FBXL10 enhancement of MAP/ERK signaling in diffuse large B-cell lymphoma

No Pathway Network information available for FBXL10 enhancement of MAP/ERK signaling in diffuse large B-cell lymphoma

Pathways in the FBXL10 enhancement of MAP/ERK signaling in diffuse large B-cell lymphoma SuperPath

Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways

Disorders associated with FBXL10 enhancement of MAP/ERK signaling in diffuse large B-cell lymphoma SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Bryant-li-bhoj neurodevelopmental syndrome 2EnrichmentH3-3A, H3-3B5.24
2Weaver syndromeEnrichmentEZH2, SUZ124.76
3Glioma susceptibility 1EnrichmentH3-3A, H3C13.80
4Luo-schoch-yamamoto syndromeEnrichmentRNF22.61
5Noonan syndrome 13EnrichmentMAPK12.61
6Imagawa-matsumoto syndromeEnrichmentSUZ122.61
7Hypogonadotropic hypogonadism 19 with or without anosmiaEnrichmentDUSP62.61
8Cohen-gibson syndromeEnrichmentEED2.61
9Bryant-li-bhoj neurodevelopmental syndrome 1EnrichmentH3-3A2.61
10Microphthalmia, syndromic 1EnrichmentBCOR2.31
11Microphthalmia, syndromic 2EnrichmentBCOR2.31
12Intravascular large b-cell lymphomaEnrichmentBCL62.31
13Brachydactyly-elbow wrist dysplasia syndromeEnrichmentMACROH2A12.31
14Primary mediastinal large b-cell lymphomaEnrichmentBCL62.31
15High-grade b-cell lymphoma double-hit/triple-hitEnrichmentBCL62.14
16Chromosome 22q11.2 deletion syndrome, distalEnrichmentMAPK12.01
17Follicular lymphomaEnrichmentBCL61.92
18Endometrial stromal sarcomaEnrichmentSUZ121.92
19Kidney clear cell sarcomaEnrichmentBCOR1.84
20Specific learning disabilityEnrichmentMAPK11.58
21Acute promyelocytic leukemiaEnrichmentBCOR1.51
22MicrocephalyEnrichmentKDM2B, MAPK11.45
23Heart, malformation ofEnrichmentMAPK11.37
24Normosmic congenital hypogonadotropic hypogonadismEnrichmentDUSP61.37
25Kallmann syndromeEnrichmentDUSP61.26
26Leukemia, acute myeloidEnrichmentBCOR1.03
27West syndromeEnrichmentKDM2B0.99
28Myeloma, multipleEnrichmentH3C10.89
29Autism spectrum disorderEnrichmentEED0.63
30Complex neurodevelopmental disorderEnrichmentRNF20.58
31Inherited cancer-predisposing syndromeEnrichmentEZH20.56

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