Incidental Mutation 'R1614:Strada'
| ID |
177010 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Strada
|
| Ensembl Gene |
ENSMUSG00000069631 |
| Gene Name |
STE20-related kinase adaptor alpha |
| Synonyms |
6030402H20Rik, 2610019A05Rik |
| MMRRC Submission |
039651-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.521)
|
| Stock # |
R1614 (G1)
|
| Quality Score |
150 |
|
Status
|
Validated
|
| Chromosome |
11 |
| Chromosomal Location |
106053739-106084460 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to C
at 106059145 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Glycine
at position 211
(V211G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000099361
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000007444]
[ENSMUST00000103072]
[ENSMUST00000152008]
|
| AlphaFold |
Q3UUJ4 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000007444
AA Change: V248G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000007444
Gene: ENSMUSG00000069631
AA Change: V248G
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Pkinase
|
69 |
379 |
2.4e-37 |
PFAM |
|
Pfam:Pkinase_Tyr
|
70 |
302 |
2.1e-24 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000103072
AA Change: V211G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000099361
Gene: ENSMUSG00000069631
AA Change: V211G
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Pkinase
|
32 |
342 |
2.2e-35 |
PFAM |
|
Pfam:Pkinase_Tyr
|
33 |
266 |
2.5e-24 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000122989
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000152008
|
| SMART Domains |
Protein: ENSMUSP00000115555
Gene: ENSMUSG00000069631
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Pkinase
|
32 |
159 |
7.4e-16 |
PFAM |
|
Pfam:Pkinase_Tyr
|
33 |
159 |
1.5e-10 |
PFAM |
|
| Meta Mutation Damage Score |
0.7999 |
| Coding Region Coverage |
- 1x: 99.0%
- 3x: 98.1%
- 10x: 95.4%
- 20x: 89.4%
|
| Validation Efficiency |
100% (53/53) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene contains a STE20-like kinase domain, but lacks several residues that are critical for catalytic activity, so it is termed a 'pseudokinase'. The protein forms a heterotrimeric complex with serine/threonine kinase 11 (STK11, also known as LKB1) and the scaffolding protein calcium binding protein 39 (CAB39, also known as MO25). The protein activates STK11 leading to the phosphorylation of both proteins and excluding STK11 from the nucleus. The protein is necessary for STK11-induced G1 cell cycle arrest. A mutation in this gene has been shown to result in polyhydramnios, megalencephaly, and symptomatic epilepsy (PMSE) syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. Additional transcript variants have been described but their full-length nature is not known. [provided by RefSeq, Sep 2009]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 46 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Arl9 |
A |
G |
5: 77,158,412 (GRCm39) |
T165A |
probably benign |
Het |
| Atpaf1 |
A |
T |
4: 115,653,954 (GRCm39) |
K201N |
possibly damaging |
Het |
| Cacna1b |
G |
T |
2: 24,580,819 (GRCm39) |
Q676K |
possibly damaging |
Het |
| Ccdc88c |
A |
T |
12: 100,879,243 (GRCm39) |
H1959Q |
probably benign |
Het |
| Cep162 |
T |
C |
9: 87,094,985 (GRCm39) |
D808G |
probably damaging |
Het |
| Chct1 |
T |
G |
11: 85,063,690 (GRCm39) |
S28A |
possibly damaging |
Het |
| Chtf18 |
A |
G |
17: 25,946,064 (GRCm39) |
L42P |
probably benign |
Het |
| Cox7c |
A |
G |
13: 86,193,904 (GRCm39) |
F40L |
probably benign |
Het |
| Dock7 |
C |
T |
4: 98,949,517 (GRCm39) |
V442I |
probably benign |
Het |
| Dst |
T |
C |
1: 34,314,344 (GRCm39) |
F4198S |
probably damaging |
Het |
| Fam13a |
T |
A |
6: 58,917,169 (GRCm39) |
D569V |
probably damaging |
Het |
| Gm6741 |
T |
A |
17: 91,544,424 (GRCm39) |
H62Q |
probably benign |
Het |
| Gnptab |
A |
G |
10: 88,250,451 (GRCm39) |
T172A |
probably benign |
Het |
| Greb1 |
A |
G |
12: 16,751,172 (GRCm39) |
S1013P |
probably damaging |
Het |
| Insl5 |
A |
T |
4: 102,883,846 (GRCm39) |
L25* |
probably null |
Het |
| Ipo13 |
A |
G |
4: 117,761,815 (GRCm39) |
S462P |
probably benign |
Het |
| Itgb1 |
G |
A |
8: 129,446,546 (GRCm39) |
C401Y |
probably damaging |
Het |
| Kcnh7 |
G |
T |
2: 62,680,948 (GRCm39) |
A213E |
probably benign |
Het |
| Kcnv1 |
G |
A |
15: 44,977,840 (GRCm39) |
T66M |
probably damaging |
Het |
| Mesp2 |
T |
C |
7: 79,461,367 (GRCm39) |
S231P |
probably benign |
Het |
| Nabp1 |
T |
C |
1: 51,510,511 (GRCm39) |
N164D |
possibly damaging |
Het |
| Nop53 |
A |
G |
7: 15,679,890 (GRCm39) |
V30A |
probably benign |
Het |
| Or1j17 |
T |
G |
2: 36,578,321 (GRCm39) |
Y102* |
probably null |
Het |
| Or4a73 |
T |
A |
2: 89,421,040 (GRCm39) |
I140L |
possibly damaging |
Het |
| Or4f54 |
T |
A |
2: 111,123,411 (GRCm39) |
V266E |
probably damaging |
Het |
| Or4f62 |
T |
A |
2: 111,986,862 (GRCm39) |
C189S |
probably damaging |
Het |
| Pcsk5 |
G |
A |
19: 17,492,620 (GRCm39) |
R918C |
probably damaging |
Het |
| Pecam1 |
T |
C |
11: 106,571,905 (GRCm39) |
D554G |
probably benign |
Het |
| Polr2a |
T |
C |
11: 69,634,199 (GRCm39) |
I744V |
possibly damaging |
Het |
| Pop1 |
C |
A |
15: 34,530,356 (GRCm39) |
A918D |
possibly damaging |
Het |
| Ppp2r5e |
C |
G |
12: 75,516,341 (GRCm39) |
A239P |
probably damaging |
Het |
| Prmt3 |
A |
T |
7: 49,476,467 (GRCm39) |
I359F |
possibly damaging |
Het |
| Proz |
G |
A |
8: 13,116,904 (GRCm39) |
C152Y |
probably damaging |
Het |
| Ptgfr |
A |
C |
3: 151,507,416 (GRCm39) |
Y316D |
probably benign |
Het |
| Ralgapa2 |
G |
T |
2: 146,230,532 (GRCm39) |
S1011Y |
probably damaging |
Het |
| Rnf43 |
C |
T |
11: 87,622,485 (GRCm39) |
R529* |
probably null |
Het |
| Slc17a6 |
G |
A |
7: 51,296,025 (GRCm39) |
|
probably benign |
Het |
| Slc25a19 |
A |
T |
11: 115,507,449 (GRCm39) |
C224* |
probably null |
Het |
| Smarcd3 |
A |
G |
5: 24,799,874 (GRCm39) |
S299P |
possibly damaging |
Het |
| Stard9 |
T |
C |
2: 120,528,156 (GRCm39) |
F1471S |
possibly damaging |
Het |
| Tom1l1 |
T |
C |
11: 90,574,080 (GRCm39) |
E68G |
probably damaging |
Het |
| Vmn2r27 |
T |
G |
6: 124,200,893 (GRCm39) |
I355L |
probably benign |
Het |
| Vmn2r68 |
A |
T |
7: 84,870,946 (GRCm39) |
M779K |
possibly damaging |
Het |
| Zbtb18 |
T |
C |
1: 177,274,736 (GRCm39) |
L23P |
probably damaging |
Het |
| Zfp112 |
G |
T |
7: 23,826,024 (GRCm39) |
C664F |
probably damaging |
Het |
| Zfp955a |
A |
T |
17: 33,461,306 (GRCm39) |
N275K |
possibly damaging |
Het |
|
| Other mutations in Strada |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00778:Strada
|
APN |
11 |
106,061,976 (GRCm39) |
splice site |
probably benign |
|
|
IGL00870:Strada
|
APN |
11 |
106,062,083 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01564:Strada
|
APN |
11 |
106,064,118 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02508:Strada
|
APN |
11 |
106,059,182 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL02816:Strada
|
APN |
11 |
106,055,251 (GRCm39) |
unclassified |
probably benign |
|
|
IGL03008:Strada
|
APN |
11 |
106,061,783 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03107:Strada
|
APN |
11 |
106,054,863 (GRCm39) |
unclassified |
probably benign |
|
|
R0587:Strada
|
UTSW |
11 |
106,061,790 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1764:Strada
|
UTSW |
11 |
106,055,010 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1852:Strada
|
UTSW |
11 |
106,062,047 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R3772:Strada
|
UTSW |
11 |
106,055,648 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4329:Strada
|
UTSW |
11 |
106,077,999 (GRCm39) |
utr 5 prime |
probably benign |
|
|
R4538:Strada
|
UTSW |
11 |
106,058,651 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5532:Strada
|
UTSW |
11 |
106,061,843 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6102:Strada
|
UTSW |
11 |
106,059,262 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6135:Strada
|
UTSW |
11 |
106,064,140 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6337:Strada
|
UTSW |
11 |
106,064,143 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R6773:Strada
|
UTSW |
11 |
106,055,733 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7155:Strada
|
UTSW |
11 |
106,061,865 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7509:Strada
|
UTSW |
11 |
106,077,920 (GRCm39) |
missense |
unknown |
|
|
R7552:Strada
|
UTSW |
11 |
106,077,830 (GRCm39) |
missense |
unknown |
|
|
R8510:Strada
|
UTSW |
11 |
106,061,984 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9262:Strada
|
UTSW |
11 |
106,075,444 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9630:Strada
|
UTSW |
11 |
106,077,781 (GRCm39) |
missense |
unknown |
|
|
RF015:Strada
|
UTSW |
11 |
106,061,846 (GRCm39) |
missense |
probably damaging |
0.98 |
|
| Predicted Primers |
PCR Primer
(F):5'- AACTGCTGTGTGAGGAGAGCCAAC -3'
(R):5'- AGTGTCAAGGCCAGCCACATTC -3'
Sequencing Primer
(F):5'- TTCAGCACAGGGATCTAAATTCCG -3'
(R):5'- ACATTCTGATCTCCACGGATGG -3'
|
| Posted On |
2014-04-24 |
Incidental Mutation