Incidental Mutation 'R0699:Adgrf5'
| ID |
62980 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Adgrf5
|
| Ensembl Gene |
ENSMUSG00000056492 |
| Gene Name |
adhesion G protein-coupled receptor F5 |
| Synonyms |
8430401C09Rik, Gpr116 |
| MMRRC Submission |
038883-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R0699 (G1)
|
| Quality Score |
189 |
|
Status
|
Validated
|
| Chromosome |
17 |
| Chromosomal Location |
43671342-43770448 bp(+) (GRCm39) |
| Type of Mutation |
splice site (5 bp from exon) |
| DNA Base Change (assembly) |
G to A
at 43733552 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000153049
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000113599]
[ENSMUST00000224278]
[ENSMUST00000225466]
[ENSMUST00000225962]
[ENSMUST00000226087]
|
| AlphaFold |
G5E8Q8 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000113599
|
| SMART Domains |
Protein: ENSMUSP00000109229
Gene: ENSMUSG00000056492
| 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 null
Transcript: ENSMUST00000224278
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000225466
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000225962
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000226087
|
| Meta Mutation Damage Score |
0.9755 |
| Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.3%
- 20x: 94.8%
|
| Validation Efficiency |
98% (120/123) |
| 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: 95 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca13 |
G |
A |
11: 9,538,508 (GRCm39) |
|
probably benign |
Het |
| Abcb6 |
C |
T |
1: 75,148,553 (GRCm39) |
E89K |
probably damaging |
Het |
| Adam25 |
C |
A |
8: 41,209,011 (GRCm39) |
T759K |
probably benign |
Het |
| Aimp1 |
A |
T |
3: 132,380,626 (GRCm39) |
|
probably benign |
Het |
| Aldh3a2 |
C |
T |
11: 61,153,148 (GRCm39) |
V193I |
probably benign |
Het |
| Ank2 |
C |
T |
3: 126,723,478 (GRCm39) |
V950I |
probably benign |
Het |
| Aspn |
A |
G |
13: 49,705,258 (GRCm39) |
D40G |
possibly damaging |
Het |
| C1rl |
A |
G |
6: 124,485,595 (GRCm39) |
D322G |
probably benign |
Het |
| Car5a |
T |
C |
8: 122,671,555 (GRCm39) |
|
probably benign |
Het |
| Cfap107 |
G |
T |
4: 144,146,322 (GRCm39) |
N110K |
probably damaging |
Het |
| Cfap157 |
T |
A |
2: 32,669,022 (GRCm39) |
K360N |
probably damaging |
Het |
| Cilp |
T |
A |
9: 65,177,608 (GRCm39) |
F117Y |
probably damaging |
Het |
| Cntnap5c |
T |
G |
17: 58,349,493 (GRCm39) |
W269G |
probably damaging |
Het |
| Col6a1 |
A |
G |
10: 76,552,114 (GRCm39) |
V459A |
unknown |
Het |
| Commd3 |
A |
G |
2: 18,679,786 (GRCm39) |
E165G |
possibly damaging |
Het |
| Cops3 |
A |
C |
11: 59,717,148 (GRCm39) |
Y244D |
probably damaging |
Het |
| Cpne5 |
T |
A |
17: 29,428,667 (GRCm39) |
K108N |
probably damaging |
Het |
| Cracdl |
T |
C |
1: 37,651,411 (GRCm39) |
D1152G |
possibly damaging |
Het |
| Ddx41 |
A |
G |
13: 55,679,112 (GRCm39) |
|
probably benign |
Het |
| Dnhd1 |
T |
C |
7: 105,301,113 (GRCm39) |
Y157H |
probably damaging |
Het |
| Dpp8 |
A |
T |
9: 64,962,176 (GRCm39) |
L405F |
probably benign |
Het |
| Dync2h1 |
G |
T |
9: 7,103,680 (GRCm39) |
A365E |
probably benign |
Het |
| Dysf |
C |
T |
6: 84,167,828 (GRCm39) |
R1757W |
probably benign |
Het |
| Eif1ad |
T |
A |
19: 5,418,726 (GRCm39) |
V93D |
possibly damaging |
Het |
| Eif2ak3 |
T |
C |
6: 70,869,514 (GRCm39) |
F734L |
probably benign |
Het |
| F8 |
T |
C |
X: 74,423,230 (GRCm39) |
|
probably benign |
Het |
| Fbxl14 |
T |
C |
6: 119,457,715 (GRCm39) |
Y299H |
probably benign |
Het |
| Fmo1 |
T |
C |
1: 162,661,341 (GRCm39) |
N314S |
probably benign |
Het |
| Fnip2 |
T |
C |
3: 79,388,446 (GRCm39) |
T762A |
probably benign |
Het |
| Gfra1 |
A |
C |
19: 58,258,555 (GRCm39) |
S271A |
probably benign |
Het |
| Gm9932 |
T |
C |
5: 100,346,931 (GRCm39) |
V43A |
probably damaging |
Het |
| Herc6 |
T |
C |
6: 57,558,092 (GRCm39) |
L24P |
probably damaging |
Het |
| Hmcn1 |
T |
C |
1: 150,695,161 (GRCm39) |
T248A |
probably damaging |
Het |
| Hook1 |
T |
A |
4: 95,884,077 (GRCm39) |
|
probably benign |
Het |
| Ifne |
T |
C |
4: 88,798,014 (GRCm39) |
S135G |
probably benign |
Het |
| Igkv13-84 |
G |
A |
6: 68,916,635 (GRCm39) |
|
probably benign |
Het |
| Itm2b |
T |
A |
14: 73,602,065 (GRCm39) |
N211I |
probably damaging |
Het |
| Kcnh5 |
A |
T |
12: 75,023,305 (GRCm39) |
C588S |
possibly damaging |
Het |
| Kif13a |
A |
T |
13: 46,952,689 (GRCm39) |
W699R |
possibly damaging |
Het |
| Kmt2e |
T |
C |
5: 23,678,581 (GRCm39) |
V220A |
probably benign |
Het |
| Macrod2 |
T |
C |
2: 140,260,836 (GRCm39) |
|
probably null |
Het |
| Map3k6 |
A |
G |
4: 132,975,437 (GRCm39) |
E724G |
probably damaging |
Het |
| Mgam |
T |
C |
6: 40,619,953 (GRCm39) |
L14P |
possibly damaging |
Het |
| Morc1 |
T |
A |
16: 48,412,977 (GRCm39) |
M706K |
probably benign |
Het |
| Muc2 |
T |
C |
7: 141,306,037 (GRCm39) |
V242A |
probably damaging |
Het |
| Mx2 |
T |
A |
16: 97,345,753 (GRCm39) |
V57E |
probably damaging |
Het |
| Myh14 |
C |
A |
7: 44,274,395 (GRCm39) |
A1339S |
possibly damaging |
Het |
| Myom1 |
G |
T |
17: 71,374,308 (GRCm39) |
S595I |
probably damaging |
Het |
| Nav1 |
T |
A |
1: 135,380,687 (GRCm39) |
M1471L |
probably benign |
Het |
| Ncapd2 |
A |
C |
6: 125,146,843 (GRCm39) |
S1248A |
probably benign |
Het |
| Ncbp1 |
T |
C |
4: 46,147,528 (GRCm39) |
V125A |
probably benign |
Het |
| Ncor2 |
A |
T |
5: 125,106,176 (GRCm39) |
|
probably benign |
Het |
| Nobox |
T |
A |
6: 43,284,144 (GRCm39) |
Q134L |
probably benign |
Het |
| Npc1 |
T |
C |
18: 12,343,632 (GRCm39) |
T454A |
probably benign |
Het |
| Ntng1 |
G |
T |
3: 109,779,611 (GRCm39) |
T322K |
probably damaging |
Het |
| Olfm5 |
T |
C |
7: 103,803,326 (GRCm39) |
E379G |
probably damaging |
Het |
| Oma1 |
T |
C |
4: 103,210,792 (GRCm39) |
S433P |
probably damaging |
Het |
| Or1ad6 |
T |
C |
11: 50,860,645 (GRCm39) |
S267P |
probably damaging |
Het |
| Or1b1 |
T |
C |
2: 36,995,074 (GRCm39) |
D196G |
possibly damaging |
Het |
| Or4c105 |
A |
T |
2: 88,647,568 (GRCm39) |
N18Y |
probably damaging |
Het |
| Or4c107 |
C |
T |
2: 88,788,960 (GRCm39) |
T50I |
probably benign |
Het |
| Or4c113 |
C |
T |
2: 88,885,636 (GRCm39) |
V45M |
possibly damaging |
Het |
| Parp14 |
G |
A |
16: 35,680,955 (GRCm39) |
T226M |
probably damaging |
Het |
| Parp8 |
A |
T |
13: 117,059,120 (GRCm39) |
H168Q |
probably benign |
Het |
| Pik3cg |
G |
A |
12: 32,247,341 (GRCm39) |
|
probably benign |
Het |
| Pla2g3 |
T |
C |
11: 3,442,000 (GRCm39) |
F388S |
probably damaging |
Het |
| Plaat3 |
T |
A |
19: 7,535,366 (GRCm39) |
|
probably null |
Het |
| Pllp |
T |
C |
8: 95,422,660 (GRCm39) |
|
probably null |
Het |
| Ppfibp1 |
T |
A |
6: 146,927,720 (GRCm39) |
V778E |
probably damaging |
Het |
| Prkci |
T |
C |
3: 31,104,422 (GRCm39) |
V595A |
possibly damaging |
Het |
| Prune2 |
T |
A |
19: 17,101,319 (GRCm39) |
D2274E |
probably damaging |
Het |
| Rad51ap2 |
A |
T |
12: 11,507,601 (GRCm39) |
T508S |
probably benign |
Het |
| Ranbp3l |
T |
C |
15: 9,058,850 (GRCm39) |
|
probably null |
Het |
| Rfc1 |
A |
C |
5: 65,476,742 (GRCm39) |
|
probably null |
Het |
| Rin3 |
G |
A |
12: 102,335,834 (GRCm39) |
V502I |
probably damaging |
Het |
| Rtn4rl1 |
A |
T |
11: 75,156,048 (GRCm39) |
H160L |
possibly damaging |
Het |
| Rtn4rl1 |
A |
T |
11: 75,156,050 (GRCm39) |
I161F |
probably benign |
Het |
| Serpinb9b |
A |
T |
13: 33,217,549 (GRCm39) |
M116L |
probably benign |
Het |
| Sgo2a |
C |
T |
1: 58,037,308 (GRCm39) |
R18* |
probably null |
Het |
| Sh3gl2 |
T |
A |
4: 85,265,408 (GRCm39) |
D31E |
probably benign |
Het |
| Slc38a9 |
T |
C |
13: 112,859,823 (GRCm39) |
L419S |
probably damaging |
Het |
| Sp8 |
AGCGGCGGCGGCGGCGG |
AGCGGCGGCGGCGG |
12: 118,812,555 (GRCm39) |
|
probably benign |
Het |
| Spen |
G |
T |
4: 141,201,702 (GRCm39) |
N2308K |
possibly damaging |
Het |
| Stac2 |
A |
G |
11: 97,933,611 (GRCm39) |
I156T |
possibly damaging |
Het |
| Stambp |
A |
G |
6: 83,533,303 (GRCm39) |
F320S |
probably damaging |
Het |
| Tas2r117 |
A |
T |
6: 132,780,161 (GRCm39) |
N100Y |
probably damaging |
Het |
| Tigd3 |
A |
T |
19: 5,941,974 (GRCm39) |
S385R |
probably benign |
Het |
| Tmem30c |
T |
C |
16: 57,097,152 (GRCm39) |
D136G |
possibly damaging |
Het |
| Tnfrsf21 |
C |
T |
17: 43,349,104 (GRCm39) |
H239Y |
probably benign |
Het |
| Tnrc6c |
A |
G |
11: 117,613,447 (GRCm39) |
Q535R |
probably benign |
Het |
| Trmt2a |
T |
C |
16: 18,067,393 (GRCm39) |
V22A |
probably benign |
Het |
| Tut7 |
G |
A |
13: 59,929,828 (GRCm39) |
|
probably benign |
Het |
| Wipf3 |
A |
C |
6: 54,460,817 (GRCm39) |
K88N |
probably damaging |
Het |
| Zfp974 |
T |
C |
7: 27,611,416 (GRCm39) |
E103G |
possibly damaging |
Het |
| Zscan10 |
C |
T |
17: 23,827,092 (GRCm39) |
T135I |
probably 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 |
|
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 |
|
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'- CTCATTCTGATGGACCGATGTGCC -3'
(R):5'- GACATGACATACTGAGCTGTGCCC -3'
Sequencing Primer
(F):5'- GGACCGATGTGCCTAGTATCTAC -3'
(R):5'- TGCCCACACATTGTTCAGAGG -3'
|
| Posted On |
2013-07-30 |
Incidental Mutation