Incidental Mutation 'R1777:Cntnap5b'
ID |
197077 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cntnap5b
|
Ensembl Gene |
ENSMUSG00000067028 |
Gene Name |
contactin associated protein-like 5B |
Synonyms |
C230078M14Rik, Caspr5-2 |
MMRRC Submission |
039808-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.158)
|
Stock # |
R1777 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
99700490-100413667 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 100297803 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Threonine
at position 781
(S781T)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000083944
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000086738]
[ENSMUST00000188735]
|
AlphaFold |
Q0V8T8 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000086738
AA Change: S781T
PolyPhen 2
Score 0.105 (Sensitivity: 0.93; Specificity: 0.86)
|
SMART Domains |
Protein: ENSMUSP00000083944 Gene: ENSMUSG00000067028 AA Change: S781T
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
24 |
N/A |
INTRINSIC |
FA58C
|
39 |
174 |
2.76e-16 |
SMART |
LamG
|
201 |
338 |
2.84e-27 |
SMART |
LamG
|
387 |
521 |
9.22e-27 |
SMART |
EGF
|
549 |
583 |
1.14e0 |
SMART |
Blast:FBG
|
586 |
758 |
3e-66 |
BLAST |
LamG
|
798 |
925 |
2.12e-26 |
SMART |
EGF
|
946 |
982 |
1.51e0 |
SMART |
LamG
|
1023 |
1159 |
2.14e-13 |
SMART |
transmembrane domain
|
1227 |
1249 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000185484
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000188735
|
SMART Domains |
Protein: ENSMUSP00000139877 Gene: ENSMUSG00000067028
Domain | Start | End | E-Value | Type |
LamG
|
73 |
207 |
5.9e-29 |
SMART |
EGF
|
235 |
269 |
5.6e-3 |
SMART |
Blast:FBG
|
272 |
402 |
2e-42 |
BLAST |
LamG
|
415 |
554 |
2.5e-11 |
SMART |
EGF
|
575 |
611 |
7.1e-3 |
SMART |
LamG
|
652 |
788 |
1.4e-15 |
SMART |
transmembrane domain
|
856 |
878 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 97.4%
- 3x: 96.8%
- 10x: 95.1%
- 20x: 92.1%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930444P10Rik |
T |
A |
1: 16,148,813 (GRCm39) |
D111V |
possibly damaging |
Het |
Ap2a1 |
G |
A |
7: 44,553,576 (GRCm39) |
T597M |
probably damaging |
Het |
Arhgap25 |
A |
G |
6: 87,440,289 (GRCm39) |
S364P |
probably benign |
Het |
Atp6v1a |
G |
T |
16: 43,935,068 (GRCm39) |
Y40* |
probably null |
Het |
Cdh1 |
T |
A |
8: 107,383,467 (GRCm39) |
H235Q |
probably damaging |
Het |
Cntln |
A |
G |
4: 85,048,916 (GRCm39) |
E1376G |
probably benign |
Het |
Cpne4 |
A |
G |
9: 104,749,887 (GRCm39) |
T64A |
probably damaging |
Het |
Ctsg |
T |
C |
14: 56,338,058 (GRCm39) |
Y179C |
probably damaging |
Het |
Cx3cr1 |
A |
G |
9: 119,880,659 (GRCm39) |
Y248H |
probably damaging |
Het |
Dhx37 |
T |
C |
5: 125,506,995 (GRCm39) |
E167G |
probably benign |
Het |
Dnajc21 |
C |
A |
15: 10,449,693 (GRCm39) |
A443S |
probably benign |
Het |
Drd5 |
T |
C |
5: 38,477,504 (GRCm39) |
S166P |
probably damaging |
Het |
Dscaml1 |
T |
C |
9: 45,595,054 (GRCm39) |
L719P |
possibly damaging |
Het |
Eif2ak4 |
T |
C |
2: 118,261,320 (GRCm39) |
I542T |
probably damaging |
Het |
Ephb3 |
G |
A |
16: 21,035,985 (GRCm39) |
G291E |
probably damaging |
Het |
Eva1a |
T |
A |
6: 82,069,137 (GRCm39) |
Y155N |
probably damaging |
Het |
Exog |
C |
T |
9: 119,278,884 (GRCm39) |
P189L |
probably damaging |
Het |
Fam13b |
A |
G |
18: 34,590,813 (GRCm39) |
V455A |
possibly damaging |
Het |
Fmn2 |
C |
A |
1: 174,409,488 (GRCm39) |
Q574K |
unknown |
Het |
Gm6871 |
A |
T |
7: 41,195,143 (GRCm39) |
S531R |
probably benign |
Het |
Golga2 |
T |
A |
2: 32,195,482 (GRCm39) |
|
probably null |
Het |
Hydin |
C |
T |
8: 111,316,203 (GRCm39) |
P4365L |
probably benign |
Het |
Ints8 |
A |
T |
4: 11,225,600 (GRCm39) |
|
probably null |
Het |
Kbtbd12 |
A |
C |
6: 88,595,042 (GRCm39) |
S263A |
probably benign |
Het |
Kcng4 |
T |
C |
8: 120,360,226 (GRCm39) |
D50G |
probably benign |
Het |
Klhl18 |
A |
T |
9: 110,266,469 (GRCm39) |
C217S |
probably benign |
Het |
Klk1b4 |
A |
G |
7: 43,856,875 (GRCm39) |
|
probably benign |
Het |
Klk7 |
G |
A |
7: 43,462,753 (GRCm39) |
C186Y |
probably damaging |
Het |
Krbox5 |
A |
T |
13: 67,981,984 (GRCm39) |
R65S |
probably benign |
Het |
Krit1 |
T |
C |
5: 3,886,799 (GRCm39) |
Y635H |
probably damaging |
Het |
Lipo4 |
A |
T |
19: 33,476,721 (GRCm39) |
D342E |
probably damaging |
Het |
Lsm14b |
T |
G |
2: 179,673,588 (GRCm39) |
D199E |
probably benign |
Het |
Map3k4 |
A |
T |
17: 12,490,617 (GRCm39) |
N271K |
possibly damaging |
Het |
Mast1 |
T |
A |
8: 85,638,697 (GRCm39) |
N1544I |
probably benign |
Het |
Megf6 |
T |
A |
4: 154,355,147 (GRCm39) |
C1487* |
probably null |
Het |
Mlh3 |
C |
A |
12: 85,315,528 (GRCm39) |
K219N |
possibly damaging |
Het |
Mtmr4 |
A |
G |
11: 87,493,656 (GRCm39) |
K305E |
probably damaging |
Het |
Myo15a |
A |
G |
11: 60,405,762 (GRCm39) |
M3105V |
probably benign |
Het |
Nbas |
A |
T |
12: 13,563,563 (GRCm39) |
I1958F |
probably benign |
Het |
Nepro |
A |
T |
16: 44,556,216 (GRCm39) |
Q458L |
probably damaging |
Het |
Opa3 |
T |
C |
7: 18,978,837 (GRCm39) |
Y101H |
probably damaging |
Het |
Or11g25 |
T |
A |
14: 50,723,757 (GRCm39) |
F281I |
probably benign |
Het |
Or14c41 |
T |
A |
7: 86,235,272 (GRCm39) |
I263N |
probably benign |
Het |
Or4f15 |
T |
A |
2: 111,814,042 (GRCm39) |
I126L |
possibly damaging |
Het |
Or51f1d |
T |
C |
7: 102,700,583 (GRCm39) |
I26T |
probably benign |
Het |
Or5ac16 |
A |
G |
16: 59,022,379 (GRCm39) |
S137P |
probably benign |
Het |
Or8b12 |
A |
G |
9: 37,657,607 (GRCm39) |
Y59C |
possibly damaging |
Het |
Pate3 |
T |
C |
9: 35,559,412 (GRCm39) |
N2D |
probably benign |
Het |
Pcdhb21 |
T |
A |
18: 37,648,771 (GRCm39) |
D633E |
possibly damaging |
Het |
Pgm2 |
C |
T |
5: 64,285,125 (GRCm39) |
P589L |
probably benign |
Het |
Pigg |
T |
A |
5: 108,465,257 (GRCm39) |
D163E |
probably damaging |
Het |
Polq |
A |
G |
16: 36,880,586 (GRCm39) |
T638A |
possibly damaging |
Het |
Prmt3 |
T |
A |
7: 49,448,094 (GRCm39) |
M268K |
possibly damaging |
Het |
Prmt9 |
T |
C |
8: 78,291,737 (GRCm39) |
C370R |
probably benign |
Het |
Prss57 |
A |
T |
10: 79,623,219 (GRCm39) |
V76E |
possibly damaging |
Het |
Psme3ip1 |
T |
C |
8: 95,315,439 (GRCm39) |
E31G |
probably damaging |
Het |
Pzp |
T |
C |
6: 128,467,535 (GRCm39) |
E1089G |
possibly damaging |
Het |
Qars1 |
T |
A |
9: 108,385,400 (GRCm39) |
|
probably null |
Het |
Ralgapb |
T |
C |
2: 158,304,115 (GRCm39) |
Y625H |
probably damaging |
Het |
Rgl2 |
G |
A |
17: 34,150,718 (GRCm39) |
D59N |
probably benign |
Het |
Robo1 |
T |
G |
16: 72,801,555 (GRCm39) |
W1060G |
probably benign |
Het |
Scaper |
A |
T |
9: 55,771,830 (GRCm39) |
V362E |
probably benign |
Het |
Schip1 |
T |
C |
3: 68,525,017 (GRCm39) |
F131S |
probably damaging |
Het |
Sh2b2 |
A |
T |
5: 136,256,276 (GRCm39) |
V252D |
probably damaging |
Het |
Shld2 |
C |
A |
14: 33,990,130 (GRCm39) |
V259L |
probably benign |
Het |
Slc17a6 |
A |
T |
7: 51,295,957 (GRCm39) |
H199L |
possibly damaging |
Het |
Slc29a1 |
A |
G |
17: 45,898,234 (GRCm39) |
Y325H |
probably damaging |
Het |
Slc29a4 |
G |
T |
5: 142,699,817 (GRCm39) |
W156L |
probably damaging |
Het |
Slc5a3 |
T |
A |
16: 91,874,644 (GRCm39) |
S234T |
probably benign |
Het |
Srd5a3 |
T |
G |
5: 76,297,630 (GRCm39) |
V20G |
probably damaging |
Het |
Stac |
A |
T |
9: 111,433,150 (GRCm39) |
S223T |
possibly damaging |
Het |
Sytl2 |
A |
T |
7: 90,052,260 (GRCm39) |
T766S |
probably benign |
Het |
Tas2r102 |
A |
G |
6: 132,739,254 (GRCm39) |
D54G |
probably benign |
Het |
Tbpl1 |
A |
G |
10: 22,583,742 (GRCm39) |
V105A |
probably damaging |
Het |
Tenm3 |
G |
T |
8: 48,870,214 (GRCm39) |
P193Q |
probably benign |
Het |
Tes |
G |
A |
6: 17,104,754 (GRCm39) |
V403M |
probably benign |
Het |
Tgfbr2 |
A |
C |
9: 115,938,948 (GRCm39) |
I318S |
probably damaging |
Het |
Tgfbr3 |
C |
A |
5: 107,284,796 (GRCm39) |
V618L |
probably benign |
Het |
Tmc1 |
C |
T |
19: 20,793,473 (GRCm39) |
|
probably null |
Het |
Tmem132a |
G |
A |
19: 10,835,870 (GRCm39) |
H887Y |
probably damaging |
Het |
Tmem43 |
C |
A |
6: 91,454,312 (GRCm39) |
S33* |
probably null |
Het |
Tob1 |
A |
G |
11: 94,104,580 (GRCm39) |
K39E |
probably damaging |
Het |
Tut7 |
A |
T |
13: 59,939,635 (GRCm39) |
H705Q |
probably damaging |
Het |
Unc79 |
T |
A |
12: 103,078,714 (GRCm39) |
D1433E |
probably damaging |
Het |
Usp25 |
T |
C |
16: 76,878,442 (GRCm39) |
M622T |
probably damaging |
Het |
Vmn1r158 |
A |
T |
7: 22,489,855 (GRCm39) |
L118Q |
probably damaging |
Het |
Vmn1r217 |
T |
A |
13: 23,298,495 (GRCm39) |
I136L |
probably benign |
Het |
Vmn2r15 |
A |
T |
5: 109,442,136 (GRCm39) |
I99K |
possibly damaging |
Het |
Vwa7 |
T |
A |
17: 35,243,924 (GRCm39) |
V786E |
probably damaging |
Het |
Xkr5 |
A |
G |
8: 18,989,148 (GRCm39) |
F248S |
probably benign |
Het |
Zzef1 |
A |
T |
11: 72,801,098 (GRCm39) |
K2444M |
probably damaging |
Het |
|
Other mutations in Cntnap5b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00417:Cntnap5b
|
APN |
1 |
99,978,479 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00477:Cntnap5b
|
APN |
1 |
100,141,468 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00505:Cntnap5b
|
APN |
1 |
100,306,886 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL00596:Cntnap5b
|
APN |
1 |
100,306,886 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL00846:Cntnap5b
|
APN |
1 |
100,091,948 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00895:Cntnap5b
|
APN |
1 |
100,311,310 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00948:Cntnap5b
|
APN |
1 |
100,069,082 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01073:Cntnap5b
|
APN |
1 |
100,003,755 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01523:Cntnap5b
|
APN |
1 |
100,359,504 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01779:Cntnap5b
|
APN |
1 |
99,895,064 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02253:Cntnap5b
|
APN |
1 |
100,091,936 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02628:Cntnap5b
|
APN |
1 |
99,999,794 (GRCm39) |
missense |
probably damaging |
0.97 |
R0166:Cntnap5b
|
UTSW |
1 |
100,202,086 (GRCm39) |
missense |
probably benign |
0.41 |
R0211:Cntnap5b
|
UTSW |
1 |
100,406,099 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0281:Cntnap5b
|
UTSW |
1 |
99,999,878 (GRCm39) |
missense |
probably benign |
0.22 |
R0363:Cntnap5b
|
UTSW |
1 |
100,202,193 (GRCm39) |
missense |
probably benign |
0.01 |
R0514:Cntnap5b
|
UTSW |
1 |
99,700,511 (GRCm39) |
missense |
probably benign |
|
R0645:Cntnap5b
|
UTSW |
1 |
99,999,767 (GRCm39) |
splice site |
probably benign |
|
R0848:Cntnap5b
|
UTSW |
1 |
100,182,888 (GRCm39) |
missense |
probably benign |
0.22 |
R1006:Cntnap5b
|
UTSW |
1 |
100,311,342 (GRCm39) |
missense |
probably benign |
0.00 |
R1349:Cntnap5b
|
UTSW |
1 |
100,091,813 (GRCm39) |
missense |
probably benign |
0.09 |
R1372:Cntnap5b
|
UTSW |
1 |
100,091,813 (GRCm39) |
missense |
probably benign |
0.09 |
R1474:Cntnap5b
|
UTSW |
1 |
99,999,814 (GRCm39) |
missense |
probably benign |
0.25 |
R1681:Cntnap5b
|
UTSW |
1 |
100,003,832 (GRCm39) |
missense |
probably damaging |
0.98 |
R1727:Cntnap5b
|
UTSW |
1 |
100,141,469 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1760:Cntnap5b
|
UTSW |
1 |
99,700,535 (GRCm39) |
missense |
probably benign |
0.05 |
R1939:Cntnap5b
|
UTSW |
1 |
99,895,073 (GRCm39) |
missense |
probably benign |
|
R1988:Cntnap5b
|
UTSW |
1 |
99,999,865 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2069:Cntnap5b
|
UTSW |
1 |
100,286,450 (GRCm39) |
missense |
probably benign |
0.04 |
R2113:Cntnap5b
|
UTSW |
1 |
100,202,140 (GRCm39) |
missense |
probably benign |
|
R2148:Cntnap5b
|
UTSW |
1 |
100,311,199 (GRCm39) |
missense |
probably benign |
0.01 |
R2158:Cntnap5b
|
UTSW |
1 |
100,318,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R2223:Cntnap5b
|
UTSW |
1 |
100,141,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R2350:Cntnap5b
|
UTSW |
1 |
100,306,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R3840:Cntnap5b
|
UTSW |
1 |
100,311,202 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4329:Cntnap5b
|
UTSW |
1 |
99,999,888 (GRCm39) |
missense |
probably damaging |
0.99 |
R4609:Cntnap5b
|
UTSW |
1 |
99,700,572 (GRCm39) |
critical splice donor site |
probably null |
|
R4799:Cntnap5b
|
UTSW |
1 |
100,286,450 (GRCm39) |
missense |
probably benign |
0.04 |
R5129:Cntnap5b
|
UTSW |
1 |
100,306,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R5323:Cntnap5b
|
UTSW |
1 |
100,311,275 (GRCm39) |
nonsense |
probably null |
|
R5434:Cntnap5b
|
UTSW |
1 |
99,999,926 (GRCm39) |
missense |
probably benign |
0.02 |
R5579:Cntnap5b
|
UTSW |
1 |
100,311,124 (GRCm39) |
missense |
probably benign |
0.27 |
R5579:Cntnap5b
|
UTSW |
1 |
100,311,120 (GRCm39) |
nonsense |
probably null |
|
R5630:Cntnap5b
|
UTSW |
1 |
99,999,794 (GRCm39) |
missense |
probably damaging |
0.99 |
R5644:Cntnap5b
|
UTSW |
1 |
100,311,326 (GRCm39) |
missense |
probably benign |
0.00 |
R5761:Cntnap5b
|
UTSW |
1 |
100,374,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R6042:Cntnap5b
|
UTSW |
1 |
100,318,317 (GRCm39) |
missense |
probably benign |
|
R6147:Cntnap5b
|
UTSW |
1 |
99,978,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R6190:Cntnap5b
|
UTSW |
1 |
100,306,800 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6248:Cntnap5b
|
UTSW |
1 |
99,999,827 (GRCm39) |
missense |
probably benign |
0.30 |
R6286:Cntnap5b
|
UTSW |
1 |
100,182,798 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6306:Cntnap5b
|
UTSW |
1 |
100,091,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R6336:Cntnap5b
|
UTSW |
1 |
100,286,394 (GRCm39) |
missense |
probably benign |
0.00 |
R6360:Cntnap5b
|
UTSW |
1 |
100,359,461 (GRCm39) |
nonsense |
probably null |
|
R6722:Cntnap5b
|
UTSW |
1 |
100,406,211 (GRCm39) |
missense |
probably damaging |
0.98 |
R6750:Cntnap5b
|
UTSW |
1 |
100,202,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R6806:Cntnap5b
|
UTSW |
1 |
99,868,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R6933:Cntnap5b
|
UTSW |
1 |
100,311,175 (GRCm39) |
missense |
probably benign |
0.01 |
R6957:Cntnap5b
|
UTSW |
1 |
100,202,197 (GRCm39) |
missense |
probably benign |
0.08 |
R6958:Cntnap5b
|
UTSW |
1 |
100,202,197 (GRCm39) |
missense |
probably benign |
0.08 |
R6959:Cntnap5b
|
UTSW |
1 |
100,202,197 (GRCm39) |
missense |
probably benign |
0.08 |
R6961:Cntnap5b
|
UTSW |
1 |
100,202,197 (GRCm39) |
missense |
probably benign |
0.08 |
R6962:Cntnap5b
|
UTSW |
1 |
100,202,197 (GRCm39) |
missense |
probably benign |
0.08 |
R7088:Cntnap5b
|
UTSW |
1 |
100,087,802 (GRCm39) |
missense |
probably damaging |
0.99 |
R7146:Cntnap5b
|
UTSW |
1 |
99,978,519 (GRCm39) |
splice site |
probably null |
|
R7165:Cntnap5b
|
UTSW |
1 |
100,003,887 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7190:Cntnap5b
|
UTSW |
1 |
100,359,574 (GRCm39) |
splice site |
probably null |
|
R7376:Cntnap5b
|
UTSW |
1 |
99,894,994 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7385:Cntnap5b
|
UTSW |
1 |
100,306,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R8053:Cntnap5b
|
UTSW |
1 |
100,318,402 (GRCm39) |
missense |
probably damaging |
0.98 |
R8080:Cntnap5b
|
UTSW |
1 |
99,999,928 (GRCm39) |
missense |
probably benign |
0.16 |
R8082:Cntnap5b
|
UTSW |
1 |
100,306,941 (GRCm39) |
missense |
probably benign |
0.00 |
R8271:Cntnap5b
|
UTSW |
1 |
99,999,832 (GRCm39) |
missense |
probably benign |
0.00 |
R8303:Cntnap5b
|
UTSW |
1 |
100,069,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R8428:Cntnap5b
|
UTSW |
1 |
100,311,310 (GRCm39) |
missense |
probably damaging |
0.98 |
R9131:Cntnap5b
|
UTSW |
1 |
99,978,368 (GRCm39) |
missense |
probably benign |
0.22 |
R9144:Cntnap5b
|
UTSW |
1 |
99,978,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R9522:Cntnap5b
|
UTSW |
1 |
100,412,347 (GRCm39) |
missense |
probably benign |
0.00 |
R9611:Cntnap5b
|
UTSW |
1 |
99,894,935 (GRCm39) |
missense |
probably damaging |
1.00 |
RF007:Cntnap5b
|
UTSW |
1 |
100,091,795 (GRCm39) |
missense |
probably damaging |
1.00 |
X0020:Cntnap5b
|
UTSW |
1 |
100,359,573 (GRCm39) |
critical splice donor site |
probably null |
|
Z1176:Cntnap5b
|
UTSW |
1 |
100,374,565 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Cntnap5b
|
UTSW |
1 |
100,091,953 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1176:Cntnap5b
|
UTSW |
1 |
99,894,995 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Cntnap5b
|
UTSW |
1 |
99,978,431 (GRCm39) |
missense |
probably damaging |
0.96 |
|
Predicted Primers |
PCR Primer
(F):5'- AGCTTGGAGAATTGGCCCCTTG -3'
(R):5'- TCTGACAGCCAGTGGAATTAGCTTG -3'
Sequencing Primer
(F):5'- CTATGGTGACCGTGAGTACATTCC -3'
(R):5'- GCTTGATGGTAAAAAACTGTACTGG -3'
|
Posted On |
2014-05-23 |