Incidental Mutation 'R1901:Mug2'
| ID |
212201 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Mug2
|
| Ensembl Gene |
ENSMUSG00000030131 |
| Gene Name |
murinoglobulin 2 |
| Synonyms |
|
| MMRRC Submission |
039921-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.053)
|
| Stock # |
R1901 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
6 |
| Chromosomal Location |
121983720-122062924 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to A
at 122048801 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Histidine to Asparagine
at position 856
(H856N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000080469
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000081777]
|
| AlphaFold |
P28666 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000081777
AA Change: H856N
PolyPhen 2
Score 0.019 (Sensitivity: 0.95; Specificity: 0.80)
|
| SMART Domains |
Protein: ENSMUSP00000080469
Gene: ENSMUSG00000030131
AA Change: H856N
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:A2M_N
|
128 |
221 |
3.5e-21 |
PFAM |
|
A2M_N_2
|
449 |
599 |
1.05e-42 |
SMART |
|
low complexity region
|
711 |
728 |
N/A |
INTRINSIC |
|
A2M
|
740 |
830 |
7.16e-36 |
SMART |
|
Pfam:Thiol-ester_cl
|
963 |
992 |
1e-18 |
PFAM |
|
low complexity region
|
994 |
1005 |
N/A |
INTRINSIC |
|
Pfam:A2M_comp
|
1012 |
1097 |
5.8e-34 |
PFAM |
|
Pfam:A2M_comp
|
1093 |
1243 |
3e-47 |
PFAM |
|
A2M_recep
|
1353 |
1440 |
1.85e-38 |
SMART |
|
| Coding Region Coverage |
- 1x: 97.3%
- 3x: 96.8%
- 10x: 95.2%
- 20x: 92.5%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 94 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca15 |
A |
G |
7: 119,945,322 (GRCm39) |
E466G |
probably damaging |
Het |
| Acacb |
A |
T |
5: 114,303,795 (GRCm39) |
R73* |
probably null |
Het |
| Acta1 |
A |
T |
8: 124,619,900 (GRCm39) |
S147T |
probably benign |
Het |
| Adh1 |
G |
A |
3: 137,994,558 (GRCm39) |
V293I |
probably benign |
Het |
| Aldh3b3 |
T |
C |
19: 4,015,130 (GRCm39) |
Y170H |
probably damaging |
Het |
| Ank3 |
A |
T |
10: 69,658,167 (GRCm39) |
T198S |
probably damaging |
Het |
| Ankrd12 |
A |
T |
17: 66,293,698 (GRCm39) |
N578K |
possibly damaging |
Het |
| Ano2 |
A |
T |
6: 125,849,647 (GRCm39) |
E126D |
probably damaging |
Het |
| Anpep |
C |
T |
7: 79,488,004 (GRCm39) |
E518K |
probably benign |
Het |
| Arhgef7 |
C |
A |
8: 11,858,713 (GRCm39) |
|
probably null |
Het |
| Cfap44 |
A |
C |
16: 44,242,737 (GRCm39) |
T714P |
probably benign |
Het |
| Cnot1 |
T |
C |
8: 96,469,749 (GRCm39) |
I1369V |
possibly damaging |
Het |
| Col19a1 |
A |
T |
1: 24,576,078 (GRCm39) |
I88K |
unknown |
Het |
| Col1a1 |
G |
A |
11: 94,837,458 (GRCm39) |
|
probably null |
Het |
| Col5a1 |
A |
G |
2: 27,850,456 (GRCm39) |
T518A |
unknown |
Het |
| Cul7 |
T |
C |
17: 46,966,666 (GRCm39) |
L365P |
probably damaging |
Het |
| Dlec1 |
T |
C |
9: 118,931,712 (GRCm39) |
S44P |
probably damaging |
Het |
| Dock9 |
T |
C |
14: 121,862,565 (GRCm39) |
|
probably null |
Het |
| Fbxl9 |
T |
C |
8: 106,039,707 (GRCm39) |
N556S |
probably damaging |
Het |
| Flrt2 |
C |
A |
12: 95,745,904 (GRCm39) |
P81T |
probably damaging |
Het |
| Flrt2 |
C |
T |
12: 95,745,905 (GRCm39) |
P81L |
probably damaging |
Het |
| Ginm1 |
A |
G |
10: 7,650,980 (GRCm39) |
|
probably null |
Het |
| Glis3 |
T |
C |
19: 28,508,985 (GRCm39) |
N333S |
probably damaging |
Het |
| Glo1 |
T |
G |
17: 30,815,382 (GRCm39) |
E144D |
probably benign |
Het |
| Golga1 |
A |
T |
2: 38,937,792 (GRCm39) |
|
probably null |
Het |
| H2-Aa |
A |
G |
17: 34,502,207 (GRCm39) |
I155T |
possibly damaging |
Het |
| Haus5 |
A |
G |
7: 30,356,670 (GRCm39) |
S479P |
probably damaging |
Het |
| Il10ra |
A |
T |
9: 45,167,654 (GRCm39) |
V299D |
probably benign |
Het |
| Il17re |
T |
C |
6: 113,446,665 (GRCm39) |
V472A |
probably damaging |
Het |
| Il22ra1 |
A |
T |
4: 135,478,219 (GRCm39) |
Q430L |
probably damaging |
Het |
| Il23r |
A |
C |
6: 67,400,718 (GRCm39) |
D537E |
probably benign |
Het |
| Inppl1 |
T |
C |
7: 101,472,584 (GRCm39) |
E1237G |
possibly damaging |
Het |
| Ip6k1 |
G |
A |
9: 107,918,195 (GRCm39) |
E77K |
possibly damaging |
Het |
| Klhl35 |
T |
C |
7: 99,119,427 (GRCm39) |
L304P |
probably damaging |
Het |
| Krt78 |
A |
T |
15: 101,855,398 (GRCm39) |
C804* |
probably null |
Het |
| Med15 |
G |
T |
16: 17,491,018 (GRCm39) |
|
probably benign |
Het |
| Mettl25 |
A |
G |
10: 105,661,948 (GRCm39) |
S341P |
probably damaging |
Het |
| Mroh1 |
A |
G |
15: 76,320,249 (GRCm39) |
T1008A |
probably benign |
Het |
| Mug1 |
A |
G |
6: 121,858,780 (GRCm39) |
D1166G |
probably benign |
Het |
| Naca |
T |
A |
10: 127,879,590 (GRCm39) |
|
probably benign |
Het |
| Nagk |
G |
T |
6: 83,776,336 (GRCm39) |
V184F |
probably damaging |
Het |
| Nav1 |
T |
G |
1: 135,400,148 (GRCm39) |
N474T |
probably benign |
Het |
| Ncor2 |
T |
A |
5: 125,102,489 (GRCm39) |
H2089L |
probably benign |
Het |
| Nek6 |
A |
G |
2: 38,472,458 (GRCm39) |
I261V |
probably damaging |
Het |
| Neurod2 |
G |
A |
11: 98,218,558 (GRCm39) |
T202M |
probably damaging |
Het |
| Nlgn2 |
A |
G |
11: 69,716,726 (GRCm39) |
V605A |
probably damaging |
Het |
| Nlrp5 |
A |
C |
7: 23,123,335 (GRCm39) |
E732A |
possibly damaging |
Het |
| Nt5dc1 |
A |
T |
10: 34,189,667 (GRCm39) |
V340D |
probably damaging |
Het |
| Ntn4 |
A |
G |
10: 93,543,234 (GRCm39) |
D320G |
possibly damaging |
Het |
| Or10al3 |
T |
A |
17: 38,012,312 (GRCm39) |
H250Q |
probably damaging |
Het |
| Or10x1 |
A |
T |
1: 174,196,734 (GRCm39) |
I84L |
probably benign |
Het |
| Or52l1 |
A |
G |
7: 104,830,079 (GRCm39) |
I162T |
possibly damaging |
Het |
| Or52z15 |
T |
C |
7: 103,332,750 (GRCm39) |
I265T |
probably damaging |
Het |
| Or5ac25 |
A |
T |
16: 59,182,526 (GRCm39) |
D18E |
probably benign |
Het |
| Osbpl5 |
T |
C |
7: 143,256,918 (GRCm39) |
D404G |
possibly damaging |
Het |
| Pcdhb12 |
T |
A |
18: 37,570,683 (GRCm39) |
W610R |
possibly damaging |
Het |
| Pias2 |
T |
A |
18: 77,185,139 (GRCm39) |
C66* |
probably null |
Het |
| Plec |
T |
A |
15: 76,059,751 (GRCm39) |
E3417D |
probably damaging |
Het |
| Plekhm3 |
CCTGCTGCTGCTGCTGCTGCTGCTGC |
CCTGCTGCTGCTGCTGCTGCTGC |
1: 64,976,940 (GRCm39) |
|
probably benign |
Het |
| Ppp1r12a |
T |
A |
10: 108,034,752 (GRCm39) |
I99N |
probably damaging |
Het |
| Prpf8 |
T |
G |
11: 75,395,570 (GRCm39) |
V1899G |
probably damaging |
Het |
| Prr13 |
C |
A |
15: 102,369,133 (GRCm39) |
|
probably benign |
Het |
| Ptchd4 |
A |
T |
17: 42,814,507 (GRCm39) |
I803L |
probably benign |
Het |
| R3hdm2 |
T |
C |
10: 127,334,337 (GRCm39) |
I947T |
possibly damaging |
Het |
| Raet1d |
A |
G |
10: 22,247,350 (GRCm39) |
D142G |
probably damaging |
Het |
| Rbbp8nl |
C |
T |
2: 179,925,106 (GRCm39) |
R33Q |
probably damaging |
Het |
| Robo1 |
A |
G |
16: 72,757,092 (GRCm39) |
Q351R |
probably null |
Het |
| Rptn |
A |
T |
3: 93,304,017 (GRCm39) |
H450L |
possibly damaging |
Het |
| Scn11a |
T |
A |
9: 119,608,102 (GRCm39) |
K1010* |
probably null |
Het |
| Slc16a10 |
G |
A |
10: 39,932,602 (GRCm39) |
Q33* |
probably null |
Het |
| Slc31a1 |
C |
T |
4: 62,303,842 (GRCm39) |
|
probably benign |
Het |
| Slc34a1 |
A |
T |
13: 55,548,963 (GRCm39) |
K138* |
probably null |
Het |
| Slc6a18 |
T |
A |
13: 73,818,162 (GRCm39) |
E285V |
probably benign |
Het |
| Slco6c1 |
T |
A |
1: 97,000,707 (GRCm39) |
T515S |
probably damaging |
Het |
| Snrnp40 |
T |
A |
4: 130,279,768 (GRCm39) |
S295T |
probably damaging |
Het |
| Snx4 |
A |
T |
16: 33,104,808 (GRCm39) |
Y252F |
possibly damaging |
Het |
| Spata18 |
T |
A |
5: 73,828,482 (GRCm39) |
F348I |
probably damaging |
Het |
| Spef2 |
G |
T |
15: 9,607,463 (GRCm39) |
R1319S |
probably damaging |
Het |
| Tas2r125 |
T |
C |
6: 132,887,139 (GRCm39) |
F176L |
probably benign |
Het |
| Tcp10b |
A |
G |
17: 13,300,513 (GRCm39) |
K399E |
possibly damaging |
Het |
| Tcstv3 |
A |
G |
13: 120,779,260 (GRCm39) |
H53R |
probably damaging |
Het |
| Tnrc6c |
A |
G |
11: 117,613,831 (GRCm39) |
K823R |
probably damaging |
Het |
| Trim31 |
A |
G |
17: 37,212,692 (GRCm39) |
E221G |
probably benign |
Het |
| Trim47 |
T |
A |
11: 115,998,605 (GRCm39) |
Q338L |
probably damaging |
Het |
| Tubgcp6 |
C |
A |
15: 89,000,444 (GRCm39) |
R307L |
possibly damaging |
Het |
| Usp9y |
A |
G |
Y: 1,303,371 (GRCm39) |
|
probably null |
Het |
| Utp20 |
G |
T |
10: 88,588,888 (GRCm39) |
T2427K |
probably benign |
Het |
| Vldlr |
T |
C |
19: 27,218,709 (GRCm39) |
V147A |
probably damaging |
Het |
| Vmn1r115 |
C |
T |
7: 20,578,198 (GRCm39) |
R238H |
probably benign |
Het |
| Vmn1r175 |
C |
A |
7: 23,508,218 (GRCm39) |
R136S |
probably benign |
Het |
| Vmn1r53 |
A |
G |
6: 90,201,268 (GRCm39) |
S19P |
possibly damaging |
Het |
| Vwa5b2 |
G |
T |
16: 20,423,582 (GRCm39) |
S1165I |
possibly damaging |
Het |
| Zfp362 |
G |
T |
4: 128,684,069 (GRCm39) |
P13T |
probably damaging |
Het |
| Zfp825 |
A |
G |
13: 74,629,064 (GRCm39) |
C151R |
probably damaging |
Het |
|
| Other mutations in Mug2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00708:Mug2
|
APN |
6 |
122,024,446 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
IGL00957:Mug2
|
APN |
6 |
122,017,613 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01314:Mug2
|
APN |
6 |
122,058,238 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
IGL01338:Mug2
|
APN |
6 |
122,026,587 (GRCm39) |
splice site |
probably benign |
|
|
IGL01477:Mug2
|
APN |
6 |
122,058,643 (GRCm39) |
splice site |
probably benign |
|
|
IGL01926:Mug2
|
APN |
6 |
122,013,063 (GRCm39) |
splice site |
probably benign |
|
|
IGL02019:Mug2
|
APN |
6 |
122,024,394 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL02305:Mug2
|
APN |
6 |
122,013,015 (GRCm39) |
missense |
probably benign |
|
|
IGL02310:Mug2
|
APN |
6 |
122,036,082 (GRCm39) |
splice site |
probably benign |
|
|
IGL02484:Mug2
|
APN |
6 |
122,049,712 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02516:Mug2
|
APN |
6 |
122,047,802 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02531:Mug2
|
APN |
6 |
122,049,730 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02666:Mug2
|
APN |
6 |
122,058,285 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02936:Mug2
|
APN |
6 |
122,058,346 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0114:Mug2
|
UTSW |
6 |
122,017,607 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0119:Mug2
|
UTSW |
6 |
122,013,022 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0123:Mug2
|
UTSW |
6 |
122,051,673 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R0144:Mug2
|
UTSW |
6 |
122,047,970 (GRCm39) |
splice site |
probably benign |
|
|
R0225:Mug2
|
UTSW |
6 |
122,051,673 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R0514:Mug2
|
UTSW |
6 |
122,058,558 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0763:Mug2
|
UTSW |
6 |
122,052,253 (GRCm39) |
missense |
probably benign |
|
|
R0959:Mug2
|
UTSW |
6 |
122,062,454 (GRCm39) |
missense |
probably benign |
0.33 |
|
R1104:Mug2
|
UTSW |
6 |
122,036,014 (GRCm39) |
missense |
probably benign |
|
|
R1239:Mug2
|
UTSW |
6 |
122,058,637 (GRCm39) |
splice site |
probably benign |
|
|
R1318:Mug2
|
UTSW |
6 |
122,054,361 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1460:Mug2
|
UTSW |
6 |
122,017,492 (GRCm39) |
splice site |
probably benign |
|
|
R1706:Mug2
|
UTSW |
6 |
122,013,191 (GRCm39) |
splice site |
probably benign |
|
|
R1761:Mug2
|
UTSW |
6 |
122,051,664 (GRCm39) |
missense |
probably benign |
0.20 |
|
R1913:Mug2
|
UTSW |
6 |
122,047,829 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1943:Mug2
|
UTSW |
6 |
122,056,598 (GRCm39) |
missense |
probably benign |
|
|
R2054:Mug2
|
UTSW |
6 |
122,054,451 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2060:Mug2
|
UTSW |
6 |
122,056,571 (GRCm39) |
missense |
probably benign |
|
|
R2420:Mug2
|
UTSW |
6 |
122,060,419 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2432:Mug2
|
UTSW |
6 |
122,061,335 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R2916:Mug2
|
UTSW |
6 |
122,051,683 (GRCm39) |
splice site |
probably null |
|
|
R2918:Mug2
|
UTSW |
6 |
122,051,683 (GRCm39) |
splice site |
probably null |
|
|
R3423:Mug2
|
UTSW |
6 |
122,024,465 (GRCm39) |
splice site |
probably benign |
|
|
R3834:Mug2
|
UTSW |
6 |
122,026,746 (GRCm39) |
critical splice donor site |
probably null |
|
|
R3902:Mug2
|
UTSW |
6 |
122,052,526 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3941:Mug2
|
UTSW |
6 |
122,040,522 (GRCm39) |
missense |
probably benign |
|
|
R4227:Mug2
|
UTSW |
6 |
122,017,691 (GRCm39) |
missense |
probably benign |
0.10 |
|
R4284:Mug2
|
UTSW |
6 |
122,040,632 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4287:Mug2
|
UTSW |
6 |
122,040,632 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4377:Mug2
|
UTSW |
6 |
122,047,966 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4419:Mug2
|
UTSW |
6 |
122,056,589 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4498:Mug2
|
UTSW |
6 |
122,059,711 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4566:Mug2
|
UTSW |
6 |
122,056,597 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4690:Mug2
|
UTSW |
6 |
122,013,255 (GRCm39) |
missense |
probably benign |
|
|
R4732:Mug2
|
UTSW |
6 |
122,048,831 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4733:Mug2
|
UTSW |
6 |
122,048,831 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4741:Mug2
|
UTSW |
6 |
122,056,572 (GRCm39) |
missense |
probably benign |
|
|
R4888:Mug2
|
UTSW |
6 |
122,058,154 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5199:Mug2
|
UTSW |
6 |
122,017,619 (GRCm39) |
missense |
probably benign |
|
|
R5347:Mug2
|
UTSW |
6 |
122,058,551 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5457:Mug2
|
UTSW |
6 |
122,026,688 (GRCm39) |
nonsense |
probably null |
|
|
R5495:Mug2
|
UTSW |
6 |
122,056,609 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R5509:Mug2
|
UTSW |
6 |
122,061,340 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R6006:Mug2
|
UTSW |
6 |
122,060,459 (GRCm39) |
missense |
probably null |
0.98 |
|
R6180:Mug2
|
UTSW |
6 |
122,056,565 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6184:Mug2
|
UTSW |
6 |
122,014,005 (GRCm39) |
missense |
probably benign |
|
|
R6199:Mug2
|
UTSW |
6 |
122,024,398 (GRCm39) |
missense |
probably benign |
0.05 |
|
R6262:Mug2
|
UTSW |
6 |
122,052,214 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6416:Mug2
|
UTSW |
6 |
122,059,713 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6548:Mug2
|
UTSW |
6 |
122,024,401 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6703:Mug2
|
UTSW |
6 |
122,055,653 (GRCm39) |
missense |
probably benign |
0.25 |
|
R7106:Mug2
|
UTSW |
6 |
122,059,680 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7131:Mug2
|
UTSW |
6 |
122,052,206 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7372:Mug2
|
UTSW |
6 |
122,060,425 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R7379:Mug2
|
UTSW |
6 |
122,024,446 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R7419:Mug2
|
UTSW |
6 |
122,017,529 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R7423:Mug2
|
UTSW |
6 |
122,056,685 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7581:Mug2
|
UTSW |
6 |
122,040,670 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7582:Mug2
|
UTSW |
6 |
122,056,603 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7672:Mug2
|
UTSW |
6 |
122,017,678 (GRCm39) |
missense |
probably benign |
0.37 |
|
R7713:Mug2
|
UTSW |
6 |
122,055,754 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R7759:Mug2
|
UTSW |
6 |
122,058,317 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7834:Mug2
|
UTSW |
6 |
122,013,241 (GRCm39) |
missense |
probably benign |
|
|
R7850:Mug2
|
UTSW |
6 |
122,052,170 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8029:Mug2
|
UTSW |
6 |
122,058,504 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R8127:Mug2
|
UTSW |
6 |
122,052,567 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8335:Mug2
|
UTSW |
6 |
122,017,543 (GRCm39) |
missense |
probably benign |
|
|
R8348:Mug2
|
UTSW |
6 |
122,049,192 (GRCm39) |
nonsense |
probably null |
|
|
R8557:Mug2
|
UTSW |
6 |
122,040,660 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8798:Mug2
|
UTSW |
6 |
122,058,569 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8823:Mug2
|
UTSW |
6 |
122,040,648 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R9029:Mug2
|
UTSW |
6 |
122,061,328 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9153:Mug2
|
UTSW |
6 |
122,017,627 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R9185:Mug2
|
UTSW |
6 |
122,054,442 (GRCm39) |
missense |
probably benign |
0.06 |
|
R9186:Mug2
|
UTSW |
6 |
122,052,248 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9418:Mug2
|
UTSW |
6 |
122,017,700 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9464:Mug2
|
UTSW |
6 |
122,028,690 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9622:Mug2
|
UTSW |
6 |
122,028,751 (GRCm39) |
missense |
probably benign |
0.29 |
|
Z1177:Mug2
|
UTSW |
6 |
122,014,080 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- AACATGCTGTCCTTCCATGG -3'
(R):5'- CAAAGCCCCTAGATCTGCAG -3'
Sequencing Primer
(F):5'- GTCCTTCCATGGTGAAAATTTTTC -3'
(R):5'- AGATCTGCAGTGCCTCCTTGG -3'
|
| Posted On |
2014-06-30 |
Incidental Mutation