Incidental Mutation 'R2059:Adgrf5'
ID |
228523 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Adgrf5
|
Ensembl Gene |
ENSMUSG00000056492 |
Gene Name |
adhesion G protein-coupled receptor F5 |
Synonyms |
8430401C09Rik, Gpr116 |
MMRRC Submission |
040064-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R2059 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
17 |
Chromosomal Location |
43671342-43770448 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 43739477 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Cysteine
at position 72
(Y72C)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000153373
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000113599]
[ENSMUST00000224278]
[ENSMUST00000225004]
[ENSMUST00000225962]
[ENSMUST00000226087]
|
AlphaFold |
G5E8Q8 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000113599
AA Change: Y317C
PolyPhen 2
Score 0.848 (Sensitivity: 0.83; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000109229 Gene: ENSMUSG00000056492 AA Change: Y317C
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
24 |
N/A |
INTRINSIC |
Blast:EGF
|
118 |
161 |
8e-14 |
BLAST |
Pfam:SEA
|
165 |
263 |
9.2e-14 |
PFAM |
IG
|
276 |
366 |
1.54e-4 |
SMART |
Blast:IG_like
|
374 |
464 |
2e-31 |
BLAST |
IG
|
475 |
561 |
1.04e-1 |
SMART |
low complexity region
|
815 |
823 |
N/A |
INTRINSIC |
GPS
|
949 |
1004 |
6.49e-16 |
SMART |
Pfam:7tm_2
|
1011 |
1264 |
1.2e-35 |
PFAM |
low complexity region
|
1328 |
1347 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000224278
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000225004
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000225962
AA Change: Y72C
PolyPhen 2
Score 0.884 (Sensitivity: 0.82; Specificity: 0.94)
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000226087
AA Change: Y317C
PolyPhen 2
Score 0.848 (Sensitivity: 0.83; Specificity: 0.93)
|
Meta Mutation Damage Score |
0.1795 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 97.1%
- 20x: 94.5%
|
Validation Efficiency |
99% (99/100) |
MGI Phenotype |
PHENOTYPE: Mice homozygous for a knock-out allele exhibit premature death, decreased body weight and respiratory distress associated with pulmonary alveolar proteinosis. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrf3 |
G |
A |
5: 30,404,489 (GRCm39) |
H316Y |
possibly damaging |
Het |
Ak5 |
T |
A |
3: 152,366,274 (GRCm39) |
L42F |
probably damaging |
Het |
Alas1 |
T |
C |
9: 106,118,489 (GRCm39) |
E211G |
probably damaging |
Het |
Alkbh1 |
C |
T |
12: 87,490,520 (GRCm39) |
|
probably benign |
Het |
Als2cl |
T |
C |
9: 110,714,506 (GRCm39) |
V118A |
probably benign |
Het |
Ano1 |
G |
C |
7: 144,165,127 (GRCm39) |
L641V |
probably damaging |
Het |
Arfgef1 |
C |
T |
1: 10,258,977 (GRCm39) |
|
probably null |
Het |
Atf6b |
A |
T |
17: 34,867,549 (GRCm39) |
|
probably null |
Het |
Atf7ip |
T |
G |
6: 136,586,346 (GRCm39) |
|
probably benign |
Het |
Atp2b4 |
G |
T |
1: 133,654,275 (GRCm39) |
Q777K |
probably benign |
Het |
Baz2a |
T |
A |
10: 127,949,447 (GRCm39) |
S347R |
probably damaging |
Het |
C2cd3 |
T |
C |
7: 100,104,700 (GRCm39) |
|
probably benign |
Het |
Cage1 |
A |
G |
13: 38,207,356 (GRCm39) |
V163A |
probably benign |
Het |
Cdh12 |
T |
A |
15: 21,583,826 (GRCm39) |
N555K |
probably benign |
Het |
Cenpj |
G |
A |
14: 56,801,412 (GRCm39) |
P187L |
possibly damaging |
Het |
Cep112 |
T |
A |
11: 108,410,087 (GRCm39) |
|
probably null |
Het |
Cfap54 |
A |
T |
10: 92,778,841 (GRCm39) |
|
probably benign |
Het |
Cgref1 |
T |
G |
5: 31,090,989 (GRCm39) |
D275A |
possibly damaging |
Het |
Clgn |
A |
C |
8: 84,126,607 (GRCm39) |
N103H |
probably benign |
Het |
Corin |
A |
G |
5: 72,473,394 (GRCm39) |
V905A |
possibly damaging |
Het |
Csta1 |
A |
C |
16: 35,942,692 (GRCm39) |
D72E |
probably benign |
Het |
Cul5 |
A |
T |
9: 53,578,456 (GRCm39) |
L44Q |
probably damaging |
Het |
Dmbt1 |
G |
A |
7: 130,707,900 (GRCm39) |
A1381T |
possibly damaging |
Het |
Dync1i2 |
G |
A |
2: 71,080,197 (GRCm39) |
|
probably null |
Het |
Enoph1 |
A |
G |
5: 100,207,078 (GRCm39) |
D55G |
probably damaging |
Het |
Fat4 |
T |
A |
3: 38,945,319 (GRCm39) |
M1404K |
possibly damaging |
Het |
Fhip2b |
A |
G |
14: 70,822,489 (GRCm39) |
V744A |
possibly damaging |
Het |
Foxi2 |
G |
T |
7: 135,012,406 (GRCm39) |
G98V |
probably damaging |
Het |
Galr2 |
T |
C |
11: 116,173,765 (GRCm39) |
S132P |
probably damaging |
Het |
Gcm2 |
T |
C |
13: 41,263,430 (GRCm39) |
M1V |
probably null |
Het |
Gm15446 |
C |
T |
5: 110,090,362 (GRCm39) |
H205Y |
probably damaging |
Het |
Gm21775 |
T |
A |
Y: 10,553,910 (GRCm39) |
I153N |
probably benign |
Het |
Grip1 |
A |
G |
10: 119,874,603 (GRCm39) |
K789R |
possibly damaging |
Het |
Gsk3b |
T |
A |
16: 38,008,271 (GRCm39) |
D192E |
probably benign |
Het |
Herc2 |
T |
A |
7: 55,813,645 (GRCm39) |
H2625Q |
probably damaging |
Het |
Hoxc9 |
A |
G |
15: 102,892,555 (GRCm39) |
D256G |
probably benign |
Het |
Il7 |
A |
T |
3: 7,638,975 (GRCm39) |
N130K |
probably damaging |
Het |
Irf2 |
A |
T |
8: 47,260,380 (GRCm39) |
N104I |
probably damaging |
Het |
Kat6a |
A |
G |
8: 23,429,321 (GRCm39) |
N1559D |
possibly damaging |
Het |
Kcnq4 |
G |
T |
4: 120,555,199 (GRCm39) |
F661L |
probably benign |
Het |
Kdm5b |
T |
A |
1: 134,540,952 (GRCm39) |
D681E |
probably benign |
Het |
Khdrbs1 |
T |
C |
4: 129,619,514 (GRCm39) |
E209G |
probably damaging |
Het |
Lama3 |
A |
T |
18: 12,661,390 (GRCm39) |
R2116S |
probably damaging |
Het |
Mir124-2hg |
C |
A |
3: 17,839,877 (GRCm39) |
E65* |
probably null |
Het |
Mphosph10 |
T |
A |
7: 64,026,499 (GRCm39) |
L650F |
probably damaging |
Het |
Mrpl48 |
T |
C |
7: 100,198,540 (GRCm39) |
E204G |
probably damaging |
Het |
Msl3l2 |
T |
A |
10: 55,992,040 (GRCm39) |
L255Q |
probably damaging |
Het |
Mx1 |
T |
A |
16: 97,255,379 (GRCm39) |
K225* |
probably null |
Het |
Nf1 |
T |
C |
11: 79,447,549 (GRCm39) |
V435A |
probably damaging |
Het |
Nid1 |
A |
C |
13: 13,675,058 (GRCm39) |
H926P |
probably benign |
Het |
Nlrp9a |
T |
A |
7: 26,256,787 (GRCm39) |
I46K |
possibly damaging |
Het |
Nop2 |
T |
A |
6: 125,116,823 (GRCm39) |
M359K |
probably null |
Het |
Nox1 |
T |
C |
X: 132,995,993 (GRCm39) |
|
probably benign |
Het |
Ogdhl |
G |
A |
14: 32,054,841 (GRCm39) |
R263K |
probably damaging |
Het |
Or14c40 |
A |
T |
7: 86,313,591 (GRCm39) |
K240N |
probably damaging |
Het |
Or2y16 |
T |
A |
11: 49,335,278 (GRCm39) |
V200E |
probably damaging |
Het |
Pbsn |
T |
C |
X: 76,891,582 (GRCm39) |
K72E |
probably damaging |
Het |
Pde12 |
T |
C |
14: 26,390,035 (GRCm39) |
I225V |
probably benign |
Het |
Ppt2 |
A |
T |
17: 34,841,818 (GRCm39) |
|
probably benign |
Het |
Prl3a1 |
A |
G |
13: 27,454,127 (GRCm39) |
D35G |
probably benign |
Het |
Prss3b |
G |
A |
6: 41,009,315 (GRCm39) |
T173I |
probably benign |
Het |
Ptprk |
T |
A |
10: 28,442,599 (GRCm39) |
I893N |
probably damaging |
Het |
Ptprz1 |
T |
C |
6: 22,986,322 (GRCm39) |
|
probably benign |
Het |
Rab3c |
A |
G |
13: 110,397,050 (GRCm39) |
V72A |
probably damaging |
Het |
Rbms2 |
A |
G |
10: 127,973,387 (GRCm39) |
S251P |
probably benign |
Het |
Rfwd3 |
A |
G |
8: 112,024,127 (GRCm39) |
V65A |
probably benign |
Het |
Rps6kl1 |
T |
A |
12: 85,186,397 (GRCm39) |
Y211F |
probably benign |
Het |
Saal1 |
T |
C |
7: 46,348,880 (GRCm39) |
Q317R |
probably damaging |
Het |
Scg3 |
T |
C |
9: 75,572,998 (GRCm39) |
D311G |
probably damaging |
Het |
Sdk2 |
C |
A |
11: 113,745,158 (GRCm39) |
M712I |
probably damaging |
Het |
Serinc2 |
T |
G |
4: 130,154,578 (GRCm39) |
Y158S |
probably damaging |
Het |
Serpinb9c |
A |
T |
13: 33,340,854 (GRCm39) |
C81* |
probably null |
Het |
Sgpp2 |
T |
A |
1: 78,393,588 (GRCm39) |
L197Q |
probably damaging |
Het |
Shroom3 |
A |
T |
5: 92,831,643 (GRCm39) |
T40S |
probably damaging |
Het |
Sik1 |
A |
G |
17: 32,067,771 (GRCm39) |
S435P |
probably benign |
Het |
Slc7a3 |
A |
G |
X: 100,124,373 (GRCm39) |
V464A |
probably benign |
Het |
Snd1 |
T |
C |
6: 28,745,206 (GRCm39) |
F517S |
probably damaging |
Het |
Spata13 |
A |
C |
14: 60,997,040 (GRCm39) |
I1165L |
possibly damaging |
Het |
St8sia5 |
A |
T |
18: 77,342,459 (GRCm39) |
I390F |
probably damaging |
Het |
Stat5b |
A |
T |
11: 100,678,158 (GRCm39) |
S652T |
probably benign |
Het |
Stom |
A |
G |
2: 35,206,037 (GRCm39) |
S231P |
probably damaging |
Het |
Sult1b1 |
A |
G |
5: 87,682,892 (GRCm39) |
Y18H |
probably damaging |
Het |
Tgm4 |
T |
C |
9: 122,890,835 (GRCm39) |
I54T |
probably damaging |
Het |
Tmem176b |
G |
A |
6: 48,813,267 (GRCm39) |
T64I |
probably damaging |
Het |
Tmem87a |
A |
T |
2: 120,199,773 (GRCm39) |
I457N |
probably damaging |
Het |
Trim12c |
A |
G |
7: 103,997,398 (GRCm39) |
F53L |
possibly damaging |
Het |
Ttc6 |
T |
A |
12: 57,784,479 (GRCm39) |
D1849E |
probably benign |
Het |
Ubap2l |
A |
T |
3: 89,938,683 (GRCm39) |
|
probably benign |
Het |
Ush2a |
T |
G |
1: 188,113,746 (GRCm39) |
|
probably null |
Het |
Usp17la |
A |
C |
7: 104,510,378 (GRCm39) |
T328P |
probably damaging |
Het |
Ust |
A |
G |
10: 8,083,330 (GRCm39) |
Y349H |
probably damaging |
Het |
V1rd19 |
A |
T |
7: 23,703,259 (GRCm39) |
M242L |
probably benign |
Het |
Vmn1r33 |
T |
A |
6: 66,589,186 (GRCm39) |
M123L |
probably benign |
Het |
Vps13c |
A |
T |
9: 67,768,115 (GRCm39) |
K111N |
probably damaging |
Het |
Vwa3a |
A |
G |
7: 120,358,172 (GRCm39) |
D81G |
probably damaging |
Het |
Zfp318 |
G |
A |
17: 46,707,950 (GRCm39) |
R336Q |
probably damaging |
Het |
Zfp609 |
A |
G |
9: 65,611,716 (GRCm39) |
S416P |
possibly damaging |
Het |
|
Other mutations in Adgrf5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00501:Adgrf5
|
APN |
17 |
43,760,806 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL00590:Adgrf5
|
APN |
17 |
43,764,038 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01128:Adgrf5
|
APN |
17 |
43,733,400 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01131:Adgrf5
|
APN |
17 |
43,733,400 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01132:Adgrf5
|
APN |
17 |
43,733,400 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01392:Adgrf5
|
APN |
17 |
43,760,903 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01475:Adgrf5
|
APN |
17 |
43,761,245 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01614:Adgrf5
|
APN |
17 |
43,735,362 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01654:Adgrf5
|
APN |
17 |
43,762,061 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02053:Adgrf5
|
APN |
17 |
43,761,058 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02175:Adgrf5
|
APN |
17 |
43,761,901 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02416:Adgrf5
|
APN |
17 |
43,755,871 (GRCm39) |
splice site |
probably null |
|
IGL02525:Adgrf5
|
APN |
17 |
43,760,854 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03035:Adgrf5
|
APN |
17 |
43,741,518 (GRCm39) |
missense |
possibly damaging |
0.80 |
duct_tape
|
UTSW |
17 |
43,756,006 (GRCm39) |
missense |
probably benign |
0.04 |
Flypaper
|
UTSW |
17 |
43,733,552 (GRCm39) |
splice site |
probably benign |
|
goop
|
UTSW |
17 |
43,752,860 (GRCm39) |
missense |
probably damaging |
0.99 |
Heaped
|
UTSW |
17 |
43,757,927 (GRCm39) |
missense |
possibly damaging |
0.93 |
la_brea
|
UTSW |
17 |
43,763,214 (GRCm39) |
critical splice donor site |
probably null |
|
Motel
|
UTSW |
17 |
43,761,271 (GRCm39) |
missense |
probably damaging |
1.00 |
noel
|
UTSW |
17 |
43,741,503 (GRCm39) |
missense |
probably damaging |
1.00 |
Schmutzfinger
|
UTSW |
17 |
43,735,709 (GRCm39) |
nonsense |
probably null |
|
sticky
|
UTSW |
17 |
43,748,462 (GRCm39) |
missense |
probably damaging |
0.98 |
sweetie
|
UTSW |
17 |
43,761,874 (GRCm39) |
missense |
probably damaging |
0.96 |
PIT4812001:Adgrf5
|
UTSW |
17 |
43,761,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R0699:Adgrf5
|
UTSW |
17 |
43,733,552 (GRCm39) |
splice site |
probably null |
|
R0972:Adgrf5
|
UTSW |
17 |
43,761,874 (GRCm39) |
missense |
probably damaging |
0.96 |
R1521:Adgrf5
|
UTSW |
17 |
43,741,443 (GRCm39) |
missense |
probably benign |
0.03 |
R1523:Adgrf5
|
UTSW |
17 |
43,761,044 (GRCm39) |
missense |
probably benign |
0.00 |
R1758:Adgrf5
|
UTSW |
17 |
43,735,484 (GRCm39) |
critical splice donor site |
probably null |
|
R1767:Adgrf5
|
UTSW |
17 |
43,761,455 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1799:Adgrf5
|
UTSW |
17 |
43,750,958 (GRCm39) |
missense |
probably damaging |
0.98 |
R1800:Adgrf5
|
UTSW |
17 |
43,761,973 (GRCm39) |
missense |
probably damaging |
1.00 |
R1888:Adgrf5
|
UTSW |
17 |
43,737,896 (GRCm39) |
splice site |
probably null |
|
R1888:Adgrf5
|
UTSW |
17 |
43,737,896 (GRCm39) |
splice site |
probably null |
|
R2057:Adgrf5
|
UTSW |
17 |
43,739,477 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2058:Adgrf5
|
UTSW |
17 |
43,739,477 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2410:Adgrf5
|
UTSW |
17 |
43,766,157 (GRCm39) |
missense |
probably benign |
0.11 |
R2568:Adgrf5
|
UTSW |
17 |
43,748,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R2847:Adgrf5
|
UTSW |
17 |
43,733,531 (GRCm39) |
missense |
possibly damaging |
0.69 |
R2848:Adgrf5
|
UTSW |
17 |
43,733,531 (GRCm39) |
missense |
possibly damaging |
0.69 |
R3800:Adgrf5
|
UTSW |
17 |
43,757,951 (GRCm39) |
splice site |
probably benign |
|
R3856:Adgrf5
|
UTSW |
17 |
43,757,927 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4021:Adgrf5
|
UTSW |
17 |
43,741,605 (GRCm39) |
splice site |
probably benign |
|
R4075:Adgrf5
|
UTSW |
17 |
43,761,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R4366:Adgrf5
|
UTSW |
17 |
43,752,860 (GRCm39) |
missense |
probably damaging |
0.99 |
R4409:Adgrf5
|
UTSW |
17 |
43,752,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R4570:Adgrf5
|
UTSW |
17 |
43,756,006 (GRCm39) |
missense |
probably benign |
0.04 |
R4616:Adgrf5
|
UTSW |
17 |
43,763,331 (GRCm39) |
missense |
probably benign |
0.38 |
R4623:Adgrf5
|
UTSW |
17 |
43,761,874 (GRCm39) |
missense |
probably benign |
0.16 |
R4645:Adgrf5
|
UTSW |
17 |
43,748,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R5211:Adgrf5
|
UTSW |
17 |
43,733,511 (GRCm39) |
missense |
probably benign |
0.32 |
R5268:Adgrf5
|
UTSW |
17 |
43,761,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R5280:Adgrf5
|
UTSW |
17 |
43,737,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R5326:Adgrf5
|
UTSW |
17 |
43,750,965 (GRCm39) |
missense |
probably damaging |
0.98 |
R5762:Adgrf5
|
UTSW |
17 |
43,741,586 (GRCm39) |
missense |
probably null |
0.16 |
R5856:Adgrf5
|
UTSW |
17 |
43,757,011 (GRCm39) |
missense |
probably benign |
0.09 |
R6007:Adgrf5
|
UTSW |
17 |
43,748,462 (GRCm39) |
missense |
probably damaging |
0.98 |
R6153:Adgrf5
|
UTSW |
17 |
43,761,974 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6451:Adgrf5
|
UTSW |
17 |
43,735,709 (GRCm39) |
nonsense |
probably null |
|
R6535:Adgrf5
|
UTSW |
17 |
43,750,920 (GRCm39) |
missense |
probably benign |
0.05 |
R6536:Adgrf5
|
UTSW |
17 |
43,733,552 (GRCm39) |
splice site |
probably benign |
|
R6602:Adgrf5
|
UTSW |
17 |
43,761,195 (GRCm39) |
missense |
probably benign |
0.32 |
R6882:Adgrf5
|
UTSW |
17 |
43,761,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R6992:Adgrf5
|
UTSW |
17 |
43,763,214 (GRCm39) |
critical splice donor site |
probably null |
|
R7137:Adgrf5
|
UTSW |
17 |
43,761,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R7170:Adgrf5
|
UTSW |
17 |
43,757,029 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7313:Adgrf5
|
UTSW |
17 |
43,763,368 (GRCm39) |
critical splice donor site |
probably null |
|
R7313:Adgrf5
|
UTSW |
17 |
43,755,974 (GRCm39) |
missense |
probably benign |
0.01 |
R7331:Adgrf5
|
UTSW |
17 |
43,748,484 (GRCm39) |
missense |
probably damaging |
0.99 |
R7346:Adgrf5
|
UTSW |
17 |
43,762,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R7350:Adgrf5
|
UTSW |
17 |
43,739,335 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7667:Adgrf5
|
UTSW |
17 |
43,756,930 (GRCm39) |
missense |
probably benign |
0.01 |
R7717:Adgrf5
|
UTSW |
17 |
43,761,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R7731:Adgrf5
|
UTSW |
17 |
43,761,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R7877:Adgrf5
|
UTSW |
17 |
43,752,729 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7950:Adgrf5
|
UTSW |
17 |
43,762,048 (GRCm39) |
missense |
probably damaging |
0.99 |
R7988:Adgrf5
|
UTSW |
17 |
43,750,704 (GRCm39) |
intron |
probably benign |
|
R8188:Adgrf5
|
UTSW |
17 |
43,741,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R8219:Adgrf5
|
UTSW |
17 |
43,760,750 (GRCm39) |
missense |
probably benign |
0.13 |
R8284:Adgrf5
|
UTSW |
17 |
43,766,161 (GRCm39) |
missense |
unknown |
|
R8460:Adgrf5
|
UTSW |
17 |
43,750,699 (GRCm39) |
intron |
probably benign |
|
R8504:Adgrf5
|
UTSW |
17 |
43,757,840 (GRCm39) |
missense |
probably benign |
0.01 |
R8751:Adgrf5
|
UTSW |
17 |
43,748,574 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8852:Adgrf5
|
UTSW |
17 |
43,763,989 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9196:Adgrf5
|
UTSW |
17 |
43,755,995 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9418:Adgrf5
|
UTSW |
17 |
43,737,864 (GRCm39) |
missense |
probably benign |
0.00 |
R9671:Adgrf5
|
UTSW |
17 |
43,760,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R9734:Adgrf5
|
UTSW |
17 |
43,763,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R9756:Adgrf5
|
UTSW |
17 |
43,761,137 (GRCm39) |
missense |
probably benign |
0.01 |
R9765:Adgrf5
|
UTSW |
17 |
43,748,491 (GRCm39) |
missense |
probably damaging |
1.00 |
X0017:Adgrf5
|
UTSW |
17 |
43,737,936 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Adgrf5
|
UTSW |
17 |
43,755,944 (GRCm39) |
missense |
probably benign |
0.00 |
Z1191:Adgrf5
|
UTSW |
17 |
43,755,926 (GRCm39) |
missense |
probably benign |
0.17 |
|
Predicted Primers |
PCR Primer
(F):5'- AGCCCCACAGTTTGCATCAC -3'
(R):5'- TGGAATAGGCTTCTTGTGAACAGC -3'
Sequencing Primer
(F):5'- CACAGTTTGCATCACTGATGTG -3'
(R):5'- GCTCACCCTCCAACCCCTG -3'
|
Posted On |
2014-09-17 |