Incidental Mutation 'R0616:Cntnap5a'
ID |
58280 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cntnap5a
|
Ensembl Gene |
ENSMUSG00000070695 |
Gene Name |
contactin associated protein-like 5A |
Synonyms |
Caspr5-1 |
MMRRC Submission |
038805-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R0616 (G1)
|
Quality Score |
220 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
115612486-116515053 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 116508279 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Histidine to Tyrosine
at position 1264
(H1264Y)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000035732
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000043725]
|
AlphaFold |
Q0V8T9 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000043725
AA Change: H1264Y
PolyPhen 2
Score 0.803 (Sensitivity: 0.84; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000035732 Gene: ENSMUSG00000070695 AA Change: H1264Y
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
24 |
N/A |
INTRINSIC |
FA58C
|
33 |
174 |
1.63e-13 |
SMART |
LamG
|
201 |
338 |
1.4e-26 |
SMART |
LamG
|
388 |
522 |
1.5e-26 |
SMART |
EGF
|
550 |
584 |
2.16e-1 |
SMART |
Blast:FBG
|
587 |
772 |
2e-81 |
BLAST |
LamG
|
812 |
939 |
1.54e-28 |
SMART |
EGF
|
960 |
996 |
2.28e0 |
SMART |
LamG
|
1037 |
1173 |
4.73e-15 |
SMART |
transmembrane domain
|
1241 |
1263 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 99.4%
- 3x: 98.9%
- 10x: 97.5%
- 20x: 95.1%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene product belongs to the neurexin family, members of which function in the vertebrate nervous system as cell adhesion molecules and receptors. This protein, like other neurexin proteins, contains epidermal growth factor repeats and laminin G domains. In addition, it includes an F5/8 type C domain, discoidin/neuropilin- and fibrinogen-like domains, and thrombospondin N-terminal-like domains. [provided by RefSeq, Jul 2008]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
G |
T |
1: 71,341,830 (GRCm39) |
Q1044K |
probably damaging |
Het |
Abi3bp |
A |
T |
16: 56,474,433 (GRCm39) |
T723S |
probably damaging |
Het |
Ackr3 |
G |
A |
1: 90,142,191 (GRCm39) |
V217I |
probably benign |
Het |
Acnat2 |
A |
G |
4: 49,380,269 (GRCm39) |
S370P |
probably damaging |
Het |
Arap1 |
A |
G |
7: 101,050,857 (GRCm39) |
R1152G |
possibly damaging |
Het |
Arhgap15 |
G |
A |
2: 44,006,729 (GRCm39) |
|
probably null |
Het |
Arhgap5 |
C |
T |
12: 52,563,848 (GRCm39) |
T273I |
possibly damaging |
Het |
Armh4 |
G |
T |
14: 50,011,113 (GRCm39) |
T198K |
possibly damaging |
Het |
C1s2 |
T |
C |
6: 124,605,723 (GRCm39) |
E332G |
probably damaging |
Het |
Camp |
G |
A |
9: 109,677,707 (GRCm39) |
R88W |
probably benign |
Het |
Cdkl2 |
A |
G |
5: 92,156,863 (GRCm39) |
M564T |
probably benign |
Het |
Ceacam20 |
A |
G |
7: 19,704,321 (GRCm39) |
H124R |
probably benign |
Het |
Cep19 |
C |
T |
16: 31,922,829 (GRCm39) |
R32C |
probably damaging |
Het |
Cep295 |
G |
A |
9: 15,243,618 (GRCm39) |
Q1565* |
probably null |
Het |
Chd3 |
T |
C |
11: 69,236,313 (GRCm39) |
E1932G |
probably damaging |
Het |
Cibar1 |
G |
A |
4: 12,168,234 (GRCm39) |
R210* |
probably null |
Het |
Cnr2 |
G |
T |
4: 135,644,873 (GRCm39) |
W317L |
probably benign |
Het |
Depdc7 |
T |
A |
2: 104,557,650 (GRCm39) |
N200I |
probably benign |
Het |
Dock4 |
T |
C |
12: 40,754,414 (GRCm39) |
S468P |
probably benign |
Het |
Dscc1 |
C |
A |
15: 54,946,966 (GRCm39) |
C253F |
probably benign |
Het |
Fam217a |
C |
A |
13: 35,097,666 (GRCm39) |
S55I |
probably benign |
Het |
Farp1 |
G |
A |
14: 121,514,434 (GRCm39) |
R921H |
probably damaging |
Het |
Fat4 |
A |
G |
3: 38,997,019 (GRCm39) |
D1746G |
probably damaging |
Het |
Fbxw5 |
T |
C |
2: 25,392,517 (GRCm39) |
F100L |
probably damaging |
Het |
Gli3 |
C |
A |
13: 15,836,991 (GRCm39) |
T458K |
possibly damaging |
Het |
Gm4841 |
T |
C |
18: 60,404,009 (GRCm39) |
Y28C |
probably benign |
Het |
Gprc5d |
T |
C |
6: 135,093,430 (GRCm39) |
E159G |
probably benign |
Het |
Grm4 |
A |
T |
17: 27,653,538 (GRCm39) |
I757N |
probably damaging |
Het |
Hagh |
A |
G |
17: 25,076,551 (GRCm39) |
Y94C |
probably damaging |
Het |
Hycc1 |
T |
C |
5: 24,191,770 (GRCm39) |
T44A |
probably damaging |
Het |
Itpkb |
T |
C |
1: 180,249,301 (GRCm39) |
I892T |
probably damaging |
Het |
Kcmf1 |
T |
C |
6: 72,827,467 (GRCm39) |
I58V |
probably benign |
Het |
Khdrbs2 |
A |
G |
1: 32,506,856 (GRCm39) |
I167V |
possibly damaging |
Het |
Kmt2c |
A |
G |
5: 25,504,250 (GRCm39) |
I275T |
probably benign |
Het |
Lingo4 |
A |
G |
3: 94,310,388 (GRCm39) |
K442R |
probably benign |
Het |
Mak |
T |
C |
13: 41,195,661 (GRCm39) |
N382D |
probably benign |
Het |
Maob |
G |
A |
X: 16,576,402 (GRCm39) |
T480I |
possibly damaging |
Het |
Mcoln1 |
A |
G |
8: 3,565,025 (GRCm39) |
E573G |
probably benign |
Het |
Ms4a6b |
G |
A |
19: 11,504,262 (GRCm39) |
|
probably null |
Het |
Muc5ac |
A |
G |
7: 141,349,981 (GRCm39) |
M576V |
probably benign |
Het |
Nme8 |
T |
A |
13: 19,875,029 (GRCm39) |
D126V |
probably benign |
Het |
Npy2r |
T |
A |
3: 82,448,670 (GRCm39) |
D35V |
possibly damaging |
Het |
Nrxn1 |
T |
C |
17: 90,670,285 (GRCm39) |
D193G |
probably damaging |
Het |
Or2g7 |
A |
C |
17: 38,378,131 (GRCm39) |
E23A |
probably damaging |
Het |
Or2y1e |
T |
C |
11: 49,218,583 (GRCm39) |
L115P |
probably damaging |
Het |
Or4c10b |
T |
A |
2: 89,711,935 (GRCm39) |
V255E |
probably benign |
Het |
Or4d5 |
A |
T |
9: 40,012,283 (GRCm39) |
F168I |
probably damaging |
Het |
Or52b4i |
T |
A |
7: 102,191,761 (GRCm39) |
M206K |
possibly damaging |
Het |
Or6d14 |
A |
G |
6: 116,533,889 (GRCm39) |
I168V |
probably benign |
Het |
Or8b3b |
A |
T |
9: 38,584,776 (GRCm39) |
M1K |
probably null |
Het |
Or8c17 |
G |
T |
9: 38,180,630 (GRCm39) |
V266L |
probably benign |
Het |
Or8g18 |
G |
A |
9: 39,148,946 (GRCm39) |
T258M |
probably benign |
Het |
Pabpc2 |
A |
T |
18: 39,906,792 (GRCm39) |
H19L |
possibly damaging |
Het |
Pcdhb9 |
A |
T |
18: 37,535,028 (GRCm39) |
K341* |
probably null |
Het |
Pde4dip |
T |
C |
3: 97,654,849 (GRCm39) |
I859M |
probably benign |
Het |
Pfkfb2 |
T |
C |
1: 130,634,159 (GRCm39) |
|
probably null |
Het |
Pigg |
C |
T |
5: 108,461,951 (GRCm39) |
T94M |
probably damaging |
Het |
Pik3c2b |
T |
C |
1: 133,028,569 (GRCm39) |
F1353L |
probably damaging |
Het |
Prg4 |
T |
C |
1: 150,336,462 (GRCm39) |
D87G |
probably damaging |
Het |
Prkdc |
A |
T |
16: 15,508,271 (GRCm39) |
D974V |
probably damaging |
Het |
Prmt3 |
A |
G |
7: 49,437,076 (GRCm39) |
Y217C |
probably damaging |
Het |
Proser1 |
A |
G |
3: 53,382,118 (GRCm39) |
T192A |
probably damaging |
Het |
Rab3d |
G |
A |
9: 21,826,060 (GRCm39) |
T118M |
probably damaging |
Het |
Rb1cc1 |
A |
G |
1: 6,314,486 (GRCm39) |
K386R |
possibly damaging |
Het |
Rcn2 |
A |
G |
9: 55,963,534 (GRCm39) |
D221G |
probably benign |
Het |
Rhbdl3 |
T |
G |
11: 80,222,687 (GRCm39) |
H245Q |
probably damaging |
Het |
Ribc1 |
T |
C |
X: 150,788,787 (GRCm39) |
E204G |
probably damaging |
Het |
Rpap1 |
G |
A |
2: 119,608,601 (GRCm39) |
L254F |
probably damaging |
Het |
Rrp12 |
A |
G |
19: 41,880,988 (GRCm39) |
F148L |
possibly damaging |
Het |
Rusf1 |
A |
T |
7: 127,871,803 (GRCm39) |
|
probably null |
Het |
Setdb1 |
A |
T |
3: 95,249,109 (GRCm39) |
I333K |
probably damaging |
Het |
Simc1 |
A |
G |
13: 54,694,845 (GRCm39) |
I1210V |
probably benign |
Het |
Smchd1 |
T |
A |
17: 71,686,569 (GRCm39) |
D1379V |
probably benign |
Het |
Snap29 |
A |
T |
16: 17,240,370 (GRCm39) |
K159* |
probably null |
Het |
Spdye4c |
A |
T |
2: 128,436,132 (GRCm39) |
K176M |
possibly damaging |
Het |
Stk31 |
T |
A |
6: 49,400,419 (GRCm39) |
W415R |
probably damaging |
Het |
Supt6 |
C |
T |
11: 78,100,321 (GRCm39) |
R1497Q |
probably damaging |
Het |
Tenm3 |
A |
G |
8: 48,729,191 (GRCm39) |
I1605T |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,676,967 (GRCm39) |
|
probably null |
Het |
Ttn |
A |
G |
2: 76,728,011 (GRCm39) |
|
probably benign |
Het |
Ucp3 |
A |
T |
7: 100,129,368 (GRCm39) |
T68S |
probably benign |
Het |
Ugt2b36 |
T |
C |
5: 87,237,336 (GRCm39) |
N316D |
probably benign |
Het |
Usp4 |
T |
G |
9: 108,244,003 (GRCm39) |
S247A |
probably benign |
Het |
Utp20 |
A |
T |
10: 88,606,613 (GRCm39) |
V1653D |
probably benign |
Het |
Vmn1r183 |
A |
G |
7: 23,754,250 (GRCm39) |
I18V |
probably benign |
Het |
Vmn1r237 |
A |
G |
17: 21,534,885 (GRCm39) |
M203V |
probably damaging |
Het |
Vmn1r61 |
A |
T |
7: 5,613,998 (GRCm39) |
F105L |
possibly damaging |
Het |
Zfp462 |
T |
C |
4: 55,011,951 (GRCm39) |
C158R |
probably damaging |
Het |
Zfyve16 |
C |
G |
13: 92,657,637 (GRCm39) |
R758P |
probably damaging |
Het |
|
Other mutations in Cntnap5a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00763:Cntnap5a
|
APN |
1 |
116,045,407 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL00929:Cntnap5a
|
APN |
1 |
115,988,004 (GRCm39) |
splice site |
probably null |
|
IGL00959:Cntnap5a
|
APN |
1 |
116,112,057 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01721:Cntnap5a
|
APN |
1 |
116,085,367 (GRCm39) |
missense |
probably benign |
|
IGL02009:Cntnap5a
|
APN |
1 |
116,085,224 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02111:Cntnap5a
|
APN |
1 |
116,017,082 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02198:Cntnap5a
|
APN |
1 |
116,508,262 (GRCm39) |
missense |
probably benign |
|
IGL02751:Cntnap5a
|
APN |
1 |
116,112,187 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02752:Cntnap5a
|
APN |
1 |
116,508,261 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02989:Cntnap5a
|
APN |
1 |
116,339,813 (GRCm39) |
splice site |
probably benign |
|
IGL03195:Cntnap5a
|
APN |
1 |
116,085,178 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4142001:Cntnap5a
|
UTSW |
1 |
115,612,686 (GRCm39) |
start gained |
probably benign |
|
R0294:Cntnap5a
|
UTSW |
1 |
115,843,046 (GRCm39) |
missense |
probably benign |
|
R0377:Cntnap5a
|
UTSW |
1 |
116,220,259 (GRCm39) |
missense |
probably benign |
0.04 |
R0597:Cntnap5a
|
UTSW |
1 |
116,112,191 (GRCm39) |
splice site |
probably benign |
|
R0725:Cntnap5a
|
UTSW |
1 |
116,220,206 (GRCm39) |
missense |
probably benign |
0.25 |
R0842:Cntnap5a
|
UTSW |
1 |
116,369,953 (GRCm39) |
missense |
probably damaging |
0.96 |
R1103:Cntnap5a
|
UTSW |
1 |
116,508,399 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1265:Cntnap5a
|
UTSW |
1 |
116,356,248 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1467:Cntnap5a
|
UTSW |
1 |
115,612,898 (GRCm39) |
nonsense |
probably null |
|
R1467:Cntnap5a
|
UTSW |
1 |
115,612,898 (GRCm39) |
nonsense |
probably null |
|
R1470:Cntnap5a
|
UTSW |
1 |
116,187,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Cntnap5a
|
UTSW |
1 |
116,187,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R1474:Cntnap5a
|
UTSW |
1 |
116,370,103 (GRCm39) |
nonsense |
probably null |
|
R1476:Cntnap5a
|
UTSW |
1 |
115,828,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R1481:Cntnap5a
|
UTSW |
1 |
116,045,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R1512:Cntnap5a
|
UTSW |
1 |
115,828,680 (GRCm39) |
missense |
probably benign |
|
R1526:Cntnap5a
|
UTSW |
1 |
116,356,207 (GRCm39) |
missense |
probably benign |
|
R1589:Cntnap5a
|
UTSW |
1 |
115,987,930 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1603:Cntnap5a
|
UTSW |
1 |
116,339,831 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1728:Cntnap5a
|
UTSW |
1 |
116,382,873 (GRCm39) |
missense |
probably benign |
0.01 |
R1728:Cntnap5a
|
UTSW |
1 |
116,382,734 (GRCm39) |
missense |
probably benign |
0.00 |
R1728:Cntnap5a
|
UTSW |
1 |
116,382,831 (GRCm39) |
missense |
probably benign |
0.00 |
R1729:Cntnap5a
|
UTSW |
1 |
116,382,873 (GRCm39) |
missense |
probably benign |
0.01 |
R1729:Cntnap5a
|
UTSW |
1 |
116,382,734 (GRCm39) |
missense |
probably benign |
0.00 |
R1729:Cntnap5a
|
UTSW |
1 |
116,382,831 (GRCm39) |
missense |
probably benign |
0.00 |
R1730:Cntnap5a
|
UTSW |
1 |
116,382,873 (GRCm39) |
missense |
probably benign |
0.01 |
R1730:Cntnap5a
|
UTSW |
1 |
116,382,734 (GRCm39) |
missense |
probably benign |
0.00 |
R1730:Cntnap5a
|
UTSW |
1 |
116,382,831 (GRCm39) |
missense |
probably benign |
0.00 |
R1739:Cntnap5a
|
UTSW |
1 |
116,382,873 (GRCm39) |
missense |
probably benign |
0.01 |
R1739:Cntnap5a
|
UTSW |
1 |
116,382,734 (GRCm39) |
missense |
probably benign |
0.00 |
R1739:Cntnap5a
|
UTSW |
1 |
116,382,831 (GRCm39) |
missense |
probably benign |
0.00 |
R1762:Cntnap5a
|
UTSW |
1 |
116,382,831 (GRCm39) |
missense |
probably benign |
0.00 |
R1762:Cntnap5a
|
UTSW |
1 |
116,382,873 (GRCm39) |
missense |
probably benign |
0.01 |
R1762:Cntnap5a
|
UTSW |
1 |
116,382,734 (GRCm39) |
missense |
probably benign |
0.00 |
R1783:Cntnap5a
|
UTSW |
1 |
116,382,873 (GRCm39) |
missense |
probably benign |
0.01 |
R1783:Cntnap5a
|
UTSW |
1 |
116,382,734 (GRCm39) |
missense |
probably benign |
0.00 |
R1783:Cntnap5a
|
UTSW |
1 |
116,382,831 (GRCm39) |
missense |
probably benign |
0.00 |
R1785:Cntnap5a
|
UTSW |
1 |
116,382,734 (GRCm39) |
missense |
probably benign |
0.00 |
R1785:Cntnap5a
|
UTSW |
1 |
116,382,831 (GRCm39) |
missense |
probably benign |
0.00 |
R1785:Cntnap5a
|
UTSW |
1 |
116,382,873 (GRCm39) |
missense |
probably benign |
0.01 |
R1816:Cntnap5a
|
UTSW |
1 |
116,356,618 (GRCm39) |
missense |
probably benign |
0.19 |
R1872:Cntnap5a
|
UTSW |
1 |
116,016,940 (GRCm39) |
missense |
probably benign |
0.02 |
R2095:Cntnap5a
|
UTSW |
1 |
116,369,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R2113:Cntnap5a
|
UTSW |
1 |
116,116,095 (GRCm39) |
missense |
probably damaging |
0.98 |
R2144:Cntnap5a
|
UTSW |
1 |
116,029,440 (GRCm39) |
missense |
probably benign |
0.14 |
R2171:Cntnap5a
|
UTSW |
1 |
116,116,132 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2219:Cntnap5a
|
UTSW |
1 |
116,508,369 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2220:Cntnap5a
|
UTSW |
1 |
116,508,369 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2571:Cntnap5a
|
UTSW |
1 |
116,112,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R3019:Cntnap5a
|
UTSW |
1 |
116,029,299 (GRCm39) |
missense |
probably benign |
|
R3827:Cntnap5a
|
UTSW |
1 |
116,045,409 (GRCm39) |
missense |
probably benign |
0.14 |
R3870:Cntnap5a
|
UTSW |
1 |
115,987,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R3871:Cntnap5a
|
UTSW |
1 |
115,987,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R4041:Cntnap5a
|
UTSW |
1 |
116,112,129 (GRCm39) |
missense |
probably benign |
0.00 |
R4080:Cntnap5a
|
UTSW |
1 |
116,029,304 (GRCm39) |
missense |
probably benign |
0.01 |
R4260:Cntnap5a
|
UTSW |
1 |
116,374,325 (GRCm39) |
missense |
probably benign |
0.31 |
R4685:Cntnap5a
|
UTSW |
1 |
116,374,410 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4781:Cntnap5a
|
UTSW |
1 |
116,339,931 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4785:Cntnap5a
|
UTSW |
1 |
116,029,295 (GRCm39) |
missense |
probably benign |
0.00 |
R5057:Cntnap5a
|
UTSW |
1 |
115,612,943 (GRCm39) |
missense |
probably benign |
0.10 |
R5059:Cntnap5a
|
UTSW |
1 |
116,356,224 (GRCm39) |
missense |
probably benign |
0.44 |
R5101:Cntnap5a
|
UTSW |
1 |
116,370,026 (GRCm39) |
missense |
probably benign |
0.00 |
R5302:Cntnap5a
|
UTSW |
1 |
116,085,300 (GRCm39) |
missense |
probably benign |
0.15 |
R5451:Cntnap5a
|
UTSW |
1 |
115,612,873 (GRCm39) |
missense |
probably benign |
|
R5473:Cntnap5a
|
UTSW |
1 |
116,016,986 (GRCm39) |
missense |
probably benign |
0.12 |
R5886:Cntnap5a
|
UTSW |
1 |
116,499,402 (GRCm39) |
critical splice donor site |
probably null |
|
R6311:Cntnap5a
|
UTSW |
1 |
116,339,836 (GRCm39) |
nonsense |
probably null |
|
R6464:Cntnap5a
|
UTSW |
1 |
116,112,138 (GRCm39) |
missense |
probably benign |
|
R6497:Cntnap5a
|
UTSW |
1 |
116,505,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R6781:Cntnap5a
|
UTSW |
1 |
116,220,127 (GRCm39) |
missense |
probably benign |
0.05 |
R7137:Cntnap5a
|
UTSW |
1 |
116,017,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R7290:Cntnap5a
|
UTSW |
1 |
116,149,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R7342:Cntnap5a
|
UTSW |
1 |
115,987,852 (GRCm39) |
missense |
probably benign |
0.00 |
R7367:Cntnap5a
|
UTSW |
1 |
116,370,025 (GRCm39) |
missense |
probably benign |
0.00 |
R7373:Cntnap5a
|
UTSW |
1 |
116,508,367 (GRCm39) |
missense |
probably benign |
0.20 |
R7426:Cntnap5a
|
UTSW |
1 |
116,370,110 (GRCm39) |
missense |
probably benign |
0.03 |
R7444:Cntnap5a
|
UTSW |
1 |
116,220,079 (GRCm39) |
missense |
probably benign |
|
R7582:Cntnap5a
|
UTSW |
1 |
116,374,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R7745:Cntnap5a
|
UTSW |
1 |
116,370,013 (GRCm39) |
missense |
probably benign |
|
R7948:Cntnap5a
|
UTSW |
1 |
116,508,258 (GRCm39) |
missense |
probably benign |
0.01 |
R7995:Cntnap5a
|
UTSW |
1 |
116,499,277 (GRCm39) |
missense |
probably damaging |
0.99 |
R8041:Cntnap5a
|
UTSW |
1 |
116,187,209 (GRCm39) |
missense |
probably damaging |
0.99 |
R8262:Cntnap5a
|
UTSW |
1 |
116,116,140 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8273:Cntnap5a
|
UTSW |
1 |
116,499,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R8320:Cntnap5a
|
UTSW |
1 |
116,374,466 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9242:Cntnap5a
|
UTSW |
1 |
116,220,109 (GRCm39) |
missense |
probably benign |
0.06 |
R9470:Cntnap5a
|
UTSW |
1 |
116,374,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R9601:Cntnap5a
|
UTSW |
1 |
116,508,217 (GRCm39) |
missense |
probably damaging |
0.96 |
R9616:Cntnap5a
|
UTSW |
1 |
116,029,323 (GRCm39) |
missense |
probably benign |
|
R9623:Cntnap5a
|
UTSW |
1 |
116,369,985 (GRCm39) |
nonsense |
probably null |
|
Z1088:Cntnap5a
|
UTSW |
1 |
115,987,981 (GRCm39) |
missense |
probably benign |
0.08 |
Z1176:Cntnap5a
|
UTSW |
1 |
116,356,246 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Cntnap5a
|
UTSW |
1 |
116,339,898 (GRCm39) |
missense |
probably benign |
0.03 |
Z1188:Cntnap5a
|
UTSW |
1 |
116,445,935 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
Predicted Primers |
PCR Primer
(F):5'- AGCTTCTGCACAGGCTCTTATGTC -3'
(R):5'- TGTCAGTGGGTTACAGTAGCCACAG -3'
Sequencing Primer
(F):5'- TCTGGATACAGAGTAGATTTGTGC -3'
(R):5'- AGTAGCCACAGCTATATGATCTC -3'
|
Posted On |
2013-07-11 |