Incidental Mutation 'R4872:Vmn2r129'
| ID |
426174 |
| 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 |
042482-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.701)
|
| Stock # |
R4872 (G1)
|
| Quality Score |
27 |
|
Status
|
Validated
|
| Chromosome |
4 |
| Chromosomal Location |
156683398-156691794 bp(+) (GRCm39) |
| Type of Mutation |
exon |
| DNA Base Change (assembly) |
G to T
at 156686692 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
|
| Meta Mutation Damage Score |
0.0869 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.9%
- 20x: 94.1%
|
| Validation Efficiency |
98% (81/83) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 73 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcd2 |
C |
A |
15: 91,075,514 (GRCm39) |
V100L |
probably benign |
Het |
| Acad11 |
G |
A |
9: 103,963,465 (GRCm39) |
|
probably benign |
Het |
| Actb |
C |
T |
5: 142,891,307 (GRCm39) |
|
probably benign |
Het |
| Ano9 |
G |
A |
7: 140,687,117 (GRCm39) |
A374V |
probably damaging |
Het |
| Baz2b |
T |
C |
2: 59,773,103 (GRCm39) |
|
probably null |
Het |
| Bltp3a |
G |
T |
17: 28,109,110 (GRCm39) |
D1110Y |
probably benign |
Het |
| Bpifb9b |
T |
A |
2: 154,155,551 (GRCm39) |
L350Q |
probably damaging |
Het |
| Cd27 |
T |
A |
6: 125,211,281 (GRCm39) |
|
probably null |
Het |
| Cd72 |
A |
G |
4: 43,449,563 (GRCm39) |
|
probably benign |
Het |
| Cdadc1 |
A |
T |
14: 59,801,973 (GRCm39) |
S516T |
probably benign |
Het |
| Chst5 |
T |
A |
8: 112,617,192 (GRCm39) |
I143F |
possibly damaging |
Het |
| Col20a1 |
T |
C |
2: 180,639,156 (GRCm39) |
V452A |
possibly damaging |
Het |
| Cox11 |
C |
A |
11: 90,535,229 (GRCm39) |
Q227K |
probably benign |
Het |
| Cpa6 |
A |
G |
1: 10,665,843 (GRCm39) |
|
probably null |
Het |
| Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Het |
| Dpm2 |
T |
C |
2: 32,461,203 (GRCm39) |
|
probably benign |
Het |
| Dync1h1 |
C |
A |
12: 110,624,560 (GRCm39) |
T3700N |
probably damaging |
Het |
| Frem1 |
A |
C |
4: 82,881,387 (GRCm39) |
N1273K |
probably damaging |
Het |
| Fry |
T |
C |
5: 150,317,704 (GRCm39) |
|
probably null |
Het |
| Gm10306 |
G |
T |
4: 94,445,069 (GRCm39) |
|
probably benign |
Het |
| Gm5565 |
T |
C |
5: 146,094,913 (GRCm39) |
T278A |
probably benign |
Het |
| Gm8180 |
A |
G |
14: 44,019,802 (GRCm39) |
I40T |
probably benign |
Het |
| Iah1 |
T |
C |
12: 21,367,426 (GRCm39) |
V44A |
probably benign |
Het |
| Iqgap3 |
C |
T |
3: 88,020,435 (GRCm39) |
P360S |
probably damaging |
Het |
| Klhl28 |
T |
A |
12: 65,003,896 (GRCm39) |
I206F |
possibly damaging |
Het |
| Krt13 |
A |
G |
11: 100,012,332 (GRCm39) |
|
probably benign |
Het |
| Lipo2 |
T |
A |
19: 33,726,914 (GRCm39) |
D41V |
probably benign |
Het |
| Lrig2 |
C |
G |
3: 104,398,842 (GRCm39) |
V229L |
possibly damaging |
Het |
| Lrrc32 |
C |
T |
7: 98,147,727 (GRCm39) |
T169I |
probably damaging |
Het |
| Lrriq1 |
T |
C |
10: 103,014,649 (GRCm39) |
N1053S |
possibly damaging |
Het |
| Mfng |
C |
T |
15: 78,648,588 (GRCm39) |
R163H |
probably benign |
Het |
| Mgat4c |
G |
C |
10: 102,224,599 (GRCm39) |
R271P |
probably damaging |
Het |
| Mylk |
A |
G |
16: 34,735,360 (GRCm39) |
N780S |
possibly damaging |
Het |
| N4bp1 |
T |
C |
8: 87,587,676 (GRCm39) |
T421A |
probably benign |
Het |
| Nat8f1 |
T |
C |
6: 85,887,295 (GRCm39) |
T222A |
probably benign |
Het |
| Nsun2 |
T |
C |
13: 69,691,992 (GRCm39) |
|
probably benign |
Het |
| Oas2 |
T |
A |
5: 120,876,599 (GRCm39) |
D448V |
probably damaging |
Het |
| Or10al7 |
C |
A |
17: 38,366,467 (GRCm39) |
V6F |
probably benign |
Het |
| Or2l13b |
A |
T |
16: 19,349,383 (GRCm39) |
C96S |
probably damaging |
Het |
| Or5ak22 |
T |
C |
2: 85,230,772 (GRCm39) |
Y35C |
probably damaging |
Het |
| Pgm2l1 |
T |
A |
7: 99,877,204 (GRCm39) |
L25Q |
probably damaging |
Het |
| Pigp |
A |
T |
16: 94,166,309 (GRCm39) |
V133D |
probably benign |
Het |
| Pnkp |
C |
T |
7: 44,511,827 (GRCm39) |
S113L |
probably damaging |
Het |
| Pomt2 |
C |
T |
12: 87,156,881 (GRCm39) |
D752N |
possibly damaging |
Het |
| Ppat |
T |
C |
5: 77,074,640 (GRCm39) |
K65E |
probably damaging |
Het |
| Ptprn2 |
T |
C |
12: 117,125,314 (GRCm39) |
L616P |
probably damaging |
Het |
| Rad54l2 |
A |
G |
9: 106,595,091 (GRCm39) |
S289P |
probably damaging |
Het |
| Rbm39 |
G |
A |
2: 156,019,266 (GRCm39) |
R31C |
possibly damaging |
Het |
| Rhbdf2 |
C |
A |
11: 116,492,771 (GRCm39) |
V417L |
probably benign |
Het |
| Rnf157 |
T |
A |
11: 116,246,298 (GRCm39) |
E255D |
possibly damaging |
Het |
| Rpl6l |
A |
T |
10: 110,962,304 (GRCm39) |
|
noncoding transcript |
Het |
| Sec24c |
A |
G |
14: 20,743,813 (GRCm39) |
D1006G |
probably damaging |
Het |
| Sh3bp1 |
G |
T |
15: 78,792,237 (GRCm39) |
A401S |
probably benign |
Het |
| Slc17a8 |
A |
T |
10: 89,412,367 (GRCm39) |
D539E |
probably benign |
Het |
| Slc38a9 |
T |
A |
13: 112,826,098 (GRCm39) |
S136R |
probably damaging |
Het |
| Smoc2 |
A |
C |
17: 14,589,295 (GRCm39) |
T255P |
probably benign |
Het |
| Smyd2 |
T |
C |
1: 189,628,847 (GRCm39) |
D152G |
probably damaging |
Het |
| Stab1 |
A |
G |
14: 30,862,350 (GRCm39) |
V2328A |
probably damaging |
Het |
| Taar2 |
A |
G |
10: 23,816,591 (GRCm39) |
I44V |
probably benign |
Het |
| Tbc1d4 |
T |
C |
14: 101,682,144 (GRCm39) |
K1251E |
probably benign |
Het |
| Thada |
G |
A |
17: 84,754,027 (GRCm39) |
L315F |
probably damaging |
Het |
| Trbv14 |
T |
C |
6: 41,112,259 (GRCm39) |
S19P |
probably benign |
Het |
| Ttc39c |
T |
C |
18: 12,820,173 (GRCm39) |
|
probably benign |
Het |
| Ttc39d |
A |
G |
17: 80,524,527 (GRCm39) |
I395M |
probably benign |
Het |
| Ttn |
T |
C |
2: 76,548,728 (GRCm39) |
E31891G |
probably damaging |
Het |
| Ubr3 |
T |
C |
2: 69,800,527 (GRCm39) |
V950A |
probably damaging |
Het |
| Usp9y |
T |
A |
Y: 1,307,920 (GRCm39) |
K2305N |
probably damaging |
Het |
| Vmn1r158 |
G |
A |
7: 22,490,179 (GRCm39) |
T10I |
possibly damaging |
Het |
| Vmn2r78 |
T |
A |
7: 86,603,916 (GRCm39) |
I698K |
possibly damaging |
Het |
| Vmn2r86 |
G |
T |
10: 130,289,460 (GRCm39) |
T145K |
probably damaging |
Het |
| Zfp51 |
T |
C |
17: 21,684,933 (GRCm39) |
V516A |
probably benign |
Het |
| Zfp654 |
A |
T |
16: 64,606,145 (GRCm39) |
S686T |
probably benign |
Het |
| Zfp846 |
T |
A |
9: 20,502,111 (GRCm39) |
C55S |
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 |
|
|
R4840:Vmn2r129
|
UTSW |
4 |
156,685,733 (GRCm39) |
intron |
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'- GCAGATATACATGACAAGGGCTAC -3'
(R):5'- GCAGTGATGTCCATTCCAAGG -3'
Sequencing Primer
(F):5'- ATGACATCTTCAGCAAAGGTTG -3'
(R):5'- CAGTGATGTCCATTCCAAGGTGTTG -3'
|
| Posted On |
2016-08-16 |
Incidental Mutation