Incidental Mutation 'R2147:Vmn2r129'
| ID |
233899 |
| 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 |
040150-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.711)
|
| Stock # |
R2147 (G1)
|
| Quality Score |
191 |
|
Status
|
Not validated
|
| Chromosome |
4 |
| Chromosomal Location |
156683398-156691794 bp(+) (GRCm39) |
| Type of Mutation |
critical splice donor site |
| DNA Base Change (assembly) |
T to C
at 156687014 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: 98.7%
- 10x: 97.5%
- 20x: 95.7%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 76 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930523C07Rik |
T |
A |
1: 159,903,003 (GRCm39) |
M91K |
probably benign |
Het |
| Abr |
T |
C |
11: 76,346,474 (GRCm39) |
R437G |
probably damaging |
Het |
| Acaca |
T |
G |
11: 84,167,362 (GRCm39) |
D1045E |
probably benign |
Het |
| Adam23 |
A |
T |
1: 63,573,521 (GRCm39) |
|
probably null |
Het |
| Adam34 |
A |
G |
8: 44,105,538 (GRCm39) |
Y36H |
probably benign |
Het |
| Alg11 |
G |
A |
8: 22,555,309 (GRCm39) |
G108D |
probably damaging |
Het |
| Alox12e |
A |
T |
11: 70,210,771 (GRCm39) |
I316N |
probably damaging |
Het |
| Arid1a |
A |
T |
4: 133,408,677 (GRCm39) |
F1943L |
unknown |
Het |
| Armh4 |
T |
C |
14: 49,989,028 (GRCm39) |
D647G |
probably benign |
Het |
| Auh |
G |
A |
13: 52,989,532 (GRCm39) |
P308L |
probably benign |
Het |
| BC035044 |
T |
C |
6: 128,867,867 (GRCm39) |
|
probably benign |
Het |
| Bcor |
G |
A |
X: 11,923,862 (GRCm39) |
A578V |
possibly damaging |
Het |
| C1qtnf12 |
A |
G |
4: 156,050,922 (GRCm39) |
N297S |
probably benign |
Het |
| Cadps2 |
G |
T |
6: 23,838,998 (GRCm39) |
|
probably benign |
Het |
| Ccnf |
A |
T |
17: 24,449,288 (GRCm39) |
|
probably null |
Het |
| Cdadc1 |
A |
G |
14: 59,835,202 (GRCm39) |
|
probably null |
Het |
| Cep57l1 |
A |
G |
10: 41,616,895 (GRCm39) |
Y131H |
probably damaging |
Het |
| Cfap251 |
T |
C |
5: 123,394,254 (GRCm39) |
V381A |
probably benign |
Het |
| Cfap44 |
A |
G |
16: 44,272,047 (GRCm39) |
R1267G |
probably benign |
Het |
| Chd3 |
A |
T |
11: 69,239,854 (GRCm39) |
L1658Q |
probably benign |
Het |
| Chl1 |
T |
C |
6: 103,692,362 (GRCm39) |
|
probably null |
Het |
| Chpf2 |
T |
A |
5: 24,797,033 (GRCm39) |
F660I |
probably damaging |
Het |
| Cmas |
T |
A |
6: 142,717,015 (GRCm39) |
D302E |
probably benign |
Het |
| Cpne3 |
T |
A |
4: 19,536,562 (GRCm39) |
M233L |
probably benign |
Het |
| Csmd3 |
CCTTTGCGCTT |
CCTT |
15: 47,604,632 (GRCm39) |
|
probably null |
Het |
| Dennd3 |
T |
G |
15: 73,395,336 (GRCm39) |
L143R |
probably damaging |
Het |
| Dnah2 |
T |
C |
11: 69,406,587 (GRCm39) |
M552V |
probably benign |
Het |
| Dock2 |
A |
G |
11: 34,179,472 (GRCm39) |
|
probably null |
Het |
| Ergic1 |
A |
G |
17: 26,855,024 (GRCm39) |
|
probably null |
Het |
| Fbxl15 |
A |
T |
19: 46,317,627 (GRCm39) |
D103V |
probably damaging |
Het |
| Gm4781 |
C |
A |
10: 100,232,414 (GRCm39) |
|
noncoding transcript |
Het |
| Hpca |
A |
G |
4: 129,012,278 (GRCm39) |
I86T |
possibly damaging |
Het |
| Katnip |
T |
A |
7: 125,464,492 (GRCm39) |
H1286Q |
probably damaging |
Het |
| Lamb3 |
T |
C |
1: 193,010,212 (GRCm39) |
V275A |
probably benign |
Het |
| Lipe |
G |
T |
7: 25,087,946 (GRCm39) |
A38E |
probably benign |
Het |
| Lrrk1 |
A |
T |
7: 65,935,159 (GRCm39) |
|
probably null |
Het |
| Lrsam1 |
T |
C |
2: 32,835,891 (GRCm39) |
K292R |
probably damaging |
Het |
| Mbtps1 |
A |
T |
8: 120,265,598 (GRCm39) |
H316Q |
probably benign |
Het |
| Mms22l |
T |
A |
4: 24,580,063 (GRCm39) |
Y525* |
probably null |
Het |
| Mrps14 |
T |
C |
1: 160,022,862 (GRCm39) |
L9P |
possibly damaging |
Het |
| Mycbp2 |
G |
A |
14: 103,393,358 (GRCm39) |
H3068Y |
probably damaging |
Het |
| Myo15a |
A |
G |
11: 60,401,055 (GRCm39) |
D2992G |
possibly damaging |
Het |
| N4bp2 |
T |
A |
5: 65,966,543 (GRCm39) |
L1327Q |
probably damaging |
Het |
| Nradd |
A |
T |
9: 110,451,243 (GRCm39) |
F42I |
probably benign |
Het |
| Or5k8 |
T |
A |
16: 58,644,842 (GRCm39) |
I77F |
probably damaging |
Het |
| Pank1 |
T |
C |
19: 34,804,754 (GRCm39) |
H134R |
probably benign |
Het |
| Pcdh7 |
T |
A |
5: 58,286,458 (GRCm39) |
M1178K |
possibly damaging |
Het |
| Pcnx3 |
A |
T |
19: 5,717,633 (GRCm39) |
I1084N |
probably damaging |
Het |
| Pdcd11 |
A |
G |
19: 47,093,191 (GRCm39) |
M490V |
probably benign |
Het |
| Phf2 |
T |
C |
13: 48,958,165 (GRCm39) |
K950E |
unknown |
Het |
| Pitpnc1 |
C |
T |
11: 107,103,344 (GRCm39) |
A252T |
probably damaging |
Het |
| Prickle2 |
A |
G |
6: 92,402,652 (GRCm39) |
L112P |
probably damaging |
Het |
| Prpf8 |
A |
G |
11: 75,381,357 (GRCm39) |
I231V |
probably benign |
Het |
| Scin |
T |
A |
12: 40,130,984 (GRCm39) |
M310L |
probably benign |
Het |
| Serpina3m |
T |
A |
12: 104,355,483 (GRCm39) |
I50N |
probably benign |
Het |
| Skint8 |
C |
G |
4: 111,794,274 (GRCm39) |
N221K |
probably damaging |
Het |
| Slc22a23 |
C |
T |
13: 34,366,990 (GRCm39) |
V673M |
probably benign |
Het |
| Slc24a5 |
A |
G |
2: 124,929,361 (GRCm39) |
D368G |
probably damaging |
Het |
| Slc28a1 |
A |
T |
7: 80,776,015 (GRCm39) |
Q237L |
possibly damaging |
Het |
| Smchd1 |
T |
A |
17: 71,705,583 (GRCm39) |
K1005N |
possibly damaging |
Het |
| Stim2 |
T |
C |
5: 54,262,717 (GRCm39) |
Y320H |
probably damaging |
Het |
| Syne3 |
T |
A |
12: 104,919,357 (GRCm39) |
D512V |
probably damaging |
Het |
| Tada2a |
T |
C |
11: 83,970,455 (GRCm39) |
D432G |
probably damaging |
Het |
| Tcp10a |
T |
C |
17: 7,601,701 (GRCm39) |
S216P |
probably damaging |
Het |
| Tmem178b |
A |
T |
6: 40,184,435 (GRCm39) |
Q111L |
probably damaging |
Het |
| Tmem236 |
A |
G |
2: 14,223,861 (GRCm39) |
I217V |
probably benign |
Het |
| Tmem45b |
A |
G |
9: 31,340,277 (GRCm39) |
V128A |
probably benign |
Het |
| Tnfaip2 |
T |
C |
12: 111,412,456 (GRCm39) |
Y286H |
probably damaging |
Het |
| Tsc2 |
T |
A |
17: 24,840,116 (GRCm39) |
I427L |
possibly damaging |
Het |
| Ttc17 |
T |
A |
2: 94,132,139 (GRCm39) |
N1180I |
possibly damaging |
Het |
| Ubr1 |
T |
G |
2: 120,694,811 (GRCm39) |
D1707A |
probably damaging |
Het |
| Vmn1r11 |
A |
G |
6: 57,114,583 (GRCm39) |
I82M |
probably benign |
Het |
| Vps41 |
G |
T |
13: 19,023,904 (GRCm39) |
|
probably null |
Het |
| Wnt5a |
A |
G |
14: 28,235,274 (GRCm39) |
Y86C |
probably damaging |
Het |
| Zfp629 |
T |
C |
7: 127,209,616 (GRCm39) |
H731R |
probably damaging |
Het |
| Zfp712 |
T |
C |
13: 67,189,960 (GRCm39) |
E189G |
possibly damaging |
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 |
|
|
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 |
|
|
R4840:Vmn2r129
|
UTSW |
4 |
156,685,733 (GRCm39) |
intron |
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'- CTTGGAATGGACATCACTGCAC -3'
(R):5'- GTTGAGACACCTTTTCACAAAACTC -3'
Sequencing Primer
(F):5'- CTGCACAACTATGATATGGCG -3'
(R):5'- CCTTTTCACAAAACTCACTGATATTC -3'
|
| Posted On |
2014-10-01 |
Incidental Mutation