Incidental Mutation 'R4680:Rab11fip2'
| ID |
350007 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Rab11fip2
|
| Ensembl Gene |
ENSMUSG00000040022 |
| Gene Name |
RAB11 family interacting protein 2 (class I) |
| Synonyms |
nRip11, Rab11-FIP2, 4930470G04Rik, A830046J09Rik |
| MMRRC Submission |
041933-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.180)
|
| Stock # |
R4680 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
19 |
| Chromosomal Location |
59891316-59932086 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 59924452 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Asparagine to Serine
at position 284
(N284S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000133151
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000051996]
[ENSMUST00000170819]
[ENSMUST00000171986]
|
| AlphaFold |
G3XA57 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000051996
AA Change: N284S
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000059978
Gene: ENSMUSG00000040022
AA Change: N284S
| Domain | Start | End | E-Value | Type |
|---|
|
C2
|
14 |
117 |
1.75e-11 |
SMART |
|
low complexity region
|
344 |
358 |
N/A |
INTRINSIC |
|
Pfam:RBD-FIP
|
452 |
499 |
3.7e-24 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000170819
AA Change: N284S
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000133151
Gene: ENSMUSG00000040022
AA Change: N284S
| Domain | Start | End | E-Value | Type |
|---|
|
C2
|
14 |
117 |
1.75e-11 |
SMART |
|
low complexity region
|
344 |
358 |
N/A |
INTRINSIC |
|
Pfam:RBD-FIP
|
452 |
499 |
3.5e-24 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000171986
AA Change: N142S
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000128813
Gene: ENSMUSG00000040022
AA Change: N142S
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
202 |
216 |
N/A |
INTRINSIC |
|
Pfam:RBD-FIP
|
310 |
357 |
3.9e-24 |
PFAM |
|
| Meta Mutation Damage Score |
0.0682 |
| Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.5%
- 10x: 96.9%
- 20x: 94.3%
|
| Validation Efficiency |
96% (48/50) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 38 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4921509C19Rik |
A |
T |
2: 151,315,390 (GRCm39) |
L96Q |
probably damaging |
Het |
| 4931414P19Rik |
T |
C |
14: 54,822,533 (GRCm39) |
Y368C |
probably damaging |
Het |
| Acin1 |
T |
C |
14: 54,924,215 (GRCm39) |
N8S |
probably benign |
Het |
| Aspm |
T |
C |
1: 139,408,409 (GRCm39) |
V2432A |
probably benign |
Het |
| Atf2 |
A |
T |
2: 73,659,025 (GRCm39) |
|
probably null |
Het |
| B3gnt2 |
A |
G |
11: 22,787,105 (GRCm39) |
S28P |
probably damaging |
Het |
| Chil5 |
A |
G |
3: 105,942,191 (GRCm39) |
|
probably benign |
Het |
| Crybg2 |
CTTCCAGAGCCATGGACCCATCTTTTCCA |
CTTCCA |
4: 133,800,029 (GRCm39) |
|
probably null |
Het |
| Dennd3 |
A |
T |
15: 73,405,225 (GRCm39) |
H326L |
possibly damaging |
Het |
| Dysf |
C |
A |
6: 84,074,697 (GRCm39) |
D499E |
probably damaging |
Het |
| Eprs1 |
T |
C |
1: 185,118,475 (GRCm39) |
V461A |
possibly damaging |
Het |
| Fhad1 |
G |
A |
4: 141,738,858 (GRCm39) |
Q31* |
probably null |
Het |
| Gpr26 |
A |
G |
7: 131,576,082 (GRCm39) |
T249A |
probably benign |
Het |
| Gtf2ird1 |
T |
A |
5: 134,386,735 (GRCm39) |
M958L |
probably damaging |
Het |
| Kat2b-ps |
A |
G |
5: 93,539,299 (GRCm39) |
|
noncoding transcript |
Het |
| Kdm2b |
A |
T |
5: 123,072,849 (GRCm39) |
V343E |
probably damaging |
Het |
| Lipi |
A |
G |
16: 75,362,417 (GRCm39) |
|
probably null |
Het |
| Ltb4r1 |
T |
C |
14: 56,004,925 (GRCm39) |
F76S |
probably damaging |
Het |
| Msantd2 |
A |
G |
9: 37,434,387 (GRCm39) |
Y209C |
probably damaging |
Het |
| Nid1 |
G |
A |
13: 13,647,437 (GRCm39) |
C401Y |
probably damaging |
Het |
| Obox1 |
A |
T |
7: 15,290,089 (GRCm39) |
N144I |
probably damaging |
Het |
| Or14j7 |
T |
C |
17: 38,234,813 (GRCm39) |
S119P |
probably damaging |
Het |
| Or8h9 |
T |
C |
2: 86,789,665 (GRCm39) |
I46V |
possibly damaging |
Het |
| Or8k20 |
T |
A |
2: 86,106,517 (GRCm39) |
I105F |
possibly damaging |
Het |
| Plec |
T |
C |
15: 76,064,775 (GRCm39) |
E1630G |
unknown |
Het |
| Ppp2r5e |
C |
T |
12: 75,516,533 (GRCm39) |
R218Q |
probably damaging |
Het |
| Prkdc |
A |
G |
16: 15,589,894 (GRCm39) |
T2586A |
probably benign |
Het |
| Ptprj |
T |
C |
2: 90,290,840 (GRCm39) |
N633S |
probably benign |
Het |
| Rlig1 |
T |
C |
10: 100,414,243 (GRCm39) |
I139V |
probably benign |
Het |
| Ropn1 |
A |
G |
16: 34,497,675 (GRCm39) |
Q189R |
possibly damaging |
Het |
| Rwdd2b |
A |
G |
16: 87,233,950 (GRCm39) |
|
probably null |
Het |
| Ryr2 |
A |
T |
13: 11,610,119 (GRCm39) |
S4236T |
probably benign |
Het |
| Sigmar1 |
A |
G |
4: 41,741,251 (GRCm39) |
M1T |
probably null |
Het |
| Sncg |
T |
A |
14: 34,095,268 (GRCm39) |
N79I |
probably benign |
Het |
| Traf3ip2 |
C |
T |
10: 39,515,256 (GRCm39) |
P345S |
possibly damaging |
Het |
| Ttn |
C |
T |
2: 76,763,021 (GRCm39) |
G3213S |
probably damaging |
Het |
| Uqcrc1 |
G |
A |
9: 108,776,929 (GRCm39) |
R77H |
probably damaging |
Het |
| Vps13d |
A |
C |
4: 144,835,080 (GRCm39) |
L2756R |
possibly damaging |
Het |
|
| Other mutations in Rab11fip2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02883:Rab11fip2
|
APN |
19 |
59,895,430 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0081:Rab11fip2
|
UTSW |
19 |
59,895,567 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R0466:Rab11fip2
|
UTSW |
19 |
59,894,675 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R1690:Rab11fip2
|
UTSW |
19 |
59,925,732 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1718:Rab11fip2
|
UTSW |
19 |
59,924,081 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1884:Rab11fip2
|
UTSW |
19 |
59,925,762 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4196:Rab11fip2
|
UTSW |
19 |
59,924,213 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4746:Rab11fip2
|
UTSW |
19 |
59,925,542 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4934:Rab11fip2
|
UTSW |
19 |
59,924,290 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5032:Rab11fip2
|
UTSW |
19 |
59,925,799 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5721:Rab11fip2
|
UTSW |
19 |
59,924,042 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6294:Rab11fip2
|
UTSW |
19 |
59,925,531 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6602:Rab11fip2
|
UTSW |
19 |
59,931,288 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6694:Rab11fip2
|
UTSW |
19 |
59,925,707 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6752:Rab11fip2
|
UTSW |
19 |
59,895,475 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6850:Rab11fip2
|
UTSW |
19 |
59,925,441 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
R7350:Rab11fip2
|
UTSW |
19 |
59,925,853 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7636:Rab11fip2
|
UTSW |
19 |
59,931,317 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R7875:Rab11fip2
|
UTSW |
19 |
59,925,655 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R8252:Rab11fip2
|
UTSW |
19 |
59,925,422 (GRCm39) |
missense |
probably benign |
0.01 |
|
| Predicted Primers |
PCR Primer
(F):5'- CTTGCCAGTCACTCTTTCAAAG -3'
(R):5'- TCATGTGATCGGTTCTGAGCC -3'
Sequencing Primer
(F):5'- TCCTGACTTCAATTGGTTTTGAG -3'
(R):5'- TCGGTTCTGAGCCAAAGAAG -3'
|
| Posted On |
2015-10-08 |
Incidental Mutation