Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aim2 |
A |
G |
1: 173,287,372 (GRCm39) |
D124G |
probably benign |
Het |
Akr1c6 |
T |
C |
13: 4,504,494 (GRCm39) |
M293T |
probably damaging |
Het |
Albfm1 |
A |
G |
5: 90,709,158 (GRCm39) |
T23A |
probably benign |
Het |
Ankhd1 |
A |
G |
18: 36,722,505 (GRCm39) |
T343A |
probably damaging |
Het |
Ano2 |
T |
C |
6: 125,880,018 (GRCm39) |
|
probably benign |
Het |
Arfgap2 |
G |
A |
2: 91,104,004 (GRCm39) |
G353R |
probably damaging |
Het |
Armc3 |
A |
G |
2: 19,297,791 (GRCm39) |
|
probably null |
Het |
Atp11b |
T |
C |
3: 35,889,528 (GRCm39) |
|
probably null |
Het |
Brd4 |
A |
G |
17: 32,418,214 (GRCm39) |
M13T |
probably benign |
Het |
Btd |
T |
A |
14: 31,384,044 (GRCm39) |
M10K |
possibly damaging |
Het |
C1s2 |
T |
C |
6: 124,602,649 (GRCm39) |
K515E |
probably benign |
Het |
Cars1 |
A |
T |
7: 143,123,587 (GRCm39) |
Y455N |
probably damaging |
Het |
Ccdc110 |
A |
G |
8: 46,396,460 (GRCm39) |
S784G |
probably benign |
Het |
Chic2 |
A |
G |
5: 75,171,872 (GRCm39) |
|
probably benign |
Het |
Chka |
A |
T |
19: 3,942,105 (GRCm39) |
|
probably null |
Het |
Chrne |
A |
G |
11: 70,506,101 (GRCm39) |
I420T |
possibly damaging |
Het |
Clstn1 |
T |
C |
4: 149,729,486 (GRCm39) |
V747A |
probably benign |
Het |
Cobll1 |
A |
G |
2: 64,929,602 (GRCm39) |
S575P |
possibly damaging |
Het |
Col6a6 |
A |
T |
9: 105,666,147 (GRCm39) |
L3Q |
probably damaging |
Het |
Comtd1 |
A |
T |
14: 21,898,813 (GRCm39) |
|
probably benign |
Het |
Cpsf2 |
T |
C |
12: 101,948,243 (GRCm39) |
V13A |
probably benign |
Het |
Creb3l4 |
T |
A |
3: 90,149,521 (GRCm39) |
I115L |
probably benign |
Het |
Cyp2j12 |
C |
T |
4: 95,990,346 (GRCm39) |
A407T |
possibly damaging |
Het |
Ddr2 |
A |
G |
1: 169,825,498 (GRCm39) |
|
probably null |
Het |
Dennd4c |
T |
C |
4: 86,725,775 (GRCm39) |
L743P |
probably damaging |
Het |
Egfl8 |
T |
C |
17: 34,833,171 (GRCm39) |
T192A |
probably benign |
Het |
Elapor1 |
C |
T |
3: 108,379,284 (GRCm39) |
|
probably null |
Het |
Elf3 |
A |
G |
1: 135,184,473 (GRCm39) |
|
probably benign |
Het |
Etv3 |
T |
G |
3: 87,443,223 (GRCm39) |
L269R |
possibly damaging |
Het |
Fah |
C |
A |
7: 84,251,260 (GRCm39) |
|
probably benign |
Het |
Fbll1 |
C |
A |
11: 35,688,407 (GRCm39) |
L285F |
probably benign |
Het |
Fcrla |
A |
T |
1: 170,748,682 (GRCm39) |
F154I |
probably damaging |
Het |
Fnip2 |
T |
A |
3: 79,396,701 (GRCm39) |
|
probably null |
Het |
Focad |
T |
C |
4: 88,115,083 (GRCm39) |
|
probably benign |
Het |
Gabrr1 |
T |
A |
4: 33,162,820 (GRCm39) |
I462N |
possibly damaging |
Het |
Gm57859 |
C |
A |
11: 113,579,805 (GRCm39) |
T400K |
probably benign |
Het |
Gnptab |
A |
G |
10: 88,265,485 (GRCm39) |
T366A |
probably benign |
Het |
Hnrnpu |
G |
A |
1: 178,159,017 (GRCm39) |
|
probably benign |
Het |
Il17ra |
T |
A |
6: 120,454,406 (GRCm39) |
V299E |
possibly damaging |
Het |
Impg1 |
G |
A |
9: 80,252,360 (GRCm39) |
Q607* |
probably null |
Het |
Impg1 |
T |
A |
9: 80,252,827 (GRCm39) |
E374V |
probably damaging |
Het |
Itgax |
C |
T |
7: 127,747,700 (GRCm39) |
L1039F |
probably benign |
Het |
Kcnk2 |
A |
T |
1: 189,072,133 (GRCm39) |
V65D |
probably damaging |
Het |
Kif20b |
A |
C |
19: 34,918,611 (GRCm39) |
|
probably null |
Het |
Krt9 |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
11: 100,079,903 (GRCm39) |
|
probably benign |
Het |
Lama5 |
T |
G |
2: 179,825,942 (GRCm39) |
I2372L |
probably benign |
Het |
Lilrb4a |
A |
G |
10: 51,368,139 (GRCm39) |
T85A |
possibly damaging |
Het |
Mapk13 |
C |
A |
17: 28,997,197 (GRCm39) |
H330N |
probably benign |
Het |
Mars1 |
C |
A |
10: 127,132,549 (GRCm39) |
|
probably benign |
Het |
Mdga1 |
C |
A |
17: 30,057,052 (GRCm39) |
R818L |
probably damaging |
Het |
Mdn1 |
T |
A |
4: 32,671,608 (GRCm39) |
L476Q |
possibly damaging |
Het |
Mup21 |
T |
C |
4: 62,066,202 (GRCm39) |
E178G |
probably benign |
Het |
Myg1 |
A |
G |
15: 102,240,288 (GRCm39) |
N38S |
probably benign |
Het |
Ncam1 |
A |
T |
9: 49,416,779 (GRCm39) |
D837E |
probably benign |
Het |
Ncam2 |
C |
T |
16: 81,386,679 (GRCm39) |
P686L |
possibly damaging |
Het |
Nck2 |
T |
C |
1: 43,500,231 (GRCm39) |
|
probably benign |
Het |
Nfya |
T |
C |
17: 48,707,563 (GRCm39) |
|
probably benign |
Het |
Npat |
A |
G |
9: 53,482,330 (GRCm39) |
K1346R |
probably damaging |
Het |
Odad2 |
C |
G |
18: 7,181,787 (GRCm39) |
D846H |
probably damaging |
Het |
Or12j3 |
G |
T |
7: 139,952,920 (GRCm39) |
T201K |
probably benign |
Het |
Or4a72 |
T |
C |
2: 89,406,023 (GRCm39) |
T16A |
probably damaging |
Het |
Or6c212 |
A |
G |
10: 129,558,681 (GRCm39) |
V244A |
probably benign |
Het |
Pde7b |
G |
T |
10: 20,288,873 (GRCm39) |
Q325K |
probably damaging |
Het |
Pla2r1 |
A |
T |
2: 60,253,056 (GRCm39) |
M1345K |
probably benign |
Het |
Prkcz |
T |
C |
4: 155,441,946 (GRCm39) |
D62G |
probably damaging |
Het |
Pros1 |
T |
A |
16: 62,723,935 (GRCm39) |
C228S |
possibly damaging |
Het |
Ptprc |
A |
G |
1: 138,006,236 (GRCm39) |
M782T |
possibly damaging |
Het |
Rcn1 |
T |
C |
2: 105,219,518 (GRCm39) |
D225G |
probably benign |
Het |
Recql4 |
G |
A |
15: 76,594,381 (GRCm39) |
R46C |
probably damaging |
Het |
Rnf220 |
C |
T |
4: 117,346,797 (GRCm39) |
R205Q |
possibly damaging |
Het |
Samd13 |
T |
C |
3: 146,368,502 (GRCm39) |
D11G |
probably benign |
Het |
Scp2d1 |
T |
A |
2: 144,666,030 (GRCm39) |
I123K |
probably benign |
Het |
Skap1 |
A |
T |
11: 96,644,870 (GRCm39) |
Y311F |
probably damaging |
Het |
Slc2a10 |
T |
C |
2: 165,356,676 (GRCm39) |
I112T |
possibly damaging |
Het |
Slc34a1 |
G |
A |
13: 24,003,078 (GRCm39) |
V243M |
probably benign |
Het |
Slc39a2 |
G |
A |
14: 52,132,711 (GRCm39) |
G218D |
probably damaging |
Het |
Sos1 |
T |
C |
17: 80,742,381 (GRCm39) |
N382S |
probably benign |
Het |
Spam1 |
C |
T |
6: 24,796,655 (GRCm39) |
T202I |
probably damaging |
Het |
Tas2r138 |
T |
A |
6: 40,589,820 (GRCm39) |
Q142L |
possibly damaging |
Het |
Tec |
T |
A |
5: 72,939,365 (GRCm39) |
R217* |
probably null |
Het |
Tmeff2 |
T |
A |
1: 50,969,804 (GRCm39) |
V90D |
probably benign |
Het |
Tmem119 |
T |
C |
5: 113,933,405 (GRCm39) |
Y132C |
probably damaging |
Het |
Topbp1 |
A |
G |
9: 103,190,035 (GRCm39) |
I204V |
probably benign |
Het |
Trappc14 |
A |
T |
5: 138,260,641 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
T |
2: 76,601,232 (GRCm39) |
I17001N |
probably damaging |
Het |
Vit |
T |
A |
17: 78,894,270 (GRCm39) |
M224K |
probably benign |
Het |
Vmn1r179 |
T |
G |
7: 23,628,491 (GRCm39) |
H227Q |
possibly damaging |
Het |
Vmn1r84 |
T |
C |
7: 12,095,743 (GRCm39) |
N305D |
probably benign |
Het |
Vmn2r61 |
A |
G |
7: 41,916,520 (GRCm39) |
N378D |
probably damaging |
Het |
Vmn2r87 |
A |
G |
10: 130,314,435 (GRCm39) |
Y384H |
probably damaging |
Het |
Wiz |
C |
T |
17: 32,580,570 (GRCm39) |
A294T |
probably benign |
Het |
Xdh |
C |
A |
17: 74,231,931 (GRCm39) |
V260L |
possibly damaging |
Het |
Xirp2 |
A |
G |
2: 67,343,237 (GRCm39) |
K1826R |
probably benign |
Het |
Zfp445 |
A |
C |
9: 122,681,358 (GRCm39) |
I861R |
probably benign |
Het |
Zfp691 |
T |
C |
4: 119,027,999 (GRCm39) |
T78A |
probably benign |
Het |
|
Other mutations in Entrep2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02053:Entrep2
|
APN |
7 |
64,469,590 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02567:Entrep2
|
APN |
7 |
64,436,479 (GRCm39) |
missense |
possibly damaging |
0.95 |
thick
|
UTSW |
7 |
64,409,116 (GRCm39) |
nonsense |
probably null |
|
R0612:Entrep2
|
UTSW |
7 |
64,411,549 (GRCm39) |
missense |
probably benign |
0.17 |
R0720:Entrep2
|
UTSW |
7 |
64,469,658 (GRCm39) |
splice site |
probably benign |
|
R1368:Entrep2
|
UTSW |
7 |
64,469,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R1716:Entrep2
|
UTSW |
7 |
64,426,633 (GRCm39) |
splice site |
probably null |
|
R1840:Entrep2
|
UTSW |
7 |
64,408,943 (GRCm39) |
missense |
probably benign |
0.37 |
R1972:Entrep2
|
UTSW |
7 |
64,425,516 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1973:Entrep2
|
UTSW |
7 |
64,425,516 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2201:Entrep2
|
UTSW |
7 |
64,409,141 (GRCm39) |
missense |
probably benign |
0.01 |
R2230:Entrep2
|
UTSW |
7 |
64,408,970 (GRCm39) |
missense |
probably damaging |
0.97 |
R2232:Entrep2
|
UTSW |
7 |
64,408,970 (GRCm39) |
missense |
probably damaging |
0.97 |
R2340:Entrep2
|
UTSW |
7 |
64,425,565 (GRCm39) |
missense |
probably benign |
0.00 |
R4809:Entrep2
|
UTSW |
7 |
64,426,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R4928:Entrep2
|
UTSW |
7 |
64,409,116 (GRCm39) |
nonsense |
probably null |
|
R5556:Entrep2
|
UTSW |
7 |
64,505,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R5852:Entrep2
|
UTSW |
7 |
64,425,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R6169:Entrep2
|
UTSW |
7 |
64,409,147 (GRCm39) |
missense |
probably benign |
0.00 |
R7029:Entrep2
|
UTSW |
7 |
64,409,075 (GRCm39) |
missense |
probably benign |
0.00 |
R7455:Entrep2
|
UTSW |
7 |
64,409,161 (GRCm39) |
missense |
probably benign |
0.00 |
R7512:Entrep2
|
UTSW |
7 |
64,805,918 (GRCm39) |
missense |
probably benign |
0.23 |
R7896:Entrep2
|
UTSW |
7 |
64,426,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R8166:Entrep2
|
UTSW |
7 |
64,409,153 (GRCm39) |
missense |
probably benign |
0.01 |
R9729:Entrep2
|
UTSW |
7 |
64,806,056 (GRCm39) |
missense |
probably benign |
|
|