Incidental Mutation 'R0610:Marf1'
ID |
54658 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Marf1
|
Ensembl Gene |
ENSMUSG00000060657 |
Gene Name |
meiosis regulator and mRNA stability 1 |
Synonyms |
4921513D23Rik |
MMRRC Submission |
038799-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.219)
|
Stock # |
R0610 (G1)
|
Quality Score |
208 |
Status
|
Validated
|
Chromosome |
16 |
Chromosomal Location |
13927030-13977157 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 13960398 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Alanine to Threonine
at position 549
(A549T)
|
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: A549T
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000087770 Gene: ENSMUSG00000060657 AA Change: A549T
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 damaging
Transcript: ENSMUST00000229614
AA Change: A370T
PolyPhen 2
Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000231032
|
Meta Mutation Damage Score |
0.5302 |
Coding Region Coverage |
- 1x: 99.4%
- 3x: 98.9%
- 10x: 97.4%
- 20x: 94.7%
|
Validation Efficiency |
99% (97/98) |
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 |
4930433I11Rik |
A |
T |
7: 40,642,480 (GRCm39) |
T141S |
probably benign |
Het |
4930578I06Rik |
G |
A |
14: 64,223,714 (GRCm39) |
R21* |
probably null |
Het |
Abca15 |
A |
G |
7: 119,965,009 (GRCm39) |
E757G |
possibly damaging |
Het |
Abca5 |
T |
C |
11: 110,192,353 (GRCm39) |
T720A |
probably benign |
Het |
Actr5 |
T |
A |
2: 158,474,376 (GRCm39) |
|
probably null |
Het |
Adgrl3 |
T |
C |
5: 81,841,563 (GRCm39) |
|
probably benign |
Het |
Adra1a |
A |
G |
14: 66,875,241 (GRCm39) |
D72G |
probably damaging |
Het |
Ahcyl |
T |
C |
16: 45,974,264 (GRCm39) |
E371G |
probably damaging |
Het |
Ahnak |
G |
T |
19: 8,985,242 (GRCm39) |
L2175F |
probably benign |
Het |
AK157302 |
A |
G |
13: 21,679,833 (GRCm39) |
T120A |
possibly damaging |
Het |
Apol7a |
G |
A |
15: 77,273,454 (GRCm39) |
A336V |
probably benign |
Het |
Asic1 |
C |
A |
15: 99,596,780 (GRCm39) |
H525Q |
probably benign |
Het |
Atxn7l2 |
T |
C |
3: 108,112,090 (GRCm39) |
D335G |
possibly damaging |
Het |
Bpgm |
G |
T |
6: 34,481,284 (GRCm39) |
R227L |
possibly damaging |
Het |
Calm4 |
T |
A |
13: 3,888,320 (GRCm39) |
V142E |
possibly damaging |
Het |
Catsperg1 |
A |
T |
7: 28,890,044 (GRCm39) |
L721Q |
probably damaging |
Het |
Cdh26 |
A |
G |
2: 178,091,691 (GRCm39) |
I83M |
probably damaging |
Het |
Cep295 |
A |
C |
9: 15,234,050 (GRCm39) |
S2249A |
possibly damaging |
Het |
Cfhr4 |
G |
A |
1: 139,629,584 (GRCm39) |
T799I |
probably benign |
Het |
Cln3 |
A |
G |
7: 126,179,361 (GRCm39) |
F139L |
probably damaging |
Het |
Cmpk2 |
T |
A |
12: 26,528,055 (GRCm39) |
L424Q |
possibly damaging |
Het |
Col12a1 |
A |
T |
9: 79,615,130 (GRCm39) |
V53E |
probably benign |
Het |
Csmd1 |
G |
A |
8: 15,968,208 (GRCm39) |
R3140C |
possibly damaging |
Het |
Dagla |
A |
G |
19: 10,248,922 (GRCm39) |
W11R |
probably damaging |
Het |
Dbx2 |
C |
T |
15: 95,522,778 (GRCm39) |
V310M |
probably benign |
Het |
Disp2 |
T |
A |
2: 118,622,717 (GRCm39) |
C1150S |
probably benign |
Het |
Dock3 |
T |
C |
9: 106,900,987 (GRCm39) |
D326G |
probably damaging |
Het |
Dph1 |
G |
T |
11: 75,076,783 (GRCm39) |
|
probably benign |
Het |
Dyrk1b |
C |
A |
7: 27,886,059 (GRCm39) |
T594K |
probably damaging |
Het |
Evx2 |
C |
A |
2: 74,486,331 (GRCm39) |
A353S |
probably benign |
Het |
Garin1b |
T |
A |
6: 29,326,576 (GRCm39) |
V231E |
probably benign |
Het |
Greb1 |
A |
C |
12: 16,746,443 (GRCm39) |
S1276A |
probably benign |
Het |
Hhipl1 |
T |
A |
12: 108,285,661 (GRCm39) |
C490* |
probably null |
Het |
Hmmr |
G |
T |
11: 40,606,729 (GRCm39) |
T231K |
probably damaging |
Het |
Hspa4l |
A |
C |
3: 40,733,832 (GRCm39) |
E526D |
probably benign |
Het |
Ibsp |
A |
G |
5: 104,458,000 (GRCm39) |
E179G |
probably benign |
Het |
Ift140 |
C |
T |
17: 25,254,777 (GRCm39) |
A150V |
probably benign |
Het |
Igf2bp2 |
A |
G |
16: 21,889,059 (GRCm39) |
S416P |
probably benign |
Het |
Ighe |
T |
C |
12: 113,235,363 (GRCm39) |
K294E |
unknown |
Het |
Ino80 |
G |
A |
2: 119,213,441 (GRCm39) |
R1249C |
probably damaging |
Het |
Iqca1 |
C |
A |
1: 90,070,453 (GRCm39) |
G133V |
probably null |
Het |
Kng2 |
T |
A |
16: 22,819,344 (GRCm39) |
N231Y |
possibly damaging |
Het |
Lca5 |
A |
T |
9: 83,281,792 (GRCm39) |
C331S |
probably benign |
Het |
Lrrc1 |
A |
G |
9: 77,379,488 (GRCm39) |
I101T |
possibly damaging |
Het |
Lrrk2 |
A |
T |
15: 91,699,619 (GRCm39) |
I2489L |
probably benign |
Het |
Lyz3 |
A |
G |
10: 117,073,635 (GRCm39) |
F66S |
probably benign |
Het |
Mapk9 |
A |
C |
11: 49,754,400 (GRCm39) |
N51T |
probably benign |
Het |
Nek2 |
T |
A |
1: 191,554,627 (GRCm39) |
V113D |
probably damaging |
Het |
Nr4a3 |
C |
A |
4: 48,051,903 (GRCm39) |
A248E |
probably benign |
Het |
Nrp1 |
T |
C |
8: 129,229,099 (GRCm39) |
I859T |
probably damaging |
Het |
Olfm5 |
A |
T |
7: 103,803,652 (GRCm39) |
Y195* |
probably null |
Het |
Or13j1 |
T |
A |
4: 43,706,400 (GRCm39) |
H56L |
possibly damaging |
Het |
Or1n2 |
T |
A |
2: 36,797,671 (GRCm39) |
W238R |
probably damaging |
Het |
Or8g35 |
A |
G |
9: 39,381,119 (GRCm39) |
L301P |
probably damaging |
Het |
Oxtr |
C |
T |
6: 112,454,138 (GRCm39) |
R42Q |
probably benign |
Het |
Pcnx2 |
A |
G |
8: 126,566,426 (GRCm39) |
W1006R |
probably damaging |
Het |
Pdpk1 |
T |
C |
17: 24,317,145 (GRCm39) |
|
probably null |
Het |
Ryr2 |
T |
A |
13: 11,637,838 (GRCm39) |
H3731L |
probably damaging |
Het |
Sdr16c5 |
T |
G |
4: 4,016,116 (GRCm39) |
E103D |
possibly damaging |
Het |
Setdb2 |
A |
C |
14: 59,654,919 (GRCm39) |
S324A |
possibly damaging |
Het |
Slc17a3 |
C |
T |
13: 24,039,841 (GRCm39) |
S293F |
probably damaging |
Het |
Slc17a8 |
A |
T |
10: 89,412,488 (GRCm39) |
I499K |
probably damaging |
Het |
Slc2a9 |
T |
A |
5: 38,537,285 (GRCm39) |
I389F |
probably damaging |
Het |
Slc30a1 |
T |
C |
1: 191,641,536 (GRCm39) |
V394A |
probably damaging |
Het |
Slc41a2 |
A |
G |
10: 83,119,592 (GRCm39) |
I390T |
possibly damaging |
Het |
Slco1a1 |
A |
G |
6: 141,864,187 (GRCm39) |
|
probably null |
Het |
Slit2 |
A |
G |
5: 48,433,016 (GRCm39) |
K1053E |
possibly damaging |
Het |
Smarca2 |
T |
A |
19: 26,668,791 (GRCm39) |
L930Q |
probably damaging |
Het |
Snx6 |
T |
C |
12: 54,798,574 (GRCm39) |
H387R |
probably damaging |
Het |
Sox5 |
A |
T |
6: 143,779,165 (GRCm39) |
M622K |
possibly damaging |
Het |
Ston1 |
C |
A |
17: 88,942,709 (GRCm39) |
N38K |
possibly damaging |
Het |
Strbp |
C |
T |
2: 37,474,089 (GRCm39) |
V658I |
probably damaging |
Het |
Strn3 |
T |
C |
12: 51,657,231 (GRCm39) |
|
probably null |
Het |
Suco |
T |
G |
1: 161,687,072 (GRCm39) |
D96A |
probably benign |
Het |
Suco |
A |
G |
1: 161,691,601 (GRCm39) |
|
probably benign |
Het |
Sytl2 |
A |
T |
7: 90,030,061 (GRCm39) |
|
probably benign |
Het |
Tmem41b |
T |
A |
7: 109,580,290 (GRCm39) |
M25L |
probably benign |
Het |
Tmem41b |
T |
A |
7: 109,580,292 (GRCm39) |
D91V |
probably damaging |
Het |
Tmem50b |
C |
T |
16: 91,380,174 (GRCm39) |
A68T |
probably damaging |
Het |
Tmprss11e |
G |
A |
5: 86,855,206 (GRCm39) |
Q400* |
probably null |
Het |
Tnfsf13b |
G |
A |
8: 10,081,661 (GRCm39) |
|
probably null |
Het |
Trappc8 |
A |
G |
18: 20,970,245 (GRCm39) |
V916A |
probably damaging |
Het |
Trdn |
G |
T |
10: 33,350,449 (GRCm39) |
V673F |
probably damaging |
Het |
Trim28 |
G |
T |
7: 12,759,711 (GRCm39) |
|
probably benign |
Het |
Txnrd2 |
T |
C |
16: 18,291,632 (GRCm39) |
V427A |
probably damaging |
Het |
Uggt1 |
T |
C |
1: 36,204,587 (GRCm39) |
|
probably benign |
Het |
Vmn1r36 |
A |
G |
6: 66,693,404 (GRCm39) |
L51P |
probably damaging |
Het |
Vmn1r63 |
T |
A |
7: 5,806,063 (GRCm39) |
M190L |
possibly damaging |
Het |
Vmn2r116 |
T |
A |
17: 23,606,286 (GRCm39) |
N399K |
probably damaging |
Het |
Vmn2r117 |
T |
C |
17: 23,694,488 (GRCm39) |
N453S |
probably benign |
Het |
Wbp1l |
T |
A |
19: 46,643,109 (GRCm39) |
I370N |
probably damaging |
Het |
Zfp445 |
T |
C |
9: 122,682,046 (GRCm39) |
K632E |
probably benign |
Het |
Zfp850 |
C |
T |
7: 27,688,819 (GRCm39) |
R463H |
probably damaging |
Het |
Zyg11a |
A |
G |
4: 108,062,054 (GRCm39) |
L249P |
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 |
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 |
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'- CAGAATTTGCCTGCAACACTTTCCC -3'
(R):5'- GCCTAGCCGATTATTGGAAGCAGC -3'
Sequencing Primer
(F):5'- CTGGCATGGCTTTGACAC -3'
(R):5'- CTGAAGTGCAGACATGACTTGTTC -3'
|
Posted On |
2013-07-11 |