Incidental Mutation 'R2004:Fndc1'
| ID |
223493 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Fndc1
|
| Ensembl Gene |
ENSMUSG00000071984 |
| Gene Name |
fibronectin type III domain containing 1 |
| Synonyms |
1110027O12Rik |
| MMRRC Submission |
040013-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.073)
|
| Stock # |
R2004 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
17 |
| Chromosomal Location |
7957401-8046134 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 8023761 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Glycine
at position 65
(R65G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000126701
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000097425]
[ENSMUST00000167580]
[ENSMUST00000169126]
|
| AlphaFold |
A0A6I8MWX0 |
| Predicted Effect |
unknown
Transcript: ENSMUST00000097425
AA Change: R16G
|
| SMART Domains |
Protein: ENSMUSP00000095036
Gene: ENSMUSG00000071984
AA Change: R16G
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:FN3
|
1 |
50 |
6e-25 |
BLAST |
|
FN3
|
54 |
137 |
7.82e-4 |
SMART |
|
FN3
|
156 |
240 |
1.48e-4 |
SMART |
|
FN3
|
256 |
340 |
3.67e-9 |
SMART |
|
low complexity region
|
377 |
388 |
N/A |
INTRINSIC |
|
low complexity region
|
579 |
601 |
N/A |
INTRINSIC |
|
low complexity region
|
646 |
676 |
N/A |
INTRINSIC |
|
low complexity region
|
766 |
777 |
N/A |
INTRINSIC |
|
low complexity region
|
868 |
884 |
N/A |
INTRINSIC |
|
low complexity region
|
1021 |
1027 |
N/A |
INTRINSIC |
|
low complexity region
|
1036 |
1050 |
N/A |
INTRINSIC |
|
low complexity region
|
1076 |
1090 |
N/A |
INTRINSIC |
|
Blast:FN3
|
1227 |
1276 |
2e-18 |
BLAST |
|
low complexity region
|
1277 |
1354 |
N/A |
INTRINSIC |
|
low complexity region
|
1395 |
1403 |
N/A |
INTRINSIC |
|
low complexity region
|
1407 |
1423 |
N/A |
INTRINSIC |
|
FN3
|
1494 |
1577 |
4.32e-6 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000167580
|
| SMART Domains |
Protein: ENSMUSP00000130996
Gene: ENSMUSG00000071984
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
29 |
N/A |
INTRINSIC |
|
FN3
|
38 |
121 |
7.82e-4 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000169126
AA Change: R65G
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000126701
Gene: ENSMUSG00000071984
AA Change: R65G
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
30 |
N/A |
INTRINSIC |
|
FN3
|
37 |
117 |
1.22e-5 |
SMART |
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.2%
- 20x: 94.9%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 92 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aass |
A |
T |
6: 23,092,561 (GRCm39) |
Y146* |
probably null |
Het |
| Adcy2 |
A |
G |
13: 68,944,722 (GRCm39) |
L220P |
probably damaging |
Het |
| Agl |
T |
C |
3: 116,574,914 (GRCm39) |
Y660C |
probably damaging |
Het |
| Ak1 |
A |
G |
2: 32,519,622 (GRCm39) |
T17A |
probably benign |
Het |
| Amph |
G |
A |
13: 19,326,198 (GRCm39) |
V643M |
probably damaging |
Het |
| Ankrd11 |
A |
T |
8: 123,629,161 (GRCm39) |
|
probably null |
Het |
| Ap5b1 |
T |
C |
19: 5,620,502 (GRCm39) |
S641P |
possibly damaging |
Het |
| Apoc4 |
A |
G |
7: 19,415,304 (GRCm39) |
M1T |
probably null |
Het |
| Arhgap5 |
T |
C |
12: 52,564,817 (GRCm39) |
V596A |
probably benign |
Het |
| Ascc3 |
A |
G |
10: 50,493,838 (GRCm39) |
E91G |
probably damaging |
Het |
| Bach2 |
T |
A |
4: 32,580,055 (GRCm39) |
V637E |
probably benign |
Het |
| Bicd2 |
T |
G |
13: 49,532,881 (GRCm39) |
L489R |
possibly damaging |
Het |
| Bltp1 |
C |
T |
3: 36,949,527 (GRCm39) |
T2I |
possibly damaging |
Het |
| Boc |
A |
T |
16: 44,322,007 (GRCm39) |
|
probably null |
Het |
| Cbln2 |
T |
A |
18: 86,734,791 (GRCm39) |
V188D |
probably damaging |
Het |
| Ccl11 |
A |
C |
11: 81,953,123 (GRCm39) |
T94P |
probably damaging |
Het |
| Cd109 |
A |
T |
9: 78,611,044 (GRCm39) |
H1220L |
probably benign |
Het |
| Cd226 |
A |
G |
18: 89,265,435 (GRCm39) |
I125V |
probably benign |
Het |
| Cep135 |
T |
A |
5: 76,780,176 (GRCm39) |
|
probably null |
Het |
| Cgnl1 |
T |
G |
9: 71,537,821 (GRCm39) |
E1233A |
probably damaging |
Het |
| Ckap5 |
T |
A |
2: 91,437,891 (GRCm39) |
D1597E |
possibly damaging |
Het |
| Clptm1 |
A |
G |
7: 19,380,762 (GRCm39) |
I63T |
possibly damaging |
Het |
| Cpsf7 |
C |
T |
19: 10,518,073 (GRCm39) |
P428S |
probably damaging |
Het |
| Cuedc1 |
C |
T |
11: 88,068,216 (GRCm39) |
P155S |
probably damaging |
Het |
| Dgkb |
T |
C |
12: 38,134,228 (GRCm39) |
Y45H |
probably damaging |
Het |
| Dglucy |
T |
C |
12: 100,823,181 (GRCm39) |
F459L |
probably damaging |
Het |
| Dmp1 |
T |
A |
5: 104,359,790 (GRCm39) |
D155E |
possibly damaging |
Het |
| Dnah1 |
T |
A |
14: 31,023,813 (GRCm39) |
I960F |
possibly damaging |
Het |
| Drosha |
G |
T |
15: 12,915,467 (GRCm39) |
M795I |
probably damaging |
Het |
| Dsg1b |
A |
G |
18: 20,529,532 (GRCm39) |
T326A |
probably damaging |
Het |
| Dusp16 |
T |
G |
6: 134,695,802 (GRCm39) |
N343T |
probably benign |
Het |
| Faim2 |
T |
C |
15: 99,398,127 (GRCm39) |
S274G |
possibly damaging |
Het |
| Fhip2a |
G |
T |
19: 57,370,324 (GRCm39) |
V523L |
probably benign |
Het |
| Fnip2 |
A |
T |
3: 79,419,632 (GRCm39) |
|
probably benign |
Het |
| Grm3 |
T |
C |
5: 9,639,793 (GRCm39) |
Y84C |
possibly damaging |
Het |
| Herc2 |
T |
C |
7: 55,787,607 (GRCm39) |
F1755L |
probably damaging |
Het |
| Hivep1 |
C |
T |
13: 42,313,625 (GRCm39) |
T1955I |
possibly damaging |
Het |
| Ift20 |
T |
C |
11: 78,431,797 (GRCm39) |
I97T |
probably damaging |
Het |
| Il36rn |
T |
C |
2: 24,171,376 (GRCm39) |
C155R |
probably damaging |
Het |
| Lca5l |
T |
A |
16: 95,963,849 (GRCm39) |
K358N |
probably damaging |
Het |
| Lca5l |
T |
C |
16: 95,977,218 (GRCm39) |
N196S |
possibly damaging |
Het |
| Maf1 |
G |
A |
15: 76,237,563 (GRCm39) |
D175N |
probably damaging |
Het |
| Mical3 |
T |
C |
6: 120,928,283 (GRCm39) |
K996E |
probably damaging |
Het |
| Midn |
A |
G |
10: 79,990,983 (GRCm39) |
N331S |
probably benign |
Het |
| Mki67 |
T |
A |
7: 135,300,238 (GRCm39) |
K1599* |
probably null |
Het |
| Mlx |
A |
G |
11: 100,979,805 (GRCm39) |
Q162R |
possibly damaging |
Het |
| Nalf1 |
A |
G |
8: 9,820,607 (GRCm39) |
S138P |
probably benign |
Het |
| Ngp |
T |
C |
9: 110,249,929 (GRCm39) |
C76R |
probably damaging |
Het |
| Nin |
C |
T |
12: 70,072,251 (GRCm39) |
G1210D |
probably benign |
Het |
| Nlgn1 |
A |
G |
3: 25,488,034 (GRCm39) |
I738T |
probably benign |
Het |
| Nop53 |
A |
C |
7: 15,672,153 (GRCm39) |
F465C |
probably damaging |
Het |
| Npas3 |
A |
G |
12: 54,114,680 (GRCm39) |
D503G |
possibly damaging |
Het |
| Npbwr1 |
T |
A |
1: 5,986,570 (GRCm39) |
S315C |
probably damaging |
Het |
| Nup42 |
G |
T |
5: 24,386,989 (GRCm39) |
G260* |
probably null |
Het |
| Ogdh |
G |
C |
11: 6,284,626 (GRCm39) |
R200P |
possibly damaging |
Het |
| Or4b13 |
T |
A |
2: 90,083,036 (GRCm39) |
I99L |
probably benign |
Het |
| Or52n20 |
A |
G |
7: 104,320,808 (GRCm39) |
T300A |
possibly damaging |
Het |
| Or5m13b |
T |
G |
2: 85,753,939 (GRCm39) |
|
probably null |
Het |
| Or6ae1 |
C |
T |
7: 139,742,729 (GRCm39) |
V45I |
probably damaging |
Het |
| Or7g16 |
G |
A |
9: 18,726,801 (GRCm39) |
S263L |
probably benign |
Het |
| Or7g33 |
A |
T |
9: 19,448,688 (GRCm39) |
C179* |
probably null |
Het |
| Ovgp1 |
T |
A |
3: 105,894,309 (GRCm39) |
|
probably benign |
Het |
| Papln |
T |
A |
12: 83,819,992 (GRCm39) |
C150S |
probably damaging |
Het |
| Pde1c |
A |
T |
6: 56,135,996 (GRCm39) |
L316Q |
probably damaging |
Het |
| Pdlim2 |
C |
T |
14: 70,402,228 (GRCm39) |
R296H |
probably damaging |
Het |
| Piezo2 |
G |
T |
18: 63,277,997 (GRCm39) |
D302E |
probably damaging |
Het |
| Pirb |
A |
T |
7: 3,720,637 (GRCm39) |
L287Q |
probably benign |
Het |
| Plin1 |
A |
G |
7: 79,375,378 (GRCm39) |
|
probably benign |
Het |
| Plxnc1 |
A |
G |
10: 94,688,484 (GRCm39) |
I698T |
probably damaging |
Het |
| Ppp1r12c |
G |
T |
7: 4,485,974 (GRCm39) |
C572* |
probably null |
Het |
| Ptgis |
T |
C |
2: 167,056,769 (GRCm39) |
M273V |
possibly damaging |
Het |
| Samd14 |
C |
A |
11: 94,914,110 (GRCm39) |
T283K |
probably damaging |
Het |
| Scnn1g |
A |
T |
7: 121,337,411 (GRCm39) |
K91* |
probably null |
Het |
| Slc24a4 |
A |
G |
12: 102,180,166 (GRCm39) |
Q95R |
probably damaging |
Het |
| Slfn9 |
T |
G |
11: 82,879,027 (GRCm39) |
D34A |
probably benign |
Het |
| Smarca4 |
A |
T |
9: 21,588,776 (GRCm39) |
I1193F |
probably damaging |
Het |
| Spata31e5 |
A |
G |
1: 28,816,260 (GRCm39) |
W591R |
probably damaging |
Het |
| Sphkap |
T |
C |
1: 83,255,632 (GRCm39) |
M706V |
probably benign |
Het |
| Stard9 |
C |
A |
2: 120,504,117 (GRCm39) |
S221R |
probably damaging |
Het |
| Stxbp1 |
T |
C |
2: 32,688,201 (GRCm39) |
D488G |
probably damaging |
Het |
| Sugp2 |
C |
T |
8: 70,695,306 (GRCm39) |
|
probably null |
Het |
| Tekt5 |
T |
C |
16: 10,213,070 (GRCm39) |
I72V |
probably benign |
Het |
| Themis |
T |
A |
10: 28,658,720 (GRCm39) |
N582K |
probably benign |
Het |
| Tmed11 |
C |
A |
5: 108,934,000 (GRCm39) |
M65I |
possibly damaging |
Het |
| Top3a |
G |
T |
11: 60,633,315 (GRCm39) |
P927Q |
probably damaging |
Het |
| Trpa1 |
A |
T |
1: 14,976,207 (GRCm39) |
N165K |
possibly damaging |
Het |
| Tsfm |
A |
G |
10: 126,866,663 (GRCm39) |
S2P |
probably damaging |
Het |
| Wdr47 |
C |
A |
3: 108,534,758 (GRCm39) |
S559* |
probably null |
Het |
| Wnt2b |
T |
C |
3: 104,860,331 (GRCm39) |
Y192C |
probably damaging |
Het |
| Zfp280b |
A |
G |
10: 75,874,370 (GRCm39) |
D83G |
probably benign |
Het |
| Zfp345 |
T |
C |
2: 150,314,038 (GRCm39) |
T500A |
possibly damaging |
Het |
| Zfp78 |
T |
A |
7: 6,382,074 (GRCm39) |
C343S |
probably damaging |
Het |
|
| Other mutations in Fndc1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00513:Fndc1
|
APN |
17 |
7,984,086 (GRCm39) |
missense |
unknown |
|
|
IGL00590:Fndc1
|
APN |
17 |
7,983,933 (GRCm39) |
missense |
unknown |
|
|
IGL00765:Fndc1
|
APN |
17 |
7,991,525 (GRCm39) |
missense |
unknown |
|
|
IGL00904:Fndc1
|
APN |
17 |
7,975,195 (GRCm39) |
missense |
probably benign |
0.35 |
|
IGL01153:Fndc1
|
APN |
17 |
7,998,874 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL01557:Fndc1
|
APN |
17 |
7,975,221 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02493:Fndc1
|
APN |
17 |
7,994,377 (GRCm39) |
missense |
unknown |
|
|
IGL02501:Fndc1
|
APN |
17 |
7,984,230 (GRCm39) |
missense |
unknown |
|
|
IGL02503:Fndc1
|
APN |
17 |
7,990,348 (GRCm39) |
missense |
unknown |
|
|
IGL02887:Fndc1
|
APN |
17 |
7,992,470 (GRCm39) |
missense |
unknown |
|
|
IGL03348:Fndc1
|
APN |
17 |
7,991,479 (GRCm39) |
missense |
unknown |
|
|
pinnacle
|
UTSW |
17 |
7,992,154 (GRCm39) |
missense |
unknown |
|
|
spire
|
UTSW |
17 |
7,990,312 (GRCm39) |
missense |
unknown |
|
|
IGL02988:Fndc1
|
UTSW |
17 |
7,972,355 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
PIT4466001:Fndc1
|
UTSW |
17 |
7,969,206 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0336:Fndc1
|
UTSW |
17 |
7,983,939 (GRCm39) |
missense |
unknown |
|
|
R0403:Fndc1
|
UTSW |
17 |
7,994,420 (GRCm39) |
splice site |
probably null |
|
|
R0403:Fndc1
|
UTSW |
17 |
7,972,555 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0538:Fndc1
|
UTSW |
17 |
8,003,173 (GRCm39) |
splice site |
probably benign |
|
|
R0646:Fndc1
|
UTSW |
17 |
7,960,505 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R1140:Fndc1
|
UTSW |
17 |
7,994,258 (GRCm39) |
missense |
unknown |
|
|
R1523:Fndc1
|
UTSW |
17 |
7,992,041 (GRCm39) |
missense |
unknown |
|
|
R1609:Fndc1
|
UTSW |
17 |
7,991,598 (GRCm39) |
missense |
unknown |
|
|
R1632:Fndc1
|
UTSW |
17 |
7,992,032 (GRCm39) |
missense |
unknown |
|
|
R1888:Fndc1
|
UTSW |
17 |
7,990,621 (GRCm39) |
missense |
unknown |
|
|
R1888:Fndc1
|
UTSW |
17 |
7,990,621 (GRCm39) |
missense |
unknown |
|
|
R2007:Fndc1
|
UTSW |
17 |
7,997,580 (GRCm39) |
unclassified |
probably benign |
|
|
R2128:Fndc1
|
UTSW |
17 |
7,997,497 (GRCm39) |
unclassified |
probably benign |
|
|
R2187:Fndc1
|
UTSW |
17 |
7,960,604 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2251:Fndc1
|
UTSW |
17 |
7,972,439 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2322:Fndc1
|
UTSW |
17 |
8,007,847 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2425:Fndc1
|
UTSW |
17 |
8,023,850 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2921:Fndc1
|
UTSW |
17 |
8,023,707 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2985:Fndc1
|
UTSW |
17 |
7,975,155 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R3436:Fndc1
|
UTSW |
17 |
7,969,189 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3499:Fndc1
|
UTSW |
17 |
7,972,416 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R3508:Fndc1
|
UTSW |
17 |
7,983,940 (GRCm39) |
nonsense |
probably null |
|
|
R3766:Fndc1
|
UTSW |
17 |
8,003,253 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3813:Fndc1
|
UTSW |
17 |
7,992,154 (GRCm39) |
missense |
unknown |
|
|
R3814:Fndc1
|
UTSW |
17 |
7,992,154 (GRCm39) |
missense |
unknown |
|
|
R4031:Fndc1
|
UTSW |
17 |
7,988,584 (GRCm39) |
nonsense |
probably null |
|
|
R4544:Fndc1
|
UTSW |
17 |
7,992,376 (GRCm39) |
missense |
unknown |
|
|
R4583:Fndc1
|
UTSW |
17 |
7,958,081 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4619:Fndc1
|
UTSW |
17 |
7,984,036 (GRCm39) |
missense |
unknown |
|
|
R4700:Fndc1
|
UTSW |
17 |
7,990,312 (GRCm39) |
missense |
unknown |
|
|
R4743:Fndc1
|
UTSW |
17 |
7,991,111 (GRCm39) |
nonsense |
probably null |
|
|
R4803:Fndc1
|
UTSW |
17 |
7,972,538 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4862:Fndc1
|
UTSW |
17 |
7,988,567 (GRCm39) |
missense |
unknown |
|
|
R4876:Fndc1
|
UTSW |
17 |
7,990,471 (GRCm39) |
missense |
unknown |
|
|
R5057:Fndc1
|
UTSW |
17 |
7,990,802 (GRCm39) |
nonsense |
probably null |
|
|
R5327:Fndc1
|
UTSW |
17 |
7,991,540 (GRCm39) |
missense |
unknown |
|
|
R5372:Fndc1
|
UTSW |
17 |
7,984,042 (GRCm39) |
missense |
unknown |
|
|
R5533:Fndc1
|
UTSW |
17 |
7,991,608 (GRCm39) |
missense |
unknown |
|
|
R5754:Fndc1
|
UTSW |
17 |
7,988,585 (GRCm39) |
missense |
unknown |
|
|
R5762:Fndc1
|
UTSW |
17 |
7,990,366 (GRCm39) |
missense |
unknown |
|
|
R5830:Fndc1
|
UTSW |
17 |
8,007,918 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R5924:Fndc1
|
UTSW |
17 |
7,992,442 (GRCm39) |
missense |
unknown |
|
|
R6147:Fndc1
|
UTSW |
17 |
7,972,594 (GRCm39) |
splice site |
probably null |
|
|
R6175:Fndc1
|
UTSW |
17 |
7,991,479 (GRCm39) |
missense |
unknown |
|
|
R6303:Fndc1
|
UTSW |
17 |
7,977,317 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6377:Fndc1
|
UTSW |
17 |
7,988,567 (GRCm39) |
missense |
unknown |
|
|
R6704:Fndc1
|
UTSW |
17 |
7,990,642 (GRCm39) |
missense |
unknown |
|
|
R6857:Fndc1
|
UTSW |
17 |
7,991,002 (GRCm39) |
missense |
unknown |
|
|
R6865:Fndc1
|
UTSW |
17 |
7,991,672 (GRCm39) |
missense |
unknown |
|
|
R7069:Fndc1
|
UTSW |
17 |
7,988,567 (GRCm39) |
missense |
unknown |
|
|
R7153:Fndc1
|
UTSW |
17 |
8,020,477 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7159:Fndc1
|
UTSW |
17 |
8,019,763 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R7359:Fndc1
|
UTSW |
17 |
8,032,318 (GRCm39) |
splice site |
probably null |
|
|
R7731:Fndc1
|
UTSW |
17 |
7,992,271 (GRCm39) |
missense |
unknown |
|
|
R7743:Fndc1
|
UTSW |
17 |
7,983,969 (GRCm39) |
missense |
unknown |
|
|
R7884:Fndc1
|
UTSW |
17 |
7,992,029 (GRCm39) |
missense |
unknown |
|
|
R8071:Fndc1
|
UTSW |
17 |
7,991,362 (GRCm39) |
missense |
unknown |
|
|
R8100:Fndc1
|
UTSW |
17 |
7,990,685 (GRCm39) |
missense |
unknown |
|
|
R8317:Fndc1
|
UTSW |
17 |
8,019,720 (GRCm39) |
nonsense |
probably null |
|
|
R8362:Fndc1
|
UTSW |
17 |
8,001,207 (GRCm39) |
missense |
unknown |
|
|
R8835:Fndc1
|
UTSW |
17 |
7,958,111 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8841:Fndc1
|
UTSW |
17 |
7,992,181 (GRCm39) |
missense |
unknown |
|
|
R8912:Fndc1
|
UTSW |
17 |
8,019,778 (GRCm39) |
missense |
probably null |
0.26 |
|
R9236:Fndc1
|
UTSW |
17 |
7,992,460 (GRCm39) |
missense |
unknown |
|
|
R9392:Fndc1
|
UTSW |
17 |
7,991,957 (GRCm39) |
missense |
unknown |
|
|
R9412:Fndc1
|
UTSW |
17 |
7,991,198 (GRCm39) |
missense |
unknown |
|
|
R9618:Fndc1
|
UTSW |
17 |
7,990,313 (GRCm39) |
missense |
unknown |
|
|
R9632:Fndc1
|
UTSW |
17 |
7,991,622 (GRCm39) |
missense |
unknown |
|
|
R9748:Fndc1
|
UTSW |
17 |
7,991,929 (GRCm39) |
missense |
unknown |
|
|
Z1088:Fndc1
|
UTSW |
17 |
8,001,311 (GRCm39) |
missense |
probably damaging |
0.96 |
|
Z1176:Fndc1
|
UTSW |
17 |
8,023,709 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
Z1176:Fndc1
|
UTSW |
17 |
7,992,425 (GRCm39) |
nonsense |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- TATCCTAAGTGCACAGCTGC -3'
(R):5'- ATGGTTGCACGCAAATCTTTAGG -3'
Sequencing Primer
(F):5'- AGCTGCAACTGTTGATGCAC -3'
(R):5'- GCACGCAAATCTTTAGGATCAG -3'
|
| Posted On |
2014-08-25 |
Incidental Mutation