Incidental Mutation 'R7030:Mink1'
ID |
546256 |
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 |
045131-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R7030 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
11 |
Chromosomal Location |
70453707-70505309 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 70498601 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Isoleucine
at position 589
(V589I)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000099618
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000072237]
[ENSMUST00000072873]
[ENSMUST00000079244]
[ENSMUST00000102558]
[ENSMUST00000102559]
|
AlphaFold |
Q9JM52 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000072237
AA Change: V589I
PolyPhen 2
Score 0.408 (Sensitivity: 0.89; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000072091 Gene: ENSMUSG00000020827 AA Change: V589I
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
AA Change: V589I
PolyPhen 2
Score 0.326 (Sensitivity: 0.90; Specificity: 0.89)
|
SMART Domains |
Protein: ENSMUSP00000072649 Gene: ENSMUSG00000020827 AA Change: V589I
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
AA Change: V586I
PolyPhen 2
Score 0.326 (Sensitivity: 0.90; Specificity: 0.89)
|
SMART Domains |
Protein: ENSMUSP00000078234 Gene: ENSMUSG00000020827 AA Change: V586I
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 |
possibly damaging
Transcript: ENSMUST00000102558
AA Change: V589I
PolyPhen 2
Score 0.455 (Sensitivity: 0.89; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000099618 Gene: ENSMUSG00000020827 AA Change: V589I
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 |
probably benign
Transcript: ENSMUST00000102559
AA Change: V589I
PolyPhen 2
Score 0.326 (Sensitivity: 0.90; Specificity: 0.89)
|
SMART Domains |
Protein: ENSMUSP00000099619 Gene: ENSMUSG00000020827 AA Change: V589I
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 |
|
SMART Domains |
Protein: ENSMUSP00000117959 Gene: ENSMUSG00000020827 AA Change: V442I
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 |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000149845
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000178764
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 98.9%
|
Validation Efficiency |
98% (92/94) |
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: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AAdacl4fm3 |
G |
T |
4: 144,430,173 (GRCm39) |
A272D |
possibly damaging |
Het |
Abr |
A |
T |
11: 76,350,038 (GRCm39) |
I347N |
probably damaging |
Het |
Acbd4 |
T |
A |
11: 102,994,985 (GRCm39) |
L50Q |
probably damaging |
Het |
Acsl5 |
T |
G |
19: 55,261,251 (GRCm39) |
Y69* |
probably null |
Het |
Agtpbp1 |
G |
A |
13: 59,652,108 (GRCm39) |
T401I |
probably damaging |
Het |
Ap3m2 |
C |
T |
8: 23,289,807 (GRCm39) |
E99K |
probably damaging |
Het |
Arhgef28 |
A |
T |
13: 98,124,769 (GRCm39) |
S504R |
possibly damaging |
Het |
Arsj |
T |
A |
3: 126,232,752 (GRCm39) |
D499E |
probably damaging |
Het |
Bach1 |
G |
A |
16: 87,516,179 (GRCm39) |
R240Q |
probably benign |
Het |
Camk2b |
T |
C |
11: 5,939,575 (GRCm39) |
D232G |
probably damaging |
Het |
Casc3 |
C |
T |
11: 98,713,359 (GRCm39) |
P258S |
possibly damaging |
Het |
Catspere2 |
T |
A |
1: 177,845,280 (GRCm39) |
I100N |
probably damaging |
Het |
Ccdc80 |
T |
A |
16: 44,943,252 (GRCm39) |
N787K |
possibly damaging |
Het |
Celsr1 |
C |
A |
15: 85,789,679 (GRCm39) |
C2653F |
probably damaging |
Het |
Cep170 |
T |
C |
1: 176,584,051 (GRCm39) |
E11G |
probably damaging |
Het |
Chia1 |
A |
C |
3: 106,022,641 (GRCm39) |
N12H |
probably damaging |
Het |
Chrna4 |
T |
C |
2: 180,671,334 (GRCm39) |
T141A |
probably damaging |
Het |
Col25a1 |
T |
C |
3: 130,272,671 (GRCm39) |
|
probably null |
Het |
Dcstamp |
A |
T |
15: 39,622,929 (GRCm39) |
I417F |
probably damaging |
Het |
Dnah5 |
A |
G |
15: 28,238,738 (GRCm39) |
I427V |
probably benign |
Het |
Dnah5 |
A |
G |
15: 28,333,208 (GRCm39) |
E2203G |
probably benign |
Het |
Dnmt3c |
A |
T |
2: 153,559,345 (GRCm39) |
S409C |
probably damaging |
Het |
Dock6 |
A |
T |
9: 21,724,375 (GRCm39) |
M1541K |
probably damaging |
Het |
Dzip1l |
C |
T |
9: 99,547,888 (GRCm39) |
T714I |
probably benign |
Het |
Exoc6b |
T |
C |
6: 84,825,807 (GRCm39) |
R535G |
probably damaging |
Het |
Fam83h |
A |
G |
15: 75,876,588 (GRCm39) |
S250P |
probably benign |
Het |
Fat4 |
C |
T |
3: 39,036,107 (GRCm39) |
T3253I |
probably damaging |
Het |
Fer1l6 |
T |
A |
15: 58,501,227 (GRCm39) |
F1302I |
probably damaging |
Het |
Fmnl1 |
T |
G |
11: 103,085,600 (GRCm39) |
|
probably benign |
Het |
Gckr |
C |
A |
5: 31,459,554 (GRCm39) |
F201L |
possibly damaging |
Het |
Gm10036 |
A |
G |
18: 15,966,292 (GRCm39) |
T148A |
probably benign |
Het |
Gm5142 |
G |
A |
14: 59,415,909 (GRCm39) |
S83F |
probably benign |
Het |
Gpr37 |
A |
T |
6: 25,689,004 (GRCm39) |
V31D |
possibly damaging |
Het |
Gramd2b |
A |
T |
18: 56,618,321 (GRCm39) |
Y207F |
probably damaging |
Het |
Hr |
T |
C |
14: 70,801,124 (GRCm39) |
|
probably null |
Het |
Igf2r |
A |
G |
17: 12,952,753 (GRCm39) |
L231P |
probably damaging |
Het |
Ighv1-66 |
A |
T |
12: 115,557,157 (GRCm39) |
W3R |
probably damaging |
Het |
Insyn2b |
T |
A |
11: 34,352,030 (GRCm39) |
V24E |
probably damaging |
Het |
Kcnu1 |
T |
C |
8: 26,408,491 (GRCm39) |
S101P |
probably benign |
Het |
Klhl23 |
T |
G |
2: 69,664,310 (GRCm39) |
V553G |
probably damaging |
Het |
Lrp1 |
T |
C |
10: 127,388,745 (GRCm39) |
I3235V |
probably damaging |
Het |
Mb |
A |
T |
15: 76,900,256 (GRCm39) |
I57N |
probably damaging |
Het |
Micu1 |
T |
C |
10: 59,624,843 (GRCm39) |
I295T |
possibly damaging |
Het |
Mndal |
T |
C |
1: 173,703,160 (GRCm39) |
K82E |
probably damaging |
Het |
Mroh1 |
A |
C |
15: 76,321,517 (GRCm39) |
K1066T |
probably benign |
Het |
Muc5b |
T |
A |
7: 141,396,192 (GRCm39) |
N149K |
unknown |
Het |
Myo7b |
G |
T |
18: 32,104,626 (GRCm39) |
L1404I |
probably damaging |
Het |
Nlrc4 |
A |
G |
17: 74,753,001 (GRCm39) |
S461P |
probably damaging |
Het |
Nudt12 |
A |
T |
17: 59,310,348 (GRCm39) |
D418E |
probably benign |
Het |
Or2g7 |
T |
A |
17: 38,378,948 (GRCm39) |
D295E |
probably benign |
Het |
Or5g27 |
G |
T |
2: 85,409,746 (GRCm39) |
R54S |
possibly damaging |
Het |
Pcdha1 |
A |
G |
18: 37,292,326 (GRCm39) |
H817R |
probably damaging |
Het |
Pcdha4 |
A |
G |
18: 37,087,080 (GRCm39) |
Y421C |
probably damaging |
Het |
Pcf11 |
T |
C |
7: 92,306,886 (GRCm39) |
D1094G |
probably benign |
Het |
Pck2 |
A |
T |
14: 55,785,223 (GRCm39) |
D427V |
probably damaging |
Het |
Pclo |
A |
G |
5: 14,726,421 (GRCm39) |
T1760A |
probably benign |
Het |
Pdzk1ip1 |
T |
A |
4: 114,950,188 (GRCm39) |
Y83N |
probably damaging |
Het |
Pgs1 |
T |
C |
11: 117,893,312 (GRCm39) |
I213T |
probably damaging |
Het |
Plin4 |
T |
A |
17: 56,410,969 (GRCm39) |
T1021S |
probably damaging |
Het |
Plxnb1 |
T |
A |
9: 108,941,375 (GRCm39) |
I1677N |
probably damaging |
Het |
Pm20d2 |
T |
C |
4: 33,174,752 (GRCm39) |
E378G |
possibly damaging |
Het |
Prkcq |
T |
G |
2: 11,231,661 (GRCm39) |
|
probably null |
Het |
Psmd2 |
C |
T |
16: 20,480,883 (GRCm39) |
P780L |
probably damaging |
Het |
Pvr |
A |
G |
7: 19,639,105 (GRCm39) |
S392P |
possibly damaging |
Het |
Rad51ap2 |
G |
C |
12: 11,507,432 (GRCm39) |
L451F |
possibly damaging |
Het |
Rbm20 |
A |
G |
19: 53,823,197 (GRCm39) |
E598G |
probably damaging |
Het |
Rho |
A |
T |
6: 115,912,504 (GRCm39) |
N123Y |
possibly damaging |
Het |
Rictor |
T |
C |
15: 6,737,934 (GRCm39) |
|
probably null |
Het |
Rilpl2 |
T |
G |
5: 124,606,656 (GRCm39) |
K186T |
probably damaging |
Het |
Rps6ka4 |
A |
C |
19: 6,816,992 (GRCm39) |
L61R |
probably damaging |
Het |
Sds |
C |
A |
5: 120,618,890 (GRCm39) |
Q118K |
probably benign |
Het |
Septin1 |
C |
T |
7: 126,816,157 (GRCm39) |
R91K |
probably benign |
Het |
Sf3a3 |
A |
G |
4: 124,616,673 (GRCm39) |
Y185C |
probably damaging |
Het |
Shtn1 |
T |
C |
19: 58,998,266 (GRCm39) |
M376V |
possibly damaging |
Het |
Slc6a9 |
A |
G |
4: 117,714,633 (GRCm39) |
T189A |
possibly damaging |
Het |
Slc7a6 |
T |
G |
8: 106,922,606 (GRCm39) |
V464G |
possibly damaging |
Het |
Smg8 |
T |
A |
11: 86,975,919 (GRCm39) |
D554V |
probably damaging |
Het |
Sox8 |
A |
G |
17: 25,789,082 (GRCm39) |
|
probably null |
Het |
Spata31e4 |
G |
T |
13: 50,857,019 (GRCm39) |
V886L |
possibly damaging |
Het |
Spats2l |
T |
A |
1: 57,918,689 (GRCm39) |
V41D |
probably damaging |
Het |
Sult2a3 |
A |
T |
7: 13,801,493 (GRCm39) |
F282Y |
probably damaging |
Het |
Svs3a |
T |
G |
2: 164,132,091 (GRCm39) |
Y220D |
probably damaging |
Het |
Teddm1a |
T |
A |
1: 153,768,369 (GRCm39) |
Y278N |
probably damaging |
Het |
Tlk1 |
T |
C |
2: 70,552,272 (GRCm39) |
Y526C |
probably damaging |
Het |
Tmc3 |
T |
A |
7: 83,266,025 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
A |
2: 76,596,583 (GRCm39) |
E20110V |
probably damaging |
Het |
Tulp4 |
A |
G |
17: 6,264,941 (GRCm39) |
D235G |
probably damaging |
Het |
Usp50 |
T |
C |
2: 126,622,395 (GRCm39) |
Y55C |
possibly damaging |
Het |
Vmn1r224 |
T |
C |
17: 20,639,789 (GRCm39) |
L122P |
probably benign |
Het |
Vmn2r62 |
A |
G |
7: 42,438,473 (GRCm39) |
L121P |
possibly damaging |
Het |
Whrn |
G |
T |
4: 63,413,368 (GRCm39) |
|
probably benign |
Het |
Zer1 |
G |
T |
2: 30,001,033 (GRCm39) |
H129Q |
probably benign |
Het |
Zfand4 |
G |
A |
6: 116,282,618 (GRCm39) |
A64T |
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 |
R5888:Mink1
|
UTSW |
11 |
70,500,885 (GRCm39) |
unclassified |
probably benign |
|
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 |
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'- GTGTCTTCTGCGCACTACAG -3'
(R):5'- TCATTATCAGGCCGAACCCAG -3'
Sequencing Primer
(F):5'- GCGCACTACAGGGCACATC -3'
(R):5'- TGGCCCTTCAGAGGTGG -3'
|
Posted On |
2019-05-13 |