Other mutations in this stock |
Total: 28 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
T |
G |
11: 110,200,264 (GRCm39) |
I483L |
probably benign |
Het |
Bmpr1b |
A |
C |
3: 141,546,488 (GRCm39) |
M466R |
probably damaging |
Het |
Casp8ap2 |
G |
A |
4: 32,630,246 (GRCm39) |
D42N |
probably null |
Het |
Ddx27 |
A |
G |
2: 166,868,124 (GRCm39) |
H319R |
probably damaging |
Het |
Dync2i2 |
T |
A |
2: 29,923,314 (GRCm39) |
D263V |
possibly damaging |
Het |
Gckr |
A |
G |
5: 31,462,374 (GRCm39) |
M236V |
probably benign |
Het |
Gm28044 |
A |
C |
13: 67,469,025 (GRCm39) |
|
probably benign |
Het |
Gmnc |
T |
A |
16: 26,781,641 (GRCm39) |
|
probably benign |
Het |
Gpx3 |
C |
A |
11: 54,800,433 (GRCm39) |
D210E |
possibly damaging |
Het |
Lpin2 |
A |
G |
17: 71,545,693 (GRCm39) |
N513S |
probably damaging |
Het |
Myh3 |
C |
T |
11: 66,974,227 (GRCm39) |
R170C |
probably damaging |
Het |
Nrxn3 |
G |
T |
12: 89,478,682 (GRCm39) |
|
probably benign |
Het |
Nynrin |
A |
G |
14: 56,101,449 (GRCm39) |
I373V |
probably benign |
Het |
Or13a21 |
T |
C |
7: 139,998,862 (GRCm39) |
T275A |
probably benign |
Het |
Or6b6 |
A |
G |
7: 106,570,756 (GRCm39) |
I265T |
possibly damaging |
Het |
Padi3 |
A |
G |
4: 140,525,467 (GRCm39) |
V172A |
probably benign |
Het |
Pdzd2 |
C |
A |
15: 12,411,105 (GRCm39) |
G554W |
probably damaging |
Het |
Plekhg6 |
G |
A |
6: 125,347,563 (GRCm39) |
R464* |
probably null |
Het |
Rnf123 |
G |
A |
9: 107,945,501 (GRCm39) |
R390* |
probably null |
Het |
Serinc1 |
A |
G |
10: 57,399,127 (GRCm39) |
S259P |
probably benign |
Het |
Slfn4 |
T |
A |
11: 83,077,832 (GRCm39) |
S207T |
possibly damaging |
Het |
Stab2 |
C |
T |
10: 86,790,123 (GRCm39) |
G548R |
probably damaging |
Het |
Tmem229b-ps |
T |
C |
10: 53,351,052 (GRCm39) |
|
noncoding transcript |
Het |
Ttn |
G |
A |
2: 76,570,509 (GRCm39) |
P26795S |
probably damaging |
Het |
Vmn2r96 |
A |
G |
17: 18,817,829 (GRCm39) |
M661V |
probably benign |
Het |
Ybey |
G |
A |
10: 76,300,165 (GRCm39) |
|
probably benign |
Het |
Zbtb17 |
A |
G |
4: 141,194,196 (GRCm39) |
D715G |
possibly damaging |
Het |
Zgrf1 |
T |
C |
3: 127,394,623 (GRCm39) |
|
probably benign |
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 |
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 |
R8958:Crebbp
|
UTSW |
16 |
4,031,172 (GRCm39) |
start gained |
probably benign |
|
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 |
|