Incidental Mutation 'R1470:Frem3'
ID |
197969 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Frem3
|
Ensembl Gene |
ENSMUSG00000042353 |
Gene Name |
Fras1 related extracellular matrix protein 3 |
Synonyms |
LOC333315 |
MMRRC Submission |
039523-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.133)
|
Stock # |
R1470 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
8 |
Chromosomal Location |
81337709-81421985 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 81337820 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Leucine
at position 38
(V38L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000038015
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000039695]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000039695
AA Change: V38L
PolyPhen 2
Score 0.050 (Sensitivity: 0.94; Specificity: 0.83)
|
SMART Domains |
Protein: ENSMUSP00000038015 Gene: ENSMUSG00000042353 AA Change: V38L
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
27 |
N/A |
INTRINSIC |
Pfam:Cadherin_3
|
369 |
515 |
9.5e-31 |
PFAM |
Pfam:Cadherin_3
|
495 |
596 |
9.4e-20 |
PFAM |
Pfam:Cadherin_3
|
637 |
786 |
4.2e-20 |
PFAM |
Pfam:Cadherin_3
|
788 |
913 |
5.5e-23 |
PFAM |
Pfam:Cadherin_3
|
998 |
1163 |
1.8e-20 |
PFAM |
Pfam:Cadherin_3
|
1129 |
1254 |
1.3e-19 |
PFAM |
Pfam:Cadherin_3
|
1250 |
1395 |
9.5e-34 |
PFAM |
Pfam:Cadherin_3
|
1397 |
1508 |
2.7e-21 |
PFAM |
Pfam:Cadherin_3
|
1493 |
1617 |
1.2e-27 |
PFAM |
Pfam:Cadherin_3
|
1622 |
1748 |
4.8e-17 |
PFAM |
Calx_beta
|
1754 |
1853 |
1.45e-7 |
SMART |
Calx_beta
|
1866 |
1977 |
3.35e-12 |
SMART |
Calx_beta
|
1991 |
2098 |
1.61e-5 |
SMART |
|
Meta Mutation Damage Score |
0.0898 |
Coding Region Coverage |
- 1x: 97.5%
- 3x: 97.0%
- 10x: 95.5%
- 20x: 93.0%
|
Validation Efficiency |
97% (125/129) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes an integral membrane protein containing numerous CSPG (chondroitin sulfate proteoglycan element) repeats and Calx-beta domains. The protein belongs to the family of FRAS1/FREM extracellular matrix proteins and may play a role cell adhesion. [provided by RefSeq, Feb 2017]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 142 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aak1 |
T |
A |
6: 86,944,337 (GRCm39) |
S749T |
unknown |
Het |
Abcb4 |
A |
T |
5: 8,990,968 (GRCm39) |
I843F |
probably damaging |
Het |
Abcb6 |
A |
T |
1: 75,149,323 (GRCm39) |
|
probably benign |
Het |
AC238840.1 |
A |
T |
7: 38,467,377 (GRCm39) |
|
noncoding transcript |
Het |
Actr8 |
T |
A |
14: 29,708,926 (GRCm39) |
H244Q |
possibly damaging |
Het |
Acyp2 |
A |
G |
11: 30,456,452 (GRCm39) |
|
probably benign |
Het |
Adgrv1 |
A |
G |
13: 81,530,417 (GRCm39) |
Y5886H |
probably benign |
Het |
Afap1 |
C |
T |
5: 36,119,081 (GRCm39) |
|
probably benign |
Het |
Agk |
T |
A |
6: 40,363,751 (GRCm39) |
W244R |
probably damaging |
Het |
Akirin1 |
T |
A |
4: 123,631,883 (GRCm39) |
|
probably benign |
Het |
Ankrd11 |
C |
A |
8: 123,626,463 (GRCm39) |
V161L |
probably damaging |
Het |
Arap3 |
T |
C |
18: 38,122,249 (GRCm39) |
|
probably null |
Het |
Arhgap29 |
A |
G |
3: 121,785,968 (GRCm39) |
|
probably benign |
Het |
Armc3 |
A |
G |
2: 19,243,547 (GRCm39) |
M88V |
probably benign |
Het |
Atp13a5 |
G |
T |
16: 29,167,833 (GRCm39) |
P109T |
probably benign |
Het |
Avpr1b |
T |
A |
1: 131,528,323 (GRCm39) |
V282D |
probably damaging |
Het |
Baz2b |
T |
C |
2: 59,808,890 (GRCm39) |
K120E |
possibly damaging |
Het |
Bltp1 |
T |
C |
3: 37,052,480 (GRCm39) |
M3060T |
probably benign |
Het |
Cacna1a |
T |
A |
8: 85,241,579 (GRCm39) |
|
probably benign |
Het |
Cacng6 |
G |
A |
7: 3,473,404 (GRCm39) |
C76Y |
probably damaging |
Het |
Cactin |
G |
T |
10: 81,158,985 (GRCm39) |
E279* |
probably null |
Het |
Car9 |
A |
G |
4: 43,510,222 (GRCm39) |
Y268C |
probably damaging |
Het |
Ccdc146 |
T |
A |
5: 21,524,564 (GRCm39) |
I263F |
probably damaging |
Het |
Cdc16 |
A |
T |
8: 13,808,992 (GRCm39) |
|
probably benign |
Het |
Cdh16 |
T |
G |
8: 105,345,003 (GRCm39) |
S429R |
probably benign |
Het |
Cep250 |
A |
G |
2: 155,832,995 (GRCm39) |
E1639G |
probably damaging |
Het |
Ces1d |
A |
T |
8: 93,921,649 (GRCm39) |
V38D |
possibly damaging |
Het |
Chd1 |
A |
T |
17: 15,946,545 (GRCm39) |
Q97L |
possibly damaging |
Het |
Ciita |
G |
A |
16: 10,332,332 (GRCm39) |
D898N |
possibly damaging |
Het |
Clstn1 |
A |
G |
4: 149,719,179 (GRCm39) |
N336S |
possibly damaging |
Het |
Cntnap5a |
A |
G |
1: 116,187,249 (GRCm39) |
D607G |
probably damaging |
Het |
Col1a2 |
G |
A |
6: 4,518,822 (GRCm39) |
|
probably benign |
Het |
Col20a1 |
C |
T |
2: 180,636,753 (GRCm39) |
H245Y |
probably benign |
Het |
Coq8b |
A |
T |
7: 26,951,734 (GRCm39) |
T399S |
probably benign |
Het |
Cpn2 |
A |
G |
16: 30,079,003 (GRCm39) |
S233P |
probably benign |
Het |
Cryz |
G |
A |
3: 154,312,113 (GRCm39) |
G70D |
probably damaging |
Het |
Csmd1 |
G |
T |
8: 16,207,218 (GRCm39) |
|
probably benign |
Het |
Def6 |
T |
A |
17: 28,444,956 (GRCm39) |
D451E |
possibly damaging |
Het |
Dnah8 |
T |
A |
17: 30,966,251 (GRCm39) |
C2480* |
probably null |
Het |
Dnah9 |
T |
C |
11: 65,818,648 (GRCm39) |
N3230S |
probably benign |
Het |
Dyrk4 |
G |
T |
6: 126,893,337 (GRCm39) |
S15* |
probably null |
Het |
Erc1 |
T |
C |
6: 119,671,563 (GRCm39) |
R917G |
probably damaging |
Het |
Fgd2 |
T |
A |
17: 29,593,082 (GRCm39) |
|
probably benign |
Het |
Gas2l3 |
T |
C |
10: 89,249,796 (GRCm39) |
I441V |
probably benign |
Het |
Gm14393 |
T |
A |
2: 174,905,774 (GRCm39) |
Y6F |
probably damaging |
Het |
Gm1527 |
A |
G |
3: 28,969,417 (GRCm39) |
K256E |
possibly damaging |
Het |
Gm21905 |
G |
T |
5: 68,103,740 (GRCm39) |
|
probably benign |
Het |
Gtf2ird1 |
T |
A |
5: 134,424,656 (GRCm39) |
|
probably null |
Het |
Hmces |
C |
A |
6: 87,913,121 (GRCm39) |
T292K |
probably benign |
Het |
Hpse2 |
G |
A |
19: 43,376,692 (GRCm39) |
S20L |
probably benign |
Het |
Ift70b |
G |
T |
2: 75,768,155 (GRCm39) |
S199R |
probably benign |
Het |
Ikbke |
A |
T |
1: 131,204,224 (GRCm39) |
V23E |
probably null |
Het |
Ino80 |
A |
T |
2: 119,210,130 (GRCm39) |
V1387E |
probably damaging |
Het |
Islr |
G |
T |
9: 58,064,589 (GRCm39) |
A306D |
probably damaging |
Het |
Jakmip1 |
G |
A |
5: 37,258,182 (GRCm39) |
G276D |
probably damaging |
Het |
Jchain |
A |
G |
5: 88,673,979 (GRCm39) |
V55A |
probably benign |
Het |
Kalrn |
T |
C |
16: 34,007,841 (GRCm39) |
K1350E |
probably damaging |
Het |
Kansl1l |
T |
C |
1: 66,841,156 (GRCm39) |
Q48R |
possibly damaging |
Het |
Kmt5a |
T |
C |
5: 124,585,334 (GRCm39) |
L23P |
probably damaging |
Het |
Lrba |
C |
T |
3: 86,644,449 (GRCm39) |
H381Y |
probably damaging |
Het |
Lrch3 |
T |
C |
16: 32,808,865 (GRCm39) |
|
probably benign |
Het |
Lrrc32 |
T |
C |
7: 98,148,564 (GRCm39) |
V448A |
probably benign |
Het |
Mapkbp1 |
T |
C |
2: 119,848,301 (GRCm39) |
M617T |
probably damaging |
Het |
Megf6 |
C |
T |
4: 154,336,876 (GRCm39) |
|
probably benign |
Het |
Mfap1a |
T |
C |
2: 121,333,282 (GRCm39) |
M50V |
probably benign |
Het |
Mgam |
G |
T |
6: 40,736,062 (GRCm39) |
A854S |
probably damaging |
Het |
Myh3 |
A |
C |
11: 66,988,885 (GRCm39) |
|
probably benign |
Het |
Myo18b |
C |
A |
5: 112,840,899 (GRCm39) |
R2298L |
probably damaging |
Het |
Myo1h |
T |
A |
5: 114,457,765 (GRCm39) |
M92K |
probably damaging |
Het |
Nfkbib |
T |
C |
7: 28,461,447 (GRCm39) |
|
probably null |
Het |
Nlrp2 |
T |
A |
7: 5,303,950 (GRCm39) |
T192S |
probably benign |
Het |
Nr2f1 |
A |
T |
13: 78,346,284 (GRCm39) |
Y137N |
possibly damaging |
Het |
Nup98 |
T |
A |
7: 101,796,513 (GRCm39) |
D841V |
probably damaging |
Het |
Nvl |
A |
G |
1: 180,966,827 (GRCm39) |
V59A |
probably damaging |
Het |
Ogdhl |
C |
A |
14: 32,068,745 (GRCm39) |
N948K |
probably damaging |
Het |
Or11g27 |
T |
C |
14: 50,771,159 (GRCm39) |
S97P |
possibly damaging |
Het |
Or12j3 |
A |
G |
7: 139,953,026 (GRCm39) |
S166P |
probably benign |
Het |
Or13a24 |
A |
G |
7: 140,154,662 (GRCm39) |
T199A |
probably benign |
Het |
Or51g1 |
A |
C |
7: 102,633,530 (GRCm39) |
Y280* |
probably null |
Het |
Orc2 |
A |
C |
1: 58,520,317 (GRCm39) |
|
probably benign |
Het |
Osgin1 |
G |
A |
8: 120,171,704 (GRCm39) |
R166H |
probably damaging |
Het |
Palb2 |
A |
T |
7: 121,706,746 (GRCm39) |
F741I |
probably benign |
Het |
Palb2 |
G |
T |
7: 121,706,747 (GRCm39) |
Y740* |
probably null |
Het |
Parvb |
G |
A |
15: 84,155,453 (GRCm39) |
G46D |
probably damaging |
Het |
Parvb |
G |
A |
15: 84,155,509 (GRCm39) |
D65N |
probably benign |
Het |
Pcsk2 |
A |
T |
2: 143,388,438 (GRCm39) |
K10* |
probably null |
Het |
Pde3a |
C |
T |
6: 141,411,932 (GRCm39) |
A502V |
probably benign |
Het |
Pfas |
T |
C |
11: 68,882,185 (GRCm39) |
I893V |
probably benign |
Het |
Pla2g4a |
A |
T |
1: 149,716,471 (GRCm39) |
D663E |
probably damaging |
Het |
Prickle2 |
G |
A |
6: 92,435,583 (GRCm39) |
P6L |
probably damaging |
Het |
Prx |
T |
A |
7: 27,217,026 (GRCm39) |
M648K |
probably benign |
Het |
Ptpn21 |
T |
C |
12: 98,654,735 (GRCm39) |
N744S |
probably benign |
Het |
Ptprq |
C |
T |
10: 107,554,435 (GRCm39) |
V97M |
probably damaging |
Het |
Pvr |
T |
C |
7: 19,652,549 (GRCm39) |
E122G |
possibly damaging |
Het |
Racgap1 |
T |
C |
15: 99,537,656 (GRCm39) |
K15E |
probably damaging |
Het |
Rock1 |
C |
T |
18: 10,136,091 (GRCm39) |
|
probably null |
Het |
Rorc |
T |
A |
3: 94,304,609 (GRCm39) |
Y331* |
probably null |
Het |
Rpl37 |
T |
C |
15: 5,148,096 (GRCm39) |
V91A |
probably benign |
Het |
Rrp36 |
T |
A |
17: 46,983,306 (GRCm39) |
K103* |
probably null |
Het |
Ryr3 |
T |
A |
2: 112,483,352 (GRCm39) |
M4142L |
probably benign |
Het |
Sash1 |
A |
T |
10: 8,665,357 (GRCm39) |
L125H |
probably damaging |
Het |
Scn5a |
T |
C |
9: 119,365,541 (GRCm39) |
M369V |
possibly damaging |
Het |
Siglec1 |
A |
T |
2: 130,912,307 (GRCm39) |
N1678K |
probably benign |
Het |
Slc15a5 |
A |
T |
6: 138,049,992 (GRCm39) |
V141E |
probably benign |
Het |
Slc43a1 |
T |
C |
2: 84,690,020 (GRCm39) |
|
probably benign |
Het |
Slc8a3 |
A |
T |
12: 81,246,484 (GRCm39) |
H856Q |
probably benign |
Het |
Spmip11 |
T |
C |
15: 98,483,142 (GRCm39) |
|
probably benign |
Het |
Sptlc2 |
T |
A |
12: 87,402,414 (GRCm39) |
M171L |
probably benign |
Het |
Srcap |
T |
A |
7: 127,158,899 (GRCm39) |
|
probably benign |
Het |
St6gal2 |
A |
G |
17: 55,797,944 (GRCm39) |
D310G |
probably damaging |
Het |
Susd2 |
T |
A |
10: 75,473,888 (GRCm39) |
D689V |
probably damaging |
Het |
Suz12 |
A |
T |
11: 79,910,558 (GRCm39) |
E303V |
possibly damaging |
Het |
Taldo1 |
C |
A |
7: 140,978,500 (GRCm39) |
T150K |
probably damaging |
Het |
Tex14 |
T |
C |
11: 87,440,355 (GRCm39) |
|
probably benign |
Het |
Tg |
T |
A |
15: 66,721,312 (GRCm39) |
F274I |
possibly damaging |
Het |
Tmem151b |
T |
C |
17: 45,856,663 (GRCm39) |
D259G |
probably damaging |
Het |
Tmem179 |
G |
T |
12: 112,468,288 (GRCm39) |
H64Q |
probably benign |
Het |
Tmem236 |
A |
G |
2: 14,223,732 (GRCm39) |
T174A |
probably benign |
Het |
Tmtc1 |
T |
A |
6: 148,207,483 (GRCm39) |
|
probably benign |
Het |
Tnc |
A |
T |
4: 63,884,811 (GRCm39) |
N1821K |
probably damaging |
Het |
Tnfrsf11a |
A |
G |
1: 105,752,773 (GRCm39) |
N261S |
probably damaging |
Het |
Traf6 |
G |
T |
2: 101,526,994 (GRCm39) |
|
probably benign |
Het |
Trank1 |
C |
A |
9: 111,172,300 (GRCm39) |
F96L |
possibly damaging |
Het |
Trim56 |
T |
A |
5: 137,142,017 (GRCm39) |
I500F |
probably damaging |
Het |
Ttll5 |
A |
G |
12: 85,926,168 (GRCm39) |
I321V |
possibly damaging |
Het |
Ttn |
C |
A |
2: 76,608,367 (GRCm39) |
W17852L |
probably damaging |
Het |
Twnk |
G |
A |
19: 44,997,820 (GRCm39) |
V450M |
probably damaging |
Het |
Uba52 |
A |
G |
8: 70,962,206 (GRCm39) |
I127T |
possibly damaging |
Het |
Ubr4 |
T |
A |
4: 139,148,537 (GRCm39) |
|
probably null |
Het |
Uggt1 |
A |
T |
1: 36,215,877 (GRCm39) |
M130K |
probably benign |
Het |
Ulk4 |
T |
A |
9: 120,910,722 (GRCm39) |
T1101S |
probably benign |
Het |
Urb1 |
A |
G |
16: 90,548,902 (GRCm39) |
S2269P |
probably benign |
Het |
Ush2a |
G |
T |
1: 188,132,403 (GRCm39) |
R875L |
probably benign |
Het |
Usp9y |
T |
A |
Y: 1,332,471 (GRCm39) |
H1624L |
probably benign |
Homo |
Vipr1 |
T |
C |
9: 121,494,586 (GRCm39) |
L308S |
possibly damaging |
Het |
Vps50 |
G |
A |
6: 3,517,777 (GRCm39) |
|
probably benign |
Het |
Xdh |
T |
G |
17: 74,198,107 (GRCm39) |
K1260T |
probably damaging |
Het |
Yipf4 |
A |
G |
17: 74,800,963 (GRCm39) |
I94V |
probably benign |
Het |
Zfhx4 |
A |
G |
3: 5,478,206 (GRCm39) |
*3582W |
probably null |
Het |
Zfp58 |
T |
C |
13: 67,640,144 (GRCm39) |
N116D |
possibly damaging |
Het |
Zfp750 |
C |
A |
11: 121,402,819 (GRCm39) |
R643L |
probably benign |
Het |
Znfx1 |
A |
G |
2: 166,884,507 (GRCm39) |
V51A |
possibly damaging |
Het |
|
Other mutations in Frem3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00481:Frem3
|
APN |
8 |
81,395,439 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL01019:Frem3
|
APN |
8 |
81,341,763 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01470:Frem3
|
APN |
8 |
81,340,944 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01609:Frem3
|
APN |
8 |
81,339,333 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01622:Frem3
|
APN |
8 |
81,340,544 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01623:Frem3
|
APN |
8 |
81,340,544 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01751:Frem3
|
APN |
8 |
81,342,372 (GRCm39) |
missense |
probably benign |
0.33 |
IGL02037:Frem3
|
APN |
8 |
81,338,118 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02039:Frem3
|
APN |
8 |
81,339,600 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02084:Frem3
|
APN |
8 |
81,339,072 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02124:Frem3
|
APN |
8 |
81,339,723 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02140:Frem3
|
APN |
8 |
81,340,736 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02836:Frem3
|
APN |
8 |
81,341,010 (GRCm39) |
missense |
probably benign |
|
IGL03090:Frem3
|
APN |
8 |
81,344,858 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03102:Frem3
|
APN |
8 |
81,339,661 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL03116:Frem3
|
APN |
8 |
81,339,435 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03165:Frem3
|
APN |
8 |
81,339,158 (GRCm39) |
missense |
probably benign |
0.26 |
IGL03224:Frem3
|
APN |
8 |
81,340,092 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03401:Frem3
|
APN |
8 |
81,341,170 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03403:Frem3
|
APN |
8 |
81,337,719 (GRCm39) |
missense |
probably benign |
0.04 |
FR4340:Frem3
|
UTSW |
8 |
81,341,870 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Frem3
|
UTSW |
8 |
81,341,870 (GRCm39) |
small insertion |
probably benign |
|
IGL02991:Frem3
|
UTSW |
8 |
81,395,511 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03052:Frem3
|
UTSW |
8 |
81,341,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R0089:Frem3
|
UTSW |
8 |
81,342,507 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0647:Frem3
|
UTSW |
8 |
81,341,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R0690:Frem3
|
UTSW |
8 |
81,340,581 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0766:Frem3
|
UTSW |
8 |
81,341,951 (GRCm39) |
missense |
probably benign |
|
R0834:Frem3
|
UTSW |
8 |
81,413,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R0909:Frem3
|
UTSW |
8 |
81,390,035 (GRCm39) |
missense |
probably benign |
0.45 |
R1033:Frem3
|
UTSW |
8 |
81,421,786 (GRCm39) |
missense |
probably benign |
0.00 |
R1144:Frem3
|
UTSW |
8 |
81,338,513 (GRCm39) |
missense |
probably benign |
0.01 |
R1312:Frem3
|
UTSW |
8 |
81,341,951 (GRCm39) |
missense |
probably benign |
|
R1330:Frem3
|
UTSW |
8 |
81,395,468 (GRCm39) |
missense |
probably damaging |
0.99 |
R1355:Frem3
|
UTSW |
8 |
81,417,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R1390:Frem3
|
UTSW |
8 |
81,417,402 (GRCm39) |
missense |
probably damaging |
0.99 |
R1413:Frem3
|
UTSW |
8 |
81,395,430 (GRCm39) |
missense |
probably benign |
|
R1470:Frem3
|
UTSW |
8 |
81,337,820 (GRCm39) |
missense |
probably benign |
0.05 |
R1503:Frem3
|
UTSW |
8 |
81,413,647 (GRCm39) |
missense |
probably damaging |
0.99 |
R1538:Frem3
|
UTSW |
8 |
81,339,764 (GRCm39) |
missense |
probably benign |
0.00 |
R1538:Frem3
|
UTSW |
8 |
81,339,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R1612:Frem3
|
UTSW |
8 |
81,341,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R1793:Frem3
|
UTSW |
8 |
81,339,741 (GRCm39) |
missense |
probably benign |
0.03 |
R1872:Frem3
|
UTSW |
8 |
81,339,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R1879:Frem3
|
UTSW |
8 |
81,338,567 (GRCm39) |
nonsense |
probably null |
|
R1886:Frem3
|
UTSW |
8 |
81,340,514 (GRCm39) |
missense |
probably benign |
0.00 |
R1933:Frem3
|
UTSW |
8 |
81,339,519 (GRCm39) |
missense |
probably benign |
0.00 |
R2027:Frem3
|
UTSW |
8 |
81,421,966 (GRCm39) |
missense |
possibly damaging |
0.75 |
R2040:Frem3
|
UTSW |
8 |
81,342,455 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2050:Frem3
|
UTSW |
8 |
81,341,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R2079:Frem3
|
UTSW |
8 |
81,341,732 (GRCm39) |
missense |
probably benign |
0.03 |
R2099:Frem3
|
UTSW |
8 |
81,342,488 (GRCm39) |
missense |
probably benign |
0.06 |
R2120:Frem3
|
UTSW |
8 |
81,342,086 (GRCm39) |
missense |
probably benign |
0.20 |
R2842:Frem3
|
UTSW |
8 |
81,395,978 (GRCm39) |
splice site |
probably null |
|
R2845:Frem3
|
UTSW |
8 |
81,339,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R3015:Frem3
|
UTSW |
8 |
81,417,402 (GRCm39) |
missense |
probably damaging |
0.99 |
R3442:Frem3
|
UTSW |
8 |
81,339,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R3724:Frem3
|
UTSW |
8 |
81,341,900 (GRCm39) |
missense |
probably benign |
0.06 |
R3730:Frem3
|
UTSW |
8 |
81,342,545 (GRCm39) |
missense |
probably damaging |
0.99 |
R3939:Frem3
|
UTSW |
8 |
81,341,649 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3940:Frem3
|
UTSW |
8 |
81,341,649 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3941:Frem3
|
UTSW |
8 |
81,341,649 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4089:Frem3
|
UTSW |
8 |
81,341,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R4282:Frem3
|
UTSW |
8 |
81,340,770 (GRCm39) |
missense |
probably benign |
0.00 |
R4437:Frem3
|
UTSW |
8 |
81,339,236 (GRCm39) |
missense |
probably benign |
0.30 |
R4480:Frem3
|
UTSW |
8 |
81,337,986 (GRCm39) |
missense |
probably benign |
0.10 |
R4575:Frem3
|
UTSW |
8 |
81,342,704 (GRCm39) |
missense |
probably benign |
0.17 |
R4583:Frem3
|
UTSW |
8 |
81,340,143 (GRCm39) |
missense |
probably benign |
0.03 |
R4620:Frem3
|
UTSW |
8 |
81,395,586 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4621:Frem3
|
UTSW |
8 |
81,395,820 (GRCm39) |
splice site |
probably null |
|
R4644:Frem3
|
UTSW |
8 |
81,340,356 (GRCm39) |
missense |
probably benign |
0.33 |
R4667:Frem3
|
UTSW |
8 |
81,390,049 (GRCm39) |
missense |
probably damaging |
0.97 |
R4748:Frem3
|
UTSW |
8 |
81,338,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R4823:Frem3
|
UTSW |
8 |
81,340,587 (GRCm39) |
missense |
probably benign |
0.25 |
R4836:Frem3
|
UTSW |
8 |
81,390,026 (GRCm39) |
missense |
probably damaging |
0.99 |
R4867:Frem3
|
UTSW |
8 |
81,339,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R4921:Frem3
|
UTSW |
8 |
81,339,765 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5030:Frem3
|
UTSW |
8 |
81,339,876 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5035:Frem3
|
UTSW |
8 |
81,342,543 (GRCm39) |
missense |
probably damaging |
0.97 |
R5172:Frem3
|
UTSW |
8 |
81,339,195 (GRCm39) |
missense |
probably benign |
0.44 |
R5289:Frem3
|
UTSW |
8 |
81,338,948 (GRCm39) |
missense |
probably benign |
0.00 |
R5492:Frem3
|
UTSW |
8 |
81,339,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R5655:Frem3
|
UTSW |
8 |
81,339,323 (GRCm39) |
missense |
probably benign |
0.00 |
R5685:Frem3
|
UTSW |
8 |
81,421,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R5723:Frem3
|
UTSW |
8 |
81,340,026 (GRCm39) |
missense |
probably benign |
0.02 |
R5743:Frem3
|
UTSW |
8 |
81,342,407 (GRCm39) |
missense |
probably damaging |
0.98 |
R5889:Frem3
|
UTSW |
8 |
81,340,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R6048:Frem3
|
UTSW |
8 |
81,340,062 (GRCm39) |
missense |
probably benign |
0.03 |
R6057:Frem3
|
UTSW |
8 |
81,342,216 (GRCm39) |
missense |
probably damaging |
0.99 |
R6137:Frem3
|
UTSW |
8 |
81,341,676 (GRCm39) |
missense |
probably benign |
|
R6264:Frem3
|
UTSW |
8 |
81,341,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R6339:Frem3
|
UTSW |
8 |
81,339,644 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6418:Frem3
|
UTSW |
8 |
81,337,781 (GRCm39) |
missense |
probably benign |
0.08 |
R6680:Frem3
|
UTSW |
8 |
81,395,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R6773:Frem3
|
UTSW |
8 |
81,338,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R6838:Frem3
|
UTSW |
8 |
81,338,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R6928:Frem3
|
UTSW |
8 |
81,337,911 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6939:Frem3
|
UTSW |
8 |
81,341,774 (GRCm39) |
missense |
probably benign |
0.23 |
R6995:Frem3
|
UTSW |
8 |
81,339,208 (GRCm39) |
missense |
probably damaging |
0.98 |
R7112:Frem3
|
UTSW |
8 |
81,338,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R7155:Frem3
|
UTSW |
8 |
81,342,668 (GRCm39) |
missense |
probably benign |
0.01 |
R7235:Frem3
|
UTSW |
8 |
81,417,354 (GRCm39) |
missense |
probably benign |
0.00 |
R7282:Frem3
|
UTSW |
8 |
81,338,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R7403:Frem3
|
UTSW |
8 |
81,342,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R7422:Frem3
|
UTSW |
8 |
81,342,392 (GRCm39) |
missense |
probably benign |
0.00 |
R7485:Frem3
|
UTSW |
8 |
81,339,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R7516:Frem3
|
UTSW |
8 |
81,338,712 (GRCm39) |
missense |
probably damaging |
0.99 |
R7858:Frem3
|
UTSW |
8 |
81,338,350 (GRCm39) |
nonsense |
probably null |
|
R7976:Frem3
|
UTSW |
8 |
81,338,231 (GRCm39) |
nonsense |
probably null |
|
R8171:Frem3
|
UTSW |
8 |
81,341,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R8185:Frem3
|
UTSW |
8 |
81,338,933 (GRCm39) |
nonsense |
probably null |
|
R8306:Frem3
|
UTSW |
8 |
81,338,840 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8478:Frem3
|
UTSW |
8 |
81,338,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R8518:Frem3
|
UTSW |
8 |
81,339,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R8794:Frem3
|
UTSW |
8 |
81,342,851 (GRCm39) |
missense |
probably benign |
0.02 |
R8794:Frem3
|
UTSW |
8 |
81,338,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R8806:Frem3
|
UTSW |
8 |
81,390,064 (GRCm39) |
missense |
probably benign |
0.30 |
R8833:Frem3
|
UTSW |
8 |
81,339,401 (GRCm39) |
missense |
probably benign |
0.29 |
R8879:Frem3
|
UTSW |
8 |
81,339,777 (GRCm39) |
missense |
probably damaging |
0.98 |
R8897:Frem3
|
UTSW |
8 |
81,339,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R8983:Frem3
|
UTSW |
8 |
81,395,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R9207:Frem3
|
UTSW |
8 |
81,340,071 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9277:Frem3
|
UTSW |
8 |
81,417,402 (GRCm39) |
missense |
probably damaging |
0.96 |
R9536:Frem3
|
UTSW |
8 |
81,342,048 (GRCm39) |
missense |
probably benign |
0.00 |
R9596:Frem3
|
UTSW |
8 |
81,341,951 (GRCm39) |
missense |
probably benign |
|
R9649:Frem3
|
UTSW |
8 |
81,341,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R9671:Frem3
|
UTSW |
8 |
81,339,134 (GRCm39) |
missense |
probably benign |
0.00 |
R9723:Frem3
|
UTSW |
8 |
81,341,352 (GRCm39) |
missense |
probably benign |
|
R9790:Frem3
|
UTSW |
8 |
81,339,890 (GRCm39) |
missense |
probably benign |
0.01 |
R9791:Frem3
|
UTSW |
8 |
81,339,890 (GRCm39) |
missense |
probably benign |
0.01 |
RF030:Frem3
|
UTSW |
8 |
81,341,867 (GRCm39) |
small insertion |
probably benign |
|
RF034:Frem3
|
UTSW |
8 |
81,341,867 (GRCm39) |
small insertion |
probably benign |
|
RF042:Frem3
|
UTSW |
8 |
81,341,867 (GRCm39) |
small insertion |
probably benign |
|
X0024:Frem3
|
UTSW |
8 |
81,339,710 (GRCm39) |
missense |
possibly damaging |
0.76 |
X0027:Frem3
|
UTSW |
8 |
81,339,017 (GRCm39) |
nonsense |
probably null |
|
Z1088:Frem3
|
UTSW |
8 |
81,342,055 (GRCm39) |
missense |
probably benign |
0.04 |
Z1176:Frem3
|
UTSW |
8 |
81,342,060 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Frem3
|
UTSW |
8 |
81,338,132 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Frem3
|
UTSW |
8 |
81,342,758 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
Predicted Primers |
PCR Primer
(F):5'- CAGCTCAGGTGGAGACTTGGAATG -3'
(R):5'- GCTGCACTCGAATCACTAGATCCC -3'
Sequencing Primer
(F):5'- ACAGAGAGAGCTTGTCCGTTG -3'
(R):5'- CTAGATCCCGCAGTGGGTTAAG -3'
|
Posted On |
2014-05-23 |