Incidental Mutation 'IGL01535:Fig4'
| ID |
89922 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Fig4
|
| Ensembl Gene |
ENSMUSG00000038417 |
| Gene Name |
FIG4 phosphoinositide 5-phosphatase |
| Synonyms |
A530089I17Rik |
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.530)
|
| Stock # |
IGL01535
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
10 |
| Chromosomal Location |
41064168-41179237 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to G
at 41132490 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Arginine
at position 439
(S439R)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000039598
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000043814]
|
| AlphaFold |
Q91WF7 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000043814
AA Change: S439R
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000039598
Gene: ENSMUSG00000038417
AA Change: S439R
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Syja_N
|
93 |
424 |
1.7e-79 |
PFAM |
|
Blast:Lactamase_B
|
533 |
610 |
6e-21 |
BLAST |
|
low complexity region
|
742 |
771 |
N/A |
INTRINSIC |
|
low complexity region
|
805 |
813 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs to the SAC domain-containing protein gene family. The SAC domain, approximately 400 amino acids in length and consisting of seven conserved motifs, has been shown to possess phosphoinositide phosphatase activity. The yeast homolog, Sac1p, is involved in the regulation of various phosphoinositides, and affects diverse cellular functions such as actin cytoskeleton organization, Golgi function, and maintenance of vacuole morphology. Membrane-bound phosphoinositides function as signaling molecules and play a key role in vesicle trafficking in eukaryotic cells. Mutations in this gene have been associated with Charcot-Marie-Tooth disease, type 4J. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a spontaneous allele exhibit premature death, severe tremors, diluted coat color, neurodegeneration, impaired coordination, muscle weakness, small size and reduced spleen. [provided by MGI curators]
|
| Allele List at MGI |
All alleles(16) : Targeted(3) Gene trapped(12) Spontaneous(1)
|
| Other mutations in this stock |
Total: 27 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adamts19 |
T |
A |
18: 59,101,891 (GRCm39) |
S654T |
probably benign |
Het |
| Brd10 |
T |
C |
19: 29,731,212 (GRCm39) |
H600R |
possibly damaging |
Het |
| Cacnb3 |
A |
T |
15: 98,537,469 (GRCm39) |
Q49L |
probably benign |
Het |
| Dapk1 |
A |
G |
13: 60,878,845 (GRCm39) |
|
probably benign |
Het |
| Dop1b |
T |
A |
16: 93,566,846 (GRCm39) |
L1091* |
probably null |
Het |
| Epb42 |
A |
G |
2: 120,858,169 (GRCm39) |
V263A |
probably damaging |
Het |
| Gatc |
A |
T |
5: 115,479,048 (GRCm39) |
V54E |
possibly damaging |
Het |
| Hook2 |
T |
C |
8: 85,729,618 (GRCm39) |
L686P |
probably benign |
Het |
| Med12l |
A |
T |
3: 59,169,680 (GRCm39) |
T1615S |
probably damaging |
Het |
| Msr1 |
C |
T |
8: 40,064,714 (GRCm39) |
G320D |
probably benign |
Het |
| Nbeal1 |
T |
A |
1: 60,256,414 (GRCm39) |
F220I |
probably damaging |
Het |
| Or14j2 |
T |
A |
17: 37,885,679 (GRCm39) |
I212F |
possibly damaging |
Het |
| Or2l5 |
G |
A |
16: 19,334,228 (GRCm39) |
H53Y |
probably benign |
Het |
| Pcdh10 |
A |
T |
3: 45,334,078 (GRCm39) |
I131F |
probably damaging |
Het |
| Phlpp2 |
A |
G |
8: 110,660,697 (GRCm39) |
E784G |
possibly damaging |
Het |
| Prr36 |
A |
T |
8: 4,264,043 (GRCm39) |
|
probably benign |
Het |
| Ptprq |
G |
A |
10: 107,535,457 (GRCm39) |
S436L |
probably benign |
Het |
| Rock1 |
T |
A |
18: 10,132,119 (GRCm39) |
|
probably benign |
Het |
| Sash1 |
T |
G |
10: 8,617,341 (GRCm39) |
T522P |
probably damaging |
Het |
| Serpinb2 |
T |
C |
1: 107,447,503 (GRCm39) |
|
probably null |
Het |
| Supt16 |
T |
C |
14: 52,414,647 (GRCm39) |
K422E |
probably damaging |
Het |
| Syt14 |
T |
G |
1: 192,669,073 (GRCm39) |
D60A |
probably damaging |
Het |
| Tbc1d2b |
A |
C |
9: 90,097,526 (GRCm39) |
|
probably benign |
Het |
| Thsd7b |
T |
C |
1: 129,605,954 (GRCm39) |
I565T |
possibly damaging |
Het |
| Ttn |
A |
G |
2: 76,564,536 (GRCm39) |
Y28534H |
probably damaging |
Het |
| Vmn1r177 |
T |
A |
7: 23,565,765 (GRCm39) |
H37L |
probably damaging |
Het |
| Vps13b |
A |
T |
15: 35,455,103 (GRCm39) |
N671Y |
possibly damaging |
Het |
|
| Other mutations in Fig4 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00972:Fig4
|
APN |
10 |
41,127,784 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01013:Fig4
|
APN |
10 |
41,143,782 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01066:Fig4
|
APN |
10 |
41,161,413 (GRCm39) |
splice site |
probably benign |
|
|
IGL01501:Fig4
|
APN |
10 |
41,146,370 (GRCm39) |
missense |
probably benign |
|
|
IGL01503:Fig4
|
APN |
10 |
41,132,514 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01733:Fig4
|
APN |
10 |
41,153,389 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
IGL01782:Fig4
|
APN |
10 |
41,146,396 (GRCm39) |
missense |
probably benign |
0.18 |
|
IGL01866:Fig4
|
APN |
10 |
41,108,160 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
IGL01934:Fig4
|
APN |
10 |
41,104,108 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL01966:Fig4
|
APN |
10 |
41,108,098 (GRCm39) |
splice site |
probably null |
|
|
IGL02032:Fig4
|
APN |
10 |
41,179,002 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02225:Fig4
|
APN |
10 |
41,132,448 (GRCm39) |
missense |
probably benign |
|
|
IGL02345:Fig4
|
APN |
10 |
41,143,770 (GRCm39) |
missense |
probably null |
1.00 |
|
IGL02532:Fig4
|
APN |
10 |
41,161,277 (GRCm39) |
splice site |
probably benign |
|
|
IGL02686:Fig4
|
APN |
10 |
41,140,000 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02965:Fig4
|
APN |
10 |
41,161,661 (GRCm39) |
missense |
probably damaging |
0.98 |
|
P0021:Fig4
|
UTSW |
10 |
41,127,821 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0017:Fig4
|
UTSW |
10 |
41,149,003 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R0017:Fig4
|
UTSW |
10 |
41,149,003 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R0117:Fig4
|
UTSW |
10 |
41,106,037 (GRCm39) |
nonsense |
probably null |
|
|
R0144:Fig4
|
UTSW |
10 |
41,134,045 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0655:Fig4
|
UTSW |
10 |
41,161,673 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0701:Fig4
|
UTSW |
10 |
41,116,508 (GRCm39) |
nonsense |
probably null |
|
|
R0751:Fig4
|
UTSW |
10 |
41,148,978 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1540:Fig4
|
UTSW |
10 |
41,064,582 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R1586:Fig4
|
UTSW |
10 |
41,141,423 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2916:Fig4
|
UTSW |
10 |
41,134,071 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R3927:Fig4
|
UTSW |
10 |
41,139,135 (GRCm39) |
missense |
probably benign |
|
|
R4304:Fig4
|
UTSW |
10 |
41,132,423 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4586:Fig4
|
UTSW |
10 |
41,064,628 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4678:Fig4
|
UTSW |
10 |
41,148,994 (GRCm39) |
missense |
probably benign |
0.27 |
|
R4858:Fig4
|
UTSW |
10 |
41,109,586 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5614:Fig4
|
UTSW |
10 |
41,148,981 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5896:Fig4
|
UTSW |
10 |
41,130,881 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R6126:Fig4
|
UTSW |
10 |
41,141,443 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7056:Fig4
|
UTSW |
10 |
41,096,928 (GRCm39) |
missense |
probably benign |
0.09 |
|
R7350:Fig4
|
UTSW |
10 |
41,127,752 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7452:Fig4
|
UTSW |
10 |
41,116,633 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R7481:Fig4
|
UTSW |
10 |
41,106,001 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7610:Fig4
|
UTSW |
10 |
41,129,709 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7818:Fig4
|
UTSW |
10 |
41,139,162 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7830:Fig4
|
UTSW |
10 |
41,132,462 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8263:Fig4
|
UTSW |
10 |
41,143,711 (GRCm39) |
nonsense |
probably null |
|
|
R8319:Fig4
|
UTSW |
10 |
41,139,097 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8409:Fig4
|
UTSW |
10 |
41,141,427 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8435:Fig4
|
UTSW |
10 |
41,161,670 (GRCm39) |
missense |
probably benign |
|
|
R8474:Fig4
|
UTSW |
10 |
41,108,170 (GRCm39) |
missense |
probably benign |
0.30 |
|
R9086:Fig4
|
UTSW |
10 |
41,161,399 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R9131:Fig4
|
UTSW |
10 |
41,141,407 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R9248:Fig4
|
UTSW |
10 |
41,153,478 (GRCm39) |
missense |
probably benign |
|
|
R9401:Fig4
|
UTSW |
10 |
41,143,733 (GRCm39) |
missense |
probably benign |
|
|
R9564:Fig4
|
UTSW |
10 |
41,161,387 (GRCm39) |
missense |
probably benign |
0.20 |
|
R9627:Fig4
|
UTSW |
10 |
41,108,178 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9649:Fig4
|
UTSW |
10 |
41,143,763 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1088:Fig4
|
UTSW |
10 |
41,129,727 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2013-12-03 |
Incidental Mutation