Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agl |
A |
T |
3: 116,587,485 (GRCm39) |
|
probably null |
Het |
Arhgap29 |
G |
A |
3: 121,782,586 (GRCm39) |
V91I |
possibly damaging |
Het |
Aste1 |
T |
A |
9: 105,273,823 (GRCm39) |
L21* |
probably null |
Het |
Bpifb5 |
A |
T |
2: 154,072,268 (GRCm39) |
D325V |
probably damaging |
Het |
Btbd10 |
G |
A |
7: 112,924,988 (GRCm39) |
Q287* |
probably null |
Het |
Cdc20 |
T |
A |
4: 118,292,686 (GRCm39) |
H354L |
probably damaging |
Het |
Cdhr3 |
G |
A |
12: 33,132,263 (GRCm39) |
T120I |
probably damaging |
Het |
Col5a2 |
G |
A |
1: 45,422,843 (GRCm39) |
R1125* |
probably null |
Het |
Col9a3 |
A |
G |
2: 180,261,549 (GRCm39) |
D613G |
probably damaging |
Het |
Coro7 |
C |
T |
16: 4,451,168 (GRCm39) |
R507H |
probably benign |
Het |
Cracdl |
C |
T |
1: 37,667,326 (GRCm39) |
R240Q |
probably damaging |
Het |
Cryga |
T |
C |
1: 65,142,382 (GRCm39) |
I4V |
probably damaging |
Het |
D930020B18Rik |
A |
G |
10: 121,507,675 (GRCm39) |
T138A |
probably damaging |
Het |
Dclre1b |
G |
T |
3: 103,710,464 (GRCm39) |
H482Q |
probably benign |
Het |
Dpy19l2 |
A |
G |
9: 24,607,420 (GRCm39) |
S14P |
probably benign |
Het |
Elavl3 |
C |
A |
9: 21,948,167 (GRCm39) |
|
probably benign |
Het |
Ephb6 |
T |
C |
6: 41,591,503 (GRCm39) |
V220A |
probably damaging |
Het |
Exoc7 |
A |
T |
11: 116,188,408 (GRCm39) |
I297N |
possibly damaging |
Het |
Gdpd4 |
A |
T |
7: 97,632,082 (GRCm39) |
N332Y |
probably damaging |
Het |
Ggct |
C |
A |
6: 54,962,887 (GRCm39) |
E175* |
probably null |
Het |
Gm5316 |
T |
C |
6: 122,877,354 (GRCm39) |
|
noncoding transcript |
Het |
Hoxa7 |
T |
C |
6: 52,194,363 (GRCm39) |
N8S |
probably damaging |
Het |
Ifi208 |
A |
G |
1: 173,510,612 (GRCm39) |
T256A |
possibly damaging |
Het |
Il12rb2 |
A |
G |
6: 67,275,903 (GRCm39) |
F630S |
probably damaging |
Het |
Kit |
A |
G |
5: 75,783,657 (GRCm39) |
N378S |
probably benign |
Het |
Lmntd1 |
T |
A |
6: 145,375,716 (GRCm39) |
Y74F |
probably benign |
Het |
Lrp1b |
A |
T |
2: 40,888,050 (GRCm39) |
|
probably benign |
Het |
Ltbp1 |
T |
A |
17: 75,671,355 (GRCm39) |
V1194D |
probably damaging |
Het |
Mc5r |
T |
G |
18: 68,471,853 (GRCm39) |
S71A |
probably benign |
Het |
Mcm7 |
T |
C |
5: 138,162,981 (GRCm39) |
*390W |
probably null |
Het |
Myo18a |
T |
C |
11: 77,734,059 (GRCm39) |
|
probably null |
Het |
Naa25 |
C |
A |
5: 121,556,039 (GRCm39) |
L276M |
probably damaging |
Het |
Nlrp1a |
T |
G |
11: 71,014,207 (GRCm39) |
T348P |
probably damaging |
Het |
Nlrp1b |
T |
G |
11: 71,052,755 (GRCm39) |
K888T |
possibly damaging |
Het |
Or4f53 |
A |
G |
2: 111,087,994 (GRCm39) |
Y178C |
probably benign |
Het |
Pabpc6 |
A |
T |
17: 9,888,145 (GRCm39) |
N135K |
probably benign |
Het |
Pdzd2 |
G |
A |
15: 12,371,691 (GRCm39) |
A2568V |
possibly damaging |
Het |
Pik3r2 |
A |
G |
8: 71,223,545 (GRCm39) |
F346S |
probably damaging |
Het |
Pkd1 |
T |
C |
17: 24,813,793 (GRCm39) |
W4086R |
probably damaging |
Het |
Plekhb2 |
G |
A |
1: 34,905,320 (GRCm39) |
|
probably benign |
Het |
Plxnb2 |
A |
G |
15: 89,047,479 (GRCm39) |
|
probably null |
Het |
Pmfbp1 |
C |
T |
8: 110,252,039 (GRCm39) |
R395W |
probably damaging |
Het |
Pnldc1 |
A |
G |
17: 13,109,006 (GRCm39) |
Y497H |
probably damaging |
Het |
Ppp1ca |
T |
G |
19: 4,244,580 (GRCm39) |
V213G |
possibly damaging |
Het |
Rapgef2 |
G |
A |
3: 78,995,207 (GRCm39) |
R814C |
probably damaging |
Het |
Relch |
T |
A |
1: 105,619,627 (GRCm39) |
|
probably benign |
Het |
Rnasel |
A |
T |
1: 153,636,521 (GRCm39) |
I634F |
probably damaging |
Het |
Rnf157 |
A |
T |
11: 116,240,276 (GRCm39) |
|
probably benign |
Het |
Ryr3 |
A |
G |
2: 112,471,011 (GRCm39) |
S4567P |
probably damaging |
Het |
Smcr8 |
T |
A |
11: 60,671,185 (GRCm39) |
W778R |
probably damaging |
Het |
Stat1 |
T |
A |
1: 52,179,789 (GRCm39) |
L333Q |
probably damaging |
Het |
Strc |
A |
G |
2: 121,198,874 (GRCm39) |
L1391P |
probably damaging |
Het |
Tek |
G |
A |
4: 94,725,509 (GRCm39) |
V592M |
probably damaging |
Het |
Top1 |
A |
C |
2: 160,544,719 (GRCm39) |
K278N |
possibly damaging |
Het |
Utrn |
C |
T |
10: 12,585,700 (GRCm39) |
|
probably benign |
Het |
Wdr7 |
T |
C |
18: 63,910,705 (GRCm39) |
I699T |
probably damaging |
Het |
Zfp30 |
A |
G |
7: 29,491,860 (GRCm39) |
E119G |
possibly damaging |
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 |
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 |
|