Incidental Mutation 'R0514:Mug2'
| ID |
48099 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Mug2
|
| Ensembl Gene |
ENSMUSG00000030131 |
| Gene Name |
murinoglobulin 2 |
| Synonyms |
|
| MMRRC Submission |
038708-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.054)
|
| Stock # |
R0514 (G1)
|
| Quality Score |
176 |
|
Status
|
Not validated
|
| Chromosome |
6 |
| Chromosomal Location |
122006761-122085965 bp(+) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 122081599 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Leucine to Proline
at position 1320
(L1320P)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000080469
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000081777]
|
| AlphaFold |
P28666 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000081777
AA Change: L1320P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000080469
Gene: ENSMUSG00000030131
AA Change: L1320P
| 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: 99.2%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 94.1%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 91 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acpp |
T |
A |
9: 104,319,978 (GRCm38) |
Y154F |
probably damaging |
Het |
| Acsl6 |
A |
T |
11: 54,350,580 (GRCm38) |
D579V |
probably damaging |
Het |
| Adamts18 |
C |
T |
8: 113,738,769 (GRCm38) |
|
probably null |
Het |
| Adamts20 |
A |
T |
15: 94,270,376 (GRCm38) |
V1882D |
probably damaging |
Het |
| Add3 |
A |
T |
19: 53,236,843 (GRCm38) |
K465* |
probably null |
Het |
| Ago1 |
T |
G |
4: 126,439,595 (GRCm38) |
I524L |
probably benign |
Het |
| Akr1c18 |
A |
G |
13: 4,137,191 (GRCm38) |
M208T |
probably benign |
Het |
| Anapc1 |
C |
A |
2: 128,632,655 (GRCm38) |
L1413F |
probably damaging |
Het |
| Arid4b |
A |
T |
13: 14,184,317 (GRCm38) |
D646V |
probably damaging |
Het |
| Arnt2 |
T |
C |
7: 84,304,859 (GRCm38) |
E261G |
probably benign |
Het |
| Bccip |
C |
T |
7: 133,719,130 (GRCm38) |
T211I |
possibly damaging |
Het |
| Bsn |
T |
C |
9: 108,125,782 (GRCm38) |
S475G |
probably benign |
Het |
| Cdh26 |
G |
A |
2: 178,466,828 (GRCm38) |
|
probably null |
Het |
| Ceacam2 |
A |
G |
7: 25,520,931 (GRCm38) |
F414S |
probably benign |
Het |
| Cfb |
T |
C |
17: 34,860,898 (GRCm38) |
R172G |
probably damaging |
Het |
| Cntnap5b |
A |
C |
1: 99,772,786 (GRCm38) |
T8P |
probably benign |
Het |
| Cpne9 |
A |
T |
6: 113,290,013 (GRCm38) |
I136L |
probably damaging |
Het |
| Crtc1 |
A |
T |
8: 70,402,429 (GRCm38) |
|
probably null |
Het |
| Dcdc2a |
A |
T |
13: 25,119,386 (GRCm38) |
H300L |
probably benign |
Het |
| Dhdh |
C |
T |
7: 45,488,706 (GRCm38) |
V20M |
probably benign |
Het |
| Dhx34 |
T |
C |
7: 16,210,537 (GRCm38) |
Q584R |
probably benign |
Het |
| Dis3l2 |
A |
G |
1: 87,047,092 (GRCm38) |
Y701C |
probably damaging |
Het |
| Dmrt2 |
T |
C |
19: 25,675,655 (GRCm38) |
|
probably null |
Het |
| Dnah5 |
A |
G |
15: 28,366,321 (GRCm38) |
T2727A |
probably damaging |
Het |
| Dopey1 |
A |
G |
9: 86,520,734 (GRCm38) |
E1329G |
probably damaging |
Het |
| Evpl |
A |
G |
11: 116,223,291 (GRCm38) |
V1191A |
probably damaging |
Het |
| Fam198a |
A |
G |
9: 121,978,352 (GRCm38) |
T521A |
possibly damaging |
Het |
| Fgfr1op |
A |
G |
17: 8,191,434 (GRCm38) |
N342S |
possibly damaging |
Het |
| Fhl4 |
T |
C |
10: 85,098,386 (GRCm38) |
D177G |
probably damaging |
Het |
| Heg1 |
A |
G |
16: 33,726,756 (GRCm38) |
T662A |
possibly damaging |
Het |
| Ifih1 |
A |
G |
2: 62,623,391 (GRCm38) |
|
probably null |
Het |
| Il13 |
T |
C |
11: 53,632,518 (GRCm38) |
R87G |
possibly damaging |
Het |
| Kcnc3 |
T |
A |
7: 44,595,928 (GRCm38) |
Y547* |
probably null |
Het |
| Krt81 |
C |
A |
15: 101,463,627 (GRCm38) |
R24L |
possibly damaging |
Het |
| Lama1 |
G |
A |
17: 67,764,698 (GRCm38) |
G860D |
probably benign |
Het |
| Lmo7 |
A |
T |
14: 101,896,559 (GRCm38) |
K447I |
probably damaging |
Het |
| Lmo7 |
T |
C |
14: 101,887,173 (GRCm38) |
L356P |
probably damaging |
Het |
| Lrp2bp |
A |
G |
8: 46,011,958 (GRCm38) |
H38R |
probably damaging |
Het |
| Magi3 |
G |
A |
3: 104,015,022 (GRCm38) |
P1460S |
probably damaging |
Het |
| Megf8 |
T |
A |
7: 25,364,303 (GRCm38) |
C2695S |
possibly damaging |
Het |
| Mrgprb2 |
T |
G |
7: 48,551,970 (GRCm38) |
S336R |
probably benign |
Het |
| Mrgprx2 |
C |
T |
7: 48,482,964 (GRCm38) |
M1I |
probably null |
Het |
| Noxred1 |
A |
G |
12: 87,227,064 (GRCm38) |
S68P |
probably benign |
Het |
| Olfr504 |
T |
A |
7: 108,565,672 (GRCm38) |
Y41F |
probably damaging |
Het |
| Olfr561 |
T |
A |
7: 102,775,332 (GRCm38) |
H269Q |
probably benign |
Het |
| Os9 |
C |
T |
10: 127,119,639 (GRCm38) |
C123Y |
probably damaging |
Het |
| Ostf1 |
T |
A |
19: 18,596,359 (GRCm38) |
T42S |
probably benign |
Het |
| Parg |
C |
A |
14: 32,254,560 (GRCm38) |
T186K |
possibly damaging |
Het |
| Pcnx |
T |
A |
12: 81,995,110 (GRCm38) |
M2172K |
probably benign |
Het |
| Pip4k2a |
A |
G |
2: 18,845,936 (GRCm38) |
I360T |
probably damaging |
Het |
| Pkn2 |
T |
C |
3: 142,810,458 (GRCm38) |
D568G |
possibly damaging |
Het |
| Plch2 |
A |
G |
4: 154,998,886 (GRCm38) |
S431P |
probably damaging |
Het |
| Prl8a6 |
A |
T |
13: 27,433,007 (GRCm38) |
C233* |
probably null |
Het |
| Prox1 |
G |
A |
1: 190,161,456 (GRCm38) |
T264I |
probably damaging |
Het |
| Prr5 |
A |
G |
15: 84,702,766 (GRCm38) |
N248S |
probably benign |
Het |
| Psip1 |
A |
C |
4: 83,460,037 (GRCm38) |
S407R |
probably damaging |
Het |
| Rab32 |
A |
T |
10: 10,550,896 (GRCm38) |
V102E |
probably damaging |
Het |
| Rap1gap2 |
T |
G |
11: 74,388,854 (GRCm38) |
K687Q |
possibly damaging |
Het |
| Rbak |
A |
T |
5: 143,173,414 (GRCm38) |
V628E |
probably damaging |
Het |
| Rnf148 |
T |
C |
6: 23,654,793 (GRCm38) |
E68G |
possibly damaging |
Het |
| Rnf212 |
A |
T |
5: 108,749,442 (GRCm38) |
S3T |
probably damaging |
Het |
| Rrad |
T |
G |
8: 104,628,627 (GRCm38) |
I250L |
probably benign |
Het |
| Sall4 |
T |
C |
2: 168,755,705 (GRCm38) |
H405R |
probably damaging |
Het |
| Scn9a |
T |
C |
2: 66,483,678 (GRCm38) |
R1888G |
probably damaging |
Het |
| Setd5 |
G |
T |
6: 113,119,437 (GRCm38) |
E535* |
probably null |
Het |
| Slc20a1 |
C |
T |
2: 129,199,891 (GRCm38) |
S58L |
probably damaging |
Het |
| Slc31a1 |
A |
G |
4: 62,385,604 (GRCm38) |
|
probably benign |
Het |
| Slc38a11 |
G |
T |
2: 65,316,865 (GRCm38) |
Q423K |
probably benign |
Het |
| Snrpd1 |
A |
T |
18: 10,626,846 (GRCm38) |
T38S |
possibly damaging |
Het |
| Taar4 |
A |
G |
10: 23,960,882 (GRCm38) |
D130G |
probably damaging |
Het |
| Tfb2m |
C |
T |
1: 179,531,304 (GRCm38) |
R338H |
probably benign |
Het |
| Tm2d2 |
A |
G |
8: 25,022,726 (GRCm38) |
I197V |
possibly damaging |
Het |
| Tmem132a |
C |
T |
19: 10,858,991 (GRCm38) |
G725D |
probably damaging |
Het |
| Tmem67 |
T |
C |
4: 12,089,317 (GRCm38) |
T38A |
probably benign |
Het |
| Tmprss15 |
A |
T |
16: 78,968,267 (GRCm38) |
S816T |
probably benign |
Het |
| Tnfrsf11a |
A |
G |
1: 105,826,992 (GRCm38) |
E263G |
probably damaging |
Het |
| Tnfrsf17 |
C |
T |
16: 11,315,327 (GRCm38) |
L90F |
probably benign |
Het |
| Tpr |
A |
G |
1: 150,402,273 (GRCm38) |
K117E |
possibly damaging |
Het |
| Trim43a |
C |
T |
9: 88,584,336 (GRCm38) |
Q5* |
probably null |
Het |
| Ubn1 |
A |
T |
16: 5,073,071 (GRCm38) |
D498V |
probably damaging |
Het |
| Vipr1 |
T |
A |
9: 121,658,049 (GRCm38) |
C63S |
probably damaging |
Het |
| Vmn1r237 |
T |
A |
17: 21,314,670 (GRCm38) |
H218Q |
possibly damaging |
Het |
| Vmn2r100 |
C |
A |
17: 19,522,120 (GRCm38) |
P252Q |
possibly damaging |
Het |
| Vmn2r95 |
T |
C |
17: 18,451,582 (GRCm38) |
V527A |
probably benign |
Het |
| Vmn2r97 |
A |
T |
17: 18,914,472 (GRCm38) |
T51S |
probably benign |
Het |
| Vwa8 |
G |
A |
14: 78,947,189 (GRCm38) |
V376I |
probably benign |
Het |
| Wdfy4 |
T |
A |
14: 33,080,775 (GRCm38) |
T1838S |
probably benign |
Het |
| Zcwpw1 |
A |
T |
5: 137,796,683 (GRCm38) |
E47V |
probably benign |
Het |
| Zeb2 |
T |
C |
2: 45,002,647 (GRCm38) |
E130G |
possibly damaging |
Het |
| Zfp111 |
A |
G |
7: 24,199,143 (GRCm38) |
Y348H |
probably damaging |
Het |
| Zfp53 |
T |
C |
17: 21,509,009 (GRCm38) |
S435P |
probably damaging |
Het |
|
| Other mutations in Mug2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00708:Mug2
|
APN |
6 |
122,047,487 (GRCm38) |
missense |
possibly damaging |
0.83 |
|
IGL00957:Mug2
|
APN |
6 |
122,040,654 (GRCm38) |
missense |
probably damaging |
0.99 |
|
IGL01314:Mug2
|
APN |
6 |
122,081,279 (GRCm38) |
missense |
possibly damaging |
0.62 |
|
IGL01338:Mug2
|
APN |
6 |
122,049,628 (GRCm38) |
splice site |
probably benign |
|
|
IGL01477:Mug2
|
APN |
6 |
122,081,684 (GRCm38) |
splice site |
probably benign |
|
|
IGL01926:Mug2
|
APN |
6 |
122,036,104 (GRCm38) |
splice site |
probably benign |
|
|
IGL02019:Mug2
|
APN |
6 |
122,047,435 (GRCm38) |
missense |
probably benign |
0.02 |
|
IGL02305:Mug2
|
APN |
6 |
122,036,056 (GRCm38) |
missense |
probably benign |
|
|
IGL02310:Mug2
|
APN |
6 |
122,059,123 (GRCm38) |
splice site |
probably benign |
|
|
IGL02484:Mug2
|
APN |
6 |
122,072,753 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02516:Mug2
|
APN |
6 |
122,070,843 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02531:Mug2
|
APN |
6 |
122,072,771 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02666:Mug2
|
APN |
6 |
122,081,326 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02936:Mug2
|
APN |
6 |
122,081,387 (GRCm38) |
critical splice donor site |
probably null |
|
|
R0114:Mug2
|
UTSW |
6 |
122,040,648 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0119:Mug2
|
UTSW |
6 |
122,036,063 (GRCm38) |
missense |
probably benign |
0.00 |
|
R0123:Mug2
|
UTSW |
6 |
122,074,714 (GRCm38) |
missense |
possibly damaging |
0.89 |
|
R0144:Mug2
|
UTSW |
6 |
122,071,011 (GRCm38) |
splice site |
probably benign |
|
|
R0225:Mug2
|
UTSW |
6 |
122,074,714 (GRCm38) |
missense |
possibly damaging |
0.89 |
|
R0763:Mug2
|
UTSW |
6 |
122,075,294 (GRCm38) |
missense |
probably benign |
|
|
R0959:Mug2
|
UTSW |
6 |
122,085,495 (GRCm38) |
missense |
probably benign |
0.33 |
|
R1104:Mug2
|
UTSW |
6 |
122,059,055 (GRCm38) |
missense |
probably benign |
|
|
R1239:Mug2
|
UTSW |
6 |
122,081,678 (GRCm38) |
splice site |
probably benign |
|
|
R1318:Mug2
|
UTSW |
6 |
122,077,402 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1460:Mug2
|
UTSW |
6 |
122,040,533 (GRCm38) |
splice site |
probably benign |
|
|
R1706:Mug2
|
UTSW |
6 |
122,036,232 (GRCm38) |
splice site |
probably benign |
|
|
R1761:Mug2
|
UTSW |
6 |
122,074,705 (GRCm38) |
missense |
probably benign |
0.20 |
|
R1901:Mug2
|
UTSW |
6 |
122,071,842 (GRCm38) |
missense |
probably benign |
0.02 |
|
R1913:Mug2
|
UTSW |
6 |
122,070,870 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1943:Mug2
|
UTSW |
6 |
122,079,639 (GRCm38) |
missense |
probably benign |
|
|
R2054:Mug2
|
UTSW |
6 |
122,077,492 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2060:Mug2
|
UTSW |
6 |
122,079,612 (GRCm38) |
missense |
probably benign |
|
|
R2420:Mug2
|
UTSW |
6 |
122,083,460 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2432:Mug2
|
UTSW |
6 |
122,084,376 (GRCm38) |
missense |
possibly damaging |
0.93 |
|
R2916:Mug2
|
UTSW |
6 |
122,074,724 (GRCm38) |
splice site |
probably null |
|
|
R2918:Mug2
|
UTSW |
6 |
122,074,724 (GRCm38) |
splice site |
probably null |
|
|
R3423:Mug2
|
UTSW |
6 |
122,047,506 (GRCm38) |
splice site |
probably benign |
|
|
R3834:Mug2
|
UTSW |
6 |
122,049,787 (GRCm38) |
critical splice donor site |
probably null |
|
|
R3902:Mug2
|
UTSW |
6 |
122,075,567 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R3941:Mug2
|
UTSW |
6 |
122,063,563 (GRCm38) |
missense |
probably benign |
|
|
R4227:Mug2
|
UTSW |
6 |
122,040,732 (GRCm38) |
missense |
probably benign |
0.10 |
|
R4284:Mug2
|
UTSW |
6 |
122,063,673 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4287:Mug2
|
UTSW |
6 |
122,063,673 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4377:Mug2
|
UTSW |
6 |
122,071,007 (GRCm38) |
critical splice donor site |
probably null |
|
|
R4419:Mug2
|
UTSW |
6 |
122,079,630 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4498:Mug2
|
UTSW |
6 |
122,082,752 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R4566:Mug2
|
UTSW |
6 |
122,079,638 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4690:Mug2
|
UTSW |
6 |
122,036,296 (GRCm38) |
missense |
probably benign |
|
|
R4732:Mug2
|
UTSW |
6 |
122,071,872 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R4733:Mug2
|
UTSW |
6 |
122,071,872 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R4741:Mug2
|
UTSW |
6 |
122,079,613 (GRCm38) |
missense |
probably benign |
|
|
R4888:Mug2
|
UTSW |
6 |
122,081,195 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5199:Mug2
|
UTSW |
6 |
122,040,660 (GRCm38) |
missense |
probably benign |
|
|
R5347:Mug2
|
UTSW |
6 |
122,081,592 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5457:Mug2
|
UTSW |
6 |
122,049,729 (GRCm38) |
nonsense |
probably null |
|
|
R5495:Mug2
|
UTSW |
6 |
122,079,650 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R5509:Mug2
|
UTSW |
6 |
122,084,381 (GRCm38) |
missense |
possibly damaging |
0.84 |
|
R6006:Mug2
|
UTSW |
6 |
122,083,500 (GRCm38) |
missense |
probably null |
0.98 |
|
R6180:Mug2
|
UTSW |
6 |
122,079,606 (GRCm38) |
missense |
probably benign |
0.01 |
|
R6184:Mug2
|
UTSW |
6 |
122,037,046 (GRCm38) |
missense |
probably benign |
|
|
R6199:Mug2
|
UTSW |
6 |
122,047,439 (GRCm38) |
missense |
probably benign |
0.05 |
|
R6262:Mug2
|
UTSW |
6 |
122,075,255 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6416:Mug2
|
UTSW |
6 |
122,082,754 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6548:Mug2
|
UTSW |
6 |
122,047,442 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6703:Mug2
|
UTSW |
6 |
122,078,694 (GRCm38) |
missense |
probably benign |
0.25 |
|
R7106:Mug2
|
UTSW |
6 |
122,082,721 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7131:Mug2
|
UTSW |
6 |
122,075,247 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7372:Mug2
|
UTSW |
6 |
122,083,466 (GRCm38) |
missense |
possibly damaging |
0.88 |
|
R7379:Mug2
|
UTSW |
6 |
122,047,487 (GRCm38) |
missense |
possibly damaging |
0.83 |
|
R7419:Mug2
|
UTSW |
6 |
122,040,570 (GRCm38) |
missense |
possibly damaging |
0.86 |
|
R7423:Mug2
|
UTSW |
6 |
122,079,726 (GRCm38) |
missense |
probably benign |
0.00 |
|
R7581:Mug2
|
UTSW |
6 |
122,063,711 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7582:Mug2
|
UTSW |
6 |
122,079,644 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R7672:Mug2
|
UTSW |
6 |
122,040,719 (GRCm38) |
missense |
probably benign |
0.37 |
|
R7713:Mug2
|
UTSW |
6 |
122,078,795 (GRCm38) |
missense |
possibly damaging |
0.83 |
|
R7759:Mug2
|
UTSW |
6 |
122,081,358 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7834:Mug2
|
UTSW |
6 |
122,036,282 (GRCm38) |
missense |
probably benign |
|
|
R7850:Mug2
|
UTSW |
6 |
122,075,211 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8029:Mug2
|
UTSW |
6 |
122,081,545 (GRCm38) |
critical splice acceptor site |
probably null |
|
|
R8127:Mug2
|
UTSW |
6 |
122,075,608 (GRCm38) |
missense |
probably benign |
0.01 |
|
R8335:Mug2
|
UTSW |
6 |
122,040,584 (GRCm38) |
missense |
probably benign |
|
|
R8348:Mug2
|
UTSW |
6 |
122,072,233 (GRCm38) |
nonsense |
probably null |
|
|
R8557:Mug2
|
UTSW |
6 |
122,063,701 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R8798:Mug2
|
UTSW |
6 |
122,081,610 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8823:Mug2
|
UTSW |
6 |
122,063,689 (GRCm38) |
missense |
possibly damaging |
0.89 |
|
R9029:Mug2
|
UTSW |
6 |
122,084,369 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9153:Mug2
|
UTSW |
6 |
122,040,668 (GRCm38) |
missense |
possibly damaging |
0.71 |
|
R9185:Mug2
|
UTSW |
6 |
122,077,483 (GRCm38) |
missense |
probably benign |
0.06 |
|
R9186:Mug2
|
UTSW |
6 |
122,075,289 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R9418:Mug2
|
UTSW |
6 |
122,040,741 (GRCm38) |
missense |
probably benign |
0.00 |
|
R9464:Mug2
|
UTSW |
6 |
122,051,731 (GRCm38) |
missense |
probably benign |
0.01 |
|
R9622:Mug2
|
UTSW |
6 |
122,051,792 (GRCm38) |
missense |
probably benign |
0.29 |
|
Z1177:Mug2
|
UTSW |
6 |
122,037,121 (GRCm38) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- CTGTGAGCCTTCTTCCCCAAAATGG -3'
(R):5'- ACAGCCTGATAGTAGCTGAGGGAC -3'
Sequencing Primer
(F):5'- ATGGAAAGTCTGACTTTGCCTACC -3'
(R):5'- TCATACAGGGACAAGACAGATTC -3'
|
| Posted On |
2013-06-12 |
Incidental Mutation