Incidental Mutation 'R1445:Marf1'
| ID |
158825 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Marf1
|
| Ensembl Gene |
ENSMUSG00000060657 |
| Gene Name |
meiosis regulator and mRNA stability 1 |
| Synonyms |
4921513D23Rik |
| MMRRC Submission |
039500-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.222)
|
| Stock # |
R1445 (G1)
|
| Quality Score |
119 |
|
Status
|
Validated
|
| Chromosome |
16 |
| Chromosomal Location |
13927030-13977157 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 13933688 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Asparagine
at position 1567
(D1567N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000087770
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000090300]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000090300
AA Change: D1567N
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000087770
Gene: ENSMUSG00000060657
AA Change: D1567N
| 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 |
|
| Meta Mutation Damage Score |
0.0898 |
| Coding Region Coverage |
- 1x: 98.8%
- 3x: 97.7%
- 10x: 93.9%
- 20x: 84.0%
|
| Validation Efficiency |
96% (101/105) |
| 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: 94 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700061I17Rik |
G |
T |
3: 116,861,385 (GRCm39) |
|
noncoding transcript |
Het |
| 2300003K06Rik |
G |
T |
11: 99,728,793 (GRCm39) |
Q17K |
probably benign |
Het |
| Abca16 |
T |
C |
7: 120,119,256 (GRCm39) |
V999A |
probably benign |
Het |
| Actn3 |
C |
T |
19: 4,915,483 (GRCm39) |
|
probably benign |
Het |
| Agap2 |
T |
A |
10: 126,926,981 (GRCm39) |
|
probably benign |
Het |
| Ago3 |
C |
A |
4: 126,265,580 (GRCm39) |
R278L |
probably benign |
Het |
| Aldh1a2 |
T |
C |
9: 71,192,492 (GRCm39) |
V449A |
possibly damaging |
Het |
| Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
| Aplnr |
A |
G |
2: 84,967,353 (GRCm39) |
Y126C |
probably damaging |
Het |
| Apob |
T |
C |
12: 8,066,084 (GRCm39) |
I4351T |
possibly damaging |
Het |
| Ash1l |
T |
C |
3: 88,914,659 (GRCm39) |
L1763P |
probably benign |
Het |
| Aspn |
T |
C |
13: 49,710,849 (GRCm39) |
S165P |
possibly damaging |
Het |
| Atg13 |
A |
T |
2: 91,510,335 (GRCm39) |
V349E |
probably damaging |
Het |
| Atp1b2 |
T |
A |
11: 69,493,309 (GRCm39) |
|
probably null |
Het |
| B3glct |
A |
T |
5: 149,677,604 (GRCm39) |
D411V |
probably damaging |
Het |
| Bcar3 |
A |
T |
3: 122,316,840 (GRCm39) |
I255F |
probably damaging |
Het |
| Cacna1b |
G |
A |
2: 24,608,148 (GRCm39) |
|
probably benign |
Het |
| Cep164 |
T |
G |
9: 45,690,198 (GRCm39) |
E675A |
possibly damaging |
Het |
| Chd1l |
C |
T |
3: 97,490,047 (GRCm39) |
E503K |
probably benign |
Het |
| Chst8 |
C |
A |
7: 34,447,593 (GRCm39) |
M8I |
possibly damaging |
Het |
| Clec4n |
A |
G |
6: 123,212,475 (GRCm39) |
E67G |
probably benign |
Het |
| Cobll1 |
A |
T |
2: 64,929,480 (GRCm39) |
D653E |
probably damaging |
Het |
| Col9a1 |
T |
C |
1: 24,276,579 (GRCm39) |
|
probably null |
Het |
| Crip2 |
T |
C |
12: 113,107,124 (GRCm39) |
L30P |
probably damaging |
Het |
| Ctbp1 |
C |
T |
5: 33,418,407 (GRCm39) |
V22I |
probably benign |
Het |
| Cwc22 |
T |
C |
2: 77,747,521 (GRCm39) |
|
probably benign |
Het |
| Cyp4a32 |
C |
A |
4: 115,460,147 (GRCm39) |
Y119* |
probably null |
Het |
| Dido1 |
G |
T |
2: 180,313,263 (GRCm39) |
A463E |
possibly damaging |
Het |
| Dnah7a |
G |
A |
1: 53,567,956 (GRCm39) |
P1880L |
probably benign |
Het |
| Dock2 |
T |
A |
11: 34,189,705 (GRCm39) |
T1489S |
probably benign |
Het |
| Dsp |
A |
G |
13: 38,375,907 (GRCm39) |
T1231A |
probably damaging |
Het |
| Eif2ak1 |
G |
T |
5: 143,810,717 (GRCm39) |
|
probably benign |
Het |
| Entrep1 |
G |
A |
19: 23,998,998 (GRCm39) |
T140M |
probably damaging |
Het |
| Epc1 |
A |
T |
18: 6,452,360 (GRCm39) |
M233K |
probably damaging |
Het |
| Gigyf2 |
A |
G |
1: 87,371,360 (GRCm39) |
|
probably benign |
Het |
| Greb1 |
T |
G |
12: 16,757,852 (GRCm39) |
H58P |
probably damaging |
Het |
| Gtpbp1 |
T |
C |
15: 79,597,649 (GRCm39) |
I348T |
possibly damaging |
Het |
| Hck |
A |
T |
2: 152,970,192 (GRCm39) |
N64Y |
probably benign |
Het |
| Herc2 |
T |
C |
7: 55,818,744 (GRCm39) |
S2812P |
probably damaging |
Het |
| Inpp4b |
T |
A |
8: 82,679,463 (GRCm39) |
|
probably null |
Het |
| Kcnq5 |
A |
C |
1: 21,475,248 (GRCm39) |
S473A |
probably benign |
Het |
| Lrat |
T |
G |
3: 82,810,676 (GRCm39) |
D115A |
probably damaging |
Het |
| Lyst |
A |
G |
13: 13,814,639 (GRCm39) |
I1131M |
possibly damaging |
Het |
| Man2a2 |
T |
C |
7: 80,018,310 (GRCm39) |
D160G |
probably benign |
Het |
| Mars1 |
T |
C |
10: 127,133,857 (GRCm39) |
D680G |
possibly damaging |
Het |
| Mat1a |
T |
C |
14: 40,843,797 (GRCm39) |
S339P |
probably damaging |
Het |
| Megf8 |
T |
C |
7: 25,042,081 (GRCm39) |
S1300P |
probably damaging |
Het |
| Mga |
T |
C |
2: 119,733,179 (GRCm39) |
L9S |
probably damaging |
Het |
| Mllt6 |
T |
C |
11: 97,563,277 (GRCm39) |
|
probably benign |
Het |
| Mrpl37 |
A |
G |
4: 106,921,692 (GRCm39) |
L179P |
probably benign |
Het |
| Mtnr1a |
G |
T |
8: 45,540,782 (GRCm39) |
V248L |
probably benign |
Het |
| Mylk |
T |
C |
16: 34,635,835 (GRCm39) |
S19P |
possibly damaging |
Het |
| Or11g1 |
A |
G |
14: 50,651,858 (GRCm39) |
T286A |
probably damaging |
Het |
| Pacc1 |
A |
G |
1: 191,080,559 (GRCm39) |
|
probably benign |
Het |
| Parp8 |
A |
T |
13: 117,161,886 (GRCm39) |
|
probably null |
Het |
| Pcnx2 |
T |
C |
8: 126,479,023 (GRCm39) |
D2075G |
probably damaging |
Het |
| Pigo |
A |
T |
4: 43,021,460 (GRCm39) |
I494K |
probably benign |
Het |
| Pkd1l1 |
A |
T |
11: 8,820,313 (GRCm39) |
D1217E |
probably benign |
Het |
| Pkhd1l1 |
T |
C |
15: 44,369,040 (GRCm39) |
V895A |
probably benign |
Het |
| Plcb4 |
A |
T |
2: 135,842,109 (GRCm39) |
H1031L |
possibly damaging |
Het |
| Plxnb1 |
A |
G |
9: 108,937,989 (GRCm39) |
K1245R |
probably null |
Het |
| Pold1 |
C |
T |
7: 44,192,181 (GRCm39) |
|
probably benign |
Het |
| Ptprq |
T |
C |
10: 107,498,423 (GRCm39) |
I885V |
probably damaging |
Het |
| Ptprz1 |
A |
G |
6: 23,050,473 (GRCm39) |
D1398G |
probably damaging |
Het |
| Pygm |
G |
A |
19: 6,439,917 (GRCm39) |
A364T |
probably benign |
Het |
| Rbl1 |
T |
C |
2: 157,035,018 (GRCm39) |
N354S |
probably benign |
Het |
| Scgb2b19 |
C |
T |
7: 32,979,037 (GRCm39) |
|
probably null |
Het |
| Slc26a8 |
C |
T |
17: 28,867,187 (GRCm39) |
V545M |
possibly damaging |
Het |
| Slc27a1 |
T |
A |
8: 72,036,757 (GRCm39) |
|
probably null |
Het |
| Smpd1 |
A |
G |
7: 105,205,881 (GRCm39) |
D416G |
possibly damaging |
Het |
| Sorbs3 |
A |
G |
14: 70,431,095 (GRCm39) |
V284A |
probably benign |
Het |
| Stfa2l1 |
T |
C |
16: 35,982,154 (GRCm39) |
V75A |
probably damaging |
Het |
| Syndig1 |
A |
G |
2: 149,772,841 (GRCm39) |
D166G |
probably damaging |
Het |
| Tcp10a |
G |
A |
17: 7,593,406 (GRCm39) |
|
probably null |
Het |
| Themis2 |
T |
A |
4: 132,510,212 (GRCm39) |
I663F |
possibly damaging |
Het |
| Thrap3 |
T |
C |
4: 126,070,129 (GRCm39) |
Q586R |
probably damaging |
Het |
| Tinag |
C |
A |
9: 76,952,798 (GRCm39) |
C62F |
probably damaging |
Het |
| Tmod1 |
T |
C |
4: 46,090,884 (GRCm39) |
Y146H |
probably damaging |
Het |
| Tmprss4 |
T |
A |
9: 45,095,683 (GRCm39) |
I54F |
possibly damaging |
Het |
| Tnks |
A |
C |
8: 35,301,757 (GRCm39) |
|
probably benign |
Het |
| Trim43a |
GATTTATTTATTTATTTATTTATTTATTTATTTATTTATT |
GATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATT |
9: 88,465,042 (GRCm39) |
|
probably benign |
Het |
| Trpc6 |
A |
G |
9: 8,680,538 (GRCm39) |
E844G |
probably benign |
Het |
| Ubtd2 |
C |
T |
11: 32,466,125 (GRCm39) |
R115W |
probably damaging |
Het |
| Ubxn6 |
T |
C |
17: 56,376,042 (GRCm39) |
D373G |
probably benign |
Het |
| Upf1 |
T |
A |
8: 70,794,174 (GRCm39) |
Q244L |
probably benign |
Het |
| Usp33 |
A |
G |
3: 152,074,271 (GRCm39) |
I372M |
probably damaging |
Het |
| Usp34 |
A |
G |
11: 23,301,629 (GRCm39) |
E351G |
probably damaging |
Het |
| Utrn |
A |
G |
10: 12,554,318 (GRCm39) |
|
probably benign |
Het |
| Vmn1r78 |
A |
G |
7: 11,886,508 (GRCm39) |
K40E |
possibly damaging |
Het |
| Vmn2r7 |
T |
A |
3: 64,632,223 (GRCm39) |
M80L |
probably benign |
Het |
| Vps13a |
G |
T |
19: 16,678,602 (GRCm39) |
Y1126* |
probably null |
Het |
| Wfdc11 |
T |
C |
2: 164,506,366 (GRCm39) |
N60S |
probably benign |
Het |
| Wnk2 |
C |
T |
13: 49,224,586 (GRCm39) |
D992N |
probably damaging |
Het |
| Zpbp2 |
C |
A |
11: 98,444,670 (GRCm39) |
T66K |
probably damaging |
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 |
|
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 |
|
R5503:Marf1
|
UTSW |
16 |
13,970,095 (GRCm39) |
missense |
probably damaging |
0.99 |
|
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'- CAAACACCCTCTGAACTTGAAGGCT -3'
(R):5'- TCTGACCCTGGTATGTGAGAAGCA -3'
Sequencing Primer
(F):5'- AGGCTTTGTCTACTTCCTTCATC -3'
(R):5'- CACTGCTTAACCAGGAGTATGTC -3'
|
| Posted On |
2014-03-14 |
Incidental Mutation