Incidental Mutation 'IGL02355:Selplg'
| ID |
289639 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Selplg
|
| Ensembl Gene |
ENSMUSG00000048163 |
| Gene Name |
selectin, platelet (p-selectin) ligand |
| Synonyms |
Psgl-1, CD162, Psgl1 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.066)
|
| Stock # |
IGL02355
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
5 |
| Chromosomal Location |
113956597-113970705 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 113957467 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Proline
at position 280
(S280P)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000098436
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000100874]
[ENSMUST00000199109]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000100874
AA Change: S280P
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000098436
Gene: ENSMUSG00000048163
AA Change: S280P
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
17 |
N/A |
INTRINSIC |
|
low complexity region
|
102 |
115 |
N/A |
INTRINSIC |
|
internal_repeat_2
|
130 |
182 |
2.38e-13 |
PROSPERO |
|
internal_repeat_1
|
133 |
186 |
5.75e-16 |
PROSPERO |
|
internal_repeat_1
|
193 |
246 |
5.75e-16 |
PROSPERO |
|
internal_repeat_2
|
200 |
252 |
2.38e-13 |
PROSPERO |
|
transmembrane domain
|
328 |
350 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000198920
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000199109
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000201194
|
| Predicted Effect |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000202555
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a glycoprotein that functions as a high affinity counter-receptor for the cell adhesion molecules P-, E- and L- selectin expressed on myeloid cells and stimulated T lymphocytes. As such, this protein plays a critical role in leukocyte trafficking during inflammation by tethering of leukocytes to activated platelets or endothelia expressing selectins. This protein requires two post-translational modifications, tyrosine sulfation and the addition of the sialyl Lewis x tetrasaccharide (sLex) to its O-linked glycans, for its high-affinity binding activity. Aberrant expression of this gene and polymorphisms in this gene are associated with defects in the innate and adaptive immune response. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Apr 2011]
PHENOTYPE: Mice homozygous for a null allele exhibit neutrophillia and impaired leukocyte adhesion and rolling. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 42 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam3 |
C |
A |
8: 25,187,207 (GRCm39) |
C428F |
probably damaging |
Het |
| Alas1 |
T |
C |
9: 106,113,838 (GRCm39) |
Y469C |
probably damaging |
Het |
| Asxl1 |
C |
T |
2: 153,243,706 (GRCm39) |
L1419F |
probably benign |
Het |
| Bcan |
C |
T |
3: 87,901,449 (GRCm39) |
D418N |
possibly damaging |
Het |
| Cdc42bpg |
A |
G |
19: 6,360,839 (GRCm39) |
D199G |
possibly damaging |
Het |
| Chst15 |
T |
C |
7: 131,868,401 (GRCm39) |
N340D |
probably benign |
Het |
| Col12a1 |
T |
G |
9: 79,537,993 (GRCm39) |
|
probably benign |
Het |
| Cyp2c67 |
T |
A |
19: 39,631,849 (GRCm39) |
H116L |
probably benign |
Het |
| Cyp2c67 |
G |
A |
19: 39,605,826 (GRCm39) |
R357* |
probably null |
Het |
| Ears2 |
T |
C |
7: 121,643,773 (GRCm39) |
D395G |
probably benign |
Het |
| Fam227a |
A |
T |
15: 79,528,139 (GRCm39) |
|
probably benign |
Het |
| Fap |
A |
G |
2: 62,403,842 (GRCm39) |
V11A |
probably benign |
Het |
| Ganc |
A |
G |
2: 120,264,238 (GRCm39) |
D397G |
probably damaging |
Het |
| Gjb6 |
C |
A |
14: 57,361,752 (GRCm39) |
G170C |
possibly damaging |
Het |
| Gria2 |
A |
T |
3: 80,614,244 (GRCm39) |
W599R |
probably damaging |
Het |
| Gvin-ps5 |
T |
C |
7: 105,929,480 (GRCm39) |
|
noncoding transcript |
Het |
| Ighv1-64 |
A |
G |
12: 115,471,236 (GRCm39) |
S94P |
probably benign |
Het |
| Kifc3 |
C |
T |
8: 95,836,507 (GRCm39) |
A85T |
probably damaging |
Het |
| Lifr |
G |
A |
15: 7,194,174 (GRCm39) |
|
probably null |
Het |
| Lonp2 |
T |
G |
8: 87,350,874 (GRCm39) |
S21R |
probably benign |
Het |
| Nxpe3 |
A |
G |
16: 55,710,949 (GRCm39) |
V30A |
probably benign |
Het |
| Olfml1 |
T |
C |
7: 107,167,010 (GRCm39) |
V13A |
probably benign |
Het |
| Or10w1 |
T |
C |
19: 13,632,597 (GRCm39) |
V268A |
probably benign |
Het |
| Or1af1 |
A |
G |
2: 37,109,681 (GRCm39) |
Y60C |
probably damaging |
Het |
| Pcnt |
G |
A |
10: 76,210,996 (GRCm39) |
Q2376* |
probably null |
Het |
| Pglyrp2 |
A |
G |
17: 32,635,996 (GRCm39) |
L380P |
probably damaging |
Het |
| Plin3 |
A |
G |
17: 56,593,636 (GRCm39) |
V26A |
probably benign |
Het |
| Potefam1 |
T |
C |
2: 111,041,996 (GRCm39) |
|
probably benign |
Het |
| Pramel25 |
A |
G |
4: 143,519,580 (GRCm39) |
S114G |
probably damaging |
Het |
| Rims1 |
A |
G |
1: 22,522,288 (GRCm39) |
I470T |
probably damaging |
Het |
| Rora |
T |
C |
9: 69,281,374 (GRCm39) |
Y329H |
probably damaging |
Het |
| Scnn1b |
G |
A |
7: 121,516,770 (GRCm39) |
R503H |
probably damaging |
Het |
| Sec14l1 |
A |
G |
11: 117,035,675 (GRCm39) |
D237G |
possibly damaging |
Het |
| Serpina12 |
A |
G |
12: 104,004,140 (GRCm39) |
L164P |
probably benign |
Het |
| Sik2 |
C |
T |
9: 50,828,903 (GRCm39) |
W176* |
probably null |
Het |
| Slc2a1 |
T |
C |
4: 118,993,612 (GRCm39) |
F483S |
possibly damaging |
Het |
| Speg |
A |
G |
1: 75,400,559 (GRCm39) |
D2573G |
possibly damaging |
Het |
| Stil |
C |
T |
4: 114,867,308 (GRCm39) |
S239L |
probably damaging |
Het |
| Tmem94 |
C |
A |
11: 115,685,571 (GRCm39) |
S941R |
probably damaging |
Het |
| Tnfrsf11b |
T |
A |
15: 54,115,778 (GRCm39) |
D273V |
probably damaging |
Het |
| Tns2 |
A |
G |
15: 102,020,725 (GRCm39) |
T864A |
probably benign |
Het |
| Zfpm2 |
A |
G |
15: 40,962,890 (GRCm39) |
H184R |
probably damaging |
Het |
|
| Other mutations in Selplg |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01412:Selplg
|
APN |
5 |
113,957,529 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01488:Selplg
|
APN |
5 |
113,957,697 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
IGL02362:Selplg
|
APN |
5 |
113,957,467 (GRCm39) |
missense |
probably benign |
0.00 |
|
PIT4142001:Selplg
|
UTSW |
5 |
113,957,689 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0375:Selplg
|
UTSW |
5 |
113,958,069 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1222:Selplg
|
UTSW |
5 |
113,957,434 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1840:Selplg
|
UTSW |
5 |
113,957,905 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R2925:Selplg
|
UTSW |
5 |
113,958,240 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R4512:Selplg
|
UTSW |
5 |
113,957,124 (GRCm39) |
missense |
probably benign |
0.05 |
|
R4702:Selplg
|
UTSW |
5 |
113,957,094 (GRCm39) |
missense |
probably benign |
0.31 |
|
R4703:Selplg
|
UTSW |
5 |
113,957,094 (GRCm39) |
missense |
probably benign |
0.31 |
|
R4704:Selplg
|
UTSW |
5 |
113,957,094 (GRCm39) |
missense |
probably benign |
0.31 |
|
R4968:Selplg
|
UTSW |
5 |
113,957,787 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R5075:Selplg
|
UTSW |
5 |
113,958,045 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6159:Selplg
|
UTSW |
5 |
113,957,162 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6345:Selplg
|
UTSW |
5 |
113,958,210 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6550:Selplg
|
UTSW |
5 |
113,958,210 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6554:Selplg
|
UTSW |
5 |
113,958,210 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6997:Selplg
|
UTSW |
5 |
113,957,756 (GRCm39) |
unclassified |
probably benign |
|
|
R7050:Selplg
|
UTSW |
5 |
113,957,756 (GRCm39) |
unclassified |
probably benign |
|
|
R7094:Selplg
|
UTSW |
5 |
113,957,756 (GRCm39) |
unclassified |
probably benign |
|
|
R7235:Selplg
|
UTSW |
5 |
113,957,756 (GRCm39) |
unclassified |
probably benign |
|
|
R7481:Selplg
|
UTSW |
5 |
113,957,756 (GRCm39) |
unclassified |
probably benign |
|
|
R7604:Selplg
|
UTSW |
5 |
113,957,756 (GRCm39) |
unclassified |
probably benign |
|
|
R7674:Selplg
|
UTSW |
5 |
113,957,756 (GRCm39) |
unclassified |
probably benign |
|
|
R7846:Selplg
|
UTSW |
5 |
113,957,481 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7887:Selplg
|
UTSW |
5 |
113,957,756 (GRCm39) |
unclassified |
probably benign |
|
|
R8051:Selplg
|
UTSW |
5 |
113,957,502 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8823:Selplg
|
UTSW |
5 |
113,957,756 (GRCm39) |
unclassified |
probably benign |
|
|
R8834:Selplg
|
UTSW |
5 |
113,957,691 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R8955:Selplg
|
UTSW |
5 |
113,957,756 (GRCm39) |
unclassified |
probably benign |
|
|
R9036:Selplg
|
UTSW |
5 |
113,957,756 (GRCm39) |
unclassified |
probably benign |
|
|
R9152:Selplg
|
UTSW |
5 |
113,957,467 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9241:Selplg
|
UTSW |
5 |
113,957,647 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R9249:Selplg
|
UTSW |
5 |
113,957,756 (GRCm39) |
unclassified |
probably benign |
|
|
R9361:Selplg
|
UTSW |
5 |
113,957,756 (GRCm39) |
unclassified |
probably benign |
|
|
R9381:Selplg
|
UTSW |
5 |
113,957,917 (GRCm39) |
missense |
probably benign |
0.05 |
|
R9434:Selplg
|
UTSW |
5 |
113,957,756 (GRCm39) |
unclassified |
probably benign |
|
|
R9446:Selplg
|
UTSW |
5 |
113,957,756 (GRCm39) |
unclassified |
probably benign |
|
|
R9482:Selplg
|
UTSW |
5 |
113,957,756 (GRCm39) |
unclassified |
probably benign |
|
|
R9670:Selplg
|
UTSW |
5 |
113,957,756 (GRCm39) |
unclassified |
probably benign |
|
|
R9779:Selplg
|
UTSW |
5 |
113,957,756 (GRCm39) |
unclassified |
probably benign |
|
|
Z1177:Selplg
|
UTSW |
5 |
113,957,412 (GRCm39) |
missense |
probably benign |
0.30 |
|
| Posted On |
2015-04-16 |
Incidental Mutation