Incidental Mutation 'R8955:Adgra3'
| ID |
681913 |
| 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 |
068791-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R8955 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
5 |
| Chromosomal Location |
50117293-50216338 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 50118731 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Phenylalanine
at position 939
(Y939F)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000030971
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000030971]
|
| AlphaFold |
Q7TT36 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000030971
AA Change: Y939F
PolyPhen 2
Score 0.051 (Sensitivity: 0.94; Specificity: 0.83)
|
| SMART Domains |
Protein: ENSMUSP00000030971
Gene: ENSMUSG00000029090
AA Change: Y939F
| 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 |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.7%
|
| Validation Efficiency |
|
| 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: 87 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adcy8 |
C |
T |
15: 64,576,554 (GRCm39) |
V1003I |
possibly damaging |
Het |
| Adra2b |
T |
C |
2: 127,205,504 (GRCm39) |
V2A |
probably benign |
Het |
| Aga |
T |
A |
8: 53,974,164 (GRCm39) |
Y296N |
possibly damaging |
Het |
| Apc |
A |
G |
18: 34,401,370 (GRCm39) |
Q52R |
probably damaging |
Het |
| Arfgef1 |
A |
T |
1: 10,270,062 (GRCm39) |
S362R |
probably benign |
Het |
| Arhgef7 |
C |
T |
8: 11,808,451 (GRCm39) |
|
probably benign |
Het |
| Bmp5 |
A |
T |
9: 75,805,835 (GRCm39) |
M446L |
probably damaging |
Het |
| Carmil3 |
C |
T |
14: 55,733,534 (GRCm39) |
T350I |
probably damaging |
Het |
| Cd44 |
T |
A |
2: 102,683,363 (GRCm39) |
T224S |
probably damaging |
Het |
| Cep112 |
A |
T |
11: 108,643,260 (GRCm39) |
I7F |
possibly damaging |
Het |
| Chrna2 |
G |
A |
14: 66,379,681 (GRCm39) |
A7T |
probably benign |
Het |
| Cldn16 |
G |
A |
16: 26,301,270 (GRCm39) |
V193I |
probably benign |
Het |
| Clec4a3 |
G |
A |
6: 122,943,479 (GRCm39) |
E100K |
possibly damaging |
Het |
| Cntln |
C |
T |
4: 84,986,110 (GRCm39) |
T1026I |
possibly damaging |
Het |
| Cyp4v3 |
T |
A |
8: 45,761,564 (GRCm39) |
I420F |
probably benign |
Het |
| Dcbld2 |
G |
A |
16: 58,271,125 (GRCm39) |
A301T |
|
Het |
| Dnah1 |
A |
T |
14: 31,007,950 (GRCm39) |
D2152E |
probably benign |
Het |
| Dpy19l4 |
A |
G |
4: 11,290,195 (GRCm39) |
V179A |
probably benign |
Het |
| Dusp4 |
T |
A |
8: 35,284,462 (GRCm39) |
I259N |
probably damaging |
Het |
| Enpp1 |
T |
A |
10: 24,544,926 (GRCm39) |
I318F |
probably benign |
Het |
| Entpd6 |
T |
C |
2: 150,595,005 (GRCm39) |
V15A |
possibly damaging |
Het |
| Epb41l1 |
C |
G |
2: 156,363,923 (GRCm39) |
Q811E |
probably benign |
Het |
| Epb41l5 |
T |
C |
1: 119,570,292 (GRCm39) |
H32R |
probably damaging |
Het |
| Fam135b |
C |
T |
15: 71,334,063 (GRCm39) |
V1044I |
possibly damaging |
Het |
| Fat4 |
A |
T |
3: 39,037,778 (GRCm39) |
H3810L |
probably benign |
Het |
| Fbxw28 |
T |
A |
9: 109,167,857 (GRCm39) |
|
probably null |
Het |
| Flnb |
T |
G |
14: 7,892,874 (GRCm38) |
V648G |
probably damaging |
Het |
| Flnb |
T |
A |
14: 7,904,688 (GRCm38) |
Y1030* |
probably null |
Het |
| Fndc3a |
T |
C |
14: 72,794,410 (GRCm39) |
T787A |
probably benign |
Het |
| Gli2 |
T |
A |
1: 118,783,187 (GRCm39) |
H106L |
probably damaging |
Het |
| Gm10283 |
T |
A |
8: 60,954,390 (GRCm39) |
|
probably null |
Het |
| Gm3336 |
C |
T |
8: 71,174,545 (GRCm39) |
R67* |
probably null |
Het |
| Gsr |
T |
G |
8: 34,183,936 (GRCm39) |
I399M |
possibly damaging |
Het |
| Gtf2ird2 |
T |
A |
5: 134,245,596 (GRCm39) |
M618K |
probably damaging |
Het |
| Gtf3c3 |
T |
A |
1: 54,462,722 (GRCm39) |
D347V |
probably benign |
Het |
| Hspa12a |
T |
C |
19: 58,788,058 (GRCm39) |
Y588C |
probably damaging |
Het |
| Il20ra |
A |
G |
10: 19,635,160 (GRCm39) |
E467G |
possibly damaging |
Het |
| Inf2 |
A |
G |
12: 112,576,998 (GRCm39) |
I991V |
unknown |
Het |
| Irag2 |
A |
T |
6: 145,117,390 (GRCm39) |
M376L |
probably benign |
Het |
| Irx6 |
T |
C |
8: 93,405,040 (GRCm39) |
C303R |
probably damaging |
Het |
| Kcnmb4 |
T |
A |
10: 116,309,381 (GRCm39) |
K16* |
probably null |
Het |
| Kirrel3 |
T |
C |
9: 34,855,738 (GRCm39) |
L86P |
probably damaging |
Het |
| Lipo5 |
A |
C |
19: 33,450,530 (GRCm39) |
F21V |
|
Het |
| Lrrc31 |
T |
A |
3: 30,733,267 (GRCm39) |
R482S |
probably benign |
Het |
| Lrrc3b |
C |
T |
14: 15,358,159 (GRCm38) |
C149Y |
probably damaging |
Het |
| Lrrk1 |
A |
G |
7: 65,919,573 (GRCm39) |
M446T |
probably benign |
Het |
| Macroh2a2 |
A |
T |
10: 61,593,610 (GRCm39) |
I22N |
probably damaging |
Het |
| Mettl14 |
C |
T |
3: 123,167,693 (GRCm39) |
D222N |
probably benign |
Het |
| Mfsd4b3-ps |
G |
A |
10: 39,824,072 (GRCm39) |
H63Y |
probably benign |
Het |
| Myo16 |
T |
C |
8: 10,426,175 (GRCm39) |
W311R |
probably damaging |
Het |
| Nccrp1 |
A |
T |
7: 28,245,628 (GRCm39) |
N151K |
probably benign |
Het |
| Obsl1 |
T |
C |
1: 75,480,493 (GRCm39) |
D377G |
probably damaging |
Het |
| Or5b97 |
T |
A |
19: 12,878,578 (GRCm39) |
T189S |
probably benign |
Het |
| Or5p80 |
T |
A |
7: 108,229,506 (GRCm39) |
C102* |
probably null |
Het |
| Or7c19 |
T |
A |
8: 85,957,913 (GRCm39) |
I263N |
probably benign |
Het |
| Or7c70 |
G |
T |
10: 78,683,576 (GRCm39) |
P58T |
probably damaging |
Het |
| Pigb |
T |
C |
9: 72,945,983 (GRCm39) |
N63S |
probably damaging |
Het |
| Plch2 |
T |
C |
4: 155,077,023 (GRCm39) |
E577G |
probably benign |
Het |
| Prkab2 |
T |
C |
3: 97,573,943 (GRCm39) |
V194A |
probably benign |
Het |
| Psd3 |
T |
C |
8: 68,416,461 (GRCm39) |
I479V |
probably benign |
Het |
| Ralgapb |
C |
A |
2: 158,279,264 (GRCm39) |
P117T |
probably benign |
Het |
| Ralgapb |
C |
G |
2: 158,337,389 (GRCm39) |
T1116R |
probably damaging |
Het |
| Rpap2 |
T |
A |
5: 107,768,361 (GRCm39) |
S400T |
possibly damaging |
Het |
| Rpgrip1l |
C |
A |
8: 92,007,456 (GRCm39) |
W378L |
possibly damaging |
Het |
| Rps20 |
T |
A |
4: 3,834,617 (GRCm39) |
M82L |
probably benign |
Het |
| Rps5 |
T |
C |
7: 12,659,440 (GRCm39) |
M77T |
possibly damaging |
Het |
| Scaf11 |
A |
G |
15: 96,318,371 (GRCm39) |
S398P |
probably damaging |
Het |
| Sdf2 |
T |
A |
11: 78,145,763 (GRCm39) |
D153E |
probably benign |
Het |
| Selplg |
GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT |
GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT |
5: 113,957,756 (GRCm39) |
|
probably benign |
Het |
| Slc12a9 |
T |
C |
5: 137,329,270 (GRCm39) |
N128S |
probably damaging |
Het |
| Slc25a32 |
C |
A |
15: 38,960,946 (GRCm39) |
G246C |
probably damaging |
Het |
| Slc38a4 |
C |
T |
15: 96,914,662 (GRCm39) |
A64T |
probably benign |
Het |
| Slit3 |
T |
C |
11: 35,589,207 (GRCm39) |
V1254A |
probably damaging |
Het |
| Slx4 |
T |
C |
16: 3,808,111 (GRCm39) |
K481R |
probably benign |
Het |
| Tcea1 |
A |
G |
1: 4,959,732 (GRCm39) |
T136A |
probably benign |
Het |
| Thra |
A |
G |
11: 98,644,449 (GRCm39) |
D13G |
possibly damaging |
Het |
| Tmed9 |
G |
A |
13: 55,744,775 (GRCm39) |
S227N |
probably benign |
Het |
| Trim80 |
C |
A |
11: 115,331,538 (GRCm39) |
T20K |
probably benign |
Het |
| Trmt61a |
G |
T |
12: 111,649,256 (GRCm39) |
V276L |
probably benign |
Het |
| Trpc4ap |
T |
C |
2: 155,508,171 (GRCm39) |
D160G |
possibly damaging |
Het |
| Ubr5 |
C |
T |
15: 38,029,825 (GRCm39) |
E467K |
|
Het |
| Vars2 |
C |
A |
17: 35,972,541 (GRCm39) |
G26W |
probably damaging |
Het |
| Vmn1r226 |
G |
T |
17: 20,908,287 (GRCm39) |
R173L |
possibly damaging |
Het |
| Vmn1r29 |
G |
T |
6: 58,284,284 (GRCm39) |
M1I |
probably null |
Het |
| Vmn2r3 |
G |
T |
3: 64,168,803 (GRCm39) |
P578Q |
possibly damaging |
Het |
| Vmn2r57 |
A |
T |
7: 41,049,571 (GRCm39) |
I726N |
possibly damaging |
Het |
| Zfp39 |
A |
T |
11: 58,780,946 (GRCm39) |
Y605* |
probably null |
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 |
|
|
R0137:Adgra3
|
UTSW |
5 |
50,121,182 (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 |
|
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'- TACAGAGAAACAGCCATGGC -3'
(R):5'- GCTGGTGCCAATCTCCTAAG -3'
Sequencing Primer
(F):5'- GCCATGGCCCCAAACATC -3'
(R):5'- GTGCTTTATTGAACTACAGAGCGTC -3'
|
| Posted On |
2021-08-31 |
Incidental Mutation