Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A930011G23Rik |
A |
G |
5: 99,377,236 (GRCm39) |
S404P |
probably damaging |
Het |
A930011G23Rik |
G |
A |
5: 99,377,241 (GRCm39) |
P402L |
probably damaging |
Het |
Abca7 |
T |
A |
10: 79,844,223 (GRCm39) |
S1410T |
probably damaging |
Het |
Abhd12 |
T |
C |
2: 150,676,289 (GRCm39) |
D356G |
probably benign |
Het |
BC004004 |
T |
C |
17: 29,517,671 (GRCm39) |
L295P |
probably damaging |
Het |
Bpifc |
T |
C |
10: 85,824,595 (GRCm39) |
S215G |
probably damaging |
Het |
Bptf |
C |
T |
11: 106,965,521 (GRCm39) |
M1109I |
probably benign |
Het |
Brat1 |
C |
T |
5: 140,698,563 (GRCm39) |
A245V |
possibly damaging |
Het |
Cask |
G |
A |
X: 13,403,860 (GRCm39) |
T16I |
probably damaging |
Het |
Cemip2 |
T |
C |
19: 21,789,342 (GRCm39) |
|
probably null |
Het |
Cibar2 |
T |
C |
8: 120,901,525 (GRCm39) |
E60G |
probably damaging |
Het |
Clic6 |
A |
T |
16: 92,327,817 (GRCm39) |
I541F |
probably damaging |
Het |
Clnk |
C |
T |
5: 38,931,909 (GRCm39) |
|
probably null |
Het |
Cntnap1 |
T |
A |
11: 101,077,677 (GRCm39) |
I1113N |
probably damaging |
Het |
Csgalnact1 |
C |
A |
8: 68,854,144 (GRCm39) |
G219V |
probably damaging |
Het |
Cyp26a1 |
T |
C |
19: 37,686,943 (GRCm39) |
S132P |
probably benign |
Het |
Cyp4f13 |
G |
T |
17: 33,149,582 (GRCm39) |
H85N |
probably benign |
Het |
Dcaf15 |
C |
T |
8: 84,828,445 (GRCm39) |
G215D |
probably damaging |
Het |
Dip2a |
T |
C |
10: 76,134,101 (GRCm39) |
T500A |
probably benign |
Het |
Gbe1 |
T |
A |
16: 70,231,546 (GRCm39) |
|
probably benign |
Het |
Gli2 |
T |
A |
1: 118,763,733 (GRCm39) |
I1473F |
probably damaging |
Het |
Gm5129 |
A |
T |
5: 29,940,861 (GRCm39) |
|
probably benign |
Het |
Hdgf |
C |
T |
3: 87,821,792 (GRCm39) |
R168C |
probably damaging |
Het |
Heph |
A |
G |
X: 95,516,633 (GRCm39) |
T342A |
probably benign |
Het |
Kdelr3 |
T |
C |
15: 79,409,988 (GRCm39) |
Y158H |
probably damaging |
Het |
Lamb3 |
C |
T |
1: 193,010,253 (GRCm39) |
R289C |
probably damaging |
Het |
Leng8 |
C |
T |
7: 4,145,092 (GRCm39) |
A164V |
probably damaging |
Het |
Ltn1 |
T |
C |
16: 87,194,889 (GRCm39) |
T1337A |
probably benign |
Het |
Mast3 |
C |
A |
8: 71,233,202 (GRCm39) |
R316L |
possibly damaging |
Het |
Nampt |
A |
G |
12: 32,880,215 (GRCm39) |
Y36C |
probably damaging |
Het |
Ncapd3 |
T |
A |
9: 26,975,264 (GRCm39) |
|
probably benign |
Het |
Nipbl |
T |
C |
15: 8,388,558 (GRCm39) |
D354G |
probably damaging |
Het |
Nsd1 |
A |
T |
13: 55,461,254 (GRCm39) |
R2494W |
probably damaging |
Het |
Nt5c1a |
A |
G |
4: 123,108,034 (GRCm39) |
N239S |
probably benign |
Het |
Ogfr |
A |
G |
2: 180,231,329 (GRCm39) |
E19G |
possibly damaging |
Het |
Or11h4b |
A |
T |
14: 50,918,657 (GRCm39) |
S145T |
probably benign |
Het |
Or4c58 |
A |
G |
2: 89,675,128 (GRCm39) |
L63P |
probably damaging |
Het |
Pcna |
A |
T |
2: 132,093,155 (GRCm39) |
|
probably benign |
Het |
Pdia3 |
T |
A |
2: 121,264,129 (GRCm39) |
V326E |
probably damaging |
Het |
Phf8 |
T |
A |
X: 150,414,356 (GRCm39) |
L1002Q |
possibly damaging |
Het |
Rhobtb2 |
T |
C |
14: 70,033,365 (GRCm39) |
E535G |
probably damaging |
Het |
Rusc2 |
G |
T |
4: 43,415,545 (GRCm39) |
D284Y |
probably damaging |
Het |
Samd8 |
A |
G |
14: 21,825,491 (GRCm39) |
Y212C |
probably benign |
Het |
Sash3 |
C |
A |
X: 47,247,672 (GRCm39) |
Q169K |
probably benign |
Het |
Scyl1 |
C |
T |
19: 5,816,224 (GRCm39) |
G324S |
probably damaging |
Het |
Sec62 |
G |
A |
3: 30,872,996 (GRCm39) |
G360R |
unknown |
Het |
Sis |
T |
C |
3: 72,826,947 (GRCm39) |
|
probably null |
Het |
Slc6a1 |
T |
A |
6: 114,285,578 (GRCm39) |
I338N |
probably damaging |
Het |
Snrnp200 |
A |
G |
2: 127,058,030 (GRCm39) |
D264G |
probably damaging |
Het |
Tgm3 |
G |
T |
2: 129,871,961 (GRCm39) |
|
probably null |
Het |
Tnrc6b |
T |
G |
15: 80,764,658 (GRCm39) |
L720R |
probably damaging |
Het |
Tspyl4 |
A |
T |
10: 34,174,228 (GRCm39) |
Q240L |
probably damaging |
Het |
Tube1 |
G |
A |
10: 39,016,846 (GRCm39) |
V80I |
probably damaging |
Het |
Uap1l1 |
C |
T |
2: 25,253,945 (GRCm39) |
V304M |
probably damaging |
Het |
Wtap |
T |
C |
17: 13,186,620 (GRCm39) |
N309S |
probably benign |
Het |
Zfp518a |
G |
A |
19: 40,903,061 (GRCm39) |
G997R |
probably damaging |
Het |
Zfyve26 |
T |
C |
12: 79,315,621 (GRCm39) |
D1285G |
probably benign |
Het |
Zscan20 |
G |
A |
4: 128,482,210 (GRCm39) |
T484I |
probably damaging |
Het |
|
Other mutations in Abca16 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00417:Abca16
|
APN |
7 |
120,022,982 (GRCm39) |
missense |
probably benign |
0.08 |
IGL00590:Abca16
|
APN |
7 |
120,023,038 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01320:Abca16
|
APN |
7 |
120,038,422 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01322:Abca16
|
APN |
7 |
120,038,422 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01613:Abca16
|
APN |
7 |
120,140,500 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01774:Abca16
|
APN |
7 |
120,021,024 (GRCm39) |
splice site |
probably benign |
|
IGL01774:Abca16
|
APN |
7 |
120,077,058 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01797:Abca16
|
APN |
7 |
120,113,760 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02406:Abca16
|
APN |
7 |
120,139,825 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02541:Abca16
|
APN |
7 |
120,113,881 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02576:Abca16
|
APN |
7 |
120,032,678 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02578:Abca16
|
APN |
7 |
120,023,179 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03156:Abca16
|
APN |
7 |
120,023,074 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL03381:Abca16
|
APN |
7 |
120,127,041 (GRCm39) |
missense |
probably benign |
0.12 |
PIT4802001:Abca16
|
UTSW |
7 |
120,139,351 (GRCm39) |
missense |
probably benign |
0.31 |
R0024:Abca16
|
UTSW |
7 |
120,032,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R0026:Abca16
|
UTSW |
7 |
120,077,146 (GRCm39) |
splice site |
probably benign |
|
R0026:Abca16
|
UTSW |
7 |
120,077,146 (GRCm39) |
splice site |
probably benign |
|
R0123:Abca16
|
UTSW |
7 |
120,139,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R0134:Abca16
|
UTSW |
7 |
120,139,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R0225:Abca16
|
UTSW |
7 |
120,139,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R0346:Abca16
|
UTSW |
7 |
120,035,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R0355:Abca16
|
UTSW |
7 |
120,023,021 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0358:Abca16
|
UTSW |
7 |
120,143,939 (GRCm39) |
missense |
probably benign |
0.01 |
R0525:Abca16
|
UTSW |
7 |
120,065,033 (GRCm39) |
nonsense |
probably null |
|
R0617:Abca16
|
UTSW |
7 |
120,032,834 (GRCm39) |
splice site |
probably benign |
|
R0625:Abca16
|
UTSW |
7 |
120,035,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R0835:Abca16
|
UTSW |
7 |
120,065,007 (GRCm39) |
missense |
probably benign |
0.42 |
R1445:Abca16
|
UTSW |
7 |
120,119,256 (GRCm39) |
missense |
probably benign |
0.41 |
R1535:Abca16
|
UTSW |
7 |
120,139,928 (GRCm39) |
missense |
probably benign |
0.30 |
R1567:Abca16
|
UTSW |
7 |
120,030,352 (GRCm39) |
missense |
probably benign |
0.08 |
R1694:Abca16
|
UTSW |
7 |
120,119,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R1860:Abca16
|
UTSW |
7 |
120,133,986 (GRCm39) |
missense |
probably benign |
0.02 |
R1876:Abca16
|
UTSW |
7 |
120,032,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R1913:Abca16
|
UTSW |
7 |
120,140,463 (GRCm39) |
missense |
probably benign |
0.04 |
R1940:Abca16
|
UTSW |
7 |
120,032,832 (GRCm39) |
splice site |
probably benign |
|
R2042:Abca16
|
UTSW |
7 |
120,143,941 (GRCm39) |
missense |
probably benign |
|
R2115:Abca16
|
UTSW |
7 |
120,139,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R2122:Abca16
|
UTSW |
7 |
120,119,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R2265:Abca16
|
UTSW |
7 |
120,030,383 (GRCm39) |
missense |
probably benign |
0.03 |
R2267:Abca16
|
UTSW |
7 |
120,030,383 (GRCm39) |
missense |
probably benign |
0.03 |
R2269:Abca16
|
UTSW |
7 |
120,030,383 (GRCm39) |
missense |
probably benign |
0.03 |
R2993:Abca16
|
UTSW |
7 |
120,134,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R3055:Abca16
|
UTSW |
7 |
120,035,074 (GRCm39) |
missense |
probably benign |
0.05 |
R3956:Abca16
|
UTSW |
7 |
120,126,975 (GRCm39) |
missense |
probably damaging |
0.96 |
R4114:Abca16
|
UTSW |
7 |
120,126,290 (GRCm39) |
missense |
probably benign |
0.06 |
R4441:Abca16
|
UTSW |
7 |
120,127,024 (GRCm39) |
missense |
probably benign |
0.04 |
R4601:Abca16
|
UTSW |
7 |
120,035,920 (GRCm39) |
missense |
probably damaging |
0.98 |
R4706:Abca16
|
UTSW |
7 |
120,064,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R4807:Abca16
|
UTSW |
7 |
120,139,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R4824:Abca16
|
UTSW |
7 |
120,074,702 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4937:Abca16
|
UTSW |
7 |
120,126,309 (GRCm39) |
missense |
probably damaging |
0.98 |
R5152:Abca16
|
UTSW |
7 |
120,139,846 (GRCm39) |
missense |
probably benign |
0.02 |
R5257:Abca16
|
UTSW |
7 |
120,035,992 (GRCm39) |
critical splice donor site |
probably null |
|
R5258:Abca16
|
UTSW |
7 |
120,035,992 (GRCm39) |
critical splice donor site |
probably null |
|
R5330:Abca16
|
UTSW |
7 |
120,102,600 (GRCm39) |
missense |
probably benign |
0.15 |
R5388:Abca16
|
UTSW |
7 |
120,139,969 (GRCm39) |
critical splice donor site |
probably null |
|
R5590:Abca16
|
UTSW |
7 |
120,143,995 (GRCm39) |
missense |
probably damaging |
0.98 |
R5810:Abca16
|
UTSW |
7 |
120,035,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R6030:Abca16
|
UTSW |
7 |
120,133,021 (GRCm39) |
missense |
probably benign |
|
R6030:Abca16
|
UTSW |
7 |
120,133,021 (GRCm39) |
missense |
probably benign |
|
R6161:Abca16
|
UTSW |
7 |
120,139,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R6313:Abca16
|
UTSW |
7 |
120,126,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R6485:Abca16
|
UTSW |
7 |
120,026,390 (GRCm39) |
nonsense |
probably null |
|
R6527:Abca16
|
UTSW |
7 |
120,076,995 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6772:Abca16
|
UTSW |
7 |
120,126,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R6885:Abca16
|
UTSW |
7 |
120,119,332 (GRCm39) |
missense |
probably benign |
0.07 |
R6899:Abca16
|
UTSW |
7 |
120,126,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R6941:Abca16
|
UTSW |
7 |
120,140,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R6990:Abca16
|
UTSW |
7 |
120,126,950 (GRCm39) |
missense |
probably benign |
0.00 |
R7059:Abca16
|
UTSW |
7 |
120,020,971 (GRCm39) |
missense |
probably benign |
0.00 |
R7144:Abca16
|
UTSW |
7 |
120,032,796 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7146:Abca16
|
UTSW |
7 |
120,126,974 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7193:Abca16
|
UTSW |
7 |
120,026,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R7308:Abca16
|
UTSW |
7 |
120,022,993 (GRCm39) |
missense |
probably benign |
0.01 |
R7449:Abca16
|
UTSW |
7 |
120,035,131 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7571:Abca16
|
UTSW |
7 |
120,119,211 (GRCm39) |
missense |
probably benign |
0.11 |
R7617:Abca16
|
UTSW |
7 |
120,102,694 (GRCm39) |
nonsense |
probably null |
|
R7646:Abca16
|
UTSW |
7 |
120,113,937 (GRCm39) |
missense |
probably benign |
0.04 |
R7750:Abca16
|
UTSW |
7 |
120,113,928 (GRCm39) |
missense |
probably benign |
0.09 |
R7763:Abca16
|
UTSW |
7 |
120,113,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R7840:Abca16
|
UTSW |
7 |
120,074,689 (GRCm39) |
missense |
probably benign |
0.00 |
R7946:Abca16
|
UTSW |
7 |
120,126,398 (GRCm39) |
missense |
probably benign |
0.01 |
R8018:Abca16
|
UTSW |
7 |
120,132,866 (GRCm39) |
missense |
probably benign |
0.04 |
R8170:Abca16
|
UTSW |
7 |
120,065,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R8413:Abca16
|
UTSW |
7 |
120,023,123 (GRCm39) |
missense |
probably benign |
0.06 |
R8461:Abca16
|
UTSW |
7 |
120,035,918 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8858:Abca16
|
UTSW |
7 |
120,052,327 (GRCm39) |
missense |
probably benign |
|
R8881:Abca16
|
UTSW |
7 |
120,074,794 (GRCm39) |
missense |
probably benign |
0.18 |
R9272:Abca16
|
UTSW |
7 |
120,076,993 (GRCm39) |
missense |
probably benign |
0.13 |
R9303:Abca16
|
UTSW |
7 |
120,126,989 (GRCm39) |
missense |
probably benign |
0.25 |
R9305:Abca16
|
UTSW |
7 |
120,126,989 (GRCm39) |
missense |
probably benign |
0.25 |
R9320:Abca16
|
UTSW |
7 |
120,139,320 (GRCm39) |
missense |
probably damaging |
0.98 |
R9413:Abca16
|
UTSW |
7 |
120,126,422 (GRCm39) |
missense |
probably benign |
0.01 |
R9512:Abca16
|
UTSW |
7 |
120,022,963 (GRCm39) |
missense |
probably benign |
0.01 |
R9559:Abca16
|
UTSW |
7 |
120,021,019 (GRCm39) |
critical splice donor site |
probably null |
|
R9615:Abca16
|
UTSW |
7 |
120,126,404 (GRCm39) |
missense |
probably benign |
0.01 |
R9641:Abca16
|
UTSW |
7 |
120,126,308 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9643:Abca16
|
UTSW |
7 |
120,065,023 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9674:Abca16
|
UTSW |
7 |
120,074,668 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9714:Abca16
|
UTSW |
7 |
120,030,383 (GRCm39) |
missense |
probably benign |
0.01 |
R9799:Abca16
|
UTSW |
7 |
120,132,998 (GRCm39) |
missense |
probably benign |
0.00 |
R9800:Abca16
|
UTSW |
7 |
120,119,283 (GRCm39) |
missense |
possibly damaging |
0.68 |
RF020:Abca16
|
UTSW |
7 |
120,132,880 (GRCm39) |
missense |
possibly damaging |
0.90 |
X0066:Abca16
|
UTSW |
7 |
120,102,609 (GRCm39) |
missense |
probably benign |
0.00 |
|