Incidental Mutation 'R1775:Vmn2r72'
| ID |
204328 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Vmn2r72
|
| Ensembl Gene |
ENSMUSG00000051877 |
| Gene Name |
vomeronasal 2, receptor 72 |
| Synonyms |
EG244114, Vmn2r72-ps |
| MMRRC Submission |
039806-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.087)
|
| Stock # |
R1775 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
7 |
| Chromosomal Location |
85386992-85404189 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 85387378 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Methionine to Valine
at position 729
(M729V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000133014
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000063425]
|
| AlphaFold |
D3Z4N8 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000063425
AA Change: M729V
PolyPhen 2
Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
|
| SMART Domains |
Protein: ENSMUSP00000133014
Gene: ENSMUSG00000051877
AA Change: M729V
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
|
Pfam:ANF_receptor
|
82 |
469 |
2.3e-28 |
PFAM |
|
Pfam:NCD3G
|
512 |
564 |
1.2e-18 |
PFAM |
|
Pfam:7tm_3
|
594 |
832 |
4e-53 |
PFAM |
|
| Meta Mutation Damage Score |
0.0898 |
| Coding Region Coverage |
- 1x: 97.5%
- 3x: 97.0%
- 10x: 95.5%
- 20x: 92.9%
|
| Validation Efficiency |
98% (95/97) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 93 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700034J04Rik |
A |
G |
12: 11,272,143 (GRCm39) |
S20P |
unknown |
Het |
| 4921528I07Rik |
G |
A |
9: 114,108,386 (GRCm39) |
|
noncoding transcript |
Het |
| 4930562C15Rik |
G |
A |
16: 4,669,422 (GRCm39) |
|
probably null |
Het |
| 4933427I04Rik |
A |
G |
4: 123,754,286 (GRCm39) |
T67A |
possibly damaging |
Het |
| Abcc2 |
A |
T |
19: 43,786,858 (GRCm39) |
N160Y |
possibly damaging |
Het |
| Acaca |
A |
G |
11: 84,191,248 (GRCm39) |
D155G |
possibly damaging |
Het |
| Afg3l1 |
G |
A |
8: 124,219,639 (GRCm39) |
R389Q |
possibly damaging |
Het |
| Ank2 |
G |
A |
3: 126,728,196 (GRCm39) |
T799M |
probably benign |
Het |
| Anxa2 |
T |
C |
9: 69,395,363 (GRCm39) |
Y202H |
possibly damaging |
Het |
| Arhgef33 |
A |
G |
17: 80,681,172 (GRCm39) |
T771A |
probably benign |
Het |
| Atp12a |
T |
C |
14: 56,610,046 (GRCm39) |
V182A |
probably benign |
Het |
| Birc6 |
T |
C |
17: 74,919,281 (GRCm39) |
L210S |
probably damaging |
Het |
| Car3 |
A |
G |
3: 14,929,492 (GRCm39) |
T73A |
probably benign |
Het |
| Cd5l |
T |
C |
3: 87,275,966 (GRCm39) |
L312P |
probably damaging |
Het |
| Celf5 |
A |
G |
10: 81,303,138 (GRCm39) |
|
probably benign |
Het |
| Cep290 |
T |
A |
10: 100,332,672 (GRCm39) |
V257E |
probably damaging |
Het |
| Cntrob |
T |
C |
11: 69,211,693 (GRCm39) |
D177G |
possibly damaging |
Het |
| Copg2 |
A |
T |
6: 30,787,271 (GRCm39) |
F658I |
probably damaging |
Het |
| Csmd3 |
T |
C |
15: 47,763,135 (GRCm39) |
T1234A |
probably damaging |
Het |
| Dhx35 |
A |
G |
2: 158,648,357 (GRCm39) |
T72A |
probably damaging |
Het |
| Dmrtc2 |
A |
T |
7: 24,573,792 (GRCm39) |
H209L |
possibly damaging |
Het |
| Eml5 |
G |
T |
12: 98,818,963 (GRCm39) |
|
probably null |
Het |
| Evpl |
T |
C |
11: 116,114,486 (GRCm39) |
E1068G |
possibly damaging |
Het |
| Ezh2 |
A |
G |
6: 47,553,594 (GRCm39) |
M41T |
probably damaging |
Het |
| Fmo3 |
A |
G |
1: 162,796,294 (GRCm39) |
S93P |
possibly damaging |
Het |
| Gdi2 |
A |
G |
13: 3,610,018 (GRCm39) |
Y213C |
possibly damaging |
Het |
| Gpr15 |
A |
T |
16: 58,538,921 (GRCm39) |
I56K |
probably benign |
Het |
| Gria2 |
G |
T |
3: 80,598,645 (GRCm39) |
S796R |
probably benign |
Het |
| Hectd4 |
T |
A |
5: 121,429,254 (GRCm39) |
|
probably benign |
Het |
| Hgfac |
T |
C |
5: 35,200,194 (GRCm39) |
|
probably benign |
Het |
| Hspg2 |
C |
T |
4: 137,247,467 (GRCm39) |
R1200W |
probably damaging |
Het |
| Ift52 |
G |
A |
2: 162,867,275 (GRCm39) |
D78N |
possibly damaging |
Het |
| Iqca1 |
C |
A |
1: 90,009,138 (GRCm39) |
W415L |
probably damaging |
Het |
| Ism1 |
A |
T |
2: 139,587,963 (GRCm39) |
K236N |
probably damaging |
Het |
| Itgb6 |
C |
T |
2: 60,502,988 (GRCm39) |
W43* |
probably null |
Het |
| Kcnk18 |
T |
A |
19: 59,223,773 (GRCm39) |
I306N |
probably damaging |
Het |
| Kctd8 |
T |
C |
5: 69,497,903 (GRCm39) |
K248E |
probably damaging |
Het |
| Layn |
T |
A |
9: 50,970,833 (GRCm39) |
I237F |
probably benign |
Het |
| Lce3f |
C |
T |
3: 92,900,248 (GRCm39) |
P23L |
unknown |
Het |
| Lct |
A |
G |
1: 128,228,038 (GRCm39) |
F1152L |
probably damaging |
Het |
| Mettl25b |
A |
G |
3: 87,831,124 (GRCm39) |
S404P |
probably damaging |
Het |
| Mxra8 |
T |
C |
4: 155,927,531 (GRCm39) |
I413T |
probably damaging |
Het |
| Nedd9 |
A |
G |
13: 41,471,438 (GRCm39) |
V187A |
probably benign |
Het |
| Net1 |
A |
G |
13: 3,937,642 (GRCm39) |
L207P |
probably damaging |
Het |
| Neurod1 |
G |
T |
2: 79,284,781 (GRCm39) |
P201T |
probably benign |
Het |
| Nlrp1b |
A |
G |
11: 71,052,647 (GRCm39) |
F927S |
probably damaging |
Het |
| Ntrk3 |
T |
A |
7: 78,005,789 (GRCm39) |
H524L |
possibly damaging |
Het |
| Nup98 |
A |
C |
7: 101,784,144 (GRCm39) |
S1063A |
probably benign |
Het |
| Or10ak11 |
T |
A |
4: 118,687,065 (GRCm39) |
M191L |
probably benign |
Het |
| Or11h4b |
G |
T |
14: 50,918,623 (GRCm39) |
P156Q |
possibly damaging |
Het |
| Or56b1 |
G |
A |
7: 104,285,366 (GRCm39) |
V162I |
probably benign |
Het |
| Or5b97 |
C |
A |
19: 12,878,599 (GRCm39) |
V182F |
probably benign |
Het |
| Or5m9b |
G |
A |
2: 85,905,104 (GRCm39) |
V7I |
possibly damaging |
Het |
| Or6d15 |
T |
C |
6: 116,559,925 (GRCm39) |
|
probably benign |
Het |
| Pdzd2 |
G |
A |
15: 12,592,546 (GRCm39) |
R33W |
probably damaging |
Het |
| Phf21a |
G |
A |
2: 92,160,860 (GRCm39) |
V243I |
probably damaging |
Het |
| Ppp1r12b |
A |
G |
1: 134,821,086 (GRCm39) |
|
probably null |
Het |
| Rexo5 |
T |
C |
7: 119,444,634 (GRCm39) |
V703A |
probably benign |
Het |
| Rgs4 |
A |
G |
1: 169,572,847 (GRCm39) |
S30P |
probably benign |
Het |
| Rxra |
C |
A |
2: 27,646,256 (GRCm39) |
D340E |
probably damaging |
Het |
| Samhd1 |
A |
G |
2: 156,949,467 (GRCm39) |
V473A |
probably benign |
Het |
| Scn3a |
T |
A |
2: 65,302,686 (GRCm39) |
K1253N |
probably damaging |
Het |
| Scn7a |
T |
C |
2: 66,511,299 (GRCm39) |
N1207S |
probably benign |
Het |
| Sec24d |
T |
A |
3: 123,130,166 (GRCm39) |
I443N |
probably damaging |
Het |
| Sema4g |
T |
A |
19: 44,987,681 (GRCm39) |
|
probably null |
Het |
| Sema5b |
A |
G |
16: 35,480,694 (GRCm39) |
K787R |
probably benign |
Het |
| Serpinc1 |
A |
G |
1: 160,817,217 (GRCm39) |
N104D |
probably benign |
Het |
| Sfn |
T |
C |
4: 133,328,542 (GRCm39) |
H180R |
probably damaging |
Het |
| Slc22a6 |
G |
T |
19: 8,596,471 (GRCm39) |
|
probably null |
Het |
| Slc9a8 |
T |
C |
2: 167,299,278 (GRCm39) |
S217P |
probably benign |
Het |
| Smc6 |
A |
G |
12: 11,359,270 (GRCm39) |
N965D |
probably benign |
Het |
| Sod2 |
T |
A |
17: 13,233,919 (GRCm39) |
I177N |
probably damaging |
Het |
| Sp4 |
A |
T |
12: 118,263,335 (GRCm39) |
I237K |
probably damaging |
Het |
| Sulf2 |
T |
C |
2: 165,921,532 (GRCm39) |
K697R |
probably benign |
Het |
| Svs4 |
A |
T |
2: 164,119,005 (GRCm39) |
D110E |
unknown |
Het |
| Tas1r1 |
T |
A |
4: 152,122,675 (GRCm39) |
R57* |
probably null |
Het |
| Tlr5 |
T |
C |
1: 182,801,287 (GRCm39) |
I197T |
probably damaging |
Het |
| Tmc3 |
T |
C |
7: 83,261,740 (GRCm39) |
V606A |
probably benign |
Het |
| Tmem241 |
T |
A |
18: 12,251,469 (GRCm39) |
L37F |
probably damaging |
Het |
| Tmem59l |
A |
T |
8: 70,938,903 (GRCm39) |
N90K |
probably damaging |
Het |
| Tram1 |
A |
C |
1: 13,646,680 (GRCm39) |
|
probably benign |
Het |
| Trim15 |
T |
A |
17: 37,176,061 (GRCm39) |
H162L |
probably benign |
Het |
| Ttc28 |
T |
A |
5: 111,424,677 (GRCm39) |
Y1501N |
probably benign |
Het |
| Ttc34 |
T |
C |
4: 154,946,671 (GRCm39) |
V857A |
probably benign |
Het |
| Tulp4 |
A |
G |
17: 6,189,321 (GRCm39) |
T48A |
probably damaging |
Het |
| Usp9y |
T |
C |
Y: 1,368,089 (GRCm39) |
E939G |
probably damaging |
Het |
| Utp20 |
A |
G |
10: 88,606,670 (GRCm39) |
I1634T |
probably benign |
Het |
| Vps13c |
C |
T |
9: 67,788,729 (GRCm39) |
T334M |
probably damaging |
Het |
| Wnk4 |
C |
G |
11: 101,167,166 (GRCm39) |
|
probably benign |
Het |
| Xpo1 |
A |
G |
11: 23,221,193 (GRCm39) |
N97D |
probably benign |
Het |
| Xpo4 |
A |
T |
14: 57,841,129 (GRCm39) |
F518Y |
probably benign |
Het |
| Zfp668 |
C |
T |
7: 127,465,778 (GRCm39) |
V469I |
possibly damaging |
Het |
| Zfp85 |
C |
A |
13: 67,897,823 (GRCm39) |
C83F |
probably damaging |
Het |
|
| Other mutations in Vmn2r72 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00931:Vmn2r72
|
APN |
7 |
85,398,854 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01019:Vmn2r72
|
APN |
7 |
85,387,542 (GRCm39) |
missense |
probably benign |
0.26 |
|
IGL01445:Vmn2r72
|
APN |
7 |
85,398,854 (GRCm39) |
missense |
probably benign |
0.06 |
|
IGL02076:Vmn2r72
|
APN |
7 |
85,387,575 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02082:Vmn2r72
|
APN |
7 |
85,387,374 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02086:Vmn2r72
|
APN |
7 |
85,387,374 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02089:Vmn2r72
|
APN |
7 |
85,387,374 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02125:Vmn2r72
|
APN |
7 |
85,399,919 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02146:Vmn2r72
|
APN |
7 |
85,387,170 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02272:Vmn2r72
|
APN |
7 |
85,399,901 (GRCm39) |
missense |
probably benign |
|
|
IGL02514:Vmn2r72
|
APN |
7 |
85,387,907 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
IGL02662:Vmn2r72
|
APN |
7 |
85,387,391 (GRCm39) |
missense |
probably benign |
0.26 |
|
IGL02697:Vmn2r72
|
APN |
7 |
85,387,879 (GRCm39) |
missense |
probably benign |
0.36 |
|
IGL02733:Vmn2r72
|
APN |
7 |
85,401,021 (GRCm39) |
missense |
probably benign |
0.05 |
|
IGL03070:Vmn2r72
|
APN |
7 |
85,401,249 (GRCm39) |
splice site |
probably benign |
|
|
IGL03150:Vmn2r72
|
APN |
7 |
85,400,384 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03159:Vmn2r72
|
APN |
7 |
85,404,162 (GRCm39) |
missense |
probably benign |
0.05 |
|
IGL03333:Vmn2r72
|
APN |
7 |
85,400,075 (GRCm39) |
missense |
probably benign |
0.10 |
|
R0081:Vmn2r72
|
UTSW |
7 |
85,401,044 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0090:Vmn2r72
|
UTSW |
7 |
85,404,084 (GRCm39) |
missense |
probably benign |
|
|
R0655:Vmn2r72
|
UTSW |
7 |
85,387,319 (GRCm39) |
nonsense |
probably null |
|
|
R0778:Vmn2r72
|
UTSW |
7 |
85,398,947 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1169:Vmn2r72
|
UTSW |
7 |
85,400,517 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1172:Vmn2r72
|
UTSW |
7 |
85,401,152 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1173:Vmn2r72
|
UTSW |
7 |
85,401,152 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1175:Vmn2r72
|
UTSW |
7 |
85,401,152 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1248:Vmn2r72
|
UTSW |
7 |
85,398,396 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1302:Vmn2r72
|
UTSW |
7 |
85,387,465 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1506:Vmn2r72
|
UTSW |
7 |
85,398,419 (GRCm39) |
missense |
probably benign |
|
|
R1632:Vmn2r72
|
UTSW |
7 |
85,401,000 (GRCm39) |
missense |
probably benign |
0.13 |
|
R1962:Vmn2r72
|
UTSW |
7 |
85,398,369 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2201:Vmn2r72
|
UTSW |
7 |
85,387,444 (GRCm39) |
missense |
probably benign |
0.12 |
|
R2290:Vmn2r72
|
UTSW |
7 |
85,387,549 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2327:Vmn2r72
|
UTSW |
7 |
85,387,464 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2424:Vmn2r72
|
UTSW |
7 |
85,400,161 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2655:Vmn2r72
|
UTSW |
7 |
85,400,477 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R2860:Vmn2r72
|
UTSW |
7 |
85,400,044 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2861:Vmn2r72
|
UTSW |
7 |
85,400,044 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2862:Vmn2r72
|
UTSW |
7 |
85,400,044 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3009:Vmn2r72
|
UTSW |
7 |
85,398,850 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3797:Vmn2r72
|
UTSW |
7 |
85,387,285 (GRCm39) |
missense |
probably benign |
0.44 |
|
R3798:Vmn2r72
|
UTSW |
7 |
85,387,285 (GRCm39) |
missense |
probably benign |
0.44 |
|
R3902:Vmn2r72
|
UTSW |
7 |
85,398,943 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R3959:Vmn2r72
|
UTSW |
7 |
85,400,339 (GRCm39) |
missense |
probably benign |
0.36 |
|
R3974:Vmn2r72
|
UTSW |
7 |
85,399,017 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4399:Vmn2r72
|
UTSW |
7 |
85,387,708 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4421:Vmn2r72
|
UTSW |
7 |
85,387,708 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4426:Vmn2r72
|
UTSW |
7 |
85,387,036 (GRCm39) |
nonsense |
probably null |
|
|
R4522:Vmn2r72
|
UTSW |
7 |
85,401,134 (GRCm39) |
missense |
probably benign |
0.44 |
|
R4523:Vmn2r72
|
UTSW |
7 |
85,401,134 (GRCm39) |
missense |
probably benign |
0.44 |
|
R4533:Vmn2r72
|
UTSW |
7 |
85,401,134 (GRCm39) |
missense |
probably benign |
0.44 |
|
R4691:Vmn2r72
|
UTSW |
7 |
85,387,119 (GRCm39) |
nonsense |
probably null |
|
|
R4781:Vmn2r72
|
UTSW |
7 |
85,387,069 (GRCm39) |
missense |
probably benign |
0.14 |
|
R4863:Vmn2r72
|
UTSW |
7 |
85,399,806 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R4952:Vmn2r72
|
UTSW |
7 |
85,400,317 (GRCm39) |
missense |
probably benign |
|
|
R4991:Vmn2r72
|
UTSW |
7 |
85,400,338 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4995:Vmn2r72
|
UTSW |
7 |
85,387,693 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5095:Vmn2r72
|
UTSW |
7 |
85,387,061 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5174:Vmn2r72
|
UTSW |
7 |
85,387,048 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5276:Vmn2r72
|
UTSW |
7 |
85,387,462 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R5395:Vmn2r72
|
UTSW |
7 |
85,400,105 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R5560:Vmn2r72
|
UTSW |
7 |
85,401,150 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R5933:Vmn2r72
|
UTSW |
7 |
85,387,058 (GRCm39) |
missense |
probably benign |
0.05 |
|
R6033:Vmn2r72
|
UTSW |
7 |
85,387,137 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6033:Vmn2r72
|
UTSW |
7 |
85,387,137 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6354:Vmn2r72
|
UTSW |
7 |
85,399,747 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6362:Vmn2r72
|
UTSW |
7 |
85,400,382 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6594:Vmn2r72
|
UTSW |
7 |
85,398,892 (GRCm39) |
missense |
probably benign |
0.32 |
|
R6794:Vmn2r72
|
UTSW |
7 |
85,387,204 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7113:Vmn2r72
|
UTSW |
7 |
85,399,011 (GRCm39) |
splice site |
probably null |
|
|
R7189:Vmn2r72
|
UTSW |
7 |
85,404,125 (GRCm39) |
missense |
probably benign |
0.36 |
|
R7266:Vmn2r72
|
UTSW |
7 |
85,387,482 (GRCm39) |
nonsense |
probably null |
|
|
R7323:Vmn2r72
|
UTSW |
7 |
85,399,771 (GRCm39) |
missense |
probably benign |
|
|
R7426:Vmn2r72
|
UTSW |
7 |
85,400,348 (GRCm39) |
missense |
probably benign |
|
|
R7606:Vmn2r72
|
UTSW |
7 |
85,400,362 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R7651:Vmn2r72
|
UTSW |
7 |
85,401,146 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7688:Vmn2r72
|
UTSW |
7 |
85,404,098 (GRCm39) |
missense |
probably benign |
0.32 |
|
R7753:Vmn2r72
|
UTSW |
7 |
85,399,834 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7843:Vmn2r72
|
UTSW |
7 |
85,398,838 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8157:Vmn2r72
|
UTSW |
7 |
85,400,441 (GRCm39) |
missense |
probably benign |
0.09 |
|
R8254:Vmn2r72
|
UTSW |
7 |
85,400,227 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8389:Vmn2r72
|
UTSW |
7 |
85,401,168 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8444:Vmn2r72
|
UTSW |
7 |
85,387,383 (GRCm39) |
missense |
probably benign |
|
|
R8989:Vmn2r72
|
UTSW |
7 |
85,404,134 (GRCm39) |
missense |
probably benign |
0.10 |
|
R9015:Vmn2r72
|
UTSW |
7 |
85,398,388 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9080:Vmn2r72
|
UTSW |
7 |
85,387,464 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9269:Vmn2r72
|
UTSW |
7 |
85,400,411 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9317:Vmn2r72
|
UTSW |
7 |
85,404,022 (GRCm39) |
missense |
probably benign |
0.04 |
|
R9509:Vmn2r72
|
UTSW |
7 |
85,404,075 (GRCm39) |
missense |
probably benign |
|
|
Z1176:Vmn2r72
|
UTSW |
7 |
85,398,399 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Predicted Primers |
PCR Primer
(F):5'- AACACCAGCATGCTGAATGTC -3'
(R):5'- CAGACCACTTTTGCCATTGC -3'
Sequencing Primer
(F):5'- CATGCTGAATGTCAAGAGCTTGGC -3'
(R):5'- ACCTCTACTATTTTGGCTAAGACG -3'
|
| Posted On |
2014-06-23 |
Incidental Mutation