Incidental Mutation 'R7356:Nek1'
ID |
570969 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Nek1
|
Ensembl Gene |
ENSMUSG00000031644 |
Gene Name |
NIMA (never in mitosis gene a)-related expressed kinase 1 |
Synonyms |
kat, D8Ertd790e, kidney, anemia and testis |
MMRRC Submission |
045442-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R7356 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
8 |
Chromosomal Location |
61446229-61584380 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 61573994 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Methionine to Leucine
at position 1081
(M1081L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000147809
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000034065]
[ENSMUST00000120689]
[ENSMUST00000211256]
[ENSMUST00000211672]
|
AlphaFold |
P51954 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000034065
AA Change: M1009L
PolyPhen 2
Score 0.007 (Sensitivity: 0.96; Specificity: 0.75)
|
SMART Domains |
Protein: ENSMUSP00000034065 Gene: ENSMUSG00000031644 AA Change: M1009L
Domain | Start | End | E-Value | Type |
S_TKc
|
4 |
258 |
4.23e-95 |
SMART |
Blast:S_TKc
|
266 |
303 |
3e-7 |
BLAST |
low complexity region
|
321 |
337 |
N/A |
INTRINSIC |
coiled coil region
|
372 |
402 |
N/A |
INTRINSIC |
coiled coil region
|
556 |
592 |
N/A |
INTRINSIC |
coiled coil region
|
647 |
685 |
N/A |
INTRINSIC |
low complexity region
|
767 |
780 |
N/A |
INTRINSIC |
low complexity region
|
1130 |
1141 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000120689
AA Change: M1037L
PolyPhen 2
Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)
|
SMART Domains |
Protein: ENSMUSP00000113932 Gene: ENSMUSG00000031644 AA Change: M1037L
Domain | Start | End | E-Value | Type |
S_TKc
|
4 |
258 |
4.23e-95 |
SMART |
Blast:S_TKc
|
266 |
303 |
3e-7 |
BLAST |
low complexity region
|
321 |
337 |
N/A |
INTRINSIC |
coiled coil region
|
372 |
402 |
N/A |
INTRINSIC |
coiled coil region
|
487 |
510 |
N/A |
INTRINSIC |
low complexity region
|
521 |
533 |
N/A |
INTRINSIC |
coiled coil region
|
584 |
620 |
N/A |
INTRINSIC |
coiled coil region
|
675 |
713 |
N/A |
INTRINSIC |
low complexity region
|
795 |
808 |
N/A |
INTRINSIC |
low complexity region
|
1158 |
1169 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000211256
AA Change: M984L
PolyPhen 2
Score 0.007 (Sensitivity: 0.96; Specificity: 0.75)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000211672
AA Change: M1081L
PolyPhen 2
Score 0.021 (Sensitivity: 0.95; Specificity: 0.80)
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.2%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a serine/threonine kinase involved in cell cycle regulation. The encoded protein is found in a centrosomal complex with FEZ1, a neuronal protein that plays a role in axonal development. Defects in this gene are a cause of polycystic kidney disease (PKD). Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2010] PHENOTYPE: Spontaneous mutations of this gene result in pleiotropic effects that include facial dysmorphism, dwarfism, male sterility, anemia, cystic choroid plexus, a late-onset slowly progressive polycystic kidney disease, and premature death. Postnatal survival is sensitive to genetic background. [provided by MGI curators]
|
Allele List at MGI |
All alleles(4) : Targeted(1) Gene trapped(1) Spontaneous(2)
|
Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acnat2 |
A |
T |
4: 49,383,507 (GRCm39) |
D15E |
probably damaging |
Het |
Adamts16 |
G |
A |
13: 70,984,399 (GRCm39) |
T88I |
probably benign |
Het |
Akap6 |
A |
C |
12: 52,958,647 (GRCm39) |
N801H |
probably damaging |
Het |
Ankfn1 |
G |
T |
11: 89,325,599 (GRCm39) |
N524K |
probably damaging |
Het |
Ap5s1 |
A |
G |
2: 131,054,582 (GRCm39) |
N131S |
probably damaging |
Het |
Astn2 |
A |
T |
4: 66,103,503 (GRCm39) |
D303E |
unknown |
Het |
Babam1 |
T |
C |
8: 71,852,208 (GRCm39) |
V132A |
probably benign |
Het |
BC028528 |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
3: 95,795,448 (GRCm39) |
|
probably benign |
Het |
BC028528 |
CACTGGTT |
CACTGGTTCTATGGTGACTGGTT |
3: 95,795,495 (GRCm39) |
|
probably benign |
Het |
BC028528 |
TCTGTGGTCACTGGT |
TCTGTGGTCACTGGTCCTGTGGTCACTGGT |
3: 95,795,487 (GRCm39) |
|
probably benign |
Het |
BC028528 |
GGTCACTGGTTCTGT |
GGTCACTGGTTCTGTAGTCACTGGTTCTGT |
3: 95,795,477 (GRCm39) |
|
probably benign |
Het |
BC028528 |
GTTCTGTGGTCACTGGTTCTGTGGTCACTG |
GTTCTGTGGTCACTGCTTCTGTGGTCACTGGTTCTGTGGTCACTG |
3: 95,795,470 (GRCm39) |
|
probably benign |
Het |
BC028528 |
TGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCAC |
TGGTTCTGTGGTCACGGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCAC |
3: 95,795,453 (GRCm39) |
|
probably benign |
Het |
Cnst |
C |
T |
1: 179,434,095 (GRCm39) |
P304S |
probably benign |
Het |
Cog4 |
A |
T |
8: 111,576,498 (GRCm39) |
|
probably null |
Het |
Cyp2j13 |
A |
T |
4: 95,965,655 (GRCm39) |
H17Q |
probably benign |
Het |
Dock6 |
G |
A |
9: 21,721,195 (GRCm39) |
T1662I |
probably damaging |
Het |
Dysf |
T |
C |
6: 84,044,443 (GRCm39) |
F270S |
probably damaging |
Het |
Erbb4 |
A |
G |
1: 68,378,514 (GRCm39) |
|
probably null |
Het |
Fam120b |
A |
T |
17: 15,627,958 (GRCm39) |
Q550L |
probably benign |
Het |
Fam83b |
A |
T |
9: 76,400,135 (GRCm39) |
F323I |
probably benign |
Het |
Far1 |
T |
A |
7: 113,167,349 (GRCm39) |
I478N |
possibly damaging |
Het |
Gdpd5 |
T |
A |
7: 99,108,085 (GRCm39) |
I554N |
probably damaging |
Het |
Glrx3 |
T |
C |
7: 137,054,453 (GRCm39) |
S79P |
probably damaging |
Het |
Hltf |
T |
C |
3: 20,163,534 (GRCm39) |
I888T |
probably damaging |
Het |
Hpx |
A |
G |
7: 105,240,917 (GRCm39) |
V452A |
probably damaging |
Het |
Itk |
T |
G |
11: 46,258,659 (GRCm39) |
Q81P |
possibly damaging |
Het |
Kdm6b |
G |
A |
11: 69,292,991 (GRCm39) |
Q1262* |
probably null |
Het |
Lpcat2 |
T |
C |
8: 93,591,611 (GRCm39) |
V85A |
probably benign |
Het |
Lrrk2 |
A |
T |
15: 91,622,947 (GRCm39) |
H1039L |
probably benign |
Het |
Mapk3 |
T |
C |
7: 126,360,087 (GRCm39) |
|
probably null |
Het |
Masp1 |
A |
T |
16: 23,288,993 (GRCm39) |
N602K |
possibly damaging |
Het |
Myo7a |
T |
A |
7: 97,751,890 (GRCm39) |
Q40L |
probably benign |
Het |
Nes |
T |
C |
3: 87,885,058 (GRCm39) |
S1106P |
possibly damaging |
Het |
Nkpd1 |
A |
T |
7: 19,257,699 (GRCm39) |
I493F |
probably damaging |
Het |
Npsr1 |
C |
G |
9: 24,009,557 (GRCm39) |
S21C |
probably benign |
Het |
Oog1 |
G |
A |
12: 87,653,047 (GRCm39) |
|
probably null |
Het |
Or11g1 |
G |
A |
14: 50,651,159 (GRCm39) |
V53M |
probably damaging |
Het |
Or5g24-ps1 |
G |
A |
2: 85,463,782 (GRCm39) |
R3K |
probably benign |
Het |
Or5k8 |
A |
T |
16: 58,644,718 (GRCm39) |
M118K |
probably damaging |
Het |
Osbpl9 |
G |
T |
4: 108,925,677 (GRCm39) |
Y340* |
probably null |
Het |
Pcyox1l |
A |
T |
18: 61,840,621 (GRCm39) |
L11Q |
probably null |
Het |
Pdxdc1 |
G |
A |
16: 13,677,867 (GRCm39) |
R255C |
probably damaging |
Het |
Pgap1 |
A |
G |
1: 54,569,293 (GRCm39) |
S358P |
probably benign |
Het |
Pgm2l1 |
A |
G |
7: 99,917,326 (GRCm39) |
Y481C |
possibly damaging |
Het |
Plekhf1 |
T |
C |
7: 37,921,545 (GRCm39) |
T8A |
possibly damaging |
Het |
Plg |
G |
T |
17: 12,629,798 (GRCm39) |
G611C |
probably damaging |
Het |
Prf1 |
A |
C |
10: 61,139,059 (GRCm39) |
D339A |
possibly damaging |
Het |
Prph |
A |
G |
15: 98,954,807 (GRCm39) |
Y291C |
probably damaging |
Het |
Rasal1 |
A |
G |
5: 120,792,890 (GRCm39) |
S48G |
possibly damaging |
Het |
Rigi |
A |
G |
4: 40,226,600 (GRCm39) |
S231P |
probably benign |
Het |
Ripk4 |
T |
A |
16: 97,544,349 (GRCm39) |
Q766L |
probably damaging |
Het |
Scaf1 |
T |
C |
7: 44,657,208 (GRCm39) |
D557G |
unknown |
Het |
Scaper |
A |
T |
9: 55,799,495 (GRCm39) |
M190K |
unknown |
Het |
Scn8a |
A |
T |
15: 100,855,460 (GRCm39) |
I202F |
probably damaging |
Het |
Siglecf |
A |
G |
7: 43,005,855 (GRCm39) |
I505V |
probably benign |
Het |
Sirpb1c |
A |
G |
3: 15,886,297 (GRCm39) |
S360P |
probably benign |
Het |
Sla2 |
C |
A |
2: 156,720,623 (GRCm39) |
|
probably null |
Het |
Slc11a1 |
G |
T |
1: 74,424,648 (GRCm39) |
V544L |
probably benign |
Het |
Slco1a5 |
T |
A |
6: 142,180,458 (GRCm39) |
K648I |
probably benign |
Het |
Sorcs1 |
T |
A |
19: 50,163,595 (GRCm39) |
I1020F |
possibly damaging |
Het |
Spen |
C |
A |
4: 141,199,235 (GRCm39) |
E3131* |
probably null |
Het |
Sult2a7 |
A |
T |
7: 14,211,031 (GRCm39) |
W162R |
probably damaging |
Het |
Sult3a1 |
G |
A |
10: 33,742,579 (GRCm39) |
E69K |
probably benign |
Het |
Tcof1 |
G |
T |
18: 60,951,166 (GRCm39) |
D1119E |
unknown |
Het |
Tom1l2 |
A |
T |
11: 60,139,853 (GRCm39) |
I272K |
probably damaging |
Het |
Tspan5 |
C |
T |
3: 138,448,193 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
G |
2: 76,698,244 (GRCm39) |
L186P |
|
Het |
Uap1l1 |
T |
C |
2: 25,251,696 (GRCm39) |
E496G |
possibly damaging |
Het |
Ube2v1 |
A |
T |
2: 167,451,115 (GRCm39) |
I117N |
possibly damaging |
Het |
Usp42 |
A |
G |
5: 143,702,842 (GRCm39) |
V593A |
possibly damaging |
Het |
Virma |
T |
A |
4: 11,513,595 (GRCm39) |
I483N |
probably damaging |
Het |
Vwde |
T |
A |
6: 13,192,641 (GRCm39) |
I421F |
probably damaging |
Het |
Zfp345 |
G |
A |
2: 150,314,209 (GRCm39) |
H443Y |
probably damaging |
Het |
Zfp760 |
A |
G |
17: 21,941,601 (GRCm39) |
T259A |
probably benign |
Het |
Zfp941 |
T |
C |
7: 140,392,028 (GRCm39) |
I444V |
possibly damaging |
Het |
Zfyve9 |
A |
C |
4: 108,576,212 (GRCm39) |
S290A |
probably benign |
Het |
|
Other mutations in Nek1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00471:Nek1
|
APN |
8 |
61,496,318 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01075:Nek1
|
APN |
8 |
61,577,166 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL01122:Nek1
|
APN |
8 |
61,574,000 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01151:Nek1
|
APN |
8 |
61,473,111 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01286:Nek1
|
APN |
8 |
61,577,250 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL01377:Nek1
|
APN |
8 |
61,542,490 (GRCm39) |
missense |
probably benign |
|
IGL01485:Nek1
|
APN |
8 |
61,502,860 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01688:Nek1
|
APN |
8 |
61,558,631 (GRCm39) |
nonsense |
probably null |
|
IGL01806:Nek1
|
APN |
8 |
61,577,246 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02006:Nek1
|
APN |
8 |
61,557,226 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02304:Nek1
|
APN |
8 |
61,465,201 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02659:Nek1
|
APN |
8 |
61,542,514 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02662:Nek1
|
APN |
8 |
61,557,218 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02801:Nek1
|
APN |
8 |
61,574,095 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02806:Nek1
|
APN |
8 |
61,497,120 (GRCm39) |
missense |
probably benign |
0.15 |
IGL03037:Nek1
|
APN |
8 |
61,487,086 (GRCm39) |
missense |
probably benign |
0.16 |
IGL03252:Nek1
|
APN |
8 |
61,525,364 (GRCm39) |
nonsense |
probably null |
|
P0014:Nek1
|
UTSW |
8 |
61,524,781 (GRCm39) |
splice site |
probably benign |
|
R0019:Nek1
|
UTSW |
8 |
61,542,768 (GRCm39) |
missense |
probably benign |
0.01 |
R0403:Nek1
|
UTSW |
8 |
61,559,889 (GRCm39) |
missense |
probably damaging |
0.99 |
R0464:Nek1
|
UTSW |
8 |
61,525,307 (GRCm39) |
splice site |
probably benign |
|
R0726:Nek1
|
UTSW |
8 |
61,542,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R0761:Nek1
|
UTSW |
8 |
61,542,489 (GRCm39) |
missense |
probably benign |
|
R0827:Nek1
|
UTSW |
8 |
61,558,682 (GRCm39) |
splice site |
probably benign |
|
R0972:Nek1
|
UTSW |
8 |
61,542,465 (GRCm39) |
splice site |
probably null |
|
R1268:Nek1
|
UTSW |
8 |
61,475,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R1343:Nek1
|
UTSW |
8 |
61,481,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R1415:Nek1
|
UTSW |
8 |
61,542,720 (GRCm39) |
missense |
probably benign |
0.00 |
R1466:Nek1
|
UTSW |
8 |
61,578,170 (GRCm39) |
splice site |
probably benign |
|
R1480:Nek1
|
UTSW |
8 |
61,577,360 (GRCm39) |
splice site |
probably null |
|
R1526:Nek1
|
UTSW |
8 |
61,502,975 (GRCm39) |
missense |
probably benign |
0.26 |
R1552:Nek1
|
UTSW |
8 |
61,459,771 (GRCm39) |
missense |
probably damaging |
0.99 |
R1606:Nek1
|
UTSW |
8 |
61,577,310 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1650:Nek1
|
UTSW |
8 |
61,489,110 (GRCm39) |
missense |
probably benign |
0.00 |
R1757:Nek1
|
UTSW |
8 |
61,542,847 (GRCm39) |
splice site |
probably null |
|
R1808:Nek1
|
UTSW |
8 |
61,469,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R1966:Nek1
|
UTSW |
8 |
61,469,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R2067:Nek1
|
UTSW |
8 |
61,460,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R2111:Nek1
|
UTSW |
8 |
61,577,360 (GRCm39) |
splice site |
probably null |
|
R2113:Nek1
|
UTSW |
8 |
61,469,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R2143:Nek1
|
UTSW |
8 |
61,481,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R2255:Nek1
|
UTSW |
8 |
61,542,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R2422:Nek1
|
UTSW |
8 |
61,472,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R3848:Nek1
|
UTSW |
8 |
61,525,349 (GRCm39) |
missense |
probably damaging |
0.99 |
R3849:Nek1
|
UTSW |
8 |
61,525,349 (GRCm39) |
missense |
probably damaging |
0.99 |
R3850:Nek1
|
UTSW |
8 |
61,525,349 (GRCm39) |
missense |
probably damaging |
0.99 |
R4418:Nek1
|
UTSW |
8 |
61,559,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R4526:Nek1
|
UTSW |
8 |
61,559,978 (GRCm39) |
missense |
probably damaging |
0.99 |
R4533:Nek1
|
UTSW |
8 |
61,460,247 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4544:Nek1
|
UTSW |
8 |
61,469,338 (GRCm39) |
nonsense |
probably null |
|
R4677:Nek1
|
UTSW |
8 |
61,481,840 (GRCm39) |
missense |
probably damaging |
0.99 |
R4739:Nek1
|
UTSW |
8 |
61,551,545 (GRCm39) |
missense |
probably benign |
0.32 |
R5068:Nek1
|
UTSW |
8 |
61,469,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R5421:Nek1
|
UTSW |
8 |
61,459,711 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5516:Nek1
|
UTSW |
8 |
61,542,523 (GRCm39) |
missense |
probably benign |
0.03 |
R5855:Nek1
|
UTSW |
8 |
61,469,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R6125:Nek1
|
UTSW |
8 |
61,481,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R6267:Nek1
|
UTSW |
8 |
61,525,343 (GRCm39) |
nonsense |
probably null |
|
R6292:Nek1
|
UTSW |
8 |
61,507,770 (GRCm39) |
splice site |
probably null |
|
R6296:Nek1
|
UTSW |
8 |
61,525,343 (GRCm39) |
nonsense |
probably null |
|
R6458:Nek1
|
UTSW |
8 |
61,553,046 (GRCm39) |
missense |
probably benign |
0.00 |
R6568:Nek1
|
UTSW |
8 |
61,559,855 (GRCm39) |
missense |
probably benign |
0.00 |
R6629:Nek1
|
UTSW |
8 |
61,507,367 (GRCm39) |
splice site |
probably null |
|
R6867:Nek1
|
UTSW |
8 |
61,525,364 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7122:Nek1
|
UTSW |
8 |
61,559,829 (GRCm39) |
missense |
probably benign |
0.00 |
R7193:Nek1
|
UTSW |
8 |
61,526,612 (GRCm39) |
missense |
probably damaging |
0.99 |
R7272:Nek1
|
UTSW |
8 |
61,578,120 (GRCm39) |
missense |
probably benign |
0.34 |
R7368:Nek1
|
UTSW |
8 |
61,542,741 (GRCm39) |
missense |
probably benign |
0.24 |
R7478:Nek1
|
UTSW |
8 |
61,583,179 (GRCm39) |
missense |
probably benign |
0.03 |
R7479:Nek1
|
UTSW |
8 |
61,583,179 (GRCm39) |
missense |
probably benign |
0.03 |
R7512:Nek1
|
UTSW |
8 |
61,583,179 (GRCm39) |
missense |
probably benign |
0.03 |
R7715:Nek1
|
UTSW |
8 |
61,459,794 (GRCm39) |
missense |
probably damaging |
0.98 |
R7984:Nek1
|
UTSW |
8 |
61,574,087 (GRCm39) |
nonsense |
probably null |
|
R8271:Nek1
|
UTSW |
8 |
61,558,646 (GRCm39) |
missense |
probably benign |
0.04 |
R8431:Nek1
|
UTSW |
8 |
61,487,066 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9076:Nek1
|
UTSW |
8 |
61,481,768 (GRCm39) |
missense |
probably damaging |
0.96 |
R9149:Nek1
|
UTSW |
8 |
61,574,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R9250:Nek1
|
UTSW |
8 |
61,465,151 (GRCm39) |
missense |
probably damaging |
0.99 |
R9429:Nek1
|
UTSW |
8 |
61,559,892 (GRCm39) |
missense |
probably benign |
|
R9563:Nek1
|
UTSW |
8 |
61,577,157 (GRCm39) |
missense |
probably benign |
0.36 |
R9616:Nek1
|
UTSW |
8 |
61,473,107 (GRCm39) |
missense |
probably damaging |
0.99 |
RF023:Nek1
|
UTSW |
8 |
61,525,779 (GRCm39) |
splice site |
probably null |
|
X0028:Nek1
|
UTSW |
8 |
61,496,292 (GRCm39) |
missense |
probably benign |
0.19 |
X0066:Nek1
|
UTSW |
8 |
61,578,162 (GRCm39) |
critical splice donor site |
probably null |
|
|
Predicted Primers |
PCR Primer
(F):5'- AAGTCTATCTAGTGTTGCTCATGTG -3'
(R):5'- GCTGTAGACCATGCTCACTCTC -3'
Sequencing Primer
(F):5'- CTCATGTGAGCTGAACTTTAAGAAAG -3'
(R):5'- CTCTCTGGACTTTGAAGAAAATCCC -3'
|
Posted On |
2019-09-13 |