Homo sapiens inositol 1,4,5-triphosphate receptor, type 1 (ITPR1), RefSeqGene on chromosome 3 |
NG_016144.1 |
253/254 (99%) |
1.00E-127 |
269954693 |
ITPR1 |
3p26-p25 |
Homo sapiens notch 2 (NOTCH2), RefSeqGene on chromosome 1 |
NG_008163.1 |
512/514 (99%) |
0 |
4853 |
NOTCH2 |
1p13-p11 |
Homo sapiens nuclear receptor corepressor 1 (NCOR1), transcript variant 3, mRNA |
NM_001190440.1 |
213/214 (99%) |
1.00E-106 |
9611 |
NCOR1 |
17p11.2 |
Homo sapiens retinoblastoma 1 (RB1), mRNA |
NM_000321.2 |
269/270 (99%) |
1.00E-137 |
5925 |
RB1 |
13q14.2 |
Homo sapiens CREB binding protein (CREBBP), RefSeqGene on chromosome |
NG_009873.1 |
197/198 (99%) |
1.00E-96 |
1387 |
CREBBP |
16p13.3 |
Homo sapiens SMAD family member 1 (SMAD1), transcript variant 2, mRNA |
NM_001003688.1 |
262/263 (99%) |
1.00E-133 |
4086 |
SMAD1 |
7p15 |
Homo sapiens Niemann-Pick disease, type C1 (NPC1), RefSeqGene on chromosome 18 |
NG_012795.1 |
174/175 (99%) |
3.00E-83 |
4864 |
NPC1 |
18q11-q12 |
Homo sapiens epidermal growth factor receptor (EGFR), RefSeqGene on chromosome 7 |
NG_007726.1 |
207/208 (99%) |
3.00E-102 |
1956 |
EGFR |
7p12 |
Homo sapiens septin 9 (SEPT9), transcript variant 4, mRNA |
NM_001113495.1 |
379/380 (99%) |
0 |
10801 SEPT9 |
SEPT9 |
17q25 |