Incidental Mutation 'R7030:Cep170'
ID |
546212 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cep170
|
Ensembl Gene |
ENSMUSG00000057335 |
Gene Name |
centrosomal protein 170 |
Synonyms |
A330004A13Rik, 4933426L22Rik |
MMRRC Submission |
045131-MU
|
Accession Numbers |
|
Essential gene? |
Possibly essential
(E-score: 0.728)
|
Stock # |
R7030 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
1 |
Chromosomal Location |
176561219-176641633 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 176584051 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamic Acid to Glycine
at position 11
(E11G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000142032
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000057037]
[ENSMUST00000192927]
[ENSMUST00000194727]
[ENSMUST00000195433]
[ENSMUST00000195717]
|
AlphaFold |
Q6A065 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000057037
AA Change: E776G
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
SMART Domains |
Protein: ENSMUSP00000059562 Gene: ENSMUSG00000057335 AA Change: E776G
Domain | Start | End | E-Value | Type |
FHA
|
22 |
73 |
1.27e-7 |
SMART |
low complexity region
|
118 |
133 |
N/A |
INTRINSIC |
low complexity region
|
717 |
731 |
N/A |
INTRINSIC |
low complexity region
|
738 |
750 |
N/A |
INTRINSIC |
low complexity region
|
770 |
782 |
N/A |
INTRINSIC |
Pfam:CEP170_C
|
801 |
1496 |
3.3e-264 |
PFAM |
low complexity region
|
1533 |
1545 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000192664
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000192927
AA Change: E11G
PolyPhen 2
Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000142032 Gene: ENSMUSG00000057335 AA Change: E11G
Domain | Start | End | E-Value | Type |
low complexity region
|
5 |
17 |
N/A |
INTRINSIC |
Pfam:CEP170_C
|
30 |
469 |
3.4e-129 |
PFAM |
Pfam:CEP170_C
|
449 |
708 |
7.4e-102 |
PFAM |
low complexity region
|
742 |
754 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000194727
AA Change: E776G
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
SMART Domains |
Protein: ENSMUSP00000141793 Gene: ENSMUSG00000057335 AA Change: E776G
Domain | Start | End | E-Value | Type |
FHA
|
22 |
73 |
1.27e-7 |
SMART |
low complexity region
|
118 |
133 |
N/A |
INTRINSIC |
low complexity region
|
717 |
731 |
N/A |
INTRINSIC |
low complexity region
|
738 |
750 |
N/A |
INTRINSIC |
low complexity region
|
770 |
782 |
N/A |
INTRINSIC |
Pfam:CEP170_C
|
795 |
1509 |
8e-260 |
PFAM |
low complexity region
|
1543 |
1555 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000195433
|
SMART Domains |
Protein: ENSMUSP00000142108 Gene: ENSMUSG00000057335
Domain | Start | End | E-Value | Type |
FHA
|
22 |
73 |
6.1e-10 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000195717
AA Change: E776G
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
SMART Domains |
Protein: ENSMUSP00000141769 Gene: ENSMUSG00000057335 AA Change: E776G
Domain | Start | End | E-Value | Type |
FHA
|
22 |
73 |
1.27e-7 |
SMART |
low complexity region
|
118 |
133 |
N/A |
INTRINSIC |
low complexity region
|
717 |
731 |
N/A |
INTRINSIC |
low complexity region
|
738 |
750 |
N/A |
INTRINSIC |
low complexity region
|
770 |
782 |
N/A |
INTRINSIC |
Pfam:CEP170_C
|
795 |
1499 |
1.8e-261 |
PFAM |
low complexity region
|
1533 |
1545 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 98.9%
|
Validation Efficiency |
98% (92/94) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The product of this gene is a component of the centrosome, a non-membraneous organelle that functions as the major microtubule-organizing center in animal cells. During interphase, the encoded protein localizes to the sub-distal appendages of mature centrioles, which are microtubule-based structures thought to help organize centrosomes. During mitosis, the protein associates with spindle microtubules near the centrosomes. The protein interacts with and is phosphorylated by polo-like kinase 1, and functions in maintaining microtubule organization and cell morphology. The human genome contains a putative transcribed pseudogene. Several alternatively spliced transcript variants of this gene have been found, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jul 2008]
|
Allele List at MGI |
All alleles(29) : Gene trapped(29)
|
Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AAdacl4fm3 |
G |
T |
4: 144,430,173 (GRCm39) |
A272D |
possibly damaging |
Het |
Abr |
A |
T |
11: 76,350,038 (GRCm39) |
I347N |
probably damaging |
Het |
Acbd4 |
T |
A |
11: 102,994,985 (GRCm39) |
L50Q |
probably damaging |
Het |
Acsl5 |
T |
G |
19: 55,261,251 (GRCm39) |
Y69* |
probably null |
Het |
Agtpbp1 |
G |
A |
13: 59,652,108 (GRCm39) |
T401I |
probably damaging |
Het |
Ap3m2 |
C |
T |
8: 23,289,807 (GRCm39) |
E99K |
probably damaging |
Het |
Arhgef28 |
A |
T |
13: 98,124,769 (GRCm39) |
S504R |
possibly damaging |
Het |
Arsj |
T |
A |
3: 126,232,752 (GRCm39) |
D499E |
probably damaging |
Het |
Bach1 |
G |
A |
16: 87,516,179 (GRCm39) |
R240Q |
probably benign |
Het |
Camk2b |
T |
C |
11: 5,939,575 (GRCm39) |
D232G |
probably damaging |
Het |
Casc3 |
C |
T |
11: 98,713,359 (GRCm39) |
P258S |
possibly damaging |
Het |
Catspere2 |
T |
A |
1: 177,845,280 (GRCm39) |
I100N |
probably damaging |
Het |
Ccdc80 |
T |
A |
16: 44,943,252 (GRCm39) |
N787K |
possibly damaging |
Het |
Celsr1 |
C |
A |
15: 85,789,679 (GRCm39) |
C2653F |
probably damaging |
Het |
Chia1 |
A |
C |
3: 106,022,641 (GRCm39) |
N12H |
probably damaging |
Het |
Chrna4 |
T |
C |
2: 180,671,334 (GRCm39) |
T141A |
probably damaging |
Het |
Col25a1 |
T |
C |
3: 130,272,671 (GRCm39) |
|
probably null |
Het |
Dcstamp |
A |
T |
15: 39,622,929 (GRCm39) |
I417F |
probably damaging |
Het |
Dnah5 |
A |
G |
15: 28,238,738 (GRCm39) |
I427V |
probably benign |
Het |
Dnah5 |
A |
G |
15: 28,333,208 (GRCm39) |
E2203G |
probably benign |
Het |
Dnmt3c |
A |
T |
2: 153,559,345 (GRCm39) |
S409C |
probably damaging |
Het |
Dock6 |
A |
T |
9: 21,724,375 (GRCm39) |
M1541K |
probably damaging |
Het |
Dzip1l |
C |
T |
9: 99,547,888 (GRCm39) |
T714I |
probably benign |
Het |
Exoc6b |
T |
C |
6: 84,825,807 (GRCm39) |
R535G |
probably damaging |
Het |
Fam83h |
A |
G |
15: 75,876,588 (GRCm39) |
S250P |
probably benign |
Het |
Fat4 |
C |
T |
3: 39,036,107 (GRCm39) |
T3253I |
probably damaging |
Het |
Fer1l6 |
T |
A |
15: 58,501,227 (GRCm39) |
F1302I |
probably damaging |
Het |
Fmnl1 |
T |
G |
11: 103,085,600 (GRCm39) |
|
probably benign |
Het |
Gckr |
C |
A |
5: 31,459,554 (GRCm39) |
F201L |
possibly damaging |
Het |
Gm10036 |
A |
G |
18: 15,966,292 (GRCm39) |
T148A |
probably benign |
Het |
Gm5142 |
G |
A |
14: 59,415,909 (GRCm39) |
S83F |
probably benign |
Het |
Gpr37 |
A |
T |
6: 25,689,004 (GRCm39) |
V31D |
possibly damaging |
Het |
Gramd2b |
A |
T |
18: 56,618,321 (GRCm39) |
Y207F |
probably damaging |
Het |
Hr |
T |
C |
14: 70,801,124 (GRCm39) |
|
probably null |
Het |
Igf2r |
A |
G |
17: 12,952,753 (GRCm39) |
L231P |
probably damaging |
Het |
Ighv1-66 |
A |
T |
12: 115,557,157 (GRCm39) |
W3R |
probably damaging |
Het |
Insyn2b |
T |
A |
11: 34,352,030 (GRCm39) |
V24E |
probably damaging |
Het |
Kcnu1 |
T |
C |
8: 26,408,491 (GRCm39) |
S101P |
probably benign |
Het |
Klhl23 |
T |
G |
2: 69,664,310 (GRCm39) |
V553G |
probably damaging |
Het |
Lrp1 |
T |
C |
10: 127,388,745 (GRCm39) |
I3235V |
probably damaging |
Het |
Mb |
A |
T |
15: 76,900,256 (GRCm39) |
I57N |
probably damaging |
Het |
Micu1 |
T |
C |
10: 59,624,843 (GRCm39) |
I295T |
possibly damaging |
Het |
Mink1 |
G |
A |
11: 70,498,601 (GRCm39) |
V589I |
possibly damaging |
Het |
Mndal |
T |
C |
1: 173,703,160 (GRCm39) |
K82E |
probably damaging |
Het |
Mroh1 |
A |
C |
15: 76,321,517 (GRCm39) |
K1066T |
probably benign |
Het |
Muc5b |
T |
A |
7: 141,396,192 (GRCm39) |
N149K |
unknown |
Het |
Myo7b |
G |
T |
18: 32,104,626 (GRCm39) |
L1404I |
probably damaging |
Het |
Nlrc4 |
A |
G |
17: 74,753,001 (GRCm39) |
S461P |
probably damaging |
Het |
Nudt12 |
A |
T |
17: 59,310,348 (GRCm39) |
D418E |
probably benign |
Het |
Or2g7 |
T |
A |
17: 38,378,948 (GRCm39) |
D295E |
probably benign |
Het |
Or5g27 |
G |
T |
2: 85,409,746 (GRCm39) |
R54S |
possibly damaging |
Het |
Pcdha1 |
A |
G |
18: 37,292,326 (GRCm39) |
H817R |
probably damaging |
Het |
Pcdha4 |
A |
G |
18: 37,087,080 (GRCm39) |
Y421C |
probably damaging |
Het |
Pcf11 |
T |
C |
7: 92,306,886 (GRCm39) |
D1094G |
probably benign |
Het |
Pck2 |
A |
T |
14: 55,785,223 (GRCm39) |
D427V |
probably damaging |
Het |
Pclo |
A |
G |
5: 14,726,421 (GRCm39) |
T1760A |
probably benign |
Het |
Pdzk1ip1 |
T |
A |
4: 114,950,188 (GRCm39) |
Y83N |
probably damaging |
Het |
Pgs1 |
T |
C |
11: 117,893,312 (GRCm39) |
I213T |
probably damaging |
Het |
Plin4 |
T |
A |
17: 56,410,969 (GRCm39) |
T1021S |
probably damaging |
Het |
Plxnb1 |
T |
A |
9: 108,941,375 (GRCm39) |
I1677N |
probably damaging |
Het |
Pm20d2 |
T |
C |
4: 33,174,752 (GRCm39) |
E378G |
possibly damaging |
Het |
Prkcq |
T |
G |
2: 11,231,661 (GRCm39) |
|
probably null |
Het |
Psmd2 |
C |
T |
16: 20,480,883 (GRCm39) |
P780L |
probably damaging |
Het |
Pvr |
A |
G |
7: 19,639,105 (GRCm39) |
S392P |
possibly damaging |
Het |
Rad51ap2 |
G |
C |
12: 11,507,432 (GRCm39) |
L451F |
possibly damaging |
Het |
Rbm20 |
A |
G |
19: 53,823,197 (GRCm39) |
E598G |
probably damaging |
Het |
Rho |
A |
T |
6: 115,912,504 (GRCm39) |
N123Y |
possibly damaging |
Het |
Rictor |
T |
C |
15: 6,737,934 (GRCm39) |
|
probably null |
Het |
Rilpl2 |
T |
G |
5: 124,606,656 (GRCm39) |
K186T |
probably damaging |
Het |
Rps6ka4 |
A |
C |
19: 6,816,992 (GRCm39) |
L61R |
probably damaging |
Het |
Sds |
C |
A |
5: 120,618,890 (GRCm39) |
Q118K |
probably benign |
Het |
Septin1 |
C |
T |
7: 126,816,157 (GRCm39) |
R91K |
probably benign |
Het |
Sf3a3 |
A |
G |
4: 124,616,673 (GRCm39) |
Y185C |
probably damaging |
Het |
Shtn1 |
T |
C |
19: 58,998,266 (GRCm39) |
M376V |
possibly damaging |
Het |
Slc6a9 |
A |
G |
4: 117,714,633 (GRCm39) |
T189A |
possibly damaging |
Het |
Slc7a6 |
T |
G |
8: 106,922,606 (GRCm39) |
V464G |
possibly damaging |
Het |
Smg8 |
T |
A |
11: 86,975,919 (GRCm39) |
D554V |
probably damaging |
Het |
Sox8 |
A |
G |
17: 25,789,082 (GRCm39) |
|
probably null |
Het |
Spata31e4 |
G |
T |
13: 50,857,019 (GRCm39) |
V886L |
possibly damaging |
Het |
Spats2l |
T |
A |
1: 57,918,689 (GRCm39) |
V41D |
probably damaging |
Het |
Sult2a3 |
A |
T |
7: 13,801,493 (GRCm39) |
F282Y |
probably damaging |
Het |
Svs3a |
T |
G |
2: 164,132,091 (GRCm39) |
Y220D |
probably damaging |
Het |
Teddm1a |
T |
A |
1: 153,768,369 (GRCm39) |
Y278N |
probably damaging |
Het |
Tlk1 |
T |
C |
2: 70,552,272 (GRCm39) |
Y526C |
probably damaging |
Het |
Tmc3 |
T |
A |
7: 83,266,025 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
A |
2: 76,596,583 (GRCm39) |
E20110V |
probably damaging |
Het |
Tulp4 |
A |
G |
17: 6,264,941 (GRCm39) |
D235G |
probably damaging |
Het |
Usp50 |
T |
C |
2: 126,622,395 (GRCm39) |
Y55C |
possibly damaging |
Het |
Vmn1r224 |
T |
C |
17: 20,639,789 (GRCm39) |
L122P |
probably benign |
Het |
Vmn2r62 |
A |
G |
7: 42,438,473 (GRCm39) |
L121P |
possibly damaging |
Het |
Whrn |
G |
T |
4: 63,413,368 (GRCm39) |
|
probably benign |
Het |
Zer1 |
G |
T |
2: 30,001,033 (GRCm39) |
H129Q |
probably benign |
Het |
Zfand4 |
G |
A |
6: 116,282,618 (GRCm39) |
A64T |
probably benign |
Het |
|
Other mutations in Cep170 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00773:Cep170
|
APN |
1 |
176,582,965 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00925:Cep170
|
APN |
1 |
176,621,090 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00972:Cep170
|
APN |
1 |
176,563,262 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01488:Cep170
|
APN |
1 |
176,583,941 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01916:Cep170
|
APN |
1 |
176,567,476 (GRCm39) |
splice site |
probably benign |
|
IGL02212:Cep170
|
APN |
1 |
176,563,502 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02269:Cep170
|
APN |
1 |
176,596,932 (GRCm39) |
missense |
probably benign |
|
IGL02732:Cep170
|
APN |
1 |
176,564,440 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02740:Cep170
|
APN |
1 |
176,621,166 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02812:Cep170
|
APN |
1 |
176,570,080 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03036:Cep170
|
APN |
1 |
176,596,903 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03201:Cep170
|
APN |
1 |
176,564,454 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03333:Cep170
|
APN |
1 |
176,597,092 (GRCm39) |
missense |
possibly damaging |
0.64 |
BB003:Cep170
|
UTSW |
1 |
176,588,979 (GRCm39) |
missense |
probably damaging |
0.97 |
BB013:Cep170
|
UTSW |
1 |
176,588,979 (GRCm39) |
missense |
probably damaging |
0.97 |
PIT4520001:Cep170
|
UTSW |
1 |
176,607,765 (GRCm39) |
missense |
unknown |
|
R0031:Cep170
|
UTSW |
1 |
176,583,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R0039:Cep170
|
UTSW |
1 |
176,610,061 (GRCm39) |
critical splice donor site |
probably null |
|
R0053:Cep170
|
UTSW |
1 |
176,609,946 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0053:Cep170
|
UTSW |
1 |
176,609,946 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0113:Cep170
|
UTSW |
1 |
176,586,021 (GRCm39) |
missense |
probably damaging |
0.97 |
R0144:Cep170
|
UTSW |
1 |
176,620,161 (GRCm39) |
missense |
probably benign |
0.01 |
R0613:Cep170
|
UTSW |
1 |
176,602,246 (GRCm39) |
missense |
probably benign |
|
R0755:Cep170
|
UTSW |
1 |
176,583,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R1132:Cep170
|
UTSW |
1 |
176,577,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R1367:Cep170
|
UTSW |
1 |
176,563,290 (GRCm39) |
missense |
probably damaging |
0.99 |
R1399:Cep170
|
UTSW |
1 |
176,585,969 (GRCm39) |
missense |
probably damaging |
0.98 |
R1462:Cep170
|
UTSW |
1 |
176,584,211 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1462:Cep170
|
UTSW |
1 |
176,584,211 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1481:Cep170
|
UTSW |
1 |
176,609,951 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1526:Cep170
|
UTSW |
1 |
176,616,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R1540:Cep170
|
UTSW |
1 |
176,567,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R1552:Cep170
|
UTSW |
1 |
176,610,060 (GRCm39) |
splice site |
probably benign |
|
R1570:Cep170
|
UTSW |
1 |
176,583,367 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1846:Cep170
|
UTSW |
1 |
176,583,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R1884:Cep170
|
UTSW |
1 |
176,602,245 (GRCm39) |
missense |
probably benign |
0.12 |
R1945:Cep170
|
UTSW |
1 |
176,621,100 (GRCm39) |
nonsense |
probably null |
|
R1954:Cep170
|
UTSW |
1 |
176,583,950 (GRCm39) |
missense |
probably benign |
|
R1957:Cep170
|
UTSW |
1 |
176,597,013 (GRCm39) |
missense |
probably benign |
0.24 |
R2184:Cep170
|
UTSW |
1 |
176,584,542 (GRCm39) |
missense |
probably benign |
0.00 |
R2280:Cep170
|
UTSW |
1 |
176,602,071 (GRCm39) |
missense |
probably benign |
0.17 |
R2426:Cep170
|
UTSW |
1 |
176,602,201 (GRCm39) |
missense |
probably benign |
|
R3415:Cep170
|
UTSW |
1 |
176,583,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R3417:Cep170
|
UTSW |
1 |
176,583,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R3752:Cep170
|
UTSW |
1 |
176,610,061 (GRCm39) |
critical splice donor site |
probably benign |
|
R3848:Cep170
|
UTSW |
1 |
176,583,409 (GRCm39) |
missense |
probably benign |
0.14 |
R3849:Cep170
|
UTSW |
1 |
176,583,409 (GRCm39) |
missense |
probably benign |
0.14 |
R4752:Cep170
|
UTSW |
1 |
176,584,254 (GRCm39) |
missense |
probably benign |
0.00 |
R4910:Cep170
|
UTSW |
1 |
176,609,829 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5007:Cep170
|
UTSW |
1 |
176,597,380 (GRCm39) |
missense |
probably benign |
0.28 |
R5052:Cep170
|
UTSW |
1 |
176,621,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R5093:Cep170
|
UTSW |
1 |
176,596,896 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5530:Cep170
|
UTSW |
1 |
176,597,076 (GRCm39) |
missense |
probably benign |
0.00 |
R5622:Cep170
|
UTSW |
1 |
176,563,433 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5892:Cep170
|
UTSW |
1 |
176,582,953 (GRCm39) |
splice site |
probably null |
|
R5942:Cep170
|
UTSW |
1 |
176,583,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R6083:Cep170
|
UTSW |
1 |
176,602,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R6091:Cep170
|
UTSW |
1 |
176,583,397 (GRCm39) |
missense |
probably damaging |
0.98 |
R6190:Cep170
|
UTSW |
1 |
176,609,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R6253:Cep170
|
UTSW |
1 |
176,607,960 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6476:Cep170
|
UTSW |
1 |
176,607,917 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6622:Cep170
|
UTSW |
1 |
176,583,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R6932:Cep170
|
UTSW |
1 |
176,589,003 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7163:Cep170
|
UTSW |
1 |
176,602,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R7352:Cep170
|
UTSW |
1 |
176,597,423 (GRCm39) |
missense |
probably benign |
0.11 |
R7499:Cep170
|
UTSW |
1 |
176,602,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R7502:Cep170
|
UTSW |
1 |
176,583,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R7773:Cep170
|
UTSW |
1 |
176,567,642 (GRCm39) |
missense |
|
|
R7926:Cep170
|
UTSW |
1 |
176,588,979 (GRCm39) |
missense |
probably damaging |
0.97 |
R8043:Cep170
|
UTSW |
1 |
176,596,808 (GRCm39) |
missense |
probably damaging |
0.96 |
R8203:Cep170
|
UTSW |
1 |
176,596,877 (GRCm39) |
missense |
probably benign |
0.28 |
R8350:Cep170
|
UTSW |
1 |
176,564,445 (GRCm39) |
missense |
|
|
R8450:Cep170
|
UTSW |
1 |
176,564,445 (GRCm39) |
missense |
|
|
R8835:Cep170
|
UTSW |
1 |
176,584,429 (GRCm39) |
missense |
probably benign |
0.00 |
R8931:Cep170
|
UTSW |
1 |
176,597,377 (GRCm39) |
missense |
probably benign |
0.02 |
R9108:Cep170
|
UTSW |
1 |
176,616,051 (GRCm39) |
nonsense |
probably null |
|
R9323:Cep170
|
UTSW |
1 |
176,586,068 (GRCm39) |
missense |
probably benign |
|
R9586:Cep170
|
UTSW |
1 |
176,563,463 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9629:Cep170
|
UTSW |
1 |
176,583,821 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
Predicted Primers |
PCR Primer
(F):5'- ATGGTGAAACTCCCTTGGCG -3'
(R):5'- ATGGTGAGAGTCCTAAAACTGGTG -3'
Sequencing Primer
(F):5'- GCGCACTAACGATTTGGAAGACTC -3'
(R):5'- TGGAGATGGTAAAGCCCTCCTTC -3'
|
Posted On |
2019-05-13 |