Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
T |
C |
6: 142,584,979 (GRCm39) |
D865G |
possibly damaging |
Het |
Acy1 |
A |
T |
9: 106,313,070 (GRCm39) |
|
probably null |
Het |
Adcy4 |
A |
T |
14: 56,010,104 (GRCm39) |
|
probably benign |
Het |
Anpep |
T |
G |
7: 79,489,047 (GRCm39) |
D347A |
probably damaging |
Het |
Arhgap28 |
C |
T |
17: 68,203,159 (GRCm39) |
|
probably null |
Het |
Ccdc32 |
A |
G |
2: 118,857,610 (GRCm39) |
|
probably benign |
Het |
Cdc42bpa |
A |
G |
1: 179,972,400 (GRCm39) |
T1401A |
possibly damaging |
Het |
Celsr2 |
A |
G |
3: 108,319,939 (GRCm39) |
Y958H |
probably damaging |
Het |
Cenpe |
A |
G |
3: 134,923,066 (GRCm39) |
E137G |
probably damaging |
Het |
Chd8 |
T |
C |
14: 52,450,890 (GRCm39) |
D1399G |
probably damaging |
Het |
Cntn3 |
T |
C |
6: 102,145,908 (GRCm39) |
T978A |
possibly damaging |
Het |
Col10a1 |
A |
G |
10: 34,271,692 (GRCm39) |
T555A |
possibly damaging |
Het |
Crybg3 |
A |
C |
16: 59,385,574 (GRCm39) |
|
probably null |
Het |
Cts7 |
A |
G |
13: 61,503,548 (GRCm39) |
F139L |
probably damaging |
Het |
Dera |
T |
C |
6: 137,773,745 (GRCm39) |
|
probably benign |
Het |
Dgka |
A |
G |
10: 128,559,129 (GRCm39) |
|
probably benign |
Het |
Dhrs7 |
T |
A |
12: 72,699,125 (GRCm39) |
I286F |
probably damaging |
Het |
Dtwd2 |
A |
G |
18: 49,861,424 (GRCm39) |
|
probably benign |
Het |
Fermt1 |
A |
G |
2: 132,748,653 (GRCm39) |
S657P |
probably damaging |
Het |
Fhip2b |
T |
C |
14: 70,825,727 (GRCm39) |
D351G |
probably damaging |
Het |
Flnb |
T |
C |
14: 7,890,810 (GRCm38) |
V564A |
probably benign |
Het |
Garnl3 |
A |
G |
2: 32,975,919 (GRCm39) |
F16L |
probably damaging |
Het |
Gck |
T |
C |
11: 5,856,691 (GRCm39) |
R191G |
probably damaging |
Het |
Gucy1b1 |
A |
T |
3: 81,952,941 (GRCm39) |
|
probably benign |
Het |
Ifna2 |
A |
C |
4: 88,601,895 (GRCm39) |
L41R |
probably damaging |
Het |
Krt33a |
T |
G |
11: 99,903,541 (GRCm39) |
E197A |
probably damaging |
Het |
Lce1e |
G |
A |
3: 92,615,063 (GRCm39) |
R95C |
unknown |
Het |
Lrp2 |
A |
T |
2: 69,281,724 (GRCm39) |
N3882K |
probably benign |
Het |
Mcc |
G |
T |
18: 44,578,927 (GRCm39) |
T652K |
possibly damaging |
Het |
Mier1 |
A |
G |
4: 102,996,699 (GRCm39) |
S109G |
probably benign |
Het |
Nfat5 |
A |
G |
8: 108,082,237 (GRCm39) |
N469S |
probably damaging |
Het |
Or1e23 |
C |
A |
11: 73,407,670 (GRCm39) |
M118I |
possibly damaging |
Het |
Or6c214 |
G |
A |
10: 129,591,271 (GRCm39) |
T16I |
probably damaging |
Het |
Piwil1 |
G |
T |
5: 128,820,371 (GRCm39) |
R256M |
probably null |
Het |
Rgma |
T |
C |
7: 73,059,160 (GRCm39) |
V88A |
probably damaging |
Het |
Sdk2 |
T |
C |
11: 113,685,746 (GRCm39) |
|
probably null |
Het |
Sec22b |
A |
G |
3: 97,819,990 (GRCm39) |
E94G |
probably damaging |
Het |
Snrnp70 |
T |
C |
7: 45,036,669 (GRCm39) |
R131G |
possibly damaging |
Het |
Spata31d1a |
A |
G |
13: 59,848,199 (GRCm39) |
S1310P |
possibly damaging |
Het |
Spint1 |
A |
G |
2: 119,076,948 (GRCm39) |
E344G |
probably damaging |
Het |
Srrm1 |
G |
A |
4: 135,052,302 (GRCm39) |
Q141* |
probably null |
Het |
Tecta |
A |
T |
9: 42,295,637 (GRCm39) |
L286Q |
probably damaging |
Het |
Tep1 |
T |
A |
14: 51,104,301 (GRCm39) |
K198* |
probably null |
Het |
Tk2 |
A |
G |
8: 104,957,824 (GRCm39) |
V174A |
probably benign |
Het |
Txndc5 |
T |
C |
13: 38,691,872 (GRCm39) |
K165E |
probably damaging |
Het |
Ubr4 |
G |
A |
4: 139,151,217 (GRCm39) |
R1884Q |
probably damaging |
Het |
Vmn2r61 |
T |
C |
7: 41,949,844 (GRCm39) |
Y755H |
probably damaging |
Het |
Xrn1 |
T |
A |
9: 95,855,592 (GRCm39) |
H296Q |
probably damaging |
Het |
Zar1l |
A |
T |
5: 150,436,407 (GRCm39) |
V223D |
probably damaging |
Het |
|
Other mutations in Lct |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00777:Lct
|
APN |
1 |
128,215,293 (GRCm39) |
missense |
probably benign |
0.09 |
IGL00970:Lct
|
APN |
1 |
128,231,805 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01022:Lct
|
APN |
1 |
128,228,596 (GRCm39) |
missense |
probably benign |
|
IGL01878:Lct
|
APN |
1 |
128,222,003 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01892:Lct
|
APN |
1 |
128,235,342 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02307:Lct
|
APN |
1 |
128,214,327 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02434:Lct
|
APN |
1 |
128,231,527 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02559:Lct
|
APN |
1 |
128,222,003 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02623:Lct
|
APN |
1 |
128,235,988 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02818:Lct
|
APN |
1 |
128,227,905 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02949:Lct
|
APN |
1 |
128,240,869 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02951:Lct
|
APN |
1 |
128,227,948 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03087:Lct
|
APN |
1 |
128,228,112 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL03227:Lct
|
APN |
1 |
128,255,426 (GRCm39) |
missense |
probably benign |
0.09 |
ANU18:Lct
|
UTSW |
1 |
128,235,784 (GRCm39) |
nonsense |
probably null |
|
R0071:Lct
|
UTSW |
1 |
128,219,755 (GRCm39) |
nonsense |
probably null |
|
R0071:Lct
|
UTSW |
1 |
128,219,755 (GRCm39) |
nonsense |
probably null |
|
R0135:Lct
|
UTSW |
1 |
128,212,860 (GRCm39) |
missense |
probably damaging |
0.98 |
R0145:Lct
|
UTSW |
1 |
128,255,632 (GRCm39) |
missense |
probably benign |
0.00 |
R0179:Lct
|
UTSW |
1 |
128,255,422 (GRCm39) |
missense |
probably benign |
|
R0331:Lct
|
UTSW |
1 |
128,226,479 (GRCm39) |
splice site |
probably benign |
|
R0366:Lct
|
UTSW |
1 |
128,214,199 (GRCm39) |
missense |
probably benign |
0.03 |
R0399:Lct
|
UTSW |
1 |
128,228,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R0492:Lct
|
UTSW |
1 |
128,228,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R0548:Lct
|
UTSW |
1 |
128,212,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R0755:Lct
|
UTSW |
1 |
128,221,872 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0839:Lct
|
UTSW |
1 |
128,214,346 (GRCm39) |
missense |
probably benign |
0.00 |
R1128:Lct
|
UTSW |
1 |
128,229,046 (GRCm39) |
missense |
probably damaging |
0.99 |
R1135:Lct
|
UTSW |
1 |
128,221,861 (GRCm39) |
critical splice donor site |
probably null |
|
R1321:Lct
|
UTSW |
1 |
128,227,759 (GRCm39) |
missense |
probably benign |
|
R1448:Lct
|
UTSW |
1 |
128,235,559 (GRCm39) |
missense |
probably damaging |
0.99 |
R1450:Lct
|
UTSW |
1 |
128,235,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R1572:Lct
|
UTSW |
1 |
128,221,932 (GRCm39) |
missense |
probably benign |
0.25 |
R1582:Lct
|
UTSW |
1 |
128,228,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R1668:Lct
|
UTSW |
1 |
128,215,459 (GRCm39) |
splice site |
probably null |
|
R1757:Lct
|
UTSW |
1 |
128,228,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R1775:Lct
|
UTSW |
1 |
128,228,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R1792:Lct
|
UTSW |
1 |
128,255,679 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1815:Lct
|
UTSW |
1 |
128,227,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R1932:Lct
|
UTSW |
1 |
128,221,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R2325:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R2381:Lct
|
UTSW |
1 |
128,231,858 (GRCm39) |
nonsense |
probably null |
|
R3001:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R3002:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R3003:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R3011:Lct
|
UTSW |
1 |
128,229,109 (GRCm39) |
missense |
possibly damaging |
0.74 |
R3082:Lct
|
UTSW |
1 |
128,215,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R3683:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R3684:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R3726:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R3886:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R3887:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R3888:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R4019:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R4027:Lct
|
UTSW |
1 |
128,212,918 (GRCm39) |
missense |
probably benign |
0.00 |
R4226:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R4409:Lct
|
UTSW |
1 |
128,231,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R4514:Lct
|
UTSW |
1 |
128,228,251 (GRCm39) |
missense |
probably benign |
|
R4570:Lct
|
UTSW |
1 |
128,227,641 (GRCm39) |
missense |
probably benign |
0.01 |
R4776:Lct
|
UTSW |
1 |
128,228,124 (GRCm39) |
missense |
probably damaging |
0.99 |
R5001:Lct
|
UTSW |
1 |
128,235,978 (GRCm39) |
missense |
probably damaging |
0.96 |
R5021:Lct
|
UTSW |
1 |
128,228,302 (GRCm39) |
missense |
probably benign |
0.38 |
R5318:Lct
|
UTSW |
1 |
128,232,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R5330:Lct
|
UTSW |
1 |
128,226,266 (GRCm39) |
missense |
probably benign |
0.06 |
R5385:Lct
|
UTSW |
1 |
128,239,354 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5499:Lct
|
UTSW |
1 |
128,214,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R5508:Lct
|
UTSW |
1 |
128,221,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R5642:Lct
|
UTSW |
1 |
128,222,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R5724:Lct
|
UTSW |
1 |
128,228,073 (GRCm39) |
missense |
probably benign |
|
R6026:Lct
|
UTSW |
1 |
128,227,755 (GRCm39) |
missense |
probably benign |
|
R6044:Lct
|
UTSW |
1 |
128,235,717 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6175:Lct
|
UTSW |
1 |
128,255,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R6277:Lct
|
UTSW |
1 |
128,231,974 (GRCm39) |
missense |
probably benign |
0.01 |
R6412:Lct
|
UTSW |
1 |
128,255,455 (GRCm39) |
missense |
probably benign |
0.00 |
R6480:Lct
|
UTSW |
1 |
128,222,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R6526:Lct
|
UTSW |
1 |
128,228,215 (GRCm39) |
missense |
probably benign |
0.05 |
R6620:Lct
|
UTSW |
1 |
128,222,809 (GRCm39) |
critical splice donor site |
probably null |
|
R7214:Lct
|
UTSW |
1 |
128,228,197 (GRCm39) |
missense |
probably benign |
0.00 |
R7308:Lct
|
UTSW |
1 |
128,246,824 (GRCm39) |
missense |
probably benign |
0.00 |
R7577:Lct
|
UTSW |
1 |
128,228,469 (GRCm39) |
missense |
probably damaging |
0.99 |
R7626:Lct
|
UTSW |
1 |
128,212,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R7737:Lct
|
UTSW |
1 |
128,226,430 (GRCm39) |
missense |
probably benign |
0.12 |
R7901:Lct
|
UTSW |
1 |
128,216,722 (GRCm39) |
missense |
probably benign |
0.44 |
R8033:Lct
|
UTSW |
1 |
128,212,996 (GRCm39) |
missense |
probably benign |
0.03 |
R8373:Lct
|
UTSW |
1 |
128,231,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R8504:Lct
|
UTSW |
1 |
128,215,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R8751:Lct
|
UTSW |
1 |
128,221,534 (GRCm39) |
missense |
probably benign |
0.18 |
R8781:Lct
|
UTSW |
1 |
128,215,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R8797:Lct
|
UTSW |
1 |
128,231,684 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8926:Lct
|
UTSW |
1 |
128,228,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R8949:Lct
|
UTSW |
1 |
128,221,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R8992:Lct
|
UTSW |
1 |
128,228,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R9138:Lct
|
UTSW |
1 |
128,227,894 (GRCm39) |
missense |
probably benign |
0.03 |
R9260:Lct
|
UTSW |
1 |
128,227,704 (GRCm39) |
nonsense |
probably null |
|
R9416:Lct
|
UTSW |
1 |
128,228,329 (GRCm39) |
missense |
possibly damaging |
0.74 |
R9531:Lct
|
UTSW |
1 |
128,235,598 (GRCm39) |
missense |
probably benign |
0.00 |
X0052:Lct
|
UTSW |
1 |
128,235,367 (GRCm39) |
missense |
probably damaging |
1.00 |
YA93:Lct
|
UTSW |
1 |
128,229,057 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Lct
|
UTSW |
1 |
128,215,348 (GRCm39) |
nonsense |
probably null |
|
|