Incidental Mutation 'R1476:Megf6'
| ID |
164052 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Megf6
|
| Ensembl Gene |
ENSMUSG00000057751 |
| Gene Name |
multiple EGF-like-domains 6 |
| Synonyms |
2600001P17Rik, Egfl3 |
| MMRRC Submission |
039529-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R1476 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
4 |
| Chromosomal Location |
154255187-154360170 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to T
at 154261578 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Leucine
at position 68
(V68L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000030897
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000030897]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000030897
AA Change: V68L
PolyPhen 2
Score 0.391 (Sensitivity: 0.90; Specificity: 0.89)
|
| SMART Domains |
Protein: ENSMUSP00000030897
Gene: ENSMUSG00000057751
AA Change: V68L
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
28 |
N/A |
INTRINSIC |
|
EGF_CA
|
122 |
162 |
1.54e-6 |
SMART |
|
EGF_CA
|
163 |
203 |
2.08e-12 |
SMART |
|
EGF
|
207 |
245 |
5.4e-2 |
SMART |
|
EGF
|
249 |
286 |
2.39e-3 |
SMART |
|
EGF_CA
|
287 |
327 |
4.96e-10 |
SMART |
|
EGF
|
336 |
373 |
1.64e-1 |
SMART |
|
EGF
|
377 |
413 |
1.99e1 |
SMART |
|
EGF_CA
|
414 |
454 |
7.4e-9 |
SMART |
|
EGF
|
521 |
554 |
4.26e0 |
SMART |
|
EGF_Lam
|
570 |
609 |
1.19e-3 |
SMART |
|
EGF_like
|
613 |
652 |
5.29e-1 |
SMART |
|
EGF
|
642 |
685 |
2.2e1 |
SMART |
|
EGF_Lam
|
656 |
697 |
1.04e-3 |
SMART |
|
EGF
|
687 |
730 |
1.59e1 |
SMART |
|
EGF_like
|
701 |
742 |
2.27e0 |
SMART |
|
EGF_Lam
|
746 |
784 |
1.33e-1 |
SMART |
|
EGF
|
783 |
816 |
2.85e-1 |
SMART |
|
EGF_Lam
|
832 |
871 |
3.88e-3 |
SMART |
|
EGF_Lam
|
875 |
915 |
3.25e-5 |
SMART |
|
EGF
|
914 |
946 |
4.7e-2 |
SMART |
|
EGF_like
|
962 |
1001 |
1.69e-1 |
SMART |
|
EGF
|
1000 |
1032 |
7.02e-1 |
SMART |
|
EGF_Lam
|
1048 |
1087 |
3.1e-2 |
SMART |
|
EGF
|
1077 |
1118 |
7.53e-1 |
SMART |
|
EGF_like
|
1091 |
1130 |
5.59e-1 |
SMART |
|
EGF
|
1129 |
1161 |
5.04e-2 |
SMART |
|
EGF_Lam
|
1177 |
1216 |
2.94e-3 |
SMART |
|
EGF
|
1206 |
1248 |
1.87e1 |
SMART |
|
EGF_Lam
|
1220 |
1260 |
3.1e-2 |
SMART |
|
EGF
|
1259 |
1291 |
1.73e0 |
SMART |
|
EGF
|
1302 |
1334 |
6.55e-1 |
SMART |
|
EGF
|
1345 |
1377 |
4.39e-2 |
SMART |
|
EGF_Lam
|
1393 |
1432 |
7.64e-2 |
SMART |
|
EGF_Lam
|
1436 |
1475 |
2.64e-5 |
SMART |
|
EGF_like
|
1465 |
1506 |
4.2e1 |
SMART |
|
EGF_Lam
|
1479 |
1518 |
1.19e-3 |
SMART |
|
EGF
|
1517 |
1549 |
1.84e1 |
SMART |
|
| Meta Mutation Damage Score |
0.0895 |
| Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.4%
- 10x: 96.5%
- 20x: 93.1%
|
| Validation Efficiency |
95% (80/84) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 78 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2310033P09Rik |
A |
G |
11: 59,099,528 (GRCm39) |
|
probably benign |
Het |
| A730015C16Rik |
G |
A |
4: 108,705,205 (GRCm39) |
V40M |
probably damaging |
Het |
| Abcg2 |
A |
G |
6: 58,655,322 (GRCm39) |
D419G |
probably benign |
Het |
| Adamts17 |
A |
C |
7: 66,725,091 (GRCm39) |
E777A |
probably damaging |
Het |
| Ak1 |
A |
G |
2: 32,523,478 (GRCm39) |
K166R |
probably benign |
Het |
| Ankrd12 |
T |
C |
17: 66,293,300 (GRCm39) |
K711R |
probably damaging |
Het |
| Ate1 |
A |
T |
7: 130,020,301 (GRCm39) |
|
probably null |
Het |
| Atp5f1a |
A |
G |
18: 77,869,625 (GRCm39) |
H519R |
probably benign |
Het |
| Best1 |
G |
T |
19: 9,967,853 (GRCm39) |
Y284* |
probably null |
Het |
| C2cd6 |
A |
G |
1: 59,115,887 (GRCm39) |
|
probably benign |
Het |
| Casz1 |
G |
T |
4: 149,030,628 (GRCm39) |
V1216L |
probably benign |
Het |
| Cdc42bpg |
A |
G |
19: 6,363,812 (GRCm39) |
D493G |
probably damaging |
Het |
| Ces2f |
A |
G |
8: 105,679,134 (GRCm39) |
D317G |
possibly damaging |
Het |
| Chst15 |
A |
T |
7: 131,872,002 (GRCm39) |
M93K |
possibly damaging |
Het |
| Cntnap5a |
T |
C |
1: 115,828,750 (GRCm39) |
L58P |
probably damaging |
Het |
| Crip3 |
T |
C |
17: 46,741,702 (GRCm39) |
|
probably benign |
Het |
| Csmd2 |
G |
A |
4: 128,380,794 (GRCm39) |
E2117K |
probably benign |
Het |
| Cstf3 |
A |
G |
2: 104,478,564 (GRCm39) |
D212G |
possibly damaging |
Het |
| Cttnbp2 |
T |
C |
6: 18,434,220 (GRCm39) |
K546R |
probably damaging |
Het |
| Cubn |
A |
G |
2: 13,480,931 (GRCm39) |
I308T |
probably benign |
Het |
| Cxcl9 |
T |
A |
5: 92,472,972 (GRCm39) |
D75V |
probably damaging |
Het |
| Dcdc5 |
C |
T |
2: 106,188,977 (GRCm39) |
|
noncoding transcript |
Het |
| Defa30 |
C |
A |
8: 21,624,752 (GRCm39) |
T25K |
possibly damaging |
Het |
| Dock7 |
A |
T |
4: 98,967,672 (GRCm39) |
H239Q |
possibly damaging |
Het |
| Dpp4 |
A |
G |
2: 62,178,245 (GRCm39) |
V629A |
possibly damaging |
Het |
| Fam83a |
T |
C |
15: 57,873,341 (GRCm39) |
M390T |
probably benign |
Het |
| Fem1c |
A |
G |
18: 46,657,552 (GRCm39) |
L54P |
probably damaging |
Het |
| Fntb |
T |
A |
12: 76,957,007 (GRCm39) |
M282K |
probably benign |
Het |
| Galnt2l |
A |
G |
8: 122,996,323 (GRCm39) |
|
probably benign |
Het |
| Gm11099 |
G |
A |
2: 58,749,482 (GRCm39) |
|
probably benign |
Het |
| Gm1527 |
T |
C |
3: 28,980,705 (GRCm39) |
S602P |
probably benign |
Het |
| Gm5478 |
T |
A |
15: 101,553,080 (GRCm39) |
I331F |
probably damaging |
Het |
| Gm7853 |
C |
A |
14: 35,811,540 (GRCm39) |
|
noncoding transcript |
Het |
| Gsta2 |
A |
T |
9: 78,249,147 (GRCm39) |
C18S |
probably benign |
Het |
| H1f8 |
T |
C |
6: 115,924,701 (GRCm39) |
V69A |
possibly damaging |
Het |
| Hecw1 |
T |
C |
13: 14,480,671 (GRCm39) |
E465G |
probably damaging |
Het |
| Herc1 |
A |
G |
9: 66,415,548 (GRCm39) |
D4841G |
probably damaging |
Het |
| Hus1b |
A |
G |
13: 31,130,984 (GRCm39) |
V225A |
probably benign |
Het |
| Keg1 |
A |
T |
19: 12,693,387 (GRCm39) |
M137L |
probably benign |
Het |
| Kmt2a |
C |
T |
9: 44,735,932 (GRCm39) |
|
probably benign |
Het |
| Mga |
T |
A |
2: 119,772,156 (GRCm39) |
V1672E |
probably damaging |
Het |
| Mios |
T |
C |
6: 8,234,237 (GRCm39) |
S803P |
probably benign |
Het |
| Mrtfa |
T |
C |
15: 80,902,409 (GRCm39) |
|
probably benign |
Het |
| Msh4 |
A |
T |
3: 153,569,021 (GRCm39) |
Y851N |
probably damaging |
Het |
| Mybl1 |
A |
C |
1: 9,742,886 (GRCm39) |
|
probably null |
Het |
| Myo5c |
A |
G |
9: 75,183,221 (GRCm39) |
Y865C |
probably damaging |
Het |
| Naip1 |
T |
C |
13: 100,563,378 (GRCm39) |
S596G |
probably benign |
Het |
| Nek5 |
G |
T |
8: 22,586,747 (GRCm39) |
Q355K |
possibly damaging |
Het |
| Nphp3 |
G |
T |
9: 103,903,126 (GRCm39) |
R701L |
possibly damaging |
Het |
| Or52n2 |
A |
T |
7: 104,542,444 (GRCm39) |
Y130* |
probably null |
Het |
| Or5j3 |
T |
C |
2: 86,128,823 (GRCm39) |
I221T |
probably damaging |
Het |
| Or5m10 |
T |
A |
2: 85,717,592 (GRCm39) |
Y149* |
probably null |
Het |
| Or5t9 |
T |
C |
2: 86,659,542 (GRCm39) |
S149P |
probably benign |
Het |
| Or9g4 |
T |
A |
2: 85,505,262 (GRCm39) |
T78S |
possibly damaging |
Het |
| Palm |
A |
G |
10: 79,651,021 (GRCm39) |
N149D |
possibly damaging |
Het |
| Pot1b |
T |
C |
17: 55,960,451 (GRCm39) |
I626M |
possibly damaging |
Het |
| Ptprt |
T |
A |
2: 161,769,404 (GRCm39) |
D487V |
probably damaging |
Het |
| Qpct |
A |
G |
17: 79,378,201 (GRCm39) |
I124V |
probably benign |
Het |
| Rbm12b1 |
T |
A |
4: 12,145,817 (GRCm39) |
D596E |
possibly damaging |
Het |
| Rnf157 |
A |
G |
11: 116,245,585 (GRCm39) |
C277R |
probably damaging |
Het |
| Rnf169 |
A |
G |
7: 99,574,535 (GRCm39) |
S687P |
possibly damaging |
Het |
| Sfxn1 |
T |
A |
13: 54,246,469 (GRCm39) |
|
probably null |
Het |
| Slc6a21 |
T |
C |
7: 44,922,052 (GRCm39) |
V649A |
probably benign |
Het |
| Slit3 |
A |
T |
11: 35,577,126 (GRCm39) |
T1120S |
probably damaging |
Het |
| Spem2 |
A |
T |
11: 69,708,896 (GRCm39) |
M58K |
probably benign |
Het |
| Sprr2k |
T |
A |
3: 92,340,703 (GRCm39) |
|
probably benign |
Het |
| Sspo |
T |
C |
6: 48,440,334 (GRCm39) |
|
probably null |
Het |
| Sv2b |
A |
T |
7: 74,769,791 (GRCm39) |
F584I |
possibly damaging |
Het |
| Tkfc |
A |
T |
19: 10,572,690 (GRCm39) |
M317K |
probably null |
Het |
| Tnni3k |
C |
T |
3: 154,735,942 (GRCm39) |
G134S |
probably benign |
Het |
| Ttn |
C |
T |
2: 76,570,124 (GRCm39) |
R26923H |
probably damaging |
Het |
| Tuba3b |
T |
C |
6: 145,564,179 (GRCm39) |
V75A |
possibly damaging |
Het |
| Unc79 |
T |
C |
12: 103,149,784 (GRCm39) |
L2626P |
probably damaging |
Het |
| Usp24 |
A |
T |
4: 106,219,130 (GRCm39) |
I491F |
probably damaging |
Het |
| V1ra8 |
A |
T |
6: 90,180,132 (GRCm39) |
I112F |
probably damaging |
Het |
| Vmn1r29 |
T |
G |
6: 58,284,663 (GRCm39) |
F128V |
probably benign |
Het |
| Wdr87-ps |
A |
G |
7: 29,234,315 (GRCm39) |
|
noncoding transcript |
Het |
| Zfp157 |
T |
A |
5: 138,453,357 (GRCm39) |
|
probably null |
Het |
|
| Other mutations in Megf6 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01122:Megf6
|
APN |
4 |
154,338,264 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01410:Megf6
|
APN |
4 |
154,337,020 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL01512:Megf6
|
APN |
4 |
154,347,040 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
IGL01824:Megf6
|
APN |
4 |
154,336,691 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02172:Megf6
|
APN |
4 |
154,355,149 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02727:Megf6
|
APN |
4 |
154,337,606 (GRCm39) |
splice site |
probably null |
|
|
IGL02966:Megf6
|
APN |
4 |
154,338,234 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Didactic
|
UTSW |
4 |
154,339,044 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0118:Megf6
|
UTSW |
4 |
154,339,098 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0220:Megf6
|
UTSW |
4 |
154,342,672 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0347:Megf6
|
UTSW |
4 |
154,339,092 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R0383:Megf6
|
UTSW |
4 |
154,349,783 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0417:Megf6
|
UTSW |
4 |
154,352,424 (GRCm39) |
missense |
probably benign |
0.06 |
|
R0526:Megf6
|
UTSW |
4 |
154,343,398 (GRCm39) |
missense |
probably benign |
|
|
R0528:Megf6
|
UTSW |
4 |
154,343,630 (GRCm39) |
missense |
probably benign |
0.04 |
|
R0928:Megf6
|
UTSW |
4 |
154,261,504 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1311:Megf6
|
UTSW |
4 |
154,348,239 (GRCm39) |
splice site |
probably null |
|
|
R1458:Megf6
|
UTSW |
4 |
154,261,578 (GRCm39) |
missense |
probably benign |
0.39 |
|
R1470:Megf6
|
UTSW |
4 |
154,336,876 (GRCm39) |
splice site |
probably benign |
|
|
R1479:Megf6
|
UTSW |
4 |
154,261,578 (GRCm39) |
missense |
probably benign |
0.39 |
|
R1624:Megf6
|
UTSW |
4 |
154,261,578 (GRCm39) |
missense |
probably benign |
0.39 |
|
R1626:Megf6
|
UTSW |
4 |
154,261,578 (GRCm39) |
missense |
probably benign |
0.39 |
|
R1638:Megf6
|
UTSW |
4 |
154,346,967 (GRCm39) |
splice site |
probably benign |
|
|
R1777:Megf6
|
UTSW |
4 |
154,355,147 (GRCm39) |
nonsense |
probably null |
|
|
R1831:Megf6
|
UTSW |
4 |
154,355,134 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1944:Megf6
|
UTSW |
4 |
154,340,523 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R1984:Megf6
|
UTSW |
4 |
154,352,124 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2109:Megf6
|
UTSW |
4 |
154,261,578 (GRCm39) |
missense |
probably benign |
0.39 |
|
R2448:Megf6
|
UTSW |
4 |
154,351,102 (GRCm39) |
splice site |
probably null |
|
|
R2880:Megf6
|
UTSW |
4 |
154,337,006 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4032:Megf6
|
UTSW |
4 |
154,261,550 (GRCm39) |
nonsense |
probably null |
|
|
R4058:Megf6
|
UTSW |
4 |
154,326,989 (GRCm39) |
splice site |
probably benign |
|
|
R4672:Megf6
|
UTSW |
4 |
154,333,909 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4688:Megf6
|
UTSW |
4 |
154,338,271 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4752:Megf6
|
UTSW |
4 |
154,336,895 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4863:Megf6
|
UTSW |
4 |
154,338,738 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4909:Megf6
|
UTSW |
4 |
154,349,848 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4942:Megf6
|
UTSW |
4 |
154,338,277 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4981:Megf6
|
UTSW |
4 |
154,351,907 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4990:Megf6
|
UTSW |
4 |
154,351,683 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R5001:Megf6
|
UTSW |
4 |
154,352,517 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5189:Megf6
|
UTSW |
4 |
154,336,980 (GRCm39) |
missense |
probably benign |
0.31 |
|
R5210:Megf6
|
UTSW |
4 |
154,354,273 (GRCm39) |
intron |
probably benign |
|
|
R5220:Megf6
|
UTSW |
4 |
154,338,295 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5250:Megf6
|
UTSW |
4 |
154,340,467 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R5697:Megf6
|
UTSW |
4 |
154,342,686 (GRCm39) |
missense |
probably null |
0.15 |
|
R5808:Megf6
|
UTSW |
4 |
154,352,119 (GRCm39) |
missense |
probably benign |
|
|
R5916:Megf6
|
UTSW |
4 |
154,333,882 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R6054:Megf6
|
UTSW |
4 |
154,347,636 (GRCm39) |
missense |
probably benign |
0.06 |
|
R6075:Megf6
|
UTSW |
4 |
154,347,056 (GRCm39) |
nonsense |
probably null |
|
|
R6515:Megf6
|
UTSW |
4 |
154,343,376 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R6599:Megf6
|
UTSW |
4 |
154,342,544 (GRCm39) |
splice site |
probably null |
|
|
R6811:Megf6
|
UTSW |
4 |
154,336,618 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6925:Megf6
|
UTSW |
4 |
154,339,044 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7023:Megf6
|
UTSW |
4 |
154,338,602 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7117:Megf6
|
UTSW |
4 |
154,343,379 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R7163:Megf6
|
UTSW |
4 |
154,351,898 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7345:Megf6
|
UTSW |
4 |
154,351,772 (GRCm39) |
missense |
probably benign |
|
|
R7580:Megf6
|
UTSW |
4 |
154,355,201 (GRCm39) |
nonsense |
probably null |
|
|
R7649:Megf6
|
UTSW |
4 |
154,349,542 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R7702:Megf6
|
UTSW |
4 |
154,354,927 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8010:Megf6
|
UTSW |
4 |
154,354,964 (GRCm39) |
missense |
probably benign |
0.13 |
|
R8175:Megf6
|
UTSW |
4 |
154,353,076 (GRCm39) |
nonsense |
probably null |
|
|
R8231:Megf6
|
UTSW |
4 |
154,336,975 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8436:Megf6
|
UTSW |
4 |
154,349,649 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8460:Megf6
|
UTSW |
4 |
154,350,634 (GRCm39) |
nonsense |
probably null |
|
|
R8738:Megf6
|
UTSW |
4 |
154,352,436 (GRCm39) |
missense |
probably benign |
|
|
R8854:Megf6
|
UTSW |
4 |
154,352,469 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8896:Megf6
|
UTSW |
4 |
154,326,860 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9098:Megf6
|
UTSW |
4 |
154,354,160 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9147:Megf6
|
UTSW |
4 |
154,339,130 (GRCm39) |
missense |
probably benign |
0.18 |
|
R9148:Megf6
|
UTSW |
4 |
154,339,130 (GRCm39) |
missense |
probably benign |
0.18 |
|
R9161:Megf6
|
UTSW |
4 |
154,352,172 (GRCm39) |
missense |
probably benign |
0.44 |
|
R9355:Megf6
|
UTSW |
4 |
154,338,282 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9386:Megf6
|
UTSW |
4 |
154,340,534 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9404:Megf6
|
UTSW |
4 |
154,348,225 (GRCm39) |
missense |
|
|
|
R9469:Megf6
|
UTSW |
4 |
154,335,369 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9472:Megf6
|
UTSW |
4 |
154,333,910 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9777:Megf6
|
UTSW |
4 |
154,343,617 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Megf6
|
UTSW |
4 |
154,322,283 (GRCm39) |
missense |
probably benign |
0.12 |
|
Z1177:Megf6
|
UTSW |
4 |
154,354,198 (GRCm39) |
nonsense |
probably null |
|
|
Z1177:Megf6
|
UTSW |
4 |
154,352,204 (GRCm39) |
nonsense |
probably null |
|
|
Z1177:Megf6
|
UTSW |
4 |
154,352,139 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Z1177:Megf6
|
UTSW |
4 |
154,352,138 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
Z1177:Megf6
|
UTSW |
4 |
154,335,306 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- TTATTAGGGACAGCCCCATGCAGC -3'
(R):5'- TGAAAGGCCATGCCCTCAGTAAAG -3'
Sequencing Primer
(F):5'- CTTGTCCTGGAGTCCCAAGTG -3'
(R):5'- CATGCCCTCAGTAAAGGGAATG -3'
|
| Posted On |
2014-03-28 |
Incidental Mutation