Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Myosin Type I [NCBI]

Gene


 Gene Link Information
Gain		 01
NEWENTRY [NCBI] 0.000138571
MYO1A [NCBI] 5.81532e-05
MYO1C [NCBI] 4.52656e-05
MYO1B [NCBI] 1.05171e-05
MYO1E [NCBI] 5.00835e-06
MYO6 [NCBI] 3.32572e-06
ACTR3 [NCBI] 3.32243e-06
ACTR2 [NCBI] 3.30947e-06
ACTB [NCBI] 3.22113e-06
RIBIN [NCBI] 2.59236e-06
MYH4 [NCBI] 2.26329e-06
ALPK1 [NCBI] 2.26329e-06
HSPA4L [NCBI] 2.13943e-06
MYOM1 [NCBI] 2.10246e-06
RRN3 [NCBI] 2.06998e-06
POLR1B [NCBI] 2.04103e-06
HERPUD1 [NCBI] 1.88075e-06
WASF1 [NCBI] 1.72104e-06
SLC6A12 [NCBI] 1.61611e-06
TEAD1 [NCBI] 1.59204e-06
RAB27A [NCBI] 1.54956e-06
SI [NCBI] 1.54523e-06
PFN1 [NCBI] 1.4757e-06
MYO7A [NCBI] 1.43869e-06
PAK1 [NCBI] 1.27267e-06
CS [NCBI] 1.24694e-06
WAS [NCBI] 1.19492e-06
PLEK [NCBI] 1.16142e-06
UCP3 [NCBI] 1.10453e-06
MLL [NCBI] 1.07401e-06



OMIM


 OMIM Link Information
gain		 01
deafness, autosomal dominant nonsyndromic sensorineural, due to mutation in myo1a [NCBI] 0.000211547
GS2 [NCBI] 0.000177719
GS1 [NCBI] 0.000174453
MYO1D [NCBI] 9.82657e-05
ALPK1 [NCBI] 4.59472e-05
MYO1A [NCBI] 4.59472e-05
MYO1F [NCBI] 4.41278e-05
GNB5 [NCBI] 4.16968e-05
RAB27A [NCBI] 3.58087e-05
CDH23 [NCBI] 3.41483e-05
MYO5A [NCBI] 3.32725e-05
SI [NCBI] 2.53098e-05



Database Center for Life Science