Incidental Mutation 'R6185:Tanc1'
ID |
502075 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Tanc1
|
Ensembl Gene |
ENSMUSG00000035168 |
Gene Name |
tetratricopeptide repeat, ankyrin repeat and coiled-coil containing 1 |
Synonyms |
1200003E16Rik |
MMRRC Submission |
044325-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R6185 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
2 |
Chromosomal Location |
59442386-59676493 bp(+) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
T to A
at 59621929 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000123345
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000037526]
[ENSMUST00000037526]
[ENSMUST00000112568]
[ENSMUST00000112568]
[ENSMUST00000139863]
[ENSMUST00000139863]
|
AlphaFold |
Q0VGY8 |
Predicted Effect |
probably null
Transcript: ENSMUST00000037526
|
SMART Domains |
Protein: ENSMUSP00000036003 Gene: ENSMUSG00000035168
Domain | Start | End | E-Value | Type |
low complexity region
|
7 |
22 |
N/A |
INTRINSIC |
low complexity region
|
60 |
78 |
N/A |
INTRINSIC |
low complexity region
|
171 |
191 |
N/A |
INTRINSIC |
low complexity region
|
229 |
240 |
N/A |
INTRINSIC |
low complexity region
|
439 |
451 |
N/A |
INTRINSIC |
low complexity region
|
455 |
475 |
N/A |
INTRINSIC |
ANK
|
893 |
925 |
1.06e3 |
SMART |
ANK
|
929 |
960 |
2.43e3 |
SMART |
ANK
|
964 |
993 |
1.12e-3 |
SMART |
Blast:ANK
|
997 |
1028 |
7e-12 |
BLAST |
ANK
|
1037 |
1066 |
1.78e3 |
SMART |
ANK
|
1075 |
1104 |
2.34e-1 |
SMART |
ANK
|
1108 |
1137 |
3.71e-4 |
SMART |
ANK
|
1141 |
1170 |
1.51e-4 |
SMART |
ANK
|
1174 |
1203 |
4.89e-4 |
SMART |
ANK
|
1207 |
1236 |
3.01e-4 |
SMART |
ANK
|
1240 |
1269 |
1.99e2 |
SMART |
TPR
|
1286 |
1319 |
7.49e1 |
SMART |
TPR
|
1333 |
1366 |
2.35e-1 |
SMART |
TPR
|
1367 |
1400 |
6.29e-2 |
SMART |
low complexity region
|
1416 |
1432 |
N/A |
INTRINSIC |
low complexity region
|
1454 |
1483 |
N/A |
INTRINSIC |
low complexity region
|
1656 |
1686 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000037526
|
SMART Domains |
Protein: ENSMUSP00000036003 Gene: ENSMUSG00000035168
Domain | Start | End | E-Value | Type |
low complexity region
|
7 |
22 |
N/A |
INTRINSIC |
low complexity region
|
60 |
78 |
N/A |
INTRINSIC |
low complexity region
|
171 |
191 |
N/A |
INTRINSIC |
low complexity region
|
229 |
240 |
N/A |
INTRINSIC |
low complexity region
|
439 |
451 |
N/A |
INTRINSIC |
low complexity region
|
455 |
475 |
N/A |
INTRINSIC |
ANK
|
893 |
925 |
1.06e3 |
SMART |
ANK
|
929 |
960 |
2.43e3 |
SMART |
ANK
|
964 |
993 |
1.12e-3 |
SMART |
Blast:ANK
|
997 |
1028 |
7e-12 |
BLAST |
ANK
|
1037 |
1066 |
1.78e3 |
SMART |
ANK
|
1075 |
1104 |
2.34e-1 |
SMART |
ANK
|
1108 |
1137 |
3.71e-4 |
SMART |
ANK
|
1141 |
1170 |
1.51e-4 |
SMART |
ANK
|
1174 |
1203 |
4.89e-4 |
SMART |
ANK
|
1207 |
1236 |
3.01e-4 |
SMART |
ANK
|
1240 |
1269 |
1.99e2 |
SMART |
TPR
|
1286 |
1319 |
7.49e1 |
SMART |
TPR
|
1333 |
1366 |
2.35e-1 |
SMART |
TPR
|
1367 |
1400 |
6.29e-2 |
SMART |
low complexity region
|
1416 |
1432 |
N/A |
INTRINSIC |
low complexity region
|
1454 |
1483 |
N/A |
INTRINSIC |
low complexity region
|
1656 |
1686 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000056900
|
Predicted Effect |
probably null
Transcript: ENSMUST00000112568
|
SMART Domains |
Protein: ENSMUSP00000108187 Gene: ENSMUSG00000035168
Domain | Start | End | E-Value | Type |
low complexity region
|
7 |
22 |
N/A |
INTRINSIC |
low complexity region
|
60 |
78 |
N/A |
INTRINSIC |
low complexity region
|
171 |
191 |
N/A |
INTRINSIC |
low complexity region
|
229 |
240 |
N/A |
INTRINSIC |
low complexity region
|
432 |
444 |
N/A |
INTRINSIC |
low complexity region
|
448 |
468 |
N/A |
INTRINSIC |
ANK
|
886 |
918 |
1.06e3 |
SMART |
ANK
|
922 |
953 |
2.43e3 |
SMART |
ANK
|
957 |
986 |
1.12e-3 |
SMART |
Blast:ANK
|
990 |
1021 |
7e-12 |
BLAST |
ANK
|
1030 |
1059 |
1.78e3 |
SMART |
ANK
|
1068 |
1097 |
2.34e-1 |
SMART |
ANK
|
1101 |
1130 |
3.71e-4 |
SMART |
ANK
|
1134 |
1163 |
1.51e-4 |
SMART |
ANK
|
1167 |
1196 |
4.89e-4 |
SMART |
ANK
|
1200 |
1229 |
3.01e-4 |
SMART |
ANK
|
1233 |
1262 |
1.99e2 |
SMART |
TPR
|
1279 |
1312 |
7.49e1 |
SMART |
TPR
|
1326 |
1359 |
2.35e-1 |
SMART |
TPR
|
1360 |
1393 |
6.29e-2 |
SMART |
low complexity region
|
1409 |
1425 |
N/A |
INTRINSIC |
low complexity region
|
1447 |
1476 |
N/A |
INTRINSIC |
low complexity region
|
1649 |
1679 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000112568
|
SMART Domains |
Protein: ENSMUSP00000108187 Gene: ENSMUSG00000035168
Domain | Start | End | E-Value | Type |
low complexity region
|
7 |
22 |
N/A |
INTRINSIC |
low complexity region
|
60 |
78 |
N/A |
INTRINSIC |
low complexity region
|
171 |
191 |
N/A |
INTRINSIC |
low complexity region
|
229 |
240 |
N/A |
INTRINSIC |
low complexity region
|
432 |
444 |
N/A |
INTRINSIC |
low complexity region
|
448 |
468 |
N/A |
INTRINSIC |
ANK
|
886 |
918 |
1.06e3 |
SMART |
ANK
|
922 |
953 |
2.43e3 |
SMART |
ANK
|
957 |
986 |
1.12e-3 |
SMART |
Blast:ANK
|
990 |
1021 |
7e-12 |
BLAST |
ANK
|
1030 |
1059 |
1.78e3 |
SMART |
ANK
|
1068 |
1097 |
2.34e-1 |
SMART |
ANK
|
1101 |
1130 |
3.71e-4 |
SMART |
ANK
|
1134 |
1163 |
1.51e-4 |
SMART |
ANK
|
1167 |
1196 |
4.89e-4 |
SMART |
ANK
|
1200 |
1229 |
3.01e-4 |
SMART |
ANK
|
1233 |
1262 |
1.99e2 |
SMART |
TPR
|
1279 |
1312 |
7.49e1 |
SMART |
TPR
|
1326 |
1359 |
2.35e-1 |
SMART |
TPR
|
1360 |
1393 |
6.29e-2 |
SMART |
low complexity region
|
1409 |
1425 |
N/A |
INTRINSIC |
low complexity region
|
1447 |
1476 |
N/A |
INTRINSIC |
low complexity region
|
1649 |
1679 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000139863
|
SMART Domains |
Protein: ENSMUSP00000123345 Gene: ENSMUSG00000035168
Domain | Start | End | E-Value | Type |
low complexity region
|
7 |
22 |
N/A |
INTRINSIC |
low complexity region
|
60 |
78 |
N/A |
INTRINSIC |
low complexity region
|
171 |
191 |
N/A |
INTRINSIC |
low complexity region
|
229 |
240 |
N/A |
INTRINSIC |
low complexity region
|
439 |
451 |
N/A |
INTRINSIC |
low complexity region
|
455 |
475 |
N/A |
INTRINSIC |
ANK
|
893 |
925 |
1.06e3 |
SMART |
ANK
|
929 |
960 |
2.43e3 |
SMART |
ANK
|
964 |
993 |
1.12e-3 |
SMART |
Blast:ANK
|
997 |
1028 |
7e-12 |
BLAST |
ANK
|
1037 |
1066 |
1.78e3 |
SMART |
ANK
|
1075 |
1104 |
2.34e-1 |
SMART |
ANK
|
1108 |
1137 |
3.71e-4 |
SMART |
ANK
|
1141 |
1170 |
1.51e-4 |
SMART |
ANK
|
1174 |
1203 |
4.89e-4 |
SMART |
ANK
|
1207 |
1236 |
3.01e-4 |
SMART |
ANK
|
1240 |
1269 |
1.99e2 |
SMART |
TPR
|
1286 |
1319 |
7.49e1 |
SMART |
TPR
|
1333 |
1366 |
2.35e-1 |
SMART |
TPR
|
1367 |
1400 |
6.29e-2 |
SMART |
low complexity region
|
1416 |
1432 |
N/A |
INTRINSIC |
low complexity region
|
1454 |
1483 |
N/A |
INTRINSIC |
low complexity region
|
1656 |
1686 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000139863
|
SMART Domains |
Protein: ENSMUSP00000123345 Gene: ENSMUSG00000035168
Domain | Start | End | E-Value | Type |
low complexity region
|
7 |
22 |
N/A |
INTRINSIC |
low complexity region
|
60 |
78 |
N/A |
INTRINSIC |
low complexity region
|
171 |
191 |
N/A |
INTRINSIC |
low complexity region
|
229 |
240 |
N/A |
INTRINSIC |
low complexity region
|
439 |
451 |
N/A |
INTRINSIC |
low complexity region
|
455 |
475 |
N/A |
INTRINSIC |
ANK
|
893 |
925 |
1.06e3 |
SMART |
ANK
|
929 |
960 |
2.43e3 |
SMART |
ANK
|
964 |
993 |
1.12e-3 |
SMART |
Blast:ANK
|
997 |
1028 |
7e-12 |
BLAST |
ANK
|
1037 |
1066 |
1.78e3 |
SMART |
ANK
|
1075 |
1104 |
2.34e-1 |
SMART |
ANK
|
1108 |
1137 |
3.71e-4 |
SMART |
ANK
|
1141 |
1170 |
1.51e-4 |
SMART |
ANK
|
1174 |
1203 |
4.89e-4 |
SMART |
ANK
|
1207 |
1236 |
3.01e-4 |
SMART |
ANK
|
1240 |
1269 |
1.99e2 |
SMART |
TPR
|
1286 |
1319 |
7.49e1 |
SMART |
TPR
|
1333 |
1366 |
2.35e-1 |
SMART |
TPR
|
1367 |
1400 |
6.29e-2 |
SMART |
low complexity region
|
1416 |
1432 |
N/A |
INTRINSIC |
low complexity region
|
1454 |
1483 |
N/A |
INTRINSIC |
low complexity region
|
1656 |
1686 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
Validation Efficiency |
96% (80/83) |
MGI Phenotype |
PHENOTYPE: Mice homozygous for a gene trap vector exhibit decreased spine density in the CA3 region and impaired spatial memory. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca1 |
A |
T |
4: 53,078,089 (GRCm39) |
H894Q |
probably benign |
Het |
Abca4 |
A |
T |
3: 121,919,789 (GRCm39) |
I1024F |
probably damaging |
Het |
Acadl |
A |
G |
1: 66,877,522 (GRCm39) |
V343A |
possibly damaging |
Het |
Akr1e1 |
T |
A |
13: 4,651,252 (GRCm39) |
I123L |
probably benign |
Het |
Angptl2 |
T |
C |
2: 33,119,026 (GRCm39) |
S267P |
probably benign |
Het |
Ap2a1 |
T |
G |
7: 44,565,594 (GRCm39) |
K91T |
probably damaging |
Het |
Bend7 |
A |
T |
2: 4,793,333 (GRCm39) |
Q379L |
probably damaging |
Het |
Bicdl1 |
C |
T |
5: 115,808,212 (GRCm39) |
|
probably null |
Het |
Cachd1 |
C |
A |
4: 100,838,228 (GRCm39) |
Y830* |
probably null |
Het |
Ccdc158 |
T |
A |
5: 92,814,713 (GRCm39) |
I38F |
possibly damaging |
Het |
Cep97 |
T |
A |
16: 55,735,455 (GRCm39) |
M448L |
probably benign |
Het |
Chd9 |
A |
G |
8: 91,775,765 (GRCm39) |
D2572G |
probably damaging |
Het |
Clcnkb |
C |
T |
4: 141,141,825 (GRCm39) |
V54M |
probably benign |
Het |
Cln8 |
A |
G |
8: 14,946,544 (GRCm39) |
D186G |
probably benign |
Het |
Crxos |
C |
T |
7: 15,636,805 (GRCm39) |
S22L |
possibly damaging |
Het |
Cx3cr1 |
A |
T |
9: 119,880,444 (GRCm39) |
H319Q |
probably benign |
Het |
Cyp2j6 |
G |
C |
4: 96,424,323 (GRCm39) |
L145V |
probably damaging |
Het |
Dmrta1 |
A |
G |
4: 89,580,005 (GRCm39) |
R322G |
probably damaging |
Het |
Dpf1 |
A |
G |
7: 29,010,696 (GRCm39) |
E103G |
possibly damaging |
Het |
Dsg1b |
T |
G |
18: 20,532,543 (GRCm39) |
V529G |
probably benign |
Het |
Dst |
G |
A |
1: 34,212,161 (GRCm39) |
V1361I |
probably damaging |
Het |
Epha4 |
T |
C |
1: 77,483,743 (GRCm39) |
I89V |
probably damaging |
Het |
Etfdh |
G |
T |
3: 79,513,114 (GRCm39) |
H370N |
probably benign |
Het |
Fam186a |
A |
G |
15: 99,845,530 (GRCm39) |
I238T |
unknown |
Het |
Fbxl5 |
T |
A |
5: 43,978,894 (GRCm39) |
S19C |
probably benign |
Het |
Fkbpl |
G |
A |
17: 34,864,303 (GRCm39) |
A24T |
probably benign |
Het |
Fryl |
A |
G |
5: 73,270,131 (GRCm39) |
V367A |
probably benign |
Het |
Gm19410 |
T |
A |
8: 36,274,664 (GRCm39) |
L1495H |
possibly damaging |
Het |
Gm19965 |
A |
G |
1: 116,749,003 (GRCm39) |
E228G |
possibly damaging |
Het |
Gpr89 |
C |
A |
3: 96,798,149 (GRCm39) |
C169F |
probably damaging |
Het |
Hmcn1 |
A |
T |
1: 150,491,189 (GRCm39) |
|
probably null |
Het |
Hsph1 |
A |
T |
5: 149,541,160 (GRCm39) |
C753S |
probably damaging |
Het |
Igf2 |
T |
A |
7: 142,212,118 (GRCm39) |
S4C |
possibly damaging |
Het |
Kansl3 |
A |
T |
1: 36,385,099 (GRCm39) |
S486T |
probably damaging |
Het |
Khdrbs1 |
G |
C |
4: 129,636,068 (GRCm39) |
|
probably benign |
Het |
Lnx1 |
A |
T |
5: 74,846,269 (GRCm39) |
C60* |
probably null |
Het |
Lrpprc |
T |
C |
17: 85,074,452 (GRCm39) |
D485G |
probably benign |
Het |
Ly6i |
A |
T |
15: 74,851,879 (GRCm39) |
S97T |
possibly damaging |
Het |
Me2 |
G |
A |
18: 73,924,199 (GRCm39) |
Q338* |
probably null |
Het |
Med16 |
A |
T |
10: 79,732,197 (GRCm39) |
L790Q |
probably damaging |
Het |
Muc16 |
G |
T |
9: 18,565,769 (GRCm39) |
T2250K |
unknown |
Het |
Myo10 |
T |
G |
15: 25,726,596 (GRCm39) |
F273C |
probably damaging |
Het |
Neil3 |
T |
A |
8: 54,052,182 (GRCm39) |
H472L |
probably benign |
Het |
Nrxn1 |
T |
A |
17: 90,344,564 (GRCm39) |
S57C |
probably damaging |
Het |
Nup188 |
A |
T |
2: 30,231,722 (GRCm39) |
T1439S |
probably damaging |
Het |
Or10g3 |
T |
C |
14: 52,610,019 (GRCm39) |
T164A |
possibly damaging |
Het |
Or10g7 |
T |
C |
9: 39,905,420 (GRCm39) |
F105L |
probably benign |
Het |
Or5w10 |
A |
G |
2: 87,375,087 (GRCm39) |
M267T |
possibly damaging |
Het |
Otud7a |
T |
A |
7: 63,408,133 (GRCm39) |
L812Q |
probably damaging |
Het |
Paip2b |
C |
T |
6: 83,786,952 (GRCm39) |
A95T |
probably benign |
Het |
Pax4 |
C |
T |
6: 28,446,347 (GRCm39) |
V49I |
probably damaging |
Het |
Plek |
C |
T |
11: 16,931,829 (GRCm39) |
A341T |
probably damaging |
Het |
Prkag1 |
G |
A |
15: 98,723,595 (GRCm39) |
P10L |
probably benign |
Het |
R3hdm1 |
A |
C |
1: 128,079,598 (GRCm39) |
D15A |
possibly damaging |
Het |
Rad54b |
A |
T |
4: 11,593,804 (GRCm39) |
D144V |
possibly damaging |
Het |
Rmi2 |
C |
T |
16: 10,704,073 (GRCm39) |
T138I |
probably benign |
Het |
Sbf1 |
A |
G |
15: 89,189,814 (GRCm39) |
L379P |
probably damaging |
Het |
Sec14l3 |
A |
T |
11: 4,025,244 (GRCm39) |
I285F |
probably damaging |
Het |
Sec31b |
A |
T |
19: 44,531,723 (GRCm39) |
I62N |
possibly damaging |
Het |
Selp |
A |
G |
1: 163,953,915 (GRCm39) |
N72D |
probably damaging |
Het |
Sipa1l1 |
T |
A |
12: 82,471,802 (GRCm39) |
S1261T |
probably damaging |
Het |
Sipa1l2 |
A |
T |
8: 126,194,992 (GRCm39) |
Y915* |
probably null |
Het |
Slc22a27 |
A |
T |
19: 7,903,953 (GRCm39) |
D61E |
probably benign |
Het |
Slc2a7 |
A |
G |
4: 150,233,450 (GRCm39) |
T8A |
probably benign |
Het |
Slc5a2 |
T |
C |
7: 127,870,349 (GRCm39) |
I529T |
probably damaging |
Het |
Spart |
A |
C |
3: 55,024,640 (GRCm39) |
Q78H |
probably damaging |
Het |
Spocd1 |
T |
C |
4: 129,850,242 (GRCm39) |
I756T |
probably benign |
Het |
Stc1 |
G |
A |
14: 69,275,813 (GRCm39) |
C202Y |
probably damaging |
Het |
Stk10 |
A |
G |
11: 32,527,749 (GRCm39) |
T166A |
probably benign |
Het |
Syt6 |
A |
T |
3: 103,492,844 (GRCm39) |
D32V |
probably damaging |
Het |
Tanc2 |
T |
A |
11: 105,803,865 (GRCm39) |
N297K |
probably damaging |
Het |
Telo2 |
A |
G |
17: 25,321,014 (GRCm39) |
S734P |
probably benign |
Het |
Tfrc |
T |
A |
16: 32,437,090 (GRCm39) |
Y250N |
probably benign |
Het |
Tmem97 |
C |
T |
11: 78,434,388 (GRCm39) |
W65* |
probably null |
Het |
Ubr3 |
T |
C |
2: 69,768,621 (GRCm39) |
M476T |
probably damaging |
Het |
Ubtf |
T |
C |
11: 102,204,849 (GRCm39) |
T117A |
probably damaging |
Het |
Usp17lb |
T |
A |
7: 104,490,631 (GRCm39) |
M99L |
probably benign |
Het |
Uvrag |
A |
C |
7: 98,790,039 (GRCm39) |
|
probably null |
Het |
Vmn2r63 |
A |
G |
7: 42,578,435 (GRCm39) |
S153P |
probably damaging |
Het |
Vmn2r90 |
A |
T |
17: 17,953,644 (GRCm39) |
T603S |
probably damaging |
Het |
Vps8 |
C |
A |
16: 21,288,891 (GRCm39) |
L417I |
probably damaging |
Het |
|
Other mutations in Tanc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00340:Tanc1
|
APN |
2 |
59,621,185 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL00484:Tanc1
|
APN |
2 |
59,623,520 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00688:Tanc1
|
APN |
2 |
59,645,735 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00765:Tanc1
|
APN |
2 |
59,636,645 (GRCm39) |
missense |
probably benign |
0.15 |
IGL01576:Tanc1
|
APN |
2 |
59,628,079 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01590:Tanc1
|
APN |
2 |
59,615,817 (GRCm39) |
missense |
probably benign |
|
IGL02016:Tanc1
|
APN |
2 |
59,673,934 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02373:Tanc1
|
APN |
2 |
59,626,372 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02539:Tanc1
|
APN |
2 |
59,663,602 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02540:Tanc1
|
APN |
2 |
59,663,602 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02541:Tanc1
|
APN |
2 |
59,663,602 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02543:Tanc1
|
APN |
2 |
59,663,602 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02559:Tanc1
|
APN |
2 |
59,554,998 (GRCm39) |
splice site |
probably benign |
|
IGL02626:Tanc1
|
APN |
2 |
59,630,216 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02669:Tanc1
|
APN |
2 |
59,630,330 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02902:Tanc1
|
APN |
2 |
59,623,431 (GRCm39) |
splice site |
probably benign |
|
Oreja
|
UTSW |
2 |
59,622,148 (GRCm39) |
synonymous |
silent |
|
R0178:Tanc1
|
UTSW |
2 |
59,665,791 (GRCm39) |
nonsense |
probably null |
|
R0347:Tanc1
|
UTSW |
2 |
59,673,335 (GRCm39) |
missense |
probably benign |
|
R0570:Tanc1
|
UTSW |
2 |
59,626,382 (GRCm39) |
splice site |
probably benign |
|
R0660:Tanc1
|
UTSW |
2 |
59,674,228 (GRCm39) |
nonsense |
probably null |
|
R0664:Tanc1
|
UTSW |
2 |
59,674,228 (GRCm39) |
nonsense |
probably null |
|
R0898:Tanc1
|
UTSW |
2 |
59,621,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R1333:Tanc1
|
UTSW |
2 |
59,673,835 (GRCm39) |
missense |
probably benign |
|
R1575:Tanc1
|
UTSW |
2 |
59,621,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R1608:Tanc1
|
UTSW |
2 |
59,628,038 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1616:Tanc1
|
UTSW |
2 |
59,615,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R1703:Tanc1
|
UTSW |
2 |
59,673,365 (GRCm39) |
missense |
probably benign |
0.02 |
R1727:Tanc1
|
UTSW |
2 |
59,621,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R1809:Tanc1
|
UTSW |
2 |
59,630,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R1812:Tanc1
|
UTSW |
2 |
59,622,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R1925:Tanc1
|
UTSW |
2 |
59,555,095 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1951:Tanc1
|
UTSW |
2 |
59,622,156 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2174:Tanc1
|
UTSW |
2 |
59,674,177 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2228:Tanc1
|
UTSW |
2 |
59,555,068 (GRCm39) |
missense |
probably benign |
0.04 |
R2267:Tanc1
|
UTSW |
2 |
59,667,563 (GRCm39) |
critical splice donor site |
probably null |
|
R4191:Tanc1
|
UTSW |
2 |
59,669,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R4476:Tanc1
|
UTSW |
2 |
59,672,340 (GRCm39) |
splice site |
probably null |
|
R4632:Tanc1
|
UTSW |
2 |
59,626,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R4825:Tanc1
|
UTSW |
2 |
59,529,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R4982:Tanc1
|
UTSW |
2 |
59,630,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R5338:Tanc1
|
UTSW |
2 |
59,626,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R5657:Tanc1
|
UTSW |
2 |
59,665,051 (GRCm39) |
splice site |
probably null |
|
R5672:Tanc1
|
UTSW |
2 |
59,602,697 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5703:Tanc1
|
UTSW |
2 |
59,626,341 (GRCm39) |
missense |
probably damaging |
0.98 |
R5707:Tanc1
|
UTSW |
2 |
59,588,874 (GRCm39) |
missense |
probably benign |
|
R5778:Tanc1
|
UTSW |
2 |
59,529,691 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5795:Tanc1
|
UTSW |
2 |
59,637,926 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5831:Tanc1
|
UTSW |
2 |
59,615,685 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5849:Tanc1
|
UTSW |
2 |
59,630,248 (GRCm39) |
missense |
probably benign |
0.00 |
R5912:Tanc1
|
UTSW |
2 |
59,622,030 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5944:Tanc1
|
UTSW |
2 |
59,667,564 (GRCm39) |
critical splice donor site |
probably null |
|
R6057:Tanc1
|
UTSW |
2 |
59,647,837 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6142:Tanc1
|
UTSW |
2 |
59,663,566 (GRCm39) |
nonsense |
probably null |
|
R6179:Tanc1
|
UTSW |
2 |
59,673,320 (GRCm39) |
missense |
probably benign |
0.42 |
R6192:Tanc1
|
UTSW |
2 |
59,669,305 (GRCm39) |
splice site |
probably null |
|
R6196:Tanc1
|
UTSW |
2 |
59,674,366 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6197:Tanc1
|
UTSW |
2 |
59,674,366 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6230:Tanc1
|
UTSW |
2 |
59,672,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R6275:Tanc1
|
UTSW |
2 |
59,673,854 (GRCm39) |
missense |
probably benign |
0.22 |
R6415:Tanc1
|
UTSW |
2 |
59,667,458 (GRCm39) |
missense |
probably benign |
0.02 |
R6480:Tanc1
|
UTSW |
2 |
59,637,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R6578:Tanc1
|
UTSW |
2 |
59,626,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R6786:Tanc1
|
UTSW |
2 |
59,622,150 (GRCm39) |
missense |
probably benign |
0.00 |
R7006:Tanc1
|
UTSW |
2 |
59,626,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R7133:Tanc1
|
UTSW |
2 |
59,627,953 (GRCm39) |
missense |
probably benign |
0.16 |
R7381:Tanc1
|
UTSW |
2 |
59,615,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R7422:Tanc1
|
UTSW |
2 |
59,636,688 (GRCm39) |
missense |
probably benign |
0.02 |
R8392:Tanc1
|
UTSW |
2 |
59,636,651 (GRCm39) |
missense |
probably damaging |
0.99 |
R8692:Tanc1
|
UTSW |
2 |
59,673,989 (GRCm39) |
missense |
probably benign |
0.01 |
R8730:Tanc1
|
UTSW |
2 |
59,601,590 (GRCm39) |
missense |
probably benign |
0.00 |
R8731:Tanc1
|
UTSW |
2 |
59,673,596 (GRCm39) |
missense |
probably benign |
0.01 |
R8813:Tanc1
|
UTSW |
2 |
59,630,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R8815:Tanc1
|
UTSW |
2 |
59,621,185 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8933:Tanc1
|
UTSW |
2 |
59,615,800 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9015:Tanc1
|
UTSW |
2 |
59,622,224 (GRCm39) |
missense |
probably benign |
|
R9042:Tanc1
|
UTSW |
2 |
59,673,766 (GRCm39) |
missense |
probably benign |
0.00 |
R9154:Tanc1
|
UTSW |
2 |
59,630,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R9269:Tanc1
|
UTSW |
2 |
59,630,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R9283:Tanc1
|
UTSW |
2 |
59,630,174 (GRCm39) |
missense |
probably damaging |
0.99 |
R9380:Tanc1
|
UTSW |
2 |
59,665,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R9422:Tanc1
|
UTSW |
2 |
59,637,933 (GRCm39) |
missense |
probably benign |
0.08 |
R9428:Tanc1
|
UTSW |
2 |
59,601,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R9694:Tanc1
|
UTSW |
2 |
59,626,196 (GRCm39) |
missense |
probably damaging |
1.00 |
RF028:Tanc1
|
UTSW |
2 |
59,673,613 (GRCm39) |
small deletion |
probably benign |
|
RF049:Tanc1
|
UTSW |
2 |
59,673,613 (GRCm39) |
small deletion |
probably benign |
|
X0063:Tanc1
|
UTSW |
2 |
59,674,324 (GRCm39) |
nonsense |
probably null |
|
X0064:Tanc1
|
UTSW |
2 |
59,674,456 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Tanc1
|
UTSW |
2 |
59,602,873 (GRCm39) |
missense |
possibly damaging |
0.93 |
Z1177:Tanc1
|
UTSW |
2 |
59,622,174 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Tanc1
|
UTSW |
2 |
59,621,231 (GRCm39) |
missense |
probably benign |
|
|
Predicted Primers |
PCR Primer
(F):5'- GACATGACTGGGGCTTTTGC -3'
(R):5'- GATGGCTGTCTTCCCAAATCC -3'
Sequencing Primer
(F):5'- GCTTTCTCTGTGTGCTTGAAAATAAC -3'
(R):5'- ACGACCACGGCTCCTCTG -3'
|
Posted On |
2018-02-27 |