Incidental Mutation 'R5256:Vmn2r6'
ID |
399597 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Vmn2r6
|
Ensembl Gene |
ENSMUSG00000090581 |
Gene Name |
vomeronasal 2, receptor 6 |
Synonyms |
EG667069, EG620718 |
MMRRC Submission |
042827-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.198)
|
Stock # |
R5256 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
3 |
Chromosomal Location |
64444916-64472855 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 64464263 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Asparagine to Lysine
at position 190
(N190K)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000135148
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000165012]
[ENSMUST00000176481]
|
AlphaFold |
H3BK29 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000165012
AA Change: N101K
PolyPhen 2
Score 0.008 (Sensitivity: 0.96; Specificity: 0.76)
|
SMART Domains |
Protein: ENSMUSP00000131831 Gene: ENSMUSG00000090581 AA Change: N101K
Domain | Start | End | E-Value | Type |
Pfam:ANF_receptor
|
1 |
416 |
1.4e-72 |
PFAM |
Pfam:Peripla_BP_6
|
58 |
244 |
1.2e-10 |
PFAM |
Pfam:NCD3G
|
458 |
511 |
1.8e-17 |
PFAM |
Pfam:7tm_3
|
542 |
779 |
3.9e-76 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000176481
AA Change: N190K
PolyPhen 2
Score 0.326 (Sensitivity: 0.90; Specificity: 0.89)
|
SMART Domains |
Protein: ENSMUSP00000135148 Gene: ENSMUSG00000090581 AA Change: N190K
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
22 |
N/A |
INTRINSIC |
Pfam:ANF_receptor
|
88 |
505 |
9.8e-77 |
PFAM |
Pfam:Peripla_BP_6
|
142 |
331 |
3.4e-10 |
PFAM |
Pfam:NCD3G
|
547 |
600 |
5.4e-17 |
PFAM |
Pfam:7tm_3
|
633 |
867 |
3.9e-47 |
PFAM |
|
Meta Mutation Damage Score |
0.0898 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.3%
- 10x: 96.4%
- 20x: 92.8%
|
Validation Efficiency |
97% (95/98) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A730015C16Rik |
C |
A |
4: 108,705,262 (GRCm39) |
|
probably benign |
Het |
Actr1b |
T |
C |
1: 36,739,173 (GRCm39) |
H372R |
probably benign |
Het |
Ampd2 |
C |
A |
3: 107,986,865 (GRCm39) |
|
probably benign |
Het |
Anapc4 |
A |
G |
5: 53,020,936 (GRCm39) |
S612G |
probably benign |
Het |
Arhgef7 |
T |
C |
8: 11,850,811 (GRCm39) |
L141P |
probably damaging |
Het |
Atl1 |
A |
G |
12: 70,006,107 (GRCm39) |
D471G |
probably damaging |
Het |
Atrn |
A |
G |
2: 130,787,939 (GRCm39) |
D247G |
probably benign |
Het |
Bag1 |
T |
A |
4: 40,948,022 (GRCm39) |
R61W |
probably damaging |
Het |
Card10 |
C |
T |
15: 78,662,451 (GRCm39) |
R898H |
probably damaging |
Het |
Cct6b |
G |
A |
11: 82,655,046 (GRCm39) |
A3V |
probably damaging |
Het |
Cfap54 |
A |
T |
10: 92,770,953 (GRCm39) |
L2097* |
probably null |
Het |
Cfap54 |
T |
C |
10: 92,880,885 (GRCm39) |
|
probably null |
Het |
Chd5 |
T |
C |
4: 152,456,554 (GRCm39) |
F964L |
probably benign |
Het |
Cog5 |
A |
G |
12: 31,936,204 (GRCm39) |
T584A |
probably benign |
Het |
Cpa2 |
T |
A |
6: 30,547,196 (GRCm39) |
N157K |
probably damaging |
Het |
Cpeb1 |
A |
T |
7: 81,001,587 (GRCm39) |
M440K |
probably damaging |
Het |
Cracr2a |
G |
A |
6: 127,580,992 (GRCm39) |
C56Y |
probably damaging |
Het |
Ddb2 |
A |
C |
2: 91,067,073 (GRCm39) |
L30R |
probably damaging |
Het |
Dlk1 |
T |
A |
12: 109,425,697 (GRCm39) |
I190N |
probably damaging |
Het |
Dnaaf4 |
T |
C |
9: 72,879,362 (GRCm39) |
|
probably null |
Het |
Dnajc13 |
T |
A |
9: 104,080,528 (GRCm39) |
Y851F |
possibly damaging |
Het |
Dop1a |
T |
A |
9: 86,397,381 (GRCm39) |
L895Q |
probably damaging |
Het |
F7 |
G |
A |
8: 13,080,763 (GRCm39) |
C122Y |
probably damaging |
Het |
Frrs1 |
T |
C |
3: 116,696,749 (GRCm39) |
V573A |
possibly damaging |
Het |
Galnt2l |
T |
C |
8: 122,997,175 (GRCm39) |
|
probably benign |
Het |
Gm17541 |
A |
T |
12: 4,739,672 (GRCm39) |
|
probably benign |
Het |
Gm5519 |
A |
T |
19: 33,800,576 (GRCm39) |
H90L |
probably damaging |
Het |
Gm5526 |
T |
A |
1: 45,896,569 (GRCm39) |
|
noncoding transcript |
Het |
Gm5709 |
A |
T |
3: 59,509,971 (GRCm39) |
|
noncoding transcript |
Het |
Golga4 |
T |
A |
9: 118,385,569 (GRCm39) |
V869D |
possibly damaging |
Het |
Grm7 |
A |
T |
6: 111,335,182 (GRCm39) |
Q531L |
probably benign |
Het |
Hnrnpu |
C |
A |
1: 178,163,458 (GRCm39) |
C265F |
unknown |
Het |
Hoxd3 |
G |
A |
2: 74,577,211 (GRCm39) |
V364I |
possibly damaging |
Het |
Hspb8 |
T |
C |
5: 116,547,532 (GRCm39) |
D150G |
probably damaging |
Het |
Hydin |
C |
A |
8: 111,313,855 (GRCm39) |
N4244K |
possibly damaging |
Het |
Ik |
A |
G |
18: 36,881,926 (GRCm39) |
D136G |
probably benign |
Het |
Il11ra1 |
T |
C |
4: 41,767,932 (GRCm39) |
|
probably benign |
Het |
Jph1 |
T |
C |
1: 17,161,622 (GRCm39) |
I347V |
probably benign |
Het |
Klk1 |
T |
A |
7: 43,870,985 (GRCm39) |
|
probably benign |
Het |
Lmcd1 |
T |
A |
6: 112,265,087 (GRCm39) |
|
probably benign |
Het |
Lnx1 |
C |
T |
5: 74,846,315 (GRCm39) |
C45Y |
probably damaging |
Het |
Macc1 |
T |
A |
12: 119,410,264 (GRCm39) |
M344K |
possibly damaging |
Het |
Madcam1 |
A |
G |
10: 79,500,779 (GRCm39) |
E32G |
possibly damaging |
Het |
Mat2a |
T |
C |
6: 72,411,316 (GRCm39) |
D383G |
probably benign |
Het |
Mpst |
T |
A |
15: 78,297,849 (GRCm39) |
I289N |
probably damaging |
Het |
Myh6 |
C |
T |
14: 55,190,118 (GRCm39) |
R1055Q |
probably damaging |
Het |
Myh7 |
T |
C |
14: 55,216,965 (GRCm39) |
K1131E |
probably damaging |
Het |
Ndrg3 |
A |
T |
2: 156,773,125 (GRCm39) |
|
probably benign |
Het |
Nebl |
A |
G |
2: 17,438,786 (GRCm39) |
S209P |
probably benign |
Het |
Nid2 |
A |
G |
14: 19,818,276 (GRCm39) |
|
probably null |
Het |
Nup188 |
A |
T |
2: 30,220,761 (GRCm39) |
S945C |
probably damaging |
Het |
Or1j21 |
A |
G |
2: 36,683,685 (GRCm39) |
M146V |
probably benign |
Het |
Or5g23 |
C |
T |
2: 85,438,817 (GRCm39) |
V146I |
probably benign |
Het |
Or8c11 |
A |
G |
9: 38,289,213 (GRCm39) |
N12S |
probably benign |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Patl2 |
A |
G |
2: 121,959,368 (GRCm39) |
L32P |
probably damaging |
Het |
Pcdh20 |
T |
A |
14: 88,705,813 (GRCm39) |
M496L |
probably benign |
Het |
Pdzd2 |
A |
G |
15: 12,373,028 (GRCm39) |
V2369A |
possibly damaging |
Het |
Pfn2 |
A |
G |
3: 57,754,812 (GRCm39) |
V31A |
probably damaging |
Het |
Plxna4 |
T |
C |
6: 32,228,007 (GRCm39) |
N533S |
probably benign |
Het |
Plxnb1 |
T |
C |
9: 108,943,661 (GRCm39) |
F1916S |
probably damaging |
Het |
Ppp4r3b |
T |
C |
11: 29,138,293 (GRCm39) |
F214L |
probably benign |
Het |
Prox1 |
T |
C |
1: 189,893,638 (GRCm39) |
D269G |
probably benign |
Het |
Rapgef4 |
T |
C |
2: 71,864,378 (GRCm39) |
F71S |
probably damaging |
Het |
Rft1 |
A |
G |
14: 30,383,243 (GRCm39) |
I94M |
probably benign |
Het |
S100z |
T |
C |
13: 95,615,127 (GRCm39) |
I13V |
probably damaging |
Het |
Serhl |
T |
A |
15: 82,986,835 (GRCm39) |
V117E |
probably damaging |
Het |
Shroom1 |
G |
A |
11: 53,356,334 (GRCm39) |
R336Q |
probably benign |
Het |
Sik3 |
A |
T |
9: 46,123,552 (GRCm39) |
Q1067L |
probably damaging |
Het |
Slc22a30 |
G |
A |
19: 8,321,757 (GRCm39) |
Q436* |
probably null |
Het |
Slc28a1 |
G |
A |
7: 80,771,869 (GRCm39) |
V118M |
probably damaging |
Het |
Slco1a6 |
T |
A |
6: 142,078,427 (GRCm39) |
I153F |
probably benign |
Het |
Ss18l1 |
T |
C |
2: 179,703,735 (GRCm39) |
Y323H |
unknown |
Het |
Susd4 |
G |
T |
1: 182,719,824 (GRCm39) |
A480S |
possibly damaging |
Het |
Syne3 |
A |
T |
12: 104,942,139 (GRCm39) |
M1K |
probably null |
Het |
Synpo2l |
A |
T |
14: 20,711,082 (GRCm39) |
S513T |
probably benign |
Het |
Tat |
A |
T |
8: 110,724,966 (GRCm39) |
N388I |
probably benign |
Het |
Tbc1d1 |
A |
G |
5: 64,439,352 (GRCm39) |
Y619C |
probably damaging |
Het |
Tbk1 |
G |
A |
10: 121,406,590 (GRCm39) |
T216M |
probably damaging |
Het |
Tns1 |
C |
T |
1: 74,034,585 (GRCm39) |
|
probably benign |
Het |
Trbv5 |
T |
C |
6: 41,039,318 (GRCm39) |
V9A |
possibly damaging |
Het |
Trpm5 |
A |
G |
7: 142,636,040 (GRCm39) |
Y575H |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,570,045 (GRCm39) |
Y25203* |
probably null |
Het |
Tubb3 |
C |
A |
8: 124,148,391 (GRCm39) |
D441E |
probably benign |
Het |
Usp33 |
T |
A |
3: 152,097,333 (GRCm39) |
C850* |
probably null |
Het |
Vdac1 |
G |
A |
11: 52,274,905 (GRCm39) |
|
probably null |
Het |
Vmn1r232 |
T |
C |
17: 21,133,846 (GRCm39) |
I251M |
probably damaging |
Het |
Vmn2r11 |
T |
G |
5: 109,202,658 (GRCm39) |
I140L |
probably benign |
Het |
Vps51 |
T |
A |
19: 6,120,518 (GRCm39) |
H465L |
probably benign |
Het |
Zfp318 |
T |
G |
17: 46,722,995 (GRCm39) |
I1666S |
probably benign |
Het |
Zfp446 |
C |
T |
7: 12,713,231 (GRCm39) |
R90* |
probably null |
Het |
Zgrf1 |
T |
A |
3: 127,396,094 (GRCm39) |
F547I |
probably damaging |
Het |
|
Other mutations in Vmn2r6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01547:Vmn2r6
|
APN |
3 |
64,445,525 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01968:Vmn2r6
|
APN |
3 |
64,463,766 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02009:Vmn2r6
|
APN |
3 |
64,445,323 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02039:Vmn2r6
|
APN |
3 |
64,463,610 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02652:Vmn2r6
|
APN |
3 |
64,463,749 (GRCm39) |
missense |
probably benign |
0.24 |
IGL02737:Vmn2r6
|
APN |
3 |
64,463,911 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02808:Vmn2r6
|
APN |
3 |
64,463,917 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03066:Vmn2r6
|
APN |
3 |
64,472,574 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03331:Vmn2r6
|
APN |
3 |
64,445,428 (GRCm39) |
missense |
probably damaging |
1.00 |
BB010:Vmn2r6
|
UTSW |
3 |
64,467,224 (GRCm39) |
missense |
probably benign |
0.02 |
BB020:Vmn2r6
|
UTSW |
3 |
64,467,224 (GRCm39) |
missense |
probably benign |
0.02 |
R0010:Vmn2r6
|
UTSW |
3 |
64,466,966 (GRCm39) |
nonsense |
probably null |
|
R0206:Vmn2r6
|
UTSW |
3 |
64,447,333 (GRCm39) |
missense |
probably benign |
|
R0206:Vmn2r6
|
UTSW |
3 |
64,447,333 (GRCm39) |
missense |
probably benign |
|
R0208:Vmn2r6
|
UTSW |
3 |
64,447,333 (GRCm39) |
missense |
probably benign |
|
R0427:Vmn2r6
|
UTSW |
3 |
64,467,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R0466:Vmn2r6
|
UTSW |
3 |
64,463,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R1018:Vmn2r6
|
UTSW |
3 |
64,464,261 (GRCm39) |
missense |
probably benign |
0.00 |
R1104:Vmn2r6
|
UTSW |
3 |
64,445,487 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1186:Vmn2r6
|
UTSW |
3 |
64,472,488 (GRCm39) |
missense |
probably benign |
0.01 |
R1245:Vmn2r6
|
UTSW |
3 |
64,464,211 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1295:Vmn2r6
|
UTSW |
3 |
64,445,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R1473:Vmn2r6
|
UTSW |
3 |
64,445,579 (GRCm39) |
nonsense |
probably null |
|
R1498:Vmn2r6
|
UTSW |
3 |
64,463,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R1925:Vmn2r6
|
UTSW |
3 |
64,463,698 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2044:Vmn2r6
|
UTSW |
3 |
64,445,262 (GRCm39) |
missense |
probably damaging |
0.96 |
R2069:Vmn2r6
|
UTSW |
3 |
64,463,519 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2253:Vmn2r6
|
UTSW |
3 |
64,467,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R2261:Vmn2r6
|
UTSW |
3 |
64,464,090 (GRCm39) |
missense |
probably benign |
0.24 |
R2262:Vmn2r6
|
UTSW |
3 |
64,464,090 (GRCm39) |
missense |
probably benign |
0.24 |
R2350:Vmn2r6
|
UTSW |
3 |
64,463,773 (GRCm39) |
missense |
probably benign |
0.01 |
R2680:Vmn2r6
|
UTSW |
3 |
64,445,707 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2846:Vmn2r6
|
UTSW |
3 |
64,464,211 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2860:Vmn2r6
|
UTSW |
3 |
64,454,760 (GRCm39) |
missense |
probably benign |
0.00 |
R2861:Vmn2r6
|
UTSW |
3 |
64,454,760 (GRCm39) |
missense |
probably benign |
0.00 |
R3766:Vmn2r6
|
UTSW |
3 |
64,463,929 (GRCm39) |
missense |
probably benign |
0.19 |
R3870:Vmn2r6
|
UTSW |
3 |
64,464,042 (GRCm39) |
missense |
probably damaging |
0.96 |
R4018:Vmn2r6
|
UTSW |
3 |
64,463,893 (GRCm39) |
missense |
probably benign |
0.05 |
R4024:Vmn2r6
|
UTSW |
3 |
64,445,671 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4026:Vmn2r6
|
UTSW |
3 |
64,445,671 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4227:Vmn2r6
|
UTSW |
3 |
64,445,369 (GRCm39) |
missense |
probably damaging |
0.99 |
R4526:Vmn2r6
|
UTSW |
3 |
64,445,145 (GRCm39) |
missense |
probably benign |
0.32 |
R4570:Vmn2r6
|
UTSW |
3 |
64,467,068 (GRCm39) |
missense |
probably benign |
0.31 |
R4894:Vmn2r6
|
UTSW |
3 |
64,454,829 (GRCm39) |
missense |
probably benign |
|
R4934:Vmn2r6
|
UTSW |
3 |
64,463,766 (GRCm39) |
missense |
probably damaging |
0.99 |
R5057:Vmn2r6
|
UTSW |
3 |
64,445,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R5059:Vmn2r6
|
UTSW |
3 |
64,445,044 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5148:Vmn2r6
|
UTSW |
3 |
64,464,015 (GRCm39) |
missense |
probably damaging |
0.99 |
R5155:Vmn2r6
|
UTSW |
3 |
64,445,935 (GRCm39) |
missense |
probably benign |
0.44 |
R5179:Vmn2r6
|
UTSW |
3 |
64,445,411 (GRCm39) |
missense |
probably benign |
0.00 |
R5861:Vmn2r6
|
UTSW |
3 |
64,463,454 (GRCm39) |
missense |
probably benign |
0.00 |
R5950:Vmn2r6
|
UTSW |
3 |
64,472,652 (GRCm39) |
missense |
probably benign |
0.05 |
R6081:Vmn2r6
|
UTSW |
3 |
64,463,953 (GRCm39) |
missense |
probably benign |
0.25 |
R6173:Vmn2r6
|
UTSW |
3 |
64,467,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R6190:Vmn2r6
|
UTSW |
3 |
64,445,424 (GRCm39) |
missense |
probably benign |
0.04 |
R6240:Vmn2r6
|
UTSW |
3 |
64,464,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R6433:Vmn2r6
|
UTSW |
3 |
64,454,801 (GRCm39) |
nonsense |
probably null |
|
R6645:Vmn2r6
|
UTSW |
3 |
64,464,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R6791:Vmn2r6
|
UTSW |
3 |
64,445,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R7265:Vmn2r6
|
UTSW |
3 |
64,464,195 (GRCm39) |
missense |
probably benign |
0.00 |
R7503:Vmn2r6
|
UTSW |
3 |
64,447,372 (GRCm39) |
nonsense |
probably null |
|
R7562:Vmn2r6
|
UTSW |
3 |
64,463,941 (GRCm39) |
missense |
probably benign |
0.00 |
R7584:Vmn2r6
|
UTSW |
3 |
64,472,683 (GRCm39) |
missense |
probably benign |
0.07 |
R7611:Vmn2r6
|
UTSW |
3 |
64,472,563 (GRCm39) |
missense |
probably damaging |
0.98 |
R7759:Vmn2r6
|
UTSW |
3 |
64,463,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R7834:Vmn2r6
|
UTSW |
3 |
64,445,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R7933:Vmn2r6
|
UTSW |
3 |
64,467,224 (GRCm39) |
missense |
probably benign |
0.02 |
R7982:Vmn2r6
|
UTSW |
3 |
64,467,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R8024:Vmn2r6
|
UTSW |
3 |
64,467,245 (GRCm39) |
missense |
probably benign |
0.40 |
R8074:Vmn2r6
|
UTSW |
3 |
64,455,064 (GRCm39) |
intron |
probably benign |
|
R8169:Vmn2r6
|
UTSW |
3 |
64,447,310 (GRCm39) |
missense |
probably benign |
0.01 |
R8337:Vmn2r6
|
UTSW |
3 |
64,463,526 (GRCm39) |
nonsense |
probably null |
|
R8736:Vmn2r6
|
UTSW |
3 |
64,467,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R8962:Vmn2r6
|
UTSW |
3 |
64,463,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R9139:Vmn2r6
|
UTSW |
3 |
64,464,277 (GRCm39) |
missense |
probably benign |
0.12 |
R9206:Vmn2r6
|
UTSW |
3 |
64,467,032 (GRCm39) |
missense |
probably damaging |
0.97 |
R9295:Vmn2r6
|
UTSW |
3 |
64,463,484 (GRCm39) |
missense |
probably benign |
0.00 |
R9332:Vmn2r6
|
UTSW |
3 |
64,454,671 (GRCm39) |
missense |
probably benign |
0.01 |
R9616:Vmn2r6
|
UTSW |
3 |
64,445,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R9663:Vmn2r6
|
UTSW |
3 |
64,463,549 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9685:Vmn2r6
|
UTSW |
3 |
64,464,081 (GRCm39) |
missense |
probably benign |
0.19 |
X0020:Vmn2r6
|
UTSW |
3 |
64,445,871 (GRCm39) |
missense |
probably benign |
|
X0066:Vmn2r6
|
UTSW |
3 |
64,454,799 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Vmn2r6
|
UTSW |
3 |
64,463,746 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Predicted Primers |
PCR Primer
(F):5'- ACACAAAGGTTGGCCCTCTC -3'
(R):5'- GAGTTGTCAAAATTGTCCCCATCTAC -3'
Sequencing Primer
(F):5'- AAAGGTTGGCCCTCTCCATTTC -3'
(R):5'- AGATTAAACAGGAAGTCACTGTCTAC -3'
|
Posted On |
2016-07-06 |