Incidental Mutation 'R7165:Camta1'
| ID |
557860 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Camta1
|
| Ensembl Gene |
ENSMUSG00000014592 |
| Gene Name |
calmodulin binding transcription activator 1 |
| Synonyms |
2310058O09Rik, 1810059M14Rik |
| MMRRC Submission |
045262-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.551)
|
| Stock # |
R7165 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
4 |
| Chromosomal Location |
151143980-151946225 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 151169157 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Leucine to Serine
at position 198
(L198S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000101295
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000049790]
[ENSMUST00000097774]
[ENSMUST00000105667]
[ENSMUST00000105668]
[ENSMUST00000105670]
[ENSMUST00000131948]
[ENSMUST00000140030]
[ENSMUST00000169423]
|
| AlphaFold |
A2A891 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000049790
AA Change: L1176S
PolyPhen 2
Score 0.131 (Sensitivity: 0.93; Specificity: 0.86)
|
| SMART Domains |
Protein: ENSMUSP00000054804
Gene: ENSMUSG00000014592
AA Change: L1176S
| Domain | Start | End | E-Value | Type |
|---|
|
CG-1
|
67 |
183 |
1.39e-91 |
SMART |
|
low complexity region
|
550 |
583 |
N/A |
INTRINSIC |
|
low complexity region
|
677 |
688 |
N/A |
INTRINSIC |
|
Pfam:TIG
|
874 |
954 |
3e-13 |
PFAM |
|
low complexity region
|
997 |
1030 |
N/A |
INTRINSIC |
|
ANK
|
1066 |
1095 |
1.7e2 |
SMART |
|
ANK
|
1111 |
1141 |
4.73e2 |
SMART |
|
low complexity region
|
1301 |
1319 |
N/A |
INTRINSIC |
|
IQ
|
1548 |
1564 |
2.38e2 |
SMART |
|
IQ
|
1578 |
1600 |
5.42e0 |
SMART |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000097774
AA Change: L1176S
PolyPhen 2
Score 0.886 (Sensitivity: 0.82; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000095381
Gene: ENSMUSG00000014592
AA Change: L1176S
| Domain | Start | End | E-Value | Type |
|---|
|
CG-1
|
67 |
183 |
1.39e-91 |
SMART |
|
low complexity region
|
550 |
583 |
N/A |
INTRINSIC |
|
low complexity region
|
677 |
688 |
N/A |
INTRINSIC |
|
Pfam:TIG
|
874 |
954 |
3.1e-11 |
PFAM |
|
low complexity region
|
997 |
1030 |
N/A |
INTRINSIC |
|
ANK
|
1066 |
1095 |
1.7e2 |
SMART |
|
ANK
|
1111 |
1141 |
4.73e2 |
SMART |
|
low complexity region
|
1301 |
1319 |
N/A |
INTRINSIC |
|
IQ
|
1548 |
1570 |
5.45e1 |
SMART |
|
IQ
|
1571 |
1593 |
5.42e0 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000105667
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000105668
AA Change: L198S
PolyPhen 2
Score 0.228 (Sensitivity: 0.91; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000101293
Gene: ENSMUSG00000014592
AA Change: L198S
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
19 |
52 |
N/A |
INTRINSIC |
|
ANK
|
88 |
117 |
1.7e2 |
SMART |
|
ANK
|
133 |
163 |
4.73e2 |
SMART |
|
Blast:ANK
|
167 |
197 |
6e-10 |
BLAST |
|
IQ
|
457 |
473 |
2.38e2 |
SMART |
|
IQ
|
487 |
509 |
5.42e0 |
SMART |
|
Pfam:IQ
|
512 |
527 |
5.1e-4 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000105670
AA Change: L198S
PolyPhen 2
Score 0.633 (Sensitivity: 0.87; Specificity: 0.91)
|
| SMART Domains |
Protein: ENSMUSP00000101295
Gene: ENSMUSG00000014592
AA Change: L198S
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
19 |
52 |
N/A |
INTRINSIC |
|
ANK
|
88 |
117 |
1.7e2 |
SMART |
|
ANK
|
133 |
163 |
4.73e2 |
SMART |
|
Blast:ANK
|
167 |
197 |
5e-10 |
BLAST |
|
IQ
|
457 |
479 |
5.45e1 |
SMART |
|
IQ
|
480 |
502 |
5.42e0 |
SMART |
|
Pfam:IQ
|
505 |
520 |
5.1e-4 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000131948
|
| SMART Domains |
Protein: ENSMUSP00000118969
Gene: ENSMUSG00000014592
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
19 |
52 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000140030
|
| SMART Domains |
Protein: ENSMUSP00000119067
Gene: ENSMUSG00000014592
| Domain | Start | End | E-Value | Type |
|---|
|
IQ
|
111 |
133 |
5.45e1 |
SMART |
|
IQ
|
134 |
156 |
5.42e0 |
SMART |
|
Pfam:IQ
|
159 |
174 |
8.5e-4 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000169423
AA Change: L1176S
PolyPhen 2
Score 0.131 (Sensitivity: 0.93; Specificity: 0.86)
|
| SMART Domains |
Protein: ENSMUSP00000127916
Gene: ENSMUSG00000014592
AA Change: L1176S
| Domain | Start | End | E-Value | Type |
|---|
|
CG-1
|
67 |
183 |
1.39e-91 |
SMART |
|
low complexity region
|
550 |
583 |
N/A |
INTRINSIC |
|
low complexity region
|
677 |
688 |
N/A |
INTRINSIC |
|
Pfam:TIG
|
874 |
954 |
3.1e-11 |
PFAM |
|
low complexity region
|
997 |
1030 |
N/A |
INTRINSIC |
|
ANK
|
1066 |
1095 |
1.7e2 |
SMART |
|
ANK
|
1111 |
1141 |
4.73e2 |
SMART |
|
low complexity region
|
1301 |
1319 |
N/A |
INTRINSIC |
|
IQ
|
1548 |
1564 |
2.38e2 |
SMART |
|
IQ
|
1578 |
1600 |
5.42e0 |
SMART |
|
| Meta Mutation Damage Score |
0.1795 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 98.8%
|
| Validation Efficiency |
98% (79/81) |
| MGI Phenotype |
PHENOTYPE: Global or nervous system deletion of this gene results in decreased body size, severe ataxia, progressive Purkinje cell degeneration, and cerebellar atrophy. [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 |
|---|
| Acoxl |
C |
A |
2: 127,965,028 (GRCm39) |
A624E |
probably benign |
Het |
| Adnp |
A |
G |
2: 168,024,287 (GRCm39) |
S1003P |
probably benign |
Het |
| Akap8l |
T |
C |
17: 32,557,386 (GRCm39) |
D75G |
probably damaging |
Het |
| Ap4e1 |
A |
T |
2: 126,905,238 (GRCm39) |
T970S |
possibly damaging |
Het |
| Asb3 |
T |
A |
11: 30,979,029 (GRCm39) |
N106K |
probably damaging |
Het |
| Atp1a3 |
T |
C |
7: 24,678,390 (GRCm39) |
I988V |
probably benign |
Het |
| Ccdc77 |
A |
G |
6: 120,327,193 (GRCm39) |
L84P |
probably damaging |
Het |
| Ccne1 |
C |
T |
7: 37,798,726 (GRCm39) |
A298T |
probably damaging |
Het |
| Cdc42bpb |
T |
A |
12: 111,287,951 (GRCm39) |
E532V |
probably damaging |
Het |
| Clasp2 |
G |
A |
9: 113,615,467 (GRCm39) |
|
probably null |
Het |
| Cntnap5b |
C |
A |
1: 100,003,887 (GRCm39) |
T289N |
possibly damaging |
Het |
| Dcun1d4 |
A |
G |
5: 73,648,538 (GRCm39) |
|
probably null |
Het |
| Dnah14 |
A |
G |
1: 181,532,100 (GRCm39) |
T2296A |
probably benign |
Het |
| Dnaja4 |
A |
T |
9: 54,616,516 (GRCm39) |
Q173L |
probably damaging |
Het |
| Dync2h1 |
G |
A |
9: 7,050,479 (GRCm39) |
A3190V |
probably benign |
Het |
| Frrs1 |
T |
A |
3: 116,671,920 (GRCm39) |
I6N |
probably benign |
Het |
| Fscn1 |
T |
C |
5: 142,957,801 (GRCm39) |
V477A |
probably benign |
Het |
| Fsip2 |
G |
A |
2: 82,811,541 (GRCm39) |
G2620E |
possibly damaging |
Het |
| Glp1r |
C |
T |
17: 31,128,297 (GRCm39) |
A92V |
probably benign |
Het |
| Gpr137b |
A |
T |
13: 13,542,205 (GRCm39) |
M204K |
probably damaging |
Het |
| Gstm1 |
A |
G |
3: 107,923,693 (GRCm39) |
V104A |
probably benign |
Het |
| Gtf2e1 |
A |
T |
16: 37,356,228 (GRCm39) |
N101K |
probably damaging |
Het |
| Igsf9b |
T |
C |
9: 27,245,536 (GRCm39) |
F1168L |
probably benign |
Het |
| Itpr2 |
A |
T |
6: 146,195,589 (GRCm39) |
V1629E |
probably damaging |
Het |
| Kat14 |
A |
G |
2: 144,235,918 (GRCm39) |
T428A |
probably benign |
Het |
| Kif21b |
T |
C |
1: 136,077,186 (GRCm39) |
Y403H |
probably damaging |
Het |
| Lpcat1 |
G |
C |
13: 73,662,649 (GRCm39) |
A533P |
probably benign |
Het |
| Lrp2 |
A |
T |
2: 69,336,917 (GRCm39) |
I1285N |
probably damaging |
Het |
| Mboat1 |
A |
T |
13: 30,408,398 (GRCm39) |
Y187F |
probably damaging |
Het |
| Mkx |
T |
C |
18: 7,002,525 (GRCm39) |
N7S |
probably damaging |
Het |
| Mrps27 |
A |
T |
13: 99,551,307 (GRCm39) |
T357S |
possibly damaging |
Het |
| Muc21 |
A |
G |
17: 35,932,870 (GRCm39) |
S439P |
unknown |
Het |
| Naa35 |
A |
G |
13: 59,733,997 (GRCm39) |
D9G |
probably benign |
Het |
| Ncoa4 |
T |
A |
14: 31,897,940 (GRCm39) |
N253K |
probably damaging |
Het |
| Neb |
A |
G |
2: 52,160,318 (GRCm39) |
Y2232H |
probably damaging |
Het |
| Nlk |
G |
A |
11: 78,481,793 (GRCm39) |
Q223* |
probably null |
Het |
| Npas2 |
T |
A |
1: 39,331,798 (GRCm39) |
I71N |
possibly damaging |
Het |
| Nup107 |
T |
A |
10: 117,609,267 (GRCm39) |
Q364L |
probably damaging |
Het |
| Or8g17 |
T |
A |
9: 38,934,566 (GRCm39) |
|
probably benign |
Het |
| Otof |
C |
T |
5: 30,532,964 (GRCm39) |
G1593S |
probably damaging |
Het |
| Panx3 |
G |
T |
9: 37,575,381 (GRCm39) |
H160Q |
probably damaging |
Het |
| Pappa |
T |
A |
4: 65,180,110 (GRCm39) |
H990Q |
probably damaging |
Het |
| Pax4 |
G |
A |
6: 28,446,136 (GRCm39) |
P119L |
probably damaging |
Het |
| Pcdhb20 |
T |
A |
18: 37,638,123 (GRCm39) |
D216E |
probably damaging |
Het |
| Pcdhgb8 |
T |
A |
18: 37,896,231 (GRCm39) |
S434T |
possibly damaging |
Het |
| Pf4 |
T |
C |
5: 90,920,448 (GRCm39) |
V3A |
probably benign |
Het |
| Phf24 |
T |
C |
4: 42,938,325 (GRCm39) |
S229P |
probably benign |
Het |
| Plcd3 |
A |
G |
11: 102,970,439 (GRCm39) |
F200S |
probably damaging |
Het |
| Ppp1r16a |
A |
G |
15: 76,575,104 (GRCm39) |
H4R |
probably damaging |
Het |
| Pramel15 |
A |
G |
4: 144,099,389 (GRCm39) |
C459R |
probably damaging |
Het |
| Prdm10 |
A |
G |
9: 31,227,738 (GRCm39) |
|
probably null |
Het |
| Prim2 |
A |
G |
1: 33,667,474 (GRCm39) |
|
probably null |
Het |
| Prkg1 |
T |
A |
19: 30,562,599 (GRCm39) |
H550L |
probably damaging |
Het |
| Prrc2c |
G |
T |
1: 162,501,086 (GRCm39) |
T2809N |
possibly damaging |
Het |
| Ptx3 |
A |
G |
3: 66,132,391 (GRCm39) |
E304G |
probably benign |
Het |
| Ralgps2 |
A |
G |
1: 156,655,818 (GRCm39) |
F369L |
probably benign |
Het |
| Rasgrp1 |
G |
A |
2: 117,168,885 (GRCm39) |
T31I |
probably benign |
Het |
| Rbsn |
A |
T |
6: 92,168,315 (GRCm39) |
M373K |
probably benign |
Het |
| Rnf168 |
C |
G |
16: 32,101,179 (GRCm39) |
R120G |
probably benign |
Het |
| Rp1 |
A |
G |
1: 4,420,140 (GRCm39) |
I324T |
probably damaging |
Het |
| Samd11 |
T |
C |
4: 156,336,747 (GRCm39) |
S31G |
probably benign |
Het |
| Sart3 |
A |
T |
5: 113,884,056 (GRCm39) |
L652Q |
probably benign |
Het |
| Scrn2 |
A |
G |
11: 96,924,634 (GRCm39) |
E421G |
probably benign |
Het |
| Sik2 |
A |
T |
9: 50,828,397 (GRCm39) |
L215Q |
probably damaging |
Het |
| Speer4a3 |
AACT |
A |
5: 26,155,849 (GRCm39) |
|
probably benign |
Het |
| Stard9 |
A |
T |
2: 120,534,639 (GRCm39) |
K3632M |
probably damaging |
Het |
| Swt1 |
A |
T |
1: 151,264,428 (GRCm39) |
D695E |
probably damaging |
Het |
| Tead3 |
T |
A |
17: 28,552,228 (GRCm39) |
M357L |
probably benign |
Het |
| Tgfbi |
A |
T |
13: 56,775,829 (GRCm39) |
T292S |
probably damaging |
Het |
| Tmc7 |
T |
C |
7: 118,155,157 (GRCm39) |
H247R |
probably benign |
Het |
| Trmt10b |
T |
A |
4: 45,308,549 (GRCm39) |
D236E |
probably damaging |
Het |
| Tshz1 |
C |
A |
18: 84,034,052 (GRCm39) |
V119L |
probably damaging |
Het |
| Ttn |
A |
C |
2: 76,658,258 (GRCm39) |
V12374G |
unknown |
Het |
| Tubgcp2 |
A |
G |
7: 139,585,274 (GRCm39) |
Y484H |
probably damaging |
Het |
| Ubr4 |
G |
C |
4: 139,177,824 (GRCm39) |
A1947P |
|
Het |
| Uggt1 |
A |
C |
1: 36,194,188 (GRCm39) |
V1350G |
probably benign |
Het |
| Vmn1r173 |
A |
T |
7: 23,402,076 (GRCm39) |
M104L |
probably benign |
Het |
| Xirp1 |
A |
T |
9: 119,848,113 (GRCm39) |
C257S |
probably damaging |
Het |
| Zfyve26 |
A |
G |
12: 79,327,179 (GRCm39) |
S724P |
probably damaging |
Het |
| Zmpste24 |
A |
T |
4: 120,940,091 (GRCm39) |
L185Q |
probably null |
Het |
| Zpld1 |
G |
A |
16: 55,052,594 (GRCm39) |
A340V |
probably benign |
Het |
|
| Other mutations in Camta1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00552:Camta1
|
APN |
4 |
151,155,881 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL00823:Camta1
|
APN |
4 |
151,169,058 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL01361:Camta1
|
APN |
4 |
151,229,149 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01523:Camta1
|
APN |
4 |
151,229,507 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
IGL01730:Camta1
|
APN |
4 |
151,147,302 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02045:Camta1
|
APN |
4 |
151,158,442 (GRCm39) |
splice site |
probably null |
|
|
IGL02541:Camta1
|
APN |
4 |
151,169,112 (GRCm39) |
missense |
probably benign |
0.12 |
|
IGL02839:Camta1
|
APN |
4 |
151,228,969 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03012:Camta1
|
APN |
4 |
151,537,756 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Bonus
|
UTSW |
4 |
151,222,832 (GRCm39) |
missense |
probably damaging |
1.00 |
|
BB010:Camta1
|
UTSW |
4 |
151,168,214 (GRCm39) |
missense |
probably damaging |
0.99 |
|
BB020:Camta1
|
UTSW |
4 |
151,168,214 (GRCm39) |
missense |
probably damaging |
0.99 |
|
PIT4449001:Camta1
|
UTSW |
4 |
151,216,043 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0136:Camta1
|
UTSW |
4 |
151,163,426 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0239:Camta1
|
UTSW |
4 |
151,228,187 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0239:Camta1
|
UTSW |
4 |
151,228,187 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0276:Camta1
|
UTSW |
4 |
151,159,597 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0346:Camta1
|
UTSW |
4 |
151,159,597 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0347:Camta1
|
UTSW |
4 |
151,159,597 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0348:Camta1
|
UTSW |
4 |
151,670,888 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R0385:Camta1
|
UTSW |
4 |
151,159,597 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0386:Camta1
|
UTSW |
4 |
151,159,597 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0388:Camta1
|
UTSW |
4 |
151,159,597 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0410:Camta1
|
UTSW |
4 |
151,159,597 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0456:Camta1
|
UTSW |
4 |
151,159,597 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0478:Camta1
|
UTSW |
4 |
151,159,597 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0510:Camta1
|
UTSW |
4 |
151,159,597 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0511:Camta1
|
UTSW |
4 |
151,159,597 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0683:Camta1
|
UTSW |
4 |
151,159,597 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0724:Camta1
|
UTSW |
4 |
151,162,349 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0732:Camta1
|
UTSW |
4 |
151,670,941 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R1549:Camta1
|
UTSW |
4 |
151,670,920 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1670:Camta1
|
UTSW |
4 |
151,164,228 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1704:Camta1
|
UTSW |
4 |
151,159,681 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1718:Camta1
|
UTSW |
4 |
151,168,481 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1941:Camta1
|
UTSW |
4 |
151,159,612 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1967:Camta1
|
UTSW |
4 |
151,173,430 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1998:Camta1
|
UTSW |
4 |
151,162,337 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2081:Camta1
|
UTSW |
4 |
151,228,699 (GRCm39) |
missense |
probably benign |
0.24 |
|
R2104:Camta1
|
UTSW |
4 |
151,537,751 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2240:Camta1
|
UTSW |
4 |
151,169,032 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R4516:Camta1
|
UTSW |
4 |
151,229,177 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R4539:Camta1
|
UTSW |
4 |
151,169,269 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4552:Camta1
|
UTSW |
4 |
151,876,959 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R4610:Camta1
|
UTSW |
4 |
151,169,284 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4658:Camta1
|
UTSW |
4 |
151,228,367 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4725:Camta1
|
UTSW |
4 |
151,232,953 (GRCm39) |
missense |
probably benign |
0.11 |
|
R4786:Camta1
|
UTSW |
4 |
151,374,496 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4812:Camta1
|
UTSW |
4 |
151,215,999 (GRCm39) |
missense |
probably null |
0.25 |
|
R4840:Camta1
|
UTSW |
4 |
151,228,864 (GRCm39) |
missense |
probably benign |
0.23 |
|
R5038:Camta1
|
UTSW |
4 |
151,229,926 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5112:Camta1
|
UTSW |
4 |
151,158,511 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5251:Camta1
|
UTSW |
4 |
151,248,341 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5388:Camta1
|
UTSW |
4 |
151,159,695 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5487:Camta1
|
UTSW |
4 |
151,229,211 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R6343:Camta1
|
UTSW |
4 |
151,164,306 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6462:Camta1
|
UTSW |
4 |
151,170,621 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6550:Camta1
|
UTSW |
4 |
151,222,832 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6990:Camta1
|
UTSW |
4 |
151,229,501 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R7190:Camta1
|
UTSW |
4 |
151,232,980 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R7215:Camta1
|
UTSW |
4 |
151,229,194 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7264:Camta1
|
UTSW |
4 |
151,537,856 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7403:Camta1
|
UTSW |
4 |
151,537,752 (GRCm39) |
nonsense |
probably null |
|
|
R7445:Camta1
|
UTSW |
4 |
151,228,748 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R7447:Camta1
|
UTSW |
4 |
151,168,327 (GRCm39) |
missense |
probably benign |
0.31 |
|
R7585:Camta1
|
UTSW |
4 |
151,229,287 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7751:Camta1
|
UTSW |
4 |
151,232,863 (GRCm39) |
splice site |
probably null |
|
|
R7881:Camta1
|
UTSW |
4 |
151,920,333 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7933:Camta1
|
UTSW |
4 |
151,168,214 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7960:Camta1
|
UTSW |
4 |
151,232,990 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8057:Camta1
|
UTSW |
4 |
151,228,489 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8073:Camta1
|
UTSW |
4 |
151,163,281 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8241:Camta1
|
UTSW |
4 |
151,168,282 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8247:Camta1
|
UTSW |
4 |
151,159,721 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8466:Camta1
|
UTSW |
4 |
151,170,577 (GRCm39) |
nonsense |
probably null |
|
|
R9035:Camta1
|
UTSW |
4 |
151,229,159 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9332:Camta1
|
UTSW |
4 |
151,228,474 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R9358:Camta1
|
UTSW |
4 |
151,222,881 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9626:Camta1
|
UTSW |
4 |
151,168,287 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9649:Camta1
|
UTSW |
4 |
151,216,004 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
X0063:Camta1
|
UTSW |
4 |
151,229,704 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Camta1
|
UTSW |
4 |
151,228,842 (GRCm39) |
missense |
probably benign |
0.06 |
|
Z1177:Camta1
|
UTSW |
4 |
151,162,382 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- CTTCTAAGGGAAGCTGCAGAC -3'
(R):5'- CTGCCTGGCTTTCAGATGTG -3'
Sequencing Primer
(F):5'- CTGCAGACAGCCAATGGG -3'
(R):5'- CAGATGTGGGCCTGTGC -3'
|
| Posted On |
2019-06-26 |
Incidental Mutation