Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr1a |
A |
T |
19: 46,368,186 (GRCm39) |
S254T |
probably benign |
Het |
Adam12 |
G |
A |
7: 133,826,542 (GRCm39) |
A22V |
unknown |
Het |
Adarb2 |
A |
G |
13: 8,619,775 (GRCm39) |
D87G |
possibly damaging |
Het |
Aldh6a1 |
A |
T |
12: 84,488,855 (GRCm39) |
I59N |
probably benign |
Het |
Ankrd50 |
C |
T |
3: 38,536,870 (GRCm39) |
C161Y |
probably damaging |
Het |
Ankrd7 |
A |
G |
6: 18,879,515 (GRCm39) |
|
probably null |
Het |
Anks1 |
T |
A |
17: 28,257,115 (GRCm39) |
I707N |
probably damaging |
Het |
Atoh1 |
A |
T |
6: 64,706,904 (GRCm39) |
M200L |
possibly damaging |
Het |
Bmp1 |
C |
T |
14: 70,730,284 (GRCm39) |
R416H |
probably damaging |
Het |
Caprin1 |
A |
G |
2: 103,602,099 (GRCm39) |
S548P |
probably benign |
Het |
Ccdc167 |
T |
A |
17: 29,924,247 (GRCm39) |
Y63F |
possibly damaging |
Het |
Cfap99 |
T |
A |
5: 34,465,284 (GRCm39) |
D174E |
probably benign |
Het |
Chil3 |
T |
G |
3: 106,056,161 (GRCm39) |
N331T |
probably benign |
Het |
Chmp5 |
T |
A |
4: 40,949,488 (GRCm39) |
I35N |
probably damaging |
Het |
Cpt1c |
A |
T |
7: 44,611,689 (GRCm39) |
S537T |
probably benign |
Het |
Dctn1 |
A |
T |
6: 83,163,123 (GRCm39) |
|
probably benign |
Het |
Dhx57 |
T |
A |
17: 80,546,287 (GRCm39) |
M1366L |
probably benign |
Het |
Dnah9 |
T |
A |
11: 65,802,656 (GRCm39) |
Y3478F |
probably damaging |
Het |
Efna3 |
A |
G |
3: 89,223,947 (GRCm39) |
Y81H |
probably damaging |
Het |
Eif4enif1 |
T |
C |
11: 3,192,608 (GRCm39) |
V812A |
probably damaging |
Het |
Erg |
A |
T |
16: 95,178,216 (GRCm39) |
I237N |
probably benign |
Het |
Fem1c |
G |
T |
18: 46,657,185 (GRCm39) |
N176K |
probably damaging |
Het |
Fgd4 |
T |
C |
16: 16,293,018 (GRCm39) |
Y233C |
probably benign |
Het |
Foxd2 |
G |
A |
4: 114,765,009 (GRCm39) |
A337V |
unknown |
Het |
Gsdma2 |
T |
C |
11: 98,548,547 (GRCm39) |
L433P |
unknown |
Het |
Hmcn2 |
C |
A |
2: 31,343,045 (GRCm39) |
|
probably null |
Het |
Hnrnpul2 |
T |
C |
19: 8,797,788 (GRCm39) |
V48A |
probably benign |
Het |
Hsf1 |
T |
A |
15: 76,383,387 (GRCm39) |
S396T |
probably benign |
Het |
Htr5b |
G |
T |
1: 121,455,487 (GRCm39) |
N144K |
probably damaging |
Het |
Igkv9-120 |
T |
C |
6: 68,027,172 (GRCm39) |
S29P |
probably damaging |
Het |
Igsf10 |
T |
A |
3: 59,236,549 (GRCm39) |
N1211Y |
possibly damaging |
Het |
Kcnh1 |
A |
C |
1: 191,959,447 (GRCm39) |
I334L |
probably benign |
Het |
Laptm4b |
T |
C |
15: 34,276,346 (GRCm39) |
I158T |
probably benign |
Het |
Mgat4f |
A |
T |
1: 134,318,250 (GRCm39) |
M341L |
probably benign |
Het |
Muc5ac |
G |
C |
7: 141,363,040 (GRCm39) |
G2117A |
unknown |
Het |
Nav3 |
T |
C |
10: 109,539,213 (GRCm39) |
T2063A |
probably damaging |
Het |
Nceh1 |
T |
A |
3: 27,261,531 (GRCm39) |
D47E |
probably benign |
Het |
Nckap5 |
A |
G |
1: 125,952,383 (GRCm39) |
S1390P |
probably damaging |
Het |
Npepps |
T |
G |
11: 97,158,454 (GRCm39) |
I104L |
probably benign |
Het |
Opn1sw |
T |
A |
6: 29,380,168 (GRCm39) |
I83F |
probably benign |
Het |
Or13p4 |
T |
C |
4: 118,547,425 (GRCm39) |
S75G |
probably damaging |
Het |
Or5b95 |
A |
T |
19: 12,657,576 (GRCm39) |
I35F |
probably benign |
Het |
Or5l13 |
G |
A |
2: 87,779,822 (GRCm39) |
H252Y |
probably damaging |
Het |
Pigg |
T |
G |
5: 108,484,162 (GRCm39) |
C603G |
probably benign |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Pkhd1l1 |
C |
A |
15: 44,391,133 (GRCm39) |
H1504N |
probably benign |
Het |
Plcd4 |
A |
G |
1: 74,604,292 (GRCm39) |
N757D |
possibly damaging |
Het |
Ppia |
A |
G |
11: 6,369,569 (GRCm39) |
T152A |
probably benign |
Het |
Psmd8 |
G |
A |
7: 28,878,346 (GRCm39) |
|
probably null |
Het |
Pxn |
T |
A |
5: 115,686,575 (GRCm39) |
Y356N |
probably benign |
Het |
Rhoa |
G |
C |
9: 108,213,914 (GRCm39) |
C159S |
probably damaging |
Het |
Rictor |
C |
T |
15: 6,801,635 (GRCm39) |
S441L |
probably benign |
Het |
Rita1 |
C |
T |
5: 120,749,506 (GRCm39) |
C69Y |
probably benign |
Het |
Satb1 |
A |
G |
17: 52,074,961 (GRCm39) |
S512P |
possibly damaging |
Het |
Sectm1b |
A |
G |
11: 120,945,768 (GRCm39) |
I191T |
possibly damaging |
Het |
Slc22a6 |
A |
G |
19: 8,599,260 (GRCm39) |
K297R |
possibly damaging |
Het |
Snrnp48 |
T |
C |
13: 38,405,263 (GRCm39) |
Y287H |
probably benign |
Het |
Sntg2 |
A |
T |
12: 30,276,910 (GRCm39) |
C381S |
probably benign |
Het |
Syngap1 |
T |
A |
17: 27,178,938 (GRCm39) |
M649K |
probably damaging |
Het |
Taf4 |
G |
A |
2: 179,573,822 (GRCm39) |
T682M |
probably damaging |
Het |
Thap2 |
T |
C |
10: 115,212,289 (GRCm39) |
I79V |
probably damaging |
Het |
Thap7 |
T |
C |
16: 17,346,467 (GRCm39) |
N172S |
probably benign |
Het |
Ticrr |
A |
G |
7: 79,328,844 (GRCm39) |
Y661C |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,606,659 (GRCm39) |
N18084D |
probably damaging |
Het |
Usp48 |
A |
T |
4: 137,377,728 (GRCm39) |
K1020M |
probably damaging |
Het |
Vmn2r12 |
T |
C |
5: 109,233,920 (GRCm39) |
N764S |
probably damaging |
Het |
Vmn2r91 |
A |
G |
17: 18,356,540 (GRCm39) |
I736V |
possibly damaging |
Het |
Wfdc6b |
T |
A |
2: 164,459,339 (GRCm39) |
C134S |
probably damaging |
Het |
Zcchc2 |
A |
T |
1: 105,946,003 (GRCm39) |
D481V |
probably damaging |
Het |
Zfp949 |
G |
A |
9: 88,451,923 (GRCm39) |
G498R |
probably damaging |
Het |
|
Other mutations in Numb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00335:Numb
|
APN |
12 |
83,854,906 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01979:Numb
|
APN |
12 |
83,889,051 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02318:Numb
|
APN |
12 |
83,878,692 (GRCm39) |
splice site |
probably null |
|
IGL02716:Numb
|
APN |
12 |
83,847,982 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL03206:Numb
|
APN |
12 |
83,872,070 (GRCm39) |
splice site |
probably benign |
|
PIT4468001:Numb
|
UTSW |
12 |
83,854,921 (GRCm39) |
missense |
probably damaging |
0.99 |
R0086:Numb
|
UTSW |
12 |
83,842,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R0626:Numb
|
UTSW |
12 |
83,842,614 (GRCm39) |
missense |
probably damaging |
0.97 |
R0652:Numb
|
UTSW |
12 |
83,842,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R1201:Numb
|
UTSW |
12 |
83,848,059 (GRCm39) |
missense |
probably damaging |
0.99 |
R1295:Numb
|
UTSW |
12 |
83,842,935 (GRCm39) |
splice site |
probably benign |
|
R1433:Numb
|
UTSW |
12 |
83,844,033 (GRCm39) |
missense |
probably damaging |
0.98 |
R1489:Numb
|
UTSW |
12 |
83,842,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R1606:Numb
|
UTSW |
12 |
83,847,784 (GRCm39) |
splice site |
probably null |
|
R1980:Numb
|
UTSW |
12 |
83,844,118 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3771:Numb
|
UTSW |
12 |
83,846,350 (GRCm39) |
missense |
probably damaging |
0.99 |
R5382:Numb
|
UTSW |
12 |
83,854,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R5818:Numb
|
UTSW |
12 |
83,872,028 (GRCm39) |
splice site |
probably null |
|
R5846:Numb
|
UTSW |
12 |
83,923,521 (GRCm39) |
utr 5 prime |
probably benign |
|
R6360:Numb
|
UTSW |
12 |
83,844,036 (GRCm39) |
missense |
probably damaging |
0.99 |
R6384:Numb
|
UTSW |
12 |
83,850,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R7186:Numb
|
UTSW |
12 |
83,842,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R7469:Numb
|
UTSW |
12 |
83,850,578 (GRCm39) |
missense |
probably benign |
0.37 |
R8342:Numb
|
UTSW |
12 |
83,854,990 (GRCm39) |
missense |
probably benign |
0.02 |
R8370:Numb
|
UTSW |
12 |
83,854,974 (GRCm39) |
nonsense |
probably null |
|
R9448:Numb
|
UTSW |
12 |
83,888,990 (GRCm39) |
critical splice donor site |
probably null |
|
|