Incidental Mutation 'R5888:Mink1'
ID |
457817 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Mink1
|
Ensembl Gene |
ENSMUSG00000020827 |
Gene Name |
misshapen-like kinase 1 (zebrafish) |
Synonyms |
Misshapen/NIKs-related kinase, Map4k6, Ysk2, MINK |
MMRRC Submission |
044089-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R5888 (G1)
|
Quality Score |
191 |
Status
|
Validated
|
Chromosome |
11 |
Chromosomal Location |
70453707-70505309 bp(+) (GRCm39) |
Type of Mutation |
unclassified |
DNA Base Change (assembly) |
A to T
at 70500885 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000014753]
[ENSMUST00000072237]
[ENSMUST00000072873]
[ENSMUST00000079244]
[ENSMUST00000102556]
[ENSMUST00000102558]
[ENSMUST00000102559]
|
AlphaFold |
Q9JM52 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000014753
|
SMART Domains |
Protein: ENSMUSP00000014753 Gene: ENSMUSG00000014609
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
Pfam:Neur_chan_LBD
|
24 |
240 |
2.9e-65 |
PFAM |
Pfam:Neur_chan_memb
|
247 |
475 |
6.5e-58 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000072237
|
SMART Domains |
Protein: ENSMUSP00000072091 Gene: ENSMUSG00000020827
Domain | Start | End | E-Value | Type |
S_TKc
|
25 |
289 |
1.86e-91 |
SMART |
low complexity region
|
307 |
338 |
N/A |
INTRINSIC |
coiled coil region
|
351 |
496 |
N/A |
INTRINSIC |
low complexity region
|
557 |
569 |
N/A |
INTRINSIC |
low complexity region
|
620 |
633 |
N/A |
INTRINSIC |
low complexity region
|
646 |
659 |
N/A |
INTRINSIC |
low complexity region
|
719 |
738 |
N/A |
INTRINSIC |
low complexity region
|
837 |
874 |
N/A |
INTRINSIC |
CNH
|
1026 |
1324 |
1.58e-113 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000072873
|
SMART Domains |
Protein: ENSMUSP00000072649 Gene: ENSMUSG00000020827
Domain | Start | End | E-Value | Type |
S_TKc
|
25 |
289 |
1.86e-91 |
SMART |
low complexity region
|
307 |
338 |
N/A |
INTRINSIC |
coiled coil region
|
351 |
496 |
N/A |
INTRINSIC |
low complexity region
|
557 |
569 |
N/A |
INTRINSIC |
low complexity region
|
620 |
633 |
N/A |
INTRINSIC |
low complexity region
|
646 |
659 |
N/A |
INTRINSIC |
low complexity region
|
719 |
738 |
N/A |
INTRINSIC |
low complexity region
|
829 |
853 |
N/A |
INTRINSIC |
CNH
|
1019 |
1317 |
1.58e-113 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000079244
|
SMART Domains |
Protein: ENSMUSP00000078234 Gene: ENSMUSG00000020827
Domain | Start | End | E-Value | Type |
S_TKc
|
25 |
289 |
1.86e-91 |
SMART |
low complexity region
|
314 |
338 |
N/A |
INTRINSIC |
coiled coil region
|
348 |
493 |
N/A |
INTRINSIC |
low complexity region
|
554 |
566 |
N/A |
INTRINSIC |
low complexity region
|
617 |
630 |
N/A |
INTRINSIC |
low complexity region
|
643 |
656 |
N/A |
INTRINSIC |
low complexity region
|
716 |
735 |
N/A |
INTRINSIC |
low complexity region
|
826 |
850 |
N/A |
INTRINSIC |
CNH
|
1016 |
1314 |
1.58e-113 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000102556
|
SMART Domains |
Protein: ENSMUSP00000099616 Gene: ENSMUSG00000014609
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
Pfam:Neur_chan_LBD
|
24 |
240 |
5.4e-65 |
PFAM |
Pfam:Neur_chan_memb
|
247 |
474 |
2.9e-53 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000102558
|
SMART Domains |
Protein: ENSMUSP00000099618 Gene: ENSMUSG00000020827
Domain | Start | End | E-Value | Type |
S_TKc
|
25 |
289 |
1.86e-91 |
SMART |
low complexity region
|
307 |
338 |
N/A |
INTRINSIC |
coiled coil region
|
351 |
496 |
N/A |
INTRINSIC |
low complexity region
|
557 |
569 |
N/A |
INTRINSIC |
low complexity region
|
620 |
633 |
N/A |
INTRINSIC |
low complexity region
|
646 |
659 |
N/A |
INTRINSIC |
low complexity region
|
792 |
816 |
N/A |
INTRINSIC |
CNH
|
982 |
1280 |
1.58e-113 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000142650
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000153503
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000152857
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000134836
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000125853
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000132208
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000135920
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000149845
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000178764
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000102559
|
SMART Domains |
Protein: ENSMUSP00000099619 Gene: ENSMUSG00000020827
Domain | Start | End | E-Value | Type |
S_TKc
|
25 |
289 |
1.86e-91 |
SMART |
low complexity region
|
307 |
338 |
N/A |
INTRINSIC |
coiled coil region
|
351 |
496 |
N/A |
INTRINSIC |
low complexity region
|
557 |
569 |
N/A |
INTRINSIC |
low complexity region
|
620 |
633 |
N/A |
INTRINSIC |
low complexity region
|
646 |
659 |
N/A |
INTRINSIC |
low complexity region
|
800 |
824 |
N/A |
INTRINSIC |
CNH
|
990 |
1288 |
1.58e-113 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000136663
|
SMART Domains |
Protein: ENSMUSP00000117959 Gene: ENSMUSG00000020827
Domain | Start | End | E-Value | Type |
Pfam:Pkinase_Tyr
|
1 |
140 |
2.3e-22 |
PFAM |
Pfam:Pkinase
|
1 |
143 |
1.6e-30 |
PFAM |
low complexity region
|
161 |
192 |
N/A |
INTRINSIC |
coiled coil region
|
204 |
349 |
N/A |
INTRINSIC |
low complexity region
|
411 |
423 |
N/A |
INTRINSIC |
low complexity region
|
474 |
487 |
N/A |
INTRINSIC |
low complexity region
|
500 |
513 |
N/A |
INTRINSIC |
low complexity region
|
573 |
592 |
N/A |
INTRINSIC |
low complexity region
|
691 |
728 |
N/A |
INTRINSIC |
CNH
|
880 |
1178 |
1.58e-113 |
SMART |
|
Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.6%
- 10x: 98.2%
- 20x: 94.9%
|
Validation Efficiency |
94% (96/102) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a serine/threonine kinase belonging to the germinal center kinase (GCK) family. The protein is structurally similar to the kinases that are related to NIK and may belong to a distinct subfamily of NIK-related kinases within the GCK family. Studies of the mouse homolog indicate an up-regulation of expression in the course of postnatal mouse cerebral development and activation of the cJun N-terminal kinase (JNK) and the p38 pathways. [provided by RefSeq, Mar 2016]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy1 |
T |
A |
11: 7,089,095 (GRCm39) |
V503E |
possibly damaging |
Het |
Alk |
C |
A |
17: 72,181,938 (GRCm39) |
V1362L |
probably damaging |
Het |
Ankrd55 |
T |
A |
13: 112,492,453 (GRCm39) |
I208N |
possibly damaging |
Het |
Asap2 |
T |
A |
12: 21,268,191 (GRCm39) |
I319N |
probably damaging |
Het |
Atp11b |
T |
C |
3: 35,891,696 (GRCm39) |
I1036T |
probably benign |
Het |
B4gat1 |
T |
C |
19: 5,089,560 (GRCm39) |
F186L |
probably benign |
Het |
C3 |
T |
A |
17: 57,521,831 (GRCm39) |
T1079S |
probably damaging |
Het |
Cacul1 |
G |
T |
19: 60,525,902 (GRCm39) |
T287K |
possibly damaging |
Het |
Cbr3 |
G |
C |
16: 93,487,614 (GRCm39) |
G266R |
probably damaging |
Het |
Cd63 |
T |
A |
10: 128,748,160 (GRCm39) |
|
probably null |
Het |
Chd7 |
G |
A |
4: 8,866,382 (GRCm39) |
M851I |
probably damaging |
Het |
Chst13 |
T |
A |
6: 90,286,554 (GRCm39) |
H136L |
probably benign |
Het |
Cyp2d22 |
T |
C |
15: 82,258,014 (GRCm39) |
T179A |
probably benign |
Het |
Dclre1b |
A |
T |
3: 103,711,053 (GRCm39) |
V286E |
probably damaging |
Het |
Defb45 |
G |
A |
2: 152,435,154 (GRCm39) |
|
probably benign |
Het |
Dlg1 |
T |
C |
16: 31,610,704 (GRCm39) |
|
probably null |
Het |
Dock3 |
A |
G |
9: 106,901,002 (GRCm39) |
V321A |
probably benign |
Het |
Dytn |
A |
T |
1: 63,716,396 (GRCm39) |
V59E |
possibly damaging |
Het |
Efcab3 |
T |
C |
11: 104,612,227 (GRCm39) |
|
probably benign |
Het |
Eif2ak1 |
A |
G |
5: 143,823,733 (GRCm39) |
I393M |
probably damaging |
Het |
Fam83g |
A |
T |
11: 61,593,420 (GRCm39) |
E318V |
probably benign |
Het |
Fbxo34 |
T |
A |
14: 47,767,176 (GRCm39) |
F179I |
probably damaging |
Het |
Fmo5 |
T |
A |
3: 97,549,041 (GRCm39) |
Y230N |
probably benign |
Het |
Fzd9 |
T |
G |
5: 135,278,317 (GRCm39) |
|
probably null |
Het |
Gata2 |
T |
C |
6: 88,177,722 (GRCm39) |
S251P |
probably benign |
Het |
Gigyf1 |
A |
G |
5: 137,523,959 (GRCm39) |
D1043G |
probably damaging |
Het |
Gm10322 |
T |
A |
10: 59,452,125 (GRCm39) |
S81T |
probably benign |
Het |
Gm15517 |
A |
T |
7: 43,910,066 (GRCm39) |
|
probably benign |
Het |
Haus4 |
T |
C |
14: 54,781,676 (GRCm39) |
T232A |
probably benign |
Het |
Hgfac |
A |
T |
5: 35,202,751 (GRCm39) |
H417L |
probably damaging |
Het |
Iqgap2 |
T |
C |
13: 95,772,118 (GRCm39) |
K1354E |
possibly damaging |
Het |
Kcnk12 |
C |
A |
17: 88,054,077 (GRCm39) |
R195L |
probably benign |
Het |
Kcnn2 |
A |
T |
18: 45,725,412 (GRCm39) |
I303F |
probably damaging |
Het |
Kcnt1 |
T |
C |
2: 25,798,122 (GRCm39) |
F879S |
probably damaging |
Het |
Kndc1 |
T |
C |
7: 139,475,133 (GRCm39) |
F11L |
probably benign |
Het |
Kpna7 |
A |
G |
5: 144,926,605 (GRCm39) |
F449S |
probably damaging |
Het |
Krt77 |
G |
T |
15: 101,773,888 (GRCm39) |
N255K |
probably benign |
Het |
Lair1 |
A |
T |
7: 4,013,844 (GRCm39) |
D134E |
probably damaging |
Het |
Loxhd1 |
T |
C |
18: 77,490,211 (GRCm39) |
V1318A |
probably damaging |
Het |
Marchf10 |
A |
T |
11: 105,292,972 (GRCm39) |
V145D |
possibly damaging |
Het |
Mcpt1 |
T |
A |
14: 56,256,969 (GRCm39) |
M169K |
probably benign |
Het |
Mdc1 |
T |
A |
17: 36,158,712 (GRCm39) |
V364E |
probably benign |
Het |
Mfsd11 |
T |
C |
11: 116,762,210 (GRCm39) |
F270S |
probably damaging |
Het |
Mfsd4b2 |
T |
G |
10: 39,798,031 (GRCm39) |
D108A |
probably benign |
Het |
Mmp25 |
T |
C |
17: 23,850,048 (GRCm39) |
Y504C |
probably damaging |
Het |
Ms4a13 |
C |
T |
19: 11,168,870 (GRCm39) |
V52I |
probably benign |
Het |
Msh4 |
C |
T |
3: 153,573,360 (GRCm39) |
|
probably null |
Het |
Muc5b |
T |
G |
7: 141,412,158 (GRCm39) |
S1701R |
unknown |
Het |
Naalad2 |
A |
T |
9: 18,241,937 (GRCm39) |
S656T |
probably benign |
Het |
Ncapd2 |
T |
C |
6: 125,164,052 (GRCm39) |
Y64C |
probably damaging |
Het |
Ncapg2 |
T |
A |
12: 116,389,420 (GRCm39) |
S347T |
possibly damaging |
Het |
Ndufb11b |
T |
C |
15: 81,864,872 (GRCm39) |
S38P |
probably benign |
Het |
Nipal4 |
T |
C |
11: 46,042,166 (GRCm39) |
T172A |
probably damaging |
Het |
Nrros |
T |
C |
16: 31,961,905 (GRCm39) |
K652R |
probably benign |
Het |
Nrxn3 |
G |
T |
12: 89,478,855 (GRCm39) |
A983S |
possibly damaging |
Het |
Or4a76 |
T |
A |
2: 89,461,143 (GRCm39) |
Y33F |
probably damaging |
Het |
Or4ac1-ps1 |
T |
C |
2: 88,370,588 (GRCm39) |
|
noncoding transcript |
Het |
Or4c115 |
T |
A |
2: 88,928,269 (GRCm39) |
M1L |
probably damaging |
Het |
Or4k77 |
T |
C |
2: 111,199,088 (GRCm39) |
M37T |
probably benign |
Het |
Or51m1 |
A |
G |
7: 103,578,239 (GRCm39) |
T70A |
possibly damaging |
Het |
Or8g24 |
A |
T |
9: 38,989,263 (GRCm39) |
Y259* |
probably null |
Het |
Or8k37 |
A |
C |
2: 86,469,488 (GRCm39) |
L188R |
probably damaging |
Het |
P2rx4 |
T |
A |
5: 122,857,228 (GRCm39) |
S155T |
probably benign |
Het |
P2rx4 |
T |
G |
5: 122,865,271 (GRCm39) |
Y299D |
probably damaging |
Het |
Pcsk6 |
A |
T |
7: 65,693,372 (GRCm39) |
L7F |
probably null |
Het |
Pdss2 |
T |
C |
10: 43,097,793 (GRCm39) |
|
silent |
Het |
Pfkl |
A |
G |
10: 77,827,204 (GRCm39) |
V494A |
possibly damaging |
Het |
Prep |
G |
T |
10: 44,943,460 (GRCm39) |
D12Y |
possibly damaging |
Het |
Prg4 |
A |
G |
1: 150,328,101 (GRCm39) |
F188S |
probably damaging |
Het |
Ripor3 |
T |
C |
2: 167,839,207 (GRCm39) |
Y98C |
probably damaging |
Het |
Rnf216 |
T |
A |
5: 143,054,069 (GRCm39) |
|
probably null |
Het |
Rnf24 |
A |
G |
2: 131,164,165 (GRCm39) |
|
probably benign |
Het |
Rps18-ps6 |
G |
A |
13: 97,896,901 (GRCm39) |
R66* |
probably null |
Het |
Scn3a |
A |
G |
2: 65,327,742 (GRCm39) |
M916T |
probably benign |
Het |
Scnm1 |
T |
C |
3: 95,037,596 (GRCm39) |
I157V |
probably benign |
Het |
Sh2b3 |
C |
G |
5: 121,967,084 (GRCm39) |
R10P |
possibly damaging |
Het |
Slc25a27 |
T |
C |
17: 43,960,585 (GRCm39) |
D211G |
probably damaging |
Het |
Slc36a4 |
A |
T |
9: 15,638,324 (GRCm39) |
Y250F |
probably damaging |
Het |
Slc4a1 |
T |
A |
11: 102,247,351 (GRCm39) |
E448V |
probably damaging |
Het |
Slit1 |
C |
A |
19: 41,731,735 (GRCm39) |
C38F |
probably damaging |
Het |
Spock3 |
T |
A |
8: 63,808,334 (GRCm39) |
N410K |
unknown |
Het |
Supt20 |
G |
T |
3: 54,619,628 (GRCm39) |
W370L |
probably benign |
Het |
Tas2r139 |
T |
A |
6: 42,118,430 (GRCm39) |
N187K |
probably damaging |
Het |
Tbc1d9b |
G |
A |
11: 50,031,311 (GRCm39) |
V111I |
probably benign |
Het |
Thsd7b |
T |
A |
1: 130,138,057 (GRCm39) |
Y1578* |
probably null |
Het |
Tln2 |
T |
A |
9: 67,136,685 (GRCm39) |
I1267F |
probably damaging |
Het |
Tnk2 |
G |
A |
16: 32,490,185 (GRCm39) |
V363I |
probably damaging |
Het |
Ttc32 |
A |
G |
12: 9,085,870 (GRCm39) |
K139R |
possibly damaging |
Het |
Vmn1r30 |
G |
C |
6: 58,412,550 (GRCm39) |
T94S |
possibly damaging |
Het |
Vmn1r90 |
G |
A |
7: 14,295,780 (GRCm39) |
T106I |
probably damaging |
Het |
Zfp677 |
T |
A |
17: 21,618,520 (GRCm39) |
C526S |
probably damaging |
Het |
Zfp831 |
T |
G |
2: 174,485,420 (GRCm39) |
S32A |
probably benign |
Het |
|
Other mutations in Mink1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00501:Mink1
|
APN |
11 |
70,494,638 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00709:Mink1
|
APN |
11 |
70,503,845 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01064:Mink1
|
APN |
11 |
70,494,307 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02612:Mink1
|
APN |
11 |
70,488,052 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02797:Mink1
|
APN |
11 |
70,501,176 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03056:Mink1
|
APN |
11 |
70,503,409 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03066:Mink1
|
APN |
11 |
70,499,715 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03185:Mink1
|
APN |
11 |
70,494,686 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4498001:Mink1
|
UTSW |
11 |
70,489,714 (GRCm39) |
missense |
probably benign |
0.05 |
R0025:Mink1
|
UTSW |
11 |
70,503,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R0025:Mink1
|
UTSW |
11 |
70,503,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R0488:Mink1
|
UTSW |
11 |
70,488,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R0637:Mink1
|
UTSW |
11 |
70,492,502 (GRCm39) |
missense |
probably damaging |
0.96 |
R0828:Mink1
|
UTSW |
11 |
70,500,971 (GRCm39) |
nonsense |
probably null |
|
R1081:Mink1
|
UTSW |
11 |
70,497,861 (GRCm39) |
missense |
probably benign |
0.07 |
R1175:Mink1
|
UTSW |
11 |
70,502,166 (GRCm39) |
missense |
probably benign |
0.02 |
R1441:Mink1
|
UTSW |
11 |
70,497,940 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1532:Mink1
|
UTSW |
11 |
70,492,833 (GRCm39) |
missense |
probably null |
1.00 |
R1545:Mink1
|
UTSW |
11 |
70,489,717 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1634:Mink1
|
UTSW |
11 |
70,499,706 (GRCm39) |
missense |
probably benign |
0.00 |
R1932:Mink1
|
UTSW |
11 |
70,499,254 (GRCm39) |
critical splice donor site |
probably null |
|
R2033:Mink1
|
UTSW |
11 |
70,503,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R2184:Mink1
|
UTSW |
11 |
70,494,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R2267:Mink1
|
UTSW |
11 |
70,492,550 (GRCm39) |
splice site |
probably null |
|
R2268:Mink1
|
UTSW |
11 |
70,492,550 (GRCm39) |
splice site |
probably null |
|
R2859:Mink1
|
UTSW |
11 |
70,503,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R3713:Mink1
|
UTSW |
11 |
70,499,776 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3714:Mink1
|
UTSW |
11 |
70,499,776 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3715:Mink1
|
UTSW |
11 |
70,499,776 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3716:Mink1
|
UTSW |
11 |
70,498,587 (GRCm39) |
missense |
probably damaging |
0.98 |
R3717:Mink1
|
UTSW |
11 |
70,498,587 (GRCm39) |
missense |
probably damaging |
0.98 |
R4607:Mink1
|
UTSW |
11 |
70,496,893 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4735:Mink1
|
UTSW |
11 |
70,500,086 (GRCm39) |
splice site |
probably null |
|
R4790:Mink1
|
UTSW |
11 |
70,489,867 (GRCm39) |
missense |
probably damaging |
0.99 |
R4847:Mink1
|
UTSW |
11 |
70,492,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R4860:Mink1
|
UTSW |
11 |
70,502,418 (GRCm39) |
missense |
probably damaging |
0.98 |
R4860:Mink1
|
UTSW |
11 |
70,502,418 (GRCm39) |
missense |
probably damaging |
0.98 |
R5081:Mink1
|
UTSW |
11 |
70,495,970 (GRCm39) |
missense |
probably damaging |
0.98 |
R5310:Mink1
|
UTSW |
11 |
70,498,169 (GRCm39) |
missense |
probably benign |
0.33 |
R5677:Mink1
|
UTSW |
11 |
70,495,991 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5767:Mink1
|
UTSW |
11 |
70,496,901 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5795:Mink1
|
UTSW |
11 |
70,498,616 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5950:Mink1
|
UTSW |
11 |
70,500,412 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6024:Mink1
|
UTSW |
11 |
70,489,915 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6034:Mink1
|
UTSW |
11 |
70,497,866 (GRCm39) |
small deletion |
probably benign |
|
R6034:Mink1
|
UTSW |
11 |
70,497,866 (GRCm39) |
small deletion |
probably benign |
|
R6058:Mink1
|
UTSW |
11 |
70,502,546 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6144:Mink1
|
UTSW |
11 |
70,501,478 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6154:Mink1
|
UTSW |
11 |
70,500,927 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6218:Mink1
|
UTSW |
11 |
70,489,720 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6262:Mink1
|
UTSW |
11 |
70,494,151 (GRCm39) |
splice site |
probably null |
|
R6269:Mink1
|
UTSW |
11 |
70,489,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R6273:Mink1
|
UTSW |
11 |
70,502,261 (GRCm39) |
nonsense |
probably null |
|
R6301:Mink1
|
UTSW |
11 |
70,503,120 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6603:Mink1
|
UTSW |
11 |
70,500,419 (GRCm39) |
missense |
probably damaging |
0.96 |
R6876:Mink1
|
UTSW |
11 |
70,498,261 (GRCm39) |
missense |
probably benign |
0.02 |
R7030:Mink1
|
UTSW |
11 |
70,498,601 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7050:Mink1
|
UTSW |
11 |
70,503,158 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7094:Mink1
|
UTSW |
11 |
70,500,901 (GRCm39) |
splice site |
probably null |
|
R7135:Mink1
|
UTSW |
11 |
70,494,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R7238:Mink1
|
UTSW |
11 |
70,502,305 (GRCm39) |
critical splice donor site |
probably null |
|
R7320:Mink1
|
UTSW |
11 |
70,489,899 (GRCm39) |
missense |
probably benign |
0.23 |
R7396:Mink1
|
UTSW |
11 |
70,495,994 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7446:Mink1
|
UTSW |
11 |
70,500,455 (GRCm39) |
missense |
probably benign |
0.18 |
R7723:Mink1
|
UTSW |
11 |
70,503,736 (GRCm39) |
missense |
probably benign |
0.16 |
R7896:Mink1
|
UTSW |
11 |
70,503,108 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8058:Mink1
|
UTSW |
11 |
70,494,594 (GRCm39) |
nonsense |
probably null |
|
R8082:Mink1
|
UTSW |
11 |
70,504,103 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8160:Mink1
|
UTSW |
11 |
70,496,907 (GRCm39) |
nonsense |
probably null |
|
R8335:Mink1
|
UTSW |
11 |
70,500,401 (GRCm39) |
missense |
probably damaging |
0.97 |
R8353:Mink1
|
UTSW |
11 |
70,501,154 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8453:Mink1
|
UTSW |
11 |
70,501,154 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8732:Mink1
|
UTSW |
11 |
70,500,902 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9072:Mink1
|
UTSW |
11 |
70,499,207 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9073:Mink1
|
UTSW |
11 |
70,499,207 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9324:Mink1
|
UTSW |
11 |
70,502,477 (GRCm39) |
missense |
probably damaging |
0.98 |
R9596:Mink1
|
UTSW |
11 |
70,497,915 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
Predicted Primers |
PCR Primer
(F):5'- TCTATCAGCCTGAGACCCTG -3'
(R):5'- CATCAGGCAGGTTTGTGTAGC -3'
Sequencing Primer
(F):5'- AGCCTGAGACCCTGTCAGAC -3'
(R):5'- CCTCTTCAGGAGTCTAAAGTTAGAG -3'
|
Posted On |
2017-02-15 |