Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcd2 |
C |
A |
15: 91,075,514 (GRCm39) |
V100L |
probably benign |
Het |
Acad11 |
G |
A |
9: 103,963,465 (GRCm39) |
|
probably benign |
Het |
Actb |
C |
T |
5: 142,891,307 (GRCm39) |
|
probably benign |
Het |
Ano9 |
G |
A |
7: 140,687,117 (GRCm39) |
A374V |
probably damaging |
Het |
Baz2b |
T |
C |
2: 59,773,103 (GRCm39) |
|
probably null |
Het |
Bltp3a |
G |
T |
17: 28,109,110 (GRCm39) |
D1110Y |
probably benign |
Het |
Bpifb9b |
T |
A |
2: 154,155,551 (GRCm39) |
L350Q |
probably damaging |
Het |
Cd27 |
T |
A |
6: 125,211,281 (GRCm39) |
|
probably null |
Het |
Cd72 |
A |
G |
4: 43,449,563 (GRCm39) |
|
probably benign |
Het |
Cdadc1 |
A |
T |
14: 59,801,973 (GRCm39) |
S516T |
probably benign |
Het |
Chst5 |
T |
A |
8: 112,617,192 (GRCm39) |
I143F |
possibly damaging |
Het |
Col20a1 |
T |
C |
2: 180,639,156 (GRCm39) |
V452A |
possibly damaging |
Het |
Cox11 |
C |
A |
11: 90,535,229 (GRCm39) |
Q227K |
probably benign |
Het |
Cpa6 |
A |
G |
1: 10,665,843 (GRCm39) |
|
probably null |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Het |
Dpm2 |
T |
C |
2: 32,461,203 (GRCm39) |
|
probably benign |
Het |
Dync1h1 |
C |
A |
12: 110,624,560 (GRCm39) |
T3700N |
probably damaging |
Het |
Frem1 |
A |
C |
4: 82,881,387 (GRCm39) |
N1273K |
probably damaging |
Het |
Fry |
T |
C |
5: 150,317,704 (GRCm39) |
|
probably null |
Het |
Gm10306 |
G |
T |
4: 94,445,069 (GRCm39) |
|
probably benign |
Het |
Gm5565 |
T |
C |
5: 146,094,913 (GRCm39) |
T278A |
probably benign |
Het |
Gm8180 |
A |
G |
14: 44,019,802 (GRCm39) |
I40T |
probably benign |
Het |
Iah1 |
T |
C |
12: 21,367,426 (GRCm39) |
V44A |
probably benign |
Het |
Iqgap3 |
C |
T |
3: 88,020,435 (GRCm39) |
P360S |
probably damaging |
Het |
Klhl28 |
T |
A |
12: 65,003,896 (GRCm39) |
I206F |
possibly damaging |
Het |
Krt13 |
A |
G |
11: 100,012,332 (GRCm39) |
|
probably benign |
Het |
Lipo2 |
T |
A |
19: 33,726,914 (GRCm39) |
D41V |
probably benign |
Het |
Lrig2 |
C |
G |
3: 104,398,842 (GRCm39) |
V229L |
possibly damaging |
Het |
Lrrc32 |
C |
T |
7: 98,147,727 (GRCm39) |
T169I |
probably damaging |
Het |
Lrriq1 |
T |
C |
10: 103,014,649 (GRCm39) |
N1053S |
possibly damaging |
Het |
Mfng |
C |
T |
15: 78,648,588 (GRCm39) |
R163H |
probably benign |
Het |
Mgat4c |
G |
C |
10: 102,224,599 (GRCm39) |
R271P |
probably damaging |
Het |
N4bp1 |
T |
C |
8: 87,587,676 (GRCm39) |
T421A |
probably benign |
Het |
Nat8f1 |
T |
C |
6: 85,887,295 (GRCm39) |
T222A |
probably benign |
Het |
Nsun2 |
T |
C |
13: 69,691,992 (GRCm39) |
|
probably benign |
Het |
Oas2 |
T |
A |
5: 120,876,599 (GRCm39) |
D448V |
probably damaging |
Het |
Or10al7 |
C |
A |
17: 38,366,467 (GRCm39) |
V6F |
probably benign |
Het |
Or2l13b |
A |
T |
16: 19,349,383 (GRCm39) |
C96S |
probably damaging |
Het |
Or5ak22 |
T |
C |
2: 85,230,772 (GRCm39) |
Y35C |
probably damaging |
Het |
Pgm2l1 |
T |
A |
7: 99,877,204 (GRCm39) |
L25Q |
probably damaging |
Het |
Pigp |
A |
T |
16: 94,166,309 (GRCm39) |
V133D |
probably benign |
Het |
Pnkp |
C |
T |
7: 44,511,827 (GRCm39) |
S113L |
probably damaging |
Het |
Pomt2 |
C |
T |
12: 87,156,881 (GRCm39) |
D752N |
possibly damaging |
Het |
Ppat |
T |
C |
5: 77,074,640 (GRCm39) |
K65E |
probably damaging |
Het |
Ptprn2 |
T |
C |
12: 117,125,314 (GRCm39) |
L616P |
probably damaging |
Het |
Rad54l2 |
A |
G |
9: 106,595,091 (GRCm39) |
S289P |
probably damaging |
Het |
Rbm39 |
G |
A |
2: 156,019,266 (GRCm39) |
R31C |
possibly damaging |
Het |
Rhbdf2 |
C |
A |
11: 116,492,771 (GRCm39) |
V417L |
probably benign |
Het |
Rnf157 |
T |
A |
11: 116,246,298 (GRCm39) |
E255D |
possibly damaging |
Het |
Rpl6l |
A |
T |
10: 110,962,304 (GRCm39) |
|
noncoding transcript |
Het |
Sec24c |
A |
G |
14: 20,743,813 (GRCm39) |
D1006G |
probably damaging |
Het |
Sh3bp1 |
G |
T |
15: 78,792,237 (GRCm39) |
A401S |
probably benign |
Het |
Slc17a8 |
A |
T |
10: 89,412,367 (GRCm39) |
D539E |
probably benign |
Het |
Slc38a9 |
T |
A |
13: 112,826,098 (GRCm39) |
S136R |
probably damaging |
Het |
Smoc2 |
A |
C |
17: 14,589,295 (GRCm39) |
T255P |
probably benign |
Het |
Smyd2 |
T |
C |
1: 189,628,847 (GRCm39) |
D152G |
probably damaging |
Het |
Stab1 |
A |
G |
14: 30,862,350 (GRCm39) |
V2328A |
probably damaging |
Het |
Taar2 |
A |
G |
10: 23,816,591 (GRCm39) |
I44V |
probably benign |
Het |
Tbc1d4 |
T |
C |
14: 101,682,144 (GRCm39) |
K1251E |
probably benign |
Het |
Thada |
G |
A |
17: 84,754,027 (GRCm39) |
L315F |
probably damaging |
Het |
Trbv14 |
T |
C |
6: 41,112,259 (GRCm39) |
S19P |
probably benign |
Het |
Ttc39c |
T |
C |
18: 12,820,173 (GRCm39) |
|
probably benign |
Het |
Ttc39d |
A |
G |
17: 80,524,527 (GRCm39) |
I395M |
probably benign |
Het |
Ttn |
T |
C |
2: 76,548,728 (GRCm39) |
E31891G |
probably damaging |
Het |
Ubr3 |
T |
C |
2: 69,800,527 (GRCm39) |
V950A |
probably damaging |
Het |
Usp9y |
T |
A |
Y: 1,307,920 (GRCm39) |
K2305N |
probably damaging |
Het |
Vmn1r158 |
G |
A |
7: 22,490,179 (GRCm39) |
T10I |
possibly damaging |
Het |
Vmn2r129 |
G |
T |
4: 156,686,692 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r78 |
T |
A |
7: 86,603,916 (GRCm39) |
I698K |
possibly damaging |
Het |
Vmn2r86 |
G |
T |
10: 130,289,460 (GRCm39) |
T145K |
probably damaging |
Het |
Zfp51 |
T |
C |
17: 21,684,933 (GRCm39) |
V516A |
probably benign |
Het |
Zfp654 |
A |
T |
16: 64,606,145 (GRCm39) |
S686T |
probably benign |
Het |
Zfp846 |
T |
A |
9: 20,502,111 (GRCm39) |
C55S |
probably benign |
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 |
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 |
R5311:Mylk
|
UTSW |
16 |
34,742,127 (GRCm39) |
missense |
probably benign |
0.01 |
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 |
|