Incidental Mutation 'IGL02756:Nek9'
| ID |
306476 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Nek9
|
| Ensembl Gene |
ENSMUSG00000034290 |
| Gene Name |
NIMA (never in mitosis gene a)-related expressed kinase 9 |
| Synonyms |
C130021H08Rik |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL02756
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
12 |
| Chromosomal Location |
85346288-85386136 bp(-) (GRCm39) |
| Type of Mutation |
critical splice donor site (2 bp from exon) |
| DNA Base Change (assembly) |
A to C
at 85358110 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000049056
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000040992]
|
| AlphaFold |
Q8K1R7 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000040992
|
| SMART Domains |
Protein: ENSMUSP00000049056
Gene: ENSMUSG00000034290
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
19 |
49 |
N/A |
INTRINSIC |
|
S_TKc
|
52 |
308 |
1.07e-73 |
SMART |
|
Pfam:RCC1
|
389 |
441 |
1.2e-9 |
PFAM |
|
Pfam:RCC1_2
|
428 |
457 |
1.5e-8 |
PFAM |
|
Pfam:RCC1
|
444 |
495 |
3.6e-13 |
PFAM |
|
Pfam:RCC1_2
|
482 |
511 |
3.6e-11 |
PFAM |
|
Pfam:RCC1
|
499 |
547 |
7.6e-14 |
PFAM |
|
Pfam:RCC1
|
615 |
665 |
4.2e-8 |
PFAM |
|
Pfam:RCC1_2
|
652 |
681 |
4.4e-7 |
PFAM |
|
low complexity region
|
752 |
767 |
N/A |
INTRINSIC |
|
low complexity region
|
889 |
900 |
N/A |
INTRINSIC |
|
low complexity region
|
910 |
927 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the NimA (never in mitosis A) family of serine/threonine protein kinases. The encoded protein is activated in mitosis and, in turn, activates other family members during mitosis. This protein also mediates cellular processes that are essential for interphase progression. [provided by RefSeq, Jul 2016]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 55 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700113H08Rik |
A |
T |
10: 87,000,970 (GRCm39) |
D54V |
probably damaging |
Het |
| Adamts18 |
C |
A |
8: 114,440,976 (GRCm39) |
|
probably benign |
Het |
| Angptl3 |
T |
A |
4: 98,919,399 (GRCm39) |
L53Q |
probably damaging |
Het |
| Apc |
A |
G |
18: 34,447,588 (GRCm39) |
T1461A |
probably damaging |
Het |
| Arl11 |
T |
A |
14: 61,548,535 (GRCm39) |
V115D |
probably damaging |
Het |
| Cabp4 |
C |
A |
19: 4,188,560 (GRCm39) |
V173L |
possibly damaging |
Het |
| Casq1 |
T |
A |
1: 172,042,672 (GRCm39) |
D230V |
probably damaging |
Het |
| Cdc42bpa |
A |
G |
1: 179,936,824 (GRCm39) |
I821V |
possibly damaging |
Het |
| Cfap65 |
T |
C |
1: 74,944,239 (GRCm39) |
Y1494C |
probably benign |
Het |
| Chd1 |
T |
A |
17: 15,951,069 (GRCm39) |
S215T |
probably damaging |
Het |
| Csf2rb2 |
T |
C |
15: 78,169,049 (GRCm39) |
E593G |
possibly damaging |
Het |
| Cstf1 |
A |
G |
2: 172,217,795 (GRCm39) |
D136G |
probably damaging |
Het |
| Ddx19b |
T |
C |
8: 111,737,910 (GRCm39) |
|
probably benign |
Het |
| Dido1 |
A |
T |
2: 180,303,716 (GRCm39) |
L1396Q |
probably benign |
Het |
| Ermn |
A |
G |
2: 57,937,824 (GRCm39) |
I263T |
probably damaging |
Het |
| F12 |
T |
A |
13: 55,568,880 (GRCm39) |
Q294L |
possibly damaging |
Het |
| Far2 |
A |
T |
6: 148,058,889 (GRCm39) |
I192F |
probably damaging |
Het |
| Fshb |
T |
A |
2: 106,889,218 (GRCm39) |
I29F |
probably damaging |
Het |
| Gcgr |
T |
A |
11: 120,427,811 (GRCm39) |
Y251N |
probably benign |
Het |
| Gpr158 |
A |
G |
2: 21,831,890 (GRCm39) |
I997V |
possibly damaging |
Het |
| Gprc5d |
A |
G |
6: 135,093,613 (GRCm39) |
V98A |
probably damaging |
Het |
| H2-T23 |
T |
C |
17: 36,342,580 (GRCm39) |
E186G |
probably damaging |
Het |
| Khdrbs3 |
C |
T |
15: 68,896,685 (GRCm39) |
T115I |
probably benign |
Het |
| Kifap3 |
C |
T |
1: 163,689,597 (GRCm39) |
T527M |
probably damaging |
Het |
| Mfsd2a |
C |
T |
4: 122,842,332 (GRCm39) |
A512T |
probably benign |
Het |
| Mmp9 |
A |
G |
2: 164,791,235 (GRCm39) |
D135G |
probably benign |
Het |
| Mylk |
T |
C |
16: 34,784,016 (GRCm39) |
V1394A |
probably benign |
Het |
| Or51q1c |
T |
C |
7: 103,652,866 (GRCm39) |
I128T |
probably damaging |
Het |
| Or8k16 |
T |
C |
2: 85,520,402 (GRCm39) |
S210P |
probably damaging |
Het |
| P2rx2 |
T |
A |
5: 110,490,276 (GRCm39) |
|
probably benign |
Het |
| P4htm |
A |
G |
9: 108,456,977 (GRCm39) |
L410P |
probably damaging |
Het |
| Pik3c2a |
A |
T |
7: 115,963,748 (GRCm39) |
W921R |
probably benign |
Het |
| Pnisr |
T |
C |
4: 21,862,175 (GRCm39) |
F288L |
probably benign |
Het |
| Ppp4r3a |
C |
T |
12: 101,024,582 (GRCm39) |
|
probably null |
Het |
| Prss34 |
T |
C |
17: 25,518,251 (GRCm39) |
S144P |
probably damaging |
Het |
| Qrsl1 |
T |
C |
10: 43,758,110 (GRCm39) |
T328A |
probably benign |
Het |
| Rab33b |
A |
T |
3: 51,391,945 (GRCm39) |
T65S |
probably damaging |
Het |
| Rdh8 |
A |
G |
9: 20,736,637 (GRCm39) |
S235G |
possibly damaging |
Het |
| Rrp12 |
T |
C |
19: 41,884,500 (GRCm39) |
K6R |
probably benign |
Het |
| Sec24a |
T |
C |
11: 51,587,560 (GRCm39) |
D1025G |
probably benign |
Het |
| Sgo2a |
T |
G |
1: 58,055,509 (GRCm39) |
N564K |
probably damaging |
Het |
| Slc43a3 |
A |
T |
2: 84,774,612 (GRCm39) |
M130L |
probably benign |
Het |
| Soat1 |
T |
C |
1: 156,274,145 (GRCm39) |
I89V |
probably benign |
Het |
| St3gal5 |
A |
G |
6: 72,126,157 (GRCm39) |
D307G |
probably null |
Het |
| Stxbp3-ps |
C |
T |
19: 9,535,193 (GRCm39) |
|
noncoding transcript |
Het |
| Tacr2 |
A |
G |
10: 62,097,469 (GRCm39) |
|
probably benign |
Het |
| Tg |
C |
T |
15: 66,606,435 (GRCm39) |
T193I |
probably benign |
Het |
| Tnik |
A |
G |
3: 28,596,179 (GRCm39) |
T191A |
probably damaging |
Het |
| Trim27 |
T |
C |
13: 21,374,256 (GRCm39) |
|
probably benign |
Het |
| Usf2 |
A |
T |
7: 30,646,417 (GRCm39) |
C134* |
probably null |
Het |
| Usp14 |
A |
G |
18: 10,001,769 (GRCm39) |
|
probably null |
Het |
| Usp47 |
T |
C |
7: 111,692,270 (GRCm39) |
S911P |
possibly damaging |
Het |
| Vmn1r73 |
T |
A |
7: 11,490,574 (GRCm39) |
S131T |
possibly damaging |
Het |
| Vmn2r80 |
T |
C |
10: 79,030,145 (GRCm39) |
I657T |
probably damaging |
Het |
| Zfp935 |
A |
T |
13: 62,602,701 (GRCm39) |
C166* |
probably null |
Het |
|
| Other mutations in Nek9 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01431:Nek9
|
APN |
12 |
85,361,361 (GRCm39) |
missense |
probably benign |
0.23 |
|
IGL01595:Nek9
|
APN |
12 |
85,361,194 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01603:Nek9
|
APN |
12 |
85,352,379 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01893:Nek9
|
APN |
12 |
85,383,174 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02017:Nek9
|
APN |
12 |
85,376,697 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02197:Nek9
|
APN |
12 |
85,354,704 (GRCm39) |
missense |
probably null |
|
|
IGL02207:Nek9
|
APN |
12 |
85,350,257 (GRCm39) |
nonsense |
probably null |
|
|
IGL02749:Nek9
|
APN |
12 |
85,352,281 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL03343:Nek9
|
APN |
12 |
85,350,383 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Rose_colored
|
UTSW |
12 |
85,350,311 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0048:Nek9
|
UTSW |
12 |
85,348,673 (GRCm39) |
missense |
probably benign |
0.17 |
|
R0331:Nek9
|
UTSW |
12 |
85,374,149 (GRCm39) |
splice site |
probably benign |
|
|
R0499:Nek9
|
UTSW |
12 |
85,348,657 (GRCm39) |
missense |
probably benign |
0.09 |
|
R1484:Nek9
|
UTSW |
12 |
85,348,622 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1760:Nek9
|
UTSW |
12 |
85,357,184 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1760:Nek9
|
UTSW |
12 |
85,352,364 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R1883:Nek9
|
UTSW |
12 |
85,379,330 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1884:Nek9
|
UTSW |
12 |
85,379,330 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1999:Nek9
|
UTSW |
12 |
85,376,677 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2046:Nek9
|
UTSW |
12 |
85,367,481 (GRCm39) |
splice site |
probably benign |
|
|
R2096:Nek9
|
UTSW |
12 |
85,361,322 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2150:Nek9
|
UTSW |
12 |
85,376,677 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2368:Nek9
|
UTSW |
12 |
85,376,661 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R2570:Nek9
|
UTSW |
12 |
85,379,320 (GRCm39) |
nonsense |
probably null |
|
|
R4381:Nek9
|
UTSW |
12 |
85,376,632 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4570:Nek9
|
UTSW |
12 |
85,367,508 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4661:Nek9
|
UTSW |
12 |
85,367,666 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R4669:Nek9
|
UTSW |
12 |
85,360,978 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4993:Nek9
|
UTSW |
12 |
85,357,194 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5071:Nek9
|
UTSW |
12 |
85,374,233 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R5090:Nek9
|
UTSW |
12 |
85,376,616 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5248:Nek9
|
UTSW |
12 |
85,355,751 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5521:Nek9
|
UTSW |
12 |
85,374,219 (GRCm39) |
missense |
probably benign |
0.09 |
|
R5734:Nek9
|
UTSW |
12 |
85,350,289 (GRCm39) |
missense |
probably benign |
|
|
R6039:Nek9
|
UTSW |
12 |
85,359,859 (GRCm39) |
missense |
probably benign |
0.08 |
|
R6039:Nek9
|
UTSW |
12 |
85,359,859 (GRCm39) |
missense |
probably benign |
0.08 |
|
R6269:Nek9
|
UTSW |
12 |
85,379,103 (GRCm39) |
splice site |
probably null |
|
|
R6353:Nek9
|
UTSW |
12 |
85,348,603 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R6406:Nek9
|
UTSW |
12 |
85,385,946 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6744:Nek9
|
UTSW |
12 |
85,376,703 (GRCm39) |
missense |
probably benign |
0.09 |
|
R6922:Nek9
|
UTSW |
12 |
85,350,311 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7603:Nek9
|
UTSW |
12 |
85,350,288 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7686:Nek9
|
UTSW |
12 |
85,350,433 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7905:Nek9
|
UTSW |
12 |
85,352,370 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7964:Nek9
|
UTSW |
12 |
85,385,787 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8165:Nek9
|
UTSW |
12 |
85,350,417 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8330:Nek9
|
UTSW |
12 |
85,376,727 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8802:Nek9
|
UTSW |
12 |
85,374,192 (GRCm39) |
missense |
probably benign |
0.19 |
|
R8859:Nek9
|
UTSW |
12 |
85,353,120 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8997:Nek9
|
UTSW |
12 |
85,367,565 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9055:Nek9
|
UTSW |
12 |
85,348,616 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9261:Nek9
|
UTSW |
12 |
85,359,841 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9661:Nek9
|
UTSW |
12 |
85,361,253 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
X0052:Nek9
|
UTSW |
12 |
85,368,801 (GRCm39) |
critical splice donor site |
probably null |
|
|
Z1177:Nek9
|
UTSW |
12 |
85,380,819 (GRCm39) |
nonsense |
probably null |
|
|
| Posted On |
2015-04-16 |
Incidental Mutation