Incidental Mutation 'R0349:Nckap5'
ID |
36040 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Nckap5
|
Ensembl Gene |
ENSMUSG00000049690 |
Gene Name |
NCK-associated protein 5 |
Synonyms |
LOC380609, D130011D22Rik, E030049G20Rik |
MMRRC Submission |
038556-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R0349 (G1)
|
Quality Score |
219 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
125841373-126758529 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 125954171 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Proline
at position 794
(S794P)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000125624
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000057846]
[ENSMUST00000094609]
[ENSMUST00000094610]
[ENSMUST00000112583]
[ENSMUST00000161954]
[ENSMUST00000162877]
|
AlphaFold |
E9QAE1 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000057846
AA Change: S730P
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000062229 Gene: ENSMUSG00000049690 AA Change: S730P
Domain | Start | End | E-Value | Type |
low complexity region
|
2 |
25 |
N/A |
INTRINSIC |
coiled coil region
|
108 |
186 |
N/A |
INTRINSIC |
low complexity region
|
321 |
332 |
N/A |
INTRINSIC |
low complexity region
|
755 |
771 |
N/A |
INTRINSIC |
low complexity region
|
950 |
971 |
N/A |
INTRINSIC |
low complexity region
|
1070 |
1085 |
N/A |
INTRINSIC |
low complexity region
|
1181 |
1200 |
N/A |
INTRINSIC |
Pfam:NCKAP5
|
1298 |
1602 |
1.8e-120 |
PFAM |
low complexity region
|
1728 |
1742 |
N/A |
INTRINSIC |
low complexity region
|
1757 |
1771 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000094609
|
SMART Domains |
Protein: ENSMUSP00000092192 Gene: ENSMUSG00000049690
Domain | Start | End | E-Value | Type |
low complexity region
|
70 |
93 |
N/A |
INTRINSIC |
Pfam:NCKAP5
|
113 |
364 |
3.6e-36 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000094610
|
SMART Domains |
Protein: ENSMUSP00000092193 Gene: ENSMUSG00000049690
Domain | Start | End | E-Value | Type |
Pfam:NCKAP5
|
1 |
101 |
8.8e-42 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000112583
AA Change: S862P
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000108202 Gene: ENSMUSG00000049690 AA Change: S862P
Domain | Start | End | E-Value | Type |
low complexity region
|
70 |
93 |
N/A |
INTRINSIC |
coiled coil region
|
176 |
254 |
N/A |
INTRINSIC |
low complexity region
|
301 |
324 |
N/A |
INTRINSIC |
low complexity region
|
453 |
464 |
N/A |
INTRINSIC |
low complexity region
|
887 |
903 |
N/A |
INTRINSIC |
low complexity region
|
1082 |
1103 |
N/A |
INTRINSIC |
low complexity region
|
1202 |
1217 |
N/A |
INTRINSIC |
low complexity region
|
1313 |
1332 |
N/A |
INTRINSIC |
Pfam:NCKAP5
|
1431 |
1733 |
5.3e-119 |
PFAM |
low complexity region
|
1860 |
1874 |
N/A |
INTRINSIC |
low complexity region
|
1889 |
1903 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000159934
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000161954
AA Change: S794P
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000125624 Gene: ENSMUSG00000049690 AA Change: S794P
Domain | Start | End | E-Value | Type |
low complexity region
|
2 |
25 |
N/A |
INTRINSIC |
coiled coil region
|
108 |
186 |
N/A |
INTRINSIC |
low complexity region
|
233 |
256 |
N/A |
INTRINSIC |
low complexity region
|
385 |
396 |
N/A |
INTRINSIC |
low complexity region
|
819 |
835 |
N/A |
INTRINSIC |
low complexity region
|
1014 |
1035 |
N/A |
INTRINSIC |
low complexity region
|
1134 |
1149 |
N/A |
INTRINSIC |
low complexity region
|
1245 |
1264 |
N/A |
INTRINSIC |
Pfam:NCKAP5
|
1362 |
1666 |
2.1e-120 |
PFAM |
low complexity region
|
1792 |
1806 |
N/A |
INTRINSIC |
low complexity region
|
1821 |
1835 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000162877
|
SMART Domains |
Protein: ENSMUSP00000124748 Gene: ENSMUSG00000049690
Domain | Start | End | E-Value | Type |
Pfam:NCKAP5
|
9 |
296 |
6e-36 |
PFAM |
|
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.1%
- 20x: 95.3%
|
Validation Efficiency |
|
Allele List at MGI |
All alleles(1) : Gene trapped(1) |
Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A1cf |
A |
T |
19: 31,910,062 (GRCm39) |
S285C |
possibly damaging |
Het |
Abcc9 |
A |
T |
6: 142,610,351 (GRCm39) |
N604K |
probably benign |
Het |
Acsbg3 |
T |
A |
17: 57,192,169 (GRCm39) |
Y577* |
probably null |
Het |
Adgrl3 |
A |
G |
5: 81,919,491 (GRCm39) |
T1192A |
probably damaging |
Het |
Aldh1l2 |
A |
T |
10: 83,326,478 (GRCm39) |
Y800N |
probably damaging |
Het |
Ano3 |
A |
T |
2: 110,491,832 (GRCm39) |
V865D |
probably damaging |
Het |
App |
A |
T |
16: 84,810,568 (GRCm39) |
L545Q |
probably damaging |
Het |
Atp10a |
A |
G |
7: 58,453,215 (GRCm39) |
D798G |
probably damaging |
Het |
B3galnt2 |
T |
C |
13: 14,166,059 (GRCm39) |
V318A |
probably benign |
Het |
Clcn3 |
T |
A |
8: 61,394,382 (GRCm39) |
D49V |
possibly damaging |
Het |
Clcn6 |
T |
A |
4: 148,108,651 (GRCm39) |
K126M |
possibly damaging |
Het |
Cntln |
T |
A |
4: 84,914,722 (GRCm39) |
S510T |
probably damaging |
Het |
Csk |
A |
C |
9: 57,535,477 (GRCm39) |
C290W |
probably damaging |
Het |
Dmxl1 |
T |
A |
18: 50,012,349 (GRCm39) |
M1502K |
probably damaging |
Het |
Dpy19l2 |
T |
A |
9: 24,607,218 (GRCm39) |
N81I |
possibly damaging |
Het |
Dpyd |
T |
A |
3: 118,710,748 (GRCm39) |
C385* |
probably null |
Het |
Dst |
G |
A |
1: 34,238,634 (GRCm39) |
V1765I |
probably benign |
Het |
Eif5b |
A |
G |
1: 38,071,447 (GRCm39) |
S459G |
probably benign |
Het |
Fam83d |
A |
G |
2: 158,621,768 (GRCm39) |
I160V |
possibly damaging |
Het |
Fat3 |
A |
G |
9: 15,942,476 (GRCm39) |
F1299L |
probably damaging |
Het |
Fmn1 |
A |
G |
2: 113,196,141 (GRCm39) |
I614V |
unknown |
Het |
Fsd1l |
T |
A |
4: 53,679,854 (GRCm39) |
V184E |
probably damaging |
Het |
Fyco1 |
A |
G |
9: 123,626,727 (GRCm39) |
V1328A |
probably damaging |
Het |
Ganab |
T |
A |
19: 8,889,016 (GRCm39) |
N572K |
probably null |
Het |
Gbp10 |
T |
A |
5: 105,368,942 (GRCm39) |
D299V |
possibly damaging |
Het |
Gpr83 |
T |
G |
9: 14,779,563 (GRCm39) |
L205R |
probably damaging |
Het |
Hapln2 |
G |
A |
3: 87,930,936 (GRCm39) |
P152S |
probably damaging |
Het |
Htatip2 |
T |
C |
7: 49,423,140 (GRCm39) |
Y232H |
probably benign |
Het |
Itga2b |
C |
T |
11: 102,358,252 (GRCm39) |
V158I |
probably damaging |
Het |
Kansl3 |
T |
C |
1: 36,390,864 (GRCm39) |
D390G |
probably damaging |
Het |
Kcnh2 |
T |
C |
5: 24,556,235 (GRCm39) |
D16G |
probably benign |
Het |
Kctd8 |
A |
T |
5: 69,498,353 (GRCm39) |
F98I |
probably damaging |
Het |
Kif21b |
A |
T |
1: 136,077,049 (GRCm39) |
E357V |
probably damaging |
Het |
Kmt5c |
C |
T |
7: 4,749,594 (GRCm39) |
R371C |
probably damaging |
Het |
Kndc1 |
T |
C |
7: 139,490,220 (GRCm39) |
F241L |
probably benign |
Het |
Lrba |
A |
G |
3: 86,447,312 (GRCm39) |
D2052G |
probably damaging |
Het |
Lsr |
T |
A |
7: 30,658,698 (GRCm39) |
I54F |
probably damaging |
Het |
Matk |
G |
T |
10: 81,094,328 (GRCm39) |
L28F |
probably benign |
Het |
Mdn1 |
T |
C |
4: 32,750,318 (GRCm39) |
L4429P |
probably damaging |
Het |
Med29 |
CCTGCTGCTGCTGCTGC |
CCTGCTGCTGCTGC |
7: 28,091,935 (GRCm39) |
|
probably benign |
Het |
Msln |
G |
T |
17: 25,969,250 (GRCm39) |
Q407K |
possibly damaging |
Het |
Msr1 |
C |
T |
8: 40,034,868 (GRCm39) |
G428R |
probably damaging |
Het |
Myof |
A |
G |
19: 37,899,417 (GRCm39) |
I1040T |
probably damaging |
Het |
Nfkbiz |
C |
T |
16: 55,639,354 (GRCm39) |
|
probably null |
Het |
Nr2c1 |
C |
T |
10: 94,031,044 (GRCm39) |
S535L |
probably damaging |
Het |
Opn3 |
A |
C |
1: 175,519,870 (GRCm39) |
L78R |
probably damaging |
Het |
Or11h4b |
G |
A |
14: 50,918,711 (GRCm39) |
R127C |
probably benign |
Het |
Or52n3 |
A |
T |
7: 104,530,199 (GRCm39) |
D95V |
possibly damaging |
Het |
Or5b12 |
A |
T |
19: 12,897,299 (GRCm39) |
C125S |
probably damaging |
Het |
Otulinl |
T |
A |
15: 27,664,876 (GRCm39) |
I27L |
probably benign |
Het |
Pcdhb9 |
A |
G |
18: 37,535,632 (GRCm39) |
N542S |
probably damaging |
Het |
Pdc |
T |
A |
1: 150,209,178 (GRCm39) |
N220K |
probably benign |
Het |
Pde6c |
A |
T |
19: 38,150,797 (GRCm39) |
N569Y |
probably damaging |
Het |
Pgm1 |
A |
T |
4: 99,820,814 (GRCm39) |
K219M |
probably damaging |
Het |
Pitpnb |
C |
T |
5: 111,494,992 (GRCm39) |
T99M |
possibly damaging |
Het |
Pou6f2 |
T |
A |
13: 18,326,589 (GRCm39) |
Q71L |
probably damaging |
Het |
Pramel24 |
T |
G |
4: 143,453,629 (GRCm39) |
W246G |
probably benign |
Het |
Prkd1 |
C |
A |
12: 50,413,139 (GRCm39) |
L677F |
probably damaging |
Het |
Ranbp17 |
T |
C |
11: 33,450,689 (GRCm39) |
I78V |
probably benign |
Het |
Rnft2 |
T |
A |
5: 118,339,450 (GRCm39) |
K362M |
possibly damaging |
Het |
Rprd1a |
T |
A |
18: 24,639,904 (GRCm39) |
E259V |
possibly damaging |
Het |
Scara3 |
A |
T |
14: 66,169,230 (GRCm39) |
I129N |
probably damaging |
Het |
Scgb1a1 |
A |
T |
19: 9,062,753 (GRCm39) |
|
probably null |
Het |
Sec16b |
A |
T |
1: 157,359,746 (GRCm39) |
|
probably null |
Het |
Slc18a1 |
A |
T |
8: 69,524,753 (GRCm39) |
M167K |
probably damaging |
Het |
Slc6a15 |
C |
T |
10: 103,254,086 (GRCm39) |
A674V |
probably benign |
Het |
Slc6a3 |
T |
C |
13: 73,715,676 (GRCm39) |
F437S |
probably damaging |
Het |
Snrnp40 |
C |
G |
4: 130,271,836 (GRCm39) |
|
probably null |
Het |
Stag1 |
T |
A |
9: 100,658,837 (GRCm39) |
N141K |
probably damaging |
Het |
Sun2 |
T |
C |
15: 79,614,433 (GRCm39) |
E321G |
probably damaging |
Het |
Taar2 |
C |
A |
10: 23,817,327 (GRCm39) |
T289K |
possibly damaging |
Het |
Taar2 |
T |
C |
10: 23,817,407 (GRCm39) |
Y316H |
probably benign |
Het |
Tbcd |
T |
A |
11: 121,493,809 (GRCm39) |
|
probably null |
Het |
Tecr |
G |
A |
8: 84,298,904 (GRCm39) |
T106I |
probably damaging |
Het |
Thoc2l |
T |
C |
5: 104,667,842 (GRCm39) |
L788P |
possibly damaging |
Het |
Tmem60 |
T |
G |
5: 21,091,628 (GRCm39) |
V131G |
probably benign |
Het |
Uimc1 |
A |
G |
13: 55,223,804 (GRCm39) |
V156A |
probably benign |
Het |
Usp28 |
G |
A |
9: 48,921,581 (GRCm39) |
W266* |
probably null |
Het |
Vmn2r17 |
T |
A |
5: 109,576,202 (GRCm39) |
S358T |
probably damaging |
Het |
Wwc2 |
T |
A |
8: 48,321,701 (GRCm39) |
Y471F |
unknown |
Het |
Ythdc1 |
C |
T |
5: 86,983,579 (GRCm39) |
R675C |
probably damaging |
Het |
Zfp30 |
T |
C |
7: 29,493,029 (GRCm39) |
S428P |
probably damaging |
Het |
Zfp462 |
T |
A |
4: 55,008,768 (GRCm39) |
C245S |
probably benign |
Het |
Zscan30 |
T |
C |
18: 24,104,455 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Nckap5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00833:Nckap5
|
APN |
1 |
125,954,889 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00956:Nckap5
|
APN |
1 |
125,952,755 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01414:Nckap5
|
APN |
1 |
126,456,450 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01482:Nckap5
|
APN |
1 |
125,950,897 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01508:Nckap5
|
APN |
1 |
125,953,309 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02071:Nckap5
|
APN |
1 |
125,909,305 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02129:Nckap5
|
APN |
1 |
125,955,432 (GRCm39) |
nonsense |
probably null |
|
IGL02821:Nckap5
|
APN |
1 |
125,955,553 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03174:Nckap5
|
APN |
1 |
125,909,383 (GRCm39) |
missense |
probably damaging |
1.00 |
F5493:Nckap5
|
UTSW |
1 |
125,953,564 (GRCm39) |
missense |
probably benign |
|
G5030:Nckap5
|
UTSW |
1 |
125,953,591 (GRCm39) |
missense |
probably damaging |
0.96 |
R0033:Nckap5
|
UTSW |
1 |
125,867,979 (GRCm39) |
intron |
probably benign |
|
R0164:Nckap5
|
UTSW |
1 |
125,952,144 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0164:Nckap5
|
UTSW |
1 |
125,952,144 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0482:Nckap5
|
UTSW |
1 |
125,954,102 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0508:Nckap5
|
UTSW |
1 |
125,909,121 (GRCm39) |
splice site |
probably null |
|
R0541:Nckap5
|
UTSW |
1 |
126,623,459 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0609:Nckap5
|
UTSW |
1 |
125,955,025 (GRCm39) |
nonsense |
probably null |
|
R0701:Nckap5
|
UTSW |
1 |
125,953,094 (GRCm39) |
missense |
probably benign |
0.06 |
R0782:Nckap5
|
UTSW |
1 |
125,909,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R1389:Nckap5
|
UTSW |
1 |
125,954,447 (GRCm39) |
missense |
probably damaging |
0.99 |
R1401:Nckap5
|
UTSW |
1 |
125,942,398 (GRCm39) |
splice site |
probably benign |
|
R1436:Nckap5
|
UTSW |
1 |
125,953,798 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1506:Nckap5
|
UTSW |
1 |
125,953,650 (GRCm39) |
nonsense |
probably null |
|
R1528:Nckap5
|
UTSW |
1 |
125,952,659 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1942:Nckap5
|
UTSW |
1 |
125,952,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R1968:Nckap5
|
UTSW |
1 |
125,942,367 (GRCm39) |
missense |
probably damaging |
0.99 |
R2055:Nckap5
|
UTSW |
1 |
125,954,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R2105:Nckap5
|
UTSW |
1 |
125,954,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R2214:Nckap5
|
UTSW |
1 |
125,953,487 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2311:Nckap5
|
UTSW |
1 |
126,456,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R2403:Nckap5
|
UTSW |
1 |
125,955,146 (GRCm39) |
missense |
probably benign |
0.18 |
R2430:Nckap5
|
UTSW |
1 |
125,842,494 (GRCm39) |
missense |
probably damaging |
0.99 |
R2914:Nckap5
|
UTSW |
1 |
125,954,274 (GRCm39) |
splice site |
probably null |
|
R3782:Nckap5
|
UTSW |
1 |
125,952,811 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4133:Nckap5
|
UTSW |
1 |
126,150,443 (GRCm39) |
missense |
probably benign |
0.13 |
R4249:Nckap5
|
UTSW |
1 |
125,955,376 (GRCm39) |
missense |
probably benign |
0.01 |
R4448:Nckap5
|
UTSW |
1 |
125,953,463 (GRCm39) |
nonsense |
probably null |
|
R4456:Nckap5
|
UTSW |
1 |
125,842,472 (GRCm39) |
unclassified |
probably benign |
|
R4682:Nckap5
|
UTSW |
1 |
126,030,279 (GRCm39) |
critical splice donor site |
probably null |
|
R4817:Nckap5
|
UTSW |
1 |
125,954,952 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4907:Nckap5
|
UTSW |
1 |
125,953,889 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4908:Nckap5
|
UTSW |
1 |
125,955,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R4924:Nckap5
|
UTSW |
1 |
125,954,765 (GRCm39) |
nonsense |
probably null |
|
R4926:Nckap5
|
UTSW |
1 |
126,456,378 (GRCm39) |
intron |
probably benign |
|
R5032:Nckap5
|
UTSW |
1 |
125,904,786 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5133:Nckap5
|
UTSW |
1 |
125,961,697 (GRCm39) |
missense |
probably benign |
0.01 |
R5197:Nckap5
|
UTSW |
1 |
126,150,410 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5238:Nckap5
|
UTSW |
1 |
125,955,461 (GRCm39) |
missense |
probably damaging |
0.96 |
R5257:Nckap5
|
UTSW |
1 |
125,952,245 (GRCm39) |
missense |
probably damaging |
0.99 |
R5277:Nckap5
|
UTSW |
1 |
125,954,277 (GRCm39) |
nonsense |
probably null |
|
R5512:Nckap5
|
UTSW |
1 |
125,955,481 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5700:Nckap5
|
UTSW |
1 |
125,904,662 (GRCm39) |
critical splice donor site |
probably null |
|
R5789:Nckap5
|
UTSW |
1 |
125,955,439 (GRCm39) |
missense |
probably damaging |
1.00 |
R6029:Nckap5
|
UTSW |
1 |
125,953,523 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6249:Nckap5
|
UTSW |
1 |
125,952,667 (GRCm39) |
missense |
probably benign |
|
R6292:Nckap5
|
UTSW |
1 |
125,842,752 (GRCm39) |
missense |
probably damaging |
0.99 |
R6521:Nckap5
|
UTSW |
1 |
126,309,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R6875:Nckap5
|
UTSW |
1 |
125,950,931 (GRCm39) |
missense |
probably benign |
0.03 |
R7017:Nckap5
|
UTSW |
1 |
126,030,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R7018:Nckap5
|
UTSW |
1 |
125,952,785 (GRCm39) |
missense |
probably damaging |
0.99 |
R7054:Nckap5
|
UTSW |
1 |
126,186,449 (GRCm39) |
splice site |
probably null |
|
R7204:Nckap5
|
UTSW |
1 |
125,954,104 (GRCm39) |
missense |
probably benign |
|
R7336:Nckap5
|
UTSW |
1 |
125,953,786 (GRCm39) |
missense |
probably benign |
0.00 |
R7544:Nckap5
|
UTSW |
1 |
125,953,948 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7590:Nckap5
|
UTSW |
1 |
125,954,270 (GRCm39) |
missense |
probably benign |
0.00 |
R7684:Nckap5
|
UTSW |
1 |
125,954,594 (GRCm39) |
missense |
probably benign |
0.00 |
R7749:Nckap5
|
UTSW |
1 |
125,952,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R7773:Nckap5
|
UTSW |
1 |
125,954,581 (GRCm39) |
missense |
probably benign |
0.00 |
R7813:Nckap5
|
UTSW |
1 |
125,953,163 (GRCm39) |
missense |
probably benign |
0.10 |
R7970:Nckap5
|
UTSW |
1 |
125,952,758 (GRCm39) |
nonsense |
probably null |
|
R7992:Nckap5
|
UTSW |
1 |
125,954,547 (GRCm39) |
missense |
probably damaging |
0.99 |
R8278:Nckap5
|
UTSW |
1 |
125,955,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R8373:Nckap5
|
UTSW |
1 |
125,954,032 (GRCm39) |
missense |
probably benign |
0.02 |
R8414:Nckap5
|
UTSW |
1 |
125,942,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R8755:Nckap5
|
UTSW |
1 |
125,954,279 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8845:Nckap5
|
UTSW |
1 |
125,909,423 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9016:Nckap5
|
UTSW |
1 |
126,623,491 (GRCm39) |
start codon destroyed |
probably null |
0.01 |
R9209:Nckap5
|
UTSW |
1 |
125,867,928 (GRCm39) |
missense |
unknown |
|
R9214:Nckap5
|
UTSW |
1 |
125,942,376 (GRCm39) |
missense |
probably benign |
0.01 |
R9300:Nckap5
|
UTSW |
1 |
125,909,423 (GRCm39) |
nonsense |
probably null |
|
R9464:Nckap5
|
UTSW |
1 |
125,952,494 (GRCm39) |
missense |
probably benign |
0.00 |
R9572:Nckap5
|
UTSW |
1 |
125,955,454 (GRCm39) |
missense |
probably benign |
0.41 |
R9721:Nckap5
|
UTSW |
1 |
125,955,017 (GRCm39) |
missense |
probably damaging |
0.98 |
R9748:Nckap5
|
UTSW |
1 |
125,953,939 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Nckap5
|
UTSW |
1 |
125,952,569 (GRCm39) |
missense |
possibly damaging |
0.76 |
Z1176:Nckap5
|
UTSW |
1 |
126,456,418 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Nckap5
|
UTSW |
1 |
126,150,396 (GRCm39) |
nonsense |
probably null |
|
|
Predicted Primers |
PCR Primer
(F):5'- TCAACCCTGGACTTACAGCGTCTC -3'
(R):5'- CAGTGCCCTAGTGACTCCTGAAAAG -3'
Sequencing Primer
(F):5'- ACTTACAGCGTCTCCAGGG -3'
(R):5'- TAGTGACTCCTGAAAAGACACCAG -3'
|
Posted On |
2013-05-09 |