Incidental Mutation 'R9642:Peak1'
| ID |
726079 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Peak1
|
| Ensembl Gene |
ENSMUSG00000074305 |
| Gene Name |
pseudopodium-enriched atypical kinase 1 |
| Synonyms |
1110049L02Rik, C230081A13Rik, NKF3 kinase family member |
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.403)
|
| Stock # |
R9642 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
9 |
| Chromosomal Location |
56108410-56325351 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 56167205 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Alanine
at position 241
(V241A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000109901
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000061552]
[ENSMUST00000186735]
|
| AlphaFold |
Q69Z38 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000061552
AA Change: V241A
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000109901
Gene: ENSMUSG00000074305
AA Change: V241A
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
247 |
259 |
N/A |
INTRINSIC |
|
low complexity region
|
325 |
336 |
N/A |
INTRINSIC |
|
low complexity region
|
367 |
378 |
N/A |
INTRINSIC |
|
low complexity region
|
498 |
509 |
N/A |
INTRINSIC |
|
low complexity region
|
845 |
856 |
N/A |
INTRINSIC |
|
low complexity region
|
860 |
878 |
N/A |
INTRINSIC |
|
low complexity region
|
932 |
948 |
N/A |
INTRINSIC |
|
Pfam:Pkinase_Tyr
|
1437 |
1649 |
1.5e-6 |
PFAM |
|
Pfam:Pkinase
|
1440 |
1651 |
2.3e-12 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000186735
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.2%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a non-receptor tyrosine kinase that is a member of the new kinase family three (NFK3) family. In migrating cells, the encoded protein is associated with the actin cytoskeleton and focal adhesions and promotes developing focal adhesion elongation. This protein may play a role in the regulation of cell migration, proliferation and cancer metastasis. [provided by RefSeq, Mar 2014]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 75 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4921524L21Rik |
T |
C |
18: 6,619,412 (GRCm39) |
|
probably null |
Het |
| Aadacl3 |
A |
G |
4: 144,182,512 (GRCm39) |
S319P |
probably benign |
Het |
| Abcc6 |
C |
A |
7: 45,639,765 (GRCm39) |
D907Y |
probably benign |
Het |
| Apol7b |
T |
C |
15: 77,308,103 (GRCm39) |
S131G |
probably benign |
Het |
| Atg2a |
C |
T |
19: 6,300,198 (GRCm39) |
R669* |
probably null |
Het |
| Atr |
T |
A |
9: 95,821,294 (GRCm39) |
I2260N |
probably damaging |
Het |
| Bmper |
T |
A |
9: 23,395,198 (GRCm39) |
V643E |
probably benign |
Het |
| Cacna2d2 |
A |
G |
9: 107,392,627 (GRCm39) |
I524V |
possibly damaging |
Het |
| Ccdc171 |
C |
A |
4: 83,599,525 (GRCm39) |
A780E |
probably benign |
Het |
| Cdcp3 |
C |
A |
7: 130,848,257 (GRCm39) |
Q688K |
probably benign |
Het |
| Cfhr2 |
A |
G |
1: 139,738,620 (GRCm39) |
S314P |
probably damaging |
Het |
| Cops2 |
A |
T |
2: 125,682,410 (GRCm39) |
D190E |
probably benign |
Het |
| Dmxl1 |
G |
A |
18: 50,013,825 (GRCm39) |
G1538R |
probably damaging |
Het |
| Dyrk4 |
A |
T |
6: 126,893,253 (GRCm39) |
V43E |
probably benign |
Het |
| Eif4a3l2 |
A |
G |
6: 116,528,350 (GRCm39) |
R76G |
probably damaging |
Het |
| Enoph1 |
T |
C |
5: 100,188,115 (GRCm39) |
I13T |
possibly damaging |
Het |
| Eya3 |
A |
T |
4: 132,426,374 (GRCm39) |
I268F |
probably damaging |
Het |
| Ezh2 |
A |
C |
6: 47,521,453 (GRCm39) |
M439R |
probably benign |
Het |
| Fam83c |
T |
C |
2: 155,672,980 (GRCm39) |
N259S |
probably damaging |
Het |
| Gbf1 |
A |
T |
19: 46,258,707 (GRCm39) |
M963L |
probably benign |
Het |
| Ghr |
A |
T |
15: 3,355,469 (GRCm39) |
D271E |
probably benign |
Het |
| Gm40460 |
ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
7: 141,794,450 (GRCm39) |
|
probably benign |
Het |
| Gtse1 |
T |
A |
15: 85,751,697 (GRCm39) |
L297I |
probably damaging |
Het |
| Hecw1 |
T |
A |
13: 14,515,394 (GRCm39) |
H246L |
probably damaging |
Het |
| Hmox1 |
G |
A |
8: 75,823,881 (GRCm39) |
R183H |
possibly damaging |
Het |
| Ifi202b |
A |
T |
1: 173,799,850 (GRCm39) |
Y210* |
probably null |
Het |
| Ighv1-76 |
A |
T |
12: 115,811,918 (GRCm39) |
I6N |
possibly damaging |
Het |
| Ildr1 |
T |
A |
16: 36,536,490 (GRCm39) |
I173N |
probably damaging |
Het |
| Jaml |
T |
C |
9: 45,000,116 (GRCm39) |
V138A |
probably damaging |
Het |
| Kmt2b |
A |
T |
7: 30,283,340 (GRCm39) |
|
probably null |
Het |
| Krt87 |
T |
C |
15: 101,385,074 (GRCm39) |
N341D |
probably benign |
Het |
| Map3k20 |
T |
C |
2: 72,272,181 (GRCm39) |
W770R |
probably damaging |
Het |
| Mast2 |
A |
G |
4: 116,170,966 (GRCm39) |
I667T |
probably damaging |
Het |
| Mdp1 |
T |
C |
14: 55,896,933 (GRCm39) |
T71A |
probably damaging |
Het |
| Muc5ac |
A |
T |
7: 141,349,601 (GRCm39) |
T505S |
possibly damaging |
Het |
| Mx1 |
A |
G |
16: 97,256,376 (GRCm39) |
V181A |
probably damaging |
Het |
| Myo15b |
A |
G |
11: 115,772,335 (GRCm39) |
E83G |
possibly damaging |
Het |
| Ncam2 |
A |
T |
16: 81,418,251 (GRCm39) |
I769L |
probably benign |
Het |
| Notum |
T |
C |
11: 120,550,980 (GRCm39) |
D62G |
probably damaging |
Het |
| Or4c124 |
A |
T |
2: 89,155,907 (GRCm39) |
C206S |
possibly damaging |
Het |
| Or5ac22 |
A |
T |
16: 59,135,610 (GRCm39) |
H53Q |
possibly damaging |
Het |
| Or7a39 |
C |
T |
10: 78,715,395 (GRCm39) |
P130S |
probably damaging |
Het |
| Or8g32 |
T |
C |
9: 39,305,857 (GRCm39) |
S254P |
probably damaging |
Het |
| P2rx2 |
A |
G |
5: 110,489,878 (GRCm39) |
S196P |
possibly damaging |
Het |
| Pcdh7 |
A |
T |
5: 57,876,717 (GRCm39) |
I91F |
probably damaging |
Het |
| Ppl |
C |
A |
16: 4,915,602 (GRCm39) |
R623S |
probably benign |
Het |
| Prkaca |
A |
G |
8: 84,717,088 (GRCm39) |
I151V |
probably benign |
Het |
| Psmb11 |
A |
T |
14: 54,863,295 (GRCm39) |
Q171L |
probably benign |
Het |
| Rab3gap2 |
T |
G |
1: 184,967,692 (GRCm39) |
F166V |
probably benign |
Het |
| Rab7 |
G |
A |
6: 87,981,187 (GRCm39) |
A165V |
probably damaging |
Het |
| Ranbp2 |
T |
C |
10: 58,318,907 (GRCm39) |
Y2473H |
probably damaging |
Het |
| Runx3 |
A |
G |
4: 134,848,341 (GRCm39) |
|
probably benign |
Het |
| Sh3bp5l |
T |
A |
11: 58,237,085 (GRCm39) |
C347* |
probably null |
Het |
| Smc5 |
A |
G |
19: 23,238,752 (GRCm39) |
M208T |
probably damaging |
Het |
| Stk11ip |
T |
C |
1: 75,510,899 (GRCm39) |
|
probably null |
Het |
| Tas2r136 |
A |
T |
6: 132,754,462 (GRCm39) |
C222S |
probably benign |
Het |
| Themis2 |
A |
G |
4: 132,513,047 (GRCm39) |
V393A |
possibly damaging |
Het |
| Tln2 |
A |
C |
9: 67,157,826 (GRCm39) |
V1171G |
probably benign |
Het |
| Tmem63a |
T |
C |
1: 180,776,393 (GRCm39) |
F68L |
probably damaging |
Het |
| Tpst1 |
T |
A |
5: 130,130,959 (GRCm39) |
L143Q |
probably damaging |
Het |
| Trp63 |
C |
A |
16: 25,682,508 (GRCm39) |
Q284K |
probably benign |
Het |
| Ttc17 |
T |
C |
2: 94,194,735 (GRCm39) |
E546G |
probably benign |
Het |
| Ttn |
A |
G |
2: 76,804,570 (GRCm39) |
I234T |
unknown |
Het |
| Upp1 |
A |
G |
11: 9,085,206 (GRCm39) |
K231R |
probably benign |
Het |
| Uso1 |
T |
A |
5: 92,285,967 (GRCm39) |
L4H |
probably damaging |
Het |
| Vmn1r9 |
T |
A |
6: 57,048,216 (GRCm39) |
L97Q |
probably damaging |
Het |
| Vmn2r107 |
T |
C |
17: 20,580,661 (GRCm39) |
C533R |
probably damaging |
Het |
| Vps35l |
C |
A |
7: 118,437,451 (GRCm39) |
D909E |
probably benign |
Het |
| Wdr90 |
A |
G |
17: 26,072,694 (GRCm39) |
|
probably null |
Het |
| Ydjc |
A |
G |
16: 16,966,073 (GRCm39) |
H219R |
probably benign |
Het |
| Ykt6 |
T |
C |
11: 5,905,917 (GRCm39) |
L6P |
probably damaging |
Het |
| Zfp236 |
A |
G |
18: 82,622,384 (GRCm39) |
V1682A |
probably benign |
Het |
| Zfp35 |
C |
T |
18: 24,137,155 (GRCm39) |
Q500* |
probably null |
Het |
| Zfp780b |
T |
A |
7: 27,664,135 (GRCm39) |
D140V |
probably benign |
Het |
| Zyg11b |
T |
C |
4: 108,117,185 (GRCm39) |
T352A |
probably damaging |
Het |
|
| Other mutations in Peak1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00501:Peak1
|
APN |
9 |
56,134,610 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00544:Peak1
|
APN |
9 |
56,167,262 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01141:Peak1
|
APN |
9 |
56,165,811 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01743:Peak1
|
APN |
9 |
56,166,486 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01781:Peak1
|
APN |
9 |
56,167,349 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
IGL01885:Peak1
|
APN |
9 |
56,167,388 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01941:Peak1
|
APN |
9 |
56,166,059 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02455:Peak1
|
APN |
9 |
56,134,757 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
IGL02719:Peak1
|
APN |
9 |
56,134,490 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03247:Peak1
|
APN |
9 |
56,165,214 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03259:Peak1
|
APN |
9 |
56,167,251 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0060:Peak1
|
UTSW |
9 |
56,135,107 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0087:Peak1
|
UTSW |
9 |
56,165,609 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0480:Peak1
|
UTSW |
9 |
56,165,916 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0569:Peak1
|
UTSW |
9 |
56,167,373 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0605:Peak1
|
UTSW |
9 |
56,134,382 (GRCm39) |
splice site |
probably benign |
|
|
R0865:Peak1
|
UTSW |
9 |
56,165,116 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1117:Peak1
|
UTSW |
9 |
56,165,702 (GRCm39) |
missense |
probably benign |
0.05 |
|
R1922:Peak1
|
UTSW |
9 |
56,113,971 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1959:Peak1
|
UTSW |
9 |
56,114,073 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2069:Peak1
|
UTSW |
9 |
56,166,043 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2083:Peak1
|
UTSW |
9 |
56,166,233 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2154:Peak1
|
UTSW |
9 |
56,114,496 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2407:Peak1
|
UTSW |
9 |
56,166,510 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3832:Peak1
|
UTSW |
9 |
56,165,667 (GRCm39) |
missense |
probably benign |
|
|
R3938:Peak1
|
UTSW |
9 |
56,167,649 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3964:Peak1
|
UTSW |
9 |
56,167,263 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4192:Peak1
|
UTSW |
9 |
56,166,025 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4381:Peak1
|
UTSW |
9 |
56,165,711 (GRCm39) |
missense |
probably benign |
0.34 |
|
R4869:Peak1
|
UTSW |
9 |
56,134,876 (GRCm39) |
missense |
probably benign |
0.06 |
|
R4994:Peak1
|
UTSW |
9 |
56,148,560 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R5062:Peak1
|
UTSW |
9 |
56,167,573 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5435:Peak1
|
UTSW |
9 |
56,113,770 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5632:Peak1
|
UTSW |
9 |
56,165,058 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5643:Peak1
|
UTSW |
9 |
56,166,039 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5880:Peak1
|
UTSW |
9 |
56,114,894 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5898:Peak1
|
UTSW |
9 |
56,114,622 (GRCm39) |
missense |
probably benign |
0.19 |
|
R5986:Peak1
|
UTSW |
9 |
56,166,726 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6109:Peak1
|
UTSW |
9 |
56,166,567 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6284:Peak1
|
UTSW |
9 |
56,167,580 (GRCm39) |
missense |
probably benign |
0.10 |
|
R6347:Peak1
|
UTSW |
9 |
56,165,495 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6374:Peak1
|
UTSW |
9 |
56,164,950 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6471:Peak1
|
UTSW |
9 |
56,165,543 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6717:Peak1
|
UTSW |
9 |
56,114,523 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7033:Peak1
|
UTSW |
9 |
56,166,991 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7039:Peak1
|
UTSW |
9 |
56,165,093 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7100:Peak1
|
UTSW |
9 |
56,166,677 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7604:Peak1
|
UTSW |
9 |
56,148,491 (GRCm39) |
nonsense |
probably null |
|
|
R7868:Peak1
|
UTSW |
9 |
56,167,754 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7979:Peak1
|
UTSW |
9 |
56,114,676 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R8258:Peak1
|
UTSW |
9 |
56,166,677 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8259:Peak1
|
UTSW |
9 |
56,166,677 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8272:Peak1
|
UTSW |
9 |
56,166,182 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8324:Peak1
|
UTSW |
9 |
56,114,760 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8516:Peak1
|
UTSW |
9 |
56,167,284 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8847:Peak1
|
UTSW |
9 |
56,114,427 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8895:Peak1
|
UTSW |
9 |
56,113,938 (GRCm39) |
missense |
probably benign |
|
|
R9082:Peak1
|
UTSW |
9 |
56,165,504 (GRCm39) |
missense |
probably benign |
0.07 |
|
R9138:Peak1
|
UTSW |
9 |
56,164,925 (GRCm39) |
missense |
probably benign |
0.34 |
|
R9355:Peak1
|
UTSW |
9 |
56,167,454 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9548:Peak1
|
UTSW |
9 |
56,113,917 (GRCm39) |
missense |
probably benign |
0.19 |
|
R9591:Peak1
|
UTSW |
9 |
56,166,834 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
| Predicted Primers |
PCR Primer
(F):5'- TCATCATAGCTGTCGTCATAGTCC -3'
(R):5'- ATTGCTACAAACGATCGTTGG -3'
Sequencing Primer
(F):5'- CTCTGCAGAGACTTATTCCGTAAG -3'
(R):5'- TCGTTGGAAAGAAAGATCCCAC -3'
|
| Posted On |
2022-09-12 |
Incidental Mutation