Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam32 |
G |
A |
8: 25,362,646 (GRCm39) |
S17L |
probably damaging |
Het |
Akt3 |
A |
T |
1: 176,877,756 (GRCm39) |
Y337* |
probably null |
Het |
Ankrd34c |
A |
G |
9: 89,611,381 (GRCm39) |
V320A |
probably benign |
Het |
Aox1 |
C |
A |
1: 58,388,227 (GRCm39) |
L1112I |
possibly damaging |
Het |
Arap2 |
A |
C |
5: 62,834,443 (GRCm39) |
|
probably null |
Het |
Atm |
A |
T |
9: 53,401,582 (GRCm39) |
I1429N |
probably damaging |
Het |
Ccdc68 |
A |
G |
18: 70,099,861 (GRCm39) |
N290D |
probably damaging |
Het |
Chst1 |
T |
C |
2: 92,443,542 (GRCm39) |
W5R |
probably damaging |
Het |
Clip1 |
G |
T |
5: 123,752,827 (GRCm39) |
|
probably benign |
Het |
Cyp2b13 |
T |
C |
7: 25,781,236 (GRCm39) |
|
probably null |
Het |
Dnah8 |
G |
A |
17: 30,967,542 (GRCm39) |
D2585N |
probably benign |
Het |
Dock1 |
T |
A |
7: 134,358,522 (GRCm39) |
|
probably null |
Het |
Dst |
A |
G |
1: 34,333,564 (GRCm39) |
I4800V |
probably damaging |
Het |
Efcab7 |
CAAGTAAAGTAA |
CAAGTAA |
4: 99,735,161 (GRCm39) |
|
probably null |
Het |
Epb41l2 |
C |
T |
10: 25,348,990 (GRCm39) |
Q382* |
probably null |
Het |
Fam83e |
A |
G |
7: 45,376,070 (GRCm39) |
D261G |
probably damaging |
Het |
Ifnk |
T |
G |
4: 35,152,134 (GRCm39) |
S21A |
possibly damaging |
Het |
Ift122 |
A |
G |
6: 115,903,204 (GRCm39) |
H1157R |
probably benign |
Het |
Ighv1-67 |
T |
C |
12: 115,567,654 (GRCm39) |
K67R |
possibly damaging |
Het |
Inpp4a |
C |
A |
1: 37,411,422 (GRCm39) |
A97D |
probably damaging |
Het |
Insm1 |
T |
A |
2: 146,065,346 (GRCm39) |
Y387* |
probably null |
Het |
Irgm1 |
T |
C |
11: 48,756,928 (GRCm39) |
I294M |
possibly damaging |
Het |
Isoc2b |
C |
T |
7: 4,854,061 (GRCm39) |
V104M |
probably damaging |
Het |
Kif2c |
A |
C |
4: 117,024,280 (GRCm39) |
S311R |
probably benign |
Het |
Morn3 |
G |
A |
5: 123,179,270 (GRCm39) |
A60V |
probably damaging |
Het |
Oit3 |
T |
C |
10: 59,274,534 (GRCm39) |
N89D |
probably damaging |
Het |
Or14c40 |
A |
T |
7: 86,313,293 (GRCm39) |
N141I |
probably damaging |
Het |
Or4c116 |
G |
T |
2: 88,942,640 (GRCm39) |
T72N |
possibly damaging |
Het |
Or4c127 |
T |
C |
2: 89,832,876 (GRCm39) |
V42A |
probably benign |
Het |
Or5d44 |
T |
A |
2: 88,142,095 (GRCm39) |
Q15L |
noncoding transcript |
Het |
Or8b48 |
A |
C |
9: 38,493,069 (GRCm39) |
R165S |
probably damaging |
Het |
Pan2 |
C |
A |
10: 128,150,381 (GRCm39) |
N708K |
possibly damaging |
Het |
Parp1 |
T |
A |
1: 180,425,927 (GRCm39) |
V886E |
probably damaging |
Het |
Pcdha8 |
C |
A |
18: 37,127,753 (GRCm39) |
A745E |
probably benign |
Het |
Pcyox1 |
C |
T |
6: 86,371,390 (GRCm39) |
|
probably null |
Het |
Prl2c2 |
A |
T |
13: 13,176,713 (GRCm39) |
|
probably null |
Het |
Samd1 |
T |
C |
8: 84,726,361 (GRCm39) |
S473P |
possibly damaging |
Het |
Slc26a1 |
A |
T |
5: 108,819,773 (GRCm39) |
D475E |
probably damaging |
Het |
Slco1c1 |
T |
C |
6: 141,493,535 (GRCm39) |
V239A |
possibly damaging |
Het |
Smo |
T |
A |
6: 29,736,044 (GRCm39) |
L12Q |
unknown |
Homo |
Srpk1 |
C |
T |
17: 28,821,727 (GRCm39) |
R229Q |
possibly damaging |
Het |
Syn2 |
T |
A |
6: 115,216,362 (GRCm39) |
F191L |
probably damaging |
Het |
Syngr2 |
T |
C |
11: 117,704,261 (GRCm39) |
V182A |
probably benign |
Het |
Tarbp1 |
G |
A |
8: 127,174,139 (GRCm39) |
A889V |
probably benign |
Het |
Tbc1d2b |
T |
C |
9: 90,108,262 (GRCm39) |
T430A |
probably benign |
Het |
Tmem217 |
T |
A |
17: 29,745,484 (GRCm39) |
Y82F |
probably damaging |
Het |
Ttll9 |
T |
A |
2: 152,841,220 (GRCm39) |
Y272* |
probably null |
Het |
Uts2r |
A |
G |
11: 121,052,033 (GRCm39) |
Y299C |
probably damaging |
Het |
Vsig8 |
T |
A |
1: 172,388,143 (GRCm39) |
M37K |
probably benign |
Het |
Vwf |
G |
T |
6: 125,616,339 (GRCm39) |
D1218Y |
unknown |
Het |
Wdr11 |
T |
G |
7: 129,226,036 (GRCm39) |
M727R |
probably benign |
Het |
Wwc2 |
A |
G |
8: 48,353,826 (GRCm39) |
Y103H |
possibly damaging |
Het |
Yod1 |
T |
A |
1: 130,647,008 (GRCm39) |
L295* |
probably null |
Het |
Zfp113 |
G |
T |
5: 138,143,608 (GRCm39) |
S214* |
probably null |
Het |
Zfp438 |
T |
A |
18: 5,213,780 (GRCm39) |
M393L |
probably benign |
Het |
Zfp946 |
G |
A |
17: 22,674,752 (GRCm39) |
C502Y |
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 |
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 |
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 |
|