Incidental Mutation 'IGL02836:Mark2'
ID |
361682 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Mark2
|
Ensembl Gene |
ENSMUSG00000024969 |
Gene Name |
MAP/microtubule affinity regulating kinase 2 |
Synonyms |
Par-1, Emk |
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.928)
|
Stock # |
IGL02836
|
Quality Score |
|
Status
|
|
Chromosome |
19 |
Chromosomal Location |
7252761-7319222 bp(-) (GRCm39) |
Type of Mutation |
critical splice donor site (2 bp from exon) |
DNA Base Change (assembly) |
A to G
at 7255405 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000025921]
[ENSMUST00000032557]
[ENSMUST00000051711]
[ENSMUST00000066646]
[ENSMUST00000113369]
[ENSMUST00000165965]
[ENSMUST00000164205]
[ENSMUST00000167767]
[ENSMUST00000165286]
[ENSMUST00000166461]
[ENSMUST00000168872]
[ENSMUST00000171352]
[ENSMUST00000164129]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably null
Transcript: ENSMUST00000025921
|
SMART Domains |
Protein: ENSMUSP00000025921 Gene: ENSMUSG00000024969
Domain | Start | End | E-Value | Type |
S_TKc
|
20 |
271 |
1.59e-108 |
SMART |
UBA
|
292 |
329 |
7.69e-7 |
SMART |
low complexity region
|
475 |
489 |
N/A |
INTRINSIC |
low complexity region
|
532 |
545 |
N/A |
INTRINSIC |
Pfam:KA1
|
697 |
743 |
2.5e-21 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000032557
|
SMART Domains |
Protein: ENSMUSP00000032557 Gene: ENSMUSG00000024969
Domain | Start | End | E-Value | Type |
S_TKc
|
53 |
304 |
1.59e-108 |
SMART |
UBA
|
325 |
362 |
7.69e-7 |
SMART |
low complexity region
|
511 |
524 |
N/A |
INTRINSIC |
Pfam:KA1
|
685 |
731 |
5.4e-22 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000051711
|
SMART Domains |
Protein: ENSMUSP00000108969 Gene: ENSMUSG00000024969
Domain | Start | End | E-Value | Type |
S_TKc
|
53 |
304 |
1.59e-108 |
SMART |
UBA
|
325 |
362 |
7.69e-7 |
SMART |
low complexity region
|
508 |
522 |
N/A |
INTRINSIC |
low complexity region
|
565 |
578 |
N/A |
INTRINSIC |
Pfam:KA1
|
730 |
776 |
6.6e-22 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000066646
|
SMART Domains |
Protein: ENSMUSP00000063335 Gene: ENSMUSG00000024968
Domain | Start | End | E-Value | Type |
low complexity region
|
30 |
44 |
N/A |
INTRINSIC |
ELM2
|
46 |
100 |
4.36e-17 |
SMART |
SANT
|
131 |
179 |
1.32e-4 |
SMART |
low complexity region
|
249 |
260 |
N/A |
INTRINSIC |
SANT
|
328 |
376 |
5.24e-8 |
SMART |
low complexity region
|
423 |
496 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113369
|
SMART Domains |
Protein: ENSMUSP00000108996 Gene: ENSMUSG00000024968
Domain | Start | End | E-Value | Type |
ELM2
|
2 |
56 |
4.36e-17 |
SMART |
SANT
|
87 |
135 |
1.32e-4 |
SMART |
low complexity region
|
205 |
216 |
N/A |
INTRINSIC |
SANT
|
284 |
332 |
5.24e-8 |
SMART |
low complexity region
|
379 |
452 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000163345
|
SMART Domains |
Protein: ENSMUSP00000125944 Gene: ENSMUSG00000024969
Domain | Start | End | E-Value | Type |
low complexity region
|
3 |
15 |
N/A |
INTRINSIC |
low complexity region
|
58 |
71 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000171044
|
Predicted Effect |
probably null
Transcript: ENSMUST00000165965
|
SMART Domains |
Protein: ENSMUSP00000131684 Gene: ENSMUSG00000024969
Domain | Start | End | E-Value | Type |
S_TKc
|
53 |
304 |
1.59e-108 |
SMART |
UBA
|
325 |
362 |
7.69e-7 |
SMART |
low complexity region
|
508 |
522 |
N/A |
INTRINSIC |
low complexity region
|
565 |
578 |
N/A |
INTRINSIC |
Pfam:KA1
|
732 |
776 |
7.2e-24 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000165881
|
SMART Domains |
Protein: ENSMUSP00000126753 Gene: ENSMUSG00000024969
Domain | Start | End | E-Value | Type |
low complexity region
|
88 |
102 |
N/A |
INTRINSIC |
low complexity region
|
145 |
158 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000164205
|
SMART Domains |
Protein: ENSMUSP00000127827 Gene: ENSMUSG00000024969
Domain | Start | End | E-Value | Type |
S_TKc
|
53 |
304 |
1.59e-108 |
SMART |
UBA
|
325 |
362 |
7.69e-7 |
SMART |
low complexity region
|
511 |
524 |
N/A |
INTRINSIC |
Pfam:KA1
|
676 |
722 |
5.4e-22 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000171721
|
SMART Domains |
Protein: ENSMUSP00000129506 Gene: ENSMUSG00000024969
Domain | Start | End | E-Value | Type |
S_TKc
|
44 |
295 |
1.59e-108 |
SMART |
UBA
|
316 |
353 |
7.69e-7 |
SMART |
low complexity region
|
499 |
513 |
N/A |
INTRINSIC |
low complexity region
|
556 |
569 |
N/A |
INTRINSIC |
Pfam:KA1
|
732 |
776 |
7.2e-24 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000167767
|
SMART Domains |
Protein: ENSMUSP00000132482 Gene: ENSMUSG00000024969
Domain | Start | End | E-Value | Type |
low complexity region
|
53 |
66 |
N/A |
INTRINSIC |
PDB:3OSE|A
|
220 |
264 |
1e-18 |
PDB |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000165286
|
SMART Domains |
Protein: ENSMUSP00000126468 Gene: ENSMUSG00000024969
Domain | Start | End | E-Value | Type |
S_TKc
|
53 |
304 |
1.59e-108 |
SMART |
UBA
|
325 |
362 |
7.69e-7 |
SMART |
low complexity region
|
511 |
524 |
N/A |
INTRINSIC |
Pfam:KA1
|
670 |
716 |
6e-22 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000166461
|
SMART Domains |
Protein: ENSMUSP00000128549 Gene: ENSMUSG00000024969
Domain | Start | End | E-Value | Type |
low complexity region
|
45 |
59 |
N/A |
INTRINSIC |
low complexity region
|
102 |
115 |
N/A |
INTRINSIC |
Pfam:KA1
|
261 |
307 |
1.9e-22 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000168872
|
SMART Domains |
Protein: ENSMUSP00000128560 Gene: ENSMUSG00000024969
Domain | Start | End | E-Value | Type |
S_TKc
|
53 |
304 |
1.59e-108 |
SMART |
UBA
|
325 |
362 |
7.69e-7 |
SMART |
low complexity region
|
511 |
524 |
N/A |
INTRINSIC |
Pfam:KA1
|
661 |
707 |
5.9e-22 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000171352
|
SMART Domains |
Protein: ENSMUSP00000129490 Gene: ENSMUSG00000024969
Domain | Start | End | E-Value | Type |
low complexity region
|
127 |
140 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000164129
|
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 Par-1 family of serine/threonine protein kinases. The protein is an important regulator of cell polarity in epithelial and neuronal cells, and also controls the stability of microtubules through phosphorylation and inactivation of several microtubule-associating proteins. The protein localizes to cell membranes. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2009] PHENOTYPE: Homozygotes for targeted null mutations exhibit proportionate dwarfism with smaller pituitaries and reduced growth hormone and prolactin secretion. Mutants develop autoimmunity and fail to breed when mated to each other. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4 |
T |
A |
4: 144,349,782 (GRCm39) |
N346K |
possibly damaging |
Het |
Abca15 |
A |
G |
7: 119,987,439 (GRCm39) |
M1242V |
probably benign |
Het |
Abca6 |
T |
A |
11: 110,139,374 (GRCm39) |
E33D |
probably damaging |
Het |
Abca8a |
T |
C |
11: 109,961,177 (GRCm39) |
K582E |
possibly damaging |
Het |
Abcb6 |
A |
G |
1: 75,154,646 (GRCm39) |
L263P |
probably damaging |
Het |
Adamts2 |
A |
C |
11: 50,678,106 (GRCm39) |
E795A |
probably damaging |
Het |
Avil |
T |
A |
10: 126,844,864 (GRCm39) |
I292N |
probably damaging |
Het |
Cd300ld2 |
T |
C |
11: 114,904,576 (GRCm39) |
D97G |
probably benign |
Het |
Cfh |
A |
C |
1: 140,030,137 (GRCm39) |
I912R |
probably damaging |
Het |
Cyp26c1 |
A |
T |
19: 37,675,604 (GRCm39) |
Q156L |
probably benign |
Het |
Dhx57 |
T |
C |
17: 80,574,978 (GRCm39) |
I614V |
probably damaging |
Het |
Dip2c |
T |
A |
13: 9,660,826 (GRCm39) |
S896T |
probably damaging |
Het |
Dmtn |
G |
T |
14: 70,853,518 (GRCm39) |
P97Q |
probably damaging |
Het |
Dock6 |
A |
T |
9: 21,713,160 (GRCm39) |
V1931E |
probably damaging |
Het |
Dpep2 |
C |
A |
8: 106,717,227 (GRCm39) |
|
probably null |
Het |
Dsg1c |
T |
A |
18: 20,400,986 (GRCm39) |
L163Q |
probably benign |
Het |
Esyt3 |
A |
G |
9: 99,202,960 (GRCm39) |
|
probably benign |
Het |
Fcgbp |
T |
A |
7: 27,816,783 (GRCm39) |
I2415N |
possibly damaging |
Het |
Fpr-rs6 |
T |
C |
17: 20,403,307 (GRCm39) |
D18G |
probably benign |
Het |
Fras1 |
T |
C |
5: 96,682,725 (GRCm39) |
V74A |
possibly damaging |
Het |
Frem3 |
T |
C |
8: 81,341,010 (GRCm39) |
V1101A |
probably benign |
Het |
Fut8 |
T |
A |
12: 77,496,987 (GRCm39) |
V399E |
probably benign |
Het |
Galntl5 |
G |
T |
5: 25,391,237 (GRCm39) |
K45N |
probably benign |
Het |
Gbe1 |
A |
G |
16: 70,357,983 (GRCm39) |
Y669C |
possibly damaging |
Het |
Gcnt1 |
T |
C |
19: 17,307,493 (GRCm39) |
I77M |
probably benign |
Het |
Itprid1 |
T |
A |
6: 55,875,075 (GRCm39) |
W342R |
probably damaging |
Het |
Muc2 |
A |
T |
7: 141,300,450 (GRCm39) |
|
probably benign |
Het |
Nacc2 |
C |
T |
2: 25,980,329 (GRCm39) |
V36I |
probably damaging |
Het |
Nphp1 |
T |
C |
2: 127,611,543 (GRCm39) |
I268V |
probably benign |
Het |
Oosp3 |
A |
G |
19: 11,678,332 (GRCm39) |
I5V |
probably benign |
Het |
Or9m1 |
T |
G |
2: 87,733,724 (GRCm39) |
T99P |
possibly damaging |
Het |
Pex7 |
A |
G |
10: 19,769,990 (GRCm39) |
|
probably benign |
Het |
Prr14l |
T |
C |
5: 32,988,440 (GRCm39) |
K352E |
probably benign |
Het |
Rheb |
T |
A |
5: 25,008,709 (GRCm39) |
I170F |
probably benign |
Het |
Rpgrip1 |
A |
G |
14: 52,382,714 (GRCm39) |
|
probably null |
Het |
Rps2 |
T |
A |
17: 24,939,650 (GRCm39) |
L107Q |
probably damaging |
Het |
Rrp1 |
A |
T |
10: 78,240,874 (GRCm39) |
|
probably benign |
Het |
Rtcb |
A |
T |
10: 85,779,806 (GRCm39) |
V288D |
possibly damaging |
Het |
Sec14l3 |
T |
C |
11: 4,020,084 (GRCm39) |
F174L |
probably benign |
Het |
Slc28a1 |
G |
A |
7: 80,775,909 (GRCm39) |
V202M |
probably damaging |
Het |
Slc44a3 |
A |
T |
3: 121,325,366 (GRCm39) |
C32S |
probably damaging |
Het |
Syne1 |
G |
A |
10: 5,359,875 (GRCm39) |
|
probably benign |
Het |
Synrg |
C |
A |
11: 83,892,804 (GRCm39) |
|
probably benign |
Het |
Tmem219 |
A |
T |
7: 126,488,121 (GRCm39) |
F265I |
probably benign |
Het |
Tmem94 |
T |
C |
11: 115,683,765 (GRCm39) |
I726T |
probably damaging |
Het |
Trim37 |
T |
C |
11: 87,087,785 (GRCm39) |
M632T |
probably benign |
Het |
Trpm6 |
A |
T |
19: 18,790,846 (GRCm39) |
Q627L |
probably damaging |
Het |
Uvrag |
A |
G |
7: 98,628,984 (GRCm39) |
V361A |
possibly damaging |
Het |
Yipf3 |
C |
A |
17: 46,562,520 (GRCm39) |
N308K |
possibly damaging |
Het |
Zfp438 |
A |
G |
18: 5,245,427 (GRCm39) |
|
probably benign |
Het |
Zmiz1 |
T |
A |
14: 25,657,166 (GRCm39) |
|
probably benign |
Het |
Zranb3 |
A |
G |
1: 127,888,562 (GRCm39) |
V841A |
probably benign |
Het |
|
Other mutations in Mark2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00567:Mark2
|
APN |
19 |
7,318,549 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01522:Mark2
|
APN |
19 |
7,258,603 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02368:Mark2
|
APN |
19 |
7,261,855 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03233:Mark2
|
APN |
19 |
7,262,091 (GRCm39) |
missense |
possibly damaging |
0.89 |
Unprintable
|
UTSW |
19 |
7,263,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R0015:Mark2
|
UTSW |
19 |
7,263,142 (GRCm39) |
nonsense |
probably null |
|
R0025:Mark2
|
UTSW |
19 |
7,263,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R0025:Mark2
|
UTSW |
19 |
7,263,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R0035:Mark2
|
UTSW |
19 |
7,262,017 (GRCm39) |
splice site |
probably benign |
|
R0035:Mark2
|
UTSW |
19 |
7,262,017 (GRCm39) |
splice site |
probably benign |
|
R0047:Mark2
|
UTSW |
19 |
7,260,942 (GRCm39) |
splice site |
probably benign |
|
R0047:Mark2
|
UTSW |
19 |
7,260,942 (GRCm39) |
splice site |
probably benign |
|
R0335:Mark2
|
UTSW |
19 |
7,259,193 (GRCm39) |
missense |
probably benign |
0.27 |
R0627:Mark2
|
UTSW |
19 |
7,259,325 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0734:Mark2
|
UTSW |
19 |
7,263,346 (GRCm39) |
splice site |
probably benign |
|
R0744:Mark2
|
UTSW |
19 |
7,263,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R0836:Mark2
|
UTSW |
19 |
7,263,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R1099:Mark2
|
UTSW |
19 |
7,254,790 (GRCm39) |
missense |
probably benign |
0.41 |
R1861:Mark2
|
UTSW |
19 |
7,268,128 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1873:Mark2
|
UTSW |
19 |
7,261,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R2160:Mark2
|
UTSW |
19 |
7,260,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R2161:Mark2
|
UTSW |
19 |
7,260,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R2162:Mark2
|
UTSW |
19 |
7,260,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R2308:Mark2
|
UTSW |
19 |
7,259,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R2844:Mark2
|
UTSW |
19 |
7,264,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R2845:Mark2
|
UTSW |
19 |
7,264,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R2846:Mark2
|
UTSW |
19 |
7,264,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R2902:Mark2
|
UTSW |
19 |
7,260,813 (GRCm39) |
missense |
probably benign |
0.00 |
R2935:Mark2
|
UTSW |
19 |
7,263,254 (GRCm39) |
missense |
probably benign |
0.09 |
R3853:Mark2
|
UTSW |
19 |
7,254,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R4377:Mark2
|
UTSW |
19 |
7,268,054 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4522:Mark2
|
UTSW |
19 |
7,263,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R4737:Mark2
|
UTSW |
19 |
7,258,597 (GRCm39) |
missense |
probably damaging |
0.96 |
R5103:Mark2
|
UTSW |
19 |
7,261,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R5154:Mark2
|
UTSW |
19 |
7,260,439 (GRCm39) |
missense |
probably damaging |
0.99 |
R5579:Mark2
|
UTSW |
19 |
7,260,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R6163:Mark2
|
UTSW |
19 |
7,268,126 (GRCm39) |
missense |
probably benign |
0.00 |
R6186:Mark2
|
UTSW |
19 |
7,260,567 (GRCm39) |
missense |
probably benign |
0.01 |
R6387:Mark2
|
UTSW |
19 |
7,263,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R7032:Mark2
|
UTSW |
19 |
7,264,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R7949:Mark2
|
UTSW |
19 |
7,262,081 (GRCm39) |
missense |
probably benign |
0.12 |
R8792:Mark2
|
UTSW |
19 |
7,258,580 (GRCm39) |
missense |
probably benign |
0.00 |
R8825:Mark2
|
UTSW |
19 |
7,318,571 (GRCm39) |
missense |
probably benign |
0.00 |
R8854:Mark2
|
UTSW |
19 |
7,258,369 (GRCm39) |
missense |
probably benign |
0.01 |
R9374:Mark2
|
UTSW |
19 |
7,263,263 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9551:Mark2
|
UTSW |
19 |
7,263,263 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9552:Mark2
|
UTSW |
19 |
7,263,263 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
Posted On |
2015-12-18 |