Incidental Mutation 'IGL02101:Slc27a5'
| ID |
279747 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Slc27a5
|
| Ensembl Gene |
ENSMUSG00000030382 |
| Gene Name |
solute carrier family 27 (fatty acid transporter), member 5 |
| Synonyms |
VLCSH2, FACVL3, VLCS-H2, FATP5 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.138)
|
| Stock # |
IGL02101
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
12722273-12732119 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 12727270 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Asparagine
at position 384
(I384N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000112495
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000032539]
[ENSMUST00000120903]
|
| AlphaFold |
Q4LDG0 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000032539
AA Change: I384N
PolyPhen 2
Score 0.952 (Sensitivity: 0.79; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000032539
Gene: ENSMUSG00000030382
AA Change: I384N
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
|
transmembrane domain
|
29 |
51 |
N/A |
INTRINSIC |
|
transmembrane domain
|
58 |
77 |
N/A |
INTRINSIC |
|
Pfam:AMP-binding
|
119 |
557 |
1.3e-64 |
PFAM |
|
Pfam:AMP-binding_C
|
565 |
641 |
1.4e-11 |
PFAM |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000120903
AA Change: I384N
PolyPhen 2
Score 0.952 (Sensitivity: 0.79; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000112495
Gene: ENSMUSG00000030382
AA Change: I384N
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
|
transmembrane domain
|
29 |
51 |
N/A |
INTRINSIC |
|
transmembrane domain
|
58 |
77 |
N/A |
INTRINSIC |
|
Pfam:AMP-binding
|
119 |
414 |
2e-42 |
PFAM |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000133977
AA Change: I185N
|
| SMART Domains |
Protein: ENSMUSP00000117208
Gene: ENSMUSG00000030382
AA Change: I185N
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:AMP-binding
|
1 |
102 |
3.3e-8 |
PFAM |
|
Pfam:AMP-binding
|
100 |
195 |
1.3e-16 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000155192
|
| 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 an isozyme of very long-chain acyl-CoA synthetase (VLCS). It is capable of activating very long-chain fatty-acids containing 24- and 26-carbons. It is expressed in liver and associated with endoplasmic reticulum but not with peroxisomes. Its primary role is in fatty acid elongation or complex lipid synthesis rather than in degradation. This gene has a mouse ortholog. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a null allele exhibit altered lipid homeostasis. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 27 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Cd163 |
T |
A |
6: 124,284,246 (GRCm39) |
C139* |
probably null |
Het |
| Ces2g |
A |
G |
8: 105,691,769 (GRCm39) |
|
probably null |
Het |
| Ckap5 |
T |
C |
2: 91,402,885 (GRCm39) |
|
probably benign |
Het |
| Cmtm7 |
T |
C |
9: 114,592,336 (GRCm39) |
H87R |
probably damaging |
Het |
| Dennd3 |
A |
G |
15: 73,399,794 (GRCm39) |
D220G |
possibly damaging |
Het |
| Dpp10 |
T |
C |
1: 123,339,555 (GRCm39) |
Y324C |
probably damaging |
Het |
| Dsc3 |
C |
T |
18: 20,134,963 (GRCm39) |
R7Q |
probably benign |
Het |
| Ezh1 |
T |
C |
11: 101,086,392 (GRCm39) |
K598E |
possibly damaging |
Het |
| Ighv7-3 |
A |
G |
12: 114,117,045 (GRCm39) |
L39P |
probably damaging |
Het |
| Il1rap |
T |
A |
16: 26,442,932 (GRCm39) |
S9R |
possibly damaging |
Het |
| Mrgpra3 |
A |
G |
7: 47,239,300 (GRCm39) |
C209R |
probably damaging |
Het |
| Oc90 |
G |
T |
15: 65,769,638 (GRCm39) |
P73Q |
probably damaging |
Het |
| Or2m12 |
T |
C |
16: 19,105,363 (GRCm39) |
I43M |
probably benign |
Het |
| Or3a1b |
G |
A |
11: 74,012,571 (GRCm39) |
W152* |
probably null |
Het |
| Pccb |
A |
G |
9: 100,869,894 (GRCm39) |
F346L |
possibly damaging |
Het |
| Pdxdc1 |
A |
G |
16: 13,687,720 (GRCm39) |
I225T |
probably damaging |
Het |
| Pold3 |
A |
T |
7: 99,749,703 (GRCm39) |
M154K |
probably damaging |
Het |
| Polr1a |
T |
G |
6: 71,927,786 (GRCm39) |
C846G |
probably benign |
Het |
| Ppip5k1 |
C |
A |
2: 121,162,089 (GRCm39) |
R978L |
possibly damaging |
Het |
| Ptpn4 |
A |
G |
1: 119,615,408 (GRCm39) |
V582A |
probably damaging |
Het |
| Sez6l |
G |
T |
5: 112,620,612 (GRCm39) |
Q323K |
probably damaging |
Het |
| Slc39a10 |
G |
A |
1: 46,857,288 (GRCm39) |
A696V |
probably damaging |
Het |
| Slc7a2 |
T |
C |
8: 41,355,631 (GRCm39) |
F227L |
probably benign |
Het |
| Smad4 |
C |
A |
18: 73,791,723 (GRCm39) |
A273S |
probably benign |
Het |
| Spata17 |
T |
C |
1: 186,849,657 (GRCm39) |
I84V |
probably benign |
Het |
| Sphkap |
T |
C |
1: 83,268,708 (GRCm39) |
T95A |
probably damaging |
Het |
| Tie1 |
T |
C |
4: 118,329,995 (GRCm39) |
D1076G |
probably benign |
Het |
|
| Other mutations in Slc27a5 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00592:Slc27a5
|
APN |
7 |
12,722,566 (GRCm39) |
missense |
probably benign |
0.08 |
|
IGL00906:Slc27a5
|
APN |
7 |
12,724,984 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01067:Slc27a5
|
APN |
7 |
12,722,999 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02148:Slc27a5
|
APN |
7 |
12,728,878 (GRCm39) |
missense |
probably damaging |
0.97 |
|
IGL02165:Slc27a5
|
APN |
7 |
12,728,875 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02324:Slc27a5
|
APN |
7 |
12,731,487 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02879:Slc27a5
|
APN |
7 |
12,728,971 (GRCm39) |
splice site |
probably benign |
|
|
R1519:Slc27a5
|
UTSW |
7 |
12,722,386 (GRCm39) |
splice site |
probably null |
|
|
R1662:Slc27a5
|
UTSW |
7 |
12,725,173 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1774:Slc27a5
|
UTSW |
7 |
12,731,534 (GRCm39) |
nonsense |
probably null |
|
|
R2012:Slc27a5
|
UTSW |
7 |
12,731,634 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2020:Slc27a5
|
UTSW |
7 |
12,727,339 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2886:Slc27a5
|
UTSW |
7 |
12,723,487 (GRCm39) |
unclassified |
probably benign |
|
|
R4234:Slc27a5
|
UTSW |
7 |
12,722,370 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4855:Slc27a5
|
UTSW |
7 |
12,722,560 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5126:Slc27a5
|
UTSW |
7 |
12,725,247 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5450:Slc27a5
|
UTSW |
7 |
12,728,869 (GRCm39) |
missense |
probably benign |
0.04 |
|
R5712:Slc27a5
|
UTSW |
7 |
12,732,010 (GRCm39) |
unclassified |
probably benign |
|
|
R6302:Slc27a5
|
UTSW |
7 |
12,722,479 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6346:Slc27a5
|
UTSW |
7 |
12,724,899 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R6866:Slc27a5
|
UTSW |
7 |
12,731,443 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6921:Slc27a5
|
UTSW |
7 |
12,725,135 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7329:Slc27a5
|
UTSW |
7 |
12,725,089 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R8017:Slc27a5
|
UTSW |
7 |
12,723,329 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8019:Slc27a5
|
UTSW |
7 |
12,723,329 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8312:Slc27a5
|
UTSW |
7 |
12,725,214 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8793:Slc27a5
|
UTSW |
7 |
12,723,296 (GRCm39) |
missense |
probably benign |
0.16 |
|
R8966:Slc27a5
|
UTSW |
7 |
12,725,090 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8980:Slc27a5
|
UTSW |
7 |
12,725,090 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9066:Slc27a5
|
UTSW |
7 |
12,722,530 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R9106:Slc27a5
|
UTSW |
7 |
12,725,097 (GRCm39) |
missense |
probably benign |
0.21 |
|
R9191:Slc27a5
|
UTSW |
7 |
12,725,247 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9275:Slc27a5
|
UTSW |
7 |
12,731,640 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Slc27a5
|
UTSW |
7 |
12,722,782 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2015-04-16 |
Incidental Mutation