Incidental Mutation 'R8249:Arhgap12'
| ID |
640345 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Arhgap12
|
| Ensembl Gene |
ENSMUSG00000041225 |
| Gene Name |
Rho GTPase activating protein 12 |
| Synonyms |
2810011M08Rik |
| MMRRC Submission |
067649-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R8249 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
18 |
| Chromosomal Location |
6024448-6136102 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 6027635 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Asparagine
at position 736
(I736N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000076376
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000062584]
[ENSMUST00000077128]
[ENSMUST00000182066]
[ENSMUST00000182213]
[ENSMUST00000182383]
[ENSMUST00000182559]
|
| AlphaFold |
Q8C0D4 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000062584
AA Change: I719N
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000054209
Gene: ENSMUSG00000041225
AA Change: I719N
| Domain | Start | End | E-Value | Type |
|---|
|
SH3
|
13 |
71 |
1.53e-3 |
SMART |
|
low complexity region
|
208 |
224 |
N/A |
INTRINSIC |
|
WW
|
264 |
296 |
3.39e-6 |
SMART |
|
WW
|
356 |
388 |
1.06e1 |
SMART |
|
PH
|
456 |
569 |
9.56e-11 |
SMART |
|
low complexity region
|
571 |
580 |
N/A |
INTRINSIC |
|
low complexity region
|
588 |
602 |
N/A |
INTRINSIC |
|
low complexity region
|
616 |
627 |
N/A |
INTRINSIC |
|
RhoGAP
|
659 |
833 |
5.47e-64 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000077128
AA Change: I736N
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000076376
Gene: ENSMUSG00000041225
AA Change: I736N
| Domain | Start | End | E-Value | Type |
|---|
|
SH3
|
13 |
71 |
1.53e-3 |
SMART |
|
low complexity region
|
208 |
224 |
N/A |
INTRINSIC |
|
WW
|
264 |
296 |
3.39e-6 |
SMART |
|
WW
|
356 |
388 |
1.06e1 |
SMART |
|
PH
|
431 |
544 |
9.56e-11 |
SMART |
|
low complexity region
|
546 |
555 |
N/A |
INTRINSIC |
|
low complexity region
|
563 |
577 |
N/A |
INTRINSIC |
|
low complexity region
|
591 |
602 |
N/A |
INTRINSIC |
|
RhoGAP
|
634 |
808 |
5.47e-64 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000182066
AA Change: I714N
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000138496
Gene: ENSMUSG00000041225
AA Change: I714N
| Domain | Start | End | E-Value | Type |
|---|
|
SH3
|
13 |
71 |
1.53e-3 |
SMART |
|
low complexity region
|
208 |
224 |
N/A |
INTRINSIC |
|
WW
|
264 |
296 |
3.39e-6 |
SMART |
|
WW
|
309 |
341 |
5.5e0 |
SMART |
|
PH
|
409 |
522 |
9.56e-11 |
SMART |
|
low complexity region
|
524 |
533 |
N/A |
INTRINSIC |
|
low complexity region
|
541 |
555 |
N/A |
INTRINSIC |
|
low complexity region
|
569 |
580 |
N/A |
INTRINSIC |
|
RhoGAP
|
612 |
786 |
5.47e-64 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000182213
AA Change: I766N
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000138464
Gene: ENSMUSG00000041225
AA Change: I766N
| Domain | Start | End | E-Value | Type |
|---|
|
SH3
|
13 |
71 |
1.53e-3 |
SMART |
|
low complexity region
|
208 |
224 |
N/A |
INTRINSIC |
|
WW
|
264 |
296 |
3.39e-6 |
SMART |
|
WW
|
356 |
388 |
1.06e1 |
SMART |
|
PH
|
461 |
574 |
9.56e-11 |
SMART |
|
low complexity region
|
576 |
585 |
N/A |
INTRINSIC |
|
low complexity region
|
593 |
607 |
N/A |
INTRINSIC |
|
low complexity region
|
621 |
632 |
N/A |
INTRINSIC |
|
RhoGAP
|
664 |
838 |
5.47e-64 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000182383
AA Change: I689N
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000138444
Gene: ENSMUSG00000041225
AA Change: I689N
| Domain | Start | End | E-Value | Type |
|---|
|
SH3
|
13 |
71 |
1.53e-3 |
SMART |
|
low complexity region
|
208 |
224 |
N/A |
INTRINSIC |
|
WW
|
264 |
296 |
3.39e-6 |
SMART |
|
WW
|
309 |
341 |
5.5e0 |
SMART |
|
PH
|
384 |
497 |
9.56e-11 |
SMART |
|
low complexity region
|
499 |
508 |
N/A |
INTRINSIC |
|
low complexity region
|
516 |
530 |
N/A |
INTRINSIC |
|
low complexity region
|
544 |
555 |
N/A |
INTRINSIC |
|
RhoGAP
|
587 |
761 |
5.47e-64 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000182559
AA Change: I761N
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000138585
Gene: ENSMUSG00000041225
AA Change: I761N
| Domain | Start | End | E-Value | Type |
|---|
|
SH3
|
13 |
71 |
1.53e-3 |
SMART |
|
low complexity region
|
208 |
224 |
N/A |
INTRINSIC |
|
WW
|
264 |
296 |
3.39e-6 |
SMART |
|
WW
|
356 |
388 |
1.06e1 |
SMART |
|
PH
|
456 |
569 |
9.56e-11 |
SMART |
|
low complexity region
|
571 |
580 |
N/A |
INTRINSIC |
|
low complexity region
|
588 |
602 |
N/A |
INTRINSIC |
|
low complexity region
|
616 |
627 |
N/A |
INTRINSIC |
|
RhoGAP
|
659 |
833 |
5.47e-64 |
SMART |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.5%
|
| 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 a large family of proteins that activate Rho-type guanosine triphosphate (GTP) metabolizing enzymes. The encoded protein may be involved in suppressing tumor formation by regulating cell invasion and adhesion. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]
PHENOTYPE: A null gene trap mutation resulted in no notable phenotype in homozygous mutant mice. [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 |
|---|
| Abca12 |
A |
G |
1: 71,360,971 (GRCm39) |
S441P |
probably benign |
Het |
| Adck2 |
C |
T |
6: 39,562,667 (GRCm39) |
R513* |
probably null |
Het |
| Agbl2 |
G |
A |
2: 90,627,908 (GRCm39) |
G238R |
probably damaging |
Het |
| AW554918 |
C |
T |
18: 25,472,775 (GRCm39) |
T193I |
probably benign |
Het |
| Bscl2 |
T |
C |
19: 8,823,884 (GRCm39) |
Y270H |
probably damaging |
Het |
| Btd |
T |
C |
14: 31,387,905 (GRCm39) |
Y112H |
probably damaging |
Het |
| Camk2d |
C |
T |
3: 126,591,378 (GRCm39) |
H283Y |
probably damaging |
Het |
| Cnga1 |
T |
C |
5: 72,762,737 (GRCm39) |
Y259C |
probably benign |
Het |
| Dnm3 |
A |
T |
1: 162,305,312 (GRCm39) |
C27* |
probably null |
Het |
| Fbxo48 |
T |
A |
11: 16,903,433 (GRCm39) |
S20T |
possibly damaging |
Het |
| Fkbp6 |
A |
G |
5: 135,378,806 (GRCm39) |
S14P |
possibly damaging |
Het |
| Gcfc2 |
T |
C |
6: 81,933,932 (GRCm39) |
F730L |
probably benign |
Het |
| Gm136 |
C |
A |
4: 34,750,955 (GRCm39) |
R106L |
probably benign |
Het |
| Gpr165 |
C |
A |
X: 95,757,623 (GRCm39) |
D7E |
probably benign |
Het |
| Grin2c |
C |
T |
11: 115,144,663 (GRCm39) |
R621Q |
probably damaging |
Het |
| H2-M11 |
T |
A |
17: 36,859,900 (GRCm39) |
W298R |
probably damaging |
Het |
| Hars2 |
A |
T |
18: 36,921,054 (GRCm39) |
I209F |
probably damaging |
Het |
| Hmcn1 |
A |
T |
1: 150,695,117 (GRCm39) |
N262K |
probably benign |
Het |
| Hycc2 |
G |
A |
1: 58,573,796 (GRCm39) |
S336L |
probably benign |
Het |
| Ifit1 |
T |
A |
19: 34,618,389 (GRCm39) |
|
probably null |
Het |
| Ighv1-85 |
T |
C |
12: 115,963,844 (GRCm39) |
D52G |
probably benign |
Het |
| Kit |
T |
C |
5: 75,802,068 (GRCm39) |
V657A |
probably damaging |
Het |
| Krt32 |
T |
C |
11: 99,977,548 (GRCm39) |
I173V |
probably benign |
Het |
| Lrfn3 |
GC |
GCCAGGGGAGGTGAGCGGTGGGTCACCTCCC |
7: 30,059,298 (GRCm39) |
|
probably null |
Het |
| Lrp1 |
C |
A |
10: 127,441,412 (GRCm39) |
S237I |
probably benign |
Het |
| Map3k9 |
T |
C |
12: 81,827,551 (GRCm39) |
D33G |
unknown |
Het |
| Mroh7 |
T |
C |
4: 106,578,409 (GRCm39) |
T90A |
probably benign |
Het |
| Mterf1a |
A |
C |
5: 3,941,550 (GRCm39) |
I106S |
probably damaging |
Het |
| Mtrf1 |
C |
A |
14: 79,638,919 (GRCm39) |
A17E |
probably benign |
Het |
| Musk |
T |
G |
4: 58,368,926 (GRCm39) |
L635R |
probably damaging |
Het |
| Naxe |
A |
T |
3: 87,965,695 (GRCm39) |
W35R |
possibly damaging |
Het |
| Nlrp9c |
T |
A |
7: 26,074,778 (GRCm39) |
K806* |
probably null |
Het |
| Pi4k2a |
A |
G |
19: 42,103,501 (GRCm39) |
E337G |
probably benign |
Het |
| Pwwp2b |
G |
T |
7: 138,834,759 (GRCm39) |
G67C |
probably damaging |
Het |
| Rftn1 |
G |
T |
17: 50,354,408 (GRCm39) |
A318D |
probably damaging |
Het |
| Scn10a |
T |
A |
9: 119,446,840 (GRCm39) |
Y1396F |
probably damaging |
Het |
| Sdk1 |
A |
T |
5: 142,173,770 (GRCm39) |
|
probably null |
Het |
| Serpina1f |
C |
T |
12: 103,660,027 (GRCm39) |
G85E |
probably damaging |
Het |
| Tceanc2 |
G |
A |
4: 107,036,190 (GRCm39) |
|
probably benign |
Het |
| Tmem156 |
T |
A |
5: 65,232,969 (GRCm39) |
R186* |
probably null |
Het |
| Trbv16 |
A |
G |
6: 41,128,932 (GRCm39) |
T39A |
possibly damaging |
Het |
| Tti1 |
C |
G |
2: 157,842,635 (GRCm39) |
S798T |
probably benign |
Het |
| Unc80 |
A |
T |
1: 66,658,650 (GRCm39) |
M1656L |
probably benign |
Het |
| Wnt2 |
C |
A |
6: 18,030,284 (GRCm39) |
M1I |
probably null |
Het |
|
| Other mutations in Arhgap12 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01468:Arhgap12
|
APN |
18 |
6,057,576 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01652:Arhgap12
|
APN |
18 |
6,061,853 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
IGL01886:Arhgap12
|
APN |
18 |
6,027,613 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02716:Arhgap12
|
APN |
18 |
6,111,857 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL03195:Arhgap12
|
APN |
18 |
6,031,766 (GRCm39) |
missense |
probably damaging |
1.00 |
|
eelier
|
UTSW |
18 |
6,061,930 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
eerie
|
UTSW |
18 |
6,111,734 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03134:Arhgap12
|
UTSW |
18 |
6,111,936 (GRCm39) |
missense |
probably benign |
0.22 |
|
R0312:Arhgap12
|
UTSW |
18 |
6,061,982 (GRCm39) |
intron |
probably benign |
|
|
R0330:Arhgap12
|
UTSW |
18 |
6,039,382 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0600:Arhgap12
|
UTSW |
18 |
6,064,433 (GRCm39) |
intron |
probably benign |
|
|
R0891:Arhgap12
|
UTSW |
18 |
6,026,699 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1123:Arhgap12
|
UTSW |
18 |
6,031,822 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1395:Arhgap12
|
UTSW |
18 |
6,037,058 (GRCm39) |
missense |
probably benign |
0.20 |
|
R1644:Arhgap12
|
UTSW |
18 |
6,112,340 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2968:Arhgap12
|
UTSW |
18 |
6,111,732 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2970:Arhgap12
|
UTSW |
18 |
6,111,732 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3809:Arhgap12
|
UTSW |
18 |
6,037,057 (GRCm39) |
missense |
probably benign |
0.36 |
|
R3824:Arhgap12
|
UTSW |
18 |
6,061,930 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R4181:Arhgap12
|
UTSW |
18 |
6,111,734 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4182:Arhgap12
|
UTSW |
18 |
6,111,734 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4183:Arhgap12
|
UTSW |
18 |
6,111,734 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4497:Arhgap12
|
UTSW |
18 |
6,111,774 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4498:Arhgap12
|
UTSW |
18 |
6,111,774 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5456:Arhgap12
|
UTSW |
18 |
6,112,170 (GRCm39) |
nonsense |
probably null |
|
|
R5539:Arhgap12
|
UTSW |
18 |
6,111,932 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5915:Arhgap12
|
UTSW |
18 |
6,037,016 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6859:Arhgap12
|
UTSW |
18 |
6,111,803 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6960:Arhgap12
|
UTSW |
18 |
6,111,901 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7114:Arhgap12
|
UTSW |
18 |
6,028,056 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7285:Arhgap12
|
UTSW |
18 |
6,111,920 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7359:Arhgap12
|
UTSW |
18 |
6,065,709 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R8048:Arhgap12
|
UTSW |
18 |
6,052,883 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8523:Arhgap12
|
UTSW |
18 |
6,111,976 (GRCm39) |
missense |
probably benign |
0.12 |
|
R9110:Arhgap12
|
UTSW |
18 |
6,034,539 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R9444:Arhgap12
|
UTSW |
18 |
6,052,909 (GRCm39) |
nonsense |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- ACCTTCTGTGTGATGAGCATTAC -3'
(R):5'- TTGAGACAGGGTTTCCAGTC -3'
Sequencing Primer
(F):5'- TGTGATGAGCATTACACAAACAC -3'
(R):5'- CAGGGTTTCCAGTCTTATTTTTAAAC -3'
|
| Posted On |
2020-07-28 |
Incidental Mutation