Incidental Mutation 'R9756:Vmn2r71'
ID |
732733 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Vmn2r71
|
Ensembl Gene |
ENSMUSG00000091205 |
Gene Name |
vomeronasal 2, receptor 71 |
Synonyms |
EG233445 |
MMRRC Submission |
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.074)
|
Stock # |
R9756 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
7 |
Chromosomal Location |
85264670-85273755 bp(+) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
A to T
at 85268573 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Lysine to Stop codon
at position 259
(K259*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000132337
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000172338]
|
AlphaFold |
L7N2D8 |
Predicted Effect |
probably null
Transcript: ENSMUST00000172338
AA Change: K259*
|
SMART Domains |
Protein: ENSMUSP00000132337 Gene: ENSMUSG00000091205 AA Change: K259*
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
Pfam:ANF_receptor
|
77 |
468 |
2.1e-31 |
PFAM |
Pfam:NCD3G
|
511 |
563 |
8.7e-20 |
PFAM |
Pfam:7tm_3
|
593 |
831 |
2e-55 |
PFAM |
|
Coding Region Coverage |
- 1x: 99.8%
- 3x: 99.7%
- 10x: 99.2%
- 20x: 98.3%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700066M21Rik |
A |
T |
1: 57,421,906 (GRCm39) |
Y94F |
possibly damaging |
Het |
Abcb5 |
A |
G |
12: 118,881,873 (GRCm39) |
S619P |
probably damaging |
Het |
Adgrf5 |
A |
G |
17: 43,761,137 (GRCm39) |
N944S |
probably benign |
Het |
Ano1 |
T |
A |
7: 144,162,666 (GRCm39) |
M689L |
probably benign |
Het |
Antxr1 |
T |
A |
6: 87,217,936 (GRCm39) |
H314L |
probably benign |
Het |
Atp13a5 |
CA |
C |
16: 29,051,583 (GRCm39) |
|
probably null |
Het |
Blmh |
T |
A |
11: 76,859,509 (GRCm39) |
M370K |
probably damaging |
Het |
Cdh8 |
G |
A |
8: 99,759,976 (GRCm39) |
T591M |
probably damaging |
Het |
Cep290 |
G |
A |
10: 100,352,034 (GRCm39) |
E747K |
probably damaging |
Het |
Chd6 |
T |
C |
2: 160,802,259 (GRCm39) |
S2192G |
probably benign |
Het |
Cldn8 |
T |
G |
16: 88,359,917 (GRCm39) |
T3P |
probably benign |
Het |
Crtac1 |
A |
G |
19: 42,286,780 (GRCm39) |
L421P |
probably damaging |
Het |
Ddx59 |
G |
T |
1: 136,345,069 (GRCm39) |
A247S |
probably damaging |
Het |
Defa38 |
C |
T |
8: 21,585,943 (GRCm39) |
V42I |
possibly damaging |
Het |
Dennd5a |
A |
G |
7: 109,496,174 (GRCm39) |
V1164A |
possibly damaging |
Het |
Dnhd1 |
A |
T |
7: 105,353,135 (GRCm39) |
T2763S |
probably benign |
Het |
Evpl |
T |
C |
11: 116,112,077 (GRCm39) |
D1871G |
probably damaging |
Het |
Fat1 |
T |
A |
8: 45,496,974 (GRCm39) |
I4153N |
probably damaging |
Het |
Fbxl17 |
A |
G |
17: 63,367,310 (GRCm39) |
Y688H |
probably damaging |
Het |
Fntb |
A |
G |
12: 76,966,938 (GRCm39) |
E424G |
probably benign |
Het |
Gabra4 |
A |
G |
5: 71,729,067 (GRCm39) |
M571T |
probably damaging |
Het |
Hoxb5 |
T |
C |
11: 96,194,449 (GRCm39) |
Y4H |
probably damaging |
Het |
Htr1a |
T |
C |
13: 105,581,450 (GRCm39) |
V230A |
probably damaging |
Het |
Idh2 |
TCCCAGG |
T |
7: 79,748,079 (GRCm39) |
|
probably benign |
Het |
Ighv3-4 |
T |
C |
12: 114,217,448 (GRCm39) |
T48A |
probably damaging |
Het |
Il15ra |
A |
G |
2: 11,728,259 (GRCm39) |
M53V |
probably benign |
Het |
Ipo9 |
A |
C |
1: 135,314,057 (GRCm39) |
D945E |
probably benign |
Het |
Klk1b22 |
A |
T |
7: 43,765,254 (GRCm39) |
|
probably null |
Het |
Klkb1 |
T |
C |
8: 45,735,811 (GRCm39) |
N184S |
possibly damaging |
Het |
Lbhd2 |
G |
A |
12: 111,376,774 (GRCm39) |
A74T |
probably damaging |
Het |
Lpcat3 |
A |
G |
6: 124,679,967 (GRCm39) |
|
probably null |
Het |
Luzp1 |
T |
C |
4: 136,270,048 (GRCm39) |
I757T |
probably damaging |
Het |
Mbd5 |
C |
A |
2: 49,169,283 (GRCm39) |
P1485T |
probably benign |
Het |
Mfsd14b |
C |
A |
13: 65,221,414 (GRCm39) |
V293L |
probably benign |
Het |
Mical2 |
C |
T |
7: 111,902,928 (GRCm39) |
T133I |
probably damaging |
Het |
Mylk |
T |
C |
16: 34,734,387 (GRCm39) |
S663P |
probably damaging |
Het |
Or2ag13 |
A |
T |
7: 106,313,002 (GRCm39) |
N295K |
probably benign |
Het |
Or2j3 |
A |
G |
17: 38,615,971 (GRCm39) |
V127A |
probably benign |
Het |
Or4x11 |
A |
T |
2: 89,867,674 (GRCm39) |
N137I |
probably benign |
Het |
Or5ak22 |
T |
A |
2: 85,230,682 (GRCm39) |
H65L |
probably damaging |
Het |
Or5b119 |
G |
A |
19: 13,456,986 (GRCm39) |
T192I |
probably benign |
Het |
Or8b12 |
G |
A |
9: 37,658,314 (GRCm39) |
D295N |
possibly damaging |
Het |
Patj |
G |
T |
4: 98,565,535 (GRCm39) |
A1656S |
probably benign |
Het |
Peg10 |
GC |
GCGCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Pigz |
G |
T |
16: 31,763,787 (GRCm39) |
G282C |
probably damaging |
Het |
Pomk |
G |
A |
8: 26,472,918 (GRCm39) |
T345M |
possibly damaging |
Het |
Psap |
T |
C |
10: 60,130,784 (GRCm39) |
S205P |
possibly damaging |
Het |
Ptpn6 |
A |
T |
6: 124,705,592 (GRCm39) |
F186L |
probably damaging |
Het |
Rnase2b |
T |
C |
14: 51,400,302 (GRCm39) |
S128P |
probably damaging |
Het |
Rnf112 |
C |
T |
11: 61,340,667 (GRCm39) |
V536I |
probably damaging |
Het |
Rnf31 |
A |
T |
14: 55,836,582 (GRCm39) |
E805D |
probably damaging |
Het |
Rps6kc1 |
A |
T |
1: 190,604,021 (GRCm39) |
D200E |
probably benign |
Het |
Rufy2 |
T |
C |
10: 62,818,519 (GRCm39) |
L25P |
probably damaging |
Het |
Sec14l2 |
T |
A |
11: 4,053,978 (GRCm39) |
K230* |
probably null |
Het |
Senp1 |
A |
G |
15: 97,957,806 (GRCm39) |
I364T |
possibly damaging |
Het |
Sod1 |
T |
A |
16: 90,017,753 (GRCm39) |
M3K |
probably benign |
Het |
Stab2 |
T |
C |
10: 86,803,553 (GRCm39) |
D332G |
possibly damaging |
Het |
Tcf4 |
G |
T |
18: 69,790,830 (GRCm39) |
E408* |
probably null |
Het |
Tdrd1 |
T |
C |
19: 56,831,662 (GRCm39) |
M351T |
probably benign |
Het |
Tmem39a |
T |
C |
16: 38,396,126 (GRCm39) |
Y120H |
probably benign |
Het |
Trav16 |
C |
A |
14: 53,980,886 (GRCm39) |
T25K |
possibly damaging |
Het |
Unc13c |
T |
A |
9: 73,839,526 (GRCm39) |
N442Y |
probably benign |
Het |
Yipf1 |
T |
C |
4: 107,176,247 (GRCm39) |
V47A |
probably benign |
Het |
Zeb2 |
T |
C |
2: 44,887,414 (GRCm39) |
T548A |
possibly damaging |
Het |
Zmym4 |
A |
G |
4: 126,771,502 (GRCm39) |
F1291L |
probably damaging |
Het |
|
Other mutations in Vmn2r71 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00922:Vmn2r71
|
APN |
7 |
85,267,901 (GRCm39) |
missense |
probably benign |
|
IGL00960:Vmn2r71
|
APN |
7 |
85,273,582 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01372:Vmn2r71
|
APN |
7 |
85,270,022 (GRCm39) |
splice site |
probably benign |
|
IGL01690:Vmn2r71
|
APN |
7 |
85,264,782 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01909:Vmn2r71
|
APN |
7 |
85,270,001 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01950:Vmn2r71
|
APN |
7 |
85,264,827 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02570:Vmn2r71
|
APN |
7 |
85,264,748 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02650:Vmn2r71
|
APN |
7 |
85,273,535 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02901:Vmn2r71
|
APN |
7 |
85,268,470 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03128:Vmn2r71
|
APN |
7 |
85,268,795 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03328:Vmn2r71
|
APN |
7 |
85,273,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R0533:Vmn2r71
|
UTSW |
7 |
85,268,426 (GRCm39) |
frame shift |
probably null |
|
R0707:Vmn2r71
|
UTSW |
7 |
85,268,640 (GRCm39) |
missense |
probably benign |
|
R0841:Vmn2r71
|
UTSW |
7 |
85,267,749 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0865:Vmn2r71
|
UTSW |
7 |
85,268,516 (GRCm39) |
missense |
probably benign |
0.01 |
R0883:Vmn2r71
|
UTSW |
7 |
85,272,842 (GRCm39) |
missense |
probably benign |
0.19 |
R0939:Vmn2r71
|
UTSW |
7 |
85,272,889 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1597:Vmn2r71
|
UTSW |
7 |
85,273,352 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1646:Vmn2r71
|
UTSW |
7 |
85,270,476 (GRCm39) |
missense |
probably damaging |
0.99 |
R1719:Vmn2r71
|
UTSW |
7 |
85,270,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R1860:Vmn2r71
|
UTSW |
7 |
85,264,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R2013:Vmn2r71
|
UTSW |
7 |
85,269,845 (GRCm39) |
missense |
probably benign |
0.38 |
R2014:Vmn2r71
|
UTSW |
7 |
85,269,845 (GRCm39) |
missense |
probably benign |
0.38 |
R2015:Vmn2r71
|
UTSW |
7 |
85,269,845 (GRCm39) |
missense |
probably benign |
0.38 |
R2050:Vmn2r71
|
UTSW |
7 |
85,273,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R2084:Vmn2r71
|
UTSW |
7 |
85,267,945 (GRCm39) |
missense |
probably benign |
0.03 |
R2221:Vmn2r71
|
UTSW |
7 |
85,273,301 (GRCm39) |
missense |
probably benign |
0.40 |
R2223:Vmn2r71
|
UTSW |
7 |
85,273,301 (GRCm39) |
missense |
probably benign |
0.40 |
R2245:Vmn2r71
|
UTSW |
7 |
85,273,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R3115:Vmn2r71
|
UTSW |
7 |
85,272,866 (GRCm39) |
missense |
probably damaging |
0.97 |
R3122:Vmn2r71
|
UTSW |
7 |
85,264,828 (GRCm39) |
nonsense |
probably null |
|
R3609:Vmn2r71
|
UTSW |
7 |
85,268,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R4093:Vmn2r71
|
UTSW |
7 |
85,270,442 (GRCm39) |
missense |
probably benign |
0.00 |
R4305:Vmn2r71
|
UTSW |
7 |
85,273,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R4306:Vmn2r71
|
UTSW |
7 |
85,273,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R4334:Vmn2r71
|
UTSW |
7 |
85,269,042 (GRCm39) |
missense |
probably benign |
0.01 |
R4569:Vmn2r71
|
UTSW |
7 |
85,273,402 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4622:Vmn2r71
|
UTSW |
7 |
85,269,817 (GRCm39) |
missense |
probably benign |
0.00 |
R4915:Vmn2r71
|
UTSW |
7 |
85,270,476 (GRCm39) |
missense |
probably damaging |
0.99 |
R4956:Vmn2r71
|
UTSW |
7 |
85,268,436 (GRCm39) |
missense |
probably benign |
0.19 |
R5005:Vmn2r71
|
UTSW |
7 |
85,273,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R5045:Vmn2r71
|
UTSW |
7 |
85,273,597 (GRCm39) |
missense |
probably benign |
0.00 |
R5153:Vmn2r71
|
UTSW |
7 |
85,268,430 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5236:Vmn2r71
|
UTSW |
7 |
85,272,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R5373:Vmn2r71
|
UTSW |
7 |
85,267,750 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5405:Vmn2r71
|
UTSW |
7 |
85,268,622 (GRCm39) |
missense |
probably benign |
|
R5831:Vmn2r71
|
UTSW |
7 |
85,272,922 (GRCm39) |
missense |
probably benign |
0.16 |
R6061:Vmn2r71
|
UTSW |
7 |
85,268,482 (GRCm39) |
missense |
probably benign |
|
R6518:Vmn2r71
|
UTSW |
7 |
85,270,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R6751:Vmn2r71
|
UTSW |
7 |
85,269,095 (GRCm39) |
critical splice donor site |
probably null |
|
R6920:Vmn2r71
|
UTSW |
7 |
85,273,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R7358:Vmn2r71
|
UTSW |
7 |
85,273,468 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7453:Vmn2r71
|
UTSW |
7 |
85,273,297 (GRCm39) |
missense |
probably benign |
0.21 |
R7560:Vmn2r71
|
UTSW |
7 |
85,273,115 (GRCm39) |
missense |
probably benign |
0.06 |
R7871:Vmn2r71
|
UTSW |
7 |
85,272,869 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8267:Vmn2r71
|
UTSW |
7 |
85,264,704 (GRCm39) |
missense |
probably benign |
0.02 |
R8377:Vmn2r71
|
UTSW |
7 |
85,264,707 (GRCm39) |
missense |
probably benign |
|
R9278:Vmn2r71
|
UTSW |
7 |
85,269,788 (GRCm39) |
missense |
probably benign |
0.19 |
R9319:Vmn2r71
|
UTSW |
7 |
85,273,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R9329:Vmn2r71
|
UTSW |
7 |
85,267,950 (GRCm39) |
missense |
probably benign |
0.00 |
R9368:Vmn2r71
|
UTSW |
7 |
85,273,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R9636:Vmn2r71
|
UTSW |
7 |
85,268,388 (GRCm39) |
missense |
possibly damaging |
0.80 |
X0025:Vmn2r71
|
UTSW |
7 |
85,267,873 (GRCm39) |
missense |
probably benign |
|
Z1186:Vmn2r71
|
UTSW |
7 |
85,273,094 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- AGCCATGGTGTCCCTATTTG -3'
(R):5'- AAAACCAGGTATTTCAGGTTGC -3'
Sequencing Primer
(F):5'- GTTCATTTCAGATGGAACTGGATAG -3'
(R):5'- ATAAAAGTCCCAGTGTAGGAGTATAG -3'
|
Posted On |
2022-11-14 |