Incidental Mutation 'R7684:Nckap5'
ID |
592905 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Nckap5
|
Ensembl Gene |
ENSMUSG00000049690 |
Gene Name |
NCK-associated protein 5 |
Synonyms |
LOC380609, D130011D22Rik, E030049G20Rik |
MMRRC Submission |
067780-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R7684 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
1 |
Chromosomal Location |
125841373-126758529 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 125954594 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Alanine
at position 653
(T653A)
|
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: T589A
PolyPhen 2
Score 0.026 (Sensitivity: 0.95; Specificity: 0.81)
|
SMART Domains |
Protein: ENSMUSP00000062229 Gene: ENSMUSG00000049690 AA Change: T589A
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: T721A
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000108202 Gene: ENSMUSG00000049690 AA Change: T721A
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 |
probably benign
Transcript: ENSMUST00000161954
AA Change: T653A
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
SMART Domains |
Protein: ENSMUSP00000125624 Gene: ENSMUSG00000049690 AA Change: T653A
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 |
|
Meta Mutation Damage Score |
0.0898 |
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.0%
|
Validation Efficiency |
100% (73/73) |
Allele List at MGI |
All alleles(1) : Gene trapped(1) |
Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
A |
T |
13: 77,760,659 (GRCm39) |
K1239* |
probably null |
Het |
Abhd6 |
T |
C |
14: 8,039,807 (GRCm38) |
F60S |
probably damaging |
Het |
Adam6b |
G |
A |
12: 113,455,196 (GRCm39) |
W671* |
probably null |
Het |
Ankrd36 |
A |
G |
11: 5,520,113 (GRCm39) |
T63A |
possibly damaging |
Het |
Arhgef16 |
A |
G |
4: 154,366,285 (GRCm39) |
V494A |
possibly damaging |
Het |
Arhgef7 |
T |
A |
8: 11,869,663 (GRCm39) |
M659K |
probably benign |
Het |
Cacna1h |
A |
G |
17: 25,608,346 (GRCm39) |
Y854H |
probably damaging |
Het |
Chd3 |
A |
T |
11: 69,248,692 (GRCm39) |
F780I |
possibly damaging |
Het |
Cldn8 |
A |
G |
16: 88,359,335 (GRCm39) |
Y197H |
probably damaging |
Het |
Cpne8 |
A |
T |
15: 90,533,450 (GRCm39) |
D58E |
probably damaging |
Het |
Cul9 |
T |
G |
17: 46,820,815 (GRCm39) |
Y1954S |
probably damaging |
Het |
Cyp4a10 |
T |
A |
4: 115,375,549 (GRCm39) |
F11I |
probably benign |
Het |
Cysrt1 |
A |
T |
2: 25,129,094 (GRCm39) |
C139* |
probably null |
Het |
Dnajc16 |
A |
G |
4: 141,501,879 (GRCm39) |
V317A |
probably benign |
Het |
Dnmt3a |
T |
C |
12: 3,947,340 (GRCm39) |
V437A |
probably benign |
Het |
Dok5 |
T |
C |
2: 170,683,344 (GRCm39) |
C202R |
probably damaging |
Het |
Dusp11 |
T |
A |
6: 85,927,542 (GRCm39) |
R164S |
probably damaging |
Het |
Dysf |
T |
C |
6: 84,077,117 (GRCm39) |
S648P |
probably benign |
Het |
Egfem1 |
A |
T |
3: 29,744,334 (GRCm39) |
R581S |
probably damaging |
Het |
Enpep |
A |
G |
3: 129,115,094 (GRCm39) |
F226S |
probably damaging |
Het |
Ep400 |
A |
G |
5: 110,845,218 (GRCm39) |
I1541T |
unknown |
Het |
Exd1 |
A |
G |
2: 119,350,684 (GRCm39) |
S526P |
probably damaging |
Het |
Fam118a |
A |
G |
15: 84,942,982 (GRCm39) |
E337G |
possibly damaging |
Het |
Fam20b |
T |
C |
1: 156,518,215 (GRCm39) |
N193S |
probably benign |
Het |
Fat3 |
A |
G |
9: 15,899,564 (GRCm39) |
|
probably null |
Het |
Flg2 |
T |
C |
3: 93,126,956 (GRCm39) |
V1956A |
unknown |
Het |
Fzd10 |
A |
G |
5: 128,678,480 (GRCm39) |
I67V |
possibly damaging |
Het |
Gckr |
A |
T |
5: 31,465,141 (GRCm39) |
D370V |
probably damaging |
Het |
Gm8797 |
A |
T |
3: 5,816,148 (GRCm39) |
Q62L |
probably benign |
Het |
H6pd |
G |
T |
4: 150,080,519 (GRCm39) |
Q109K |
probably benign |
Het |
Higd1a |
T |
C |
9: 121,679,322 (GRCm39) |
K55R |
possibly damaging |
Het |
Il1b |
C |
T |
2: 129,209,277 (GRCm39) |
V118I |
probably benign |
Het |
Insr |
T |
C |
8: 3,219,753 (GRCm39) |
N923S |
possibly damaging |
Het |
Krit1 |
A |
G |
5: 3,880,723 (GRCm39) |
I561V |
possibly damaging |
Het |
Lamc2 |
T |
C |
1: 153,002,771 (GRCm39) |
D1070G |
probably null |
Het |
Lpcat2 |
T |
A |
8: 93,635,823 (GRCm39) |
D408E |
possibly damaging |
Het |
Mst1r |
T |
A |
9: 107,788,762 (GRCm39) |
F427Y |
probably benign |
Het |
Mtx1 |
A |
T |
3: 89,117,739 (GRCm39) |
I258K |
possibly damaging |
Het |
Npas3 |
A |
T |
12: 54,115,609 (GRCm39) |
N844Y |
probably damaging |
Het |
Nrg3 |
A |
T |
14: 39,194,522 (GRCm39) |
L79Q |
probably damaging |
Het |
Nsmce1 |
C |
A |
7: 125,070,348 (GRCm39) |
K154N |
probably damaging |
Het |
Oard1 |
T |
C |
17: 48,723,726 (GRCm39) |
L124P |
probably damaging |
Het |
Or10ag57 |
T |
C |
2: 87,218,372 (GRCm39) |
S108P |
probably damaging |
Het |
Or10ak13 |
T |
C |
4: 118,639,471 (GRCm39) |
M104V |
probably benign |
Het |
Or51a10 |
G |
A |
7: 103,698,667 (GRCm39) |
T298I |
probably damaging |
Het |
Or51ah3 |
T |
C |
7: 103,210,425 (GRCm39) |
F247S |
probably benign |
Het |
Ovgp1 |
A |
T |
3: 105,887,272 (GRCm39) |
T223S |
probably damaging |
Het |
Pik3c2a |
A |
T |
7: 115,987,312 (GRCm39) |
Y536* |
probably null |
Het |
Plekho2 |
A |
T |
9: 65,466,816 (GRCm39) |
|
probably null |
Het |
Prelid3b |
T |
C |
2: 174,310,210 (GRCm39) |
|
probably null |
Het |
Rftn1 |
G |
T |
17: 50,354,408 (GRCm39) |
A318D |
probably damaging |
Het |
Rxfp1 |
T |
A |
3: 79,578,214 (GRCm39) |
N159I |
possibly damaging |
Het |
Sfmbt1 |
A |
G |
14: 30,532,311 (GRCm39) |
Q557R |
probably damaging |
Het |
Slc22a18 |
G |
T |
7: 143,044,577 (GRCm39) |
V177L |
probably benign |
Het |
Slc22a8 |
A |
G |
19: 8,587,294 (GRCm39) |
I451M |
probably benign |
Het |
Slc39a12 |
T |
C |
2: 14,454,670 (GRCm39) |
S563P |
probably damaging |
Het |
Snx20 |
T |
C |
8: 89,353,863 (GRCm39) |
D289G |
probably benign |
Het |
Sptb |
A |
G |
12: 76,658,969 (GRCm39) |
Y1189H |
probably benign |
Het |
Tbc1d1 |
T |
A |
5: 64,473,829 (GRCm39) |
M784K |
probably benign |
Het |
Tbkbp1 |
T |
C |
11: 97,038,559 (GRCm39) |
|
probably benign |
Het |
Tfap2b |
G |
C |
1: 19,284,511 (GRCm39) |
D140H |
probably damaging |
Het |
Thy1 |
G |
A |
9: 43,957,855 (GRCm39) |
G13D |
unknown |
Het |
Ticam1 |
A |
G |
17: 56,576,984 (GRCm39) |
S704P |
unknown |
Het |
Tmem151b |
A |
G |
17: 45,857,929 (GRCm39) |
Y106H |
probably damaging |
Het |
Trappc8 |
T |
C |
18: 20,996,559 (GRCm39) |
N452S |
probably benign |
Het |
Ttc9c |
A |
G |
19: 8,789,128 (GRCm39) |
Y166H |
probably damaging |
Het |
Txndc16 |
A |
G |
14: 45,385,325 (GRCm39) |
V556A |
possibly damaging |
Het |
Tyrp1 |
C |
A |
4: 80,758,862 (GRCm39) |
S245Y |
probably damaging |
Het |
Urb1 |
A |
T |
16: 90,583,006 (GRCm39) |
L621* |
probably null |
Het |
Wdr72 |
A |
T |
9: 74,054,292 (GRCm39) |
T224S |
probably damaging |
Het |
Zc3h18 |
T |
G |
8: 123,134,165 (GRCm39) |
S544A |
unknown |
Het |
Zfp462 |
T |
A |
4: 55,008,908 (GRCm39) |
N291K |
probably benign |
Het |
Zfp609 |
T |
C |
9: 65,638,362 (GRCm39) |
N290S |
possibly damaging |
Het |
Zfp979 |
A |
T |
4: 147,697,799 (GRCm39) |
H303Q |
probably damaging |
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 |
R0349:Nckap5
|
UTSW |
1 |
125,954,171 (GRCm39) |
missense |
probably benign |
|
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 |
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'- AAGACTTGCCTCTGGAAGGG -3'
(R):5'- GAGCCAGTGGAATTCAGCTCTC -3'
Sequencing Primer
(F):5'- CTCTGGAAGGGATTTTTGTCAGACC -3'
(R):5'- CTGTCACCAGGGATGAAATTTCC -3'
|
Posted On |
2019-11-12 |