Incidental Mutation 'R7381:Adgra3'
| ID |
572706 |
| 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 |
045463-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R7381 (G1)
|
| Quality Score |
167.009 |
|
Status
|
Not validated
|
| Chromosome |
5 |
| Chromosomal Location |
50117293-50216338 bp(-) (GRCm39) |
| Type of Mutation |
start codon destroyed |
| DNA Base Change (assembly) |
A to G
at 50216116 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Methionine to Threonine
at position 1
(M1T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000030971
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000030971]
|
| AlphaFold |
Q7TT36 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000030971
AA Change: M1T
|
| SMART Domains |
Protein: ENSMUSP00000030971
Gene: ENSMUSG00000029090
AA Change: M1T
| 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: 100.0%
- 10x: 99.7%
- 20x: 99.2%
|
| Validation Efficiency |
98% (88/90) |
| 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: 93 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930550C14Rik |
T |
C |
9: 53,323,122 (GRCm39) |
Y53H |
probably damaging |
Het |
| Abca8a |
A |
T |
11: 109,920,913 (GRCm39) |
|
probably null |
Het |
| Acads |
C |
A |
5: 115,249,057 (GRCm39) |
Q365H |
probably damaging |
Het |
| Acsm3 |
A |
G |
7: 119,380,049 (GRCm39) |
D462G |
probably damaging |
Het |
| Adam39 |
T |
A |
8: 41,279,000 (GRCm39) |
C464S |
probably damaging |
Het |
| AI182371 |
T |
C |
2: 34,975,371 (GRCm39) |
Y276C |
probably damaging |
Het |
| Ank2 |
T |
A |
3: 126,730,277 (GRCm39) |
H719L |
possibly damaging |
Het |
| Ano7 |
G |
A |
1: 93,323,057 (GRCm39) |
V466I |
probably benign |
Het |
| Art5 |
A |
G |
7: 101,747,377 (GRCm39) |
L134P |
probably damaging |
Het |
| Atcay |
A |
G |
10: 81,046,431 (GRCm39) |
Y298H |
possibly damaging |
Het |
| Atp1a4 |
A |
T |
1: 172,067,682 (GRCm39) |
F527Y |
possibly damaging |
Het |
| Bpifb2 |
A |
T |
2: 153,734,268 (GRCm39) |
M428L |
probably benign |
Het |
| Brinp2 |
A |
C |
1: 158,073,913 (GRCm39) |
V736G |
probably benign |
Het |
| Cdc5l |
C |
T |
17: 45,722,849 (GRCm39) |
A437T |
probably benign |
Het |
| Cdx2 |
G |
A |
5: 147,243,440 (GRCm39) |
P118L |
possibly damaging |
Het |
| Chpt1 |
G |
A |
10: 88,311,193 (GRCm39) |
|
probably null |
Het |
| Creb3l2 |
T |
A |
6: 37,312,783 (GRCm39) |
E417V |
probably damaging |
Het |
| Csnk2a1 |
A |
G |
2: 152,100,614 (GRCm39) |
T129A |
probably benign |
Het |
| Dennd6b |
A |
T |
15: 89,070,376 (GRCm39) |
L431Q |
possibly damaging |
Het |
| Dgkz |
C |
T |
2: 91,775,180 (GRCm39) |
A260T |
probably benign |
Het |
| Dhx34 |
T |
A |
7: 15,949,373 (GRCm39) |
T352S |
probably benign |
Het |
| Elp4 |
C |
T |
2: 105,622,652 (GRCm39) |
R349Q |
not run |
Het |
| Emsy |
A |
C |
7: 98,240,010 (GRCm39) |
F1228V |
probably damaging |
Het |
| Eps8l1 |
T |
A |
7: 4,473,437 (GRCm39) |
|
probably null |
Het |
| Faf1 |
T |
A |
4: 109,719,134 (GRCm39) |
D413E |
probably damaging |
Het |
| Fat3 |
T |
C |
9: 16,158,283 (GRCm39) |
Y1109C |
probably damaging |
Het |
| Fbp1 |
T |
C |
13: 63,012,867 (GRCm39) |
K314E |
probably benign |
Het |
| Fbxl20 |
A |
G |
11: 97,981,614 (GRCm39) |
V358A |
probably benign |
Het |
| Fbxo34 |
C |
G |
14: 47,767,992 (GRCm39) |
R502G |
probably benign |
Het |
| Fxr2 |
G |
A |
11: 69,532,875 (GRCm39) |
C151Y |
possibly damaging |
Het |
| Garin5b |
C |
A |
7: 4,760,681 (GRCm39) |
R677L |
|
Het |
| Gja8 |
T |
C |
3: 96,827,338 (GRCm39) |
D108G |
probably benign |
Het |
| Gm10722 |
C |
A |
9: 3,001,235 (GRCm39) |
L104I |
probably benign |
Het |
| Grsf1 |
A |
G |
5: 88,813,666 (GRCm39) |
V361A |
probably benign |
Het |
| Gsap |
T |
A |
5: 21,431,785 (GRCm39) |
I228N |
probably damaging |
Het |
| Hagh |
T |
C |
17: 25,075,686 (GRCm39) |
I131T |
probably damaging |
Het |
| Heca |
A |
T |
10: 17,791,272 (GRCm39) |
Y261* |
probably null |
Het |
| Hipk3 |
A |
G |
2: 104,269,696 (GRCm39) |
F498L |
probably damaging |
Het |
| Hps4 |
T |
A |
5: 112,523,324 (GRCm39) |
I614N |
possibly damaging |
Het |
| Icam1 |
T |
C |
9: 20,938,886 (GRCm39) |
S450P |
probably benign |
Het |
| Il22 |
G |
A |
10: 118,041,069 (GRCm39) |
M58I |
possibly damaging |
Het |
| Khdrbs2 |
T |
A |
1: 32,372,883 (GRCm39) |
S186T |
not run |
Het |
| Kif16b |
A |
G |
2: 142,699,343 (GRCm39) |
F79S |
probably damaging |
Het |
| Kntc1 |
C |
A |
5: 123,948,971 (GRCm39) |
F1905L |
probably benign |
Het |
| Liat1 |
A |
T |
11: 75,893,833 (GRCm39) |
D70V |
probably damaging |
Het |
| Lrp1b |
C |
T |
2: 40,692,929 (GRCm39) |
G3423D |
|
Het |
| Lrp5 |
G |
T |
19: 3,643,588 (GRCm39) |
Q1346K |
probably benign |
Het |
| Map3k21 |
A |
C |
8: 126,671,717 (GRCm39) |
T1002P |
possibly damaging |
Het |
| Mdga2 |
G |
T |
12: 66,615,670 (GRCm39) |
R646S |
probably benign |
Het |
| Mex3b |
G |
T |
7: 82,518,073 (GRCm39) |
M129I |
possibly damaging |
Het |
| Mfsd10 |
G |
T |
5: 34,793,770 (GRCm39) |
N85K |
probably damaging |
Het |
| Mios |
A |
G |
6: 8,216,064 (GRCm39) |
D420G |
probably damaging |
Het |
| Mogs |
C |
A |
6: 83,092,613 (GRCm39) |
P18T |
unknown |
Het |
| Mrgpre |
A |
G |
7: 143,335,150 (GRCm39) |
C118R |
probably damaging |
Het |
| Muc4 |
A |
T |
16: 32,601,285 (GRCm39) |
H1321L |
|
Het |
| Nkapl |
T |
C |
13: 21,651,759 (GRCm39) |
K285E |
probably damaging |
Het |
| Nphp4 |
C |
T |
4: 152,583,460 (GRCm39) |
P200S |
possibly damaging |
Het |
| Piezo1 |
A |
G |
8: 123,228,397 (GRCm39) |
F297L |
|
Het |
| Pkhd1 |
T |
G |
1: 20,271,197 (GRCm39) |
S3119R |
probably damaging |
Het |
| Pla2g15 |
G |
A |
8: 106,889,576 (GRCm39) |
V283I |
probably benign |
Het |
| Ppp1r13l |
T |
A |
7: 19,102,786 (GRCm39) |
|
probably null |
Het |
| Prex1 |
A |
G |
2: 166,429,047 (GRCm39) |
Y849H |
probably damaging |
Het |
| Psg27 |
C |
A |
7: 18,301,008 (GRCm39) |
W15L |
probably benign |
Het |
| Ptar1 |
A |
T |
19: 23,686,334 (GRCm39) |
|
probably null |
Het |
| Ptpn6 |
G |
A |
6: 124,705,135 (GRCm39) |
R264C |
probably damaging |
Het |
| Ptprb |
A |
G |
10: 116,177,038 (GRCm39) |
I988V |
probably benign |
Het |
| Ptpro |
G |
A |
6: 137,376,559 (GRCm39) |
V680I |
possibly damaging |
Het |
| Rnf170 |
C |
T |
8: 26,613,876 (GRCm39) |
P28S |
probably benign |
Het |
| Rnpepl1 |
A |
G |
1: 92,846,917 (GRCm39) |
S580G |
possibly damaging |
Het |
| Rtel1 |
C |
T |
2: 180,972,608 (GRCm39) |
R29* |
probably null |
Het |
| Rtkn |
T |
C |
6: 83,128,726 (GRCm39) |
L26P |
probably damaging |
Het |
| Sdk2 |
A |
C |
11: 113,729,315 (GRCm39) |
S1087R |
probably damaging |
Het |
| Sema7a |
C |
T |
9: 57,860,852 (GRCm39) |
P71L |
probably benign |
Het |
| Sgpp1 |
C |
T |
12: 75,763,038 (GRCm39) |
C381Y |
probably damaging |
Het |
| Sis |
A |
T |
3: 72,820,625 (GRCm39) |
|
probably null |
Het |
| Slc24a5 |
A |
C |
2: 124,910,869 (GRCm39) |
D100A |
probably benign |
Het |
| Slc25a23 |
A |
T |
17: 57,360,587 (GRCm39) |
I251K |
probably damaging |
Het |
| Slc6a5 |
T |
A |
7: 49,579,804 (GRCm39) |
L394H |
probably damaging |
Het |
| Slc7a4 |
A |
T |
16: 17,392,920 (GRCm39) |
M293K |
probably damaging |
Het |
| Syne2 |
T |
A |
12: 75,973,263 (GRCm39) |
S1089T |
probably benign |
Het |
| Tanc1 |
A |
T |
2: 59,615,670 (GRCm39) |
T226S |
probably damaging |
Het |
| Tdrd6 |
T |
C |
17: 43,936,984 (GRCm39) |
T1355A |
probably benign |
Het |
| Tmem101 |
A |
G |
11: 102,044,176 (GRCm39) |
M237T |
possibly damaging |
Het |
| Ttn |
G |
A |
2: 76,749,359 (GRCm39) |
H3897Y |
possibly damaging |
Het |
| Tubb4a |
C |
T |
17: 57,387,698 (GRCm39) |
V443M |
unknown |
Het |
| Ucp2 |
G |
A |
7: 100,147,576 (GRCm39) |
R185H |
possibly damaging |
Het |
| Vmn1r116 |
G |
T |
7: 20,606,436 (GRCm39) |
E86* |
probably null |
Het |
| Vmn2r37 |
T |
C |
7: 9,213,032 (GRCm39) |
E530G |
probably benign |
Het |
| Vwa8 |
A |
G |
14: 79,333,125 (GRCm39) |
T1293A |
probably benign |
Het |
| Zfc3h1 |
T |
A |
10: 115,260,535 (GRCm39) |
Y1711N |
probably benign |
Het |
| Zfp873 |
A |
T |
10: 81,896,805 (GRCm39) |
E512V |
probably damaging |
Het |
| Zfyve16 |
T |
A |
13: 92,657,654 (GRCm39) |
K752N |
probably damaging |
Het |
| Zhx1 |
T |
C |
15: 57,916,561 (GRCm39) |
N562D |
possibly damaging |
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 |
|
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'- TGGGTTACTCACAGGGTGAC -3'
(R):5'- GTCTAGAACTTTCTTCCGCTGG -3'
Sequencing Primer
(F):5'- GTGTCCGGGGGCAGAAC -3'
(R):5'- TTCTTCCGCTGGGTCCAGG -3'
|
| Posted On |
2019-09-13 |
Incidental Mutation