Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700001J03Rik |
G |
T |
5: 146,121,691 (GRCm39) |
Y69* |
probably null |
Het |
2310011J03Rik |
A |
G |
10: 80,156,015 (GRCm39) |
|
probably null |
Het |
A2ml1 |
A |
C |
6: 128,520,262 (GRCm39) |
D1367E |
probably damaging |
Het |
Adam6a |
C |
G |
12: 113,508,334 (GRCm39) |
L236V |
probably benign |
Het |
Arf3 |
T |
C |
15: 98,638,954 (GRCm39) |
N101S |
probably benign |
Het |
Arhgap42 |
T |
C |
9: 9,180,051 (GRCm39) |
E76G |
probably damaging |
Het |
Atp2a1 |
A |
G |
7: 126,052,573 (GRCm39) |
F382S |
probably damaging |
Het |
Bud13 |
T |
A |
9: 46,199,705 (GRCm39) |
F355L |
probably benign |
Het |
C2 |
G |
A |
17: 35,083,508 (GRCm39) |
P349S |
probably damaging |
Het |
Cbl |
C |
A |
9: 44,075,526 (GRCm39) |
G373V |
probably damaging |
Het |
Ccdc3 |
T |
A |
2: 5,142,896 (GRCm39) |
L51Q |
probably damaging |
Het |
Ccdc34 |
T |
A |
2: 109,874,601 (GRCm39) |
M320K |
probably benign |
Het |
Cntln |
A |
G |
4: 85,015,000 (GRCm39) |
E1097G |
probably damaging |
Het |
Ctsc |
A |
C |
7: 87,948,750 (GRCm39) |
K195Q |
possibly damaging |
Het |
Ctsf |
C |
T |
19: 4,906,562 (GRCm39) |
P163L |
probably benign |
Het |
Dcxr |
A |
T |
11: 120,616,438 (GRCm39) |
|
probably null |
Het |
Dgki |
T |
C |
6: 37,126,509 (GRCm39) |
E157G |
possibly damaging |
Het |
Dnah8 |
T |
C |
17: 30,903,160 (GRCm39) |
L933P |
probably damaging |
Het |
Dtna |
T |
C |
18: 23,702,697 (GRCm39) |
L76P |
probably damaging |
Het |
Fcgbp |
T |
A |
7: 27,784,515 (GRCm39) |
C192S |
probably benign |
Het |
Galnt5 |
T |
A |
2: 57,916,137 (GRCm39) |
D683E |
probably benign |
Het |
Grik4 |
T |
C |
9: 42,540,322 (GRCm39) |
N286S |
probably benign |
Het |
Hrc |
A |
T |
7: 44,986,202 (GRCm39) |
E451V |
probably damaging |
Het |
Hrh3 |
G |
A |
2: 179,741,577 (GRCm39) |
|
probably benign |
Het |
Ints13 |
A |
G |
6: 146,455,695 (GRCm39) |
I152T |
probably damaging |
Het |
Irgm1 |
A |
T |
11: 48,757,259 (GRCm39) |
V184D |
probably damaging |
Het |
Itga5 |
C |
T |
15: 103,258,826 (GRCm39) |
A791T |
probably damaging |
Het |
Kcp |
T |
C |
6: 29,505,654 (GRCm39) |
T73A |
probably benign |
Het |
Kidins220 |
A |
G |
12: 25,053,008 (GRCm39) |
T433A |
probably benign |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Kmt2d |
T |
C |
15: 98,764,567 (GRCm39) |
D12G |
probably damaging |
Het |
Mms19 |
A |
G |
19: 41,954,698 (GRCm39) |
S74P |
probably damaging |
Het |
Myh1 |
G |
T |
11: 67,102,300 (GRCm39) |
E864* |
probably null |
Het |
Nek1 |
A |
G |
8: 61,469,264 (GRCm39) |
D107G |
probably damaging |
Het |
Npc1 |
T |
C |
18: 12,327,149 (GRCm39) |
N1149D |
probably damaging |
Het |
Or14j6 |
T |
A |
17: 38,214,661 (GRCm39) |
S75T |
probably damaging |
Het |
Or3a1b |
C |
A |
11: 74,012,257 (GRCm39) |
S47R |
probably damaging |
Het |
Or4k36 |
T |
C |
2: 111,146,343 (GRCm39) |
V173A |
probably benign |
Het |
Or5p79 |
A |
C |
7: 108,221,817 (GRCm39) |
K266T |
possibly damaging |
Het |
Osbp |
T |
C |
19: 11,948,142 (GRCm39) |
S150P |
probably damaging |
Het |
Paf1 |
T |
C |
7: 28,096,247 (GRCm39) |
Y287H |
probably damaging |
Het |
Pdgfrb |
T |
C |
18: 61,201,174 (GRCm39) |
V420A |
probably benign |
Het |
Pdss1 |
G |
T |
2: 22,796,846 (GRCm39) |
E120* |
probably null |
Het |
Pink1 |
A |
T |
4: 138,044,630 (GRCm39) |
V339E |
probably damaging |
Het |
Pkn3 |
C |
T |
2: 29,969,663 (GRCm39) |
R58C |
probably damaging |
Het |
Pm20d1 |
G |
A |
1: 131,730,165 (GRCm39) |
V235I |
probably benign |
Het |
Ppp2r2a |
A |
G |
14: 67,276,412 (GRCm39) |
I31T |
probably damaging |
Het |
Rbms3 |
T |
C |
9: 116,651,894 (GRCm39) |
E152G |
probably damaging |
Het |
Rfx1 |
A |
C |
8: 84,821,677 (GRCm39) |
Q804H |
probably damaging |
Het |
Rpe |
G |
T |
1: 66,754,356 (GRCm39) |
V143L |
probably benign |
Het |
Sap30l |
G |
T |
11: 57,700,771 (GRCm39) |
V142L |
probably benign |
Het |
Sh3tc1 |
T |
C |
5: 35,863,268 (GRCm39) |
Q973R |
probably benign |
Het |
Slc10a2 |
T |
C |
8: 5,154,856 (GRCm39) |
T110A |
probably damaging |
Het |
Snrnp200 |
A |
T |
2: 127,060,947 (GRCm39) |
|
probably null |
Het |
Snrnp200 |
G |
A |
2: 127,060,948 (GRCm39) |
|
probably null |
Het |
Spaca3 |
T |
A |
11: 80,758,511 (GRCm39) |
V158E |
probably damaging |
Het |
Sprtn |
C |
A |
8: 125,629,770 (GRCm39) |
N354K |
probably benign |
Het |
Stab1 |
T |
A |
14: 30,863,101 (GRCm39) |
Y2166F |
possibly damaging |
Het |
Tmem106c |
G |
A |
15: 97,866,548 (GRCm39) |
|
probably null |
Het |
Tnc |
A |
G |
4: 63,918,168 (GRCm39) |
S1248P |
probably damaging |
Het |
Tshr |
T |
C |
12: 91,504,090 (GRCm39) |
F343L |
probably benign |
Het |
Ttn |
C |
A |
2: 76,555,698 (GRCm39) |
A30436S |
probably damaging |
Het |
Ubxn2a |
A |
T |
12: 4,935,839 (GRCm39) |
M68K |
probably benign |
Het |
Ucp2 |
T |
C |
7: 100,148,021 (GRCm39) |
V238A |
probably damaging |
Het |
Urgcp |
C |
A |
11: 5,667,242 (GRCm39) |
L365F |
probably damaging |
Het |
Vezt |
A |
T |
10: 93,826,026 (GRCm39) |
D328E |
probably damaging |
Het |
Vmn1r168 |
G |
T |
7: 23,240,184 (GRCm39) |
V14L |
probably benign |
Het |
Vps13b |
T |
C |
15: 35,792,205 (GRCm39) |
F2158L |
probably benign |
Het |
|
Other mutations in Greb1l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00485:Greb1l
|
APN |
18 |
10,555,962 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01554:Greb1l
|
APN |
18 |
10,522,144 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01563:Greb1l
|
APN |
18 |
10,469,399 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01944:Greb1l
|
APN |
18 |
10,557,280 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02110:Greb1l
|
APN |
18 |
10,515,271 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02249:Greb1l
|
APN |
18 |
10,532,961 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02318:Greb1l
|
APN |
18 |
10,469,388 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02340:Greb1l
|
APN |
18 |
10,515,200 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02516:Greb1l
|
APN |
18 |
10,537,064 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02566:Greb1l
|
APN |
18 |
10,503,299 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02583:Greb1l
|
APN |
18 |
10,542,362 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02838:Greb1l
|
APN |
18 |
10,560,430 (GRCm39) |
missense |
probably damaging |
1.00 |
A4554:Greb1l
|
UTSW |
18 |
10,532,862 (GRCm39) |
missense |
possibly damaging |
0.58 |
PIT4453001:Greb1l
|
UTSW |
18 |
10,533,032 (GRCm39) |
missense |
probably benign |
0.08 |
PIT4453001:Greb1l
|
UTSW |
18 |
10,533,031 (GRCm39) |
missense |
probably damaging |
0.98 |
R0099:Greb1l
|
UTSW |
18 |
10,509,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R0226:Greb1l
|
UTSW |
18 |
10,522,076 (GRCm39) |
intron |
probably benign |
|
R0234:Greb1l
|
UTSW |
18 |
10,560,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R0234:Greb1l
|
UTSW |
18 |
10,560,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R0239:Greb1l
|
UTSW |
18 |
10,458,567 (GRCm39) |
splice site |
probably benign |
|
R0316:Greb1l
|
UTSW |
18 |
10,547,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R0369:Greb1l
|
UTSW |
18 |
10,469,375 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0394:Greb1l
|
UTSW |
18 |
10,523,374 (GRCm39) |
missense |
probably damaging |
0.99 |
R0478:Greb1l
|
UTSW |
18 |
10,509,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R0555:Greb1l
|
UTSW |
18 |
10,458,781 (GRCm39) |
splice site |
probably benign |
|
R0671:Greb1l
|
UTSW |
18 |
10,474,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R1282:Greb1l
|
UTSW |
18 |
10,547,289 (GRCm39) |
missense |
probably benign |
0.13 |
R1574:Greb1l
|
UTSW |
18 |
10,554,997 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1574:Greb1l
|
UTSW |
18 |
10,554,997 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1607:Greb1l
|
UTSW |
18 |
10,529,703 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1666:Greb1l
|
UTSW |
18 |
10,529,708 (GRCm39) |
critical splice donor site |
probably null |
|
R1666:Greb1l
|
UTSW |
18 |
10,501,080 (GRCm39) |
critical splice donor site |
probably null |
|
R1720:Greb1l
|
UTSW |
18 |
10,553,848 (GRCm39) |
missense |
probably benign |
0.19 |
R1829:Greb1l
|
UTSW |
18 |
10,509,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R1897:Greb1l
|
UTSW |
18 |
10,498,992 (GRCm39) |
missense |
probably benign |
0.00 |
R1967:Greb1l
|
UTSW |
18 |
10,501,049 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2025:Greb1l
|
UTSW |
18 |
10,515,221 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2086:Greb1l
|
UTSW |
18 |
10,523,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R2125:Greb1l
|
UTSW |
18 |
10,511,422 (GRCm39) |
missense |
probably damaging |
0.98 |
R2139:Greb1l
|
UTSW |
18 |
10,555,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R2255:Greb1l
|
UTSW |
18 |
10,554,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R2256:Greb1l
|
UTSW |
18 |
10,503,307 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2257:Greb1l
|
UTSW |
18 |
10,503,307 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2880:Greb1l
|
UTSW |
18 |
10,547,288 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3623:Greb1l
|
UTSW |
18 |
10,542,380 (GRCm39) |
missense |
probably damaging |
0.99 |
R3778:Greb1l
|
UTSW |
18 |
10,469,444 (GRCm39) |
missense |
possibly damaging |
0.60 |
R3975:Greb1l
|
UTSW |
18 |
10,522,247 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4038:Greb1l
|
UTSW |
18 |
10,515,209 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4062:Greb1l
|
UTSW |
18 |
10,522,150 (GRCm39) |
missense |
probably damaging |
0.99 |
R4134:Greb1l
|
UTSW |
18 |
10,529,708 (GRCm39) |
critical splice donor site |
probably null |
|
R4342:Greb1l
|
UTSW |
18 |
10,544,561 (GRCm39) |
missense |
probably benign |
0.12 |
R4409:Greb1l
|
UTSW |
18 |
10,503,182 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4600:Greb1l
|
UTSW |
18 |
10,553,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R4618:Greb1l
|
UTSW |
18 |
10,498,965 (GRCm39) |
missense |
probably benign |
0.00 |
R4683:Greb1l
|
UTSW |
18 |
10,529,563 (GRCm39) |
splice site |
probably null |
|
R4686:Greb1l
|
UTSW |
18 |
10,522,112 (GRCm39) |
missense |
probably damaging |
0.98 |
R4707:Greb1l
|
UTSW |
18 |
10,532,922 (GRCm39) |
missense |
probably benign |
0.02 |
R4780:Greb1l
|
UTSW |
18 |
10,541,792 (GRCm39) |
missense |
probably benign |
0.00 |
R4819:Greb1l
|
UTSW |
18 |
10,458,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R4925:Greb1l
|
UTSW |
18 |
10,547,447 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4960:Greb1l
|
UTSW |
18 |
10,547,306 (GRCm39) |
missense |
probably damaging |
0.99 |
R5150:Greb1l
|
UTSW |
18 |
10,555,950 (GRCm39) |
frame shift |
probably null |
|
R5154:Greb1l
|
UTSW |
18 |
10,458,312 (GRCm39) |
missense |
probably benign |
0.02 |
R5269:Greb1l
|
UTSW |
18 |
10,511,409 (GRCm39) |
missense |
probably benign |
|
R5290:Greb1l
|
UTSW |
18 |
10,542,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R5310:Greb1l
|
UTSW |
18 |
10,542,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R5328:Greb1l
|
UTSW |
18 |
10,553,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R5337:Greb1l
|
UTSW |
18 |
10,509,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R5393:Greb1l
|
UTSW |
18 |
10,458,312 (GRCm39) |
missense |
probably benign |
0.02 |
R5402:Greb1l
|
UTSW |
18 |
10,537,169 (GRCm39) |
missense |
probably benign |
0.26 |
R5718:Greb1l
|
UTSW |
18 |
10,542,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R5719:Greb1l
|
UTSW |
18 |
10,542,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R5720:Greb1l
|
UTSW |
18 |
10,542,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R5721:Greb1l
|
UTSW |
18 |
10,542,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R5902:Greb1l
|
UTSW |
18 |
10,538,302 (GRCm39) |
missense |
probably benign |
0.00 |
R5993:Greb1l
|
UTSW |
18 |
10,544,455 (GRCm39) |
missense |
probably benign |
0.10 |
R6035:Greb1l
|
UTSW |
18 |
10,501,025 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6035:Greb1l
|
UTSW |
18 |
10,501,025 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6045:Greb1l
|
UTSW |
18 |
10,547,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R6063:Greb1l
|
UTSW |
18 |
10,557,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R6297:Greb1l
|
UTSW |
18 |
10,469,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R6405:Greb1l
|
UTSW |
18 |
10,501,076 (GRCm39) |
missense |
probably benign |
0.30 |
R6552:Greb1l
|
UTSW |
18 |
10,541,814 (GRCm39) |
missense |
probably benign |
0.00 |
R6572:Greb1l
|
UTSW |
18 |
10,522,131 (GRCm39) |
missense |
probably benign |
0.07 |
R6575:Greb1l
|
UTSW |
18 |
10,547,347 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6922:Greb1l
|
UTSW |
18 |
10,547,482 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6957:Greb1l
|
UTSW |
18 |
10,558,786 (GRCm39) |
missense |
probably benign |
0.23 |
R6962:Greb1l
|
UTSW |
18 |
10,547,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R7012:Greb1l
|
UTSW |
18 |
10,529,707 (GRCm39) |
critical splice donor site |
probably null |
|
R7179:Greb1l
|
UTSW |
18 |
10,544,576 (GRCm39) |
missense |
probably benign |
0.00 |
R7251:Greb1l
|
UTSW |
18 |
10,515,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R7275:Greb1l
|
UTSW |
18 |
10,544,561 (GRCm39) |
missense |
probably benign |
0.12 |
R7301:Greb1l
|
UTSW |
18 |
10,544,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R7307:Greb1l
|
UTSW |
18 |
10,538,142 (GRCm39) |
missense |
probably damaging |
0.99 |
R7455:Greb1l
|
UTSW |
18 |
10,554,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R7832:Greb1l
|
UTSW |
18 |
10,542,056 (GRCm39) |
missense |
probably benign |
0.38 |
R7934:Greb1l
|
UTSW |
18 |
10,474,371 (GRCm39) |
nonsense |
probably null |
|
R8137:Greb1l
|
UTSW |
18 |
10,474,357 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8138:Greb1l
|
UTSW |
18 |
10,533,060 (GRCm39) |
missense |
probably benign |
0.13 |
R8208:Greb1l
|
UTSW |
18 |
10,510,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R8227:Greb1l
|
UTSW |
18 |
10,515,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R8312:Greb1l
|
UTSW |
18 |
10,511,587 (GRCm39) |
intron |
probably benign |
|
R8331:Greb1l
|
UTSW |
18 |
10,458,706 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8364:Greb1l
|
UTSW |
18 |
10,529,687 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8389:Greb1l
|
UTSW |
18 |
10,529,613 (GRCm39) |
missense |
probably benign |
0.00 |
R8695:Greb1l
|
UTSW |
18 |
10,544,450 (GRCm39) |
missense |
probably benign |
0.01 |
R8795:Greb1l
|
UTSW |
18 |
10,553,739 (GRCm39) |
missense |
probably damaging |
0.98 |
R8836:Greb1l
|
UTSW |
18 |
10,509,257 (GRCm39) |
missense |
probably benign |
0.30 |
R8862:Greb1l
|
UTSW |
18 |
10,555,042 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8872:Greb1l
|
UTSW |
18 |
10,529,684 (GRCm39) |
missense |
probably benign |
0.18 |
R8874:Greb1l
|
UTSW |
18 |
10,544,896 (GRCm39) |
missense |
probably benign |
0.01 |
R8886:Greb1l
|
UTSW |
18 |
10,553,843 (GRCm39) |
missense |
probably benign |
0.21 |
R8921:Greb1l
|
UTSW |
18 |
10,541,825 (GRCm39) |
missense |
probably benign |
0.01 |
R8997:Greb1l
|
UTSW |
18 |
10,510,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R9015:Greb1l
|
UTSW |
18 |
10,541,675 (GRCm39) |
missense |
probably benign |
0.00 |
R9018:Greb1l
|
UTSW |
18 |
10,542,004 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9074:Greb1l
|
UTSW |
18 |
10,558,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R9074:Greb1l
|
UTSW |
18 |
10,532,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R9117:Greb1l
|
UTSW |
18 |
10,542,422 (GRCm39) |
missense |
probably benign |
0.31 |
R9189:Greb1l
|
UTSW |
18 |
10,499,983 (GRCm39) |
missense |
probably benign |
|
R9332:Greb1l
|
UTSW |
18 |
10,532,796 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9367:Greb1l
|
UTSW |
18 |
10,522,130 (GRCm39) |
missense |
probably benign |
0.00 |
R9497:Greb1l
|
UTSW |
18 |
10,458,600 (GRCm39) |
missense |
probably benign |
0.00 |
R9796:Greb1l
|
UTSW |
18 |
10,538,233 (GRCm39) |
missense |
possibly damaging |
0.69 |
Z1176:Greb1l
|
UTSW |
18 |
10,515,305 (GRCm39) |
missense |
probably damaging |
1.00 |
|