Incidental Mutation 'IGL02272:Rap1gap'
| ID |
287202 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Rap1gap
|
| Ensembl Gene |
ENSMUSG00000041351 |
| Gene Name |
Rap1 GTPase-activating protein |
| Synonyms |
Gap, 1300019I11Rik, 2310004O14Rik, Rap1ga1 |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL02272
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
4 |
| Chromosomal Location |
137392037-137457172 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 137443877 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Cysteine
at position 163
(Y163C)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000123561
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000047243]
[ENSMUST00000097837]
[ENSMUST00000105835]
[ENSMUST00000141306]
[ENSMUST00000150928]
[ENSMUST00000152567]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000047243
AA Change: Y238C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000042473
Gene: ENSMUSG00000041351
AA Change: Y238C
| Domain | Start | End | E-Value | Type |
|---|
|
GoLoco
|
59 |
81 |
4.94e-10 |
SMART |
|
Pfam:Rap_GAP
|
274 |
461 |
1.4e-64 |
PFAM |
|
low complexity region
|
485 |
495 |
N/A |
INTRINSIC |
|
low complexity region
|
630 |
641 |
N/A |
INTRINSIC |
|
low complexity region
|
680 |
695 |
N/A |
INTRINSIC |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000097837
AA Change: Y205C
PolyPhen 2
Score 0.890 (Sensitivity: 0.82; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000095448
Gene: ENSMUSG00000041351
AA Change: Y205C
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
4 |
16 |
N/A |
INTRINSIC |
|
GoLoco
|
26 |
48 |
4.94e-10 |
SMART |
|
Pfam:Rap_GAP
|
241 |
428 |
1.2e-64 |
PFAM |
|
low complexity region
|
452 |
462 |
N/A |
INTRINSIC |
|
low complexity region
|
597 |
608 |
N/A |
INTRINSIC |
|
low complexity region
|
647 |
662 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000105835
AA Change: Y238C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000101461
Gene: ENSMUSG00000041351
AA Change: Y238C
| Domain | Start | End | E-Value | Type |
|---|
|
GoLoco
|
59 |
81 |
4.94e-10 |
SMART |
|
Pfam:Rap_GAP
|
274 |
455 |
4.5e-66 |
PFAM |
|
low complexity region
|
485 |
495 |
N/A |
INTRINSIC |
|
low complexity region
|
630 |
641 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000131536
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000139831
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000141306
|
| SMART Domains |
Protein: ENSMUSP00000122315
Gene: ENSMUSG00000041351
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Rap_GAP
|
1 |
117 |
1.4e-32 |
PFAM |
|
low complexity region
|
141 |
151 |
N/A |
INTRINSIC |
|
low complexity region
|
312 |
323 |
N/A |
INTRINSIC |
|
low complexity region
|
362 |
377 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000150928
AA Change: Y163C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000123561
Gene: ENSMUSG00000041351
AA Change: Y163C
| Domain | Start | End | E-Value | Type |
|---|
|
GoLoco
|
59 |
81 |
4.94e-10 |
SMART |
|
Pfam:Rap_GAP
|
199 |
241 |
1.3e-13 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000156683
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000152567
|
| SMART Domains |
Protein: ENSMUSP00000115391
Gene: ENSMUSG00000041351
| Domain | Start | End | E-Value | Type |
|---|
|
GoLoco
|
47 |
69 |
4.94e-10 |
SMART |
|
PDB:1SRQ|D
|
127 |
165 |
4e-20 |
PDB |
|
| 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 type of GTPase-activating-protein (GAP) that down-regulates the activity of the ras-related RAP1 protein. RAP1 acts as a molecular switch by cycling between an inactive GDP-bound form and an active GTP-bound form. The product of this gene, RAP1GAP, promotes the hydrolysis of bound GTP and hence returns RAP1 to the inactive state whereas other proteins, guanine nucleotide exchange factors (GEFs), act as RAP1 activators by facilitating the conversion of RAP1 from the GDP- to the GTP-bound form. In general, ras subfamily proteins, such as RAP1, play key roles in receptor-linked signaling pathways that control cell growth and differentiation. RAP1 plays a role in diverse processes such as cell proliferation, adhesion, differentiation, and embryogenesis. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Aug 2011]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 59 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adgre1 |
T |
A |
17: 57,757,021 (GRCm39) |
C759* |
probably null |
Het |
| Adgrg6 |
T |
A |
10: 14,344,573 (GRCm39) |
M127L |
probably damaging |
Het |
| Anxa9 |
A |
G |
3: 95,213,205 (GRCm39) |
V47A |
probably benign |
Het |
| Arhgef12 |
T |
A |
9: 42,912,748 (GRCm39) |
D483V |
probably damaging |
Het |
| Arrdc3 |
C |
A |
13: 81,039,769 (GRCm39) |
|
probably benign |
Het |
| Ccdc169 |
A |
G |
3: 55,058,169 (GRCm39) |
E67G |
probably damaging |
Het |
| Ccdc191 |
T |
A |
16: 43,780,385 (GRCm39) |
V731D |
possibly damaging |
Het |
| Cdh3 |
G |
T |
8: 107,274,468 (GRCm39) |
|
probably null |
Het |
| Cntnap1 |
G |
A |
11: 101,069,142 (GRCm39) |
V199M |
probably damaging |
Het |
| Cntnap3 |
A |
T |
13: 64,905,225 (GRCm39) |
V852E |
probably damaging |
Het |
| Csmd1 |
A |
T |
8: 16,249,907 (GRCm39) |
S1024T |
probably damaging |
Het |
| Cyp3a25 |
T |
C |
5: 145,930,075 (GRCm39) |
|
probably benign |
Het |
| Dusp6 |
T |
A |
10: 99,101,881 (GRCm39) |
V289D |
probably damaging |
Het |
| Ecpas |
A |
T |
4: 58,811,731 (GRCm39) |
N1439K |
probably benign |
Het |
| Epha6 |
C |
T |
16: 59,639,300 (GRCm39) |
R858Q |
probably damaging |
Het |
| Flrt2 |
T |
A |
12: 95,746,478 (GRCm39) |
F272Y |
probably damaging |
Het |
| Gbf1 |
T |
A |
19: 46,258,242 (GRCm39) |
W846R |
probably damaging |
Het |
| Gtpbp2 |
T |
A |
17: 46,475,707 (GRCm39) |
V152E |
probably benign |
Het |
| Hmces |
A |
G |
6: 87,894,837 (GRCm39) |
|
probably null |
Het |
| Hsph1 |
A |
G |
5: 149,540,995 (GRCm39) |
S852P |
probably benign |
Het |
| Kat6b |
A |
C |
14: 21,676,846 (GRCm39) |
K394Q |
probably damaging |
Het |
| Kdr |
G |
A |
5: 76,122,500 (GRCm39) |
T475I |
probably benign |
Het |
| Klhl25 |
A |
G |
7: 75,516,368 (GRCm39) |
T425A |
probably benign |
Het |
| Klk1b8 |
T |
A |
7: 43,602,217 (GRCm39) |
C50S |
probably damaging |
Het |
| Kri1 |
T |
C |
9: 21,187,464 (GRCm39) |
Y343C |
probably damaging |
Het |
| Lamb1 |
T |
C |
12: 31,355,768 (GRCm39) |
S953P |
probably benign |
Het |
| Lpin1 |
A |
G |
12: 16,597,601 (GRCm39) |
V681A |
probably damaging |
Het |
| Lpin3 |
A |
G |
2: 160,743,581 (GRCm39) |
T508A |
probably benign |
Het |
| Moxd1 |
T |
A |
10: 24,158,598 (GRCm39) |
Y417* |
probably null |
Het |
| Mthfd1l |
T |
G |
10: 3,991,812 (GRCm39) |
I588S |
probably damaging |
Het |
| Myo5c |
C |
A |
9: 75,173,442 (GRCm39) |
N543K |
possibly damaging |
Het |
| Myo9a |
T |
A |
9: 59,791,883 (GRCm39) |
|
probably benign |
Het |
| Nme8 |
T |
C |
13: 19,842,996 (GRCm39) |
Y393C |
probably damaging |
Het |
| Nr2e1 |
T |
G |
10: 42,443,975 (GRCm39) |
N249T |
probably damaging |
Het |
| Pex11g |
A |
G |
8: 3,515,898 (GRCm39) |
V45A |
probably benign |
Het |
| Pkhd1 |
C |
A |
1: 20,279,484 (GRCm39) |
G2945W |
probably damaging |
Het |
| Plxnd1 |
A |
G |
6: 115,970,589 (GRCm39) |
F393S |
probably damaging |
Het |
| Ppp3cc |
A |
G |
14: 70,473,938 (GRCm39) |
V353A |
probably damaging |
Het |
| Prss16 |
T |
A |
13: 22,187,205 (GRCm39) |
Q455L |
probably damaging |
Het |
| Ptpn6 |
A |
T |
6: 124,698,171 (GRCm39) |
V524E |
probably damaging |
Het |
| Rnf31 |
C |
T |
14: 55,836,239 (GRCm39) |
L598F |
probably damaging |
Het |
| Sardh |
T |
G |
2: 27,115,003 (GRCm39) |
D550A |
probably benign |
Het |
| Serpinc1 |
T |
G |
1: 160,827,562 (GRCm39) |
I387S |
probably damaging |
Het |
| Sh3d19 |
A |
T |
3: 86,028,474 (GRCm39) |
D650V |
probably benign |
Het |
| Sipa1l2 |
T |
A |
8: 126,218,750 (GRCm39) |
T196S |
probably damaging |
Het |
| Slc25a46 |
T |
C |
18: 31,716,621 (GRCm39) |
T294A |
probably benign |
Het |
| Srrm2 |
T |
C |
17: 24,034,756 (GRCm39) |
|
probably benign |
Het |
| Steap2 |
T |
A |
5: 5,727,612 (GRCm39) |
N241I |
probably benign |
Het |
| Tcaf3 |
T |
C |
6: 42,573,594 (GRCm39) |
Y206C |
probably damaging |
Het |
| Tmem259 |
T |
A |
10: 79,814,297 (GRCm39) |
Q322L |
probably damaging |
Het |
| Tnni2 |
C |
A |
7: 141,997,166 (GRCm39) |
Q52K |
possibly damaging |
Het |
| Ttn |
A |
G |
2: 76,565,372 (GRCm39) |
V28285A |
possibly damaging |
Het |
| Uba7 |
T |
A |
9: 107,853,352 (GRCm39) |
S99R |
probably benign |
Het |
| Ubxn2b |
A |
T |
4: 6,216,071 (GRCm39) |
K331N |
probably damaging |
Het |
| Usp50 |
G |
A |
2: 126,611,864 (GRCm39) |
T232I |
probably damaging |
Het |
| Vmn2r116 |
G |
A |
17: 23,604,973 (GRCm39) |
M95I |
probably benign |
Het |
| Vmn2r116 |
T |
A |
17: 23,604,978 (GRCm39) |
L97Q |
probably damaging |
Het |
| Vmn2r24 |
A |
T |
6: 123,763,843 (GRCm39) |
N240I |
possibly damaging |
Het |
| Vmn2r72 |
T |
C |
7: 85,399,901 (GRCm39) |
R383G |
probably benign |
Het |
|
| Other mutations in Rap1gap |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00771:Rap1gap
|
APN |
4 |
137,443,835 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL01810:Rap1gap
|
APN |
4 |
137,443,466 (GRCm39) |
missense |
probably benign |
0.07 |
|
IGL01944:Rap1gap
|
APN |
4 |
137,452,931 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02117:Rap1gap
|
APN |
4 |
137,454,355 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02271:Rap1gap
|
APN |
4 |
137,445,317 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02590:Rap1gap
|
APN |
4 |
137,447,611 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02626:Rap1gap
|
APN |
4 |
137,454,364 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL03211:Rap1gap
|
APN |
4 |
137,443,157 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0243:Rap1gap
|
UTSW |
4 |
137,446,662 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1239:Rap1gap
|
UTSW |
4 |
137,445,307 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1246:Rap1gap
|
UTSW |
4 |
137,439,405 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R2264:Rap1gap
|
UTSW |
4 |
137,455,034 (GRCm39) |
missense |
probably benign |
|
|
R2935:Rap1gap
|
UTSW |
4 |
137,452,042 (GRCm39) |
missense |
probably benign |
0.19 |
|
R3840:Rap1gap
|
UTSW |
4 |
137,444,758 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3841:Rap1gap
|
UTSW |
4 |
137,444,758 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4619:Rap1gap
|
UTSW |
4 |
137,443,422 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4821:Rap1gap
|
UTSW |
4 |
137,439,440 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4998:Rap1gap
|
UTSW |
4 |
137,455,595 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R5061:Rap1gap
|
UTSW |
4 |
137,447,744 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5800:Rap1gap
|
UTSW |
4 |
137,447,688 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6259:Rap1gap
|
UTSW |
4 |
137,409,068 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7082:Rap1gap
|
UTSW |
4 |
137,446,247 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7098:Rap1gap
|
UTSW |
4 |
137,443,393 (GRCm39) |
splice site |
probably null |
|
|
R7234:Rap1gap
|
UTSW |
4 |
137,455,851 (GRCm39) |
nonsense |
probably null |
|
|
R7580:Rap1gap
|
UTSW |
4 |
137,447,293 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R8097:Rap1gap
|
UTSW |
4 |
137,455,597 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8196:Rap1gap
|
UTSW |
4 |
137,445,275 (GRCm39) |
missense |
probably benign |
0.07 |
|
R8278:Rap1gap
|
UTSW |
4 |
137,444,748 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9022:Rap1gap
|
UTSW |
4 |
137,445,309 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9157:Rap1gap
|
UTSW |
4 |
137,444,742 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9290:Rap1gap
|
UTSW |
4 |
137,446,222 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Posted On |
2015-04-16 |
Incidental Mutation