Incidental Mutation 'R5503:Marf1'
| ID |
430777 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Marf1
|
| Ensembl Gene |
ENSMUSG00000060657 |
| Gene Name |
meiosis regulator and mRNA stability 1 |
| Synonyms |
4921513D23Rik |
| MMRRC Submission |
043064-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.222)
|
| Stock # |
R5503 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
16 |
| Chromosomal Location |
13927030-13977157 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to C
at 13970095 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Leucine to Arginine
at position 208
(L208R)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000087770
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000090300]
[ENSMUST00000229614]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000090300
AA Change: L208R
PolyPhen 2
Score 0.992 (Sensitivity: 0.70; Specificity: 0.97)
|
| SMART Domains |
Protein: ENSMUSP00000087770
Gene: ENSMUSG00000060657
AA Change: L208R
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
116 |
127 |
N/A |
INTRINSIC |
|
low complexity region
|
290 |
305 |
N/A |
INTRINSIC |
|
Pfam:NYN
|
351 |
492 |
1.5e-21 |
PFAM |
|
RRM
|
511 |
579 |
3.17e-1 |
SMART |
|
low complexity region
|
599 |
610 |
N/A |
INTRINSIC |
|
RRM
|
790 |
864 |
4.47e-3 |
SMART |
|
internal_repeat_2
|
871 |
914 |
1.57e-5 |
PROSPERO |
|
low complexity region
|
944 |
960 |
N/A |
INTRINSIC |
|
Pfam:OST-HTH
|
1096 |
1167 |
1e-11 |
PFAM |
|
low complexity region
|
1181 |
1186 |
N/A |
INTRINSIC |
|
Pfam:OST-HTH
|
1256 |
1328 |
1.2e-10 |
PFAM |
|
Pfam:OST-HTH
|
1332 |
1404 |
2.4e-10 |
PFAM |
|
Pfam:OST-HTH
|
1408 |
1480 |
6.8e-13 |
PFAM |
|
Pfam:OST-HTH
|
1483 |
1555 |
3e-14 |
PFAM |
|
low complexity region
|
1682 |
1701 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000229614
|
| Meta Mutation Damage Score |
0.1067 |
| Coding Region Coverage |
- 1x: 98.3%
- 3x: 97.4%
- 10x: 95.4%
- 20x: 91.5%
|
| Validation Efficiency |
96% (103/107) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a putative peroxisomal protein that appears to be conserved across Euteleostomi. In humans, it may be autoantigenic. [provided by RefSeq, Jul 2010]
PHENOTYPE: Mice homozygous for an ENU-induced mutation exhibit female infertility with abnormalities in oogenic processes including meiotic progression, genomic integrity and acquisition of developmental competence. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 88 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
| 2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
| Abca6 |
A |
G |
11: 110,109,083 (GRCm39) |
S696P |
probably damaging |
Het |
| Abca9 |
G |
A |
11: 110,032,436 (GRCm39) |
T727M |
probably damaging |
Het |
| Alpk2 |
T |
C |
18: 65,439,312 (GRCm39) |
R1161G |
probably benign |
Het |
| Amy1 |
T |
C |
3: 113,349,709 (GRCm39) |
D487G |
probably benign |
Het |
| Arap2 |
G |
A |
5: 62,787,529 (GRCm39) |
A1409V |
probably damaging |
Het |
| B4galt6 |
C |
A |
18: 20,878,409 (GRCm39) |
|
probably null |
Het |
| Cacna1s |
G |
A |
1: 136,014,480 (GRCm39) |
G382D |
probably damaging |
Het |
| Camk2a |
A |
G |
18: 61,111,072 (GRCm39) |
D87G |
probably damaging |
Het |
| Cdh18 |
A |
G |
15: 23,436,620 (GRCm39) |
Y492C |
probably damaging |
Het |
| Cert1 |
C |
T |
13: 96,679,747 (GRCm39) |
R26C |
possibly damaging |
Het |
| Col18a1 |
C |
T |
10: 76,907,454 (GRCm39) |
G861D |
probably damaging |
Het |
| Crybg1 |
C |
A |
10: 43,874,762 (GRCm39) |
S782I |
probably benign |
Het |
| Csgalnact1 |
G |
A |
8: 68,914,125 (GRCm39) |
L27F |
probably damaging |
Het |
| Dab1 |
T |
A |
4: 104,369,461 (GRCm39) |
C3S |
probably benign |
Het |
| Dapk1 |
T |
C |
13: 60,873,126 (GRCm39) |
F343L |
probably benign |
Het |
| Dgat1 |
A |
T |
15: 76,386,394 (GRCm39) |
|
probably benign |
Het |
| Dnah11 |
C |
A |
12: 117,844,186 (GRCm39) |
|
probably null |
Het |
| Dsg2 |
T |
A |
18: 20,713,708 (GRCm39) |
Y226* |
probably null |
Het |
| Epg5 |
T |
A |
18: 77,994,422 (GRCm39) |
M351K |
possibly damaging |
Het |
| F13b |
A |
G |
1: 139,450,281 (GRCm39) |
T648A |
probably benign |
Het |
| Fgf17 |
T |
C |
14: 70,874,408 (GRCm39) |
Y127C |
probably damaging |
Het |
| Fkbp15 |
G |
A |
4: 62,246,124 (GRCm39) |
P435S |
probably benign |
Het |
| Gfm1 |
G |
A |
3: 67,361,060 (GRCm39) |
|
probably null |
Het |
| Gigyf1 |
T |
C |
5: 137,521,729 (GRCm39) |
|
probably benign |
Het |
| Gm12830 |
A |
T |
4: 114,678,936 (GRCm39) |
T6S |
unknown |
Het |
| Gm6465 |
A |
T |
5: 11,898,150 (GRCm39) |
N88I |
probably damaging |
Het |
| Gpr18 |
C |
T |
14: 122,149,159 (GRCm39) |
V289I |
probably damaging |
Het |
| Ipp |
G |
T |
4: 116,395,135 (GRCm39) |
E557* |
probably null |
Het |
| Klhl12 |
T |
A |
1: 134,413,653 (GRCm39) |
|
probably null |
Het |
| Klhl38 |
A |
G |
15: 58,185,745 (GRCm39) |
V328A |
possibly damaging |
Het |
| Kndc1 |
A |
G |
7: 139,511,802 (GRCm39) |
T1470A |
probably damaging |
Het |
| Kntc1 |
T |
A |
5: 123,957,939 (GRCm39) |
D2173E |
possibly damaging |
Het |
| Lipi |
T |
C |
16: 75,370,864 (GRCm39) |
K118E |
probably benign |
Het |
| Misp |
G |
A |
10: 79,662,552 (GRCm39) |
R323K |
probably damaging |
Het |
| Mlxip |
T |
A |
5: 123,533,390 (GRCm39) |
M133K |
probably damaging |
Het |
| Mon2 |
A |
T |
10: 122,868,550 (GRCm39) |
M501K |
possibly damaging |
Het |
| Myh2 |
A |
G |
11: 67,064,275 (GRCm39) |
I77V |
probably benign |
Het |
| Napa |
C |
A |
7: 15,849,549 (GRCm39) |
Q254K |
probably benign |
Het |
| Nckap5l |
C |
A |
15: 99,323,503 (GRCm39) |
G1000V |
probably damaging |
Het |
| Neo1 |
A |
T |
9: 58,892,933 (GRCm39) |
S236R |
possibly damaging |
Het |
| Neurl4 |
T |
A |
11: 69,797,194 (GRCm39) |
Y594N |
probably damaging |
Het |
| Nmral1 |
G |
A |
16: 4,533,493 (GRCm39) |
P94L |
probably benign |
Het |
| Notch3 |
A |
T |
17: 32,366,029 (GRCm39) |
I1024N |
probably benign |
Het |
| Nsd1 |
T |
A |
13: 55,393,752 (GRCm39) |
I451K |
probably damaging |
Het |
| Nt5c3b |
T |
C |
11: 100,323,883 (GRCm39) |
D143G |
probably benign |
Het |
| Oplah |
A |
G |
15: 76,189,646 (GRCm39) |
|
probably null |
Het |
| Or13a17 |
A |
C |
7: 140,271,309 (GRCm39) |
M164L |
probably benign |
Het |
| Or2ak4 |
T |
A |
11: 58,649,154 (GRCm39) |
V221E |
probably damaging |
Het |
| Or6b2b |
C |
A |
1: 92,418,918 (GRCm39) |
K186N |
probably benign |
Het |
| Or7d10 |
A |
G |
9: 19,831,675 (GRCm39) |
T57A |
probably benign |
Het |
| Or8b48 |
T |
C |
9: 38,493,368 (GRCm39) |
V265A |
probably benign |
Het |
| Or8g19 |
A |
G |
9: 39,055,780 (GRCm39) |
N128S |
probably benign |
Het |
| Phb2 |
T |
A |
6: 124,689,985 (GRCm39) |
|
probably benign |
Het |
| Plcl2 |
A |
G |
17: 50,816,957 (GRCm39) |
I108V |
probably benign |
Het |
| Plpp6 |
T |
A |
19: 28,942,146 (GRCm39) |
M249K |
probably damaging |
Het |
| Pnpt1 |
G |
A |
11: 29,088,156 (GRCm39) |
G189E |
probably damaging |
Het |
| Pramel17 |
A |
T |
4: 101,692,999 (GRCm39) |
Y334N |
probably benign |
Het |
| Ptprn |
C |
T |
1: 75,228,519 (GRCm39) |
V853M |
probably damaging |
Het |
| Ptprq |
T |
C |
10: 107,524,189 (GRCm39) |
|
probably null |
Het |
| Rai1 |
G |
A |
11: 60,077,279 (GRCm39) |
V448I |
probably benign |
Het |
| Rbm20 |
T |
A |
19: 53,839,785 (GRCm39) |
C925S |
possibly damaging |
Het |
| Rin3 |
C |
A |
12: 102,279,314 (GRCm39) |
P41Q |
probably benign |
Het |
| Rpl31-ps21 |
T |
C |
5: 21,324,505 (GRCm39) |
|
noncoding transcript |
Het |
| Rpl39-ps |
A |
T |
15: 102,543,561 (GRCm39) |
|
noncoding transcript |
Het |
| Rtn4ip1 |
T |
A |
10: 43,783,879 (GRCm39) |
D133E |
probably benign |
Het |
| Ryr1 |
T |
C |
7: 28,768,453 (GRCm39) |
K2839E |
possibly damaging |
Het |
| Septin5 |
T |
C |
16: 18,442,118 (GRCm39) |
K268R |
probably benign |
Het |
| Serpinb6b |
T |
A |
13: 33,161,642 (GRCm39) |
D238E |
possibly damaging |
Het |
| Slc15a2 |
C |
T |
16: 36,582,747 (GRCm39) |
V214M |
probably damaging |
Het |
| Smarca2 |
T |
C |
19: 26,601,336 (GRCm39) |
M18T |
probably damaging |
Het |
| Smarca2 |
C |
A |
19: 26,659,446 (GRCm39) |
T912K |
possibly damaging |
Het |
| Smdt1 |
A |
T |
15: 82,232,101 (GRCm39) |
R46S |
possibly damaging |
Het |
| Spa17 |
A |
C |
9: 37,523,273 (GRCm39) |
F5V |
probably damaging |
Het |
| Spag17 |
A |
G |
3: 99,934,560 (GRCm39) |
E614G |
possibly damaging |
Het |
| Sstr4 |
CGAGGAGGAGGAGGA |
CGAGGAGGAGGAGGAGGA |
2: 148,237,471 (GRCm39) |
|
probably benign |
Het |
| Tlr1 |
A |
T |
5: 65,083,635 (GRCm39) |
V314D |
probably damaging |
Het |
| Trappc8 |
A |
T |
18: 20,969,957 (GRCm39) |
L1011Q |
probably benign |
Het |
| Tsga10 |
A |
G |
1: 37,800,028 (GRCm39) |
*691Q |
probably null |
Het |
| Vav1 |
A |
T |
17: 57,610,079 (GRCm39) |
K420* |
probably null |
Het |
| Vmn1r174 |
C |
G |
7: 23,453,562 (GRCm39) |
T76R |
probably benign |
Het |
| Vmn2r116 |
A |
G |
17: 23,605,778 (GRCm39) |
E230G |
probably benign |
Het |
| Vps13b |
A |
G |
15: 35,452,312 (GRCm39) |
T637A |
probably damaging |
Het |
| Zbtb7a |
A |
G |
10: 80,980,631 (GRCm39) |
E275G |
probably damaging |
Het |
| Zfp280b |
A |
G |
10: 75,875,296 (GRCm39) |
|
probably null |
Het |
| Zfp763 |
A |
G |
17: 33,238,507 (GRCm39) |
Y213H |
possibly damaging |
Het |
| Zfp78 |
T |
A |
7: 6,381,528 (GRCm39) |
W161R |
probably benign |
Het |
|
| Other mutations in Marf1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00517:Marf1
|
APN |
16 |
13,933,606 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
IGL00933:Marf1
|
APN |
16 |
13,935,221 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01101:Marf1
|
APN |
16 |
13,964,600 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
IGL02140:Marf1
|
APN |
16 |
13,959,776 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL03196:Marf1
|
APN |
16 |
13,958,123 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
PIT4283001:Marf1
|
UTSW |
16 |
13,946,432 (GRCm39) |
missense |
probably benign |
0.22 |
|
R0016:Marf1
|
UTSW |
16 |
13,970,129 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0016:Marf1
|
UTSW |
16 |
13,970,129 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0046:Marf1
|
UTSW |
16 |
13,929,591 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R0046:Marf1
|
UTSW |
16 |
13,929,591 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R0056:Marf1
|
UTSW |
16 |
13,960,398 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0057:Marf1
|
UTSW |
16 |
13,960,398 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0058:Marf1
|
UTSW |
16 |
13,960,398 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0058:Marf1
|
UTSW |
16 |
13,960,398 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0113:Marf1
|
UTSW |
16 |
13,960,398 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0115:Marf1
|
UTSW |
16 |
13,960,398 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0179:Marf1
|
UTSW |
16 |
13,969,040 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0238:Marf1
|
UTSW |
16 |
13,969,147 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0238:Marf1
|
UTSW |
16 |
13,969,147 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0294:Marf1
|
UTSW |
16 |
13,960,398 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0295:Marf1
|
UTSW |
16 |
13,960,398 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0316:Marf1
|
UTSW |
16 |
13,960,398 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0318:Marf1
|
UTSW |
16 |
13,960,398 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0375:Marf1
|
UTSW |
16 |
13,969,184 (GRCm39) |
splice site |
probably benign |
|
|
R0383:Marf1
|
UTSW |
16 |
13,960,398 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0391:Marf1
|
UTSW |
16 |
13,960,398 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0504:Marf1
|
UTSW |
16 |
13,960,398 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0589:Marf1
|
UTSW |
16 |
13,959,919 (GRCm39) |
splice site |
probably benign |
|
|
R0603:Marf1
|
UTSW |
16 |
13,960,398 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0610:Marf1
|
UTSW |
16 |
13,960,398 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1240:Marf1
|
UTSW |
16 |
13,964,626 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R1445:Marf1
|
UTSW |
16 |
13,933,688 (GRCm39) |
missense |
probably benign |
|
|
R1716:Marf1
|
UTSW |
16 |
13,960,450 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1921:Marf1
|
UTSW |
16 |
13,946,465 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R2098:Marf1
|
UTSW |
16 |
13,932,064 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2155:Marf1
|
UTSW |
16 |
13,950,293 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2177:Marf1
|
UTSW |
16 |
13,970,471 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2195:Marf1
|
UTSW |
16 |
13,929,563 (GRCm39) |
missense |
probably benign |
|
|
R2410:Marf1
|
UTSW |
16 |
13,933,691 (GRCm39) |
missense |
probably benign |
0.02 |
|
R2999:Marf1
|
UTSW |
16 |
13,960,505 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R3000:Marf1
|
UTSW |
16 |
13,960,505 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R3147:Marf1
|
UTSW |
16 |
13,943,843 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R3148:Marf1
|
UTSW |
16 |
13,943,843 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R3430:Marf1
|
UTSW |
16 |
13,958,041 (GRCm39) |
unclassified |
probably benign |
|
|
R3821:Marf1
|
UTSW |
16 |
13,960,418 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4383:Marf1
|
UTSW |
16 |
13,960,505 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R4384:Marf1
|
UTSW |
16 |
13,960,505 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R4520:Marf1
|
UTSW |
16 |
13,950,530 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4554:Marf1
|
UTSW |
16 |
13,971,841 (GRCm39) |
start gained |
probably benign |
|
|
R4557:Marf1
|
UTSW |
16 |
13,971,841 (GRCm39) |
start gained |
probably benign |
|
|
R4768:Marf1
|
UTSW |
16 |
13,949,461 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R4784:Marf1
|
UTSW |
16 |
13,970,321 (GRCm39) |
missense |
probably benign |
|
|
R4857:Marf1
|
UTSW |
16 |
13,946,475 (GRCm39) |
nonsense |
probably null |
|
|
R4863:Marf1
|
UTSW |
16 |
13,950,529 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R4994:Marf1
|
UTSW |
16 |
13,932,095 (GRCm39) |
missense |
probably benign |
|
|
R5191:Marf1
|
UTSW |
16 |
13,963,942 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5813:Marf1
|
UTSW |
16 |
13,970,449 (GRCm39) |
missense |
probably benign |
0.35 |
|
R5905:Marf1
|
UTSW |
16 |
13,945,113 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5960:Marf1
|
UTSW |
16 |
13,970,281 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6104:Marf1
|
UTSW |
16 |
13,935,319 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6387:Marf1
|
UTSW |
16 |
13,959,504 (GRCm39) |
makesense |
probably null |
|
|
R6533:Marf1
|
UTSW |
16 |
13,933,663 (GRCm39) |
missense |
probably benign |
0.16 |
|
R6608:Marf1
|
UTSW |
16 |
13,950,578 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6642:Marf1
|
UTSW |
16 |
13,950,611 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6954:Marf1
|
UTSW |
16 |
13,956,384 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6994:Marf1
|
UTSW |
16 |
13,946,721 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7010:Marf1
|
UTSW |
16 |
13,954,865 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7090:Marf1
|
UTSW |
16 |
13,929,566 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R7174:Marf1
|
UTSW |
16 |
13,954,817 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7221:Marf1
|
UTSW |
16 |
13,960,349 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7247:Marf1
|
UTSW |
16 |
13,944,957 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7557:Marf1
|
UTSW |
16 |
13,950,560 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7798:Marf1
|
UTSW |
16 |
13,956,315 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7807:Marf1
|
UTSW |
16 |
13,971,753 (GRCm39) |
nonsense |
probably null |
|
|
R7855:Marf1
|
UTSW |
16 |
13,932,065 (GRCm39) |
missense |
probably benign |
0.27 |
|
R7867:Marf1
|
UTSW |
16 |
13,946,470 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R7893:Marf1
|
UTSW |
16 |
13,964,599 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8291:Marf1
|
UTSW |
16 |
13,950,432 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8746:Marf1
|
UTSW |
16 |
13,935,168 (GRCm39) |
missense |
probably benign |
0.18 |
|
R8842:Marf1
|
UTSW |
16 |
13,935,169 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9253:Marf1
|
UTSW |
16 |
13,935,172 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9350:Marf1
|
UTSW |
16 |
13,963,789 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9440:Marf1
|
UTSW |
16 |
13,938,196 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9460:Marf1
|
UTSW |
16 |
13,947,526 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9658:Marf1
|
UTSW |
16 |
13,958,087 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9698:Marf1
|
UTSW |
16 |
13,967,077 (GRCm39) |
missense |
probably benign |
0.00 |
|
U24488:Marf1
|
UTSW |
16 |
13,950,230 (GRCm39) |
nonsense |
probably null |
|
|
X0025:Marf1
|
UTSW |
16 |
13,932,142 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Marf1
|
UTSW |
16 |
13,933,641 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- GAGCCCTTTAAACAAACCGG -3'
(R):5'- CTCTTAGACTCACCAAGCACTG -3'
Sequencing Primer
(F):5'- CGGAGGTGCCACATTTAGG -3'
(R):5'- CAGTCACGTGTCAAGTAGGGTC -3'
|
| Posted On |
2016-10-05 |
Incidental Mutation