Incidental Mutation 'R4750:Kcp'
ID |
357488 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Kcp
|
Ensembl Gene |
ENSMUSG00000059022 |
Gene Name |
kielin/chordin-like protein |
Synonyms |
Crim2, LOC333088, KCP |
MMRRC Submission |
042031-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.121)
|
Stock # |
R4750 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
6 |
Chromosomal Location |
29473161-29507951 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 29484625 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Proline to Serine
at position 1318
(P1318S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000099135
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000078112]
[ENSMUST00000091391]
[ENSMUST00000101614]
[ENSMUST00000159479]
|
AlphaFold |
Q3U492 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000078112
|
SMART Domains |
Protein: ENSMUSP00000077251 Gene: ENSMUSG00000059022
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
21 |
N/A |
INTRINSIC |
SCOP:d1fxkc_
|
64 |
91 |
7e-3 |
SMART |
VWC
|
136 |
190 |
1.41e-13 |
SMART |
VWC
|
194 |
250 |
1.24e-9 |
SMART |
VWC
|
255 |
311 |
4.55e-8 |
SMART |
VWC
|
314 |
369 |
8.88e-11 |
SMART |
VWC
|
428 |
484 |
9.15e-13 |
SMART |
VWC
|
487 |
543 |
7.61e-10 |
SMART |
VWC
|
546 |
601 |
4.05e-5 |
SMART |
VWC
|
604 |
660 |
8.28e-11 |
SMART |
VWC
|
667 |
723 |
6.58e-5 |
SMART |
VWC
|
726 |
780 |
2.14e-4 |
SMART |
VWC
|
783 |
839 |
1.98e-8 |
SMART |
VWC
|
842 |
898 |
1.35e-1 |
SMART |
VWC
|
901 |
957 |
5.77e-10 |
SMART |
VWC
|
960 |
1015 |
1.21e-3 |
SMART |
VWC
|
1018 |
1083 |
2.44e-8 |
SMART |
VWC
|
1090 |
1143 |
1.05e-3 |
SMART |
VWC
|
1150 |
1207 |
2.93e-11 |
SMART |
Pfam:VWD
|
1214 |
1254 |
4.9e-11 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000091391
|
SMART Domains |
Protein: ENSMUSP00000088954 Gene: ENSMUSG00000059022
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
21 |
N/A |
INTRINSIC |
SCOP:d1fxkc_
|
64 |
91 |
7e-3 |
SMART |
VWC
|
136 |
190 |
1.41e-13 |
SMART |
VWC
|
194 |
250 |
1.24e-9 |
SMART |
VWC
|
255 |
311 |
4.55e-8 |
SMART |
VWC
|
314 |
369 |
8.88e-11 |
SMART |
VWC
|
428 |
484 |
9.15e-13 |
SMART |
VWC
|
487 |
543 |
7.61e-10 |
SMART |
VWC
|
546 |
601 |
4.05e-5 |
SMART |
VWC
|
604 |
660 |
8.28e-11 |
SMART |
VWC
|
667 |
723 |
6.58e-5 |
SMART |
VWC
|
726 |
780 |
2.14e-4 |
SMART |
VWC
|
783 |
839 |
1.98e-8 |
SMART |
VWC
|
842 |
898 |
1.35e-1 |
SMART |
VWC
|
901 |
957 |
5.77e-10 |
SMART |
VWC
|
960 |
1015 |
1.21e-3 |
SMART |
VWC
|
1018 |
1082 |
6.53e-9 |
SMART |
VWC
|
1089 |
1142 |
1.05e-3 |
SMART |
VWC
|
1149 |
1206 |
2.93e-11 |
SMART |
Pfam:VWD
|
1213 |
1253 |
4.6e-11 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000101614
AA Change: P1318S
PolyPhen 2
Score 0.027 (Sensitivity: 0.95; Specificity: 0.81)
|
SMART Domains |
Protein: ENSMUSP00000099135 Gene: ENSMUSG00000059022 AA Change: P1318S
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
21 |
N/A |
INTRINSIC |
SCOP:d1fxkc_
|
64 |
91 |
8e-3 |
SMART |
VWC
|
136 |
190 |
1.41e-13 |
SMART |
VWC
|
194 |
250 |
1.24e-9 |
SMART |
VWC
|
255 |
311 |
4.55e-8 |
SMART |
VWC
|
314 |
369 |
8.88e-11 |
SMART |
VWC
|
428 |
484 |
9.15e-13 |
SMART |
VWC
|
487 |
543 |
7.61e-10 |
SMART |
VWC
|
546 |
601 |
4.05e-5 |
SMART |
VWC
|
604 |
660 |
8.28e-11 |
SMART |
VWC
|
667 |
723 |
6.58e-5 |
SMART |
VWC
|
726 |
780 |
2.14e-4 |
SMART |
VWC
|
783 |
839 |
1.98e-8 |
SMART |
VWC
|
842 |
898 |
1.35e-1 |
SMART |
VWC
|
901 |
957 |
5.77e-10 |
SMART |
VWC
|
960 |
1015 |
1.21e-3 |
SMART |
VWC
|
1018 |
1083 |
2.44e-8 |
SMART |
VWC
|
1090 |
1143 |
1.05e-3 |
SMART |
VWC
|
1150 |
1207 |
2.93e-11 |
SMART |
VWD
|
1201 |
1362 |
6.09e-50 |
SMART |
C8
|
1404 |
1479 |
1.55e-34 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000158018
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000159479
|
SMART Domains |
Protein: ENSMUSP00000124771 Gene: ENSMUSG00000059022
Domain | Start | End | E-Value | Type |
VWC
|
1 |
51 |
4.56e-1 |
SMART |
VWC
|
54 |
110 |
1.98e-8 |
SMART |
VWC
|
113 |
169 |
1.35e-1 |
SMART |
VWC
|
172 |
228 |
5.77e-10 |
SMART |
VWC
|
231 |
286 |
1.21e-3 |
SMART |
VWC
|
289 |
353 |
6.53e-9 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000159482
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000161655
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000161276
|
Meta Mutation Damage Score |
0.0600 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.2%
- 20x: 94.9%
|
Validation Efficiency |
97% (89/92) |
MGI Phenotype |
PHENOTYPE: Homozygous null mice display increased sensitivity to renal injury. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2510039O18Rik |
T |
A |
4: 148,025,945 (GRCm39) |
L155Q |
probably damaging |
Het |
Aadac |
T |
C |
3: 59,943,238 (GRCm39) |
F48L |
probably benign |
Het |
Aadat |
T |
A |
8: 60,979,634 (GRCm39) |
N165K |
probably benign |
Het |
Acan |
C |
A |
7: 78,742,466 (GRCm39) |
D557E |
probably damaging |
Het |
Adamts4 |
T |
A |
1: 171,078,635 (GRCm39) |
V85D |
probably benign |
Het |
Agt |
A |
G |
8: 125,283,676 (GRCm39) |
V481A |
probably benign |
Het |
Angpt1 |
T |
C |
15: 42,539,797 (GRCm39) |
N21D |
probably benign |
Het |
Ankrd52 |
A |
C |
10: 128,213,958 (GRCm39) |
D38A |
probably damaging |
Het |
Ap1g2 |
G |
T |
14: 55,341,822 (GRCm39) |
Q247K |
probably damaging |
Het |
Apaf1 |
T |
C |
10: 90,896,050 (GRCm39) |
R341G |
probably damaging |
Het |
Arf2 |
T |
C |
11: 103,870,585 (GRCm39) |
|
probably null |
Het |
Arhgef1 |
A |
G |
7: 24,618,001 (GRCm39) |
|
probably benign |
Het |
Bbln |
C |
T |
2: 32,269,425 (GRCm39) |
|
probably null |
Het |
Bbox1 |
T |
A |
2: 110,095,866 (GRCm39) |
Y366F |
possibly damaging |
Het |
Bmp3 |
A |
G |
5: 99,020,417 (GRCm39) |
E280G |
possibly damaging |
Het |
Cd109 |
CATTTATTTATTTATTTATTTATTTATTTATTTAT |
CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT |
9: 78,619,782 (GRCm39) |
|
probably benign |
Het |
Cdh12 |
T |
A |
15: 21,583,894 (GRCm39) |
V578D |
possibly damaging |
Het |
Cdk19 |
T |
C |
10: 40,352,195 (GRCm39) |
S282P |
probably damaging |
Het |
Cfap46 |
A |
G |
7: 139,259,239 (GRCm39) |
|
probably null |
Het |
Cfhr3 |
T |
A |
1: 139,512,566 (GRCm39) |
|
noncoding transcript |
Het |
Ctrc |
T |
A |
4: 141,568,834 (GRCm39) |
Y123F |
probably benign |
Het |
Dync2i2 |
T |
C |
2: 29,923,932 (GRCm39) |
T198A |
probably benign |
Het |
Enpp4 |
A |
G |
17: 44,413,246 (GRCm39) |
M96T |
probably damaging |
Het |
Exosc10 |
T |
A |
4: 148,646,851 (GRCm39) |
S154T |
possibly damaging |
Het |
Fbxo21 |
G |
A |
5: 118,138,533 (GRCm39) |
R486H |
probably benign |
Het |
Foxj3 |
C |
A |
4: 119,473,787 (GRCm39) |
A204E |
probably damaging |
Het |
Gas6 |
T |
G |
8: 13,526,227 (GRCm39) |
D237A |
probably benign |
Het |
Gimap8 |
A |
G |
6: 48,627,361 (GRCm39) |
S112G |
probably benign |
Het |
Gm4787 |
T |
C |
12: 81,425,141 (GRCm39) |
N339S |
possibly damaging |
Het |
Gm6185 |
T |
C |
1: 161,009,933 (GRCm39) |
|
noncoding transcript |
Het |
Gramd2b |
A |
G |
18: 56,565,372 (GRCm39) |
E9G |
probably benign |
Het |
Hmgxb3 |
A |
T |
18: 61,300,568 (GRCm39) |
D169E |
probably benign |
Het |
Isl2 |
T |
A |
9: 55,451,596 (GRCm39) |
V162D |
probably benign |
Het |
Kcns3 |
T |
A |
12: 11,141,655 (GRCm39) |
D348V |
probably damaging |
Het |
Kif12 |
T |
A |
4: 63,086,020 (GRCm39) |
Q415L |
probably damaging |
Het |
Lama3 |
T |
A |
18: 12,637,416 (GRCm39) |
H45Q |
probably benign |
Het |
Lonp2 |
A |
T |
8: 87,358,130 (GRCm39) |
K117M |
probably benign |
Het |
Loxl4 |
T |
A |
19: 42,593,443 (GRCm39) |
N243Y |
probably damaging |
Het |
Lrif1 |
C |
A |
3: 106,642,880 (GRCm39) |
Q662K |
probably benign |
Het |
Lrrc37a |
T |
A |
11: 103,346,306 (GRCm39) |
I3187L |
probably benign |
Het |
Lsg1 |
A |
G |
16: 30,384,267 (GRCm39) |
I521T |
probably damaging |
Het |
Mecom |
T |
G |
3: 30,011,679 (GRCm39) |
K865Q |
probably damaging |
Het |
Myh10 |
T |
C |
11: 68,676,140 (GRCm39) |
I790T |
probably damaging |
Het |
Nek7 |
C |
T |
1: 138,426,411 (GRCm39) |
S234N |
probably damaging |
Het |
Nepro |
T |
C |
16: 44,550,545 (GRCm39) |
L179P |
probably damaging |
Het |
Nexn |
A |
G |
3: 151,943,359 (GRCm39) |
C649R |
probably damaging |
Het |
Nsmf |
T |
C |
2: 24,945,038 (GRCm39) |
S34P |
probably damaging |
Het |
Or10x1 |
A |
G |
1: 174,196,488 (GRCm39) |
I2V |
probably benign |
Het |
Or13n4 |
A |
G |
7: 106,423,514 (GRCm39) |
F73S |
probably damaging |
Het |
Or13p5 |
T |
A |
4: 118,591,930 (GRCm39) |
V68D |
possibly damaging |
Het |
Or1n2 |
T |
A |
2: 36,797,728 (GRCm39) |
S257T |
probably benign |
Het |
Or1p1c |
T |
A |
11: 74,160,246 (GRCm39) |
F10L |
probably benign |
Het |
Or2w2 |
A |
G |
13: 21,757,913 (GRCm39) |
S238P |
possibly damaging |
Het |
Or52l1 |
A |
T |
7: 104,830,133 (GRCm39) |
I144N |
probably damaging |
Het |
Or5bw2 |
A |
G |
7: 6,573,850 (GRCm39) |
I287V |
probably benign |
Het |
Or5w16 |
C |
T |
2: 87,576,852 (GRCm39) |
T104I |
probably benign |
Het |
P2rx5 |
G |
T |
11: 73,055,703 (GRCm39) |
K53N |
probably damaging |
Het |
Pcdhb20 |
C |
A |
18: 37,639,184 (GRCm39) |
A570E |
possibly damaging |
Het |
Pip4k2c |
T |
C |
10: 127,047,286 (GRCm39) |
H32R |
unknown |
Het |
Pkhd1 |
T |
A |
1: 20,594,336 (GRCm39) |
D1259V |
possibly damaging |
Het |
Plekha7 |
A |
T |
7: 115,736,546 (GRCm39) |
V889E |
probably damaging |
Het |
Polr2b |
A |
C |
5: 77,479,886 (GRCm39) |
E546D |
possibly damaging |
Het |
Ppm1l |
A |
G |
3: 69,456,661 (GRCm39) |
T193A |
probably damaging |
Het |
Ppp1r37 |
G |
T |
7: 19,265,445 (GRCm39) |
D710E |
probably benign |
Het |
Prdm4 |
A |
G |
10: 85,735,085 (GRCm39) |
F679L |
probably damaging |
Het |
Prkcd |
A |
G |
14: 30,332,258 (GRCm39) |
M1T |
probably null |
Het |
Prss59 |
A |
G |
6: 40,897,955 (GRCm39) |
W243R |
probably damaging |
Het |
Rcor3 |
A |
G |
1: 191,814,749 (GRCm39) |
Y77H |
unknown |
Het |
Rdh5 |
T |
C |
10: 128,754,235 (GRCm39) |
E66G |
possibly damaging |
Het |
Slc12a5 |
A |
G |
2: 164,824,851 (GRCm39) |
M396V |
probably benign |
Het |
Slco5a1 |
T |
G |
1: 12,949,504 (GRCm39) |
T629P |
probably damaging |
Het |
Smarca5 |
A |
C |
8: 81,460,336 (GRCm39) |
N133K |
probably benign |
Het |
Spag5 |
T |
C |
11: 78,210,878 (GRCm39) |
M927T |
probably benign |
Het |
Spint4 |
A |
T |
2: 164,542,066 (GRCm39) |
D39V |
probably damaging |
Het |
Syt6 |
T |
A |
3: 103,538,233 (GRCm39) |
*512R |
probably null |
Het |
Tmem247 |
T |
C |
17: 87,229,770 (GRCm39) |
C204R |
probably damaging |
Het |
Tmem72 |
A |
G |
6: 116,672,395 (GRCm39) |
Y149H |
probably damaging |
Het |
Trpm6 |
T |
C |
19: 18,853,428 (GRCm39) |
V1816A |
probably damaging |
Het |
Usp35 |
A |
G |
7: 96,959,546 (GRCm39) |
V1008A |
possibly damaging |
Het |
Washc4 |
T |
C |
10: 83,426,916 (GRCm39) |
S1075P |
probably damaging |
Het |
Xylb |
G |
T |
9: 119,188,379 (GRCm39) |
G62* |
probably null |
Het |
Zfp142 |
T |
C |
1: 74,611,617 (GRCm39) |
E623G |
probably damaging |
Het |
Zfp239 |
A |
G |
6: 117,848,700 (GRCm39) |
Y146C |
probably damaging |
Het |
|
Other mutations in Kcp |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00474:Kcp
|
APN |
6 |
29,482,656 (GRCm39) |
missense |
probably benign |
|
IGL01344:Kcp
|
APN |
6 |
29,498,950 (GRCm39) |
splice site |
probably null |
|
IGL01404:Kcp
|
APN |
6 |
29,496,638 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01735:Kcp
|
APN |
6 |
29,498,878 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01776:Kcp
|
APN |
6 |
29,497,907 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02092:Kcp
|
APN |
6 |
29,489,031 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02252:Kcp
|
APN |
6 |
29,504,548 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02690:Kcp
|
APN |
6 |
29,484,998 (GRCm39) |
unclassified |
probably benign |
|
IGL02817:Kcp
|
APN |
6 |
29,496,968 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03074:Kcp
|
APN |
6 |
29,496,630 (GRCm39) |
missense |
probably damaging |
1.00 |
P0045:Kcp
|
UTSW |
6 |
29,498,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R0219:Kcp
|
UTSW |
6 |
29,495,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R0355:Kcp
|
UTSW |
6 |
29,496,926 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0738:Kcp
|
UTSW |
6 |
29,490,438 (GRCm39) |
missense |
probably benign |
0.24 |
R1111:Kcp
|
UTSW |
6 |
29,485,422 (GRCm39) |
missense |
probably benign |
|
R1304:Kcp
|
UTSW |
6 |
29,501,291 (GRCm39) |
unclassified |
probably benign |
|
R1663:Kcp
|
UTSW |
6 |
29,498,964 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1808:Kcp
|
UTSW |
6 |
29,505,654 (GRCm39) |
missense |
probably benign |
0.05 |
R1907:Kcp
|
UTSW |
6 |
29,497,834 (GRCm39) |
unclassified |
probably benign |
|
R2030:Kcp
|
UTSW |
6 |
29,489,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R2099:Kcp
|
UTSW |
6 |
29,496,164 (GRCm39) |
nonsense |
probably null |
|
R3411:Kcp
|
UTSW |
6 |
29,482,845 (GRCm39) |
missense |
possibly damaging |
0.68 |
R3982:Kcp
|
UTSW |
6 |
29,484,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R3983:Kcp
|
UTSW |
6 |
29,484,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R4223:Kcp
|
UTSW |
6 |
29,482,257 (GRCm39) |
missense |
possibly damaging |
0.55 |
R4377:Kcp
|
UTSW |
6 |
29,493,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R4570:Kcp
|
UTSW |
6 |
29,491,847 (GRCm39) |
nonsense |
probably null |
|
R4624:Kcp
|
UTSW |
6 |
29,482,813 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4694:Kcp
|
UTSW |
6 |
29,493,196 (GRCm39) |
missense |
probably benign |
0.29 |
R4968:Kcp
|
UTSW |
6 |
29,497,628 (GRCm39) |
nonsense |
probably null |
|
R5053:Kcp
|
UTSW |
6 |
29,496,957 (GRCm39) |
missense |
probably benign |
0.01 |
R5067:Kcp
|
UTSW |
6 |
29,492,107 (GRCm39) |
missense |
probably benign |
0.06 |
R5253:Kcp
|
UTSW |
6 |
29,498,519 (GRCm39) |
unclassified |
probably benign |
|
R5418:Kcp
|
UTSW |
6 |
29,504,283 (GRCm39) |
nonsense |
probably null |
|
R6020:Kcp
|
UTSW |
6 |
29,502,863 (GRCm39) |
missense |
probably benign |
0.03 |
R6033:Kcp
|
UTSW |
6 |
29,493,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R6033:Kcp
|
UTSW |
6 |
29,493,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R6088:Kcp
|
UTSW |
6 |
29,502,631 (GRCm39) |
missense |
probably benign |
|
R6178:Kcp
|
UTSW |
6 |
29,482,887 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6285:Kcp
|
UTSW |
6 |
29,502,364 (GRCm39) |
missense |
probably benign |
0.21 |
R6310:Kcp
|
UTSW |
6 |
29,493,257 (GRCm39) |
missense |
probably damaging |
0.98 |
R6369:Kcp
|
UTSW |
6 |
29,484,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R6860:Kcp
|
UTSW |
6 |
29,505,719 (GRCm39) |
missense |
probably benign |
0.19 |
R6949:Kcp
|
UTSW |
6 |
29,484,611 (GRCm39) |
splice site |
probably null |
|
R6962:Kcp
|
UTSW |
6 |
29,482,839 (GRCm39) |
missense |
probably benign |
0.08 |
R7006:Kcp
|
UTSW |
6 |
29,499,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R7138:Kcp
|
UTSW |
6 |
29,491,861 (GRCm39) |
nonsense |
probably null |
|
R7141:Kcp
|
UTSW |
6 |
29,487,511 (GRCm39) |
nonsense |
probably null |
|
R7153:Kcp
|
UTSW |
6 |
29,499,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R7162:Kcp
|
UTSW |
6 |
29,497,199 (GRCm39) |
splice site |
probably null |
|
R7334:Kcp
|
UTSW |
6 |
29,485,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R7565:Kcp
|
UTSW |
6 |
29,499,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R7671:Kcp
|
UTSW |
6 |
29,496,516 (GRCm39) |
missense |
probably benign |
0.02 |
R7766:Kcp
|
UTSW |
6 |
29,496,846 (GRCm39) |
missense |
probably damaging |
0.98 |
R7781:Kcp
|
UTSW |
6 |
29,497,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R8702:Kcp
|
UTSW |
6 |
29,482,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R9384:Kcp
|
UTSW |
6 |
29,496,618 (GRCm39) |
critical splice donor site |
probably null |
|
R9425:Kcp
|
UTSW |
6 |
29,489,151 (GRCm39) |
missense |
probably benign |
|
R9553:Kcp
|
UTSW |
6 |
29,485,100 (GRCm39) |
missense |
probably null |
1.00 |
R9752:Kcp
|
UTSW |
6 |
29,497,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R9755:Kcp
|
UTSW |
6 |
29,492,460 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Kcp
|
UTSW |
6 |
29,485,011 (GRCm39) |
missense |
probably benign |
0.23 |
Z1177:Kcp
|
UTSW |
6 |
29,485,524 (GRCm39) |
missense |
probably benign |
0.45 |
|
Predicted Primers |
PCR Primer
(F):5'- GCTGCGAGCAAGAGATCATC -3'
(R):5'- TCATGGTGAGCTAAGGACCC -3'
Sequencing Primer
(F):5'- CTGCGAGCAAGAGATCATCATTTTCC -3'
(R):5'- CCAGGGAAGGTCAGTGCTACAC -3'
|
Posted On |
2015-11-11 |