Incidental Mutation 'R6166:Camta2'
ID |
523285 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Camta2
|
Ensembl Gene |
ENSMUSG00000040712 |
Gene Name |
calmodulin binding transcription activator 2 |
Synonyms |
Kiaa0909-hp |
MMRRC Submission |
044312-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.461)
|
Stock # |
R6166 (G1)
|
Quality Score |
21.0411 |
Status
|
Validated
|
Chromosome |
11 |
Chromosomal Location |
70560289-70578931 bp(-) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
G to C
at 70565087 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000113667
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000018431]
[ENSMUST00000036299]
[ENSMUST00000100933]
[ENSMUST00000108544]
[ENSMUST00000108545]
[ENSMUST00000119120]
[ENSMUST00000120261]
[ENSMUST00000145823]
[ENSMUST00000129434]
|
AlphaFold |
Q80Y50 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000018431
|
SMART Domains |
Protein: ENSMUSP00000018431 Gene: ENSMUSG00000018287
Domain | Start | End | E-Value | Type |
R3H
|
31 |
109 |
3.85e-21 |
SMART |
low complexity region
|
130 |
152 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000036299
|
SMART Domains |
Protein: ENSMUSP00000043792 Gene: ENSMUSG00000040712
Domain | Start | End | E-Value | Type |
CG-1
|
34 |
155 |
1.07e-83 |
SMART |
low complexity region
|
232 |
243 |
N/A |
INTRINSIC |
low complexity region
|
273 |
291 |
N/A |
INTRINSIC |
low complexity region
|
294 |
305 |
N/A |
INTRINSIC |
low complexity region
|
314 |
329 |
N/A |
INTRINSIC |
low complexity region
|
370 |
380 |
N/A |
INTRINSIC |
low complexity region
|
417 |
435 |
N/A |
INTRINSIC |
low complexity region
|
461 |
485 |
N/A |
INTRINSIC |
low complexity region
|
501 |
514 |
N/A |
INTRINSIC |
Pfam:TIG
|
541 |
621 |
6.2e-13 |
PFAM |
low complexity region
|
660 |
679 |
N/A |
INTRINSIC |
Blast:ANK
|
717 |
750 |
7e-12 |
BLAST |
SCOP:d1myo__
|
718 |
816 |
2e-15 |
SMART |
Blast:ANK
|
762 |
792 |
4e-11 |
BLAST |
low complexity region
|
829 |
839 |
N/A |
INTRINSIC |
low complexity region
|
844 |
853 |
N/A |
INTRINSIC |
low complexity region
|
861 |
882 |
N/A |
INTRINSIC |
IQ
|
1053 |
1075 |
2.59e2 |
SMART |
IQ
|
1076 |
1092 |
2.38e2 |
SMART |
IQ
|
1106 |
1128 |
5.42e0 |
SMART |
low complexity region
|
1140 |
1157 |
N/A |
INTRINSIC |
low complexity region
|
1180 |
1190 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000100933
|
SMART Domains |
Protein: ENSMUSP00000098493 Gene: ENSMUSG00000040712
Domain | Start | End | E-Value | Type |
CG-1
|
36 |
152 |
8.08e-88 |
SMART |
low complexity region
|
229 |
240 |
N/A |
INTRINSIC |
low complexity region
|
270 |
288 |
N/A |
INTRINSIC |
low complexity region
|
291 |
302 |
N/A |
INTRINSIC |
low complexity region
|
311 |
326 |
N/A |
INTRINSIC |
low complexity region
|
367 |
377 |
N/A |
INTRINSIC |
low complexity region
|
414 |
432 |
N/A |
INTRINSIC |
low complexity region
|
458 |
482 |
N/A |
INTRINSIC |
low complexity region
|
498 |
511 |
N/A |
INTRINSIC |
Pfam:TIG
|
538 |
618 |
1.2e-8 |
PFAM |
low complexity region
|
657 |
676 |
N/A |
INTRINSIC |
Blast:ANK
|
714 |
747 |
8e-12 |
BLAST |
SCOP:d1myo__
|
715 |
813 |
2e-15 |
SMART |
Blast:ANK
|
759 |
789 |
4e-11 |
BLAST |
low complexity region
|
826 |
836 |
N/A |
INTRINSIC |
low complexity region
|
841 |
850 |
N/A |
INTRINSIC |
low complexity region
|
858 |
879 |
N/A |
INTRINSIC |
IQ
|
1050 |
1072 |
2.59e2 |
SMART |
IQ
|
1073 |
1095 |
1.18e1 |
SMART |
IQ
|
1096 |
1118 |
5.42e0 |
SMART |
low complexity region
|
1130 |
1147 |
N/A |
INTRINSIC |
low complexity region
|
1170 |
1180 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000108544
|
SMART Domains |
Protein: ENSMUSP00000104184 Gene: ENSMUSG00000040712
Domain | Start | End | E-Value | Type |
CG-1
|
34 |
150 |
8.08e-88 |
SMART |
low complexity region
|
227 |
238 |
N/A |
INTRINSIC |
low complexity region
|
268 |
286 |
N/A |
INTRINSIC |
low complexity region
|
289 |
300 |
N/A |
INTRINSIC |
low complexity region
|
309 |
324 |
N/A |
INTRINSIC |
low complexity region
|
365 |
375 |
N/A |
INTRINSIC |
low complexity region
|
412 |
430 |
N/A |
INTRINSIC |
low complexity region
|
456 |
480 |
N/A |
INTRINSIC |
low complexity region
|
496 |
509 |
N/A |
INTRINSIC |
Pfam:TIG
|
536 |
616 |
1.2e-8 |
PFAM |
low complexity region
|
655 |
674 |
N/A |
INTRINSIC |
Blast:ANK
|
712 |
745 |
7e-12 |
BLAST |
SCOP:d1myo__
|
713 |
811 |
2e-15 |
SMART |
Blast:ANK
|
757 |
787 |
4e-11 |
BLAST |
low complexity region
|
824 |
834 |
N/A |
INTRINSIC |
low complexity region
|
839 |
848 |
N/A |
INTRINSIC |
low complexity region
|
856 |
877 |
N/A |
INTRINSIC |
IQ
|
1048 |
1070 |
2.59e2 |
SMART |
IQ
|
1071 |
1087 |
2.38e2 |
SMART |
IQ
|
1101 |
1123 |
5.42e0 |
SMART |
low complexity region
|
1135 |
1152 |
N/A |
INTRINSIC |
low complexity region
|
1175 |
1185 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000108545
|
SMART Domains |
Protein: ENSMUSP00000104185 Gene: ENSMUSG00000040712
Domain | Start | End | E-Value | Type |
CG-1
|
34 |
126 |
3.23e-55 |
SMART |
low complexity region
|
203 |
214 |
N/A |
INTRINSIC |
low complexity region
|
244 |
262 |
N/A |
INTRINSIC |
low complexity region
|
265 |
276 |
N/A |
INTRINSIC |
low complexity region
|
285 |
300 |
N/A |
INTRINSIC |
low complexity region
|
341 |
351 |
N/A |
INTRINSIC |
low complexity region
|
388 |
406 |
N/A |
INTRINSIC |
low complexity region
|
432 |
456 |
N/A |
INTRINSIC |
low complexity region
|
472 |
485 |
N/A |
INTRINSIC |
Pfam:TIG
|
512 |
592 |
1.1e-8 |
PFAM |
low complexity region
|
631 |
650 |
N/A |
INTRINSIC |
Blast:ANK
|
688 |
721 |
7e-12 |
BLAST |
SCOP:d1myo__
|
689 |
787 |
2e-15 |
SMART |
Blast:ANK
|
733 |
763 |
5e-13 |
BLAST |
low complexity region
|
800 |
810 |
N/A |
INTRINSIC |
low complexity region
|
815 |
824 |
N/A |
INTRINSIC |
low complexity region
|
832 |
853 |
N/A |
INTRINSIC |
IQ
|
1024 |
1046 |
2.59e2 |
SMART |
IQ
|
1047 |
1069 |
1.18e1 |
SMART |
IQ
|
1070 |
1092 |
5.42e0 |
SMART |
low complexity region
|
1104 |
1121 |
N/A |
INTRINSIC |
low complexity region
|
1144 |
1154 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000119120
|
SMART Domains |
Protein: ENSMUSP00000113847 Gene: ENSMUSG00000040712
Domain | Start | End | E-Value | Type |
CG-1
|
34 |
150 |
8.08e-88 |
SMART |
low complexity region
|
227 |
238 |
N/A |
INTRINSIC |
low complexity region
|
268 |
286 |
N/A |
INTRINSIC |
low complexity region
|
289 |
300 |
N/A |
INTRINSIC |
low complexity region
|
309 |
324 |
N/A |
INTRINSIC |
low complexity region
|
365 |
375 |
N/A |
INTRINSIC |
low complexity region
|
412 |
430 |
N/A |
INTRINSIC |
low complexity region
|
456 |
480 |
N/A |
INTRINSIC |
low complexity region
|
496 |
509 |
N/A |
INTRINSIC |
Pfam:TIG
|
536 |
616 |
1.1e-8 |
PFAM |
low complexity region
|
655 |
674 |
N/A |
INTRINSIC |
Blast:ANK
|
712 |
745 |
7e-12 |
BLAST |
SCOP:d1myo__
|
713 |
811 |
2e-15 |
SMART |
Blast:ANK
|
757 |
787 |
8e-13 |
BLAST |
low complexity region
|
824 |
834 |
N/A |
INTRINSIC |
low complexity region
|
839 |
848 |
N/A |
INTRINSIC |
low complexity region
|
856 |
877 |
N/A |
INTRINSIC |
IQ
|
1048 |
1070 |
2.59e2 |
SMART |
IQ
|
1071 |
1093 |
1.18e1 |
SMART |
IQ
|
1094 |
1116 |
5.42e0 |
SMART |
low complexity region
|
1128 |
1145 |
N/A |
INTRINSIC |
low complexity region
|
1168 |
1178 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000120261
|
SMART Domains |
Protein: ENSMUSP00000113667 Gene: ENSMUSG00000040712
Domain | Start | End | E-Value | Type |
CG-1
|
34 |
126 |
3.23e-55 |
SMART |
low complexity region
|
203 |
214 |
N/A |
INTRINSIC |
low complexity region
|
244 |
262 |
N/A |
INTRINSIC |
low complexity region
|
265 |
276 |
N/A |
INTRINSIC |
low complexity region
|
285 |
300 |
N/A |
INTRINSIC |
low complexity region
|
341 |
351 |
N/A |
INTRINSIC |
low complexity region
|
388 |
406 |
N/A |
INTRINSIC |
low complexity region
|
432 |
456 |
N/A |
INTRINSIC |
low complexity region
|
472 |
485 |
N/A |
INTRINSIC |
Pfam:TIG
|
512 |
592 |
1e-8 |
PFAM |
low complexity region
|
631 |
650 |
N/A |
INTRINSIC |
Blast:ANK
|
688 |
721 |
7e-12 |
BLAST |
SCOP:d1myo__
|
689 |
787 |
2e-15 |
SMART |
Blast:ANK
|
733 |
763 |
7e-13 |
BLAST |
low complexity region
|
800 |
810 |
N/A |
INTRINSIC |
low complexity region
|
815 |
824 |
N/A |
INTRINSIC |
low complexity region
|
832 |
853 |
N/A |
INTRINSIC |
IQ
|
1024 |
1046 |
2.59e2 |
SMART |
IQ
|
1047 |
1063 |
2.38e2 |
SMART |
IQ
|
1077 |
1099 |
5.42e0 |
SMART |
low complexity region
|
1111 |
1128 |
N/A |
INTRINSIC |
low complexity region
|
1151 |
1161 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000145823
|
SMART Domains |
Protein: ENSMUSP00000123602 Gene: ENSMUSG00000040712
Domain | Start | End | E-Value | Type |
CG-1
|
34 |
137 |
2.55e-44 |
SMART |
low complexity region
|
146 |
165 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000124691
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000129434
|
SMART Domains |
Protein: ENSMUSP00000115098 Gene: ENSMUSG00000018287
Domain | Start | End | E-Value | Type |
R3H
|
22 |
99 |
3.06e-15 |
SMART |
low complexity region
|
120 |
142 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000125687
|
Meta Mutation Damage Score |
0.9755 |
Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.6%
- 10x: 98.1%
- 20x: 94.7%
|
Validation Efficiency |
97% (57/59) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the calmodulin-binding transcription activator protein family. Members of this family share a common domain structure that consists of a transcription activation domain, a DNA-binding domain, and a calmodulin-binding domain. The encoded protein may be a transcriptional coactivator of genes involved in cardiac growth. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Jan 2010] PHENOTYPE: Mice homozygous for a knock-out allele are viable, fertile and free of obvious cardiac defects, but show reduced pathophysiologic cardiac hypertrophy in response to diverse stress stimuli. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot2 |
A |
T |
12: 84,039,378 (GRCm39) |
N296Y |
probably damaging |
Het |
Ago2 |
T |
A |
15: 72,996,089 (GRCm39) |
I347L |
probably benign |
Het |
Aldh1l2 |
C |
T |
10: 83,329,288 (GRCm39) |
|
probably null |
Het |
Ap1ar |
A |
G |
3: 127,606,177 (GRCm39) |
|
probably null |
Het |
Arap3 |
T |
C |
18: 38,107,423 (GRCm39) |
T1365A |
probably damaging |
Het |
Arhgef17 |
A |
T |
7: 100,525,699 (GRCm39) |
H1966Q |
probably damaging |
Het |
Arpp21 |
T |
C |
9: 111,948,266 (GRCm39) |
T668A |
probably benign |
Het |
Atg13 |
G |
T |
2: 91,506,736 (GRCm39) |
Q479K |
probably damaging |
Het |
Bmp8a |
T |
C |
4: 123,218,471 (GRCm39) |
T183A |
probably benign |
Het |
Catspere2 |
A |
G |
1: 177,931,403 (GRCm39) |
T441A |
unknown |
Het |
Ccdc40 |
T |
C |
11: 119,122,827 (GRCm39) |
S210P |
probably benign |
Het |
Cnn2 |
A |
G |
10: 79,824,561 (GRCm39) |
E17G |
possibly damaging |
Het |
Cnot6l |
T |
C |
5: 96,227,799 (GRCm39) |
D478G |
possibly damaging |
Het |
Cplane1 |
A |
G |
15: 8,216,044 (GRCm39) |
H478R |
probably benign |
Het |
Csf2rb |
A |
G |
15: 78,228,766 (GRCm39) |
Y369C |
probably damaging |
Het |
Dll4 |
A |
G |
2: 119,165,107 (GRCm39) |
|
probably null |
Het |
Efcab6 |
A |
G |
15: 83,780,316 (GRCm39) |
V1039A |
probably benign |
Het |
Fam117a |
T |
C |
11: 95,271,607 (GRCm39) |
M393T |
possibly damaging |
Het |
Fancd2 |
T |
A |
6: 113,532,212 (GRCm39) |
N508K |
possibly damaging |
Het |
Fat1 |
T |
C |
8: 45,405,522 (GRCm39) |
S758P |
probably damaging |
Het |
Fgf20 |
T |
C |
8: 40,732,881 (GRCm39) |
K186E |
probably damaging |
Het |
Filip1 |
T |
C |
9: 79,726,736 (GRCm39) |
K628E |
probably damaging |
Het |
Fsip2 |
G |
T |
2: 82,811,071 (GRCm39) |
K2463N |
probably benign |
Het |
Gm15446 |
T |
A |
5: 110,090,646 (GRCm39) |
Y299* |
probably null |
Het |
Gm7363 |
A |
T |
7: 3,986,784 (GRCm39) |
|
noncoding transcript |
Het |
Gpx5 |
A |
T |
13: 21,473,435 (GRCm39) |
F104I |
probably damaging |
Het |
Grip1 |
A |
T |
10: 119,908,623 (GRCm39) |
I618F |
probably damaging |
Het |
Hmcn2 |
G |
A |
2: 31,259,274 (GRCm39) |
G1038D |
probably damaging |
Het |
Lgals9 |
C |
T |
11: 78,862,184 (GRCm39) |
A134T |
probably benign |
Het |
Lrba |
G |
A |
3: 86,261,614 (GRCm39) |
|
probably null |
Het |
Lypd10 |
A |
T |
7: 24,413,644 (GRCm39) |
Q220L |
probably benign |
Het |
Naprt |
T |
C |
15: 75,763,326 (GRCm39) |
Q439R |
possibly damaging |
Het |
Ndufs6 |
G |
A |
13: 73,466,060 (GRCm39) |
|
probably benign |
Het |
Nodal |
C |
A |
10: 61,260,337 (GRCm39) |
S329R |
probably damaging |
Het |
Olfm3 |
T |
A |
3: 114,916,074 (GRCm39) |
N315K |
probably damaging |
Het |
Or4k2 |
C |
T |
14: 50,424,225 (GRCm39) |
V150I |
probably benign |
Het |
Or6c3b |
A |
T |
10: 129,527,148 (GRCm39) |
I254K |
probably damaging |
Het |
Or6k2 |
A |
G |
1: 173,986,659 (GRCm39) |
T107A |
probably benign |
Het |
Plg |
T |
A |
17: 12,617,001 (GRCm39) |
V373E |
probably damaging |
Het |
Prdm2 |
A |
C |
4: 142,861,306 (GRCm39) |
S661R |
probably damaging |
Het |
Psg21 |
A |
T |
7: 18,390,664 (GRCm39) |
|
probably benign |
Het |
Rhobtb2 |
T |
C |
14: 70,035,627 (GRCm39) |
D148G |
probably damaging |
Het |
Rsf1 |
GCG |
GCGACGGCGACG |
7: 97,229,114 (GRCm39) |
|
probably benign |
Het |
Scaf11 |
A |
T |
15: 96,322,543 (GRCm39) |
N116K |
probably damaging |
Het |
Sf3a3 |
T |
C |
4: 124,617,177 (GRCm39) |
|
probably benign |
Homo |
Slc38a9 |
T |
G |
13: 112,831,801 (GRCm39) |
Y184D |
possibly damaging |
Het |
Sowahc |
A |
G |
10: 59,058,182 (GRCm39) |
D106G |
probably benign |
Het |
Srbd1 |
T |
C |
17: 86,406,696 (GRCm39) |
Y563C |
probably damaging |
Het |
Src |
A |
G |
2: 157,310,442 (GRCm39) |
Y359C |
probably damaging |
Het |
Tbc1d9b |
A |
G |
11: 50,026,673 (GRCm39) |
D47G |
probably damaging |
Het |
Tctn3 |
T |
C |
19: 40,585,923 (GRCm39) |
K541E |
possibly damaging |
Het |
Tgm7 |
A |
G |
2: 120,929,539 (GRCm39) |
V245A |
probably damaging |
Het |
Thbs2 |
C |
T |
17: 14,900,650 (GRCm39) |
R519H |
probably damaging |
Het |
Tm4sf19 |
T |
C |
16: 32,226,681 (GRCm39) |
S157P |
probably damaging |
Het |
Trio |
C |
T |
15: 27,818,157 (GRCm39) |
S507N |
probably damaging |
Het |
Trrap |
T |
A |
5: 144,718,791 (GRCm39) |
H152Q |
possibly damaging |
Het |
Vmn2r56 |
A |
G |
7: 12,427,947 (GRCm39) |
L773P |
probably damaging |
Het |
Vmn2r70 |
A |
G |
7: 85,215,189 (GRCm39) |
L115P |
probably benign |
Het |
Wdr59 |
C |
T |
8: 112,199,293 (GRCm39) |
R631H |
probably damaging |
Het |
|
Other mutations in Camta2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01022:Camta2
|
APN |
11 |
70,562,308 (GRCm39) |
nonsense |
probably null |
|
IGL01472:Camta2
|
APN |
11 |
70,574,950 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02548:Camta2
|
APN |
11 |
70,561,511 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02794:Camta2
|
APN |
11 |
70,566,484 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02983:Camta2
|
APN |
11 |
70,562,848 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03035:Camta2
|
APN |
11 |
70,562,335 (GRCm39) |
nonsense |
probably null |
|
weeping
|
UTSW |
11 |
70,574,134 (GRCm39) |
missense |
probably damaging |
1.00 |
Willow
|
UTSW |
11 |
70,569,151 (GRCm39) |
missense |
probably damaging |
1.00 |
P0027:Camta2
|
UTSW |
11 |
70,574,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R0360:Camta2
|
UTSW |
11 |
70,574,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R0364:Camta2
|
UTSW |
11 |
70,574,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R0541:Camta2
|
UTSW |
11 |
70,572,447 (GRCm39) |
missense |
probably benign |
0.01 |
R0600:Camta2
|
UTSW |
11 |
70,564,785 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0630:Camta2
|
UTSW |
11 |
70,569,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R1301:Camta2
|
UTSW |
11 |
70,567,230 (GRCm39) |
missense |
probably benign |
0.18 |
R1346:Camta2
|
UTSW |
11 |
70,567,293 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1826:Camta2
|
UTSW |
11 |
70,574,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R1881:Camta2
|
UTSW |
11 |
70,562,842 (GRCm39) |
missense |
probably benign |
0.00 |
R1980:Camta2
|
UTSW |
11 |
70,573,308 (GRCm39) |
missense |
probably benign |
0.43 |
R2144:Camta2
|
UTSW |
11 |
70,562,401 (GRCm39) |
missense |
probably benign |
0.31 |
R2145:Camta2
|
UTSW |
11 |
70,562,401 (GRCm39) |
missense |
probably benign |
0.31 |
R2763:Camta2
|
UTSW |
11 |
70,573,356 (GRCm39) |
nonsense |
probably null |
|
R2881:Camta2
|
UTSW |
11 |
70,570,490 (GRCm39) |
splice site |
probably null |
|
R2917:Camta2
|
UTSW |
11 |
70,571,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R4115:Camta2
|
UTSW |
11 |
70,567,300 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4321:Camta2
|
UTSW |
11 |
70,569,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R4470:Camta2
|
UTSW |
11 |
70,571,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R4499:Camta2
|
UTSW |
11 |
70,565,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R4509:Camta2
|
UTSW |
11 |
70,571,844 (GRCm39) |
missense |
probably benign |
0.28 |
R6154:Camta2
|
UTSW |
11 |
70,569,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R6287:Camta2
|
UTSW |
11 |
70,572,295 (GRCm39) |
missense |
probably damaging |
0.98 |
R6382:Camta2
|
UTSW |
11 |
70,562,867 (GRCm39) |
missense |
probably damaging |
0.99 |
R6864:Camta2
|
UTSW |
11 |
70,562,792 (GRCm39) |
missense |
probably benign |
0.00 |
R6922:Camta2
|
UTSW |
11 |
70,564,964 (GRCm39) |
missense |
probably benign |
0.04 |
R7438:Camta2
|
UTSW |
11 |
70,574,714 (GRCm39) |
critical splice donor site |
probably null |
|
R7611:Camta2
|
UTSW |
11 |
70,572,372 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7883:Camta2
|
UTSW |
11 |
70,566,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R8094:Camta2
|
UTSW |
11 |
70,576,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R8232:Camta2
|
UTSW |
11 |
70,573,841 (GRCm39) |
missense |
unknown |
|
R8271:Camta2
|
UTSW |
11 |
70,561,886 (GRCm39) |
missense |
probably benign |
0.05 |
R8973:Camta2
|
UTSW |
11 |
70,561,184 (GRCm39) |
missense |
probably benign |
0.05 |
R9072:Camta2
|
UTSW |
11 |
70,567,234 (GRCm39) |
missense |
probably benign |
0.21 |
T0722:Camta2
|
UTSW |
11 |
70,574,831 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Camta2
|
UTSW |
11 |
70,572,504 (GRCm39) |
missense |
probably benign |
0.08 |
Z1177:Camta2
|
UTSW |
11 |
70,566,047 (GRCm39) |
nonsense |
probably null |
|
|
Predicted Primers |
PCR Primer
(F):5'- GGCTTCATAGTCCATGAGGAG -3'
(R):5'- ACTGGTGAGAGCTGGCATTG -3'
Sequencing Primer
(F):5'- CCATGAGGAGTAAGGGTGTCTC -3'
(R):5'- AGAGACTGGCTGTGCTTCC -3'
|
Posted On |
2018-06-18 |