Incidental Mutation 'IGL02937:Far1'
| ID |
364384 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Far1
|
| Ensembl Gene |
ENSMUSG00000030759 |
| Gene Name |
fatty acyl CoA reductase 1 |
| Synonyms |
Mlstd2, 2600011M19Rik, 2900034E22Rik, 3732409C05Rik |
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.791)
|
| Stock # |
IGL02937
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
113113041-113170718 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 113139855 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Asparagine
at position 101
(I101N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000117131
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000033018]
[ENSMUST00000067929]
[ENSMUST00000122890]
[ENSMUST00000129087]
[ENSMUST00000136158]
[ENSMUST00000164745]
|
| AlphaFold |
Q922J9 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000033018
AA Change: I101N
PolyPhen 2
Score 0.913 (Sensitivity: 0.81; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000033018
Gene: ENSMUSG00000030759
AA Change: I101N
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Epimerase
|
13 |
177 |
1e-8 |
PFAM |
|
Pfam:NAD_binding_4
|
15 |
285 |
3.2e-80 |
PFAM |
|
Pfam:Sterile
|
356 |
448 |
3.1e-34 |
PFAM |
|
transmembrane domain
|
466 |
483 |
N/A |
INTRINSIC |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000067929
AA Change: I101N
PolyPhen 2
Score 0.913 (Sensitivity: 0.81; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000064334
Gene: ENSMUSG00000030759
AA Change: I101N
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Epimerase
|
13 |
177 |
1e-8 |
PFAM |
|
Pfam:NAD_binding_4
|
15 |
285 |
3.2e-80 |
PFAM |
|
Pfam:Sterile
|
356 |
448 |
5.4e-36 |
PFAM |
|
transmembrane domain
|
466 |
483 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000122890
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000123845
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000129087
AA Change: I101N
PolyPhen 2
Score 0.984 (Sensitivity: 0.74; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000117131
Gene: ENSMUSG00000030759
AA Change: I101N
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Polysacc_synt_2
|
13 |
159 |
1.5e-7 |
PFAM |
|
Pfam:Epimerase
|
13 |
174 |
8.5e-10 |
PFAM |
|
Pfam:NAD_binding_4
|
15 |
180 |
9.7e-52 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000136158
AA Change: I101N
PolyPhen 2
Score 0.913 (Sensitivity: 0.81; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000122643
Gene: ENSMUSG00000030759
AA Change: I101N
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Polysacc_synt_2
|
13 |
159 |
2.3e-7 |
PFAM |
|
Pfam:Epimerase
|
13 |
174 |
1.3e-9 |
PFAM |
|
Pfam:NAD_binding_4
|
15 |
207 |
7.6e-54 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000138253
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000164745
AA Change: I101N
PolyPhen 2
Score 0.913 (Sensitivity: 0.81; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000128695
Gene: ENSMUSG00000030759
AA Change: I101N
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Epimerase
|
13 |
241 |
1.5e-10 |
PFAM |
|
Pfam:NAD_binding_4
|
15 |
285 |
9.9e-78 |
PFAM |
|
Pfam:Sterile
|
355 |
448 |
5.8e-26 |
PFAM |
|
transmembrane domain
|
466 |
483 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000156875
|
| 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 is required for the reduction of fatty acids to fatty alcohols, a process that is required for the synthesis of monoesters and ether lipids. NADPH is required as a cofactor in this reaction, and 16-18 carbon saturated and unsaturated fatty acids are the preferred substrate. This is a peroxisomal membrane protein, and studies suggest that the N-terminus contains a large catalytic domain located on the outside of the peroxisome, while the C-terminus is exposed to the matrix of the peroxisome. Studies indicate that the regulation of this protein is dependent on plasmalogen levels. Mutations in this gene have been associated with individuals affected by severe intellectual disability, early-onset epilepsy, microcephaly, congenital cataracts, growth retardation, and spasticity (PMID: 25439727). A pseudogene of this gene is located on chromosome 13. [provided by RefSeq, Jan 2015]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 53 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4931406C07Rik |
C |
T |
9: 15,206,049 (GRCm39) |
C21Y |
probably damaging |
Het |
| 4933427D06Rik |
T |
C |
6: 89,085,127 (GRCm39) |
|
noncoding transcript |
Het |
| 5730480H06Rik |
A |
G |
5: 48,536,783 (GRCm39) |
I160V |
probably benign |
Het |
| Arhgap29 |
G |
A |
3: 121,767,698 (GRCm39) |
E47K |
probably damaging |
Het |
| Arhgef12 |
T |
A |
9: 42,927,216 (GRCm39) |
S303C |
probably damaging |
Het |
| Bap1 |
A |
G |
14: 30,980,284 (GRCm39) |
N644S |
probably benign |
Het |
| Cc2d1b |
A |
G |
4: 108,489,091 (GRCm39) |
E796G |
probably damaging |
Het |
| Cfh |
C |
A |
1: 140,033,180 (GRCm39) |
R788L |
probably benign |
Het |
| Cldn1 |
A |
G |
16: 26,179,623 (GRCm39) |
F148S |
probably damaging |
Het |
| Cryzl1 |
A |
G |
16: 91,487,619 (GRCm39) |
M292T |
possibly damaging |
Het |
| Cyp11b1 |
T |
C |
15: 74,708,408 (GRCm39) |
R385G |
possibly damaging |
Het |
| Cyp4f37 |
T |
C |
17: 32,844,163 (GRCm39) |
L89P |
probably benign |
Het |
| Dach1 |
A |
G |
14: 98,153,231 (GRCm39) |
|
probably null |
Het |
| Dhtkd1 |
A |
G |
2: 5,922,716 (GRCm39) |
I481T |
possibly damaging |
Het |
| Dlx5 |
A |
T |
6: 6,881,755 (GRCm39) |
D44E |
probably damaging |
Het |
| Dsg1a |
T |
A |
18: 20,464,591 (GRCm39) |
I362N |
possibly damaging |
Het |
| Ecm2 |
T |
A |
13: 49,671,952 (GRCm39) |
I151N |
probably damaging |
Het |
| Gm21985 |
T |
C |
2: 112,172,207 (GRCm39) |
S384P |
probably benign |
Het |
| Gnb5 |
T |
C |
9: 75,247,471 (GRCm39) |
Y247H |
probably damaging |
Het |
| Golgb1 |
A |
G |
16: 36,736,572 (GRCm39) |
K1940E |
probably damaging |
Het |
| Gprc5b |
A |
G |
7: 118,583,017 (GRCm39) |
V284A |
probably benign |
Het |
| Idh2 |
T |
C |
7: 79,748,661 (GRCm39) |
Y179C |
probably damaging |
Het |
| Kalrn |
G |
A |
16: 34,040,500 (GRCm39) |
Q737* |
probably null |
Het |
| Kcnj13 |
T |
C |
1: 87,314,175 (GRCm39) |
D349G |
probably damaging |
Het |
| Lgsn |
A |
T |
1: 31,243,318 (GRCm39) |
T467S |
possibly damaging |
Het |
| Map9 |
T |
A |
3: 82,270,819 (GRCm39) |
S128T |
possibly damaging |
Het |
| Mroh5 |
A |
G |
15: 73,661,827 (GRCm39) |
C455R |
probably damaging |
Het |
| Nes |
A |
G |
3: 87,887,186 (GRCm39) |
H1771R |
probably benign |
Het |
| Nkain2 |
T |
C |
10: 32,205,840 (GRCm39) |
Y65C |
probably damaging |
Het |
| Or51a43 |
T |
A |
7: 103,718,056 (GRCm39) |
M61L |
probably damaging |
Het |
| Or51b6b |
A |
T |
7: 103,310,112 (GRCm39) |
V115D |
probably damaging |
Het |
| Or6aa1 |
T |
C |
7: 86,043,798 (GRCm39) |
K303E |
possibly damaging |
Het |
| Pabpc4l |
A |
C |
3: 46,400,725 (GRCm39) |
D306E |
probably benign |
Het |
| Parp12 |
A |
T |
6: 39,079,515 (GRCm39) |
Y332N |
probably damaging |
Het |
| Parvb |
A |
T |
15: 84,193,154 (GRCm39) |
K316M |
probably damaging |
Het |
| Pde8a |
T |
A |
7: 80,945,519 (GRCm39) |
|
probably benign |
Het |
| Polq |
A |
G |
16: 36,833,471 (GRCm39) |
T55A |
probably benign |
Het |
| Ppp2r5b |
T |
A |
19: 6,281,016 (GRCm39) |
K271M |
probably damaging |
Het |
| Ralgapb |
A |
G |
2: 158,334,936 (GRCm39) |
|
probably null |
Het |
| Rigi |
C |
T |
4: 40,229,661 (GRCm39) |
C86Y |
probably benign |
Het |
| Skap2 |
T |
C |
6: 51,886,351 (GRCm39) |
N175D |
probably benign |
Het |
| Slc44a3 |
A |
G |
3: 121,303,970 (GRCm39) |
|
probably benign |
Het |
| Smurf2 |
G |
A |
11: 106,736,873 (GRCm39) |
H318Y |
probably damaging |
Het |
| Tbc1d23 |
T |
C |
16: 57,004,778 (GRCm39) |
T460A |
possibly damaging |
Het |
| Tcerg1 |
T |
C |
18: 42,657,414 (GRCm39) |
S299P |
unknown |
Het |
| Tll1 |
A |
C |
8: 64,658,319 (GRCm39) |
Y33* |
probably null |
Het |
| Tmem59 |
A |
T |
4: 107,054,782 (GRCm39) |
T196S |
probably damaging |
Het |
| Ttll4 |
C |
A |
1: 74,718,662 (GRCm39) |
A171D |
possibly damaging |
Het |
| Ttn |
T |
C |
2: 76,641,513 (GRCm39) |
T13528A |
possibly damaging |
Het |
| Ttn |
A |
G |
2: 76,717,621 (GRCm39) |
|
probably benign |
Het |
| Xpc |
C |
A |
6: 91,477,119 (GRCm39) |
G327W |
probably damaging |
Het |
| Zbtb7a |
A |
G |
10: 80,980,132 (GRCm39) |
S109G |
probably benign |
Het |
| Zfyve26 |
T |
C |
12: 79,285,794 (GRCm39) |
M2328V |
probably benign |
Het |
|
| Other mutations in Far1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00815:Far1
|
APN |
7 |
113,139,896 (GRCm39) |
missense |
probably benign |
0.07 |
|
IGL02597:Far1
|
APN |
7 |
113,150,463 (GRCm39) |
missense |
probably benign |
0.31 |
|
R0499:Far1
|
UTSW |
7 |
113,153,503 (GRCm39) |
intron |
probably benign |
|
|
R2045:Far1
|
UTSW |
7 |
113,138,478 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R2140:Far1
|
UTSW |
7 |
113,165,667 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R2852:Far1
|
UTSW |
7 |
113,152,944 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R2853:Far1
|
UTSW |
7 |
113,152,944 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4423:Far1
|
UTSW |
7 |
113,139,805 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4426:Far1
|
UTSW |
7 |
113,149,208 (GRCm39) |
missense |
probably benign |
0.08 |
|
R4801:Far1
|
UTSW |
7 |
113,138,660 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R4802:Far1
|
UTSW |
7 |
113,138,660 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R4898:Far1
|
UTSW |
7 |
113,167,432 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5762:Far1
|
UTSW |
7 |
113,167,396 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6151:Far1
|
UTSW |
7 |
113,160,603 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R6165:Far1
|
UTSW |
7 |
113,153,425 (GRCm39) |
missense |
probably benign |
|
|
R6278:Far1
|
UTSW |
7 |
113,167,344 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7269:Far1
|
UTSW |
7 |
113,160,654 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7356:Far1
|
UTSW |
7 |
113,167,349 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R7853:Far1
|
UTSW |
7 |
113,153,355 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9028:Far1
|
UTSW |
7 |
113,146,629 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9519:Far1
|
UTSW |
7 |
113,150,559 (GRCm39) |
missense |
probably benign |
0.01 |
|
| Posted On |
2015-12-18 |
Incidental Mutation