Incidental Mutation 'R8456:Camsap3'
| ID |
655026 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Camsap3
|
| Ensembl Gene |
ENSMUSG00000044433 |
| Gene Name |
calmodulin regulated spectrin-associated protein family, member 3 |
| Synonyms |
Nezha, 2310057J16Rik |
| MMRRC Submission |
067833-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.941)
|
| Stock # |
R8456 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
8 |
| Chromosomal Location |
3637293-3659075 bp(+) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
C to T
at 3650679 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Stop codon
at position 236
(R236*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000146896
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000057028]
[ENSMUST00000171962]
[ENSMUST00000207077]
[ENSMUST00000207432]
[ENSMUST00000207533]
[ENSMUST00000207712]
[ENSMUST00000207970]
[ENSMUST00000208036]
[ENSMUST00000208240]
|
| AlphaFold |
Q80VC9 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000057028
AA Change: R209*
|
| SMART Domains |
Protein: ENSMUSP00000058958
Gene: ENSMUSG00000044433
AA Change: R209*
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
30 |
45 |
N/A |
INTRINSIC |
|
low complexity region
|
90 |
109 |
N/A |
INTRINSIC |
|
Pfam:CH
|
166 |
315 |
5.5e-27 |
PFAM |
|
Pfam:CAMSAP_CH
|
214 |
296 |
1.2e-29 |
PFAM |
|
low complexity region
|
359 |
373 |
N/A |
INTRINSIC |
|
coiled coil region
|
595 |
633 |
N/A |
INTRINSIC |
|
low complexity region
|
645 |
655 |
N/A |
INTRINSIC |
|
coiled coil region
|
696 |
727 |
N/A |
INTRINSIC |
|
low complexity region
|
749 |
779 |
N/A |
INTRINSIC |
|
low complexity region
|
828 |
837 |
N/A |
INTRINSIC |
|
low complexity region
|
866 |
881 |
N/A |
INTRINSIC |
|
coiled coil region
|
900 |
943 |
N/A |
INTRINSIC |
|
low complexity region
|
944 |
965 |
N/A |
INTRINSIC |
|
low complexity region
|
1002 |
1024 |
N/A |
INTRINSIC |
|
CAMSAP_CKK
|
1111 |
1240 |
1.29e-86 |
SMART |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000171962
AA Change: R209*
|
| SMART Domains |
Protein: ENSMUSP00000125993
Gene: ENSMUSG00000044433
AA Change: R209*
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
30 |
45 |
N/A |
INTRINSIC |
|
low complexity region
|
90 |
109 |
N/A |
INTRINSIC |
|
Pfam:CAMSAP_CH
|
214 |
296 |
6e-31 |
PFAM |
|
low complexity region
|
360 |
374 |
N/A |
INTRINSIC |
|
Pfam:CAMSAP_CC1
|
587 |
645 |
1.1e-27 |
PFAM |
|
low complexity region
|
646 |
656 |
N/A |
INTRINSIC |
|
coiled coil region
|
697 |
728 |
N/A |
INTRINSIC |
|
low complexity region
|
750 |
780 |
N/A |
INTRINSIC |
|
low complexity region
|
829 |
838 |
N/A |
INTRINSIC |
|
low complexity region
|
867 |
882 |
N/A |
INTRINSIC |
|
coiled coil region
|
901 |
944 |
N/A |
INTRINSIC |
|
low complexity region
|
945 |
966 |
N/A |
INTRINSIC |
|
low complexity region
|
1003 |
1025 |
N/A |
INTRINSIC |
|
CAMSAP_CKK
|
1112 |
1241 |
1.29e-86 |
SMART |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000207077
AA Change: R225*
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000207432
AA Change: R236*
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000207533
AA Change: R225*
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000207712
AA Change: R209*
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000207970
AA Change: R220*
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000208036
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000208240
AA Change: R220*
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.1%
|
| Validation Efficiency |
|
| MGI Phenotype |
PHENOTYPE: Mice homozygous for a null allele display variable penetrance of vascular, liver, nervous system, rib and eye abnormalities. Mice homozygous for an allele with loss of microtubule binding show partial lethality, decreased body size and abnormal alignment of microtubles in polarized epithelial cells. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 52 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca7 |
A |
G |
10: 79,842,360 (GRCm39) |
E1098G |
probably benign |
Het |
| Akap1 |
T |
A |
11: 88,725,557 (GRCm39) |
|
probably null |
Het |
| Arhgap26 |
T |
C |
18: 39,244,901 (GRCm39) |
V182A |
possibly damaging |
Het |
| Arhgef19 |
A |
G |
4: 140,977,926 (GRCm39) |
K545R |
probably benign |
Het |
| Asph |
C |
T |
4: 9,537,722 (GRCm39) |
R352Q |
probably benign |
Het |
| B3glct |
T |
A |
5: 149,650,254 (GRCm39) |
I119N |
probably damaging |
Het |
| Bltp3b |
A |
G |
10: 89,647,954 (GRCm39) |
T1339A |
probably benign |
Het |
| Ccser2 |
A |
T |
14: 36,612,331 (GRCm39) |
M792K |
probably benign |
Het |
| Ceacam5 |
C |
T |
7: 17,479,624 (GRCm39) |
T247I |
possibly damaging |
Het |
| Dnah9 |
A |
G |
11: 66,047,764 (GRCm39) |
S19P |
probably damaging |
Het |
| Dtwd1 |
A |
G |
2: 126,000,451 (GRCm39) |
E129G |
probably damaging |
Het |
| Ebf3 |
T |
A |
7: 136,800,916 (GRCm39) |
M490L |
probably benign |
Het |
| Elp1 |
ACTTCTTCTTCTTCTTCTTCTTC |
ACTTCTTCTTCTTCTTCTTC |
4: 56,781,176 (GRCm39) |
|
probably benign |
Het |
| Erbb4 |
A |
G |
1: 68,110,789 (GRCm39) |
L1008S |
probably damaging |
Het |
| Ereg |
C |
T |
5: 91,237,993 (GRCm39) |
P160S |
possibly damaging |
Het |
| Exoc6b |
ATTT |
ATTTT |
6: 84,821,077 (GRCm39) |
|
probably null |
Het |
| Fmn1 |
A |
G |
2: 113,195,385 (GRCm39) |
T362A |
unknown |
Het |
| Gm14326 |
A |
T |
2: 177,590,312 (GRCm39) |
D16E |
probably benign |
Het |
| H1f8 |
A |
T |
6: 115,925,745 (GRCm39) |
M181L |
probably benign |
Het |
| H3c1 |
A |
T |
13: 23,946,083 (GRCm39) |
F85Y |
probably damaging |
Het |
| Herc6 |
A |
T |
6: 57,575,548 (GRCm39) |
T190S |
probably benign |
Het |
| Lama1 |
T |
G |
17: 68,044,491 (GRCm39) |
I130S |
|
Het |
| Letm2 |
T |
C |
8: 26,071,729 (GRCm39) |
D391G |
probably damaging |
Het |
| Map3k9 |
T |
C |
12: 81,780,892 (GRCm39) |
I423V |
probably damaging |
Het |
| Melk |
T |
A |
4: 44,312,191 (GRCm39) |
C168S |
possibly damaging |
Het |
| Naa16 |
A |
T |
14: 79,596,915 (GRCm39) |
N356K |
probably benign |
Het |
| Nup214 |
A |
G |
2: 31,929,372 (GRCm39) |
N1873S |
probably benign |
Het |
| Or2y1f |
C |
T |
11: 49,184,385 (GRCm39) |
P79L |
probably damaging |
Het |
| Or8b41 |
T |
A |
9: 38,054,981 (GRCm39) |
C178* |
probably null |
Het |
| Pom121 |
A |
G |
5: 135,410,032 (GRCm39) |
F1042L |
unknown |
Het |
| Pramel51 |
T |
A |
12: 88,143,986 (GRCm39) |
T284S |
probably benign |
Het |
| Pxdn |
T |
C |
12: 30,061,889 (GRCm39) |
S1334P |
probably damaging |
Het |
| Ranbp1 |
C |
T |
16: 18,063,170 (GRCm39) |
E69K |
probably damaging |
Het |
| Rasl11a |
T |
C |
5: 146,782,045 (GRCm39) |
S7P |
probably damaging |
Het |
| Rev1 |
G |
A |
1: 38,098,324 (GRCm39) |
R740* |
probably null |
Het |
| Rnf157 |
C |
T |
11: 116,240,246 (GRCm39) |
V443M |
probably benign |
Het |
| Scn3a |
T |
A |
2: 65,291,017 (GRCm39) |
T1910S |
probably benign |
Het |
| Sh2b1 |
TGGGGACCAGCTCAGCCACGGGGACCAGCTC |
TGGGGACCAGCTCAGCCACGGGGACCAGCTCAGCCACGGGGACCAGCTC |
7: 126,066,742 (GRCm39) |
|
probably benign |
Het |
| Sh2b1 |
C |
CAGCCACGGGGCCTAGCTA |
7: 126,066,772 (GRCm39) |
|
probably null |
Het |
| Siah2 |
T |
C |
3: 58,583,503 (GRCm39) |
N261S |
probably benign |
Het |
| Sumf2 |
T |
G |
5: 129,889,003 (GRCm39) |
W264G |
possibly damaging |
Het |
| Tal1 |
G |
T |
4: 114,920,625 (GRCm39) |
A100S |
probably benign |
Het |
| Tmprss9 |
A |
G |
10: 80,730,251 (GRCm39) |
D717G |
possibly damaging |
Het |
| Tox2 |
G |
T |
2: 163,046,550 (GRCm39) |
R9L |
unknown |
Het |
| Traj46 |
A |
G |
14: 54,409,795 (GRCm39) |
E1G |
|
Het |
| Unc80 |
A |
G |
1: 66,680,788 (GRCm39) |
D2128G |
possibly damaging |
Het |
| Usp21 |
A |
T |
1: 171,112,290 (GRCm39) |
F308I |
probably damaging |
Het |
| Vgf |
A |
T |
5: 137,061,265 (GRCm39) |
I476F |
probably damaging |
Het |
| Vps35 |
G |
A |
8: 85,987,934 (GRCm39) |
T739I |
possibly damaging |
Het |
| Wdr95 |
G |
T |
5: 149,502,572 (GRCm39) |
C279F |
probably damaging |
Het |
| Zbtb32 |
T |
C |
7: 30,289,381 (GRCm39) |
S94G |
unknown |
Het |
| Zdhhc13 |
T |
A |
7: 48,452,747 (GRCm39) |
I153N |
probably damaging |
Het |
|
| Other mutations in Camsap3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00546:Camsap3
|
APN |
8 |
3,652,077 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00797:Camsap3
|
APN |
8 |
3,652,115 (GRCm39) |
splice site |
probably benign |
|
|
IGL01457:Camsap3
|
APN |
8 |
3,654,795 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL01833:Camsap3
|
APN |
8 |
3,658,508 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02095:Camsap3
|
APN |
8 |
3,653,845 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02880:Camsap3
|
APN |
8 |
3,653,913 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0005:Camsap3
|
UTSW |
8 |
3,654,288 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0049:Camsap3
|
UTSW |
8 |
3,648,772 (GRCm39) |
missense |
probably benign |
0.11 |
|
R0049:Camsap3
|
UTSW |
8 |
3,648,772 (GRCm39) |
missense |
probably benign |
0.11 |
|
R0347:Camsap3
|
UTSW |
8 |
3,652,029 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0926:Camsap3
|
UTSW |
8 |
3,637,960 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0946:Camsap3
|
UTSW |
8 |
3,654,442 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1169:Camsap3
|
UTSW |
8 |
3,653,866 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1206:Camsap3
|
UTSW |
8 |
3,654,708 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1207:Camsap3
|
UTSW |
8 |
3,654,708 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1207:Camsap3
|
UTSW |
8 |
3,654,708 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1454:Camsap3
|
UTSW |
8 |
3,653,968 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
R1475:Camsap3
|
UTSW |
8 |
3,654,708 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1581:Camsap3
|
UTSW |
8 |
3,654,708 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1618:Camsap3
|
UTSW |
8 |
3,648,740 (GRCm39) |
missense |
probably benign |
0.25 |
|
R1820:Camsap3
|
UTSW |
8 |
3,653,485 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1899:Camsap3
|
UTSW |
8 |
3,653,922 (GRCm39) |
nonsense |
probably null |
|
|
R1914:Camsap3
|
UTSW |
8 |
3,654,708 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1952:Camsap3
|
UTSW |
8 |
3,654,789 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2338:Camsap3
|
UTSW |
8 |
3,656,808 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3725:Camsap3
|
UTSW |
8 |
3,653,785 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3726:Camsap3
|
UTSW |
8 |
3,653,785 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4528:Camsap3
|
UTSW |
8 |
3,656,515 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R4652:Camsap3
|
UTSW |
8 |
3,650,689 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R5025:Camsap3
|
UTSW |
8 |
3,654,244 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5120:Camsap3
|
UTSW |
8 |
3,650,680 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5381:Camsap3
|
UTSW |
8 |
3,653,812 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5388:Camsap3
|
UTSW |
8 |
3,654,276 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5829:Camsap3
|
UTSW |
8 |
3,647,899 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5846:Camsap3
|
UTSW |
8 |
3,653,980 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5935:Camsap3
|
UTSW |
8 |
3,651,999 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6363:Camsap3
|
UTSW |
8 |
3,651,971 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6469:Camsap3
|
UTSW |
8 |
3,653,941 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R6595:Camsap3
|
UTSW |
8 |
3,658,742 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6595:Camsap3
|
UTSW |
8 |
3,654,186 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7024:Camsap3
|
UTSW |
8 |
3,658,242 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7062:Camsap3
|
UTSW |
8 |
3,657,834 (GRCm39) |
unclassified |
probably benign |
|
|
R7109:Camsap3
|
UTSW |
8 |
3,648,087 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R7233:Camsap3
|
UTSW |
8 |
3,650,371 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7236:Camsap3
|
UTSW |
8 |
3,654,116 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7316:Camsap3
|
UTSW |
8 |
3,654,648 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
R7340:Camsap3
|
UTSW |
8 |
3,637,960 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7512:Camsap3
|
UTSW |
8 |
3,648,740 (GRCm39) |
missense |
probably benign |
0.25 |
|
R7779:Camsap3
|
UTSW |
8 |
3,647,887 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8134:Camsap3
|
UTSW |
8 |
3,648,075 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8356:Camsap3
|
UTSW |
8 |
3,650,679 (GRCm39) |
nonsense |
probably null |
|
|
R8696:Camsap3
|
UTSW |
8 |
3,653,614 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8804:Camsap3
|
UTSW |
8 |
3,652,624 (GRCm39) |
missense |
probably benign |
0.14 |
|
R9022:Camsap3
|
UTSW |
8 |
3,656,575 (GRCm39) |
missense |
probably benign |
0.08 |
|
R9380:Camsap3
|
UTSW |
8 |
3,653,999 (GRCm39) |
missense |
probably benign |
0.09 |
|
R9706:Camsap3
|
UTSW |
8 |
3,658,689 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
Z1192:Camsap3
|
UTSW |
8 |
3,654,124 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- CAGACAAGTCTTCTGCCTCTTG -3'
(R):5'- ATACTGGTCTTGCAGACTGGAG -3'
Sequencing Primer
(F):5'- AAGTCTTCTGCCTCTTGCTTCTG -3'
(R):5'- ACTGGAGATGCCTTTCCAGGATC -3'
|
| Posted On |
2020-10-20 |
Incidental Mutation