Incidental Mutation 'R0137:Adgra3'
ID |
22012 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Adgra3
|
Ensembl Gene |
ENSMUSG00000029090 |
Gene Name |
adhesion G protein-coupled receptor A3 |
Synonyms |
Tem5-like, 3830613O22Rik, Gpr125 |
MMRRC Submission |
038422-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R0137 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
5 |
Chromosomal Location |
50117293-50216338 bp(-) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
C to T
at 50121182 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000030971
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000030971]
|
AlphaFold |
Q7TT36 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000030971
|
SMART Domains |
Protein: ENSMUSP00000030971 Gene: ENSMUSG00000029090
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
27 |
N/A |
INTRINSIC |
low complexity region
|
36 |
48 |
N/A |
INTRINSIC |
LRR
|
68 |
92 |
1.71e1 |
SMART |
LRR_TYP
|
93 |
116 |
2.27e-4 |
SMART |
LRR_TYP
|
117 |
140 |
4.11e-2 |
SMART |
LRR_TYP
|
141 |
164 |
3.89e-3 |
SMART |
LRRCT
|
176 |
225 |
5.24e-5 |
SMART |
IG
|
238 |
331 |
8.26e-5 |
SMART |
GPS
|
686 |
738 |
4.81e-3 |
SMART |
Pfam:7tm_2
|
746 |
1031 |
1.6e-16 |
PFAM |
low complexity region
|
1251 |
1262 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000196177
|
Coding Region Coverage |
- 1x: 99.0%
- 3x: 98.2%
- 10x: 96.1%
- 20x: 91.8%
|
Validation Efficiency |
95% (94/99) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the G protein-coupled receptor superfamily. This membrane protein may play a role in tumor angiogenesis through its interaction with the human homolog of the Drosophila disc large tumor suppressor gene. This gene is mapped to a candidate region of chromosome 4 which may be associated with bipolar disorder and schizophrenia. [provided by RefSeq, Oct 2012] PHENOTYPE: Homozygous mutant mice are fertile and grossly normal. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6430548M08Rik |
A |
T |
8: 120,878,115 (GRCm39) |
H190L |
possibly damaging |
Het |
Adap1 |
A |
G |
5: 139,278,976 (GRCm39) |
|
probably benign |
Het |
Adgre5 |
A |
T |
8: 84,451,527 (GRCm39) |
V527E |
probably damaging |
Het |
Anapc5 |
A |
T |
5: 122,938,695 (GRCm39) |
Y360N |
probably damaging |
Het |
Angptl6 |
C |
A |
9: 20,789,683 (GRCm39) |
A70S |
probably benign |
Het |
Ankdd1a |
C |
A |
9: 65,417,610 (GRCm39) |
K137N |
probably null |
Het |
Ccdc170 |
T |
C |
10: 4,496,950 (GRCm39) |
|
probably benign |
Het |
Ccdc51 |
A |
G |
9: 108,920,698 (GRCm39) |
E195G |
probably damaging |
Het |
Cdc37 |
A |
T |
9: 21,053,426 (GRCm39) |
C204S |
possibly damaging |
Het |
Cfap36 |
T |
C |
11: 29,172,431 (GRCm39) |
|
probably benign |
Het |
Col6a2 |
C |
A |
10: 76,432,259 (GRCm39) |
G965C |
probably damaging |
Het |
Csn1s2a |
G |
A |
5: 87,926,826 (GRCm39) |
S53N |
possibly damaging |
Het |
Dab2ip |
T |
C |
2: 35,582,388 (GRCm39) |
|
probably null |
Het |
Dhx58 |
A |
G |
11: 100,587,823 (GRCm39) |
V578A |
probably damaging |
Het |
Diaph1 |
G |
T |
18: 38,024,902 (GRCm39) |
Q520K |
unknown |
Het |
Eefsec |
C |
A |
6: 88,274,631 (GRCm39) |
K444N |
probably benign |
Het |
Eftud2 |
A |
T |
11: 102,759,443 (GRCm39) |
H153Q |
possibly damaging |
Het |
Eif5b |
T |
G |
1: 38,058,324 (GRCm39) |
S209A |
probably benign |
Het |
Exosc2 |
T |
A |
2: 31,562,497 (GRCm39) |
Y46N |
probably damaging |
Het |
F2 |
C |
T |
2: 91,456,075 (GRCm39) |
G562D |
probably damaging |
Het |
Fgf23 |
G |
A |
6: 127,057,128 (GRCm39) |
G148D |
probably damaging |
Het |
Fmnl3 |
G |
C |
15: 99,220,619 (GRCm39) |
|
probably benign |
Het |
Fstl5 |
G |
A |
3: 76,614,786 (GRCm39) |
G179R |
probably damaging |
Het |
Garre1 |
A |
T |
7: 33,938,644 (GRCm39) |
W246R |
probably damaging |
Het |
Gart |
T |
A |
16: 91,422,282 (GRCm39) |
Q745L |
probably benign |
Het |
Gmeb1 |
T |
A |
4: 131,959,419 (GRCm39) |
M212L |
probably benign |
Het |
Gpaa1 |
T |
C |
15: 76,218,981 (GRCm39) |
Y548H |
probably damaging |
Het |
Gpatch1 |
T |
C |
7: 34,986,667 (GRCm39) |
E763G |
probably damaging |
Het |
Grm8 |
T |
A |
6: 27,762,389 (GRCm39) |
I279F |
probably damaging |
Het |
Hcls1 |
T |
A |
16: 36,771,536 (GRCm39) |
H147Q |
probably damaging |
Het |
Hpcal1 |
A |
C |
12: 17,836,389 (GRCm39) |
D73A |
probably damaging |
Het |
Il22ra1 |
T |
C |
4: 135,478,317 (GRCm39) |
S463P |
probably benign |
Het |
Itgbl1 |
G |
A |
14: 124,078,098 (GRCm39) |
|
probably null |
Het |
Izumo3 |
G |
T |
4: 92,035,437 (GRCm39) |
|
probably benign |
Het |
Kcna5 |
A |
T |
6: 126,510,346 (GRCm39) |
L594Q |
probably damaging |
Het |
Kif13a |
A |
T |
13: 46,918,079 (GRCm39) |
D409E |
probably benign |
Het |
Kif9 |
A |
T |
9: 110,314,106 (GRCm39) |
I39F |
probably damaging |
Het |
Klri2 |
C |
T |
6: 129,709,171 (GRCm39) |
R227H |
possibly damaging |
Het |
Lamc3 |
G |
A |
2: 31,798,628 (GRCm39) |
G445S |
probably damaging |
Het |
Lctl |
A |
G |
9: 64,024,980 (GRCm39) |
|
probably benign |
Het |
Lrp4 |
T |
C |
2: 91,325,327 (GRCm39) |
L1384P |
probably damaging |
Het |
Mcm9 |
G |
A |
10: 53,439,526 (GRCm39) |
S549L |
possibly damaging |
Het |
Ms4a15 |
G |
A |
19: 10,956,697 (GRCm39) |
|
probably benign |
Het |
Mtor |
T |
C |
4: 148,555,081 (GRCm39) |
V901A |
possibly damaging |
Het |
Nckap1l |
A |
T |
15: 103,390,391 (GRCm39) |
I721F |
probably benign |
Het |
Nemp2 |
T |
C |
1: 52,684,588 (GRCm39) |
V298A |
probably benign |
Het |
Npc1l1 |
T |
A |
11: 6,178,148 (GRCm39) |
K421* |
probably null |
Het |
Npr1 |
C |
T |
3: 90,363,244 (GRCm39) |
V879M |
probably damaging |
Het |
Odad4 |
A |
G |
11: 100,454,394 (GRCm39) |
E393G |
probably damaging |
Het |
Or2ad1 |
A |
G |
13: 21,326,336 (GRCm39) |
V297A |
possibly damaging |
Het |
Or51q1c |
A |
G |
7: 103,652,709 (GRCm39) |
T82A |
probably benign |
Het |
Osgin1 |
A |
T |
8: 120,169,219 (GRCm39) |
I39F |
possibly damaging |
Het |
Phip |
G |
C |
9: 82,809,244 (GRCm39) |
|
probably null |
Het |
Pkdrej |
G |
T |
15: 85,705,768 (GRCm39) |
P56Q |
possibly damaging |
Het |
Plcxd2 |
A |
G |
16: 45,800,889 (GRCm39) |
Y112H |
probably damaging |
Het |
Plekha1 |
C |
T |
7: 130,499,176 (GRCm39) |
T155M |
probably damaging |
Het |
Prkdc |
T |
C |
16: 15,558,196 (GRCm39) |
|
probably null |
Het |
Prss1 |
A |
G |
6: 41,439,495 (GRCm39) |
H76R |
probably damaging |
Het |
Psg23 |
T |
C |
7: 18,348,558 (GRCm39) |
D83G |
probably benign |
Het |
Ptprd |
T |
A |
4: 76,055,140 (GRCm39) |
Q196L |
probably benign |
Het |
Ranbp3l |
A |
T |
15: 9,063,067 (GRCm39) |
H292L |
probably damaging |
Het |
Ranbp6 |
T |
C |
19: 29,787,097 (GRCm39) |
E1085G |
probably benign |
Het |
Rccd1 |
A |
G |
7: 79,970,326 (GRCm39) |
V97A |
possibly damaging |
Het |
Rchy1 |
T |
C |
5: 92,105,458 (GRCm39) |
S48G |
probably benign |
Het |
Rnmt |
G |
A |
18: 68,446,771 (GRCm39) |
M265I |
probably benign |
Het |
Robo3 |
A |
T |
9: 37,336,640 (GRCm39) |
M376K |
probably benign |
Het |
Rrp12 |
T |
C |
19: 41,862,289 (GRCm39) |
D898G |
probably benign |
Het |
Scg3 |
A |
T |
9: 75,570,462 (GRCm39) |
|
probably benign |
Het |
Sec31b |
A |
T |
19: 44,522,821 (GRCm39) |
M57K |
probably damaging |
Het |
Slc17a6 |
A |
C |
7: 51,315,892 (GRCm39) |
I387L |
probably benign |
Het |
Speer4a1 |
T |
A |
5: 26,240,982 (GRCm39) |
Q170L |
possibly damaging |
Het |
Srsf9 |
A |
G |
5: 115,470,260 (GRCm39) |
D146G |
possibly damaging |
Het |
Ss18 |
A |
G |
18: 14,788,200 (GRCm39) |
M90T |
probably damaging |
Het |
Syna |
A |
T |
5: 134,588,314 (GRCm39) |
F212I |
possibly damaging |
Het |
Tex54 |
A |
G |
19: 8,718,221 (GRCm39) |
|
probably benign |
Het |
Thsd1 |
A |
G |
8: 22,733,055 (GRCm39) |
H34R |
probably damaging |
Het |
Tmem143 |
T |
C |
7: 45,547,086 (GRCm39) |
I84T |
probably benign |
Het |
Trim50 |
T |
C |
5: 135,395,487 (GRCm39) |
V281A |
probably damaging |
Het |
Trp53i11 |
C |
A |
2: 93,029,696 (GRCm39) |
|
probably benign |
Het |
Ttll4 |
C |
T |
1: 74,718,851 (GRCm39) |
T234I |
possibly damaging |
Het |
Ttyh1 |
A |
T |
7: 4,127,719 (GRCm39) |
I136F |
possibly damaging |
Het |
Ube2f |
T |
C |
1: 91,189,976 (GRCm39) |
|
probably benign |
Het |
Vcl |
T |
A |
14: 21,037,083 (GRCm39) |
L227* |
probably null |
Het |
Vmn1r222 |
A |
C |
13: 23,416,974 (GRCm39) |
C80G |
probably damaging |
Het |
Vps13b |
G |
T |
15: 35,926,365 (GRCm39) |
A3889S |
probably benign |
Het |
Vps8 |
T |
C |
16: 21,323,136 (GRCm39) |
|
probably benign |
Het |
Zbtb44 |
A |
G |
9: 30,978,006 (GRCm39) |
Y422C |
probably damaging |
Het |
Zfp180 |
A |
G |
7: 23,805,158 (GRCm39) |
S526G |
possibly damaging |
Het |
Zfp518a |
A |
C |
19: 40,904,310 (GRCm39) |
E1413A |
probably damaging |
Het |
Zfp629 |
T |
A |
7: 127,210,858 (GRCm39) |
Y317F |
probably damaging |
Het |
Zfp804b |
T |
C |
5: 6,820,534 (GRCm39) |
E843G |
probably benign |
Het |
|
Other mutations in Adgra3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00777:Adgra3
|
APN |
5 |
50,183,100 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00848:Adgra3
|
APN |
5 |
50,159,291 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01455:Adgra3
|
APN |
5 |
50,144,899 (GRCm39) |
nonsense |
probably null |
|
IGL01665:Adgra3
|
APN |
5 |
50,164,272 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL02151:Adgra3
|
APN |
5 |
50,136,484 (GRCm39) |
missense |
probably benign |
|
IGL02239:Adgra3
|
APN |
5 |
50,118,054 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02351:Adgra3
|
APN |
5 |
50,215,900 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02358:Adgra3
|
APN |
5 |
50,215,900 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02938:Adgra3
|
APN |
5 |
50,118,659 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03028:Adgra3
|
APN |
5 |
50,174,194 (GRCm39) |
missense |
probably benign |
0.30 |
aperture
|
UTSW |
5 |
50,156,487 (GRCm39) |
nonsense |
probably null |
|
saltatory
|
UTSW |
5 |
50,117,901 (GRCm39) |
missense |
probably benign |
0.09 |
ANU74:Adgra3
|
UTSW |
5 |
50,118,380 (GRCm39) |
missense |
probably benign |
0.16 |
R0041:Adgra3
|
UTSW |
5 |
50,117,901 (GRCm39) |
missense |
probably benign |
0.09 |
R0041:Adgra3
|
UTSW |
5 |
50,117,901 (GRCm39) |
missense |
probably benign |
0.09 |
R0121:Adgra3
|
UTSW |
5 |
50,183,128 (GRCm39) |
splice site |
probably benign |
|
R0125:Adgra3
|
UTSW |
5 |
50,159,194 (GRCm39) |
splice site |
probably benign |
|
R0415:Adgra3
|
UTSW |
5 |
50,119,099 (GRCm39) |
splice site |
probably benign |
|
R0479:Adgra3
|
UTSW |
5 |
50,147,607 (GRCm39) |
missense |
probably benign |
0.00 |
R0505:Adgra3
|
UTSW |
5 |
50,166,676 (GRCm39) |
critical splice donor site |
probably null |
|
R0831:Adgra3
|
UTSW |
5 |
50,128,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R0883:Adgra3
|
UTSW |
5 |
50,118,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R0920:Adgra3
|
UTSW |
5 |
50,118,503 (GRCm39) |
missense |
probably benign |
0.19 |
R1139:Adgra3
|
UTSW |
5 |
50,119,097 (GRCm39) |
splice site |
probably null |
|
R1211:Adgra3
|
UTSW |
5 |
50,164,218 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1370:Adgra3
|
UTSW |
5 |
50,118,129 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1530:Adgra3
|
UTSW |
5 |
50,118,479 (GRCm39) |
missense |
probably benign |
0.00 |
R1703:Adgra3
|
UTSW |
5 |
50,164,117 (GRCm39) |
missense |
probably benign |
0.00 |
R1782:Adgra3
|
UTSW |
5 |
50,129,404 (GRCm39) |
missense |
probably benign |
0.02 |
R1843:Adgra3
|
UTSW |
5 |
50,118,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R2157:Adgra3
|
UTSW |
5 |
50,159,283 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2281:Adgra3
|
UTSW |
5 |
50,159,222 (GRCm39) |
missense |
probably benign |
0.04 |
R2385:Adgra3
|
UTSW |
5 |
50,136,908 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2426:Adgra3
|
UTSW |
5 |
50,166,791 (GRCm39) |
missense |
possibly damaging |
0.61 |
R3084:Adgra3
|
UTSW |
5 |
50,170,733 (GRCm39) |
critical splice donor site |
probably null |
|
R3086:Adgra3
|
UTSW |
5 |
50,170,733 (GRCm39) |
critical splice donor site |
probably null |
|
R3409:Adgra3
|
UTSW |
5 |
50,159,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R3410:Adgra3
|
UTSW |
5 |
50,159,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R3411:Adgra3
|
UTSW |
5 |
50,159,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R4301:Adgra3
|
UTSW |
5 |
50,118,420 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4360:Adgra3
|
UTSW |
5 |
50,147,552 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4475:Adgra3
|
UTSW |
5 |
50,159,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R4569:Adgra3
|
UTSW |
5 |
50,117,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R4607:Adgra3
|
UTSW |
5 |
50,128,081 (GRCm39) |
missense |
probably damaging |
0.98 |
R4667:Adgra3
|
UTSW |
5 |
50,136,298 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4671:Adgra3
|
UTSW |
5 |
50,136,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R4886:Adgra3
|
UTSW |
5 |
50,156,537 (GRCm39) |
missense |
probably benign |
0.07 |
R5197:Adgra3
|
UTSW |
5 |
50,118,096 (GRCm39) |
missense |
probably benign |
0.01 |
R5208:Adgra3
|
UTSW |
5 |
50,168,857 (GRCm39) |
missense |
probably damaging |
0.99 |
R5313:Adgra3
|
UTSW |
5 |
50,118,651 (GRCm39) |
missense |
probably benign |
0.24 |
R5435:Adgra3
|
UTSW |
5 |
50,147,468 (GRCm39) |
missense |
probably damaging |
0.99 |
R5663:Adgra3
|
UTSW |
5 |
50,156,627 (GRCm39) |
missense |
probably benign |
0.14 |
R6038:Adgra3
|
UTSW |
5 |
50,156,487 (GRCm39) |
nonsense |
probably null |
|
R6038:Adgra3
|
UTSW |
5 |
50,156,487 (GRCm39) |
nonsense |
probably null |
|
R6064:Adgra3
|
UTSW |
5 |
50,117,667 (GRCm39) |
missense |
probably damaging |
0.97 |
R6259:Adgra3
|
UTSW |
5 |
50,156,483 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6272:Adgra3
|
UTSW |
5 |
50,166,791 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6293:Adgra3
|
UTSW |
5 |
50,118,189 (GRCm39) |
missense |
probably benign |
0.21 |
R6296:Adgra3
|
UTSW |
5 |
50,118,189 (GRCm39) |
missense |
probably benign |
0.21 |
R6297:Adgra3
|
UTSW |
5 |
50,118,189 (GRCm39) |
missense |
probably benign |
0.21 |
R6352:Adgra3
|
UTSW |
5 |
50,147,592 (GRCm39) |
missense |
probably benign |
0.01 |
R6352:Adgra3
|
UTSW |
5 |
50,136,478 (GRCm39) |
missense |
probably benign |
|
R6989:Adgra3
|
UTSW |
5 |
50,164,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R7026:Adgra3
|
UTSW |
5 |
50,118,083 (GRCm39) |
missense |
probably benign |
|
R7147:Adgra3
|
UTSW |
5 |
50,118,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R7206:Adgra3
|
UTSW |
5 |
50,164,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R7381:Adgra3
|
UTSW |
5 |
50,216,116 (GRCm39) |
start codon destroyed |
probably null |
|
R7508:Adgra3
|
UTSW |
5 |
50,174,209 (GRCm39) |
missense |
probably benign |
0.10 |
R7538:Adgra3
|
UTSW |
5 |
50,118,792 (GRCm39) |
missense |
probably benign |
0.01 |
R7579:Adgra3
|
UTSW |
5 |
50,144,977 (GRCm39) |
missense |
probably benign |
|
R7951:Adgra3
|
UTSW |
5 |
50,121,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R8269:Adgra3
|
UTSW |
5 |
50,121,079 (GRCm39) |
missense |
probably damaging |
0.98 |
R8458:Adgra3
|
UTSW |
5 |
50,145,013 (GRCm39) |
missense |
probably damaging |
0.99 |
R8486:Adgra3
|
UTSW |
5 |
50,147,621 (GRCm39) |
missense |
probably damaging |
0.98 |
R8912:Adgra3
|
UTSW |
5 |
50,118,273 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8955:Adgra3
|
UTSW |
5 |
50,118,731 (GRCm39) |
missense |
probably benign |
0.05 |
R9108:Adgra3
|
UTSW |
5 |
50,136,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R9112:Adgra3
|
UTSW |
5 |
50,118,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R9191:Adgra3
|
UTSW |
5 |
50,145,006 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9267:Adgra3
|
UTSW |
5 |
50,155,618 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9312:Adgra3
|
UTSW |
5 |
50,117,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R9537:Adgra3
|
UTSW |
5 |
50,118,207 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9614:Adgra3
|
UTSW |
5 |
50,164,250 (GRCm39) |
missense |
probably damaging |
1.00 |
RF005:Adgra3
|
UTSW |
5 |
50,170,729 (GRCm39) |
splice site |
probably null |
|
RF024:Adgra3
|
UTSW |
5 |
50,170,729 (GRCm39) |
splice site |
probably null |
|
RF036:Adgra3
|
UTSW |
5 |
50,215,983 (GRCm39) |
small deletion |
probably benign |
|
X0065:Adgra3
|
UTSW |
5 |
50,129,304 (GRCm39) |
missense |
probably benign |
|
Z1187:Adgra3
|
UTSW |
5 |
50,136,421 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1192:Adgra3
|
UTSW |
5 |
50,156,623 (GRCm39) |
missense |
probably benign |
0.00 |
|
Predicted Primers |
PCR Primer
(F):5'- CGCTGATGCTCATAGCACTGAGAAC -3'
(R):5'- TGGCTGAAATCACAGTCGGGTAGG -3'
Sequencing Primer
(F):5'- TGAGAACCAGTCAGCTTGC -3'
(R):5'- AATATGGCGACTCTCAGGC -3'
|
Posted On |
2013-04-12 |