Incidental Mutation 'R1754:Mtcl1'
ID |
193894 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Mtcl1
|
Ensembl Gene |
ENSMUSG00000052105 |
Gene Name |
microtubule crosslinking factor 1 |
Synonyms |
1110012J17Rik, Soga2, t8219b25 |
MMRRC Submission |
039786-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.126)
|
Stock # |
R1754 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
17 |
Chromosomal Location |
66643977-66756745 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 66687178 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Lysine to Arginine
at position 576
(K576R)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000094894
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000086693]
[ENSMUST00000097291]
[ENSMUST00000145347]
[ENSMUST00000177034]
|
AlphaFold |
Q3UHU5 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000086693
AA Change: K576R
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000083899 Gene: ENSMUSG00000052105 AA Change: K576R
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: K576R
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000094894 Gene: ENSMUSG00000052105 AA Change: K576R
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 |
noncoding transcript
Transcript: ENSMUST00000134139
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000142154
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000144492
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000145347
AA Change: K127R
PolyPhen 2
Score 0.953 (Sensitivity: 0.79; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000121387 Gene: ENSMUSG00000052105 AA Change: K127R
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: K224R
PolyPhen 2
Score 0.953 (Sensitivity: 0.79; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000135690 Gene: ENSMUSG00000052105 AA Change: K224R
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: 97.5%
- 3x: 97.0%
- 10x: 95.6%
- 20x: 93.3%
|
Validation Efficiency |
|
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: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca2 |
T |
A |
2: 25,324,345 (GRCm39) |
L234M |
probably benign |
Het |
Abca3 |
G |
A |
17: 24,596,753 (GRCm39) |
S402N |
probably benign |
Het |
Acad12 |
A |
T |
5: 121,745,544 (GRCm39) |
V249D |
probably benign |
Het |
Acp4 |
T |
C |
7: 43,904,428 (GRCm39) |
I212V |
probably benign |
Het |
Actl6a |
T |
A |
3: 32,772,723 (GRCm39) |
V233D |
probably damaging |
Het |
Aire |
T |
A |
10: 77,866,124 (GRCm39) |
Q533L |
probably damaging |
Het |
Aldh3b3 |
T |
C |
19: 4,018,517 (GRCm39) |
S411P |
probably benign |
Het |
Amer2 |
A |
G |
14: 60,617,206 (GRCm39) |
K467R |
probably damaging |
Het |
Apol9b |
A |
T |
15: 77,619,962 (GRCm39) |
I253F |
probably benign |
Het |
Arid1b |
A |
G |
17: 5,329,476 (GRCm39) |
|
probably null |
Het |
Atp6v0a4 |
T |
C |
6: 38,044,764 (GRCm39) |
T494A |
probably benign |
Het |
Atp6v1b2 |
A |
G |
8: 69,554,613 (GRCm39) |
D106G |
probably benign |
Het |
Avpr1b |
T |
C |
1: 131,527,839 (GRCm39) |
S121P |
probably damaging |
Het |
Bcl11a |
A |
C |
11: 24,114,724 (GRCm39) |
E689A |
probably damaging |
Het |
Brpf3 |
T |
G |
17: 29,040,297 (GRCm39) |
L906R |
probably benign |
Het |
Btn1a1 |
T |
C |
13: 23,644,638 (GRCm39) |
K287E |
probably benign |
Het |
Cacna1i |
A |
G |
15: 80,255,730 (GRCm39) |
H871R |
probably damaging |
Het |
Cd14 |
A |
T |
18: 36,858,567 (GRCm39) |
L296Q |
probably damaging |
Het |
Col1a2 |
G |
A |
6: 4,518,822 (GRCm39) |
|
probably benign |
Het |
Colgalt1 |
G |
T |
8: 72,075,823 (GRCm39) |
W490L |
probably damaging |
Het |
Ctnna2 |
A |
G |
6: 77,613,732 (GRCm39) |
I273T |
possibly damaging |
Het |
Dnah7a |
A |
T |
1: 53,543,344 (GRCm39) |
D2275E |
probably benign |
Het |
Dnah7a |
A |
C |
1: 53,601,059 (GRCm39) |
|
probably null |
Het |
Egfem1 |
T |
C |
3: 29,722,482 (GRCm39) |
Y404H |
possibly damaging |
Het |
Esm1 |
A |
T |
13: 113,353,230 (GRCm39) |
N171Y |
probably damaging |
Het |
Exoc1 |
T |
G |
5: 76,708,169 (GRCm39) |
|
probably null |
Het |
Fam243 |
A |
G |
16: 92,117,919 (GRCm39) |
V123A |
probably damaging |
Het |
Fcho1 |
A |
G |
8: 72,163,890 (GRCm39) |
I580T |
probably benign |
Het |
Fgfr1 |
A |
G |
8: 26,060,226 (GRCm39) |
H552R |
probably damaging |
Het |
Fsbp |
A |
G |
4: 11,583,906 (GRCm39) |
R202G |
probably damaging |
Het |
Gabra6 |
A |
G |
11: 42,207,388 (GRCm39) |
V231A |
probably damaging |
Het |
Gmeb1 |
A |
G |
4: 131,959,338 (GRCm39) |
S239P |
probably benign |
Het |
Gnpat |
T |
A |
8: 125,603,745 (GRCm39) |
Y208N |
probably damaging |
Het |
Il21 |
T |
C |
3: 37,279,674 (GRCm39) |
K114R |
possibly damaging |
Het |
Inhbc |
T |
C |
10: 127,206,162 (GRCm39) |
D35G |
possibly damaging |
Het |
Inpp4b |
A |
T |
8: 82,497,440 (GRCm39) |
T87S |
probably damaging |
Het |
Kcns2 |
T |
C |
15: 34,839,663 (GRCm39) |
I342T |
possibly damaging |
Het |
Ky |
A |
T |
9: 102,419,126 (GRCm39) |
T378S |
possibly damaging |
Het |
Lcat |
CAT |
C |
8: 106,668,446 (GRCm39) |
|
probably null |
Het |
Lrrc8d |
T |
C |
5: 105,960,523 (GRCm39) |
V311A |
probably benign |
Het |
Mief1 |
A |
G |
15: 80,133,803 (GRCm39) |
I287V |
probably damaging |
Het |
Mrpl47 |
A |
G |
3: 32,784,233 (GRCm39) |
V179A |
probably benign |
Het |
Myh10 |
C |
A |
11: 68,703,884 (GRCm39) |
A1902E |
probably damaging |
Het |
Nlrp3 |
A |
G |
11: 59,449,228 (GRCm39) |
T837A |
possibly damaging |
Het |
Nr1i3 |
T |
C |
1: 171,044,963 (GRCm39) |
Y132H |
probably damaging |
Het |
Oit3 |
T |
C |
10: 59,263,762 (GRCm39) |
|
probably null |
Het |
Or12j4 |
A |
T |
7: 140,046,773 (GRCm39) |
I220F |
probably damaging |
Het |
Or2z2 |
A |
T |
11: 58,346,088 (GRCm39) |
M229K |
probably damaging |
Het |
Or4c100 |
A |
T |
2: 88,356,159 (GRCm39) |
R77S |
probably damaging |
Het |
Or5b113 |
T |
C |
19: 13,342,717 (GRCm39) |
S242P |
probably damaging |
Het |
Or5h25 |
T |
A |
16: 58,930,944 (GRCm39) |
I10F |
probably benign |
Het |
Or6k14 |
A |
G |
1: 173,927,599 (GRCm39) |
T192A |
probably benign |
Het |
Or7a42 |
T |
A |
10: 78,791,531 (GRCm39) |
V164E |
probably damaging |
Het |
Or9k2 |
G |
A |
10: 129,999,033 (GRCm39) |
T54I |
probably benign |
Het |
Pdlim4 |
T |
C |
11: 53,946,699 (GRCm39) |
E196G |
possibly damaging |
Het |
Pigs |
A |
G |
11: 78,228,673 (GRCm39) |
Y293C |
probably damaging |
Het |
Pkd1l2 |
A |
T |
8: 117,757,458 (GRCm39) |
S1527T |
possibly damaging |
Het |
Pkd2l1 |
A |
T |
19: 44,144,040 (GRCm39) |
Y344* |
probably null |
Het |
Pmp2 |
T |
C |
3: 10,247,284 (GRCm39) |
|
probably null |
Het |
Polr3e |
T |
C |
7: 120,538,521 (GRCm39) |
|
probably null |
Het |
Ppp3ca |
C |
G |
3: 136,587,209 (GRCm39) |
I230M |
probably benign |
Het |
Ppp5c |
T |
C |
7: 16,739,235 (GRCm39) |
H463R |
probably benign |
Het |
Ptger1 |
A |
G |
8: 84,395,926 (GRCm39) |
N328D |
probably benign |
Het |
Rhno1 |
A |
T |
6: 128,334,822 (GRCm39) |
I167N |
probably benign |
Het |
Rictor |
C |
A |
15: 6,764,849 (GRCm39) |
P34H |
probably damaging |
Het |
Rnf10 |
A |
C |
5: 115,383,924 (GRCm39) |
S630R |
probably damaging |
Het |
Rnf168 |
A |
G |
16: 32,117,942 (GRCm39) |
Q501R |
probably benign |
Het |
Rngtt |
T |
G |
4: 33,329,634 (GRCm39) |
|
probably null |
Het |
Samd9l |
G |
T |
6: 3,373,126 (GRCm39) |
F1378L |
probably damaging |
Het |
Slc9c1 |
T |
A |
16: 45,409,872 (GRCm39) |
M864K |
probably benign |
Het |
Slitrk5 |
T |
C |
14: 111,917,951 (GRCm39) |
F525S |
probably damaging |
Het |
Sox6 |
T |
C |
7: 115,076,290 (GRCm39) |
M784V |
probably benign |
Het |
Spata31e4 |
A |
T |
13: 50,855,123 (GRCm39) |
T254S |
probably damaging |
Het |
Spint2 |
C |
T |
7: 28,959,791 (GRCm39) |
|
probably null |
Het |
Ssh1 |
A |
T |
5: 114,093,906 (GRCm39) |
I276N |
probably damaging |
Het |
Trank1 |
T |
A |
9: 111,221,939 (GRCm39) |
V2892D |
probably benign |
Het |
Ttn |
C |
A |
2: 76,581,384 (GRCm39) |
E21424* |
probably null |
Het |
Usp17lc |
T |
C |
7: 103,068,055 (GRCm39) |
I450T |
probably benign |
Het |
Vcan |
A |
G |
13: 89,852,854 (GRCm39) |
V702A |
probably benign |
Het |
Vmn1r36 |
TA |
TAA |
6: 66,693,517 (GRCm39) |
|
probably null |
Het |
Vmn2r51 |
G |
T |
7: 9,833,873 (GRCm39) |
D388E |
probably benign |
Het |
Zfp106 |
A |
C |
2: 120,364,245 (GRCm39) |
S721A |
probably damaging |
Het |
Zfp106 |
G |
A |
2: 120,364,244 (GRCm39) |
S721L |
probably damaging |
Het |
Zfp189 |
T |
A |
4: 49,529,342 (GRCm39) |
H148Q |
possibly damaging |
Het |
Zfp352 |
A |
T |
4: 90,112,046 (GRCm39) |
Y62F |
probably benign |
Het |
Zfp839 |
T |
C |
12: 110,821,891 (GRCm39) |
V235A |
probably damaging |
Het |
Zfp871 |
T |
C |
17: 32,994,308 (GRCm39) |
Y289C |
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 |
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 |
R9016:Mtcl1
|
UTSW |
17 |
66,651,062 (GRCm39) |
missense |
probably damaging |
1.00 |
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'- AGATGGATCTCCTCAGCAGCTCAG -3'
(R):5'- ACAGTGCGGATTTGAAGTGTCAGC -3'
Sequencing Primer
(F):5'- CAGCAGCTCAGCCTCTTC -3'
(R):5'- GTCAGCTTCAGTTTGTCAAAGAG -3'
|
Posted On |
2014-05-23 |