Incidental Mutation 'R1799:Adgrf5'
| ID |
202984 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Adgrf5
|
| Ensembl Gene |
ENSMUSG00000056492 |
| Gene Name |
adhesion G protein-coupled receptor F5 |
| Synonyms |
8430401C09Rik, Gpr116 |
| MMRRC Submission |
039829-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R1799 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
17 |
| Chromosomal Location |
43671342-43770448 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 43750958 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Phenylalanine
at position 508
(I508F)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000153049
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000113599]
[ENSMUST00000225004]
[ENSMUST00000225962]
[ENSMUST00000226087]
|
| AlphaFold |
G5E8Q8 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000113599
AA Change: I508F
PolyPhen 2
Score 0.983 (Sensitivity: 0.75; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000109229
Gene: ENSMUSG00000056492
AA Change: I508F
| 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: ENSMUST00000225004
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000225962
AA Change: I303F
PolyPhen 2
Score 0.979 (Sensitivity: 0.75; Specificity: 0.96)
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000226087
AA Change: I508F
PolyPhen 2
Score 0.983 (Sensitivity: 0.75; Specificity: 0.96)
|
| Coding Region Coverage |
- 1x: 97.5%
- 3x: 96.9%
- 10x: 95.3%
- 20x: 92.3%
|
| Validation Efficiency |
|
| 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: 102 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A930011G23Rik |
A |
G |
5: 99,382,435 (GRCm39) |
L271P |
probably benign |
Het |
| Adamts3 |
A |
C |
5: 89,923,280 (GRCm39) |
D175E |
probably benign |
Het |
| Adcy4 |
T |
C |
14: 56,008,929 (GRCm39) |
T833A |
probably benign |
Het |
| Arhgap9 |
G |
T |
10: 127,163,593 (GRCm39) |
V464L |
probably damaging |
Het |
| Atp10a |
T |
A |
7: 58,474,182 (GRCm39) |
D1156E |
probably damaging |
Het |
| Atp2a1 |
A |
T |
7: 126,049,314 (GRCm39) |
M576K |
probably benign |
Het |
| Atrx |
T |
C |
X: 104,891,235 (GRCm39) |
Q1536R |
probably damaging |
Het |
| Ccdc141 |
A |
C |
2: 76,842,015 (GRCm39) |
V1472G |
possibly damaging |
Het |
| Cd84 |
A |
G |
1: 171,700,317 (GRCm39) |
T145A |
possibly damaging |
Het |
| Celsr1 |
G |
T |
15: 85,916,886 (GRCm39) |
N362K |
probably damaging |
Het |
| Cep290 |
G |
A |
10: 100,352,058 (GRCm39) |
A755T |
probably benign |
Het |
| Cfap70 |
T |
A |
14: 20,445,067 (GRCm39) |
E1071V |
probably damaging |
Het |
| Cps1 |
T |
C |
1: 67,248,801 (GRCm39) |
V1176A |
probably damaging |
Het |
| Csf2rb2 |
A |
C |
15: 78,181,268 (GRCm39) |
N41K |
probably damaging |
Het |
| Csn1s2a |
G |
A |
5: 87,926,052 (GRCm39) |
V43M |
probably damaging |
Het |
| Cyp26b1 |
T |
C |
6: 84,561,254 (GRCm39) |
D136G |
probably benign |
Het |
| Cyp7b1 |
A |
G |
3: 18,151,616 (GRCm39) |
L199P |
probably benign |
Het |
| Dapk1 |
C |
T |
13: 60,867,468 (GRCm39) |
T225I |
probably damaging |
Het |
| Dio2 |
T |
A |
12: 90,696,680 (GRCm39) |
T103S |
probably benign |
Het |
| Dipk1a |
C |
A |
5: 108,057,713 (GRCm39) |
V237F |
probably damaging |
Het |
| Dnhd1 |
T |
A |
7: 105,304,974 (GRCm39) |
S339T |
probably benign |
Het |
| Drc1 |
A |
G |
5: 30,523,841 (GRCm39) |
N737D |
probably damaging |
Het |
| Efhc1 |
C |
T |
1: 21,049,762 (GRCm39) |
P541S |
probably benign |
Het |
| Elmo2 |
A |
T |
2: 165,134,077 (GRCm39) |
I637N |
probably damaging |
Het |
| Eps15 |
T |
A |
4: 109,240,034 (GRCm39) |
D492E |
probably damaging |
Het |
| Ermn |
G |
T |
2: 57,938,249 (GRCm39) |
N121K |
probably benign |
Het |
| F5 |
A |
G |
1: 164,021,100 (GRCm39) |
T1192A |
possibly damaging |
Het |
| Fbxo22 |
T |
C |
9: 55,130,771 (GRCm39) |
F347L |
probably benign |
Het |
| Fbxw15 |
G |
A |
9: 109,387,314 (GRCm39) |
S227F |
probably damaging |
Het |
| Foxj3 |
A |
G |
4: 119,476,548 (GRCm39) |
N242S |
probably benign |
Het |
| Gjb3 |
G |
A |
4: 127,220,224 (GRCm39) |
R103W |
probably damaging |
Het |
| Grm4 |
A |
G |
17: 27,691,914 (GRCm39) |
V235A |
probably damaging |
Het |
| Gstm4 |
T |
C |
3: 107,950,874 (GRCm39) |
N74S |
probably damaging |
Het |
| Gtf3c3 |
A |
G |
1: 54,459,583 (GRCm39) |
V393A |
possibly damaging |
Het |
| Hltf |
T |
A |
3: 20,159,855 (GRCm39) |
L702H |
probably damaging |
Het |
| Inpp4a |
T |
A |
1: 37,432,059 (GRCm39) |
V153E |
possibly damaging |
Het |
| Kmt5c |
T |
C |
7: 4,745,729 (GRCm39) |
|
probably null |
Het |
| Kynu |
A |
G |
2: 43,494,169 (GRCm39) |
R201G |
possibly damaging |
Het |
| Lrp2 |
T |
A |
2: 69,333,874 (GRCm39) |
T1456S |
probably benign |
Het |
| Lrrc40 |
G |
A |
3: 157,742,441 (GRCm39) |
V19I |
probably benign |
Het |
| M1ap |
T |
A |
6: 82,982,491 (GRCm39) |
C258* |
probably null |
Het |
| Man2a1 |
T |
C |
17: 65,059,452 (GRCm39) |
L1113P |
probably benign |
Het |
| Man2a1 |
C |
T |
17: 64,976,492 (GRCm39) |
R427W |
probably damaging |
Het |
| Meikin |
C |
A |
11: 54,308,613 (GRCm39) |
Q404K |
probably benign |
Het |
| Mfsd4a |
T |
C |
1: 131,981,334 (GRCm39) |
I222V |
possibly damaging |
Het |
| N4bp2 |
A |
G |
5: 65,964,168 (GRCm39) |
N739S |
possibly damaging |
Het |
| Ncoa2 |
A |
T |
1: 13,232,517 (GRCm39) |
|
probably null |
Het |
| Nisch |
G |
T |
14: 30,899,228 (GRCm39) |
|
probably benign |
Het |
| Nmur2 |
A |
G |
11: 55,920,447 (GRCm39) |
V266A |
probably damaging |
Het |
| Npcd |
G |
A |
15: 79,712,987 (GRCm39) |
R147C |
probably damaging |
Het |
| Or4q3 |
T |
A |
14: 50,583,537 (GRCm39) |
M121L |
probably benign |
Het |
| Or5ac25 |
T |
A |
16: 59,182,243 (GRCm39) |
I113F |
probably benign |
Het |
| Pals2 |
T |
A |
6: 50,173,525 (GRCm39) |
M463K |
probably damaging |
Het |
| Parp4 |
A |
T |
14: 56,885,589 (GRCm39) |
H1556L |
unknown |
Het |
| Pcdh9 |
G |
T |
14: 94,126,107 (GRCm39) |
A21E |
probably benign |
Het |
| Phtf1 |
A |
G |
3: 103,903,958 (GRCm39) |
E436G |
probably benign |
Het |
| Piezo2 |
C |
A |
18: 63,165,911 (GRCm39) |
|
probably null |
Het |
| Piezo2 |
T |
C |
18: 63,241,158 (GRCm39) |
Y690C |
probably damaging |
Het |
| Pla2g4f |
T |
C |
2: 120,141,549 (GRCm39) |
R183G |
possibly damaging |
Het |
| Plxnd1 |
T |
C |
6: 115,971,018 (GRCm39) |
D250G |
probably damaging |
Het |
| Ppig |
A |
G |
2: 69,579,744 (GRCm39) |
D426G |
unknown |
Het |
| Ppp3cb |
T |
C |
14: 20,574,540 (GRCm39) |
E185G |
possibly damaging |
Het |
| Qsox1 |
A |
T |
1: 155,670,364 (GRCm39) |
M151K |
probably null |
Het |
| Ralgapa2 |
T |
C |
2: 146,184,648 (GRCm39) |
E1453G |
probably benign |
Het |
| Rnf167 |
G |
A |
11: 70,540,838 (GRCm39) |
V191I |
probably benign |
Het |
| Rp1 |
T |
C |
1: 4,419,055 (GRCm39) |
K686E |
possibly damaging |
Het |
| Ryr1 |
T |
G |
7: 28,767,046 (GRCm39) |
Q2979P |
probably damaging |
Het |
| Scaf1 |
T |
A |
7: 44,657,443 (GRCm39) |
I479F |
probably damaging |
Het |
| Septin8 |
A |
G |
11: 53,425,310 (GRCm39) |
T68A |
probably benign |
Het |
| Sh3rf1 |
A |
T |
8: 61,825,661 (GRCm39) |
N552I |
probably damaging |
Het |
| Shoc1 |
A |
T |
4: 59,099,383 (GRCm39) |
V103D |
possibly damaging |
Het |
| Slc1a3 |
A |
G |
15: 8,717,888 (GRCm39) |
L68P |
probably damaging |
Het |
| Slc39a6 |
G |
A |
18: 24,718,524 (GRCm39) |
P511L |
probably benign |
Het |
| Slc9c1 |
A |
G |
16: 45,374,652 (GRCm39) |
Y339C |
probably damaging |
Het |
| Smarcal1 |
G |
T |
1: 72,625,120 (GRCm39) |
C89F |
probably damaging |
Het |
| Smu1 |
A |
T |
4: 40,745,537 (GRCm39) |
M261K |
probably damaging |
Het |
| Spag8 |
T |
G |
4: 43,653,087 (GRCm39) |
|
probably benign |
Het |
| Spag8 |
T |
C |
4: 43,653,345 (GRCm39) |
|
probably benign |
Het |
| Spata31d1a |
T |
C |
13: 59,851,216 (GRCm39) |
D304G |
probably benign |
Het |
| Spdl1 |
A |
T |
11: 34,711,856 (GRCm39) |
L298* |
probably null |
Het |
| Stac2 |
C |
T |
11: 97,930,444 (GRCm39) |
|
probably null |
Het |
| Stag1 |
A |
G |
9: 100,835,515 (GRCm39) |
|
probably null |
Het |
| Stpg2 |
C |
T |
3: 139,125,542 (GRCm39) |
P445L |
probably damaging |
Het |
| Sult2a8 |
A |
T |
7: 14,157,451 (GRCm39) |
V128E |
probably damaging |
Het |
| Synm |
A |
G |
7: 67,385,707 (GRCm39) |
F210L |
probably damaging |
Het |
| Tbck |
C |
G |
3: 132,480,263 (GRCm39) |
A714G |
probably benign |
Het |
| Tcerg1 |
A |
T |
18: 42,694,012 (GRCm39) |
Y711F |
possibly damaging |
Het |
| Tnfrsf25 |
A |
G |
4: 152,201,465 (GRCm39) |
T98A |
probably benign |
Het |
| Togaram2 |
T |
C |
17: 71,998,450 (GRCm39) |
S218P |
probably damaging |
Het |
| Tpp1 |
A |
T |
7: 105,399,515 (GRCm39) |
D84E |
probably benign |
Het |
| Trim30d |
G |
T |
7: 104,132,682 (GRCm39) |
Q202K |
probably damaging |
Het |
| Trim37 |
T |
A |
11: 87,068,845 (GRCm39) |
V397E |
probably damaging |
Het |
| Triml1 |
A |
T |
8: 43,583,512 (GRCm39) |
I363N |
probably damaging |
Het |
| Trpm6 |
T |
A |
19: 18,869,363 (GRCm39) |
|
probably null |
Het |
| Tsc2 |
T |
C |
17: 24,823,382 (GRCm39) |
S1055G |
probably benign |
Het |
| Ubr5 |
T |
C |
15: 37,989,621 (GRCm39) |
D2065G |
probably damaging |
Het |
| Uggt2 |
G |
T |
14: 119,269,688 (GRCm39) |
P948Q |
probably benign |
Het |
| Vps13c |
A |
T |
9: 67,851,399 (GRCm39) |
S2345C |
probably damaging |
Het |
| Wtap |
G |
T |
17: 13,199,771 (GRCm39) |
R48S |
possibly damaging |
Het |
| Zbtb38 |
A |
G |
9: 96,570,934 (GRCm39) |
V50A |
probably damaging |
Het |
| Zcchc2 |
T |
A |
1: 105,958,017 (GRCm39) |
S829R |
probably benign |
Het |
| Zfp385b |
T |
C |
2: 77,246,316 (GRCm39) |
D237G |
probably benign |
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 |
|
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 |
|
R2059: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'- AATGTCACTCCCGTGTCGATG -3'
(R):5'- TGTCCTGTCACCCACAAAG -3'
Sequencing Primer
(F):5'- CCCGTGTCGATGTCATCTG -3'
(R):5'- TGTCACCCACAAAGAGTAATTAATC -3'
|
| Posted On |
2014-06-23 |
Incidental Mutation