Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ap5z1 |
A |
G |
5: 142,453,442 (GRCm39) |
K137E |
possibly damaging |
Het |
Atm |
A |
C |
9: 53,429,923 (GRCm39) |
V371G |
probably benign |
Het |
Cacna2d3 |
A |
G |
14: 29,068,987 (GRCm39) |
Y247H |
probably damaging |
Het |
Ccdc180 |
T |
C |
4: 45,917,556 (GRCm39) |
V927A |
probably damaging |
Het |
Cdc45 |
C |
T |
16: 18,614,647 (GRCm39) |
R205H |
probably damaging |
Het |
Edar |
G |
A |
10: 58,443,257 (GRCm39) |
P290S |
possibly damaging |
Het |
Ext2 |
T |
C |
2: 93,526,606 (GRCm39) |
I677V |
probably benign |
Het |
Fam53a |
A |
G |
5: 33,765,080 (GRCm39) |
S209P |
probably damaging |
Het |
Fshr |
A |
T |
17: 89,318,441 (GRCm39) |
|
probably null |
Het |
Gfm2 |
G |
A |
13: 97,299,659 (GRCm39) |
A406T |
probably damaging |
Het |
Gm14295 |
A |
T |
2: 176,502,465 (GRCm39) |
I652L |
probably benign |
Het |
Gm14403 |
AAACCCTA |
AA |
2: 177,201,448 (GRCm39) |
|
probably benign |
Het |
Gm5431 |
T |
A |
11: 48,779,716 (GRCm39) |
E402V |
probably damaging |
Het |
Gm6899 |
GGAGGCCGCCCAGTGGCAGAGGCCGCCCAGTGGCAGAGGC |
GGAGGCCGCCCAGTGGCAGAGGC |
11: 26,543,725 (GRCm39) |
|
probably null |
Het |
Itih2 |
T |
C |
2: 10,115,346 (GRCm39) |
D342G |
probably benign |
Het |
Lgi2 |
A |
T |
5: 52,711,827 (GRCm39) |
D164E |
probably damaging |
Het |
Lrriq1 |
A |
G |
10: 103,050,448 (GRCm39) |
I768T |
probably damaging |
Het |
Map1a |
C |
A |
2: 121,132,868 (GRCm39) |
A990E |
probably damaging |
Het |
Mdh1b |
A |
G |
1: 63,759,163 (GRCm39) |
V143A |
probably benign |
Het |
Mrgprb3 |
C |
T |
7: 48,293,059 (GRCm39) |
C164Y |
probably damaging |
Het |
Mtpap |
T |
A |
18: 4,386,328 (GRCm39) |
V316E |
probably damaging |
Het |
Mybpc3 |
T |
A |
2: 90,959,023 (GRCm39) |
C655* |
probably null |
Het |
Myh15 |
A |
G |
16: 48,986,204 (GRCm39) |
E1558G |
possibly damaging |
Het |
Nckap1 |
T |
A |
2: 80,370,466 (GRCm39) |
D408V |
probably damaging |
Het |
Nos3 |
A |
T |
5: 24,582,343 (GRCm39) |
H605L |
probably benign |
Het |
Nrxn2 |
C |
A |
19: 6,581,428 (GRCm39) |
D411E |
probably benign |
Het |
Or1af1 |
T |
C |
2: 37,109,633 (GRCm39) |
V44A |
probably benign |
Het |
Or8j3b |
T |
A |
2: 86,205,094 (GRCm39) |
I221L |
possibly damaging |
Het |
Pde4d |
C |
A |
13: 109,769,398 (GRCm39) |
P29T |
probably benign |
Het |
Pde4d |
C |
T |
13: 109,769,399 (GRCm39) |
P29L |
probably benign |
Het |
Pkhd1 |
A |
G |
1: 20,636,094 (GRCm39) |
V412A |
possibly damaging |
Het |
Rev1 |
T |
A |
1: 38,118,474 (GRCm39) |
I480L |
probably benign |
Het |
Rimbp3 |
A |
G |
16: 17,028,708 (GRCm39) |
T711A |
probably benign |
Het |
RP23-191E1.1 |
T |
A |
3: 106,204,784 (GRCm39) |
|
noncoding transcript |
Het |
Serpina11 |
A |
T |
12: 103,952,221 (GRCm39) |
I183N |
probably damaging |
Het |
Siglec1 |
T |
C |
2: 130,921,236 (GRCm39) |
H645R |
probably damaging |
Het |
Skint7 |
G |
A |
4: 111,837,501 (GRCm39) |
R93H |
probably damaging |
Het |
Slfn8 |
T |
C |
11: 82,894,910 (GRCm39) |
E632G |
probably damaging |
Het |
Tmem8b |
G |
A |
4: 43,673,992 (GRCm39) |
V208I |
probably benign |
Het |
Trps1 |
G |
A |
15: 50,528,156 (GRCm39) |
T658I |
probably damaging |
Het |
Ubash3a |
A |
G |
17: 31,438,691 (GRCm39) |
T287A |
probably damaging |
Het |
Ugt2b35 |
G |
A |
5: 87,159,139 (GRCm39) |
W444* |
probably null |
Het |
Vmn1r219 |
T |
A |
13: 23,347,063 (GRCm39) |
V84D |
probably damaging |
Het |
Vmn2r10 |
T |
C |
5: 109,154,121 (GRCm39) |
Y61C |
probably damaging |
Het |
Vmn2r104 |
G |
A |
17: 20,250,163 (GRCm39) |
P703S |
probably damaging |
Het |
Wdsub1 |
T |
A |
2: 59,708,873 (GRCm39) |
|
probably benign |
Het |
Zfp667 |
A |
G |
7: 6,308,715 (GRCm39) |
Q461R |
probably benign |
Het |
Zfp941 |
C |
A |
7: 140,391,872 (GRCm39) |
G496* |
probably null |
Het |
|
Other mutations in Mylk |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01384:Mylk
|
APN |
16 |
34,759,322 (GRCm39) |
missense |
probably benign |
0.36 |
IGL01386:Mylk
|
APN |
16 |
34,791,610 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01684:Mylk
|
APN |
16 |
34,792,310 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL01884:Mylk
|
APN |
16 |
34,809,247 (GRCm39) |
splice site |
probably benign |
|
IGL02079:Mylk
|
APN |
16 |
34,681,001 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02104:Mylk
|
APN |
16 |
34,635,805 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02624:Mylk
|
APN |
16 |
34,750,266 (GRCm39) |
missense |
probably benign |
0.29 |
IGL02756:Mylk
|
APN |
16 |
34,784,016 (GRCm39) |
missense |
probably benign |
0.42 |
IGL02794:Mylk
|
APN |
16 |
34,806,911 (GRCm39) |
missense |
probably benign |
0.21 |
IGL02833:Mylk
|
APN |
16 |
34,735,270 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02946:Mylk
|
APN |
16 |
34,742,158 (GRCm39) |
missense |
probably benign |
0.10 |
IGL03012:Mylk
|
APN |
16 |
34,773,151 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03093:Mylk
|
APN |
16 |
34,732,562 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL03272:Mylk
|
APN |
16 |
34,799,559 (GRCm39) |
missense |
probably benign |
0.09 |
billy
|
UTSW |
16 |
34,695,990 (GRCm39) |
missense |
probably damaging |
0.97 |
brutus
|
UTSW |
16 |
34,774,065 (GRCm39) |
missense |
probably benign |
0.12 |
Club
|
UTSW |
16 |
34,732,645 (GRCm39) |
nonsense |
probably null |
|
popeye
|
UTSW |
16 |
34,783,947 (GRCm39) |
missense |
probably benign |
0.29 |
F5770:Mylk
|
UTSW |
16 |
34,815,574 (GRCm39) |
critical splice donor site |
probably null |
|
P4717OSA:Mylk
|
UTSW |
16 |
34,797,483 (GRCm39) |
splice site |
probably benign |
|
PIT4382001:Mylk
|
UTSW |
16 |
34,696,012 (GRCm39) |
missense |
probably damaging |
0.99 |
R0131:Mylk
|
UTSW |
16 |
34,695,874 (GRCm39) |
missense |
probably benign |
0.03 |
R0309:Mylk
|
UTSW |
16 |
34,732,667 (GRCm39) |
splice site |
probably benign |
|
R0358:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0381:Mylk
|
UTSW |
16 |
34,605,344 (GRCm39) |
splice site |
probably null |
|
R0390:Mylk
|
UTSW |
16 |
34,695,990 (GRCm39) |
missense |
probably damaging |
0.97 |
R0413:Mylk
|
UTSW |
16 |
34,742,314 (GRCm39) |
missense |
probably benign |
0.01 |
R0536:Mylk
|
UTSW |
16 |
34,820,757 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0544:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0545:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0546:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0547:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0548:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0627:Mylk
|
UTSW |
16 |
34,820,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R0726:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0755:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0782:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0783:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0784:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1136:Mylk
|
UTSW |
16 |
34,820,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R1170:Mylk
|
UTSW |
16 |
34,694,409 (GRCm39) |
missense |
probably benign |
0.20 |
R1222:Mylk
|
UTSW |
16 |
34,681,022 (GRCm39) |
missense |
probably benign |
0.12 |
R1445:Mylk
|
UTSW |
16 |
34,635,835 (GRCm39) |
missense |
possibly damaging |
0.57 |
R1583:Mylk
|
UTSW |
16 |
34,695,956 (GRCm39) |
missense |
probably benign |
0.29 |
R1618:Mylk
|
UTSW |
16 |
34,699,845 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1643:Mylk
|
UTSW |
16 |
34,696,005 (GRCm39) |
missense |
probably benign |
0.03 |
R1702:Mylk
|
UTSW |
16 |
34,742,314 (GRCm39) |
missense |
probably benign |
0.00 |
R1776:Mylk
|
UTSW |
16 |
34,773,152 (GRCm39) |
missense |
probably benign |
0.16 |
R1865:Mylk
|
UTSW |
16 |
34,732,600 (GRCm39) |
missense |
probably benign |
0.03 |
R1975:Mylk
|
UTSW |
16 |
34,700,673 (GRCm39) |
splice site |
probably null |
|
R2016:Mylk
|
UTSW |
16 |
34,817,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R2045:Mylk
|
UTSW |
16 |
34,774,023 (GRCm39) |
missense |
probably benign |
0.29 |
R2134:Mylk
|
UTSW |
16 |
34,806,846 (GRCm39) |
missense |
probably benign |
0.13 |
R3547:Mylk
|
UTSW |
16 |
34,700,538 (GRCm39) |
missense |
possibly damaging |
0.61 |
R3844:Mylk
|
UTSW |
16 |
34,742,247 (GRCm39) |
missense |
probably benign |
0.01 |
R4003:Mylk
|
UTSW |
16 |
34,783,947 (GRCm39) |
missense |
probably benign |
0.29 |
R4396:Mylk
|
UTSW |
16 |
34,732,645 (GRCm39) |
nonsense |
probably null |
|
R4470:Mylk
|
UTSW |
16 |
34,732,522 (GRCm39) |
missense |
probably benign |
0.09 |
R4507:Mylk
|
UTSW |
16 |
34,774,065 (GRCm39) |
missense |
probably benign |
0.12 |
R4700:Mylk
|
UTSW |
16 |
34,742,805 (GRCm39) |
missense |
probably benign |
0.16 |
R4751:Mylk
|
UTSW |
16 |
34,699,539 (GRCm39) |
missense |
probably benign |
0.29 |
R4815:Mylk
|
UTSW |
16 |
34,715,295 (GRCm39) |
missense |
probably damaging |
0.97 |
R4832:Mylk
|
UTSW |
16 |
34,742,737 (GRCm39) |
missense |
probably benign |
0.36 |
R4872:Mylk
|
UTSW |
16 |
34,735,360 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4953:Mylk
|
UTSW |
16 |
34,809,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R4969:Mylk
|
UTSW |
16 |
34,791,810 (GRCm39) |
missense |
probably damaging |
0.96 |
R5009:Mylk
|
UTSW |
16 |
34,719,877 (GRCm39) |
missense |
probably benign |
0.39 |
R5130:Mylk
|
UTSW |
16 |
34,809,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R5173:Mylk
|
UTSW |
16 |
34,797,383 (GRCm39) |
missense |
probably benign |
0.40 |
R5195:Mylk
|
UTSW |
16 |
34,799,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R5209:Mylk
|
UTSW |
16 |
34,742,995 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5418:Mylk
|
UTSW |
16 |
34,732,600 (GRCm39) |
missense |
probably benign |
0.02 |
R5481:Mylk
|
UTSW |
16 |
34,741,974 (GRCm39) |
missense |
probably benign |
0.09 |
R5590:Mylk
|
UTSW |
16 |
34,699,722 (GRCm39) |
missense |
probably benign |
0.29 |
R5603:Mylk
|
UTSW |
16 |
34,776,862 (GRCm39) |
missense |
probably benign |
0.06 |
R5823:Mylk
|
UTSW |
16 |
34,715,317 (GRCm39) |
critical splice donor site |
probably null |
|
R6290:Mylk
|
UTSW |
16 |
34,715,213 (GRCm39) |
missense |
probably benign |
0.39 |
R6351:Mylk
|
UTSW |
16 |
34,742,341 (GRCm39) |
missense |
probably benign |
0.01 |
R6365:Mylk
|
UTSW |
16 |
34,680,961 (GRCm39) |
missense |
probably benign |
0.12 |
R6490:Mylk
|
UTSW |
16 |
34,750,237 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6723:Mylk
|
UTSW |
16 |
34,750,258 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6864:Mylk
|
UTSW |
16 |
34,694,520 (GRCm39) |
missense |
probably benign |
0.03 |
R6908:Mylk
|
UTSW |
16 |
34,700,643 (GRCm39) |
missense |
probably benign |
0.18 |
R6949:Mylk
|
UTSW |
16 |
34,820,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R7018:Mylk
|
UTSW |
16 |
34,820,796 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7035:Mylk
|
UTSW |
16 |
34,797,352 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7162:Mylk
|
UTSW |
16 |
34,742,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R7236:Mylk
|
UTSW |
16 |
34,742,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R7269:Mylk
|
UTSW |
16 |
34,605,381 (GRCm39) |
missense |
probably damaging |
0.96 |
R7475:Mylk
|
UTSW |
16 |
34,734,446 (GRCm39) |
splice site |
probably null |
|
R7525:Mylk
|
UTSW |
16 |
34,809,357 (GRCm39) |
missense |
probably benign |
0.06 |
R7587:Mylk
|
UTSW |
16 |
34,742,887 (GRCm39) |
missense |
probably benign |
0.29 |
R7607:Mylk
|
UTSW |
16 |
34,715,184 (GRCm39) |
missense |
probably benign |
0.09 |
R7616:Mylk
|
UTSW |
16 |
34,699,927 (GRCm39) |
missense |
probably damaging |
0.97 |
R7647:Mylk
|
UTSW |
16 |
34,699,894 (GRCm39) |
missense |
probably benign |
0.29 |
R7648:Mylk
|
UTSW |
16 |
34,699,894 (GRCm39) |
missense |
probably benign |
0.29 |
R7764:Mylk
|
UTSW |
16 |
34,742,553 (GRCm39) |
missense |
probably benign |
0.16 |
R7890:Mylk
|
UTSW |
16 |
34,784,018 (GRCm39) |
nonsense |
probably null |
|
R7892:Mylk
|
UTSW |
16 |
34,699,894 (GRCm39) |
missense |
probably benign |
0.29 |
R7893:Mylk
|
UTSW |
16 |
34,699,894 (GRCm39) |
missense |
probably benign |
0.29 |
R8065:Mylk
|
UTSW |
16 |
34,792,389 (GRCm39) |
missense |
probably benign |
0.08 |
R8067:Mylk
|
UTSW |
16 |
34,792,389 (GRCm39) |
missense |
probably benign |
0.08 |
R8143:Mylk
|
UTSW |
16 |
34,734,525 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8210:Mylk
|
UTSW |
16 |
34,820,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R8271:Mylk
|
UTSW |
16 |
34,742,949 (GRCm39) |
missense |
probably damaging |
0.97 |
R8540:Mylk
|
UTSW |
16 |
34,750,257 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8721:Mylk
|
UTSW |
16 |
34,817,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R8743:Mylk
|
UTSW |
16 |
34,741,427 (GRCm39) |
missense |
probably benign |
0.03 |
R8798:Mylk
|
UTSW |
16 |
34,719,772 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8956:Mylk
|
UTSW |
16 |
34,791,779 (GRCm39) |
missense |
probably benign |
0.01 |
R9131:Mylk
|
UTSW |
16 |
34,776,835 (GRCm39) |
missense |
probably benign |
0.29 |
R9403:Mylk
|
UTSW |
16 |
34,696,012 (GRCm39) |
nonsense |
probably null |
|
R9624:Mylk
|
UTSW |
16 |
34,699,677 (GRCm39) |
missense |
probably benign |
0.29 |
R9735:Mylk
|
UTSW |
16 |
34,735,179 (GRCm39) |
missense |
probably benign |
0.09 |
R9756:Mylk
|
UTSW |
16 |
34,734,387 (GRCm39) |
missense |
probably damaging |
0.96 |
R9763:Mylk
|
UTSW |
16 |
34,699,482 (GRCm39) |
nonsense |
probably null |
|
RF001:Mylk
|
UTSW |
16 |
34,699,741 (GRCm39) |
missense |
probably benign |
0.03 |
V7580:Mylk
|
UTSW |
16 |
34,815,574 (GRCm39) |
critical splice donor site |
probably null |
|
V7583:Mylk
|
UTSW |
16 |
34,815,574 (GRCm39) |
critical splice donor site |
probably null |
|
X0065:Mylk
|
UTSW |
16 |
34,820,811 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Mylk
|
UTSW |
16 |
34,743,021 (GRCm39) |
missense |
possibly damaging |
0.74 |
|