Enhancer ID: | E_02_0506 |
Species: | human |
Position : | chr10:96186235-96188235 |
Biosample name: | |
Experiment class : | High+Lowthroughput |
Enhancer type: | Enhancer |
Disease: | -- |
Pubmed ID: | 30055251 |
Enhancer experiment: | Western blot, immunofluorescence staining |
Enhancer experiment description: | Functional studies involving BLNK were first car- ried out in chicken BLNK-deficient DT40 cells, which exhibited the abolishment of phospholipase C-?2 (PLC-?2) tyrosine phosphorylation, a calcium mobilization defect, and impaired activation of c-Jun N- terminal kinase (JNK) [4]. After SYK phosphorylates several critical tyrosines (Y72, Y84, Y96, Y178, and Y189), BLNK provides docking sites for intracellular sig- naling molecules including guanine nucleotide exchange factors (VAV), non-catalytic region of tyrosine kinase (NCK), Bruton's tyrosine kinase (BTK), and phospholipase C? (PLC?) [1 3]. |
Target gene : | BLNK |
Strong evidence: | qRT-PCR,qPCR,ChIP,3C |
Less strong evidence: | RNA-Seq |
Target gene experiment description: | Functional studies involving BLNK were first car- ried out in chicken BLNK-deficient DT40 cells, which exhibited the abolishment of phospholipase C-?2 (PLC-?2) tyrosine phosphorylation, a calcium mobilization defect, and impaired activation of c-Jun N- terminal kinase (JNK) [4]. After SYK phosphorylates several critical tyrosines (Y72, Y84, Y96, Y178, and Y189), BLNK provides docking sites for intracellular sig- naling molecules including guanine nucleotide exchange factors (VAV), non-catalytic region of tyrosine kinase (NCK), Bruton's tyrosine kinase (BTK), and phospholipase C? (PLC?) [1 3]. |
TF name : | -- |
TF experiment: | Western blot,?????? |
TF experiment description: | Functional studies involving BLNK were first car- ried out in chicken BLNK-deficient DT40 cells, which exhibited the abolishment of phospholipase C-?2 (PLC-?2) tyrosine phosphorylation, a calcium mobilization defect, and impaired activation of c-Jun N- terminal kinase (JNK) [4]. After SYK phosphorylates several critical tyrosines (Y72, Y84, Y96, Y178, and Y189), BLNK provides docking sites for intracellular sig- naling molecules including guanine nucleotide exchange factors (VAV), non-catalytic region of tyrosine kinase (NCK), Bruton's tyrosine kinase (BTK), and phospholipase C? (PLC?) [1 3]. |
Enhancer function : | Functional studies involving BLNK were first car- ried out in chicken BLNK-deficient DT40 cells, which exhibited the abolishment of phospholipase C-?2 (PLC-?2) tyrosine phosphorylation, a calcium mobilization defect, and impaired activation of c-Jun N- terminal kinase (JNK) [4]. After SYK phosphorylates several critical tyrosines (Y72, Y84, Y96, Y178, and Y189), BLNK provides docking sites for intracellular sig- naling molecules including guanine nucleotide exchange factors (VAV), non-catalytic region of tyrosine kinase (NCK), Bruton's tyrosine kinase (BTK), and phospholipase C? (PLC?) [1 3]. |
Enhancer function experiment: | Immunohistochemical staining |
Enhancer function experiment description: |
Functional studies involving BLNK were first car- ried out in chicken BLNK-deficient DT40 cells, which exhibited the abolishment of phospholipase C-?2 (PLC-?2) tyrosine phosphorylation, a calcium mobilization defect, and impaired activation of c-Jun N- terminal kinase (JNK) [4]. After SYK phosphorylates several critical tyrosines (Y72, Y84, Y96, Y178, and Y189), BLNK provides docking sites for intracellular sig- naling molecules including guanine nucleotide exchange factors (VAV), non-catalytic region of tyrosine kinase (NCK), Bruton's tyrosine kinase (BTK), and phospholipase C? (PLC?) [1 3]. |
SNP ID: | -- |
GeneName | Pathway Name | Source | Gene Number |
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