Incidental Mutation 'R4592:Rab3gap1'
| ID |
342874 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Rab3gap1
|
| Ensembl Gene |
ENSMUSG00000036104 |
| Gene Name |
RAB3 GTPase activating protein subunit 1 |
| Synonyms |
1700003B17Rik, 4732493F09Rik, p130 |
| MMRRC Submission |
041808-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.279)
|
| Stock # |
R4592 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
1 |
| Chromosomal Location |
127796510-127871605 bp(+) (GRCm39) |
| Type of Mutation |
intron |
| DNA Base Change (assembly) |
C to A
at 127852996 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000148357
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000037649]
[ENSMUST00000212506]
|
| AlphaFold |
Q80UJ7 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000037649
|
| SMART Domains |
Protein: ENSMUSP00000042070
Gene: ENSMUSG00000036104
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
254 |
263 |
N/A |
INTRINSIC |
|
low complexity region
|
574 |
587 |
N/A |
INTRINSIC |
|
Pfam:Rab3-GTPase_cat
|
612 |
769 |
2.9e-67 |
PFAM |
|
low complexity region
|
856 |
868 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000189259
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000212506
|
| Meta Mutation Damage Score |
0.0898 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 97.1%
- 20x: 94.8%
|
| Validation Efficiency |
98% (64/65) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes the catalytic subunit of a Rab GTPase activating protein. The encoded protein forms a heterodimer with a non-catalytic subunit to specifically regulate the activity of members of the Rab3 subfamily of small G proteins. This protein mediates the hydrolysis of GTP bound Rab3 to the GDP bound form. Mutations in this gene are associated with Warburg micro syndrome. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Feb 2010]
PHENOTYPE: Mice homozygous for a null mutation display abnormal synaptic transmission but have normal gross brain morphology. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 60 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4933430I17Rik |
T |
A |
4: 62,457,164 (GRCm39) |
V161E |
possibly damaging |
Het |
| Arhgap40 |
T |
C |
2: 158,388,629 (GRCm39) |
V521A |
possibly damaging |
Het |
| Atrn |
T |
C |
2: 130,841,050 (GRCm39) |
|
probably benign |
Het |
| Casp12 |
T |
C |
9: 5,352,923 (GRCm39) |
|
probably benign |
Het |
| Cenpf |
G |
A |
1: 189,411,230 (GRCm39) |
T318M |
probably damaging |
Het |
| Cfap119 |
C |
T |
7: 127,184,663 (GRCm39) |
R172H |
probably benign |
Het |
| Clcn2 |
T |
C |
16: 20,527,892 (GRCm39) |
K525E |
probably damaging |
Het |
| Cntln |
A |
G |
4: 84,889,419 (GRCm39) |
T301A |
probably benign |
Het |
| Crat |
T |
C |
2: 30,305,378 (GRCm39) |
|
probably benign |
Het |
| Cul5 |
A |
G |
9: 53,545,027 (GRCm39) |
|
probably benign |
Het |
| Cxcl14 |
A |
T |
13: 56,443,708 (GRCm39) |
I34N |
probably damaging |
Het |
| Cyp2b19 |
A |
G |
7: 26,470,819 (GRCm39) |
I487V |
probably benign |
Het |
| Cyp4a10 |
T |
A |
4: 115,386,690 (GRCm39) |
F446I |
probably damaging |
Het |
| D430041D05Rik |
T |
A |
2: 104,063,824 (GRCm39) |
M659L |
possibly damaging |
Het |
| Dclk3 |
T |
C |
9: 111,296,963 (GRCm39) |
F169S |
probably damaging |
Het |
| Ddx52 |
T |
C |
11: 83,848,306 (GRCm39) |
I532T |
probably damaging |
Het |
| Dnm1 |
T |
C |
2: 32,226,023 (GRCm39) |
D352G |
probably damaging |
Het |
| Eif4g2 |
T |
C |
7: 110,677,509 (GRCm39) |
E174G |
probably damaging |
Het |
| Enpp6 |
G |
T |
8: 47,546,067 (GRCm39) |
V386L |
probably damaging |
Het |
| Entr1 |
C |
A |
2: 26,278,909 (GRCm39) |
|
probably benign |
Het |
| Eps15l1 |
T |
C |
8: 73,095,238 (GRCm39) |
D904G |
probably damaging |
Het |
| Esrrb |
A |
G |
12: 86,565,604 (GRCm39) |
Y356C |
probably damaging |
Het |
| Flt3 |
A |
T |
5: 147,291,509 (GRCm39) |
S619T |
possibly damaging |
Het |
| Fndc7 |
A |
T |
3: 108,766,218 (GRCm39) |
C716S |
probably damaging |
Het |
| Gm26996 |
T |
A |
6: 130,556,448 (GRCm39) |
|
noncoding transcript |
Het |
| Grik2 |
A |
T |
10: 49,298,711 (GRCm39) |
F50I |
possibly damaging |
Het |
| Guf1 |
T |
C |
5: 69,723,786 (GRCm39) |
V367A |
possibly damaging |
Het |
| Hspg2 |
C |
T |
4: 137,246,251 (GRCm39) |
R1010C |
probably damaging |
Het |
| Ifnar2 |
T |
C |
16: 91,188,684 (GRCm39) |
V55A |
probably benign |
Het |
| Impg1 |
T |
A |
9: 80,322,907 (GRCm39) |
I33F |
probably benign |
Het |
| Ltbp4 |
A |
C |
7: 27,024,608 (GRCm39) |
V674G |
probably damaging |
Het |
| Mroh2b |
T |
A |
15: 4,947,772 (GRCm39) |
L529H |
probably damaging |
Het |
| Negr1 |
T |
C |
3: 156,914,023 (GRCm39) |
|
probably benign |
Het |
| Neurog3 |
A |
G |
10: 61,969,599 (GRCm39) |
T25A |
probably damaging |
Het |
| Or10v1 |
T |
C |
19: 11,874,126 (GRCm39) |
V247A |
probably benign |
Het |
| Or4a69 |
T |
A |
2: 89,313,100 (GRCm39) |
K126N |
probably damaging |
Het |
| Or51h1 |
A |
C |
7: 102,308,685 (GRCm39) |
Y219S |
probably damaging |
Het |
| Or5k17 |
T |
C |
16: 58,746,455 (GRCm39) |
T160A |
probably benign |
Het |
| Pax8 |
T |
A |
2: 24,333,201 (GRCm39) |
|
probably benign |
Het |
| Pcsk6 |
A |
C |
7: 65,581,480 (GRCm39) |
I254L |
possibly damaging |
Het |
| Pde3a |
A |
G |
6: 141,404,942 (GRCm39) |
K389R |
probably benign |
Het |
| Rbck1 |
G |
A |
2: 152,160,653 (GRCm39) |
Q428* |
probably null |
Het |
| Rptor |
A |
G |
11: 119,689,666 (GRCm39) |
D321G |
probably null |
Het |
| Sall2 |
C |
A |
14: 52,551,260 (GRCm39) |
R643L |
probably damaging |
Het |
| Skp1 |
T |
C |
11: 52,134,446 (GRCm39) |
I59T |
possibly damaging |
Het |
| Slc23a3 |
T |
G |
1: 75,105,200 (GRCm39) |
N456T |
probably damaging |
Het |
| Slc4a7 |
G |
A |
14: 14,778,850 (GRCm38) |
G920S |
probably damaging |
Het |
| Smarcd3 |
T |
C |
5: 24,797,802 (GRCm39) |
I467V |
probably benign |
Het |
| Spata31d1c |
C |
T |
13: 65,183,874 (GRCm39) |
A472V |
probably damaging |
Het |
| Spmap1 |
A |
G |
11: 97,662,441 (GRCm39) |
S144P |
probably damaging |
Het |
| Srsf6 |
T |
C |
2: 162,773,643 (GRCm39) |
I18T |
probably damaging |
Het |
| Stom |
C |
T |
2: 35,213,758 (GRCm39) |
G80D |
probably damaging |
Het |
| Svep1 |
A |
T |
4: 58,084,028 (GRCm39) |
Y1915N |
possibly damaging |
Het |
| Tmf1 |
C |
T |
6: 97,150,361 (GRCm39) |
V449I |
probably benign |
Het |
| Triobp |
C |
T |
15: 78,851,295 (GRCm39) |
A483V |
probably benign |
Het |
| Vdac1 |
G |
A |
11: 52,265,799 (GRCm39) |
|
probably null |
Het |
| Vmn2r75 |
T |
G |
7: 85,815,494 (GRCm39) |
E123D |
probably benign |
Het |
| Vmn2r79 |
T |
A |
7: 86,653,319 (GRCm39) |
V528D |
possibly damaging |
Het |
| Zdbf2 |
T |
G |
1: 63,345,750 (GRCm39) |
N1376K |
possibly damaging |
Het |
| Zeb1os1 |
T |
C |
18: 5,525,375 (GRCm39) |
|
noncoding transcript |
Het |
|
| Other mutations in Rab3gap1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01090:Rab3gap1
|
APN |
1 |
127,858,124 (GRCm39) |
splice site |
probably benign |
|
|
IGL01467:Rab3gap1
|
APN |
1 |
127,858,121 (GRCm39) |
splice site |
probably null |
|
|
IGL01554:Rab3gap1
|
APN |
1 |
127,855,745 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
IGL01773:Rab3gap1
|
APN |
1 |
127,845,958 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
IGL01866:Rab3gap1
|
APN |
1 |
127,818,817 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02078:Rab3gap1
|
APN |
1 |
127,796,652 (GRCm39) |
splice site |
probably benign |
|
|
IGL02251:Rab3gap1
|
APN |
1 |
127,865,237 (GRCm39) |
missense |
probably benign |
0.25 |
|
IGL02268:Rab3gap1
|
APN |
1 |
127,796,695 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02274:Rab3gap1
|
APN |
1 |
127,866,817 (GRCm39) |
missense |
probably benign |
|
|
IGL02372:Rab3gap1
|
APN |
1 |
127,847,298 (GRCm39) |
splice site |
probably benign |
|
|
IGL02399:Rab3gap1
|
APN |
1 |
127,855,840 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
IGL02629:Rab3gap1
|
APN |
1 |
127,837,600 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02700:Rab3gap1
|
APN |
1 |
127,866,342 (GRCm39) |
missense |
probably benign |
0.06 |
|
IGL02748:Rab3gap1
|
APN |
1 |
127,865,198 (GRCm39) |
missense |
probably damaging |
0.99 |
|
little_bighorn
|
UTSW |
1 |
127,818,835 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL03048:Rab3gap1
|
UTSW |
1 |
127,865,214 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0828:Rab3gap1
|
UTSW |
1 |
127,865,922 (GRCm39) |
splice site |
probably benign |
|
|
R1382:Rab3gap1
|
UTSW |
1 |
127,870,333 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R1729:Rab3gap1
|
UTSW |
1 |
127,870,223 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1809:Rab3gap1
|
UTSW |
1 |
127,862,251 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1990:Rab3gap1
|
UTSW |
1 |
127,870,166 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R2001:Rab3gap1
|
UTSW |
1 |
127,831,456 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R2041:Rab3gap1
|
UTSW |
1 |
127,865,727 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R3955:Rab3gap1
|
UTSW |
1 |
127,862,254 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4192:Rab3gap1
|
UTSW |
1 |
127,853,207 (GRCm39) |
intron |
probably benign |
|
|
R4243:Rab3gap1
|
UTSW |
1 |
127,865,304 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4244:Rab3gap1
|
UTSW |
1 |
127,865,304 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4354:Rab3gap1
|
UTSW |
1 |
127,843,378 (GRCm39) |
missense |
probably benign |
0.02 |
|
R4622:Rab3gap1
|
UTSW |
1 |
127,870,156 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4738:Rab3gap1
|
UTSW |
1 |
127,862,173 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4917:Rab3gap1
|
UTSW |
1 |
127,816,914 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R4918:Rab3gap1
|
UTSW |
1 |
127,816,914 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R5090:Rab3gap1
|
UTSW |
1 |
127,843,415 (GRCm39) |
missense |
probably benign |
0.35 |
|
R5197:Rab3gap1
|
UTSW |
1 |
127,816,931 (GRCm39) |
missense |
probably benign |
|
|
R5310:Rab3gap1
|
UTSW |
1 |
127,870,110 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R5580:Rab3gap1
|
UTSW |
1 |
127,858,727 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6670:Rab3gap1
|
UTSW |
1 |
127,858,512 (GRCm39) |
missense |
probably benign |
|
|
R6825:Rab3gap1
|
UTSW |
1 |
127,858,158 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7024:Rab3gap1
|
UTSW |
1 |
127,818,835 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7274:Rab3gap1
|
UTSW |
1 |
127,855,249 (GRCm39) |
missense |
probably benign |
|
|
R7380:Rab3gap1
|
UTSW |
1 |
127,865,727 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R7583:Rab3gap1
|
UTSW |
1 |
127,858,612 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7654:Rab3gap1
|
UTSW |
1 |
127,837,652 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8309:Rab3gap1
|
UTSW |
1 |
127,837,655 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R8392:Rab3gap1
|
UTSW |
1 |
127,866,370 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8864:Rab3gap1
|
UTSW |
1 |
127,837,630 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9190:Rab3gap1
|
UTSW |
1 |
127,858,495 (GRCm39) |
missense |
probably benign |
|
|
R9799:Rab3gap1
|
UTSW |
1 |
127,858,489 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- AACTTTGTGATTTCTCGGCATC -3'
(R):5'- AATCCAGTGCTGCCATAAAGAAG -3'
Sequencing Primer
(F):5'- CGGCATCCATGTTTCATGTAAAGC -3'
(R):5'- TGAGGCGGCTACTTACCAAG -3'
|
| Posted On |
2015-09-24 |
Incidental Mutation