Incidental Mutation 'IGL02725:Vmn2r70'
ID |
305137 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Vmn2r70
|
Ensembl Gene |
ENSMUSG00000090806 |
Gene Name |
vomeronasal 2, receptor 70 |
Synonyms |
EG620835 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.130)
|
Stock # |
IGL02725
|
Quality Score |
|
Status
|
|
Chromosome |
7 |
Chromosomal Location |
85207911-85218296 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 85214553 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Isoleucine
at position 200
(V200I)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000129703
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000168230]
|
AlphaFold |
K7N702 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000168230
AA Change: V200I
PolyPhen 2
Score 0.456 (Sensitivity: 0.89; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000129703 Gene: ENSMUSG00000090806 AA Change: V200I
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
23 |
N/A |
INTRINSIC |
Pfam:ANF_receptor
|
77 |
468 |
2.5e-28 |
PFAM |
Pfam:NCD3G
|
510 |
562 |
1.5e-19 |
PFAM |
Pfam:7tm_3
|
592 |
830 |
1.2e-52 |
PFAM |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4833420G17Rik |
T |
C |
13: 119,611,445 (GRCm39) |
I414T |
possibly damaging |
Het |
Agpat3 |
A |
C |
10: 78,113,889 (GRCm39) |
D266E |
probably benign |
Het |
Alpk3 |
G |
T |
7: 80,743,358 (GRCm39) |
Q1058H |
possibly damaging |
Het |
Atat1 |
A |
T |
17: 36,220,381 (GRCm39) |
V37E |
probably benign |
Het |
Bcl6b |
A |
G |
11: 70,119,344 (GRCm39) |
V124A |
probably damaging |
Het |
Bmt2 |
T |
C |
6: 13,628,495 (GRCm39) |
E396G |
probably damaging |
Het |
Ccdc50 |
T |
C |
16: 27,255,347 (GRCm39) |
C237R |
probably benign |
Het |
Chd9 |
A |
G |
8: 91,778,312 (GRCm39) |
I2790M |
possibly damaging |
Het |
Chkb |
A |
G |
15: 89,313,340 (GRCm39) |
L82P |
probably damaging |
Het |
Cit |
T |
C |
5: 116,123,532 (GRCm39) |
Y1458H |
probably benign |
Het |
Clp1 |
T |
A |
2: 84,554,208 (GRCm39) |
K320N |
probably benign |
Het |
Cry2 |
T |
C |
2: 92,243,605 (GRCm39) |
|
probably benign |
Het |
Cyp20a1 |
C |
T |
1: 60,405,865 (GRCm39) |
R220W |
probably benign |
Het |
Cyp27a1 |
C |
T |
1: 74,774,862 (GRCm39) |
P268S |
probably damaging |
Het |
Cyp2e1 |
T |
G |
7: 140,343,828 (GRCm39) |
I22S |
probably null |
Het |
Defb34 |
A |
G |
8: 19,173,774 (GRCm39) |
T3A |
unknown |
Het |
Dpy19l3 |
A |
T |
7: 35,411,343 (GRCm39) |
M422K |
probably benign |
Het |
Eif4g3 |
A |
T |
4: 137,897,782 (GRCm39) |
|
probably benign |
Het |
Elmod3 |
A |
G |
6: 72,571,758 (GRCm39) |
S7P |
probably damaging |
Het |
Fam151a |
T |
G |
4: 106,605,211 (GRCm39) |
S524R |
probably damaging |
Het |
Gcc1 |
A |
T |
6: 28,418,458 (GRCm39) |
V625E |
probably benign |
Het |
Glmn |
G |
A |
5: 107,723,155 (GRCm39) |
P112S |
possibly damaging |
Het |
Grm5 |
A |
C |
7: 87,723,873 (GRCm39) |
D721A |
probably damaging |
Het |
Hivep3 |
T |
C |
4: 119,953,019 (GRCm39) |
V445A |
possibly damaging |
Het |
Hmcn1 |
T |
A |
1: 150,480,654 (GRCm39) |
E4507D |
possibly damaging |
Het |
Hmcn2 |
A |
C |
2: 31,295,540 (GRCm39) |
E2583A |
probably damaging |
Het |
Ifnb1 |
T |
A |
4: 88,440,867 (GRCm39) |
I49F |
probably benign |
Het |
Ints8 |
A |
C |
4: 11,239,406 (GRCm39) |
C306W |
probably benign |
Het |
Jakmip2 |
A |
G |
18: 43,695,655 (GRCm39) |
S540P |
probably damaging |
Het |
Kctd1 |
A |
G |
18: 15,102,667 (GRCm39) |
V838A |
possibly damaging |
Het |
Klk10 |
T |
C |
7: 43,431,044 (GRCm39) |
L29P |
probably damaging |
Het |
Lyst |
T |
A |
13: 13,935,412 (GRCm39) |
I3627K |
probably damaging |
Het |
Maml3 |
A |
G |
3: 52,011,195 (GRCm39) |
S124P |
probably damaging |
Het |
Nav2 |
A |
T |
7: 49,214,843 (GRCm39) |
K1632I |
probably damaging |
Het |
Or2ab1 |
T |
C |
11: 58,488,690 (GRCm39) |
V156A |
probably benign |
Het |
Pde2a |
G |
T |
7: 101,156,425 (GRCm39) |
M616I |
probably null |
Het |
Pdia2 |
T |
C |
17: 26,415,506 (GRCm39) |
D440G |
probably benign |
Het |
Rab11fip5 |
A |
G |
6: 85,351,471 (GRCm39) |
S14P |
probably damaging |
Het |
Rhpn2 |
T |
C |
7: 35,079,031 (GRCm39) |
S383P |
probably damaging |
Het |
Rnf220 |
A |
G |
4: 117,129,576 (GRCm39) |
|
probably benign |
Het |
Rnf43 |
A |
G |
11: 87,622,411 (GRCm39) |
D504G |
probably damaging |
Het |
Setbp1 |
A |
T |
18: 78,900,589 (GRCm39) |
L1026* |
probably null |
Het |
Slc1a4 |
A |
T |
11: 20,258,408 (GRCm39) |
S264T |
probably damaging |
Het |
Snx19 |
A |
G |
9: 30,343,556 (GRCm39) |
N572S |
possibly damaging |
Het |
Sptan1 |
T |
C |
2: 29,886,055 (GRCm39) |
I739T |
probably damaging |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Stat5b |
A |
T |
11: 100,695,840 (GRCm39) |
D47E |
possibly damaging |
Het |
Taar7b |
A |
T |
10: 23,875,961 (GRCm39) |
Y42F |
probably benign |
Het |
Tfdp2 |
T |
A |
9: 96,169,748 (GRCm39) |
I33K |
possibly damaging |
Het |
Tm4sf5 |
A |
G |
11: 70,401,448 (GRCm39) |
H149R |
probably benign |
Het |
Tmco6 |
A |
G |
18: 36,871,760 (GRCm39) |
M257V |
probably benign |
Het |
Tuba8 |
G |
T |
6: 121,202,916 (GRCm39) |
G410* |
probably null |
Het |
Ubd |
T |
A |
17: 37,504,853 (GRCm39) |
V4D |
probably benign |
Het |
Ugt2b34 |
C |
T |
5: 87,054,284 (GRCm39) |
V166I |
probably benign |
Het |
Wdcp |
A |
T |
12: 4,901,206 (GRCm39) |
N354I |
probably damaging |
Het |
Wipi2 |
A |
T |
5: 142,652,618 (GRCm39) |
Y410F |
possibly damaging |
Het |
Zc3hav1 |
G |
T |
6: 38,309,127 (GRCm39) |
P565Q |
probably damaging |
Het |
Zfp398 |
T |
C |
6: 47,842,737 (GRCm39) |
V131A |
probably benign |
Het |
Zkscan3 |
T |
C |
13: 21,579,063 (GRCm39) |
D144G |
possibly damaging |
Het |
Zpbp |
T |
A |
11: 11,412,358 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Vmn2r70 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00978:Vmn2r70
|
APN |
7 |
85,213,007 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01140:Vmn2r70
|
APN |
7 |
85,214,379 (GRCm39) |
nonsense |
probably null |
|
IGL01287:Vmn2r70
|
APN |
7 |
85,218,227 (GRCm39) |
nonsense |
probably null |
|
IGL01581:Vmn2r70
|
APN |
7 |
85,213,122 (GRCm39) |
splice site |
probably null |
|
IGL01632:Vmn2r70
|
APN |
7 |
85,215,280 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01725:Vmn2r70
|
APN |
7 |
85,208,594 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02244:Vmn2r70
|
APN |
7 |
85,214,211 (GRCm39) |
missense |
probably benign |
|
IGL02288:Vmn2r70
|
APN |
7 |
85,214,342 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02313:Vmn2r70
|
APN |
7 |
85,214,376 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02591:Vmn2r70
|
APN |
7 |
85,214,153 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02797:Vmn2r70
|
APN |
7 |
85,208,295 (GRCm39) |
missense |
probably benign |
0.00 |
R0045:Vmn2r70
|
UTSW |
7 |
85,215,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R0729:Vmn2r70
|
UTSW |
7 |
85,215,112 (GRCm39) |
missense |
probably benign |
0.00 |
R0967:Vmn2r70
|
UTSW |
7 |
85,208,827 (GRCm39) |
missense |
probably damaging |
0.99 |
R1217:Vmn2r70
|
UTSW |
7 |
85,208,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R1351:Vmn2r70
|
UTSW |
7 |
85,214,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R1387:Vmn2r70
|
UTSW |
7 |
85,207,969 (GRCm39) |
missense |
probably benign |
0.12 |
R1483:Vmn2r70
|
UTSW |
7 |
85,208,375 (GRCm39) |
missense |
probably benign |
0.04 |
R1796:Vmn2r70
|
UTSW |
7 |
85,213,011 (GRCm39) |
nonsense |
probably null |
|
R1809:Vmn2r70
|
UTSW |
7 |
85,215,130 (GRCm39) |
missense |
probably benign |
0.23 |
R2154:Vmn2r70
|
UTSW |
7 |
85,212,923 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2173:Vmn2r70
|
UTSW |
7 |
85,214,290 (GRCm39) |
missense |
probably benign |
|
R2334:Vmn2r70
|
UTSW |
7 |
85,208,800 (GRCm39) |
missense |
probably benign |
0.05 |
R2871:Vmn2r70
|
UTSW |
7 |
85,208,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R2871:Vmn2r70
|
UTSW |
7 |
85,208,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R3975:Vmn2r70
|
UTSW |
7 |
85,208,540 (GRCm39) |
missense |
probably benign |
0.00 |
R4525:Vmn2r70
|
UTSW |
7 |
85,208,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R4527:Vmn2r70
|
UTSW |
7 |
85,208,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R4535:Vmn2r70
|
UTSW |
7 |
85,214,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R5181:Vmn2r70
|
UTSW |
7 |
85,208,387 (GRCm39) |
missense |
probably damaging |
0.99 |
R5600:Vmn2r70
|
UTSW |
7 |
85,212,935 (GRCm39) |
missense |
probably benign |
0.07 |
R5641:Vmn2r70
|
UTSW |
7 |
85,208,572 (GRCm39) |
missense |
probably damaging |
0.99 |
R5726:Vmn2r70
|
UTSW |
7 |
85,208,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R5943:Vmn2r70
|
UTSW |
7 |
85,215,199 (GRCm39) |
missense |
probably benign |
0.09 |
R6166:Vmn2r70
|
UTSW |
7 |
85,215,189 (GRCm39) |
missense |
probably benign |
0.25 |
R6272:Vmn2r70
|
UTSW |
7 |
85,208,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R6324:Vmn2r70
|
UTSW |
7 |
85,208,087 (GRCm39) |
missense |
probably benign |
0.01 |
R6429:Vmn2r70
|
UTSW |
7 |
85,208,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R6449:Vmn2r70
|
UTSW |
7 |
85,214,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R6512:Vmn2r70
|
UTSW |
7 |
85,215,305 (GRCm39) |
missense |
probably benign |
|
R7000:Vmn2r70
|
UTSW |
7 |
85,208,819 (GRCm39) |
missense |
probably damaging |
0.99 |
R7141:Vmn2r70
|
UTSW |
7 |
85,208,044 (GRCm39) |
missense |
probably benign |
|
R7153:Vmn2r70
|
UTSW |
7 |
85,214,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R7424:Vmn2r70
|
UTSW |
7 |
85,213,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R7565:Vmn2r70
|
UTSW |
7 |
85,214,499 (GRCm39) |
missense |
probably benign |
0.35 |
R7567:Vmn2r70
|
UTSW |
7 |
85,214,243 (GRCm39) |
missense |
probably benign |
0.41 |
R7593:Vmn2r70
|
UTSW |
7 |
85,215,312 (GRCm39) |
nonsense |
probably null |
|
R7660:Vmn2r70
|
UTSW |
7 |
85,218,130 (GRCm39) |
missense |
probably damaging |
0.99 |
R7806:Vmn2r70
|
UTSW |
7 |
85,208,401 (GRCm39) |
missense |
probably benign |
|
R7892:Vmn2r70
|
UTSW |
7 |
85,208,588 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7965:Vmn2r70
|
UTSW |
7 |
85,211,071 (GRCm39) |
missense |
probably damaging |
0.96 |
R8052:Vmn2r70
|
UTSW |
7 |
85,212,923 (GRCm39) |
missense |
probably benign |
|
R8251:Vmn2r70
|
UTSW |
7 |
85,215,186 (GRCm39) |
nonsense |
probably null |
|
R8814:Vmn2r70
|
UTSW |
7 |
85,215,169 (GRCm39) |
missense |
probably benign |
0.00 |
R8934:Vmn2r70
|
UTSW |
7 |
85,211,188 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9225:Vmn2r70
|
UTSW |
7 |
85,208,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R9322:Vmn2r70
|
UTSW |
7 |
85,208,498 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9430:Vmn2r70
|
UTSW |
7 |
85,215,240 (GRCm39) |
missense |
probably benign |
0.10 |
R9477:Vmn2r70
|
UTSW |
7 |
85,218,244 (GRCm39) |
missense |
possibly damaging |
0.50 |
Z1088:Vmn2r70
|
UTSW |
7 |
85,213,968 (GRCm39) |
missense |
possibly damaging |
0.53 |
Z1176:Vmn2r70
|
UTSW |
7 |
85,218,253 (GRCm39) |
missense |
probably benign |
0.00 |
|
Posted On |
2015-04-16 |