Incidental Mutation 'R3440:Fignl2'
ID |
334566 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Fignl2
|
Ensembl Gene |
ENSMUSG00000095440 |
Gene Name |
fidgetin-like 2 |
Synonyms |
|
MMRRC Submission |
040658-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.138)
|
Stock # |
R3440 (G1)
|
Quality Score |
40 |
Status
|
Validated
|
Chromosome |
15 |
Chromosomal Location |
100948075-100976448 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 100951004 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Phenylalanine to Serine
at position 426
(F426S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000150618
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000178140]
[ENSMUST00000213610]
|
AlphaFold |
J3QK54 |
Predicted Effect |
unknown
Transcript: ENSMUST00000178140
AA Change: F426S
|
SMART Domains |
Protein: ENSMUSP00000137256 Gene: ENSMUSG00000095440 AA Change: F426S
Domain | Start | End | E-Value | Type |
low complexity region
|
94 |
105 |
N/A |
INTRINSIC |
low complexity region
|
112 |
135 |
N/A |
INTRINSIC |
low complexity region
|
152 |
201 |
N/A |
INTRINSIC |
low complexity region
|
203 |
255 |
N/A |
INTRINSIC |
low complexity region
|
267 |
296 |
N/A |
INTRINSIC |
low complexity region
|
310 |
329 |
N/A |
INTRINSIC |
low complexity region
|
394 |
412 |
N/A |
INTRINSIC |
AAA
|
419 |
550 |
3.31e-8 |
SMART |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000213610
AA Change: F426S
|
Meta Mutation Damage Score |
0.0728 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.3%
- 20x: 95.2%
|
Validation Efficiency |
97% (29/30) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 25 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abtb2 |
C |
A |
2: 103,397,577 (GRCm39) |
A169E |
probably benign |
Het |
Adam3 |
T |
C |
8: 25,170,759 (GRCm39) |
|
probably benign |
Het |
Agmo |
C |
T |
12: 37,293,799 (GRCm39) |
T74I |
probably damaging |
Het |
Ano6 |
T |
C |
15: 95,865,602 (GRCm39) |
V862A |
probably damaging |
Het |
Bltp1 |
C |
T |
3: 37,096,061 (GRCm39) |
Q4614* |
probably null |
Het |
Cavin2 |
T |
A |
1: 51,340,565 (GRCm39) |
V414E |
probably damaging |
Het |
Clrn3 |
A |
C |
7: 135,115,854 (GRCm39) |
Y165* |
probably null |
Het |
Cp |
A |
T |
3: 20,029,121 (GRCm39) |
M533L |
probably benign |
Het |
Dhrs3 |
T |
A |
4: 144,646,628 (GRCm39) |
M226K |
probably damaging |
Het |
Fpr1 |
C |
T |
17: 18,097,420 (GRCm39) |
D190N |
probably benign |
Het |
Grik3 |
C |
A |
4: 125,587,763 (GRCm39) |
L628M |
probably damaging |
Het |
Grik3 |
T |
A |
4: 125,587,764 (GRCm39) |
L628Q |
probably damaging |
Het |
Grin2c |
T |
A |
11: 115,141,469 (GRCm39) |
D883V |
probably damaging |
Het |
Gtf3c6 |
T |
A |
10: 40,127,169 (GRCm39) |
E123V |
probably null |
Het |
H2-Eb1 |
A |
G |
17: 34,528,655 (GRCm39) |
E62G |
probably damaging |
Het |
Kif1a |
C |
T |
1: 92,964,575 (GRCm39) |
D1334N |
possibly damaging |
Het |
Lef1 |
A |
G |
3: 130,978,407 (GRCm39) |
D175G |
probably damaging |
Het |
Myom1 |
A |
G |
17: 71,352,658 (GRCm39) |
|
probably null |
Het |
Or6k2 |
A |
T |
1: 173,986,746 (GRCm39) |
M136L |
probably benign |
Het |
Pgr |
A |
T |
9: 8,922,630 (GRCm39) |
N600I |
probably damaging |
Het |
Rab36 |
G |
A |
10: 74,880,328 (GRCm39) |
V63I |
probably damaging |
Het |
Selp |
T |
C |
1: 163,951,344 (GRCm39) |
F26S |
probably benign |
Het |
Tchh |
A |
T |
3: 93,352,414 (GRCm39) |
D618V |
unknown |
Het |
Tenm4 |
A |
T |
7: 96,202,723 (GRCm39) |
M88L |
probably benign |
Het |
Zfat |
A |
T |
15: 67,956,402 (GRCm39) |
D1143E |
probably benign |
Het |
|
Other mutations in Fignl2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0068:Fignl2
|
UTSW |
15 |
100,952,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R0068:Fignl2
|
UTSW |
15 |
100,952,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R0375:Fignl2
|
UTSW |
15 |
100,951,974 (GRCm39) |
missense |
probably benign |
0.06 |
R1616:Fignl2
|
UTSW |
15 |
100,951,997 (GRCm39) |
missense |
probably damaging |
0.96 |
R2240:Fignl2
|
UTSW |
15 |
100,951,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R3976:Fignl2
|
UTSW |
15 |
100,950,467 (GRCm39) |
missense |
unknown |
|
R4418:Fignl2
|
UTSW |
15 |
100,951,830 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5869:Fignl2
|
UTSW |
15 |
100,951,161 (GRCm39) |
missense |
unknown |
|
R6249:Fignl2
|
UTSW |
15 |
100,952,060 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6894:Fignl2
|
UTSW |
15 |
100,951,854 (GRCm39) |
missense |
probably benign |
0.00 |
R7302:Fignl2
|
UTSW |
15 |
100,951,259 (GRCm39) |
missense |
unknown |
|
R7323:Fignl2
|
UTSW |
15 |
100,951,382 (GRCm39) |
missense |
unknown |
|
R7548:Fignl2
|
UTSW |
15 |
100,951,079 (GRCm39) |
missense |
unknown |
|
R7558:Fignl2
|
UTSW |
15 |
100,952,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R7776:Fignl2
|
UTSW |
15 |
100,951,301 (GRCm39) |
missense |
unknown |
|
R7782:Fignl2
|
UTSW |
15 |
100,951,188 (GRCm39) |
missense |
unknown |
|
R8708:Fignl2
|
UTSW |
15 |
100,950,734 (GRCm39) |
missense |
unknown |
|
R8936:Fignl2
|
UTSW |
15 |
100,951,339 (GRCm39) |
missense |
unknown |
|
R9328:Fignl2
|
UTSW |
15 |
100,951,271 (GRCm39) |
missense |
unknown |
|
R9393:Fignl2
|
UTSW |
15 |
100,951,466 (GRCm39) |
missense |
unknown |
|
|
Predicted Primers |
PCR Primer
(F):5'- AAAAGCCCTGAGTTCCCTGC -3'
(R):5'- TTTGACAAGTTCCCGGAGCG -3'
Sequencing Primer
(F):5'- GTCCAGCTCGCTGATGAG -3'
(R):5'- ACGGAGGCTTCGCGGAG -3'
|
Posted On |
2015-09-03 |