Incidental Mutation 'R5268:Adgrf5'
| ID |
400010 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Adgrf5
|
| Ensembl Gene |
ENSMUSG00000056492 |
| Gene Name |
adhesion G protein-coupled receptor F5 |
| Synonyms |
8430401C09Rik, Gpr116 |
| MMRRC Submission |
042860-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R5268 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
17 |
| Chromosomal Location |
43671342-43770448 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 43761890 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Alanine
at position 1195
(V1195A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000153049
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000113599]
[ENSMUST00000225962]
[ENSMUST00000226087]
|
| AlphaFold |
G5E8Q8 |
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000082648
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000113599
AA Change: V1195A
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000109229
Gene: ENSMUSG00000056492
AA Change: V1195A
| 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 damaging
Transcript: ENSMUST00000225962
AA Change: V990A
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000226087
AA Change: V1195A
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 97.0%
- 20x: 94.9%
|
| 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: 83 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aadacl2fm2 |
A |
G |
3: 59,659,444 (GRCm39) |
E299G |
probably damaging |
Het |
| Adamtsl4 |
C |
A |
3: 95,587,473 (GRCm39) |
R701L |
probably damaging |
Het |
| Agpat5 |
A |
G |
8: 18,931,878 (GRCm39) |
T333A |
possibly damaging |
Het |
| Aspm |
G |
T |
1: 139,392,033 (GRCm39) |
G795C |
probably damaging |
Het |
| Car4 |
C |
A |
11: 84,856,626 (GRCm39) |
Q305K |
probably benign |
Het |
| Catsperg1 |
T |
C |
7: 28,894,672 (GRCm39) |
N612S |
probably benign |
Het |
| Cdc5l |
G |
A |
17: 45,726,511 (GRCm39) |
R354W |
probably damaging |
Het |
| Cdh9 |
G |
A |
15: 16,851,099 (GRCm39) |
V623I |
probably benign |
Het |
| Cfap65 |
A |
G |
1: 74,964,061 (GRCm39) |
V629A |
probably benign |
Het |
| Chd1 |
G |
A |
17: 15,956,005 (GRCm39) |
V535I |
probably damaging |
Het |
| Col12a1 |
A |
G |
9: 79,585,329 (GRCm39) |
V1316A |
probably damaging |
Het |
| Col6a3 |
A |
T |
1: 90,712,965 (GRCm39) |
D1721E |
unknown |
Het |
| Cop1 |
T |
A |
1: 159,154,734 (GRCm39) |
F647L |
probably damaging |
Het |
| Corin |
A |
C |
5: 72,500,362 (GRCm39) |
S421A |
probably damaging |
Het |
| Crb2 |
T |
C |
2: 37,680,833 (GRCm39) |
V587A |
probably damaging |
Het |
| Ctc1 |
T |
A |
11: 68,920,636 (GRCm39) |
V646E |
possibly damaging |
Het |
| Cyp2a12 |
A |
T |
7: 26,730,643 (GRCm39) |
M203L |
probably benign |
Het |
| Dcdc2c |
T |
A |
12: 28,566,656 (GRCm39) |
K336M |
possibly damaging |
Het |
| Ddx39a |
G |
A |
8: 84,448,950 (GRCm39) |
R275H |
probably benign |
Het |
| Dennd2b |
A |
G |
7: 109,156,519 (GRCm39) |
L77P |
probably benign |
Het |
| Des |
A |
G |
1: 75,339,572 (GRCm39) |
N310S |
possibly damaging |
Het |
| Dlk1 |
C |
A |
12: 109,425,764 (GRCm39) |
S212R |
probably benign |
Het |
| Dnajc5b |
A |
G |
3: 19,633,224 (GRCm39) |
E149G |
probably benign |
Het |
| Dpep1 |
A |
T |
8: 123,920,828 (GRCm39) |
I3F |
probably benign |
Het |
| Eml6 |
T |
A |
11: 29,753,108 (GRCm39) |
R934S |
probably benign |
Het |
| Ercc6l2 |
T |
C |
13: 64,016,925 (GRCm39) |
L676P |
possibly damaging |
Het |
| Fkbpl |
G |
A |
17: 34,864,303 (GRCm39) |
A24T |
probably benign |
Het |
| Frem2 |
T |
A |
3: 53,560,575 (GRCm39) |
I1311F |
probably damaging |
Het |
| Gldc |
T |
A |
19: 30,123,125 (GRCm39) |
M257L |
probably damaging |
Het |
| Gm8674 |
T |
G |
13: 50,055,390 (GRCm39) |
|
noncoding transcript |
Het |
| Gnai3 |
C |
T |
3: 108,030,857 (GRCm39) |
|
probably null |
Het |
| Gtf3a |
A |
G |
5: 146,891,965 (GRCm39) |
D300G |
probably damaging |
Het |
| Haus3 |
A |
T |
5: 34,323,449 (GRCm39) |
V387D |
probably damaging |
Het |
| Hpf1 |
T |
A |
8: 61,346,768 (GRCm39) |
F28I |
possibly damaging |
Het |
| Iars1 |
A |
G |
13: 49,843,967 (GRCm39) |
D147G |
probably damaging |
Het |
| Ibtk |
A |
T |
9: 85,625,743 (GRCm39) |
D2E |
probably benign |
Het |
| Ift140 |
T |
A |
17: 25,239,601 (GRCm39) |
I86K |
possibly damaging |
Het |
| Igf2bp2 |
T |
A |
16: 21,898,241 (GRCm39) |
I235F |
probably damaging |
Het |
| Ighv3-8 |
G |
T |
12: 114,286,252 (GRCm39) |
A30E |
probably benign |
Het |
| Kcnq5 |
T |
A |
1: 21,575,949 (GRCm39) |
T252S |
probably damaging |
Het |
| Lrrc4b |
A |
T |
7: 44,110,787 (GRCm39) |
N220Y |
probably damaging |
Het |
| Ltbr |
G |
A |
6: 125,289,757 (GRCm39) |
R146W |
probably damaging |
Het |
| Mamdc4 |
T |
C |
2: 25,454,702 (GRCm39) |
T1037A |
possibly damaging |
Het |
| Mbd5 |
A |
T |
2: 49,162,106 (GRCm39) |
I863F |
possibly damaging |
Het |
| Muc4 |
T |
A |
16: 32,570,484 (GRCm39) |
S515T |
possibly damaging |
Het |
| Mylk4 |
T |
A |
13: 32,892,864 (GRCm39) |
|
probably null |
Het |
| Neu4 |
G |
A |
1: 93,952,669 (GRCm39) |
R346H |
probably benign |
Het |
| Nxpe5 |
T |
A |
5: 138,238,200 (GRCm39) |
Y253* |
probably null |
Het |
| Olfml2b |
A |
T |
1: 170,477,330 (GRCm39) |
E155V |
probably damaging |
Het |
| Or14a258 |
A |
G |
7: 86,034,867 (GRCm39) |
*334Q |
probably null |
Het |
| Or6a2 |
T |
A |
7: 106,600,111 (GRCm39) |
N319Y |
probably benign |
Het |
| Or8a1b |
T |
A |
9: 37,623,300 (GRCm39) |
I92F |
probably damaging |
Het |
| Pamr1 |
G |
A |
2: 102,417,029 (GRCm39) |
A114T |
probably damaging |
Het |
| Pdzd2 |
T |
A |
15: 12,592,263 (GRCm39) |
N127I |
probably damaging |
Het |
| Pglyrp4 |
C |
T |
3: 90,634,271 (GRCm39) |
L5F |
probably damaging |
Het |
| Plce1 |
T |
A |
19: 38,747,279 (GRCm39) |
S1667T |
possibly damaging |
Het |
| Qser1 |
A |
T |
2: 104,617,776 (GRCm39) |
V1012E |
possibly damaging |
Het |
| R3hdm4 |
C |
T |
10: 79,748,292 (GRCm39) |
E162K |
possibly damaging |
Het |
| Rcn3 |
A |
T |
7: 44,736,203 (GRCm39) |
D168E |
probably damaging |
Het |
| Rdh1 |
T |
G |
10: 127,595,832 (GRCm39) |
V9G |
possibly damaging |
Het |
| Rin2 |
A |
G |
2: 145,686,680 (GRCm39) |
T70A |
probably benign |
Het |
| Rnf207 |
T |
C |
4: 152,398,346 (GRCm39) |
D276G |
probably damaging |
Het |
| Rtel1 |
C |
T |
2: 180,982,354 (GRCm39) |
S368L |
probably benign |
Het |
| Slc15a5 |
C |
A |
6: 138,056,751 (GRCm39) |
C55F |
probably damaging |
Het |
| Slc36a4 |
T |
C |
9: 15,638,212 (GRCm39) |
F213L |
possibly damaging |
Het |
| Snhg16 |
G |
T |
11: 116,562,582 (GRCm39) |
M18I |
probably benign |
Het |
| Spata25 |
C |
T |
2: 164,669,954 (GRCm39) |
G19D |
probably damaging |
Het |
| Tas2r102 |
A |
T |
6: 132,739,360 (GRCm39) |
L89F |
probably damaging |
Het |
| Tbc1d1 |
A |
G |
5: 64,481,910 (GRCm39) |
K704E |
probably damaging |
Het |
| Tert |
T |
G |
13: 73,775,473 (GRCm39) |
S75A |
probably damaging |
Het |
| Tiparp |
T |
A |
3: 65,454,986 (GRCm39) |
L195Q |
possibly damaging |
Het |
| Tmem205 |
A |
C |
9: 21,837,380 (GRCm39) |
Y57* |
probably null |
Het |
| Tomm22 |
A |
G |
15: 79,555,428 (GRCm39) |
R5G |
probably benign |
Het |
| Trav10 |
A |
T |
14: 53,743,515 (GRCm39) |
S39C |
probably benign |
Het |
| Trav6-2 |
T |
A |
14: 52,905,205 (GRCm39) |
N75K |
probably benign |
Het |
| Trio |
T |
C |
15: 27,748,372 (GRCm39) |
S2427G |
probably benign |
Het |
| Ttc41 |
C |
A |
10: 86,580,342 (GRCm39) |
H763N |
possibly damaging |
Het |
| Usp29 |
A |
T |
7: 6,964,583 (GRCm39) |
N142I |
probably damaging |
Het |
| Vmn1r204 |
G |
T |
13: 22,740,912 (GRCm39) |
W181L |
probably damaging |
Het |
| Vmn2r76 |
G |
A |
7: 85,875,267 (GRCm39) |
T570M |
probably damaging |
Het |
| Wdr90 |
A |
G |
17: 26,069,819 (GRCm39) |
L1173P |
probably damaging |
Het |
| Wnt9a |
T |
A |
11: 59,219,396 (GRCm39) |
C141S |
probably damaging |
Het |
| Zfp462 |
A |
T |
4: 55,012,299 (GRCm39) |
I1422L |
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 |
|
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 |
|
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 |
|
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'- CAGAAAGCCATCGCATTTTCTC -3'
(R):5'- GCTTACCTGGAAGGCATTGAG -3'
Sequencing Primer
(F):5'- GAAAGCCATCGCATTTTCTCTAGGC -3'
(R):5'- CTTACCTGGAAGGCATTGAGGAGAG -3'
|
| Posted On |
2016-07-06 |
Incidental Mutation