Incidental Mutation 'R8832:Fmnl2'
| ID |
673881 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Fmnl2
|
| Ensembl Gene |
ENSMUSG00000036053 |
| Gene Name |
formin-like 2 |
| Synonyms |
man, 5430425K04Rik |
| MMRRC Submission |
068660-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R8832 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
2 |
| Chromosomal Location |
52747872-53023816 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 52944584 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Glycine
at position 188
(S188G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000117822
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000049483]
[ENSMUST00000050719]
[ENSMUST00000090952]
[ENSMUST00000127122]
[ENSMUST00000155586]
|
| AlphaFold |
A2APV2 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000049483
AA Change: S188G
PolyPhen 2
Score 0.177 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000047260
Gene: ENSMUSG00000036053
AA Change: S188G
| Domain | Start | End | E-Value | Type |
|---|
|
Drf_GBD
|
23 |
275 |
1.19e-96 |
SMART |
|
Drf_FH3
|
278 |
482 |
8.68e-76 |
SMART |
|
low complexity region
|
518 |
540 |
N/A |
INTRINSIC |
|
SCOP:d1jvr__
|
549 |
588 |
8e-3 |
SMART |
|
FH2
|
615 |
1052 |
1.66e-124 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000050719
AA Change: S188G
PolyPhen 2
Score 0.007 (Sensitivity: 0.96; Specificity: 0.75)
|
| SMART Domains |
Protein: ENSMUSP00000057084
Gene: ENSMUSG00000036053
AA Change: S188G
| Domain | Start | End | E-Value | Type |
|---|
|
Drf_GBD
|
23 |
275 |
1.19e-96 |
SMART |
|
Drf_FH3
|
278 |
482 |
8.68e-76 |
SMART |
|
low complexity region
|
518 |
540 |
N/A |
INTRINSIC |
|
low complexity region
|
549 |
568 |
N/A |
INTRINSIC |
|
FH2
|
581 |
1018 |
1.66e-124 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000090952
AA Change: S188G
PolyPhen 2
Score 0.008 (Sensitivity: 0.96; Specificity: 0.76)
|
| SMART Domains |
Protein: ENSMUSP00000088472
Gene: ENSMUSG00000036053
AA Change: S188G
| Domain | Start | End | E-Value | Type |
|---|
|
Drf_GBD
|
23 |
275 |
1.19e-96 |
SMART |
|
Drf_FH3
|
278 |
482 |
8.68e-76 |
SMART |
|
low complexity region
|
518 |
540 |
N/A |
INTRINSIC |
|
SCOP:d1jvr__
|
549 |
588 |
6e-3 |
SMART |
|
FH2
|
615 |
1052 |
1.66e-124 |
SMART |
|
low complexity region
|
1063 |
1075 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000127122
AA Change: S188G
PolyPhen 2
Score 0.177 (Sensitivity: 0.92; Specificity: 0.87)
|
| SMART Domains |
Protein: ENSMUSP00000118658
Gene: ENSMUSG00000036053
AA Change: S188G
| Domain | Start | End | E-Value | Type |
|---|
|
Drf_GBD
|
23 |
275 |
1.19e-96 |
SMART |
|
Drf_FH3
|
278 |
482 |
8.68e-76 |
SMART |
|
low complexity region
|
518 |
540 |
N/A |
INTRINSIC |
|
SCOP:d1jvr__
|
549 |
588 |
7e-3 |
SMART |
|
FH2
|
615 |
1052 |
1.66e-124 |
SMART |
|
| Predicted Effect |
|
| SMART Domains |
Protein: ENSMUSP00000117822
Gene: ENSMUSG00000036053
AA Change: S188G
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:FH2
|
1 |
131 |
2e-33 |
PFAM |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.5%
- 20x: 98.5%
|
| Validation Efficiency |
99% (81/82) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a formin-related protein. Formin-related proteins have been implicated in morphogenesis, cytokinesis, and cell polarity. Alternatively spliced transcript variants encoding different isoforms have been described but their full-length nature has yet to be determined. [provided by RefSeq, Jul 2008]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 83 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 9330159F19Rik |
A |
T |
10: 29,100,341 (GRCm39) |
E238V |
probably damaging |
Het |
| Adh6b |
T |
C |
3: 138,055,463 (GRCm39) |
V71A |
probably benign |
Het |
| Agmat |
G |
A |
4: 141,474,320 (GRCm39) |
R67H |
probably benign |
Het |
| AI182371 |
T |
C |
2: 34,985,909 (GRCm39) |
D49G |
unknown |
Het |
| Ak7 |
A |
G |
12: 105,708,598 (GRCm39) |
N351S |
possibly damaging |
Het |
| Aldh3b1 |
G |
T |
19: 3,964,025 (GRCm39) |
R426S |
probably damaging |
Het |
| Aldh4a1 |
A |
G |
4: 139,371,466 (GRCm39) |
D460G |
probably benign |
Het |
| Aox4 |
A |
T |
1: 58,294,649 (GRCm39) |
M953L |
probably benign |
Het |
| Arhgap32 |
C |
T |
9: 32,172,115 (GRCm39) |
P1632S |
possibly damaging |
Het |
| Armh1 |
A |
G |
4: 117,094,867 (GRCm39) |
F58L |
probably damaging |
Het |
| Baz1b |
C |
T |
5: 135,246,230 (GRCm39) |
R560W |
possibly damaging |
Het |
| Bbs10 |
C |
T |
10: 111,136,266 (GRCm39) |
Q460* |
probably null |
Het |
| BC034090 |
A |
C |
1: 155,102,034 (GRCm39) |
S77A |
probably damaging |
Het |
| Bltp2 |
A |
G |
11: 78,158,064 (GRCm39) |
K409E |
probably benign |
Het |
| Brca2 |
A |
G |
5: 150,465,611 (GRCm39) |
K1792E |
possibly damaging |
Het |
| Cadps2 |
A |
T |
6: 23,587,536 (GRCm39) |
L318Q |
possibly damaging |
Het |
| Catsperg2 |
A |
G |
7: 29,397,269 (GRCm39) |
V1078A |
probably benign |
Het |
| Ccno |
A |
G |
13: 113,126,239 (GRCm39) |
N236S |
probably benign |
Het |
| Chct1 |
A |
G |
11: 85,062,037 (GRCm39) |
D12G |
probably damaging |
Het |
| Cobll1 |
A |
T |
2: 64,929,602 (GRCm39) |
S575T |
probably damaging |
Het |
| Col6a4 |
A |
G |
9: 105,949,353 (GRCm39) |
Y761H |
probably benign |
Het |
| Cyp2j9 |
G |
T |
4: 96,474,121 (GRCm39) |
H106Q |
probably benign |
Het |
| Dennd2c |
T |
A |
3: 103,059,720 (GRCm39) |
|
probably null |
Het |
| Drd5 |
G |
A |
5: 38,477,078 (GRCm39) |
V24M |
probably benign |
Het |
| Dthd1 |
T |
C |
5: 62,971,608 (GRCm39) |
S144P |
probably benign |
Het |
| Fcna |
C |
A |
2: 25,516,145 (GRCm39) |
R124L |
possibly damaging |
Het |
| Ggt1 |
A |
T |
10: 75,410,173 (GRCm39) |
H35L |
possibly damaging |
Het |
| Gphn |
A |
T |
12: 78,459,174 (GRCm39) |
|
silent |
Het |
| Hic1 |
G |
A |
11: 75,057,728 (GRCm39) |
A387V |
possibly damaging |
Het |
| Hycc2 |
A |
T |
1: 58,587,832 (GRCm39) |
I127N |
possibly damaging |
Het |
| Igf1r |
T |
A |
7: 67,875,769 (GRCm39) |
F1244I |
probably damaging |
Het |
| Kcnk7 |
T |
C |
19: 5,754,736 (GRCm39) |
V78A |
probably damaging |
Het |
| Kit |
A |
G |
5: 75,799,791 (GRCm39) |
N508D |
probably benign |
Het |
| Klk1b22 |
A |
T |
7: 43,764,277 (GRCm39) |
E68D |
probably benign |
Het |
| Klra4 |
C |
T |
6: 130,021,019 (GRCm39) |
D259N |
probably benign |
Het |
| Krtap2-4 |
A |
T |
11: 99,505,246 (GRCm39) |
C122S |
unknown |
Het |
| Map3k1 |
T |
G |
13: 111,889,015 (GRCm39) |
H1314P |
possibly damaging |
Het |
| Mast2 |
C |
T |
4: 116,168,875 (GRCm39) |
|
probably null |
Het |
| Mfsd2a |
A |
G |
4: 122,843,102 (GRCm39) |
V393A |
probably benign |
Het |
| Myh7b |
T |
A |
2: 155,475,182 (GRCm39) |
V1858E |
probably benign |
Het |
| Myo1c |
G |
A |
11: 75,561,072 (GRCm39) |
V793I |
probably benign |
Het |
| Myt1l |
T |
A |
12: 29,970,351 (GRCm39) |
N1145K |
unknown |
Het |
| Nckap1l |
T |
A |
15: 103,387,242 (GRCm39) |
S706T |
probably benign |
Het |
| Nos2 |
A |
G |
11: 78,846,290 (GRCm39) |
|
probably null |
Het |
| Odf2l |
C |
T |
3: 144,833,820 (GRCm39) |
S160L |
probably benign |
Het |
| Or10ag54 |
T |
A |
2: 87,099,743 (GRCm39) |
M206K |
probably benign |
Het |
| Or2av9 |
T |
C |
11: 58,381,063 (GRCm39) |
I173V |
possibly damaging |
Het |
| Or4p18 |
A |
G |
2: 88,233,137 (GRCm39) |
I47T |
probably damaging |
Het |
| Or56b34 |
T |
C |
7: 104,937,435 (GRCm39) |
L45P |
possibly damaging |
Het |
| Or8g53 |
T |
C |
9: 39,683,886 (GRCm39) |
D70G |
probably damaging |
Het |
| Pclo |
T |
C |
5: 14,838,464 (GRCm39) |
W1424R |
|
Het |
| Pde8a |
A |
G |
7: 80,956,498 (GRCm39) |
N299S |
probably benign |
Het |
| Pi4kb |
C |
T |
3: 94,900,344 (GRCm39) |
T326M |
probably damaging |
Het |
| Pip4k2c |
A |
T |
10: 127,037,037 (GRCm39) |
H177Q |
probably damaging |
Het |
| Pld1 |
T |
A |
3: 28,177,846 (GRCm39) |
W686R |
|
Het |
| Ppp1r3b |
A |
T |
8: 35,851,419 (GRCm39) |
D86V |
probably damaging |
Het |
| Ppp1r3g |
C |
T |
13: 36,153,143 (GRCm39) |
R188* |
probably null |
Het |
| Pramel48 |
G |
T |
5: 95,630,939 (GRCm39) |
C272F |
possibly damaging |
Het |
| Ptbp1 |
A |
G |
10: 79,699,023 (GRCm39) |
E527G |
probably damaging |
Het |
| Rasef |
T |
C |
4: 73,698,558 (GRCm39) |
|
probably benign |
Het |
| Rce1 |
A |
T |
19: 4,675,532 (GRCm39) |
C34S |
unknown |
Het |
| Rnf144a |
T |
C |
12: 26,370,948 (GRCm39) |
|
probably benign |
Het |
| Rpl7 |
C |
T |
1: 16,173,485 (GRCm39) |
R88H |
possibly damaging |
Het |
| Rubcnl |
A |
T |
14: 75,269,359 (GRCm39) |
T6S |
|
Het |
| Samd9l |
A |
T |
6: 3,374,990 (GRCm39) |
V757D |
probably damaging |
Het |
| Sec22c |
A |
G |
9: 121,514,638 (GRCm39) |
V221A |
probably benign |
Het |
| Slc16a6 |
A |
G |
11: 109,345,932 (GRCm39) |
Y444H |
probably benign |
Het |
| Slc6a15 |
A |
T |
10: 103,225,179 (GRCm39) |
Y89F |
probably damaging |
Het |
| Smg1 |
A |
G |
7: 117,739,006 (GRCm39) |
V3466A |
probably benign |
Het |
| Sobp |
G |
A |
10: 43,036,824 (GRCm39) |
T38I |
probably damaging |
Het |
| Sppl2b |
TGTCACAGGT |
TGT |
10: 80,701,903 (GRCm39) |
|
probably null |
Het |
| Srsf5 |
T |
A |
12: 80,996,278 (GRCm39) |
F151I |
probably damaging |
Het |
| Taf2 |
A |
C |
15: 54,928,001 (GRCm39) |
L134R |
possibly damaging |
Het |
| Tbc1d1 |
A |
G |
5: 64,442,020 (GRCm39) |
|
probably benign |
Het |
| Thap1 |
C |
T |
8: 26,648,261 (GRCm39) |
|
probably benign |
Het |
| Tmc5 |
A |
T |
7: 118,222,332 (GRCm39) |
M11L |
probably benign |
Het |
| Tnfaip8 |
ACACACTCTCTCTCTC |
AC |
18: 50,179,908 (GRCm39) |
|
probably benign |
Het |
| Tomm7 |
T |
C |
5: 24,049,047 (GRCm39) |
K9E |
possibly damaging |
Het |
| Trem3 |
T |
C |
17: 48,556,865 (GRCm39) |
V112A |
probably benign |
Het |
| Vmn1r178 |
G |
A |
7: 23,593,264 (GRCm39) |
C104Y |
probably damaging |
Het |
| Zdhhc20 |
A |
T |
14: 58,080,721 (GRCm39) |
S263T |
possibly damaging |
Het |
| Zdhhc20 |
A |
G |
14: 58,103,089 (GRCm39) |
S87P |
probably benign |
Het |
| Zfp423 |
C |
A |
8: 88,507,827 (GRCm39) |
C839F |
probably damaging |
Het |
|
| Other mutations in Fmnl2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00401:Fmnl2
|
APN |
2 |
53,004,929 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00960:Fmnl2
|
APN |
2 |
53,013,494 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL01343:Fmnl2
|
APN |
2 |
53,013,557 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01790:Fmnl2
|
APN |
2 |
53,008,380 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02555:Fmnl2
|
APN |
2 |
53,016,863 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
IGL02613:Fmnl2
|
APN |
2 |
52,963,747 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02712:Fmnl2
|
APN |
2 |
52,926,510 (GRCm39) |
splice site |
probably benign |
|
|
IGL02715:Fmnl2
|
APN |
2 |
52,962,222 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
IGL02750:Fmnl2
|
APN |
2 |
52,993,709 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL02832:Fmnl2
|
APN |
2 |
52,748,261 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
IGL02975:Fmnl2
|
APN |
2 |
52,991,494 (GRCm39) |
missense |
probably benign |
0.45 |
|
Beefeater
|
UTSW |
2 |
52,963,666 (GRCm39) |
missense |
unknown |
|
|
waterloo
|
UTSW |
2 |
52,904,860 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4280001:Fmnl2
|
UTSW |
2 |
53,008,208 (GRCm39) |
missense |
unknown |
|
|
R0529:Fmnl2
|
UTSW |
2 |
52,932,377 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0571:Fmnl2
|
UTSW |
2 |
52,944,503 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0707:Fmnl2
|
UTSW |
2 |
52,944,498 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R1172:Fmnl2
|
UTSW |
2 |
52,962,286 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1473:Fmnl2
|
UTSW |
2 |
52,748,219 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R1533:Fmnl2
|
UTSW |
2 |
52,995,549 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1536:Fmnl2
|
UTSW |
2 |
52,995,549 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1537:Fmnl2
|
UTSW |
2 |
52,995,549 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1547:Fmnl2
|
UTSW |
2 |
52,995,549 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1548:Fmnl2
|
UTSW |
2 |
52,995,549 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1549:Fmnl2
|
UTSW |
2 |
52,995,549 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1604:Fmnl2
|
UTSW |
2 |
52,995,549 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1608:Fmnl2
|
UTSW |
2 |
52,995,549 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1615:Fmnl2
|
UTSW |
2 |
53,008,436 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1792:Fmnl2
|
UTSW |
2 |
52,932,329 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R1965:Fmnl2
|
UTSW |
2 |
53,004,880 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1970:Fmnl2
|
UTSW |
2 |
52,995,588 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R2012:Fmnl2
|
UTSW |
2 |
52,995,549 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2065:Fmnl2
|
UTSW |
2 |
52,995,549 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2111:Fmnl2
|
UTSW |
2 |
52,995,549 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2112:Fmnl2
|
UTSW |
2 |
52,995,549 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2427:Fmnl2
|
UTSW |
2 |
53,006,991 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R4084:Fmnl2
|
UTSW |
2 |
52,997,507 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R4095:Fmnl2
|
UTSW |
2 |
52,991,535 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4607:Fmnl2
|
UTSW |
2 |
52,993,728 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R4608:Fmnl2
|
UTSW |
2 |
52,993,728 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R4720:Fmnl2
|
UTSW |
2 |
52,997,552 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R4731:Fmnl2
|
UTSW |
2 |
53,007,081 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4947:Fmnl2
|
UTSW |
2 |
52,963,722 (GRCm39) |
missense |
probably benign |
0.32 |
|
R5015:Fmnl2
|
UTSW |
2 |
52,993,773 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R5402:Fmnl2
|
UTSW |
2 |
53,018,794 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5731:Fmnl2
|
UTSW |
2 |
53,008,149 (GRCm39) |
splice site |
probably null |
|
|
R5766:Fmnl2
|
UTSW |
2 |
52,991,466 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5945:Fmnl2
|
UTSW |
2 |
53,004,211 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6093:Fmnl2
|
UTSW |
2 |
53,004,880 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6210:Fmnl2
|
UTSW |
2 |
53,020,457 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R6287:Fmnl2
|
UTSW |
2 |
52,904,860 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6661:Fmnl2
|
UTSW |
2 |
52,998,297 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6967:Fmnl2
|
UTSW |
2 |
52,987,344 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R7006:Fmnl2
|
UTSW |
2 |
52,998,266 (GRCm39) |
missense |
probably benign |
0.27 |
|
R7146:Fmnl2
|
UTSW |
2 |
52,958,552 (GRCm39) |
missense |
|
|
|
R7173:Fmnl2
|
UTSW |
2 |
53,004,202 (GRCm39) |
missense |
unknown |
|
|
R7176:Fmnl2
|
UTSW |
2 |
53,004,162 (GRCm39) |
missense |
unknown |
|
|
R7182:Fmnl2
|
UTSW |
2 |
52,997,453 (GRCm39) |
missense |
unknown |
|
|
R7201:Fmnl2
|
UTSW |
2 |
52,963,666 (GRCm39) |
missense |
unknown |
|
|
R7470:Fmnl2
|
UTSW |
2 |
52,932,377 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7481:Fmnl2
|
UTSW |
2 |
52,998,443 (GRCm39) |
missense |
unknown |
|
|
R7691:Fmnl2
|
UTSW |
2 |
52,991,510 (GRCm39) |
missense |
unknown |
|
|
R7699:Fmnl2
|
UTSW |
2 |
52,926,520 (GRCm39) |
missense |
|
|
|
R7700:Fmnl2
|
UTSW |
2 |
52,926,520 (GRCm39) |
missense |
|
|
|
R7722:Fmnl2
|
UTSW |
2 |
52,944,479 (GRCm39) |
missense |
|
|
|
R7775:Fmnl2
|
UTSW |
2 |
52,963,692 (GRCm39) |
missense |
unknown |
|
|
R7824:Fmnl2
|
UTSW |
2 |
52,963,692 (GRCm39) |
missense |
unknown |
|
|
R8282:Fmnl2
|
UTSW |
2 |
52,997,678 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8774:Fmnl2
|
UTSW |
2 |
52,932,321 (GRCm39) |
missense |
|
|
|
R8774-TAIL:Fmnl2
|
UTSW |
2 |
52,932,321 (GRCm39) |
missense |
|
|
|
R8816:Fmnl2
|
UTSW |
2 |
53,004,214 (GRCm39) |
missense |
unknown |
|
|
R8868:Fmnl2
|
UTSW |
2 |
53,016,077 (GRCm39) |
missense |
unknown |
|
|
R8990:Fmnl2
|
UTSW |
2 |
53,016,971 (GRCm39) |
missense |
unknown |
|
|
R9412:Fmnl2
|
UTSW |
2 |
53,007,016 (GRCm39) |
missense |
unknown |
|
|
R9502:Fmnl2
|
UTSW |
2 |
52,998,312 (GRCm39) |
missense |
unknown |
|
|
R9532:Fmnl2
|
UTSW |
2 |
53,006,941 (GRCm39) |
missense |
unknown |
|
|
R9602:Fmnl2
|
UTSW |
2 |
53,013,587 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9760:Fmnl2
|
UTSW |
2 |
52,944,527 (GRCm39) |
missense |
|
|
|
Z1188:Fmnl2
|
UTSW |
2 |
53,004,883 (GRCm39) |
missense |
unknown |
|
|
| Predicted Primers |
PCR Primer
(F):5'- TTCCTTTGGCTGCAAACACC -3'
(R):5'- TGCTGAATCACAAGATGGCG -3'
Sequencing Primer
(F):5'- TGGCTGCAAACACCTCTCG -3'
(R):5'- CTGAATCACAAGATGGCGTTTCTAAG -3'
|
| Posted On |
2021-07-15 |
Incidental Mutation