Incidental Mutation 'R4971:Cdkl3'
| ID |
384457 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Cdkl3
|
| Ensembl Gene |
ENSMUSG00000020389 |
| Gene Name |
cyclin dependent kinase like 3 |
| Synonyms |
B230379H01Rik |
| MMRRC Submission |
042566-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.863)
|
| Stock # |
R4971 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
11 |
| Chromosomal Location |
51895048-51980611 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 51901995 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Alanine
at position 68
(V68A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000113303
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000063303]
[ENSMUST00000063321]
[ENSMUST00000109076]
[ENSMUST00000109077]
[ENSMUST00000109078]
[ENSMUST00000109079]
[ENSMUST00000109080]
[ENSMUST00000135076]
[ENSMUST00000109081]
[ENSMUST00000143228]
[ENSMUST00000121591]
[ENSMUST00000120374]
|
| AlphaFold |
Q8BLF2 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000063303
AA Change: V68A
PolyPhen 2
Score 0.201 (Sensitivity: 0.92; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000064315
Gene: ENSMUSG00000020389
AA Change: V68A
| Domain | Start | End | E-Value | Type |
|---|
|
S_TKc
|
4 |
286 |
2.27e-95 |
SMART |
|
Blast:S_TKc
|
361 |
477 |
1e-18 |
BLAST |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000063321
AA Change: V68A
PolyPhen 2
Score 0.201 (Sensitivity: 0.92; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000065128
Gene: ENSMUSG00000020389
AA Change: V68A
| Domain | Start | End | E-Value | Type |
|---|
|
S_TKc
|
4 |
286 |
2.27e-95 |
SMART |
|
Blast:S_TKc
|
361 |
477 |
9e-19 |
BLAST |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000109076
AA Change: V68A
PolyPhen 2
Score 0.201 (Sensitivity: 0.92; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000104704
Gene: ENSMUSG00000020389
AA Change: V68A
| Domain | Start | End | E-Value | Type |
|---|
|
S_TKc
|
4 |
286 |
2.27e-95 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000109077
AA Change: V68A
PolyPhen 2
Score 0.201 (Sensitivity: 0.92; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000104705
Gene: ENSMUSG00000020389
AA Change: V68A
| Domain | Start | End | E-Value | Type |
|---|
|
S_TKc
|
4 |
286 |
2.27e-95 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000109078
AA Change: V68A
PolyPhen 2
Score 0.201 (Sensitivity: 0.92; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000104706
Gene: ENSMUSG00000020389
AA Change: V68A
| Domain | Start | End | E-Value | Type |
|---|
|
S_TKc
|
4 |
286 |
2.27e-95 |
SMART |
|
Blast:S_TKc
|
361 |
457 |
8e-14 |
BLAST |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000109079
AA Change: V68A
PolyPhen 2
Score 0.201 (Sensitivity: 0.92; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000104707
Gene: ENSMUSG00000020389
AA Change: V68A
| Domain | Start | End | E-Value | Type |
|---|
|
S_TKc
|
4 |
286 |
2.27e-95 |
SMART |
|
Blast:S_TKc
|
361 |
477 |
9e-19 |
BLAST |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000109080
AA Change: V68A
PolyPhen 2
Score 0.481 (Sensitivity: 0.89; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000104708
Gene: ENSMUSG00000020389
AA Change: V68A
| Domain | Start | End | E-Value | Type |
|---|
|
S_TKc
|
4 |
286 |
2.27e-95 |
SMART |
|
Blast:S_TKc
|
361 |
477 |
1e-18 |
BLAST |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000135076
AA Change: V68A
PolyPhen 2
Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
|
| SMART Domains |
Protein: ENSMUSP00000117983
Gene: ENSMUSG00000020389
AA Change: V68A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Pkinase
|
4 |
192 |
5.6e-65 |
PFAM |
|
Pfam:Pkinase_Tyr
|
4 |
192 |
7.3e-37 |
PFAM |
|
Pfam:Kinase-like
|
49 |
192 |
3.2e-9 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000109081
AA Change: V68A
PolyPhen 2
Score 0.201 (Sensitivity: 0.92; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000104709
Gene: ENSMUSG00000020389
AA Change: V68A
| Domain | Start | End | E-Value | Type |
|---|
|
S_TKc
|
4 |
286 |
2.27e-95 |
SMART |
|
Blast:S_TKc
|
361 |
477 |
1e-18 |
BLAST |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000143228
AA Change: V68A
PolyPhen 2
Score 0.103 (Sensitivity: 0.93; Specificity: 0.86)
|
| SMART Domains |
Protein: ENSMUSP00000123279
Gene: ENSMUSG00000020389
AA Change: V68A
| Domain | Start | End | E-Value | Type |
|---|
|
S_TKc
|
4 |
286 |
2.27e-95 |
SMART |
|
Blast:S_TKc
|
361 |
477 |
1e-18 |
BLAST |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000121591
AA Change: V68A
PolyPhen 2
Score 0.201 (Sensitivity: 0.92; Specificity: 0.88)
|
| SMART Domains |
Protein: ENSMUSP00000112477
Gene: ENSMUSG00000020389
AA Change: V68A
| Domain | Start | End | E-Value | Type |
|---|
|
S_TKc
|
4 |
286 |
2.27e-95 |
SMART |
|
Blast:S_TKc
|
361 |
477 |
1e-18 |
BLAST |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000120374
AA Change: V68A
PolyPhen 2
Score 0.481 (Sensitivity: 0.89; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000113303
Gene: ENSMUSG00000020389
AA Change: V68A
| Domain | Start | End | E-Value | Type |
|---|
|
S_TKc
|
4 |
286 |
2.27e-95 |
SMART |
|
Blast:S_TKc
|
361 |
477 |
1e-18 |
BLAST |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000181262
|
| Coding Region Coverage |
- 1x: 99.0%
- 3x: 98.1%
- 10x: 95.6%
- 20x: 89.7%
|
| Validation Efficiency |
|
| 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 cyclin-dependent protein kinase (CDK) family. CDK family members are highly similar to the gene products of Saccharomyces cerevisiae cdc28, and Schizosaccharomyces pombe cdc2, and are known to be important regulators of cell cycle progression. This gene was identified as a gene absent in leukemic patients with chromosome 5q deletion. This loss may be an important determinant of dysmyelopoiesis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 57 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A2ml1 |
A |
T |
6: 128,524,190 (GRCm39) |
F1147L |
probably damaging |
Het |
| Abca2 |
T |
C |
2: 25,332,006 (GRCm39) |
S1373P |
probably damaging |
Het |
| Abca9 |
A |
T |
11: 110,042,874 (GRCm39) |
S392T |
probably benign |
Het |
| Abcd2 |
T |
C |
15: 91,047,313 (GRCm39) |
D580G |
probably benign |
Het |
| Actl9 |
T |
A |
17: 33,652,882 (GRCm39) |
L314H |
probably damaging |
Het |
| Adamtsl1 |
T |
C |
4: 86,255,168 (GRCm39) |
F746L |
probably damaging |
Het |
| Anks6 |
C |
T |
4: 47,030,795 (GRCm39) |
G601S |
probably damaging |
Het |
| Cnot1 |
A |
G |
8: 96,448,254 (GRCm39) |
F2266S |
probably damaging |
Het |
| Colq |
T |
C |
14: 31,267,034 (GRCm39) |
R159G |
probably damaging |
Het |
| Ctse |
A |
T |
1: 131,592,130 (GRCm39) |
D152V |
probably damaging |
Het |
| Cul7 |
G |
T |
17: 46,970,045 (GRCm39) |
M1011I |
probably benign |
Het |
| Cyb5r4 |
G |
T |
9: 86,939,224 (GRCm39) |
V336L |
possibly damaging |
Het |
| Dync2h1 |
A |
T |
9: 7,131,949 (GRCm39) |
H1619Q |
probably benign |
Het |
| Eif2ak1 |
A |
G |
5: 143,818,986 (GRCm39) |
K216E |
probably damaging |
Het |
| F5 |
A |
T |
1: 164,021,755 (GRCm39) |
H1410L |
probably benign |
Het |
| Frem2 |
T |
C |
3: 53,446,604 (GRCm39) |
Y2388C |
probably damaging |
Het |
| Fsip2 |
C |
T |
2: 82,816,222 (GRCm39) |
T3985M |
probably benign |
Het |
| Gak |
T |
C |
5: 108,744,672 (GRCm39) |
Y535C |
probably damaging |
Het |
| Gzmc |
G |
T |
14: 56,469,826 (GRCm39) |
P158Q |
probably damaging |
Het |
| Hook3 |
A |
G |
8: 26,572,607 (GRCm39) |
Y135H |
probably benign |
Het |
| Ikbke |
GCC |
G |
1: 131,203,004 (GRCm39) |
|
probably null |
Het |
| Ing4 |
A |
T |
6: 125,020,961 (GRCm39) |
M28L |
probably benign |
Het |
| Irs3 |
T |
A |
5: 137,642,754 (GRCm39) |
D228V |
probably damaging |
Het |
| Jade1 |
T |
A |
3: 41,555,836 (GRCm39) |
I301N |
probably damaging |
Het |
| Kif13b |
T |
A |
14: 64,995,011 (GRCm39) |
M921K |
possibly damaging |
Het |
| Kmt2c |
A |
G |
5: 25,515,870 (GRCm39) |
S2658P |
probably benign |
Het |
| Map3k4 |
A |
G |
17: 12,468,382 (GRCm39) |
|
probably null |
Het |
| Map4k5 |
C |
T |
12: 69,899,493 (GRCm39) |
V53I |
possibly damaging |
Het |
| Mdn1 |
T |
C |
4: 32,739,827 (GRCm39) |
S3694P |
probably damaging |
Het |
| Mroh7 |
A |
G |
4: 106,548,749 (GRCm39) |
V1038A |
probably benign |
Het |
| Muc5ac |
T |
C |
7: 141,370,015 (GRCm39) |
V3185A |
possibly damaging |
Het |
| Mup5 |
T |
A |
4: 61,751,297 (GRCm39) |
N117I |
probably benign |
Het |
| Myo19 |
T |
A |
11: 84,783,023 (GRCm39) |
M179K |
probably damaging |
Het |
| Myo1c |
A |
G |
11: 75,562,414 (GRCm39) |
Y902C |
probably damaging |
Het |
| Nf1 |
T |
A |
11: 79,335,469 (GRCm39) |
I977K |
probably damaging |
Het |
| Nos1 |
T |
C |
5: 118,081,899 (GRCm39) |
V1240A |
probably benign |
Het |
| Nr3c1 |
T |
C |
18: 39,619,930 (GRCm39) |
D119G |
probably damaging |
Het |
| Oga |
C |
A |
19: 45,758,485 (GRCm39) |
|
probably null |
Het |
| Or4c107 |
A |
T |
2: 88,788,863 (GRCm39) |
N18Y |
probably damaging |
Het |
| Pdlim2 |
A |
G |
14: 70,405,208 (GRCm39) |
V219A |
probably damaging |
Het |
| Pira13 |
T |
A |
7: 3,825,805 (GRCm39) |
M355L |
probably benign |
Het |
| Polr1g |
T |
C |
7: 19,091,487 (GRCm39) |
N207D |
probably benign |
Het |
| Prdx1 |
T |
C |
4: 116,549,128 (GRCm39) |
|
probably null |
Het |
| Rbfox1 |
C |
T |
16: 7,111,952 (GRCm39) |
R173C |
probably damaging |
Het |
| Rbp3 |
T |
A |
14: 33,676,427 (GRCm39) |
V125D |
probably damaging |
Het |
| Resf1 |
T |
C |
6: 149,227,097 (GRCm39) |
|
probably benign |
Het |
| Rhot1 |
T |
A |
11: 80,124,300 (GRCm39) |
I154K |
probably damaging |
Het |
| Runx1t1 |
C |
T |
4: 13,837,978 (GRCm39) |
R129C |
probably damaging |
Het |
| Setbp1 |
A |
G |
18: 78,901,382 (GRCm39) |
S762P |
probably benign |
Het |
| Slc13a3 |
A |
G |
2: 165,290,619 (GRCm39) |
I67T |
probably damaging |
Het |
| Tbc1d2b |
A |
T |
9: 90,100,923 (GRCm39) |
M689K |
probably benign |
Het |
| Top2a |
T |
C |
11: 98,884,667 (GRCm39) |
Y1517C |
probably damaging |
Het |
| Txndc2 |
A |
T |
17: 65,945,849 (GRCm39) |
N109K |
probably damaging |
Het |
| Tyk2 |
A |
G |
9: 21,031,797 (GRCm39) |
|
probably null |
Het |
| Wdfy3 |
A |
T |
5: 102,096,838 (GRCm39) |
L320* |
probably null |
Het |
| Zfp456 |
T |
C |
13: 67,514,995 (GRCm39) |
E237G |
probably benign |
Het |
| Zscan10 |
A |
G |
17: 23,826,147 (GRCm39) |
E103G |
possibly damaging |
Het |
|
| Other mutations in Cdkl3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00425:Cdkl3
|
APN |
11 |
51,920,683 (GRCm39) |
missense |
probably benign |
0.28 |
|
IGL01632:Cdkl3
|
APN |
11 |
51,895,899 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01768:Cdkl3
|
APN |
11 |
51,916,744 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01974:Cdkl3
|
APN |
11 |
51,902,064 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01981:Cdkl3
|
APN |
11 |
51,895,896 (GRCm39) |
missense |
probably benign |
0.43 |
|
IGL02510:Cdkl3
|
APN |
11 |
51,902,097 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0027:Cdkl3
|
UTSW |
11 |
51,923,176 (GRCm39) |
unclassified |
probably benign |
|
|
R0027:Cdkl3
|
UTSW |
11 |
51,923,176 (GRCm39) |
unclassified |
probably benign |
|
|
R0480:Cdkl3
|
UTSW |
11 |
51,895,882 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0499:Cdkl3
|
UTSW |
11 |
51,923,243 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R0627:Cdkl3
|
UTSW |
11 |
51,902,135 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0848:Cdkl3
|
UTSW |
11 |
51,902,094 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1510:Cdkl3
|
UTSW |
11 |
51,924,341 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R1558:Cdkl3
|
UTSW |
11 |
51,923,337 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R2046:Cdkl3
|
UTSW |
11 |
51,917,677 (GRCm39) |
missense |
probably benign |
|
|
R2077:Cdkl3
|
UTSW |
11 |
51,917,666 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2207:Cdkl3
|
UTSW |
11 |
51,918,020 (GRCm39) |
makesense |
probably null |
|
|
R2271:Cdkl3
|
UTSW |
11 |
51,923,322 (GRCm39) |
missense |
probably benign |
0.07 |
|
R2272:Cdkl3
|
UTSW |
11 |
51,923,322 (GRCm39) |
missense |
probably benign |
0.07 |
|
R4032:Cdkl3
|
UTSW |
11 |
51,902,118 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4839:Cdkl3
|
UTSW |
11 |
51,895,861 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6541:Cdkl3
|
UTSW |
11 |
51,913,571 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6559:Cdkl3
|
UTSW |
11 |
51,916,696 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7034:Cdkl3
|
UTSW |
11 |
51,918,042 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7068:Cdkl3
|
UTSW |
11 |
51,902,154 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7406:Cdkl3
|
UTSW |
11 |
51,924,369 (GRCm39) |
missense |
probably benign |
0.11 |
|
R7658:Cdkl3
|
UTSW |
11 |
51,918,009 (GRCm39) |
missense |
not run |
|
|
R7870:Cdkl3
|
UTSW |
11 |
51,909,284 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8324:Cdkl3
|
UTSW |
11 |
51,913,706 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8331:Cdkl3
|
UTSW |
11 |
51,917,704 (GRCm39) |
missense |
probably benign |
0.04 |
|
R8349:Cdkl3
|
UTSW |
11 |
51,975,260 (GRCm39) |
missense |
|
|
|
R8449:Cdkl3
|
UTSW |
11 |
51,975,260 (GRCm39) |
missense |
|
|
|
R8806:Cdkl3
|
UTSW |
11 |
51,923,295 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R9262:Cdkl3
|
UTSW |
11 |
51,916,702 (GRCm39) |
missense |
probably benign |
0.21 |
|
R9360:Cdkl3
|
UTSW |
11 |
51,924,349 (GRCm39) |
missense |
probably null |
0.00 |
|
R9385:Cdkl3
|
UTSW |
11 |
51,926,779 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9623:Cdkl3
|
UTSW |
11 |
51,895,816 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9729:Cdkl3
|
UTSW |
11 |
51,895,770 (GRCm39) |
missense |
probably benign |
0.44 |
|
| Predicted Primers |
PCR Primer
(F):5'- ATTAAGAATGTGCCAAGCCAGTTG -3'
(R):5'- AAAATAGGACTATCCCCGCGG -3'
Sequencing Primer
(F):5'- CAAGCCAGTTGAGAGCTTCTG -3'
(R):5'- AGCGGGCTCACTCTGAAG -3'
|
| Posted On |
2016-04-27 |
Incidental Mutation