Incidental Mutation 'R4840:Vmn2r129'
| ID |
371710 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Vmn2r129
|
| Ensembl Gene |
ENSMUSG00000057021 |
| Gene Name |
vomeronasal 2, receptor 129 |
| Synonyms |
Vmn2r-ps160, Vmn2r-ps159, V2r9, V2r8 |
| MMRRC Submission |
042453-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.711)
|
| Stock # |
R4840 (G1)
|
| Quality Score |
145 |
|
Status
|
Validated
|
| Chromosome |
4 |
| Chromosomal Location |
156683398-156691794 bp(+) (GRCm39) |
| Type of Mutation |
intron |
| DNA Base Change (assembly) |
G to C
at 156685733 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Gene Model |
predicted gene model for transcript(s):
|
| AlphaFold |
A0A3Q4EIC8 |
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000074107
|
| SMART Domains |
Protein: ENSMUSP00000128975
Gene: ENSMUSG00000057021
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
24 |
N/A |
INTRINSIC |
|
Pfam:ANF_receptor
|
76 |
423 |
1.4e-32 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000096792
|
| SMART Domains |
Protein: ENSMUSP00000094554
Gene: ENSMUSG00000057021
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
24 |
N/A |
INTRINSIC |
|
Pfam:ANF_receptor
|
76 |
441 |
3.7e-31 |
PFAM |
|
Pfam:NCD3G
|
510 |
563 |
1.4e-20 |
PFAM |
|
Pfam:7tm_3
|
596 |
831 |
1.9e-56 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000189559
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.9%
- 20x: 94.1%
|
| Validation Efficiency |
97% (114/117) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 103 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2810459M11Rik |
C |
A |
1: 85,974,166 (GRCm39) |
T161K |
probably benign |
Het |
| Actn3 |
G |
A |
19: 4,914,539 (GRCm39) |
R530W |
probably damaging |
Het |
| Alg11 |
C |
T |
8: 22,558,026 (GRCm39) |
A404V |
possibly damaging |
Het |
| Alkbh8 |
T |
A |
9: 3,369,751 (GRCm39) |
V340D |
probably damaging |
Het |
| Arhgef12 |
T |
C |
9: 42,886,364 (GRCm39) |
H1166R |
probably benign |
Het |
| Aspm |
T |
A |
1: 139,398,269 (GRCm39) |
D978E |
possibly damaging |
Het |
| Bod1l |
C |
T |
5: 41,975,815 (GRCm39) |
G1833D |
probably damaging |
Het |
| Brd3 |
A |
G |
2: 27,339,251 (GRCm39) |
V676A |
possibly damaging |
Het |
| Brip1 |
G |
A |
11: 86,037,009 (GRCm39) |
T454I |
possibly damaging |
Het |
| C3ar1 |
T |
C |
6: 122,827,723 (GRCm39) |
I165V |
probably benign |
Het |
| Camta1 |
T |
A |
4: 151,228,864 (GRCm39) |
Q656L |
probably benign |
Het |
| Casp14 |
A |
T |
10: 78,549,178 (GRCm39) |
L256* |
probably null |
Het |
| Cdh23 |
G |
T |
10: 60,255,556 (GRCm39) |
H773Q |
possibly damaging |
Het |
| Chd1 |
G |
T |
17: 15,989,016 (GRCm39) |
D1590Y |
probably damaging |
Het |
| Chd1 |
G |
A |
17: 15,989,015 (GRCm39) |
W1589* |
probably null |
Het |
| Cldn19 |
A |
G |
4: 119,112,951 (GRCm39) |
Q61R |
probably damaging |
Het |
| Cyp2a22 |
A |
G |
7: 26,631,949 (GRCm39) |
S436P |
probably benign |
Het |
| Emc10 |
A |
C |
7: 44,142,051 (GRCm39) |
V124G |
probably damaging |
Het |
| Enam |
A |
T |
5: 88,650,885 (GRCm39) |
D723V |
probably benign |
Het |
| Eps8 |
C |
A |
6: 137,504,128 (GRCm39) |
Q158H |
probably damaging |
Het |
| Ercc6 |
G |
A |
14: 32,263,253 (GRCm39) |
D486N |
probably damaging |
Het |
| Fasn |
T |
C |
11: 120,703,885 (GRCm39) |
E1485G |
possibly damaging |
Het |
| Fat2 |
T |
C |
11: 55,169,844 (GRCm39) |
K2972E |
probably benign |
Het |
| Fbxw28 |
T |
C |
9: 109,168,602 (GRCm39) |
K30R |
probably null |
Het |
| Flot2 |
T |
A |
11: 77,948,339 (GRCm39) |
L164Q |
probably damaging |
Het |
| Fsip2 |
A |
T |
2: 82,779,739 (GRCm39) |
I162L |
probably benign |
Het |
| Fsip2 |
A |
T |
2: 82,815,815 (GRCm39) |
L3849F |
probably benign |
Het |
| Gabrb1 |
C |
G |
5: 71,858,154 (GRCm39) |
P60R |
probably damaging |
Het |
| Galnt14 |
T |
C |
17: 73,811,893 (GRCm39) |
R443G |
probably benign |
Het |
| Gas8 |
C |
T |
8: 124,257,753 (GRCm39) |
T400M |
probably benign |
Het |
| Gfap |
T |
C |
11: 102,785,214 (GRCm39) |
Y254C |
probably damaging |
Het |
| Git2 |
A |
G |
5: 114,883,543 (GRCm39) |
S396P |
probably damaging |
Het |
| Glb1l3 |
A |
T |
9: 26,740,349 (GRCm39) |
M327K |
probably benign |
Het |
| Gm10715 |
A |
C |
9: 3,038,062 (GRCm39) |
|
probably benign |
Het |
| Gm10787 |
G |
A |
10: 76,857,841 (GRCm39) |
|
noncoding transcript |
Het |
| Gm1123 |
T |
A |
9: 98,900,622 (GRCm39) |
D78V |
probably damaging |
Het |
| Gm27013 |
T |
C |
6: 130,655,079 (GRCm39) |
T128A |
probably benign |
Het |
| Gpbp1 |
A |
G |
13: 111,577,164 (GRCm39) |
|
probably null |
Het |
| Gphn |
G |
A |
12: 78,569,729 (GRCm39) |
|
probably null |
Het |
| Gpr157 |
A |
G |
4: 150,186,823 (GRCm39) |
E317G |
probably benign |
Het |
| Gsdmc4 |
T |
A |
15: 63,765,596 (GRCm39) |
M318L |
probably benign |
Het |
| Gtf2f2 |
A |
T |
14: 76,248,131 (GRCm39) |
W19R |
probably damaging |
Het |
| Gvin-ps3 |
T |
C |
7: 105,680,627 (GRCm39) |
|
noncoding transcript |
Het |
| Helb |
A |
G |
10: 119,920,763 (GRCm39) |
V1060A |
probably benign |
Het |
| Igfn1 |
C |
T |
1: 135,895,778 (GRCm39) |
G1596D |
probably benign |
Het |
| Il1rl2 |
T |
C |
1: 40,366,547 (GRCm39) |
I27T |
possibly damaging |
Het |
| Inpp5j |
A |
G |
11: 3,449,676 (GRCm39) |
V702A |
probably damaging |
Het |
| Kmt2d |
A |
C |
15: 98,759,775 (GRCm39) |
V1161G |
unknown |
Het |
| Krtap1-3 |
T |
G |
11: 99,481,715 (GRCm39) |
Y144S |
possibly damaging |
Het |
| Layn |
C |
T |
9: 50,968,682 (GRCm39) |
V354M |
probably damaging |
Het |
| Lrba |
G |
A |
3: 86,526,816 (GRCm39) |
|
probably null |
Het |
| Lrp8 |
T |
A |
4: 107,727,234 (GRCm39) |
L893Q |
possibly damaging |
Het |
| Mrps9 |
T |
A |
1: 42,937,575 (GRCm39) |
|
probably benign |
Het |
| Mug1 |
T |
A |
6: 121,862,813 (GRCm39) |
M1387K |
probably damaging |
Het |
| Myo18b |
A |
C |
5: 113,021,895 (GRCm39) |
V499G |
probably benign |
Het |
| Nbea |
T |
C |
3: 55,618,091 (GRCm39) |
E2321G |
probably benign |
Het |
| Nrsn2 |
C |
T |
2: 152,211,552 (GRCm39) |
V160I |
probably benign |
Het |
| Nup210 |
G |
A |
6: 91,008,650 (GRCm39) |
Q510* |
probably null |
Het |
| Ofcc1 |
G |
A |
13: 40,168,864 (GRCm39) |
T841I |
probably damaging |
Het |
| Or2ag12 |
T |
G |
7: 106,277,330 (GRCm39) |
D121A |
probably damaging |
Het |
| P3h3 |
G |
T |
6: 124,827,600 (GRCm39) |
Q479K |
possibly damaging |
Het |
| Paqr9 |
T |
A |
9: 95,442,723 (GRCm39) |
F238I |
probably damaging |
Het |
| Parp3 |
A |
T |
9: 106,350,308 (GRCm39) |
L343H |
probably damaging |
Het |
| Pcdh18 |
A |
C |
3: 49,699,117 (GRCm39) |
M1115R |
probably damaging |
Het |
| Pcdh8 |
A |
G |
14: 80,008,308 (GRCm39) |
V85A |
possibly damaging |
Het |
| Pcdhb4 |
A |
G |
18: 37,441,452 (GRCm39) |
N254S |
possibly damaging |
Het |
| Pld1 |
T |
C |
3: 28,130,700 (GRCm39) |
V500A |
probably benign |
Het |
| Pramel29 |
T |
C |
4: 143,935,144 (GRCm39) |
K199R |
probably damaging |
Het |
| Prkg2 |
A |
T |
5: 99,129,002 (GRCm39) |
D311E |
probably benign |
Het |
| Prss42 |
T |
C |
9: 110,628,369 (GRCm39) |
L171P |
probably damaging |
Het |
| Pth2 |
T |
A |
7: 44,830,767 (GRCm39) |
L17H |
probably damaging |
Het |
| Reln |
A |
T |
5: 22,223,844 (GRCm39) |
|
probably null |
Het |
| Rmi2 |
G |
T |
16: 10,657,701 (GRCm39) |
V104L |
probably damaging |
Het |
| Rpusd4 |
T |
A |
9: 35,179,831 (GRCm39) |
V108D |
probably damaging |
Het |
| Rufy4 |
C |
A |
1: 74,168,198 (GRCm39) |
T82K |
possibly damaging |
Het |
| Scimp |
G |
A |
11: 70,682,294 (GRCm39) |
Q141* |
probably null |
Het |
| Sel1l2 |
T |
C |
2: 140,105,390 (GRCm39) |
T267A |
probably benign |
Het |
| Sema5a |
T |
A |
15: 32,550,400 (GRCm39) |
S146R |
possibly damaging |
Het |
| Sh2d3c |
T |
C |
2: 32,611,172 (GRCm39) |
M1T |
probably null |
Het |
| Slc30a6 |
T |
C |
17: 74,712,716 (GRCm39) |
L71P |
probably damaging |
Het |
| Srrm3 |
A |
G |
5: 135,883,449 (GRCm39) |
Y224C |
possibly damaging |
Het |
| Tacr3 |
A |
T |
3: 134,560,615 (GRCm39) |
T185S |
possibly damaging |
Het |
| Tas2r140 |
T |
A |
6: 133,032,528 (GRCm39) |
T77S |
probably benign |
Het |
| Thsd7b |
T |
C |
1: 129,523,581 (GRCm39) |
V128A |
probably benign |
Het |
| Tnfrsf10b |
T |
G |
14: 70,013,608 (GRCm39) |
H179Q |
probably damaging |
Het |
| Tonsl |
A |
G |
15: 76,517,409 (GRCm39) |
V770A |
probably benign |
Het |
| Trim42 |
G |
A |
9: 97,244,982 (GRCm39) |
P606L |
probably benign |
Het |
| Trim45 |
A |
T |
3: 100,832,804 (GRCm39) |
T346S |
possibly damaging |
Het |
| Ttc28 |
C |
A |
5: 111,433,947 (GRCm39) |
S2296Y |
probably damaging |
Het |
| Ttc41 |
C |
T |
10: 86,566,989 (GRCm39) |
R552C |
probably benign |
Het |
| Tube1 |
A |
G |
10: 39,020,842 (GRCm39) |
N243D |
probably benign |
Het |
| Tvp23b |
G |
T |
11: 62,770,424 (GRCm39) |
|
probably null |
Het |
| Ubxn11 |
T |
A |
4: 133,836,919 (GRCm39) |
I49N |
probably damaging |
Het |
| Usp17le |
T |
A |
7: 104,418,977 (GRCm39) |
E55V |
probably benign |
Het |
| Vmn2r114 |
A |
T |
17: 23,510,353 (GRCm39) |
V709D |
probably damaging |
Het |
| Vmn2r23 |
C |
T |
6: 123,690,033 (GRCm39) |
T303M |
probably damaging |
Het |
| Vmn2r60 |
C |
T |
7: 41,785,285 (GRCm39) |
P166S |
probably damaging |
Het |
| Vmn2r83 |
A |
G |
10: 79,313,682 (GRCm39) |
I97V |
possibly damaging |
Het |
| Wbp2nl |
A |
T |
15: 82,198,537 (GRCm39) |
K358M |
possibly damaging |
Het |
| Xpo1 |
T |
A |
11: 23,228,183 (GRCm39) |
I150N |
probably damaging |
Het |
| Zfp113 |
G |
A |
5: 138,143,687 (GRCm39) |
L188F |
probably damaging |
Het |
| Zfp189 |
T |
G |
4: 49,529,984 (GRCm39) |
S362R |
probably damaging |
Het |
| Zfp593os |
A |
G |
4: 133,972,587 (GRCm39) |
|
probably benign |
Het |
|
| Other mutations in Vmn2r129 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00977:Vmn2r129
|
APN |
4 |
156,686,491 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL00990:Vmn2r129
|
APN |
4 |
156,686,692 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL00990:Vmn2r129
|
APN |
4 |
156,686,558 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL00990:Vmn2r129
|
APN |
4 |
156,690,755 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL00990:Vmn2r129
|
APN |
4 |
156,690,730 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL00990:Vmn2r129
|
APN |
4 |
156,690,441 (GRCm39) |
splice site |
noncoding transcript |
|
|
IGL00990:Vmn2r129
|
APN |
4 |
156,690,779 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL00990:Vmn2r129
|
APN |
4 |
156,686,857 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01018:Vmn2r129
|
APN |
4 |
156,687,885 (GRCm39) |
intron |
noncoding transcript |
|
|
IGL01018:Vmn2r129
|
APN |
4 |
156,686,558 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01018:Vmn2r129
|
APN |
4 |
156,690,730 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01018:Vmn2r129
|
APN |
4 |
156,690,441 (GRCm39) |
splice site |
noncoding transcript |
|
|
IGL01018:Vmn2r129
|
APN |
4 |
156,686,900 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01829:Vmn2r129
|
APN |
4 |
156,685,614 (GRCm39) |
intron |
noncoding transcript |
|
|
IGL01863:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01864:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01865:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01866:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01868:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01869:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01872:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01873:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01876:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01877:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01878:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01879:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01880:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01884:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01885:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01886:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01887:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01888:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01890:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01891:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01893:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01894:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01896:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01897:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01898:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01899:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01901:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01902:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01903:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01904:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01905:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01906:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01907:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01908:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01909:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01913:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01915:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01916:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01917:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01918:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01919:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01920:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01921:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01922:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01923:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01927:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01928:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01929:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01930:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01931:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01932:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01935:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01937:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01939:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01941:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01942:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01944:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01945:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01946:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01949:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01953:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01954:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01956:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL01957:Vmn2r129
|
APN |
4 |
156,690,549 (GRCm39) |
exon |
noncoding transcript |
|
|
IGL02270:Vmn2r129
|
APN |
4 |
156,686,950 (GRCm39) |
exon |
noncoding transcript |
|
|
R1746:Vmn2r129
|
UTSW |
4 |
156,686,692 (GRCm39) |
exon |
noncoding transcript |
|
|
R1870:Vmn2r129
|
UTSW |
4 |
156,686,692 (GRCm39) |
exon |
noncoding transcript |
|
|
R2147:Vmn2r129
|
UTSW |
4 |
156,687,014 (GRCm39) |
critical splice donor site |
noncoding transcript |
|
|
R2168:Vmn2r129
|
UTSW |
4 |
156,690,673 (GRCm39) |
exon |
noncoding transcript |
|
|
R2345:Vmn2r129
|
UTSW |
4 |
156,689,334 (GRCm39) |
splice site |
noncoding transcript |
|
|
R2510:Vmn2r129
|
UTSW |
4 |
156,686,692 (GRCm39) |
exon |
noncoding transcript |
|
|
R2899:Vmn2r129
|
UTSW |
4 |
156,686,692 (GRCm39) |
exon |
noncoding transcript |
|
|
R3106:Vmn2r129
|
UTSW |
4 |
156,685,730 (GRCm39) |
intron |
noncoding transcript |
|
|
R3122:Vmn2r129
|
UTSW |
4 |
156,686,692 (GRCm39) |
exon |
noncoding transcript |
|
|
R3405:Vmn2r129
|
UTSW |
4 |
156,686,692 (GRCm39) |
exon |
noncoding transcript |
|
|
R3430:Vmn2r129
|
UTSW |
4 |
156,686,692 (GRCm39) |
exon |
noncoding transcript |
|
|
R3732:Vmn2r129
|
UTSW |
4 |
156,686,692 (GRCm39) |
exon |
noncoding transcript |
|
|
R3751:Vmn2r129
|
UTSW |
4 |
156,686,692 (GRCm39) |
exon |
noncoding transcript |
|
|
R4108:Vmn2r129
|
UTSW |
4 |
156,686,692 (GRCm39) |
exon |
noncoding transcript |
|
|
R4112:Vmn2r129
|
UTSW |
4 |
156,686,692 (GRCm39) |
exon |
noncoding transcript |
|
|
R4120:Vmn2r129
|
UTSW |
4 |
156,686,778 (GRCm39) |
exon |
noncoding transcript |
|
|
R4135:Vmn2r129
|
UTSW |
4 |
156,691,085 (GRCm39) |
exon |
noncoding transcript |
|
|
R4302:Vmn2r129
|
UTSW |
4 |
156,686,692 (GRCm39) |
exon |
noncoding transcript |
|
|
R4475:Vmn2r129
|
UTSW |
4 |
156,691,085 (GRCm39) |
exon |
noncoding transcript |
|
|
R4872:Vmn2r129
|
UTSW |
4 |
156,686,692 (GRCm39) |
exon |
noncoding transcript |
|
|
R5144:Vmn2r129
|
UTSW |
4 |
156,686,692 (GRCm39) |
exon |
noncoding transcript |
|
|
R5271:Vmn2r129
|
UTSW |
4 |
156,686,692 (GRCm39) |
exon |
noncoding transcript |
|
|
R5625:Vmn2r129
|
UTSW |
4 |
156,686,505 (GRCm39) |
exon |
noncoding transcript |
|
|
R5775:Vmn2r129
|
UTSW |
4 |
156,686,692 (GRCm39) |
exon |
noncoding transcript |
|
|
| Predicted Primers |
PCR Primer
(F):5'- TGCTATCGATGAGATCAACAGGAATC -3'
(R):5'- CTGTTTGCACAGTACATCTATGAAC -3'
Sequencing Primer
(F):5'- CGATGAGATCAACAGGAATCCTTATC -3'
(R):5'- CGTGTGTGTTTGTGTAGCAGC -3'
|
| Posted On |
2016-03-01 |
Incidental Mutation