Other mutations in this stock |
Total: 106 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgre4 |
G |
A |
17: 56,098,952 (GRCm39) |
V153I |
probably benign |
Het |
Akap13 |
G |
A |
7: 75,380,213 (GRCm39) |
R462H |
probably damaging |
Het |
Aldh16a1 |
A |
G |
7: 44,795,331 (GRCm39) |
Y443H |
probably benign |
Het |
Apbb1 |
A |
G |
7: 105,215,339 (GRCm39) |
V434A |
probably benign |
Het |
Atrip |
A |
G |
9: 108,898,422 (GRCm39) |
M199T |
probably damaging |
Het |
Atxn2 |
T |
C |
5: 121,940,330 (GRCm39) |
|
probably null |
Het |
AU040320 |
A |
G |
4: 126,708,103 (GRCm39) |
T240A |
probably benign |
Het |
Btf3l4 |
A |
T |
4: 108,675,589 (GRCm39) |
|
probably null |
Het |
Ccdc106 |
A |
G |
7: 5,063,325 (GRCm39) |
T277A |
probably damaging |
Het |
Cdk15 |
G |
T |
1: 59,328,938 (GRCm39) |
W282L |
probably null |
Het |
Cflar |
T |
A |
1: 58,765,597 (GRCm39) |
M1K |
probably null |
Het |
Champ1 |
C |
A |
8: 13,928,579 (GRCm39) |
P246T |
possibly damaging |
Het |
Crat |
A |
C |
2: 30,299,994 (GRCm39) |
F129V |
probably damaging |
Het |
Csmd3 |
T |
C |
15: 47,492,640 (GRCm39) |
N2256S |
|
Het |
Cwh43 |
C |
A |
5: 73,569,311 (GRCm39) |
Q118K |
probably damaging |
Het |
Daam1 |
A |
T |
12: 72,032,580 (GRCm39) |
K949* |
probably null |
Het |
Ddn |
C |
G |
15: 98,703,247 (GRCm39) |
E682Q |
possibly damaging |
Het |
Des |
T |
A |
1: 75,339,605 (GRCm39) |
M321K |
possibly damaging |
Het |
Dnm2 |
T |
C |
9: 21,392,672 (GRCm39) |
V460A |
probably damaging |
Het |
Dst |
G |
A |
1: 34,230,236 (GRCm39) |
E2610K |
probably benign |
Het |
Efr3a |
C |
T |
15: 65,729,360 (GRCm39) |
T660I |
possibly damaging |
Het |
Eogt |
T |
C |
6: 97,119,794 (GRCm39) |
E138G |
probably benign |
Het |
Epha8 |
G |
A |
4: 136,658,399 (GRCm39) |
A992V |
possibly damaging |
Het |
Exoc2 |
A |
T |
13: 31,109,716 (GRCm39) |
D217E |
probably damaging |
Het |
Fam222b |
T |
C |
11: 78,045,173 (GRCm39) |
S245P |
probably damaging |
Het |
Fbxo45 |
T |
C |
16: 32,057,339 (GRCm39) |
Y185C |
probably damaging |
Het |
Fbxo47 |
T |
C |
11: 97,755,993 (GRCm39) |
T170A |
probably benign |
Het |
Fbxw26 |
A |
T |
9: 109,561,765 (GRCm39) |
V143E |
probably benign |
Het |
Foxb2 |
T |
C |
19: 16,851,004 (GRCm39) |
M1V |
probably null |
Het |
Gm11596 |
C |
A |
11: 99,683,962 (GRCm39) |
V53L |
unknown |
Het |
Gm47791 |
A |
G |
1: 82,748,547 (GRCm39) |
*140Q |
probably null |
Het |
Gpr179 |
C |
T |
11: 97,226,115 (GRCm39) |
M2013I |
probably benign |
Het |
Hck |
T |
A |
2: 152,971,850 (GRCm39) |
L137* |
probably null |
Het |
Hectd4 |
T |
A |
5: 121,462,024 (GRCm39) |
C964S |
possibly damaging |
Het |
Hexa |
T |
C |
9: 59,464,683 (GRCm39) |
|
probably null |
Het |
Ifna12 |
C |
A |
4: 88,521,502 (GRCm39) |
S15I |
possibly damaging |
Het |
Kif18b |
C |
A |
11: 102,807,234 (GRCm39) |
V34L |
probably damaging |
Het |
Kif18b |
A |
T |
11: 102,803,174 (GRCm39) |
|
probably null |
Het |
Kifap3 |
A |
T |
1: 163,643,402 (GRCm39) |
H209L |
probably benign |
Het |
Klhl1 |
A |
T |
14: 96,360,713 (GRCm39) |
D712E |
probably damaging |
Het |
Kmt2c |
T |
C |
5: 25,513,530 (GRCm39) |
D3088G |
probably damaging |
Het |
Mageb3 |
A |
G |
2: 121,784,953 (GRCm39) |
Y250H |
probably damaging |
Het |
Manba |
G |
T |
3: 135,250,562 (GRCm39) |
E396D |
probably damaging |
Het |
Mapkbp1 |
T |
A |
2: 119,852,669 (GRCm39) |
V997E |
probably damaging |
Het |
Mdc1 |
A |
G |
17: 36,155,448 (GRCm39) |
H41R |
probably benign |
Het |
Mis18a |
T |
G |
16: 90,516,866 (GRCm39) |
M179L |
probably benign |
Het |
Mmp25 |
C |
G |
17: 23,863,756 (GRCm39) |
G25R |
possibly damaging |
Het |
Mmp3 |
A |
G |
9: 7,447,621 (GRCm39) |
D202G |
possibly damaging |
Het |
Mmp3 |
C |
T |
9: 7,450,125 (GRCm39) |
P286S |
probably benign |
Het |
Mrgpra2b |
G |
A |
7: 47,114,277 (GRCm39) |
H152Y |
possibly damaging |
Het |
Mslnl |
A |
T |
17: 25,955,895 (GRCm39) |
M1L |
probably benign |
Het |
Myo1d |
G |
A |
11: 80,477,743 (GRCm39) |
T880I |
probably damaging |
Het |
Ncaph |
T |
A |
2: 126,975,795 (GRCm39) |
|
probably benign |
Het |
Nln |
T |
C |
13: 104,161,530 (GRCm39) |
D680G |
possibly damaging |
Het |
Noct |
C |
T |
3: 51,132,622 (GRCm39) |
A33V |
probably benign |
Het |
Nolc1 |
A |
G |
19: 46,070,773 (GRCm39) |
T325A |
unknown |
Het |
Nr2e3 |
A |
G |
9: 59,856,434 (GRCm39) |
|
probably null |
Het |
Nrg2 |
T |
A |
18: 36,155,459 (GRCm39) |
H450L |
probably benign |
Het |
Or13a21 |
T |
C |
7: 139,999,287 (GRCm39) |
N133S |
probably benign |
Het |
Or2t43 |
A |
C |
11: 58,457,288 (GRCm39) |
N294K |
possibly damaging |
Het |
Or5ak24 |
T |
G |
2: 85,261,171 (GRCm39) |
M1L |
possibly damaging |
Het |
Or5an1 |
T |
A |
19: 12,260,839 (GRCm39) |
C142* |
probably null |
Het |
Or6b3 |
T |
A |
1: 92,439,570 (GRCm39) |
Y60F |
possibly damaging |
Het |
Pank2 |
T |
A |
2: 131,115,967 (GRCm39) |
N128K |
possibly damaging |
Het |
Pcdha3 |
T |
C |
18: 37,080,584 (GRCm39) |
V442A |
probably damaging |
Het |
Pds5b |
T |
A |
5: 150,659,792 (GRCm39) |
S252T |
probably damaging |
Het |
Pfpl |
T |
C |
19: 12,405,878 (GRCm39) |
L43S |
probably damaging |
Het |
Pigu |
T |
A |
2: 155,141,009 (GRCm39) |
I295F |
probably damaging |
Het |
Piwil4 |
T |
C |
9: 14,616,337 (GRCm39) |
Y673C |
probably damaging |
Het |
Pls1 |
A |
G |
9: 95,651,166 (GRCm39) |
Y414H |
possibly damaging |
Het |
Ppp1r13l |
A |
T |
7: 19,105,305 (GRCm39) |
Q359L |
probably damaging |
Het |
Ppp2r5c |
A |
G |
12: 110,519,317 (GRCm39) |
Y263C |
probably damaging |
Het |
Prrc2c |
A |
T |
1: 162,504,932 (GRCm39) |
S2638R |
possibly damaging |
Het |
Prss39 |
T |
A |
1: 34,538,473 (GRCm39) |
|
probably null |
Het |
Psmd1 |
G |
A |
1: 86,044,355 (GRCm39) |
V648M |
probably damaging |
Het |
Rad50 |
T |
C |
11: 53,545,735 (GRCm39) |
D1196G |
probably damaging |
Het |
Rfx1 |
T |
C |
8: 84,800,542 (GRCm39) |
Y48H |
possibly damaging |
Het |
Rgs20 |
A |
G |
1: 4,982,553 (GRCm39) |
I305T |
probably benign |
Het |
Rpl9 |
T |
C |
5: 65,548,310 (GRCm39) |
T9A |
probably benign |
Het |
Samd4 |
A |
G |
14: 47,325,313 (GRCm39) |
N598D |
probably benign |
Het |
Sema7a |
T |
C |
9: 57,868,705 (GRCm39) |
Y606H |
probably damaging |
Het |
Sf3b3 |
A |
G |
8: 111,538,088 (GRCm39) |
S1150P |
possibly damaging |
Het |
Sirt1 |
T |
C |
10: 63,157,929 (GRCm39) |
N495S |
probably benign |
Het |
Slc17a3 |
T |
C |
13: 24,030,950 (GRCm39) |
|
probably null |
Het |
Slc25a22 |
T |
C |
7: 141,013,889 (GRCm39) |
T24A |
probably benign |
Het |
Slc30a9 |
T |
C |
5: 67,502,987 (GRCm39) |
I363T |
probably benign |
Het |
Srbd1 |
A |
G |
17: 86,406,702 (GRCm39) |
V561A |
probably damaging |
Het |
Srgap2 |
T |
C |
1: 131,220,405 (GRCm39) |
S896G |
probably damaging |
Het |
Sspo |
T |
C |
6: 48,463,237 (GRCm39) |
C3730R |
probably damaging |
Het |
Stat2 |
T |
A |
10: 128,113,772 (GRCm39) |
|
probably null |
Het |
Tcof1 |
T |
C |
18: 60,964,977 (GRCm39) |
K581E |
unknown |
Het |
Tdpoz6 |
T |
A |
3: 93,600,265 (GRCm39) |
T35S |
probably benign |
Het |
Thbs1 |
T |
C |
2: 117,948,681 (GRCm39) |
S446P |
probably damaging |
Het |
Thsd7a |
T |
C |
6: 12,331,584 (GRCm39) |
Y1330C |
|
Het |
Tmem121 |
C |
A |
12: 113,152,690 (GRCm39) |
P303T |
probably benign |
Het |
Tmem87b |
T |
A |
2: 128,691,071 (GRCm39) |
|
probably null |
Het |
Tmem98 |
A |
T |
11: 80,711,011 (GRCm39) |
|
probably null |
Het |
Trpm3 |
T |
A |
19: 22,955,698 (GRCm39) |
I1091N |
possibly damaging |
Het |
Urb2 |
A |
G |
8: 124,755,250 (GRCm39) |
E319G |
probably benign |
Het |
Vmn1r170 |
A |
T |
7: 23,306,320 (GRCm39) |
M241L |
not run |
Het |
Vmn1r238 |
T |
C |
18: 3,123,393 (GRCm39) |
N7S |
probably benign |
Het |
Wdr6 |
T |
C |
9: 108,450,201 (GRCm39) |
H1109R |
probably benign |
Het |
Zdhhc13 |
T |
C |
7: 48,454,156 (GRCm39) |
V193A |
probably benign |
Het |
Zfp354c |
T |
C |
11: 50,706,253 (GRCm39) |
Y274C |
probably damaging |
Het |
Zfp738 |
T |
A |
13: 67,821,080 (GRCm39) |
E89V |
probably benign |
Het |
Zswim3 |
T |
A |
2: 164,661,795 (GRCm39) |
F92I |
possibly damaging |
Het |
|
Other mutations in Srgap1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01964:Srgap1
|
APN |
10 |
121,640,871 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02106:Srgap1
|
APN |
10 |
121,621,598 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02927:Srgap1
|
APN |
10 |
121,691,367 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03088:Srgap1
|
APN |
10 |
121,661,598 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03208:Srgap1
|
APN |
10 |
121,628,171 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03251:Srgap1
|
APN |
10 |
121,640,826 (GRCm39) |
splice site |
probably null |
|
PIT1430001:Srgap1
|
UTSW |
10 |
121,732,658 (GRCm39) |
splice site |
probably benign |
|
R0052:Srgap1
|
UTSW |
10 |
121,636,732 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0052:Srgap1
|
UTSW |
10 |
121,636,732 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0356:Srgap1
|
UTSW |
10 |
121,691,441 (GRCm39) |
splice site |
probably null |
|
R0361:Srgap1
|
UTSW |
10 |
121,883,097 (GRCm39) |
start codon destroyed |
probably null |
0.89 |
R0365:Srgap1
|
UTSW |
10 |
121,621,610 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0675:Srgap1
|
UTSW |
10 |
121,628,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R0801:Srgap1
|
UTSW |
10 |
121,643,780 (GRCm39) |
missense |
probably damaging |
0.96 |
R0815:Srgap1
|
UTSW |
10 |
121,621,379 (GRCm39) |
missense |
probably damaging |
0.99 |
R1034:Srgap1
|
UTSW |
10 |
121,621,350 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1160:Srgap1
|
UTSW |
10 |
121,691,382 (GRCm39) |
missense |
probably benign |
0.01 |
R1454:Srgap1
|
UTSW |
10 |
121,732,643 (GRCm39) |
missense |
probably damaging |
0.99 |
R1624:Srgap1
|
UTSW |
10 |
121,691,278 (GRCm39) |
missense |
probably benign |
0.03 |
R1628:Srgap1
|
UTSW |
10 |
121,706,244 (GRCm39) |
missense |
probably benign |
0.15 |
R1816:Srgap1
|
UTSW |
10 |
121,761,876 (GRCm39) |
nonsense |
probably null |
|
R1933:Srgap1
|
UTSW |
10 |
121,761,808 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2034:Srgap1
|
UTSW |
10 |
121,628,651 (GRCm39) |
missense |
probably damaging |
0.98 |
R2211:Srgap1
|
UTSW |
10 |
121,689,645 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2295:Srgap1
|
UTSW |
10 |
121,630,665 (GRCm39) |
missense |
probably benign |
0.03 |
R2368:Srgap1
|
UTSW |
10 |
121,665,194 (GRCm39) |
missense |
probably benign |
0.05 |
R3796:Srgap1
|
UTSW |
10 |
121,883,037 (GRCm39) |
missense |
probably benign |
0.06 |
R4083:Srgap1
|
UTSW |
10 |
121,621,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R4172:Srgap1
|
UTSW |
10 |
121,691,268 (GRCm39) |
missense |
probably benign |
0.00 |
R4322:Srgap1
|
UTSW |
10 |
121,705,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R4401:Srgap1
|
UTSW |
10 |
121,640,826 (GRCm39) |
splice site |
probably null |
|
R4513:Srgap1
|
UTSW |
10 |
121,706,231 (GRCm39) |
critical splice donor site |
probably null |
|
R4698:Srgap1
|
UTSW |
10 |
121,628,392 (GRCm39) |
missense |
probably benign |
0.22 |
R4776:Srgap1
|
UTSW |
10 |
121,628,256 (GRCm39) |
missense |
probably benign |
0.03 |
R4951:Srgap1
|
UTSW |
10 |
121,621,457 (GRCm39) |
missense |
probably benign |
0.20 |
R5116:Srgap1
|
UTSW |
10 |
121,628,284 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5232:Srgap1
|
UTSW |
10 |
121,676,816 (GRCm39) |
missense |
probably benign |
0.00 |
R5237:Srgap1
|
UTSW |
10 |
121,643,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R5335:Srgap1
|
UTSW |
10 |
121,621,282 (GRCm39) |
utr 3 prime |
probably benign |
|
R5402:Srgap1
|
UTSW |
10 |
121,621,665 (GRCm39) |
missense |
probably benign |
0.06 |
R5432:Srgap1
|
UTSW |
10 |
121,705,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R5456:Srgap1
|
UTSW |
10 |
121,705,716 (GRCm39) |
missense |
probably benign |
0.45 |
R5669:Srgap1
|
UTSW |
10 |
121,640,755 (GRCm39) |
missense |
probably benign |
0.00 |
R5682:Srgap1
|
UTSW |
10 |
121,640,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R5687:Srgap1
|
UTSW |
10 |
121,661,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R5773:Srgap1
|
UTSW |
10 |
121,732,614 (GRCm39) |
missense |
probably benign |
0.02 |
R5832:Srgap1
|
UTSW |
10 |
121,676,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R6028:Srgap1
|
UTSW |
10 |
121,664,635 (GRCm39) |
missense |
probably null |
|
R6240:Srgap1
|
UTSW |
10 |
121,883,061 (GRCm39) |
missense |
probably benign |
0.06 |
R6336:Srgap1
|
UTSW |
10 |
121,761,846 (GRCm39) |
missense |
probably benign |
0.01 |
R6435:Srgap1
|
UTSW |
10 |
121,636,732 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6597:Srgap1
|
UTSW |
10 |
121,628,276 (GRCm39) |
missense |
probably benign |
0.11 |
R6798:Srgap1
|
UTSW |
10 |
121,761,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R6807:Srgap1
|
UTSW |
10 |
121,664,631 (GRCm39) |
splice site |
probably null |
|
R6897:Srgap1
|
UTSW |
10 |
121,621,523 (GRCm39) |
missense |
probably damaging |
0.96 |
R7057:Srgap1
|
UTSW |
10 |
121,640,858 (GRCm39) |
missense |
probably benign |
0.20 |
R7196:Srgap1
|
UTSW |
10 |
121,676,753 (GRCm39) |
missense |
probably benign |
0.00 |
R7247:Srgap1
|
UTSW |
10 |
121,705,695 (GRCm39) |
missense |
probably damaging |
0.98 |
R7404:Srgap1
|
UTSW |
10 |
121,621,650 (GRCm39) |
missense |
probably benign |
0.18 |
R7792:Srgap1
|
UTSW |
10 |
121,761,872 (GRCm39) |
missense |
probably damaging |
0.98 |
R7846:Srgap1
|
UTSW |
10 |
121,621,397 (GRCm39) |
missense |
probably damaging |
0.97 |
R7896:Srgap1
|
UTSW |
10 |
121,689,458 (GRCm39) |
critical splice donor site |
probably benign |
|
R7912:Srgap1
|
UTSW |
10 |
121,689,458 (GRCm39) |
critical splice donor site |
probably benign |
|
R8127:Srgap1
|
UTSW |
10 |
121,691,271 (GRCm39) |
missense |
probably null |
0.04 |
R8233:Srgap1
|
UTSW |
10 |
121,661,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R8248:Srgap1
|
UTSW |
10 |
121,640,722 (GRCm39) |
missense |
probably damaging |
0.99 |
R8362:Srgap1
|
UTSW |
10 |
121,691,383 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8885:Srgap1
|
UTSW |
10 |
121,761,545 (GRCm39) |
intron |
probably benign |
|
R9074:Srgap1
|
UTSW |
10 |
121,628,257 (GRCm39) |
missense |
probably damaging |
0.99 |
R9134:Srgap1
|
UTSW |
10 |
121,883,127 (GRCm39) |
start gained |
probably benign |
|
R9338:Srgap1
|
UTSW |
10 |
121,689,458 (GRCm39) |
critical splice donor site |
probably benign |
|
R9437:Srgap1
|
UTSW |
10 |
121,636,777 (GRCm39) |
missense |
probably benign |
0.18 |
R9629:Srgap1
|
UTSW |
10 |
121,705,746 (GRCm39) |
missense |
probably benign |
0.06 |
R9747:Srgap1
|
UTSW |
10 |
121,761,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R9747:Srgap1
|
UTSW |
10 |
121,628,579 (GRCm39) |
missense |
probably benign |
|
X0063:Srgap1
|
UTSW |
10 |
121,621,317 (GRCm39) |
missense |
probably damaging |
0.97 |
|