Incidental Mutation 'R6322:Rgl1'
| ID |
510132 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Rgl1
|
| Ensembl Gene |
ENSMUSG00000026482 |
| Gene Name |
ral guanine nucleotide dissociation stimulator,-like 1 |
| Synonyms |
Rgl |
| MMRRC Submission |
044476-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.350)
|
| Stock # |
R6322 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
1 |
| Chromosomal Location |
152392513-152642089 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 152428186 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Valine
at position 348
(I348V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000107490
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000027760]
[ENSMUST00000111857]
[ENSMUST00000111859]
|
| AlphaFold |
Q60695 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000027760
AA Change: I313V
PolyPhen 2
Score 0.906 (Sensitivity: 0.82; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000027760
Gene: ENSMUSG00000026482
AA Change: I313V
| Domain | Start | End | E-Value | Type |
|---|
|
RasGEFN
|
64 |
196 |
5.86e-39 |
SMART |
|
RasGEF
|
228 |
502 |
9.56e-116 |
SMART |
|
Blast:RasGEF
|
522 |
582 |
6e-8 |
BLAST |
|
low complexity region
|
585 |
596 |
N/A |
INTRINSIC |
|
low complexity region
|
627 |
637 |
N/A |
INTRINSIC |
|
RA
|
648 |
735 |
1.7e-25 |
SMART |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000111857
AA Change: I311V
PolyPhen 2
Score 0.956 (Sensitivity: 0.79; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000107488
Gene: ENSMUSG00000026482
AA Change: I311V
| Domain | Start | End | E-Value | Type |
|---|
|
RasGEFN
|
62 |
194 |
5.86e-39 |
SMART |
|
RasGEF
|
226 |
500 |
9.56e-116 |
SMART |
|
Blast:RasGEF
|
520 |
580 |
7e-8 |
BLAST |
|
low complexity region
|
583 |
594 |
N/A |
INTRINSIC |
|
low complexity region
|
625 |
635 |
N/A |
INTRINSIC |
|
RA
|
646 |
733 |
1.7e-25 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000111859
AA Change: I348V
PolyPhen 2
Score 0.979 (Sensitivity: 0.75; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000107490
Gene: ENSMUSG00000026482
AA Change: I348V
| Domain | Start | End | E-Value | Type |
|---|
|
RasGEFN
|
99 |
231 |
5.86e-39 |
SMART |
|
RasGEF
|
263 |
537 |
9.56e-116 |
SMART |
|
Blast:RasGEF
|
557 |
617 |
6e-8 |
BLAST |
|
low complexity region
|
620 |
631 |
N/A |
INTRINSIC |
|
low complexity region
|
662 |
672 |
N/A |
INTRINSIC |
|
RA
|
683 |
770 |
1.7e-25 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000188395
|
| Meta Mutation Damage Score |
0.5397 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.3%
- 20x: 97.7%
|
| Validation Efficiency |
98% (51/52) |
| MGI Phenotype |
FUNCTION: This gene encodes a member of the Ras-like (Ral) -selective guanine nucleotide exchange factor (RalGEF) family of small GTPase activators which function both as downstream effectors of activated Ras GTPase and as regulators of certain Ral GTPases in the RalGEF - Ral GTPase signaling pathway. The encoded protein, like other RalGEFs, has an N-terminal ras exchanger motif domain, a catalytic CDC25 homology domain, and a C-terminal ras binding domain that stimulates guanine nucleotide exchange when bound to a Ral GTPase. RalGEF family members bridge the Ras and Ral signaling pathways and are thought to play a role in oncogenic transformation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 51 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4932414N04Rik |
T |
C |
2: 68,559,843 (GRCm39) |
V211A |
probably benign |
Het |
| Adora3 |
G |
A |
3: 105,814,760 (GRCm39) |
R170H |
probably benign |
Het |
| Aldh1l1 |
T |
C |
6: 90,539,680 (GRCm39) |
I203T |
probably benign |
Het |
| Alox12b |
T |
C |
11: 69,049,199 (GRCm39) |
Y83H |
possibly damaging |
Het |
| Atcay |
A |
T |
10: 81,049,125 (GRCm39) |
I159K |
probably damaging |
Het |
| Blvra |
A |
G |
2: 126,922,459 (GRCm39) |
|
probably benign |
Het |
| Catspere2 |
T |
A |
1: 177,845,296 (GRCm39) |
Y105* |
probably null |
Het |
| Celsr2 |
A |
G |
3: 108,319,890 (GRCm39) |
F974S |
probably damaging |
Het |
| Cfap44 |
C |
T |
16: 44,254,029 (GRCm39) |
R918* |
probably null |
Het |
| Cpa6 |
T |
A |
1: 10,547,346 (GRCm39) |
R181S |
possibly damaging |
Het |
| Dlg1 |
A |
G |
16: 31,675,297 (GRCm39) |
N730D |
probably damaging |
Het |
| Eif2ak1 |
A |
G |
5: 143,835,913 (GRCm39) |
T535A |
probably benign |
Het |
| Fam13c |
A |
T |
10: 70,334,721 (GRCm39) |
D149V |
probably damaging |
Het |
| Fam171a1 |
G |
A |
2: 3,227,392 (GRCm39) |
V717I |
probably benign |
Het |
| Fchsd1 |
A |
G |
18: 38,098,753 (GRCm39) |
V290A |
probably benign |
Het |
| Gm10549 |
C |
A |
18: 33,597,358 (GRCm39) |
|
probably benign |
Het |
| Gm11595 |
G |
A |
11: 99,663,381 (GRCm39) |
R100C |
unknown |
Het |
| Gm15446 |
A |
T |
5: 110,091,383 (GRCm39) |
H545L |
probably damaging |
Het |
| Heatr9 |
T |
G |
11: 83,407,538 (GRCm39) |
K215T |
possibly damaging |
Het |
| Hfe |
T |
A |
13: 23,889,879 (GRCm39) |
H210L |
probably damaging |
Het |
| Lama2 |
T |
C |
10: 27,066,543 (GRCm39) |
T1113A |
probably damaging |
Het |
| Lipe |
A |
T |
7: 25,079,961 (GRCm39) |
V686E |
probably damaging |
Het |
| Map3k20 |
T |
G |
2: 72,263,814 (GRCm39) |
L488V |
possibly damaging |
Het |
| Moxd1 |
C |
T |
10: 24,160,709 (GRCm39) |
T454I |
probably damaging |
Het |
| Mrpl58 |
C |
T |
11: 115,301,492 (GRCm39) |
R189* |
probably null |
Het |
| Myl10 |
G |
C |
5: 136,726,825 (GRCm39) |
V70L |
probably benign |
Het |
| Nkx1-1 |
T |
C |
5: 33,588,389 (GRCm39) |
N300D |
probably damaging |
Het |
| Nrm |
A |
T |
17: 36,175,605 (GRCm39) |
Q237L |
possibly damaging |
Het |
| Numa1 |
T |
C |
7: 101,650,127 (GRCm39) |
L1286P |
probably damaging |
Het |
| Or4f4-ps1 |
T |
C |
2: 111,329,729 (GRCm39) |
F44S |
possibly damaging |
Het |
| Pappa |
C |
A |
4: 65,232,896 (GRCm39) |
A1345D |
probably damaging |
Het |
| Pds5a |
T |
C |
5: 65,854,177 (GRCm39) |
I22V |
probably benign |
Het |
| Phf21b |
C |
A |
15: 84,671,580 (GRCm39) |
R438L |
possibly damaging |
Het |
| Pik3r5 |
T |
C |
11: 68,383,567 (GRCm39) |
L462P |
probably benign |
Het |
| Plagl2 |
T |
C |
2: 153,073,806 (GRCm39) |
E365G |
probably benign |
Het |
| Plxna2 |
A |
G |
1: 194,436,675 (GRCm39) |
Y677C |
possibly damaging |
Het |
| Pramel13 |
A |
G |
4: 144,119,475 (GRCm39) |
M364T |
probably benign |
Het |
| Prkcd |
C |
A |
14: 30,321,620 (GRCm39) |
G410W |
probably damaging |
Het |
| Rnmt |
C |
T |
18: 68,452,285 (GRCm39) |
P386S |
probably damaging |
Het |
| Rtn3 |
G |
A |
19: 7,435,503 (GRCm39) |
P163L |
possibly damaging |
Het |
| Sfxn1 |
T |
C |
13: 54,258,869 (GRCm39) |
C275R |
possibly damaging |
Het |
| Sh2b2 |
A |
G |
5: 136,253,042 (GRCm39) |
S377P |
probably damaging |
Het |
| Sh3bp1 |
C |
T |
15: 78,795,715 (GRCm39) |
P615S |
probably damaging |
Het |
| Simc1 |
T |
C |
13: 54,698,382 (GRCm39) |
L1334S |
probably damaging |
Het |
| Slc9a2 |
C |
A |
1: 40,781,813 (GRCm39) |
Y347* |
probably null |
Het |
| Snapc5 |
T |
A |
9: 64,089,455 (GRCm39) |
I71K |
probably damaging |
Het |
| Tmem161a |
T |
C |
8: 70,634,764 (GRCm39) |
F447S |
probably damaging |
Het |
| Tns3 |
A |
G |
11: 8,442,147 (GRCm39) |
C739R |
probably benign |
Het |
| Trappc11 |
A |
T |
8: 47,983,808 (GRCm39) |
V28D |
possibly damaging |
Het |
| Ubr3 |
C |
T |
2: 69,786,429 (GRCm39) |
Q848* |
probably null |
Het |
| Zbtb17 |
G |
A |
4: 141,190,694 (GRCm39) |
G171S |
probably benign |
Het |
|
| Other mutations in Rgl1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00569:Rgl1
|
APN |
1 |
152,447,368 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL01065:Rgl1
|
APN |
1 |
152,394,893 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01390:Rgl1
|
APN |
1 |
152,447,339 (GRCm39) |
splice site |
probably benign |
|
|
IGL01726:Rgl1
|
APN |
1 |
152,394,904 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01837:Rgl1
|
APN |
1 |
152,424,901 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02019:Rgl1
|
APN |
1 |
152,404,220 (GRCm39) |
splice site |
probably benign |
|
|
IGL02369:Rgl1
|
APN |
1 |
152,409,357 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0240:Rgl1
|
UTSW |
1 |
152,430,175 (GRCm39) |
unclassified |
probably benign |
|
|
R0255:Rgl1
|
UTSW |
1 |
152,428,347 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0562:Rgl1
|
UTSW |
1 |
152,415,696 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0648:Rgl1
|
UTSW |
1 |
152,412,016 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0734:Rgl1
|
UTSW |
1 |
152,430,051 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1187:Rgl1
|
UTSW |
1 |
152,420,184 (GRCm39) |
missense |
probably benign |
0.14 |
|
R1522:Rgl1
|
UTSW |
1 |
152,462,284 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1595:Rgl1
|
UTSW |
1 |
152,550,774 (GRCm39) |
splice site |
probably benign |
|
|
R1634:Rgl1
|
UTSW |
1 |
152,400,523 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1661:Rgl1
|
UTSW |
1 |
152,409,326 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1665:Rgl1
|
UTSW |
1 |
152,409,326 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1964:Rgl1
|
UTSW |
1 |
152,424,855 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2291:Rgl1
|
UTSW |
1 |
152,412,032 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4272:Rgl1
|
UTSW |
1 |
152,412,040 (GRCm39) |
missense |
probably benign |
0.13 |
|
R4668:Rgl1
|
UTSW |
1 |
152,397,122 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4669:Rgl1
|
UTSW |
1 |
152,397,122 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4747:Rgl1
|
UTSW |
1 |
152,400,450 (GRCm39) |
nonsense |
probably null |
|
|
R4830:Rgl1
|
UTSW |
1 |
152,430,081 (GRCm39) |
missense |
probably benign |
0.11 |
|
R4853:Rgl1
|
UTSW |
1 |
152,433,325 (GRCm39) |
missense |
probably benign |
0.07 |
|
R4969:Rgl1
|
UTSW |
1 |
152,424,813 (GRCm39) |
splice site |
probably null |
|
|
R5778:Rgl1
|
UTSW |
1 |
152,428,172 (GRCm39) |
missense |
probably benign |
0.05 |
|
R5979:Rgl1
|
UTSW |
1 |
152,433,244 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6180:Rgl1
|
UTSW |
1 |
152,394,923 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6183:Rgl1
|
UTSW |
1 |
152,462,321 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R6678:Rgl1
|
UTSW |
1 |
152,400,475 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6759:Rgl1
|
UTSW |
1 |
152,409,281 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6892:Rgl1
|
UTSW |
1 |
152,415,691 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7290:Rgl1
|
UTSW |
1 |
152,420,146 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R7363:Rgl1
|
UTSW |
1 |
152,394,914 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7610:Rgl1
|
UTSW |
1 |
152,428,371 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7774:Rgl1
|
UTSW |
1 |
152,430,101 (GRCm39) |
missense |
probably benign |
|
|
R8140:Rgl1
|
UTSW |
1 |
152,433,252 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9188:Rgl1
|
UTSW |
1 |
152,394,922 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9190:Rgl1
|
UTSW |
1 |
152,428,362 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R9297:Rgl1
|
UTSW |
1 |
152,400,454 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R9318:Rgl1
|
UTSW |
1 |
152,400,454 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R9491:Rgl1
|
UTSW |
1 |
152,424,869 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9570:Rgl1
|
UTSW |
1 |
152,430,082 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R9610:Rgl1
|
UTSW |
1 |
152,397,115 (GRCm39) |
missense |
probably benign |
0.13 |
|
R9640:Rgl1
|
UTSW |
1 |
152,397,142 (GRCm39) |
missense |
probably damaging |
1.00 |
|
RF005:Rgl1
|
UTSW |
1 |
152,397,114 (GRCm39) |
missense |
probably benign |
|
|
Z1088:Rgl1
|
UTSW |
1 |
152,550,771 (GRCm39) |
start gained |
probably benign |
|
|
| Predicted Primers |
PCR Primer
(F):5'- TGTGCCTTCCTCTACACAAGTG -3'
(R):5'- CGTGTGTTCCTGATGTCAATTC -3'
Sequencing Primer
(F):5'- GCCTTCCTCTACACAAGTGTTAGAC -3'
(R):5'- AGGTAGTGCCTCACCATTGC -3'
|
| Posted On |
2018-04-02 |
Incidental Mutation