQSLI LKLRPGGAQT LQVHVRQTED YPVDLYYLMD LSASMDDDLN TIKELGSRLS KEMSKLTSNF RLGFGSFVEK PVSPFVKTTP EEIANPCSSI PYFCLPTFGF KHILPLTNDA ERFNEIVKNQ KISANIDTPE GGFDAIMQAA VCKEKIGWRN DSLHLLVFVS DADSHFGMDS KLAGIVIPND GLCHLDSKNE YSMSTVLEYP TIGQLIDKLV QNNVLLIFAV TQEQVHLYEN YAKLIPGATV GLLQKDSGNI LQLIISAYEE LRSEVELEVL GDTEGLNLSF TAICNNGTLF QHQKKCSHMK VGDTASFSVT VNIPHCERRS RHIIIKPVGL GDALELLVSP ECNCDCQKEV EVNSSKCHHG NGSFQCGVCA CHPGHMGPRC ECGEDMLSTD SCKEAPDHPS CSGRGDCYCG QCICHLSPYG NIYGPYCQCD NFSCVRHKGL LCGGNGDCDC GECVCRSGWT GEYCNCTTST DSCVSEDGVL CSGRGDCVCG KCVCTNPGAS GPTCERCPTC GDPCNSKRSC IECHLSAAGQ AREECVDKCK LAGATISEEE DFSKDGSVSC SLQGENECLI TFLITTDNEG KTIIHSINEK DCPKPPNIPM IMLGVSLAIL LIGVVLLCIW KLLVSFHDRK EVAKFEAERS KAKWQTGTNP LYRGSTSTFK NVTYKHREKQ KVDLSTDC
Genular Protein ID: 3439987401
Symbol: B4E2B8_HUMAN
Name: N/A
UniProtKB Accession Codes:
Database IDs:
Sequence Information:
- Length: 746
- Mass: 81522
- Checksum: E435089EF5DD0367
- Sequence:
MITYKNFTHP SGVGERCDTP ANLLAKGCQL NFIENPVSQV EILKNKPLSV GRQKNSSDIV QIAPQSLILK LRPGGAQTLQ VHVRQTEDYP VDLYYLMDLS ASMDDDLNTI KELGSRLSKE MSKLTSNFRL GFGSFVEKPV SPFVKTTPEE IANPCSSIPY FCLPTFGFKH ILPLTNDAER FNEIVKNQKI SANIDTPEGG FDAIMQAAVC KEKIGWRNDS LHLLVFVSDA DSHFGMDSKL AGIVIPNDGL CHLDSKNEYS MSTVLEYPTI GQLIDKLVQN NVLLIFAVTQ EQVHLYENYA KLIPGATVGL LQKDSGNILQ LIISAYEELR SEVELEVLGD TEGLNLSFTA ICNNGTLFQH QKKCSHMKVG DTASFSVTVN IPHCERRSRH IIIKPVGLGD ALELLVSPEC NCDCQKEVEV NSSKCHHGNG SFQCGVCACH PGHMGPRCEC GEDMLSTDPC KEAPDHPSCS GRGDCYCGQC ICHLSPYGNI YGPYCQCDNF SCVRHKGLLC GGNGDCDCGE CVCRSGWTGE YCNCTTSTDS CVSEDGVLCS GRGDCVCGKC VCTNPGASGP TCERCPTCGD PCNSKRSCIE CHLSAAGQAR EECVDKCKLA GATISEEEDF SKDGSVSCSL QGENECLITF LITTDNEGKT IIHSINEKDC PKPPNIPVIM LGVSLAILLI GVVLLCIWKL LVSFHDRKEV AKFEAERSKA KWQTGTNPLY RGSTSTFKNV TYKHREKQKV DLSTDC
Genular Protein ID: 2098844688
Symbol: A0A087WXP3_HUMAN
Name: N/A
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 11237011
Title: Initial sequencing and analysis of the human genome.
PubMed ID: 11237011
DOI: 10.1038/35057062
PubMed ID: 15496913
Title: Finishing the euchromatic sequence of the human genome.
PubMed ID: 15496913
DOI: 10.1038/nature03001
PubMed ID: 15815621
Title: Generation and annotation of the DNA sequences of human chromosomes 2 and 4.
PubMed ID: 15815621
DOI: 10.1038/nature03466
Sequence Information:
- Length: 693
- Mass: 75849
- Checksum: F04FC7553E9228C7
- Sequence:
MGIELLCLFF LFLGRNDHVQ GGAQTLQVHV RQTEDYPVDL YYLMDLSASM DDDLNTIKEL GSRLSKEMSK LTSNFRLGFG SFVEKPVSPF VKTTPEEIAN PCSSIPYFCL PTFGFKHILP LTNDAERFNE IVKNQKISAN IDTPEGGFDA IMQAAVCKEK IGWRNDSLHL LVFVSDADSH FGMDSKLAGI VIPNDGLCHL DSKNEYSMST VLEYPTIGQL IDKLVQNNVL LIFAVTQEQV HLYENYAKLI PGATVGLLQK DSGNILQLII SAYEELRSEV ELEVLGDTEG LNLSFTAICN NGTLFQHQKK CSHMKVGDTA SFSVTVNIPH CERRSRHIII KPVGLGDALE LLVSPECNCD CQKEVEVNSS KCHHGNGSFQ CGVCACHPGH MGPRCECGED MLSTDSCKEA PDHPSCSGRG DCYCGQCICH LSPYGNIYGP YCQCDNFSCV RHKGLLCGGN GDCDCGECVC RSGWTGEYCN CTTSTDSCVS EDGVLCSGRG DCVCGKCVCT NPGASGPTCE RCPTCGDPCN SKRSCIECHL SAAGQAREEC VDKCKLAGAT ISEEEDFSKD GSVSCSLQGE NECLITFLIT TDNEGKTIIH SINEKDCPKP PNIPMIMLGV SLAILLIGVV LLCIWKLLVS FHDRKEVAKF EAERSKAKWQ TGTNPLYRGS TSTFKNVTYK HREKQKVDLS TDC
Genular Protein ID: 857721210
Symbol: E9PEE8_HUMAN
Name: N/A
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 11237011
Title: Initial sequencing and analysis of the human genome.
PubMed ID: 11237011
DOI: 10.1038/35057062
PubMed ID: 15496913
Title: Finishing the euchromatic sequence of the human genome.
PubMed ID: 15496913
DOI: 10.1038/nature03001
PubMed ID: 15815621
Title: Generation and annotation of the DNA sequences of human chromosomes 2 and 4.
PubMed ID: 15815621
DOI: 10.1038/nature03466
Sequence Information:
- Length: 746
- Mass: 81544
- Checksum: A3767C1EEB3DF1CD
- Sequence:
MITYKNFTHP SGVGERCDTP ANLLAKGCQL NFIENPVSQV EILKNKPLSV GRQKNSSDIV QIAPQSLILK LRPGGAQTLQ VHVRQTEDYP VDLYYLMDLS ASMDDDLNTI KELGSRLSKE MSKLTSNFRL GFGSFVEKPV SPFVKTTPEE IANPCSSIPY FCLPTFGFKH ILPLTNDAER FNEIVKNQKI SANIDTPEGG FDAIMQAAVC KEKIGWRNDS LHLLVFVSDA DSHFGMDSKL AGIVIPNDGL CHLDSKNEYS MSTVLEYPTI GQLIDKLVQN NVLLIFAVTQ EQVHLYENYA KLIPGATVGL LQKDSGNILQ LIISAYEELR SEVELEVLGD TEGLNLSFTA ICNNGTLFQH QKKCSHMKVG DTASFSVTVN IPHCERRSRH IIIKPVGLGD ALELLVSPEC NCDCQKEVEV NSSKCHHGNG SFQCGVCACH PGHMGPRCEC GEDMLSTDSC KEAPDHPSCS GRGDCYCGQC ICHLSPYGNI YGPYCQCDNF SCVRHKGLLC GGNGDCDCGE CVCRSGWTGE YCNCTTSTDS CVSEDGVLCS GRGDCVCGKC VCTNPGASGP TCERCPTCGD PCNSKRSCIE CHLSAAGQAR EECVDKCKLA GATISEEEDF SKDGSVSCSL QGENECLITF LITTDNEGKT IIHSINEKDC PKPPNIPMIM LGVSLAILLI GVVLLCIWKL LVSFHDRKEV AKFEAERSKA KWQTGTNPLY RGSTSTFKNV TYKHREKQKV DLSTDC