Incidental Mutation 'IGL03108:Mapk7'
ID |
419078 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Mapk7
|
Ensembl Gene |
ENSMUSG00000001034 |
Gene Name |
mitogen-activated protein kinase 7 |
Synonyms |
BMK1, big MAP kinase 1, ERK5, b2b2346Clo, Erk5-T |
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
IGL03108
|
Quality Score |
|
Status
|
|
Chromosome |
11 |
Chromosomal Location |
61379638-61385101 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 61382498 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Glycine
at position 68
(D68G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000098646
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000040522]
[ENSMUST00000064783]
[ENSMUST00000079080]
[ENSMUST00000101085]
[ENSMUST00000108714]
[ENSMUST00000153441]
|
AlphaFold |
Q9WVS8 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000040522
|
SMART Domains |
Protein: ENSMUSP00000038971 Gene: ENSMUSG00000042436
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
22 |
N/A |
INTRINSIC |
FBG
|
38 |
280 |
5.6e-119 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000064783
|
SMART Domains |
Protein: ENSMUSP00000070848 Gene: ENSMUSG00000042436
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
22 |
N/A |
INTRINSIC |
FBG
|
38 |
257 |
3.39e-130 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000079080
AA Change: D138G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000078087 Gene: ENSMUSG00000001034 AA Change: D138G
Domain | Start | End | E-Value | Type |
low complexity region
|
7 |
19 |
N/A |
INTRINSIC |
S_TKc
|
55 |
347 |
5.66e-96 |
SMART |
low complexity region
|
433 |
447 |
N/A |
INTRINSIC |
low complexity region
|
476 |
492 |
N/A |
INTRINSIC |
coiled coil region
|
508 |
544 |
N/A |
INTRINSIC |
low complexity region
|
578 |
603 |
N/A |
INTRINSIC |
low complexity region
|
620 |
644 |
N/A |
INTRINSIC |
low complexity region
|
675 |
692 |
N/A |
INTRINSIC |
low complexity region
|
758 |
772 |
N/A |
INTRINSIC |
low complexity region
|
791 |
803 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000101085
AA Change: D68G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000098646 Gene: ENSMUSG00000001034 AA Change: D68G
Domain | Start | End | E-Value | Type |
S_TKc
|
4 |
277 |
3.48e-73 |
SMART |
low complexity region
|
363 |
377 |
N/A |
INTRINSIC |
coiled coil region
|
405 |
441 |
N/A |
INTRINSIC |
low complexity region
|
475 |
500 |
N/A |
INTRINSIC |
low complexity region
|
517 |
541 |
N/A |
INTRINSIC |
low complexity region
|
572 |
589 |
N/A |
INTRINSIC |
low complexity region
|
655 |
669 |
N/A |
INTRINSIC |
low complexity region
|
688 |
700 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000108714
AA Change: D69G
PolyPhen 2
Score 0.884 (Sensitivity: 0.82; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000104354 Gene: ENSMUSG00000001034 AA Change: D69G
Domain | Start | End | E-Value | Type |
S_TKc
|
1 |
278 |
1.76e-74 |
SMART |
low complexity region
|
364 |
378 |
N/A |
INTRINSIC |
low complexity region
|
407 |
423 |
N/A |
INTRINSIC |
coiled coil region
|
439 |
475 |
N/A |
INTRINSIC |
low complexity region
|
509 |
534 |
N/A |
INTRINSIC |
low complexity region
|
551 |
575 |
N/A |
INTRINSIC |
low complexity region
|
606 |
623 |
N/A |
INTRINSIC |
low complexity region
|
689 |
703 |
N/A |
INTRINSIC |
low complexity region
|
722 |
734 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000123360
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000125840
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000135521
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000152755
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000128478
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000126495
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000139932
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000139663
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000126308
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000127073
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000129272
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000140779
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000153441
|
SMART Domains |
Protein: ENSMUSP00000116084 Gene: ENSMUSG00000001034
Domain | Start | End | E-Value | Type |
PDB:4IC8|B
|
1 |
49 |
2e-26 |
PDB |
low complexity region
|
51 |
65 |
N/A |
INTRINSIC |
low complexity region
|
94 |
110 |
N/A |
INTRINSIC |
coiled coil region
|
126 |
162 |
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.] The protein encoded by this gene is a member of the MAP kinase family. MAP kinases act as an integration point for multiple biochemical signals, and are involved in a wide variety of cellular processes such as proliferation, differentiation, transcription regulation and development. This kinase is specifically activated by mitogen-activated protein kinase kinase 5 (MAP2K5/MEK5). It is involved in the downstream signaling processes of various receptor molecules including receptor type kinases, and G protein-coupled receptors. In response to extracelluar signals, this kinase translocates to cell nucleus, where it regulates gene expression by phosphorylating, and activating different transcription factors. Four alternatively spliced transcript variants of this gene encoding two distinct isoforms have been reported. [provided by RefSeq, Jul 2008] PHENOTYPE: Homozygous inactivation of this gene leads to embryonic growth retardation and midgestational lethality due to multiple developmental anomalies and vascular remodelling, cardiac development, and placental defects. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
C |
A |
13: 81,707,648 (GRCm39) |
V1253F |
probably damaging |
Het |
Apbb2 |
A |
G |
5: 66,557,574 (GRCm39) |
W296R |
probably damaging |
Het |
Armh3 |
G |
A |
19: 45,808,792 (GRCm39) |
T633I |
probably damaging |
Het |
Btbd3 |
T |
C |
2: 138,126,043 (GRCm39) |
V409A |
possibly damaging |
Het |
C130050O18Rik |
A |
T |
5: 139,400,820 (GRCm39) |
D291V |
probably damaging |
Het |
Catsper3 |
A |
G |
13: 55,955,848 (GRCm39) |
N318D |
probably benign |
Het |
Chd1 |
T |
A |
17: 15,945,543 (GRCm39) |
D22E |
possibly damaging |
Het |
Chrnb2 |
G |
A |
3: 89,670,681 (GRCm39) |
|
probably benign |
Het |
Col24a1 |
G |
A |
3: 145,029,162 (GRCm39) |
G550D |
probably damaging |
Het |
Cryl1 |
T |
C |
14: 57,550,534 (GRCm39) |
D110G |
probably damaging |
Het |
Deaf1 |
A |
G |
7: 140,902,874 (GRCm39) |
I150T |
probably damaging |
Het |
Eif3a |
A |
T |
19: 60,770,747 (GRCm39) |
D33E |
possibly damaging |
Het |
Fabp12 |
C |
A |
3: 10,315,114 (GRCm39) |
G78C |
probably benign |
Het |
Fat1 |
A |
G |
8: 45,476,651 (GRCm39) |
D1899G |
probably damaging |
Het |
Galnt13 |
G |
A |
2: 54,744,660 (GRCm39) |
V120I |
probably benign |
Het |
Ganab |
G |
A |
19: 8,889,840 (GRCm39) |
A635T |
probably damaging |
Het |
Gm17509 |
G |
A |
13: 117,357,380 (GRCm39) |
|
probably benign |
Het |
Gstm3 |
A |
T |
3: 107,875,080 (GRCm39) |
|
probably null |
Het |
Hfm1 |
T |
A |
5: 107,043,800 (GRCm39) |
|
probably benign |
Het |
Hoxd13 |
A |
C |
2: 74,500,440 (GRCm39) |
D327A |
probably damaging |
Het |
Ints4 |
G |
T |
7: 97,140,137 (GRCm39) |
|
probably null |
Het |
Kcna10 |
A |
T |
3: 107,102,259 (GRCm39) |
T297S |
probably benign |
Het |
Ldb2 |
G |
A |
5: 44,699,057 (GRCm39) |
T127I |
probably damaging |
Het |
Msh3 |
A |
T |
13: 92,357,596 (GRCm39) |
|
probably benign |
Het |
Muc6 |
A |
G |
7: 141,217,402 (GRCm39) |
S2359P |
possibly damaging |
Het |
Mup6 |
A |
T |
4: 60,005,990 (GRCm39) |
I161F |
possibly damaging |
Het |
Nup160 |
G |
A |
2: 90,534,169 (GRCm39) |
V665I |
probably benign |
Het |
Or13a22 |
A |
G |
7: 140,073,034 (GRCm39) |
N161S |
possibly damaging |
Het |
Or14a258 |
T |
C |
7: 86,034,929 (GRCm39) |
Y313C |
possibly damaging |
Het |
Or4e5 |
T |
A |
14: 52,727,533 (GRCm39) |
D296V |
probably damaging |
Het |
Otog |
G |
A |
7: 45,900,762 (GRCm39) |
V352I |
probably damaging |
Het |
Oxct1 |
T |
A |
15: 4,064,764 (GRCm39) |
V34D |
probably benign |
Het |
Pcdhb21 |
T |
A |
18: 37,648,944 (GRCm39) |
|
probably null |
Het |
Pcdhb8 |
T |
G |
18: 37,490,299 (GRCm39) |
V659G |
probably damaging |
Het |
Plxnb2 |
T |
C |
15: 89,042,234 (GRCm39) |
N1590S |
probably benign |
Het |
Rnf168 |
G |
T |
16: 32,097,099 (GRCm39) |
R56L |
possibly damaging |
Het |
Scn8a |
C |
T |
15: 100,872,496 (GRCm39) |
P362S |
probably benign |
Het |
Slc1a3 |
T |
A |
15: 8,668,562 (GRCm39) |
I468F |
probably damaging |
Het |
Slc39a14 |
G |
A |
14: 70,556,368 (GRCm39) |
R3W |
probably damaging |
Het |
Slc7a6 |
T |
A |
8: 106,921,149 (GRCm39) |
N373K |
probably damaging |
Het |
Snrnp200 |
T |
C |
2: 127,080,087 (GRCm39) |
S1955P |
possibly damaging |
Het |
Stat5a |
T |
A |
11: 100,753,965 (GRCm39) |
Y98* |
probably null |
Het |
Thsd7b |
G |
T |
1: 130,138,013 (GRCm39) |
G1564C |
probably damaging |
Het |
Zc3h13 |
T |
C |
14: 75,569,206 (GRCm39) |
V1351A |
possibly damaging |
Het |
|
Other mutations in Mapk7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01510:Mapk7
|
APN |
11 |
61,381,986 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02289:Mapk7
|
APN |
11 |
61,380,785 (GRCm39) |
splice site |
probably null |
|
IGL03342:Mapk7
|
APN |
11 |
61,382,216 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4340:Mapk7
|
UTSW |
11 |
61,381,032 (GRCm39) |
intron |
probably benign |
|
FR4589:Mapk7
|
UTSW |
11 |
61,381,048 (GRCm39) |
intron |
probably benign |
|
R1497:Mapk7
|
UTSW |
11 |
61,384,689 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1866:Mapk7
|
UTSW |
11 |
61,380,239 (GRCm39) |
missense |
probably benign |
0.27 |
R2870:Mapk7
|
UTSW |
11 |
61,381,038 (GRCm39) |
intron |
probably benign |
|
R2871:Mapk7
|
UTSW |
11 |
61,381,038 (GRCm39) |
intron |
probably benign |
|
R2872:Mapk7
|
UTSW |
11 |
61,381,038 (GRCm39) |
intron |
probably benign |
|
R3831:Mapk7
|
UTSW |
11 |
61,380,680 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3832:Mapk7
|
UTSW |
11 |
61,380,680 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3833:Mapk7
|
UTSW |
11 |
61,380,680 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4378:Mapk7
|
UTSW |
11 |
61,384,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R4428:Mapk7
|
UTSW |
11 |
61,380,055 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4642:Mapk7
|
UTSW |
11 |
61,381,727 (GRCm39) |
missense |
probably damaging |
0.99 |
R4692:Mapk7
|
UTSW |
11 |
61,380,068 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4718:Mapk7
|
UTSW |
11 |
61,380,080 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4755:Mapk7
|
UTSW |
11 |
61,381,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R4916:Mapk7
|
UTSW |
11 |
61,384,475 (GRCm39) |
missense |
probably damaging |
0.97 |
R4933:Mapk7
|
UTSW |
11 |
61,384,734 (GRCm39) |
unclassified |
probably benign |
|
R5825:Mapk7
|
UTSW |
11 |
61,381,207 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5875:Mapk7
|
UTSW |
11 |
61,384,524 (GRCm39) |
missense |
probably benign |
0.13 |
R5910:Mapk7
|
UTSW |
11 |
61,384,447 (GRCm39) |
start codon destroyed |
probably benign |
0.01 |
R7201:Mapk7
|
UTSW |
11 |
61,379,998 (GRCm39) |
missense |
probably benign |
0.33 |
R7465:Mapk7
|
UTSW |
11 |
61,381,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R7797:Mapk7
|
UTSW |
11 |
61,380,241 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8867:Mapk7
|
UTSW |
11 |
61,384,632 (GRCm39) |
missense |
probably benign |
0.41 |
R8953:Mapk7
|
UTSW |
11 |
61,383,792 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9243:Mapk7
|
UTSW |
11 |
61,384,535 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9394:Mapk7
|
UTSW |
11 |
61,381,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R9671:Mapk7
|
UTSW |
11 |
61,382,498 (GRCm39) |
missense |
probably damaging |
1.00 |
RF031:Mapk7
|
UTSW |
11 |
61,381,060 (GRCm39) |
intron |
probably benign |
|
Z1177:Mapk7
|
UTSW |
11 |
61,382,188 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1186:Mapk7
|
UTSW |
11 |
61,381,053 (GRCm39) |
intron |
probably benign |
|
Z1186:Mapk7
|
UTSW |
11 |
61,381,042 (GRCm39) |
intron |
probably benign |
|
Z1186:Mapk7
|
UTSW |
11 |
61,381,038 (GRCm39) |
intron |
probably benign |
|
Z1187:Mapk7
|
UTSW |
11 |
61,381,053 (GRCm39) |
intron |
probably benign |
|
Z1187:Mapk7
|
UTSW |
11 |
61,381,038 (GRCm39) |
intron |
probably benign |
|
Z1188:Mapk7
|
UTSW |
11 |
61,381,070 (GRCm39) |
intron |
probably benign |
|
Z1188:Mapk7
|
UTSW |
11 |
61,381,053 (GRCm39) |
intron |
probably benign |
|
Z1188:Mapk7
|
UTSW |
11 |
61,381,038 (GRCm39) |
intron |
probably benign |
|
Z1189:Mapk7
|
UTSW |
11 |
61,381,053 (GRCm39) |
intron |
probably benign |
|
Z1190:Mapk7
|
UTSW |
11 |
61,381,053 (GRCm39) |
intron |
probably benign |
|
Z1191:Mapk7
|
UTSW |
11 |
61,381,053 (GRCm39) |
intron |
probably benign |
|
Z1191:Mapk7
|
UTSW |
11 |
61,381,038 (GRCm39) |
intron |
probably benign |
|
Z1192:Mapk7
|
UTSW |
11 |
61,381,053 (GRCm39) |
intron |
probably benign |
|
|
Posted On |
2016-08-02 |