Incidental Mutation 'R4623:Adgrf5'
| ID |
346371 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Adgrf5
|
| Ensembl Gene |
ENSMUSG00000056492 |
| Gene Name |
adhesion G protein-coupled receptor F5 |
| Synonyms |
8430401C09Rik, Gpr116 |
| MMRRC Submission |
041888-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R4623 (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 43761874 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Glycine
at position 1190
(S1190G)
|
| 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 benign
Transcript: ENSMUST00000113599
AA Change: S1190G
PolyPhen 2
Score 0.158 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000109229
Gene: ENSMUSG00000056492
AA Change: S1190G
| 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: ENSMUST00000225962
AA Change: S985G
PolyPhen 2
Score 0.130 (Sensitivity: 0.93; Specificity: 0.86)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000226087
AA Change: S1190G
PolyPhen 2
Score 0.158 (Sensitivity: 0.92; Specificity: 0.87)
|
| Meta Mutation Damage Score |
0.0898 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.1%
- 20x: 94.8%
|
| Validation Efficiency |
99% (88/89) |
| 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: 82 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700034J04Rik |
T |
C |
12: 11,272,141 (GRCm39) |
|
noncoding transcript |
Het |
| A930003A15Rik |
C |
T |
16: 19,702,487 (GRCm39) |
|
noncoding transcript |
Het |
| Abca13 |
A |
G |
11: 9,259,130 (GRCm39) |
Y2952C |
probably damaging |
Het |
| Actrt2 |
T |
C |
4: 154,751,747 (GRCm39) |
T130A |
probably benign |
Het |
| Adamts7 |
T |
A |
9: 90,068,515 (GRCm39) |
D475E |
probably benign |
Het |
| Adgrg6 |
A |
T |
10: 14,317,243 (GRCm39) |
C526S |
probably damaging |
Het |
| Aldoc |
T |
C |
11: 78,215,947 (GRCm39) |
V151A |
probably damaging |
Het |
| Arsj |
A |
T |
3: 126,158,445 (GRCm39) |
E8V |
probably benign |
Het |
| Asph |
T |
C |
4: 9,622,005 (GRCm39) |
K167E |
possibly damaging |
Het |
| Auts2 |
G |
A |
5: 131,469,221 (GRCm39) |
P475S |
probably benign |
Het |
| C1d |
A |
G |
11: 17,212,742 (GRCm39) |
D29G |
possibly damaging |
Het |
| Calb1 |
T |
A |
4: 15,895,721 (GRCm39) |
|
probably benign |
Het |
| Ceacam15 |
A |
T |
7: 16,407,391 (GRCm39) |
F42Y |
probably damaging |
Het |
| Cpm |
A |
G |
10: 117,506,202 (GRCm39) |
N188D |
possibly damaging |
Het |
| Cts6 |
A |
T |
13: 61,349,974 (GRCm39) |
Y36N |
possibly damaging |
Het |
| Cux1 |
T |
C |
5: 136,337,154 (GRCm39) |
K657R |
probably damaging |
Het |
| Cyp2a22 |
G |
T |
7: 26,632,916 (GRCm39) |
P429T |
probably damaging |
Het |
| Dipk2a |
T |
C |
9: 94,402,451 (GRCm39) |
N404D |
possibly damaging |
Het |
| Dock3 |
T |
C |
9: 106,939,244 (GRCm39) |
E168G |
possibly damaging |
Het |
| Dot1l |
A |
G |
10: 80,617,984 (GRCm39) |
N324S |
probably benign |
Het |
| Dusp13b |
A |
C |
14: 21,793,546 (GRCm39) |
|
probably benign |
Het |
| Eif4g1 |
T |
A |
16: 20,500,095 (GRCm39) |
|
probably benign |
Het |
| Fan1 |
G |
T |
7: 64,023,301 (GRCm39) |
Y121* |
probably null |
Het |
| Foxn4 |
T |
C |
5: 114,398,991 (GRCm39) |
E80G |
possibly damaging |
Het |
| Gal3st2c |
C |
A |
1: 93,937,178 (GRCm39) |
H374Q |
possibly damaging |
Het |
| Gm973 |
A |
T |
1: 59,595,435 (GRCm39) |
I409F |
probably damaging |
Het |
| Gpr18 |
T |
A |
14: 122,149,579 (GRCm39) |
T149S |
probably damaging |
Het |
| Gsr |
A |
G |
8: 34,170,333 (GRCm39) |
E206G |
probably damaging |
Het |
| Hal |
A |
G |
10: 93,343,301 (GRCm39) |
H515R |
probably damaging |
Het |
| Heatr5b |
A |
G |
17: 79,102,548 (GRCm39) |
S1277P |
possibly damaging |
Het |
| Hmcn2 |
A |
G |
2: 31,286,722 (GRCm39) |
E2125G |
probably damaging |
Het |
| Ikzf4 |
A |
G |
10: 128,476,988 (GRCm39) |
C108R |
probably damaging |
Het |
| Kcnh2 |
A |
G |
5: 24,553,440 (GRCm39) |
V59A |
probably benign |
Het |
| Khdrbs1 |
A |
G |
4: 129,614,635 (GRCm39) |
V306A |
probably benign |
Het |
| Kif11 |
A |
T |
19: 37,398,195 (GRCm39) |
I674L |
probably benign |
Het |
| Lrp1b |
A |
T |
2: 41,136,033 (GRCm39) |
C1646S |
probably damaging |
Het |
| Ltbp2 |
A |
G |
12: 84,856,122 (GRCm39) |
I707T |
probably damaging |
Het |
| Macf1 |
A |
G |
4: 123,266,141 (GRCm39) |
|
probably null |
Het |
| Mib1 |
C |
A |
18: 10,808,086 (GRCm39) |
N944K |
probably benign |
Het |
| Mical3 |
C |
A |
6: 120,938,586 (GRCm39) |
E262* |
probably null |
Het |
| Mms22l |
C |
T |
4: 24,502,792 (GRCm39) |
Q55* |
probably null |
Het |
| Mplkipl1 |
C |
T |
19: 61,164,364 (GRCm39) |
G24R |
unknown |
Het |
| Mrps11 |
T |
C |
7: 78,441,689 (GRCm39) |
|
probably null |
Het |
| Myh8 |
A |
G |
11: 67,177,084 (GRCm39) |
E412G |
probably damaging |
Het |
| Myo9a |
T |
A |
9: 59,778,355 (GRCm39) |
D1370E |
probably benign |
Het |
| Ncapd2 |
A |
G |
6: 125,150,572 (GRCm39) |
V843A |
probably benign |
Het |
| Nell1 |
A |
G |
7: 49,770,310 (GRCm39) |
E123G |
possibly damaging |
Het |
| Nkd1 |
A |
G |
8: 89,316,383 (GRCm39) |
D213G |
probably benign |
Het |
| Nlrp1b |
T |
C |
11: 71,052,669 (GRCm39) |
T920A |
probably benign |
Het |
| Or5k8 |
A |
T |
16: 58,644,469 (GRCm39) |
I201N |
possibly damaging |
Het |
| Or6c208 |
G |
A |
10: 129,223,915 (GRCm39) |
V138M |
probably benign |
Het |
| Or8k40 |
T |
A |
2: 86,584,906 (GRCm39) |
M59L |
possibly damaging |
Het |
| Pde8b |
C |
T |
13: 95,178,447 (GRCm39) |
A566T |
possibly damaging |
Het |
| Pds5b |
T |
A |
5: 150,724,066 (GRCm39) |
S1214R |
probably benign |
Het |
| Pld1 |
T |
C |
3: 28,083,393 (GRCm39) |
I171T |
probably benign |
Het |
| Plekha5 |
T |
A |
6: 140,496,912 (GRCm39) |
V154E |
probably damaging |
Het |
| Plxna2 |
A |
T |
1: 194,494,458 (GRCm39) |
I1892L |
probably benign |
Het |
| Ppp1r16b |
A |
G |
2: 158,603,383 (GRCm39) |
Y436C |
possibly damaging |
Het |
| Proc |
T |
A |
18: 32,260,526 (GRCm39) |
T200S |
probably benign |
Het |
| Psap |
T |
G |
10: 60,136,630 (GRCm39) |
C536W |
probably damaging |
Het |
| Ptger2 |
G |
A |
14: 45,226,471 (GRCm39) |
R17H |
possibly damaging |
Het |
| Rab42 |
A |
G |
4: 132,030,504 (GRCm39) |
F49L |
possibly damaging |
Het |
| Racgap1 |
C |
A |
15: 99,524,087 (GRCm39) |
S440I |
probably benign |
Het |
| Rdh10 |
G |
A |
1: 16,201,287 (GRCm39) |
|
probably benign |
Het |
| Rnft2 |
T |
A |
5: 118,370,471 (GRCm39) |
S244C |
probably damaging |
Het |
| Sftpc |
T |
C |
14: 70,759,718 (GRCm39) |
|
probably null |
Het |
| Shcbp1 |
A |
C |
8: 4,789,178 (GRCm39) |
V547G |
probably damaging |
Het |
| Slc6a13 |
T |
C |
6: 121,302,104 (GRCm39) |
S229P |
probably damaging |
Het |
| Soat2 |
A |
T |
15: 102,066,144 (GRCm39) |
|
probably benign |
Het |
| Swap70 |
A |
G |
7: 109,867,079 (GRCm39) |
K294E |
probably benign |
Het |
| Tcim |
C |
A |
8: 24,928,725 (GRCm39) |
R63L |
probably damaging |
Het |
| Tek |
G |
A |
4: 94,751,898 (GRCm39) |
V1013I |
probably damaging |
Het |
| Tg |
T |
A |
15: 66,607,120 (GRCm39) |
M219K |
probably benign |
Het |
| Tie1 |
A |
G |
4: 118,343,808 (GRCm39) |
S45P |
possibly damaging |
Het |
| Tmem59 |
A |
T |
4: 107,047,915 (GRCm39) |
|
probably benign |
Het |
| Togaram1 |
A |
T |
12: 65,029,224 (GRCm39) |
E882D |
possibly damaging |
Het |
| Tram1l1 |
T |
A |
3: 124,115,509 (GRCm39) |
M223K |
possibly damaging |
Het |
| Tssk5 |
C |
T |
15: 76,256,668 (GRCm39) |
R280Q |
probably benign |
Het |
| Uspl1 |
T |
A |
5: 149,151,405 (GRCm39) |
D669E |
probably damaging |
Het |
| Vav1 |
C |
A |
17: 57,606,839 (GRCm39) |
|
probably null |
Het |
| Vcl |
A |
T |
14: 21,065,007 (GRCm39) |
E634V |
probably benign |
Het |
| Zfp672 |
A |
T |
11: 58,207,281 (GRCm39) |
C347S |
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 |
|
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'- GTCCACTCAGAAAGCCATCG -3'
(R):5'- TTACCTGGAAGGCATTGAGGAG -3'
Sequencing Primer
(F):5'- CAGAAAGCCATCGCATTTTCTCTAGG -3'
(R):5'- TGGAACACAGCATTGCTTCC -3'
|
| Posted On |
2015-09-25 |
Incidental Mutation