Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Branchio-Oto-Renal Syndrome [NCBI]

Gene


 Gene Link Information
Gain		 01
EYA1 [NCBI] 0.000801653
BOS2 [NCBI] 0.000499621
SIX1 [NCBI] 0.000120538
SALL1 [NCBI] 1.96076e-05
GJB2 [NCBI] 1.67339e-05
EYA3 [NCBI] 1.40865e-05
SIX2 [NCBI] 1.26048e-05
NDUFB9 [NCBI] 1.2171e-05
EYA2 [NCBI] 1.18254e-05
DACH1 [NCBI] 1.1538e-05
GNAZ [NCBI] 1.1538e-05
SIX6 [NCBI] 1.08858e-05
EYA4 [NCBI] 1.00453e-05
CLRN1 [NCBI] 9.74176e-06
OTX2 [NCBI] 9.40603e-06
SIX5 [NCBI] 9.06198e-06
GNAI2 [NCBI] 9.00076e-06
TFAP2A [NCBI] 7.76933e-06
MYOG [NCBI] 7.52464e-06
GJB6 [NCBI] 7.08134e-06
PAX2 [NCBI] 6.52159e-06
FGF3 [NCBI] 6.46644e-06
PAX8 [NCBI] 6.41303e-06
COL2A1 [NCBI] 6.09098e-06
GDNF [NCBI] 4.83778e-06



OMIM


 OMIM Link Information
gain		 01
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging [NCBI] 0.00342726
branchiootic syndrome 2 [NCBI] 0.00200702
DURS1 [NCBI] 0.00136056
EYA1 [NCBI] 0.00119832
hydrocephalus, autosomal dominant [NCBI] 0.00092257
BOR1 [NCBI] 0.000878263
BOS1 [NCBI] 0.000696216
BOS3 [NCBI] 0.000427752
SIX1 [NCBI] 0.00021828
TBS [NCBI] 0.000157906
BOR2 [NCBI] 0.000141395
bor-duane hydrocephalus contiguous gene syndrome [NCBI] 0.000118925
cholesteatoma, congenital [NCBI] 0.000118925
DFNA23 [NCBI] 0.000118925
otofaciocervical syndrome [NCBI] 0.000110446
EYA3 [NCBI] 8.96982e-05
NDUFB9 [NCBI] 7.59186e-05
EYA2 [NCBI] 6.73416e-05
SALL1 [NCBI] 5.54947e-05
SIX5 [NCBI] 5.25308e-05



Database Center for Life Science