Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam17 |
A |
T |
12: 21,399,934 (GRCm39) |
N157K |
possibly damaging |
Het |
Adck2 |
T |
C |
6: 39,560,848 (GRCm39) |
V412A |
probably benign |
Het |
Adgrb3 |
C |
T |
1: 25,865,190 (GRCm39) |
V11I |
possibly damaging |
Het |
Arhgef17 |
T |
C |
7: 100,579,019 (GRCm39) |
D643G |
probably damaging |
Het |
Arvcf |
A |
G |
16: 18,221,376 (GRCm39) |
Q597R |
probably damaging |
Het |
Brdt |
T |
C |
5: 107,525,877 (GRCm39) |
V910A |
probably benign |
Het |
Cachd1 |
A |
G |
4: 100,851,283 (GRCm39) |
D1167G |
probably benign |
Het |
Ccdc187 |
A |
C |
2: 26,165,577 (GRCm39) |
S860A |
probably benign |
Het |
Ccdc28a |
T |
C |
10: 18,089,926 (GRCm39) |
I113M |
probably benign |
Het |
Cdc5l |
T |
C |
17: 45,704,127 (GRCm39) |
N699S |
probably benign |
Het |
Cenpf |
A |
T |
1: 189,385,350 (GRCm39) |
I2310K |
possibly damaging |
Het |
Ch25h |
A |
T |
19: 34,452,414 (GRCm39) |
I38N |
probably benign |
Het |
Chrdl2 |
C |
A |
7: 99,670,129 (GRCm39) |
P84Q |
probably damaging |
Het |
Cltc |
A |
T |
11: 86,586,403 (GRCm39) |
Y1673N |
possibly damaging |
Het |
Cr1l |
C |
G |
1: 194,812,243 (GRCm39) |
G27R |
probably damaging |
Het |
Dync1h1 |
G |
A |
12: 110,586,805 (GRCm39) |
E929K |
probably benign |
Het |
E2f7 |
C |
A |
10: 110,601,615 (GRCm39) |
P324Q |
probably damaging |
Het |
Eif3b |
A |
G |
5: 140,411,194 (GRCm39) |
D215G |
probably benign |
Het |
Ephb1 |
A |
G |
9: 102,072,614 (GRCm39) |
I55T |
probably damaging |
Het |
Fbxw14 |
A |
T |
9: 109,107,810 (GRCm39) |
L188Q |
probably damaging |
Het |
Foxg1 |
T |
C |
12: 49,431,944 (GRCm39) |
S226P |
probably damaging |
Het |
Gbe1 |
T |
C |
16: 70,275,210 (GRCm39) |
F337L |
probably damaging |
Het |
Glg1 |
A |
T |
8: 111,899,116 (GRCm39) |
C716* |
probably null |
Het |
Gp1ba |
C |
G |
11: 70,531,730 (GRCm39) |
|
probably benign |
Het |
Grm7 |
C |
T |
6: 111,472,783 (GRCm39) |
S36L |
probably damaging |
Het |
H2-M5 |
T |
A |
17: 37,299,520 (GRCm39) |
I167F |
probably damaging |
Het |
H3c6 |
T |
C |
13: 23,746,421 (GRCm39) |
H40R |
possibly damaging |
Het |
Hycc1 |
A |
G |
5: 24,169,934 (GRCm39) |
C472R |
probably benign |
Het |
Il18rap |
C |
T |
1: 40,582,177 (GRCm39) |
T366M |
probably benign |
Het |
Ino80 |
C |
T |
2: 119,213,862 (GRCm39) |
R1236H |
probably damaging |
Het |
Ism1 |
T |
A |
2: 139,573,995 (GRCm39) |
I115N |
possibly damaging |
Het |
Kdm4a |
A |
G |
4: 117,999,573 (GRCm39) |
S950P |
probably benign |
Het |
Lama5 |
T |
C |
2: 179,835,592 (GRCm39) |
T1254A |
probably benign |
Het |
Lipo2 |
T |
A |
19: 33,698,361 (GRCm39) |
K339* |
probably null |
Het |
Lrrc7 |
T |
C |
3: 157,946,138 (GRCm39) |
K187R |
probably benign |
Het |
Mkrn2os |
G |
C |
6: 115,562,317 (GRCm39) |
S215R |
probably benign |
Het |
Myzap |
G |
T |
9: 71,457,485 (GRCm39) |
D303E |
possibly damaging |
Het |
Naa11 |
T |
C |
5: 97,540,084 (GRCm39) |
N25D |
probably damaging |
Het |
Naip5 |
T |
A |
13: 100,354,117 (GRCm39) |
K1149* |
probably null |
Het |
Obscn |
C |
T |
11: 58,964,158 (GRCm39) |
V3083M |
probably damaging |
Het |
Or10d1 |
T |
C |
9: 39,484,091 (GRCm39) |
T155A |
probably benign |
Het |
Or4k48 |
T |
C |
2: 111,476,070 (GRCm39) |
T91A |
possibly damaging |
Het |
Parn |
T |
A |
16: 13,466,322 (GRCm39) |
E241D |
possibly damaging |
Het |
Pax1 |
T |
A |
2: 147,210,517 (GRCm39) |
|
probably null |
Het |
Pclo |
A |
T |
5: 14,725,369 (GRCm39) |
E1409V |
unknown |
Het |
Pclo |
A |
G |
5: 14,763,056 (GRCm39) |
Y3843C |
unknown |
Het |
Ppp2r3d |
A |
T |
9: 101,088,634 (GRCm39) |
M563K |
probably benign |
Het |
Prdm1 |
T |
G |
10: 44,316,729 (GRCm39) |
K623Q |
probably damaging |
Het |
Ptpn13 |
T |
C |
5: 103,698,973 (GRCm39) |
V1152A |
probably benign |
Het |
Ptx3 |
G |
A |
3: 66,128,391 (GRCm39) |
A151T |
probably benign |
Het |
Rab11fip1 |
T |
C |
8: 27,644,940 (GRCm39) |
S282G |
possibly damaging |
Het |
Ros1 |
G |
T |
10: 51,972,190 (GRCm39) |
N1641K |
probably damaging |
Het |
Syne1 |
T |
C |
10: 5,181,768 (GRCm39) |
K4189R |
probably benign |
Het |
Tcf3 |
T |
C |
10: 80,246,091 (GRCm39) |
K611E |
probably damaging |
Het |
Tmem215 |
A |
G |
4: 40,474,376 (GRCm39) |
Q151R |
probably benign |
Het |
Trappc8 |
T |
C |
18: 21,003,667 (GRCm39) |
I254V |
probably benign |
Het |
Trim46 |
T |
C |
3: 89,143,760 (GRCm39) |
D556G |
probably damaging |
Het |
Wdr97 |
A |
T |
15: 76,245,694 (GRCm39) |
E1310D |
|
Het |
Zfp513 |
C |
A |
5: 31,356,825 (GRCm39) |
R487L |
probably damaging |
Het |
Zmpste24 |
C |
A |
4: 120,944,508 (GRCm39) |
E97* |
probably null |
Het |
|
Other mutations in Crebbp |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01086:Crebbp
|
APN |
16 |
3,997,416 (GRCm39) |
missense |
probably benign |
|
IGL01366:Crebbp
|
APN |
16 |
3,944,370 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01457:Crebbp
|
APN |
16 |
3,942,632 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01713:Crebbp
|
APN |
16 |
3,946,512 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02382:Crebbp
|
APN |
16 |
3,925,934 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02513:Crebbp
|
APN |
16 |
3,944,469 (GRCm39) |
splice site |
probably null |
|
IGL02519:Crebbp
|
APN |
16 |
3,919,457 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02533:Crebbp
|
APN |
16 |
3,925,296 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02582:Crebbp
|
APN |
16 |
3,902,141 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02600:Crebbp
|
APN |
16 |
3,972,882 (GRCm39) |
missense |
probably benign |
|
IGL02716:Crebbp
|
APN |
16 |
3,932,742 (GRCm39) |
missense |
probably benign |
0.22 |
IGL02736:Crebbp
|
APN |
16 |
3,972,774 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03349:Crebbp
|
APN |
16 |
3,935,222 (GRCm39) |
missense |
possibly damaging |
0.69 |
enchanting
|
UTSW |
16 |
3,937,670 (GRCm39) |
missense |
possibly damaging |
0.92 |
Intriguing
|
UTSW |
16 |
3,997,886 (GRCm39) |
missense |
possibly damaging |
0.83 |
Rivetting
|
UTSW |
16 |
3,909,753 (GRCm39) |
missense |
probably damaging |
1.00 |
Stunning
|
UTSW |
16 |
3,909,792 (GRCm39) |
missense |
probably damaging |
1.00 |
Suggestive
|
UTSW |
16 |
3,925,991 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4418001:Crebbp
|
UTSW |
16 |
3,932,689 (GRCm39) |
missense |
probably benign |
0.02 |
R0022:Crebbp
|
UTSW |
16 |
3,903,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R0029:Crebbp
|
UTSW |
16 |
3,935,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R0098:Crebbp
|
UTSW |
16 |
3,909,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R0098:Crebbp
|
UTSW |
16 |
3,909,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R0125:Crebbp
|
UTSW |
16 |
3,935,105 (GRCm39) |
splice site |
probably benign |
|
R0126:Crebbp
|
UTSW |
16 |
3,901,927 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0140:Crebbp
|
UTSW |
16 |
3,935,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R0546:Crebbp
|
UTSW |
16 |
3,903,671 (GRCm39) |
missense |
probably damaging |
0.99 |
R0705:Crebbp
|
UTSW |
16 |
3,972,874 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0801:Crebbp
|
UTSW |
16 |
3,906,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R1103:Crebbp
|
UTSW |
16 |
3,901,925 (GRCm39) |
missense |
probably damaging |
0.97 |
R1225:Crebbp
|
UTSW |
16 |
3,944,820 (GRCm39) |
missense |
probably benign |
0.04 |
R1421:Crebbp
|
UTSW |
16 |
3,942,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R1513:Crebbp
|
UTSW |
16 |
3,933,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R1531:Crebbp
|
UTSW |
16 |
3,902,381 (GRCm39) |
missense |
probably benign |
0.04 |
R1860:Crebbp
|
UTSW |
16 |
3,905,600 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1941:Crebbp
|
UTSW |
16 |
3,997,555 (GRCm39) |
missense |
probably benign |
|
R1953:Crebbp
|
UTSW |
16 |
3,997,313 (GRCm39) |
missense |
probably benign |
0.23 |
R1992:Crebbp
|
UTSW |
16 |
3,946,561 (GRCm39) |
splice site |
probably null |
|
R2000:Crebbp
|
UTSW |
16 |
3,902,116 (GRCm39) |
missense |
probably damaging |
0.98 |
R2006:Crebbp
|
UTSW |
16 |
3,902,617 (GRCm39) |
unclassified |
probably benign |
|
R2022:Crebbp
|
UTSW |
16 |
3,903,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R2044:Crebbp
|
UTSW |
16 |
3,902,687 (GRCm39) |
missense |
probably benign |
0.04 |
R2185:Crebbp
|
UTSW |
16 |
3,902,002 (GRCm39) |
missense |
probably damaging |
0.99 |
R2203:Crebbp
|
UTSW |
16 |
3,956,641 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2349:Crebbp
|
UTSW |
16 |
3,956,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R2430:Crebbp
|
UTSW |
16 |
3,914,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R2438:Crebbp
|
UTSW |
16 |
3,972,722 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2842:Crebbp
|
UTSW |
16 |
3,927,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R2896:Crebbp
|
UTSW |
16 |
3,956,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R2920:Crebbp
|
UTSW |
16 |
3,936,946 (GRCm39) |
missense |
probably damaging |
0.98 |
R3118:Crebbp
|
UTSW |
16 |
3,927,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R3894:Crebbp
|
UTSW |
16 |
3,913,966 (GRCm39) |
missense |
probably benign |
0.11 |
R4177:Crebbp
|
UTSW |
16 |
3,937,663 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4692:Crebbp
|
UTSW |
16 |
3,932,727 (GRCm39) |
missense |
possibly damaging |
0.64 |
R4790:Crebbp
|
UTSW |
16 |
3,997,983 (GRCm39) |
missense |
probably damaging |
0.98 |
R4884:Crebbp
|
UTSW |
16 |
3,906,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R4957:Crebbp
|
UTSW |
16 |
3,935,231 (GRCm39) |
missense |
probably benign |
0.14 |
R5109:Crebbp
|
UTSW |
16 |
3,906,295 (GRCm39) |
intron |
probably benign |
|
R5121:Crebbp
|
UTSW |
16 |
3,911,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R5420:Crebbp
|
UTSW |
16 |
3,925,322 (GRCm39) |
missense |
probably damaging |
1.00 |
R5455:Crebbp
|
UTSW |
16 |
3,903,831 (GRCm39) |
missense |
probably benign |
0.45 |
R5485:Crebbp
|
UTSW |
16 |
3,932,777 (GRCm39) |
missense |
probably benign |
|
R5660:Crebbp
|
UTSW |
16 |
3,972,722 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5724:Crebbp
|
UTSW |
16 |
3,905,499 (GRCm39) |
unclassified |
probably benign |
|
R5771:Crebbp
|
UTSW |
16 |
3,937,636 (GRCm39) |
missense |
probably benign |
0.03 |
R5825:Crebbp
|
UTSW |
16 |
3,905,606 (GRCm39) |
missense |
probably damaging |
0.99 |
R5919:Crebbp
|
UTSW |
16 |
3,925,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R5965:Crebbp
|
UTSW |
16 |
3,905,525 (GRCm39) |
unclassified |
probably benign |
|
R6021:Crebbp
|
UTSW |
16 |
3,903,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R6146:Crebbp
|
UTSW |
16 |
3,902,487 (GRCm39) |
nonsense |
probably null |
|
R6521:Crebbp
|
UTSW |
16 |
3,936,992 (GRCm39) |
missense |
probably damaging |
0.99 |
R6571:Crebbp
|
UTSW |
16 |
3,937,670 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6617:Crebbp
|
UTSW |
16 |
3,937,670 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6618:Crebbp
|
UTSW |
16 |
3,937,670 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6634:Crebbp
|
UTSW |
16 |
3,937,670 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6646:Crebbp
|
UTSW |
16 |
3,937,670 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6647:Crebbp
|
UTSW |
16 |
3,937,670 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6766:Crebbp
|
UTSW |
16 |
3,935,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R6836:Crebbp
|
UTSW |
16 |
3,997,886 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7022:Crebbp
|
UTSW |
16 |
3,935,187 (GRCm39) |
missense |
probably damaging |
0.98 |
R7210:Crebbp
|
UTSW |
16 |
3,902,121 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7568:Crebbp
|
UTSW |
16 |
3,944,353 (GRCm39) |
missense |
probably benign |
0.34 |
R7672:Crebbp
|
UTSW |
16 |
3,902,574 (GRCm39) |
missense |
probably benign |
0.06 |
R8145:Crebbp
|
UTSW |
16 |
3,946,389 (GRCm39) |
missense |
probably benign |
0.03 |
R8152:Crebbp
|
UTSW |
16 |
3,902,945 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8374:Crebbp
|
UTSW |
16 |
3,902,175 (GRCm39) |
missense |
probably damaging |
0.99 |
R8392:Crebbp
|
UTSW |
16 |
3,902,145 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8679:Crebbp
|
UTSW |
16 |
3,902,322 (GRCm39) |
missense |
probably damaging |
0.99 |
R8738:Crebbp
|
UTSW |
16 |
3,936,952 (GRCm39) |
missense |
probably benign |
0.07 |
R8756:Crebbp
|
UTSW |
16 |
3,903,767 (GRCm39) |
missense |
probably benign |
0.01 |
R8847:Crebbp
|
UTSW |
16 |
3,902,891 (GRCm39) |
missense |
probably benign |
0.01 |
R8950:Crebbp
|
UTSW |
16 |
4,031,023 (GRCm39) |
missense |
probably damaging |
0.98 |
R8964:Crebbp
|
UTSW |
16 |
3,909,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R8972:Crebbp
|
UTSW |
16 |
3,925,935 (GRCm39) |
missense |
probably benign |
0.17 |
R9069:Crebbp
|
UTSW |
16 |
3,903,187 (GRCm39) |
missense |
probably benign |
|
R9155:Crebbp
|
UTSW |
16 |
3,914,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R9240:Crebbp
|
UTSW |
16 |
3,917,537 (GRCm39) |
critical splice donor site |
probably null |
|
R9414:Crebbp
|
UTSW |
16 |
3,925,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R9500:Crebbp
|
UTSW |
16 |
3,911,355 (GRCm39) |
missense |
probably damaging |
0.98 |
R9549:Crebbp
|
UTSW |
16 |
3,903,111 (GRCm39) |
missense |
probably benign |
0.03 |
R9663:Crebbp
|
UTSW |
16 |
3,933,654 (GRCm39) |
missense |
probably damaging |
0.99 |
X0012:Crebbp
|
UTSW |
16 |
3,905,629 (GRCm39) |
missense |
probably damaging |
1.00 |
|