Incidental Mutation 'R9016:Mtcl1'
ID |
686035 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Mtcl1
|
Ensembl Gene |
ENSMUSG00000052105 |
Gene Name |
microtubule crosslinking factor 1 |
Synonyms |
1110012J17Rik, Soga2, t8219b25 |
MMRRC Submission |
068846-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.154)
|
Stock # |
R9016 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
17 |
Chromosomal Location |
66643977-66756745 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 66651062 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Serine
at position 1468
(T1468S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000083899
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000086693]
[ENSMUST00000097291]
[ENSMUST00000145347]
[ENSMUST00000177034]
|
AlphaFold |
Q3UHU5 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000086693
AA Change: T1468S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000083899 Gene: ENSMUSG00000052105 AA Change: T1468S
Domain | Start | End | E-Value | Type |
low complexity region
|
23 |
42 |
N/A |
INTRINSIC |
low complexity region
|
54 |
98 |
N/A |
INTRINSIC |
low complexity region
|
99 |
120 |
N/A |
INTRINSIC |
low complexity region
|
127 |
132 |
N/A |
INTRINSIC |
low complexity region
|
166 |
183 |
N/A |
INTRINSIC |
low complexity region
|
240 |
259 |
N/A |
INTRINSIC |
low complexity region
|
273 |
290 |
N/A |
INTRINSIC |
SCOP:d1fxkc_
|
332 |
466 |
3e-7 |
SMART |
Blast:BRLZ
|
339 |
362 |
1e-5 |
BLAST |
Pfam:DUF3166
|
493 |
587 |
1.8e-34 |
PFAM |
Pfam:DUF3166
|
622 |
714 |
3.8e-39 |
PFAM |
low complexity region
|
843 |
859 |
N/A |
INTRINSIC |
low complexity region
|
896 |
910 |
N/A |
INTRINSIC |
low complexity region
|
962 |
973 |
N/A |
INTRINSIC |
low complexity region
|
1049 |
1062 |
N/A |
INTRINSIC |
coiled coil region
|
1120 |
1159 |
N/A |
INTRINSIC |
Pfam:DUF4482
|
1220 |
1344 |
3e-40 |
PFAM |
low complexity region
|
1464 |
1476 |
N/A |
INTRINSIC |
low complexity region
|
1672 |
1681 |
N/A |
INTRINSIC |
low complexity region
|
1912 |
1924 |
N/A |
INTRINSIC |
low complexity region
|
1931 |
1943 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000097291
AA Change: T1468S
PolyPhen 2
Score 0.964 (Sensitivity: 0.78; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000094894 Gene: ENSMUSG00000052105 AA Change: T1468S
Domain | Start | End | E-Value | Type |
low complexity region
|
23 |
42 |
N/A |
INTRINSIC |
low complexity region
|
54 |
98 |
N/A |
INTRINSIC |
low complexity region
|
99 |
120 |
N/A |
INTRINSIC |
low complexity region
|
127 |
132 |
N/A |
INTRINSIC |
low complexity region
|
166 |
183 |
N/A |
INTRINSIC |
low complexity region
|
240 |
259 |
N/A |
INTRINSIC |
low complexity region
|
273 |
290 |
N/A |
INTRINSIC |
SCOP:d1fxkc_
|
332 |
466 |
3e-7 |
SMART |
Blast:BRLZ
|
339 |
362 |
1e-5 |
BLAST |
Pfam:DUF3166
|
492 |
588 |
1.8e-43 |
PFAM |
Pfam:DUF3166
|
621 |
716 |
5e-19 |
PFAM |
low complexity region
|
843 |
859 |
N/A |
INTRINSIC |
low complexity region
|
896 |
910 |
N/A |
INTRINSIC |
low complexity region
|
962 |
973 |
N/A |
INTRINSIC |
low complexity region
|
1049 |
1062 |
N/A |
INTRINSIC |
coiled coil region
|
1120 |
1159 |
N/A |
INTRINSIC |
Pfam:DUF4482
|
1220 |
1392 |
3.9e-49 |
PFAM |
low complexity region
|
1464 |
1476 |
N/A |
INTRINSIC |
low complexity region
|
1672 |
1681 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000145347
AA Change: T1019S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000121387 Gene: ENSMUSG00000052105 AA Change: T1019S
Domain | Start | End | E-Value | Type |
Pfam:DUF3166
|
43 |
139 |
9.1e-44 |
PFAM |
Pfam:DUF3166
|
172 |
267 |
2.5e-19 |
PFAM |
low complexity region
|
394 |
410 |
N/A |
INTRINSIC |
low complexity region
|
447 |
461 |
N/A |
INTRINSIC |
low complexity region
|
513 |
524 |
N/A |
INTRINSIC |
low complexity region
|
600 |
613 |
N/A |
INTRINSIC |
coiled coil region
|
671 |
710 |
N/A |
INTRINSIC |
Pfam:DUF4482
|
771 |
910 |
4.6e-49 |
PFAM |
low complexity region
|
1015 |
1027 |
N/A |
INTRINSIC |
low complexity region
|
1223 |
1232 |
N/A |
INTRINSIC |
low complexity region
|
1463 |
1475 |
N/A |
INTRINSIC |
low complexity region
|
1482 |
1494 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000177034
AA Change: T1165S
PolyPhen 2
Score 0.955 (Sensitivity: 0.79; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000135690 Gene: ENSMUSG00000052105 AA Change: T1165S
Domain | Start | End | E-Value | Type |
Pfam:DUF3166
|
140 |
236 |
1.5e-43 |
PFAM |
Pfam:DUF3166
|
269 |
364 |
4e-19 |
PFAM |
low complexity region
|
491 |
507 |
N/A |
INTRINSIC |
low complexity region
|
544 |
558 |
N/A |
INTRINSIC |
low complexity region
|
610 |
621 |
N/A |
INTRINSIC |
coiled coil region
|
642 |
674 |
N/A |
INTRINSIC |
low complexity region
|
738 |
751 |
N/A |
INTRINSIC |
coiled coil region
|
809 |
848 |
N/A |
INTRINSIC |
Pfam:DUF4482
|
909 |
1042 |
4e-49 |
PFAM |
low complexity region
|
1161 |
1173 |
N/A |
INTRINSIC |
low complexity region
|
1369 |
1378 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.0%
|
Validation Efficiency |
100% (75/75) |
MGI Phenotype |
PHENOTYPE: Global or Purkinje cell-specific homozygous knockout affects Purkinje cell axon and dendrite morphology, resulting in abnormal motor function. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaa2 |
C |
A |
18: 74,932,154 (GRCm39) |
S264R |
probably damaging |
Het |
Agap1 |
T |
C |
1: 89,694,188 (GRCm39) |
|
probably null |
Het |
Amer2 |
G |
C |
14: 60,617,376 (GRCm39) |
D524H |
probably damaging |
Het |
Ank1 |
G |
A |
8: 23,606,264 (GRCm39) |
G1219S |
probably null |
Het |
Apob |
C |
T |
12: 8,035,408 (GRCm39) |
|
silent |
Het |
Atg2a |
G |
C |
19: 6,300,111 (GRCm39) |
A640P |
probably damaging |
Het |
AW209491 |
G |
A |
13: 14,812,193 (GRCm39) |
V349M |
probably damaging |
Het |
Bmpr2 |
C |
T |
1: 59,854,460 (GRCm39) |
T103I |
probably damaging |
Het |
Btaf1 |
A |
C |
19: 36,971,705 (GRCm39) |
E1231D |
probably benign |
Het |
Btbd7 |
T |
C |
12: 102,751,417 (GRCm39) |
R1116G |
probably damaging |
Het |
Catsperg1 |
A |
T |
7: 28,891,162 (GRCm39) |
M627K |
probably benign |
Het |
Cdk7 |
G |
A |
13: 100,854,126 (GRCm39) |
T121I |
probably benign |
Het |
Csmd3 |
T |
A |
15: 47,522,438 (GRCm39) |
T1833S |
|
Het |
Dapk3 |
A |
T |
10: 81,028,266 (GRCm39) |
R279W |
probably damaging |
Het |
Dennd2b |
A |
C |
7: 109,139,642 (GRCm39) |
D645E |
possibly damaging |
Het |
Dnah9 |
T |
C |
11: 65,998,856 (GRCm39) |
E1064G |
probably damaging |
Het |
Dner |
T |
C |
1: 84,673,226 (GRCm39) |
E75G |
probably benign |
Het |
Dnmt1 |
T |
C |
9: 20,847,855 (GRCm39) |
E229G |
possibly damaging |
Het |
Fam171a1 |
G |
A |
2: 3,227,434 (GRCm39) |
A856T |
probably benign |
Het |
Fam186b |
G |
A |
15: 99,177,616 (GRCm39) |
A570V |
probably damaging |
Het |
Fen1 |
A |
T |
19: 10,178,306 (GRCm39) |
V46D |
probably damaging |
Het |
Ffar3 |
T |
C |
7: 30,554,454 (GRCm39) |
R289G |
probably damaging |
Het |
Fhod3 |
G |
A |
18: 25,243,136 (GRCm39) |
E1165K |
possibly damaging |
Het |
Fras1 |
A |
T |
5: 96,783,923 (GRCm39) |
H809L |
probably damaging |
Het |
Gbp7 |
A |
T |
3: 142,249,870 (GRCm39) |
E447V |
probably benign |
Het |
Gja8 |
T |
C |
3: 96,827,521 (GRCm39) |
D47G |
probably damaging |
Het |
Gm5795 |
A |
G |
14: 14,883,574 (GRCm39) |
K144E |
probably benign |
Het |
Gm7298 |
A |
C |
6: 121,758,800 (GRCm39) |
Q1139H |
possibly damaging |
Het |
Gpa33 |
A |
T |
1: 165,992,730 (GRCm39) |
Y281F |
probably damaging |
Het |
H2-M10.5 |
G |
A |
17: 37,084,226 (GRCm39) |
E63K |
possibly damaging |
Het |
Hgf |
T |
C |
5: 16,823,956 (GRCm39) |
W718R |
probably damaging |
Het |
Ifna5 |
C |
G |
4: 88,754,046 (GRCm39) |
D95E |
probably benign |
Het |
Ifnar2 |
T |
C |
16: 91,201,073 (GRCm39) |
L438P |
possibly damaging |
Het |
Ints1 |
T |
C |
5: 139,744,326 (GRCm39) |
T1479A |
probably benign |
Het |
Kif1a |
C |
T |
1: 92,953,395 (GRCm39) |
R1263H |
probably damaging |
Het |
Ltbp2 |
T |
C |
12: 84,856,467 (GRCm39) |
T686A |
probably benign |
Het |
Med12l |
A |
T |
3: 59,163,294 (GRCm39) |
E1307V |
probably damaging |
Het |
Myo9a |
C |
T |
9: 59,775,427 (GRCm39) |
Q1013* |
probably null |
Het |
Nckap5 |
T |
C |
1: 126,623,491 (GRCm39) |
M1V |
probably null |
Het |
Nos3 |
G |
T |
5: 24,588,639 (GRCm39) |
V1122F |
probably damaging |
Het |
Nxt2 |
C |
T |
X: 141,020,747 (GRCm39) |
A118V |
possibly damaging |
Het |
Odad1 |
T |
G |
7: 45,585,988 (GRCm39) |
C128W |
probably damaging |
Het |
Or1x6 |
G |
A |
11: 50,938,938 (GRCm39) |
M1I |
probably null |
Het |
Or52n4 |
A |
T |
7: 104,293,828 (GRCm39) |
C250* |
probably null |
Het |
Oscar |
A |
G |
7: 3,619,072 (GRCm39) |
V2A |
probably benign |
Het |
P2rx6 |
T |
A |
16: 17,385,304 (GRCm39) |
H132Q |
possibly damaging |
Het |
Pakap |
T |
C |
4: 57,637,857 (GRCm39) |
C12R |
unknown |
Het |
Pde6b |
T |
A |
5: 108,536,592 (GRCm39) |
M96K |
possibly damaging |
Het |
Polq |
T |
A |
16: 36,843,159 (GRCm39) |
L231Q |
probably damaging |
Het |
Pramel23 |
T |
C |
4: 143,423,899 (GRCm39) |
I297V |
possibly damaging |
Het |
Prrc2a |
G |
A |
17: 35,378,844 (GRCm39) |
T399I |
unknown |
Het |
Rapsn |
A |
G |
2: 90,867,172 (GRCm39) |
D158G |
probably damaging |
Het |
Rcor1 |
T |
A |
12: 111,047,933 (GRCm39) |
|
probably benign |
Het |
Sema4d |
G |
T |
13: 51,867,794 (GRCm39) |
P186T |
probably damaging |
Het |
Skic2 |
A |
C |
17: 35,063,640 (GRCm39) |
L601R |
probably damaging |
Het |
Slc4a7 |
G |
A |
14: 14,773,241 (GRCm38) |
R737Q |
probably damaging |
Het |
Sorbs2 |
T |
G |
8: 46,248,774 (GRCm39) |
V675G |
probably benign |
Het |
Sox15 |
T |
G |
11: 69,546,529 (GRCm39) |
Y111D |
probably damaging |
Het |
Spen |
C |
T |
4: 141,200,938 (GRCm39) |
C2563Y |
probably damaging |
Het |
Taf8 |
A |
T |
17: 47,807,527 (GRCm39) |
D153E |
probably damaging |
Het |
Tet3 |
G |
A |
6: 83,345,253 (GRCm39) |
A1728V |
probably damaging |
Het |
Tmem232 |
A |
T |
17: 65,737,778 (GRCm39) |
D427E |
probably benign |
Het |
Tmem53 |
T |
C |
4: 117,125,451 (GRCm39) |
I188T |
probably benign |
Het |
Tnc |
T |
G |
4: 63,935,331 (GRCm39) |
D535A |
probably benign |
Het |
Tnfrsf11a |
G |
A |
1: 105,754,854 (GRCm39) |
A309T |
possibly damaging |
Het |
Tnik |
G |
A |
3: 28,692,544 (GRCm39) |
G867R |
probably damaging |
Het |
Uba3 |
A |
T |
6: 97,162,694 (GRCm39) |
C367* |
probably null |
Het |
Vmn1r235 |
G |
T |
17: 21,481,969 (GRCm39) |
S98I |
possibly damaging |
Het |
Vmn2r15 |
T |
C |
5: 109,442,109 (GRCm39) |
E108G |
probably benign |
Het |
Xrra1 |
T |
A |
7: 99,525,462 (GRCm39) |
I127N |
probably benign |
Het |
Zc3h18 |
G |
A |
8: 123,129,963 (GRCm39) |
R447Q |
unknown |
Het |
Zcwpw1 |
C |
A |
5: 137,798,340 (GRCm39) |
P179Q |
probably damaging |
Het |
Zfp526 |
C |
T |
7: 24,925,264 (GRCm39) |
H508Y |
probably damaging |
Het |
Zfp583 |
T |
C |
7: 6,320,404 (GRCm39) |
K203E |
probably benign |
Het |
Zfp979 |
A |
G |
4: 147,697,504 (GRCm39) |
C402R |
possibly damaging |
Het |
Zxdc |
A |
G |
6: 90,359,254 (GRCm39) |
T629A |
probably damaging |
Het |
|
Other mutations in Mtcl1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Mtcl1
|
APN |
17 |
66,651,314 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01774:Mtcl1
|
APN |
17 |
66,692,880 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01918:Mtcl1
|
APN |
17 |
66,675,263 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02000:Mtcl1
|
APN |
17 |
66,661,185 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02074:Mtcl1
|
APN |
17 |
66,673,463 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02338:Mtcl1
|
APN |
17 |
66,686,965 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02597:Mtcl1
|
APN |
17 |
66,645,016 (GRCm39) |
missense |
probably benign |
|
IGL03034:Mtcl1
|
APN |
17 |
66,651,193 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03120:Mtcl1
|
APN |
17 |
66,686,378 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03184:Mtcl1
|
APN |
17 |
66,661,209 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03240:Mtcl1
|
APN |
17 |
66,645,014 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03294:Mtcl1
|
APN |
17 |
66,645,014 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03332:Mtcl1
|
APN |
17 |
66,645,014 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4378001:Mtcl1
|
UTSW |
17 |
66,745,274 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4520001:Mtcl1
|
UTSW |
17 |
66,692,907 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0110:Mtcl1
|
UTSW |
17 |
66,665,109 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0113:Mtcl1
|
UTSW |
17 |
66,661,237 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0321:Mtcl1
|
UTSW |
17 |
66,686,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R0366:Mtcl1
|
UTSW |
17 |
66,645,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R0629:Mtcl1
|
UTSW |
17 |
66,645,137 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1466:Mtcl1
|
UTSW |
17 |
66,687,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Mtcl1
|
UTSW |
17 |
66,687,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Mtcl1
|
UTSW |
17 |
66,755,322 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Mtcl1
|
UTSW |
17 |
66,755,322 (GRCm39) |
missense |
probably damaging |
1.00 |
R1471:Mtcl1
|
UTSW |
17 |
66,686,143 (GRCm39) |
missense |
probably damaging |
0.96 |
R1650:Mtcl1
|
UTSW |
17 |
66,692,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R1754:Mtcl1
|
UTSW |
17 |
66,687,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R1855:Mtcl1
|
UTSW |
17 |
66,686,509 (GRCm39) |
missense |
probably benign |
|
R1882:Mtcl1
|
UTSW |
17 |
66,686,315 (GRCm39) |
missense |
probably benign |
0.01 |
R1935:Mtcl1
|
UTSW |
17 |
66,686,409 (GRCm39) |
missense |
probably benign |
0.10 |
R2063:Mtcl1
|
UTSW |
17 |
66,653,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R2132:Mtcl1
|
UTSW |
17 |
66,650,618 (GRCm39) |
missense |
probably benign |
0.04 |
R2197:Mtcl1
|
UTSW |
17 |
66,673,427 (GRCm39) |
missense |
probably benign |
|
R3196:Mtcl1
|
UTSW |
17 |
66,650,829 (GRCm39) |
missense |
probably benign |
0.07 |
R3877:Mtcl1
|
UTSW |
17 |
66,649,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R4116:Mtcl1
|
UTSW |
17 |
66,673,476 (GRCm39) |
missense |
probably benign |
|
R4204:Mtcl1
|
UTSW |
17 |
66,745,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R4373:Mtcl1
|
UTSW |
17 |
66,687,074 (GRCm39) |
missense |
probably benign |
0.05 |
R4396:Mtcl1
|
UTSW |
17 |
66,651,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R4591:Mtcl1
|
UTSW |
17 |
66,655,506 (GRCm39) |
missense |
probably benign |
0.07 |
R4610:Mtcl1
|
UTSW |
17 |
66,684,882 (GRCm39) |
missense |
probably benign |
0.04 |
R4681:Mtcl1
|
UTSW |
17 |
66,756,139 (GRCm39) |
missense |
unknown |
|
R4922:Mtcl1
|
UTSW |
17 |
66,655,474 (GRCm39) |
missense |
probably benign |
0.29 |
R4992:Mtcl1
|
UTSW |
17 |
66,649,834 (GRCm39) |
missense |
probably damaging |
0.99 |
R5169:Mtcl1
|
UTSW |
17 |
66,650,818 (GRCm39) |
missense |
probably benign |
0.00 |
R5542:Mtcl1
|
UTSW |
17 |
66,691,354 (GRCm39) |
intron |
probably benign |
|
R5804:Mtcl1
|
UTSW |
17 |
66,650,132 (GRCm39) |
missense |
probably benign |
0.03 |
R5998:Mtcl1
|
UTSW |
17 |
66,675,275 (GRCm39) |
missense |
probably damaging |
0.99 |
R6163:Mtcl1
|
UTSW |
17 |
66,686,326 (GRCm39) |
missense |
probably benign |
0.10 |
R6191:Mtcl1
|
UTSW |
17 |
66,650,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R6254:Mtcl1
|
UTSW |
17 |
66,665,129 (GRCm39) |
missense |
probably benign |
0.02 |
R6260:Mtcl1
|
UTSW |
17 |
66,650,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R6524:Mtcl1
|
UTSW |
17 |
66,655,280 (GRCm39) |
missense |
probably benign |
0.15 |
R6884:Mtcl1
|
UTSW |
17 |
66,745,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R7199:Mtcl1
|
UTSW |
17 |
66,647,534 (GRCm39) |
missense |
probably benign |
0.13 |
R7431:Mtcl1
|
UTSW |
17 |
66,649,901 (GRCm39) |
nonsense |
probably null |
|
R7479:Mtcl1
|
UTSW |
17 |
66,686,485 (GRCm39) |
missense |
probably benign |
|
R7564:Mtcl1
|
UTSW |
17 |
66,678,322 (GRCm39) |
missense |
probably benign |
|
R7608:Mtcl1
|
UTSW |
17 |
66,650,300 (GRCm39) |
missense |
probably damaging |
0.96 |
R7691:Mtcl1
|
UTSW |
17 |
66,687,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R7847:Mtcl1
|
UTSW |
17 |
66,651,328 (GRCm39) |
missense |
probably damaging |
0.96 |
R7908:Mtcl1
|
UTSW |
17 |
66,678,325 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8262:Mtcl1
|
UTSW |
17 |
66,650,653 (GRCm39) |
missense |
probably damaging |
0.99 |
R8324:Mtcl1
|
UTSW |
17 |
66,743,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R8477:Mtcl1
|
UTSW |
17 |
66,684,942 (GRCm39) |
missense |
probably benign |
0.10 |
R8927:Mtcl1
|
UTSW |
17 |
66,755,628 (GRCm39) |
missense |
probably benign |
0.00 |
R8928:Mtcl1
|
UTSW |
17 |
66,755,628 (GRCm39) |
missense |
probably benign |
0.00 |
R9048:Mtcl1
|
UTSW |
17 |
66,678,331 (GRCm39) |
missense |
probably benign |
0.01 |
R9059:Mtcl1
|
UTSW |
17 |
66,650,606 (GRCm39) |
missense |
probably benign |
0.04 |
R9221:Mtcl1
|
UTSW |
17 |
66,650,879 (GRCm39) |
missense |
probably benign |
0.00 |
R9327:Mtcl1
|
UTSW |
17 |
66,645,130 (GRCm39) |
missense |
probably damaging |
0.96 |
R9398:Mtcl1
|
UTSW |
17 |
66,755,462 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9762:Mtcl1
|
UTSW |
17 |
66,673,347 (GRCm39) |
missense |
probably benign |
0.00 |
X0065:Mtcl1
|
UTSW |
17 |
66,686,602 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Mtcl1
|
UTSW |
17 |
66,650,723 (GRCm39) |
missense |
probably benign |
0.20 |
Z1176:Mtcl1
|
UTSW |
17 |
66,686,455 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Mtcl1
|
UTSW |
17 |
66,651,290 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- CTCTGCTCATAGGAAAGGGG -3'
(R):5'- AAGGAGGATGTCACTCCACC -3'
Sequencing Primer
(F):5'- TCATAGGAAAGGGGCCCTC -3'
(R):5'- GTCTCCCGACGACTTGAAATACATTG -3'
|
Posted On |
2021-10-11 |