Incidental Mutation 'FR4340:Cul9'
ID |
511190 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cul9
|
Ensembl Gene |
ENSMUSG00000040327 |
Gene Name |
cullin 9 |
Synonyms |
Parc, 1810035I07Rik |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.227)
|
Stock # |
FR4340 ()
|
Quality Score |
176.468 |
Status
|
Not validated
|
Chromosome |
17 |
Chromosomal Location |
46811535-46857314 bp(-) (GRCm39) |
Type of Mutation |
small insertion (1 aa in frame mutation) |
DNA Base Change (assembly) |
TCC to TCCCCC
at 46811779 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000138418
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000046497]
[ENSMUST00000066026]
[ENSMUST00000182485]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000046497
|
SMART Domains |
Protein: ENSMUSP00000045283 Gene: ENSMUSG00000040658
Domain | Start | End | E-Value | Type |
Pfam:Nuc_deoxyrib_tr
|
12 |
144 |
3.8e-21 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000066026
|
SMART Domains |
Protein: ENSMUSP00000067736 Gene: ENSMUSG00000040327
Domain | Start | End | E-Value | Type |
low complexity region
|
46 |
61 |
N/A |
INTRINSIC |
low complexity region
|
119 |
131 |
N/A |
INTRINSIC |
low complexity region
|
345 |
357 |
N/A |
INTRINSIC |
Pfam:Cul7
|
367 |
441 |
1e-35 |
PFAM |
low complexity region
|
447 |
460 |
N/A |
INTRINSIC |
low complexity region
|
525 |
540 |
N/A |
INTRINSIC |
low complexity region
|
845 |
860 |
N/A |
INTRINSIC |
low complexity region
|
873 |
880 |
N/A |
INTRINSIC |
APC10
|
1166 |
1325 |
1.97e-56 |
SMART |
low complexity region
|
1437 |
1450 |
N/A |
INTRINSIC |
low complexity region
|
1563 |
1578 |
N/A |
INTRINSIC |
low complexity region
|
1646 |
1671 |
N/A |
INTRINSIC |
Cullin_Nedd8
|
1867 |
1950 |
7.55e-6 |
SMART |
Blast:RING
|
2074 |
2122 |
2e-13 |
BLAST |
IBR
|
2144 |
2207 |
8.99e-14 |
SMART |
IBR
|
2228 |
2283 |
4.66e-2 |
SMART |
low complexity region
|
2503 |
2520 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000181301
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000182315
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000182485
|
SMART Domains |
Protein: ENSMUSP00000138418 Gene: ENSMUSG00000040327
Domain | Start | End | E-Value | Type |
low complexity region
|
46 |
61 |
N/A |
INTRINSIC |
low complexity region
|
119 |
131 |
N/A |
INTRINSIC |
low complexity region
|
345 |
357 |
N/A |
INTRINSIC |
Pfam:Cul7
|
367 |
442 |
1.4e-33 |
PFAM |
low complexity region
|
447 |
460 |
N/A |
INTRINSIC |
low complexity region
|
525 |
540 |
N/A |
INTRINSIC |
low complexity region
|
845 |
860 |
N/A |
INTRINSIC |
low complexity region
|
873 |
880 |
N/A |
INTRINSIC |
APC10
|
1166 |
1325 |
1.97e-56 |
SMART |
low complexity region
|
1437 |
1450 |
N/A |
INTRINSIC |
low complexity region
|
1563 |
1578 |
N/A |
INTRINSIC |
low complexity region
|
1646 |
1671 |
N/A |
INTRINSIC |
Cullin_Nedd8
|
1867 |
1950 |
7.55e-6 |
SMART |
Blast:RING
|
2074 |
2122 |
3e-13 |
BLAST |
IBR
|
2144 |
2207 |
8.99e-14 |
SMART |
IBR
|
2228 |
2283 |
4.66e-2 |
SMART |
coiled coil region
|
2461 |
2497 |
N/A |
INTRINSIC |
low complexity region
|
2513 |
2530 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000182530
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000183078
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000183312
|
Coding Region Coverage |
- 1x: 99.7%
- 3x: 99.4%
- 10x: 97.8%
- 20x: 94.3%
|
Validation Efficiency |
|
MGI Phenotype |
PHENOTYPE: Mice homozygous for a knock-out allele exhibit decreased body weight, increased incidence of tumors, and decreased cellular sensitivity to radiation-induced apoptosis. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 115 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930433I11Rik |
AACC |
A |
7: 40,642,479 (GRCm39) |
|
probably benign |
Het |
4930578G10Rik |
G |
T |
4: 42,761,098 (GRCm39) |
|
probably benign |
Het |
7530416G11Rik |
T |
A |
15: 85,378,508 (GRCm39) |
E45V |
unknown |
Homo |
A530064D06Rik |
GTAGGAAGCTTAG |
GTAG |
17: 48,470,549 (GRCm39) |
|
probably benign |
Homo |
Arpc1b |
CC |
CCTGGTC |
5: 145,063,602 (GRCm39) |
|
probably null |
Het |
Arrb2 |
C |
T |
11: 70,329,497 (GRCm39) |
T269M |
probably damaging |
Homo |
Bcas3 |
G |
A |
11: 85,400,323 (GRCm39) |
V431I |
probably benign |
Homo |
Blm |
ACCT |
ACCTGCCT |
7: 80,113,515 (GRCm39) |
|
probably benign |
Het |
Blm |
TCCTCCTCCTCCTCCTCCTCCTCC |
TCCTCCTCCTCCACCTCCTCCTCCTCCTCCTCCTCC |
7: 80,162,658 (GRCm39) |
|
probably benign |
Het |
Blm |
TCCTCCTCCTCCTCCTCCTCCTCC |
TCCTCCTCCTCCGCCTCCTCCTCCTCCTCCTCCTCC |
7: 80,162,655 (GRCm39) |
|
probably benign |
Het |
Bltp1 |
TATTATTAT |
TATTATTATTATTATCATTATTAT |
3: 37,104,901 (GRCm39) |
|
probably benign |
Het |
Cacna1a |
ACC |
ACCGCC |
8: 85,365,352 (GRCm39) |
|
probably benign |
Het |
Cacna1f |
AGG |
AGGCGG |
X: 7,486,306 (GRCm39) |
|
probably benign |
Het |
Calhm1 |
CTCTGTGGCTGTGGCTGTGGCTGTG |
CTCTGTGGCTGTGTCTGTGGCTGTGGCTGTGGCTGTG |
19: 47,129,690 (GRCm39) |
|
probably benign |
Het |
Casz1 |
ACCACAGCCACAGCCACAGCCAC |
ACCACAGCCACAGCCAC |
4: 149,036,759 (GRCm39) |
|
probably benign |
Homo |
Ccdc121 |
GAGAAG |
GAG |
5: 31,644,717 (GRCm39) |
|
probably benign |
Het |
Cd164 |
G |
T |
10: 41,397,922 (GRCm39) |
A59S |
probably benign |
Het |
Cd22 |
C |
T |
7: 30,577,507 (GRCm39) |
R2H |
possibly damaging |
Homo |
Cd80 |
GAA |
GAAAAA |
16: 38,306,678 (GRCm39) |
|
probably benign |
Homo |
Cimip2b |
CAGAG |
CAG |
4: 43,427,384 (GRCm39) |
|
probably null |
Homo |
Col2a1 |
C |
A |
15: 97,886,862 (GRCm39) |
|
probably null |
Het |
Col6a5 |
A |
T |
9: 105,811,373 (GRCm39) |
N715K |
unknown |
Homo |
Crygc |
A |
T |
1: 65,110,822 (GRCm39) |
F155Y |
probably benign |
Het |
Cyp2d11 |
T |
TGGGA |
15: 82,274,223 (GRCm39) |
|
probably null |
Homo |
Dbr1 |
AGG |
AGGAGGCGG |
9: 99,465,754 (GRCm39) |
|
probably benign |
Het |
Dennd10 |
CT |
CTTTT |
19: 60,803,059 (GRCm39) |
|
probably benign |
Homo |
Dennd2b |
CACCACACTGGGGCAGCCCACACTGGGGCAG |
CCCCACACTGGGGCAG |
7: 109,156,128 (GRCm39) |
|
probably benign |
Het |
Dnah12 |
G |
T |
14: 26,571,342 (GRCm39) |
G2817V |
probably damaging |
Homo |
Dnah8 |
ACACTGCC |
AC |
17: 30,854,437 (GRCm39) |
|
probably benign |
Het |
Dthd1 |
C |
CTTA |
5: 63,000,369 (GRCm39) |
|
probably benign |
Homo |
Frem3 |
CT |
CTTTT |
8: 81,341,870 (GRCm39) |
|
probably benign |
Homo |
Frmpd2 |
G |
T |
14: 33,232,978 (GRCm39) |
L399F |
probably damaging |
Homo |
G530012D18Rik |
CACACAGAGAGAGAGAGAGAGAGAGA |
CA |
1: 85,504,873 (GRCm39) |
|
probably benign |
Het |
Gbp2b |
A |
G |
3: 142,309,413 (GRCm39) |
I175V |
probably benign |
Het |
Gm14393 |
T |
C |
2: 174,903,427 (GRCm39) |
E160G |
possibly damaging |
Het |
Gm16519 |
A |
AGAAC |
17: 71,236,333 (GRCm39) |
|
probably null |
Homo |
Gm4340 |
GCAG |
GCAACAG |
10: 104,031,959 (GRCm39) |
|
probably benign |
Het |
Gm4340 |
CAGAAG |
CAGAAGAAG |
10: 104,031,960 (GRCm39) |
|
probably benign |
Het |
Gm4340 |
CAG |
CAGTAG |
10: 104,031,936 (GRCm39) |
|
probably null |
Het |
Gpatch11 |
AGGAAG |
AGGAAGGGGAAG |
17: 79,149,603 (GRCm39) |
|
probably benign |
Het |
H2-Q4 |
G |
A |
17: 35,599,381 (GRCm39) |
D155N |
probably damaging |
Het |
Ifi208 |
ATGGTG |
ATG |
1: 173,505,264 (GRCm39) |
|
probably benign |
Homo |
Ighv5-9 |
C |
T |
12: 113,625,497 (GRCm39) |
S82N |
probably benign |
Homo |
Ipo9 |
TCC |
TCCCCC |
1: 135,314,007 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
CTC |
CTCTTC |
1: 135,314,009 (GRCm39) |
|
probably benign |
Het |
Isg20l2 |
AAG |
AAGTAG |
3: 87,839,019 (GRCm39) |
|
probably null |
Het |
Kmt2b |
TCCTCC |
TCCTCCCCCTCC |
7: 30,285,800 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
TCCTCC |
TCCTCCCCCTCC |
7: 30,285,788 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
TCCTCC |
TCCTCCCCCTCC |
7: 30,285,794 (GRCm39) |
|
probably benign |
Het |
Krt10 |
CCTCCT |
CCTCCTTCTCCT |
11: 99,280,100 (GRCm39) |
|
probably benign |
Het |
Krt10 |
CAC |
CACGAC |
11: 99,277,028 (GRCm39) |
|
probably benign |
Het |
Krt10 |
ACCG |
ACCGCCG |
11: 99,277,029 (GRCm39) |
|
probably benign |
Homo |
Las1l |
TCCTC |
TCCTCTACCTC |
X: 94,984,228 (GRCm39) |
|
probably benign |
Het |
Lce1a1 |
C |
T |
3: 92,554,151 (GRCm39) |
G108S |
unknown |
Het |
Lkaaear1 |
CCAGCTCCAG |
CCAGCTCCAGCTGCAGCTCCAG |
2: 181,339,387 (GRCm39) |
|
probably benign |
Het |
Lrit3 |
CTG |
CTGTTG |
3: 129,582,457 (GRCm39) |
|
probably benign |
Het |
Mamld1 |
CAG |
CAGAAG |
X: 70,162,452 (GRCm39) |
|
probably benign |
Het |
Mapk7 |
TGCTGGCGCTGGTGCTGGCGCTGG |
TGCTGGCGCTGGCGCTGGTGCTGGCGCTGG |
11: 61,381,032 (GRCm39) |
|
probably benign |
Het |
Mast4 |
GCA |
GCAGTGTCA |
13: 102,872,825 (GRCm39) |
|
probably benign |
Homo |
Mast4 |
TTTT |
TTTTATTT |
13: 102,871,365 (GRCm39) |
|
probably null |
Het |
Med12l |
AGC |
AGCCGC |
3: 59,183,406 (GRCm39) |
|
probably benign |
Het |
Mfsd5 |
G |
A |
15: 102,189,596 (GRCm39) |
V323I |
probably benign |
Het |
Nacad |
GTC |
GTCAGGATC |
11: 6,549,761 (GRCm39) |
|
probably benign |
Het |
Naip1 |
A |
C |
13: 100,559,584 (GRCm39) |
M1140R |
probably benign |
Het |
Nbea |
TTTA |
T |
3: 55,916,633 (GRCm39) |
|
probably benign |
Homo |
Nefh |
CTCACCTGGGGACTTGGCCTC |
CTCACCTGGGGACTTGGCCTCACCTGGGGACTTGGCCTC |
11: 4,891,040 (GRCm39) |
|
probably benign |
Homo |
Nefh |
ACTTGGCCTCACCTGGGG |
ACTTGGCCTCACCTGGGGCCTTGGCCTCACCTGGGG |
11: 4,891,033 (GRCm39) |
|
probably benign |
Het |
Nefh |
GCCTCACCTGGGGACTTGGCCTC |
GCCTCACCTGGGGACTTGGCCTCACCTGGGGACTTGGCCTC |
11: 4,891,038 (GRCm39) |
|
probably benign |
Homo |
Neu1 |
TCTTCTA |
T |
17: 35,151,534 (GRCm39) |
|
probably benign |
Het |
Nutf2 |
G |
T |
8: 106,603,202 (GRCm39) |
D78Y |
probably damaging |
Het |
Or51q1 |
TCC |
TCCC |
7: 103,629,110 (GRCm39) |
|
probably null |
Het |
Or5e1 |
AT |
ATGATATT |
7: 108,354,161 (GRCm39) |
|
probably benign |
Homo |
Or5p70 |
G |
A |
7: 107,995,105 (GRCm39) |
M259I |
probably benign |
Het |
Or5p70 |
A |
G |
7: 107,995,100 (GRCm39) |
T258A |
probably benign |
Het |
Pdik1l |
ACCAC |
ACCACCCCCAC |
4: 134,006,823 (GRCm39) |
|
probably benign |
Het |
Phaf1 |
G |
A |
8: 105,967,730 (GRCm39) |
G207E |
probably benign |
Homo |
Pik3c2g |
AG |
AGAGGG |
6: 139,612,654 (GRCm39) |
|
probably null |
Homo |
Plekhs1 |
TCCAGAC |
TCCAGACCTCCCCCCAGAC |
19: 56,468,290 (GRCm39) |
|
probably benign |
Homo |
Prag1 |
C |
CAGT |
8: 36,571,040 (GRCm39) |
|
probably benign |
Homo |
Pramel16 |
G |
A |
4: 143,676,312 (GRCm39) |
T264M |
probably damaging |
Het |
Prkn |
G |
A |
17: 12,073,650 (GRCm39) |
V323M |
probably damaging |
Homo |
Raet1d |
A |
G |
10: 22,247,458 (GRCm39) |
Q178R |
probably benign |
Het |
Serac1 |
T |
A |
17: 6,121,083 (GRCm39) |
K70N |
probably damaging |
Homo |
Serpina3i |
CGG |
CGGTGG |
12: 104,231,423 (GRCm39) |
|
probably benign |
Het |
Sfswap |
ACTCAGCCC |
ACTCAGCCCCCTCAGCCC |
5: 129,646,815 (GRCm39) |
|
probably benign |
Het |
Six3 |
CGG |
CGGGGG |
17: 85,928,784 (GRCm39) |
|
probably benign |
Het |
Sp140l1 |
A |
C |
1: 85,087,072 (GRCm39) |
N6K |
probably damaging |
Het |
Speer4a1 |
C |
A |
5: 26,241,746 (GRCm39) |
E127* |
probably null |
Het |
Sry |
GCTGCTGCTGCTG |
GCTGCTGCTGCTGCTG |
Y: 2,662,824 (GRCm39) |
|
probably benign |
Het |
Tbr1 |
A |
C |
2: 61,636,691 (GRCm39) |
|
probably benign |
Het |
Tdpoz2 |
T |
TCC |
3: 93,558,922 (GRCm39) |
|
probably null |
Homo |
Tdpoz4 |
GAA |
GA |
3: 93,704,187 (GRCm39) |
|
probably null |
Het |
Tgoln1 |
AAG |
AAGCCTCAG |
6: 72,593,334 (GRCm39) |
|
probably benign |
Homo |
Tmbim7 |
C |
T |
5: 3,720,064 (GRCm39) |
R100C |
possibly damaging |
Het |
Tob1 |
CA |
CAGAA |
11: 94,105,303 (GRCm39) |
|
probably benign |
Het |
Tob1 |
AGC |
AGCCGC |
11: 94,105,280 (GRCm39) |
|
probably benign |
Het |
Tob1 |
AGC |
AGCCGC |
11: 94,105,286 (GRCm39) |
|
probably benign |
Het |
Tomm5 |
GCATCTTCC |
GCATCTTCCACATCTTCC |
4: 45,107,973 (GRCm39) |
|
probably benign |
Het |
Triobp |
TCGG |
TCGGCGG |
15: 78,877,590 (GRCm39) |
|
probably benign |
Homo |
Tsbp1 |
GC |
GCAAC |
17: 34,679,051 (GRCm39) |
|
probably benign |
Het |
Tsbp1 |
CAG |
CAGTAG |
17: 34,679,034 (GRCm39) |
|
probably null |
Het |
Tsbp1 |
GCA |
GCATCA |
17: 34,679,042 (GRCm39) |
|
probably benign |
Het |
Tsen2 |
AGG |
AGGGGG |
6: 115,537,027 (GRCm39) |
|
probably benign |
Homo |
Tsen2 |
AGG |
AGGGGG |
6: 115,537,030 (GRCm39) |
|
probably benign |
Homo |
Ubtf |
TCC |
TCCCCC |
11: 102,197,776 (GRCm39) |
|
probably benign |
Het |
Vmn2r87 |
C |
T |
10: 130,314,583 (GRCm39) |
M334I |
probably benign |
Homo |
Zc3h13 |
CGGGATGTGCG |
CGGGATGTGCGGGATGTGCG |
14: 75,561,032 (GRCm39) |
|
probably benign |
Homo |
Zfp28 |
G |
A |
7: 6,397,862 (GRCm39) |
G766R |
probably damaging |
Het |
Zfp384 |
AAGCCCAGGCCCAGGCCCAGGCCCA |
AAGCCCAGGCCCAAGCCCAGGCCCAGGCCCAGGCCCA |
6: 125,013,426 (GRCm39) |
|
probably benign |
Het |
Zfp428 |
G |
A |
7: 24,214,506 (GRCm39) |
D41N |
probably damaging |
Homo |
Zfp598 |
CCACAGGC |
CC |
17: 24,898,346 (GRCm39) |
|
probably benign |
Het |
Zfp598 |
CCACCA |
CCACCAACACCA |
17: 24,899,757 (GRCm39) |
|
probably benign |
Het |
Zfp831 |
TCC |
TCCCCC |
2: 174,487,273 (GRCm39) |
|
probably benign |
Het |
Zfp933 |
GCTT |
GCTTTTCTT |
4: 147,910,186 (GRCm39) |
|
probably null |
Homo |
Zfp936 |
G |
A |
7: 42,838,913 (GRCm39) |
G127R |
possibly damaging |
Het |
|
Other mutations in Cul9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Cul9
|
APN |
17 |
46,836,635 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00330:Cul9
|
APN |
17 |
46,821,767 (GRCm39) |
splice site |
probably benign |
|
IGL00726:Cul9
|
APN |
17 |
46,839,022 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01020:Cul9
|
APN |
17 |
46,849,949 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01358:Cul9
|
APN |
17 |
46,849,240 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01410:Cul9
|
APN |
17 |
46,839,572 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01781:Cul9
|
APN |
17 |
46,850,230 (GRCm39) |
missense |
probably benign |
|
IGL01873:Cul9
|
APN |
17 |
46,813,378 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02117:Cul9
|
APN |
17 |
46,851,301 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02300:Cul9
|
APN |
17 |
46,831,958 (GRCm39) |
splice site |
probably benign |
|
IGL02426:Cul9
|
APN |
17 |
46,834,184 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02427:Cul9
|
APN |
17 |
46,813,558 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02496:Cul9
|
APN |
17 |
46,851,302 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL03008:Cul9
|
APN |
17 |
46,813,623 (GRCm39) |
splice site |
probably benign |
|
IGL03059:Cul9
|
APN |
17 |
46,849,913 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03302:Cul9
|
APN |
17 |
46,837,566 (GRCm39) |
missense |
probably damaging |
0.98 |
bottlenose
|
UTSW |
17 |
46,811,770 (GRCm39) |
missense |
possibly damaging |
0.79 |
flipper
|
UTSW |
17 |
46,836,818 (GRCm39) |
missense |
probably benign |
0.05 |
orca
|
UTSW |
17 |
46,836,061 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4449:Cul9
|
UTSW |
17 |
46,811,782 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Cul9
|
UTSW |
17 |
46,811,784 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Cul9
|
UTSW |
17 |
46,811,772 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Cul9
|
UTSW |
17 |
46,811,779 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Cul9
|
UTSW |
17 |
46,811,776 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Cul9
|
UTSW |
17 |
46,811,774 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Cul9
|
UTSW |
17 |
46,811,782 (GRCm39) |
small insertion |
probably benign |
|
R0012:Cul9
|
UTSW |
17 |
46,849,436 (GRCm39) |
missense |
probably benign |
0.26 |
R0079:Cul9
|
UTSW |
17 |
46,848,589 (GRCm39) |
nonsense |
probably null |
|
R0143:Cul9
|
UTSW |
17 |
46,837,336 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0390:Cul9
|
UTSW |
17 |
46,839,515 (GRCm39) |
missense |
probably benign |
0.34 |
R0401:Cul9
|
UTSW |
17 |
46,852,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R0529:Cul9
|
UTSW |
17 |
46,831,394 (GRCm39) |
splice site |
probably benign |
|
R0815:Cul9
|
UTSW |
17 |
46,848,748 (GRCm39) |
splice site |
probably null |
|
R0863:Cul9
|
UTSW |
17 |
46,848,748 (GRCm39) |
splice site |
probably null |
|
R0972:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1173:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1216:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1217:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1261:Cul9
|
UTSW |
17 |
46,836,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R1278:Cul9
|
UTSW |
17 |
46,811,775 (GRCm39) |
small deletion |
probably benign |
|
R1281:Cul9
|
UTSW |
17 |
46,822,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R1349:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1372:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1403:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1403:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1405:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1405:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Cul9
|
UTSW |
17 |
46,836,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Cul9
|
UTSW |
17 |
46,836,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R1482:Cul9
|
UTSW |
17 |
46,819,473 (GRCm39) |
missense |
probably damaging |
0.99 |
R1491:Cul9
|
UTSW |
17 |
46,849,490 (GRCm39) |
nonsense |
probably null |
|
R1618:Cul9
|
UTSW |
17 |
46,836,818 (GRCm39) |
missense |
probably benign |
0.05 |
R1641:Cul9
|
UTSW |
17 |
46,854,486 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1679:Cul9
|
UTSW |
17 |
46,832,082 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1771:Cul9
|
UTSW |
17 |
46,848,738 (GRCm39) |
missense |
probably benign |
0.41 |
R1803:Cul9
|
UTSW |
17 |
46,814,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R2020:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R2046:Cul9
|
UTSW |
17 |
46,854,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R2056:Cul9
|
UTSW |
17 |
46,854,298 (GRCm39) |
missense |
probably benign |
|
R2088:Cul9
|
UTSW |
17 |
46,837,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R2415:Cul9
|
UTSW |
17 |
46,854,364 (GRCm39) |
missense |
probably benign |
|
R2925:Cul9
|
UTSW |
17 |
46,821,907 (GRCm39) |
missense |
probably benign |
0.08 |
R2964:Cul9
|
UTSW |
17 |
46,813,154 (GRCm39) |
missense |
probably damaging |
0.96 |
R2965:Cul9
|
UTSW |
17 |
46,813,154 (GRCm39) |
missense |
probably damaging |
0.96 |
R3690:Cul9
|
UTSW |
17 |
46,814,957 (GRCm39) |
splice site |
probably null |
|
R3847:Cul9
|
UTSW |
17 |
46,836,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R4437:Cul9
|
UTSW |
17 |
46,813,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R4470:Cul9
|
UTSW |
17 |
46,849,262 (GRCm39) |
missense |
probably benign |
0.00 |
R4540:Cul9
|
UTSW |
17 |
46,814,015 (GRCm39) |
missense |
probably null |
0.98 |
R4555:Cul9
|
UTSW |
17 |
46,812,755 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4604:Cul9
|
UTSW |
17 |
46,841,072 (GRCm39) |
missense |
probably damaging |
0.99 |
R4646:Cul9
|
UTSW |
17 |
46,849,943 (GRCm39) |
nonsense |
probably null |
|
R4799:Cul9
|
UTSW |
17 |
46,811,770 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4822:Cul9
|
UTSW |
17 |
46,840,977 (GRCm39) |
missense |
probably benign |
0.01 |
R4964:Cul9
|
UTSW |
17 |
46,849,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R4965:Cul9
|
UTSW |
17 |
46,849,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R5027:Cul9
|
UTSW |
17 |
46,811,708 (GRCm39) |
missense |
probably damaging |
0.99 |
R5185:Cul9
|
UTSW |
17 |
46,836,758 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5237:Cul9
|
UTSW |
17 |
46,854,393 (GRCm39) |
missense |
probably benign |
0.00 |
R5278:Cul9
|
UTSW |
17 |
46,821,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R5361:Cul9
|
UTSW |
17 |
46,811,775 (GRCm39) |
small deletion |
probably benign |
|
R5455:Cul9
|
UTSW |
17 |
46,821,772 (GRCm39) |
splice site |
probably null |
|
R5592:Cul9
|
UTSW |
17 |
46,831,517 (GRCm39) |
missense |
probably benign |
0.00 |
R5597:Cul9
|
UTSW |
17 |
46,813,591 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5613:Cul9
|
UTSW |
17 |
46,814,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R6122:Cul9
|
UTSW |
17 |
46,832,854 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6135:Cul9
|
UTSW |
17 |
46,832,379 (GRCm39) |
missense |
probably benign |
|
R6352:Cul9
|
UTSW |
17 |
46,822,241 (GRCm39) |
missense |
probably benign |
0.00 |
R6376:Cul9
|
UTSW |
17 |
46,819,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R6868:Cul9
|
UTSW |
17 |
46,833,109 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6898:Cul9
|
UTSW |
17 |
46,821,952 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7090:Cul9
|
UTSW |
17 |
46,811,765 (GRCm39) |
missense |
probably damaging |
0.96 |
R7193:Cul9
|
UTSW |
17 |
46,849,423 (GRCm39) |
missense |
probably damaging |
0.98 |
R7221:Cul9
|
UTSW |
17 |
46,839,491 (GRCm39) |
missense |
probably damaging |
0.99 |
R7291:Cul9
|
UTSW |
17 |
46,851,359 (GRCm39) |
missense |
probably benign |
0.00 |
R7320:Cul9
|
UTSW |
17 |
46,821,835 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7348:Cul9
|
UTSW |
17 |
46,821,919 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7463:Cul9
|
UTSW |
17 |
46,831,402 (GRCm39) |
splice site |
probably null |
|
R7480:Cul9
|
UTSW |
17 |
46,848,738 (GRCm39) |
missense |
probably benign |
0.41 |
R7573:Cul9
|
UTSW |
17 |
46,830,836 (GRCm39) |
missense |
probably benign |
|
R7582:Cul9
|
UTSW |
17 |
46,821,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R7605:Cul9
|
UTSW |
17 |
46,852,658 (GRCm39) |
missense |
probably damaging |
0.99 |
R7684:Cul9
|
UTSW |
17 |
46,820,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R7830:Cul9
|
UTSW |
17 |
46,851,237 (GRCm39) |
missense |
probably benign |
0.37 |
R7834:Cul9
|
UTSW |
17 |
46,836,630 (GRCm39) |
splice site |
probably null |
|
R8131:Cul9
|
UTSW |
17 |
46,822,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R8192:Cul9
|
UTSW |
17 |
46,849,273 (GRCm39) |
missense |
probably benign |
0.01 |
R8231:Cul9
|
UTSW |
17 |
46,831,427 (GRCm39) |
missense |
probably damaging |
0.99 |
R8248:Cul9
|
UTSW |
17 |
46,840,940 (GRCm39) |
missense |
probably damaging |
0.99 |
R8504:Cul9
|
UTSW |
17 |
46,814,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R8550:Cul9
|
UTSW |
17 |
46,830,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R8716:Cul9
|
UTSW |
17 |
46,838,840 (GRCm39) |
missense |
probably benign |
0.28 |
R8769:Cul9
|
UTSW |
17 |
46,832,828 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8893:Cul9
|
UTSW |
17 |
46,811,775 (GRCm39) |
small deletion |
probably benign |
|
R8904:Cul9
|
UTSW |
17 |
46,831,427 (GRCm39) |
missense |
probably damaging |
0.99 |
R8936:Cul9
|
UTSW |
17 |
46,839,528 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8972:Cul9
|
UTSW |
17 |
46,854,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R9003:Cul9
|
UTSW |
17 |
46,836,001 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9012:Cul9
|
UTSW |
17 |
46,854,447 (GRCm39) |
missense |
probably benign |
|
R9056:Cul9
|
UTSW |
17 |
46,854,696 (GRCm39) |
missense |
probably damaging |
0.99 |
R9071:Cul9
|
UTSW |
17 |
46,837,379 (GRCm39) |
missense |
probably benign |
|
R9162:Cul9
|
UTSW |
17 |
46,837,529 (GRCm39) |
missense |
probably benign |
0.32 |
R9476:Cul9
|
UTSW |
17 |
46,821,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R9526:Cul9
|
UTSW |
17 |
46,841,026 (GRCm39) |
missense |
probably benign |
0.41 |
R9563:Cul9
|
UTSW |
17 |
46,820,897 (GRCm39) |
missense |
probably benign |
0.01 |
R9568:Cul9
|
UTSW |
17 |
46,831,044 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9610:Cul9
|
UTSW |
17 |
46,830,823 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9611:Cul9
|
UTSW |
17 |
46,830,823 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9705:Cul9
|
UTSW |
17 |
46,854,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R9765:Cul9
|
UTSW |
17 |
46,850,224 (GRCm39) |
missense |
probably benign |
0.18 |
RF011:Cul9
|
UTSW |
17 |
46,811,774 (GRCm39) |
small insertion |
probably benign |
|
RF016:Cul9
|
UTSW |
17 |
46,811,789 (GRCm39) |
nonsense |
probably null |
|
RF026:Cul9
|
UTSW |
17 |
46,811,795 (GRCm39) |
nonsense |
probably null |
|
RF027:Cul9
|
UTSW |
17 |
46,811,774 (GRCm39) |
small insertion |
probably benign |
|
RF030:Cul9
|
UTSW |
17 |
46,811,795 (GRCm39) |
small insertion |
probably benign |
|
RF033:Cul9
|
UTSW |
17 |
46,811,780 (GRCm39) |
small insertion |
probably benign |
|
RF039:Cul9
|
UTSW |
17 |
46,811,780 (GRCm39) |
small insertion |
probably benign |
|
RF041:Cul9
|
UTSW |
17 |
46,811,780 (GRCm39) |
nonsense |
probably null |
|
RF042:Cul9
|
UTSW |
17 |
46,851,541 (GRCm39) |
frame shift |
probably null |
|
RF057:Cul9
|
UTSW |
17 |
46,811,789 (GRCm39) |
nonsense |
probably null |
|
Z1176:Cul9
|
UTSW |
17 |
46,831,511 (GRCm39) |
nonsense |
probably null |
|
Z1176:Cul9
|
UTSW |
17 |
46,831,502 (GRCm39) |
nonsense |
probably null |
|
Z1177:Cul9
|
UTSW |
17 |
46,848,723 (GRCm39) |
missense |
probably benign |
0.14 |
|
Predicted Primers |
PCR Primer
(F):5'- CTTCAGACACTGGGAATCCC -3'
(R):5'- TGCAGAGTCCCTCAGTAGAGAC -3'
Sequencing Primer
(F):5'- GGAATCCCCTCTCCCATGAC -3'
(R):5'- TGAAAGGGTCCAACGTGCC -3'
|
Posted On |
2018-04-05 |