Incidental Mutation 'IGL02928:Stxbp2'
| ID |
363954 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Stxbp2
|
| Ensembl Gene |
ENSMUSG00000004626 |
| Gene Name |
syntaxin binding protein 2 |
| Synonyms |
muSec1, C79054, Sxtp2, Munc18b, Munc-18b, Munc-18-2 |
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
IGL02928
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
8 |
| Chromosomal Location |
3680955-3693644 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 3691736 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Glycine
at position 485
(D485G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000125405
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000160708]
|
| AlphaFold |
Q64324 |
| Predicted Effect |
unknown
Transcript: ENSMUST00000004745
AA Change: D484G
|
| SMART Domains |
Protein: ENSMUSP00000004745
Gene: ENSMUSG00000004626
AA Change: D484G
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Sec1
|
29 |
580 |
6.8e-113 |
PFAM |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000159370
AA Change: D15G
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000159652
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000160435
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000160708
AA Change: D485G
PolyPhen 2
Score 0.986 (Sensitivity: 0.74; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000125405
Gene: ENSMUSG00000004626
AA Change: D485G
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Sec1
|
29 |
579 |
4.9e-112 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000161629
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000162047
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000162832
|
| 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 member of the STXBP/unc-18/SEC1 family. The encoded protein is involved in intracellular trafficking, control of SNARE (soluble NSF attachment protein receptor) complex assembly, and the release of cytotoxic granules by natural killer cells. Mutations in this gene are associated with familial hemophagocytic lymphohistiocytosis. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jan 2013]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit complete preweaning lethality. Mice heterozygous for this allele exhibit decreased stimulated mucin secretion, release of histones in stimulated mast cells and decreased susceptibility to type I hypersensitivity reaction. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 47 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700018F24Rik |
A |
G |
5: 144,980,327 (GRCm39) |
Y92C |
probably damaging |
Het |
| Aadacl4fm1 |
A |
T |
4: 144,255,802 (GRCm39) |
L407F |
possibly damaging |
Het |
| Abcc3 |
G |
T |
11: 94,252,132 (GRCm39) |
T817K |
possibly damaging |
Het |
| Arhgap10 |
G |
A |
8: 77,977,539 (GRCm39) |
|
probably benign |
Het |
| Arhgef16 |
G |
T |
4: 154,367,350 (GRCm39) |
Q352K |
probably benign |
Het |
| Cep104 |
A |
G |
4: 154,065,716 (GRCm39) |
I68V |
probably benign |
Het |
| Col5a2 |
G |
A |
1: 45,424,180 (GRCm39) |
A1082V |
probably benign |
Het |
| Col6a1 |
A |
T |
10: 76,545,500 (GRCm39) |
Y991N |
possibly damaging |
Het |
| Ehmt2 |
T |
C |
17: 35,129,798 (GRCm39) |
I1021T |
probably damaging |
Het |
| Eif2ak4 |
G |
A |
2: 118,303,168 (GRCm39) |
|
probably null |
Het |
| Ern1 |
A |
G |
11: 106,296,705 (GRCm39) |
|
probably benign |
Het |
| Fgf18 |
A |
T |
11: 33,074,674 (GRCm39) |
I99N |
possibly damaging |
Het |
| Glp1r |
A |
G |
17: 31,137,911 (GRCm39) |
D114G |
probably benign |
Het |
| Gm10553 |
A |
G |
1: 85,077,933 (GRCm39) |
K17E |
possibly damaging |
Het |
| Gm5422 |
T |
A |
10: 31,126,250 (GRCm39) |
|
noncoding transcript |
Het |
| Gnb1 |
A |
C |
4: 155,637,863 (GRCm39) |
T196P |
probably benign |
Het |
| Ighv6-5 |
T |
A |
12: 114,380,412 (GRCm39) |
D35V |
probably benign |
Het |
| Il18r1 |
G |
A |
1: 40,517,711 (GRCm39) |
|
probably null |
Het |
| Ipo11 |
A |
T |
13: 107,025,863 (GRCm39) |
|
probably benign |
Het |
| Itih1 |
T |
A |
14: 30,659,715 (GRCm39) |
Q307L |
probably damaging |
Het |
| Mmp1b |
T |
A |
9: 7,368,242 (GRCm39) |
*464L |
probably null |
Het |
| Mrps7 |
C |
T |
11: 115,495,910 (GRCm39) |
Q113* |
probably null |
Het |
| Npat |
A |
C |
9: 53,478,138 (GRCm39) |
|
probably benign |
Het |
| Nrp2 |
A |
G |
1: 62,854,605 (GRCm39) |
I852V |
probably damaging |
Het |
| Or10ak14 |
A |
G |
4: 118,611,697 (GRCm39) |
F15L |
probably damaging |
Het |
| Or5ae2 |
A |
G |
7: 84,506,273 (GRCm39) |
E232G |
probably benign |
Het |
| P2rx6 |
T |
A |
16: 17,382,901 (GRCm39) |
|
probably benign |
Het |
| Parp6 |
T |
A |
9: 59,548,346 (GRCm39) |
N466K |
possibly damaging |
Het |
| Prss12 |
A |
T |
3: 123,280,805 (GRCm39) |
N497Y |
possibly damaging |
Het |
| Psg22 |
T |
C |
7: 18,453,458 (GRCm39) |
V51A |
probably damaging |
Het |
| Ptgir |
T |
C |
7: 16,642,923 (GRCm39) |
S175P |
possibly damaging |
Het |
| Rd3l |
T |
C |
12: 111,946,012 (GRCm39) |
S156G |
probably benign |
Het |
| Reck |
C |
T |
4: 43,912,078 (GRCm39) |
H196Y |
possibly damaging |
Het |
| Rft1 |
T |
A |
14: 30,385,072 (GRCm39) |
V165D |
possibly damaging |
Het |
| Rin2 |
A |
G |
2: 145,701,926 (GRCm39) |
|
probably benign |
Het |
| Rufy4 |
A |
G |
1: 74,168,241 (GRCm39) |
|
probably benign |
Het |
| Scfd2 |
G |
A |
5: 74,691,832 (GRCm39) |
T150M |
probably damaging |
Het |
| Sgca |
A |
G |
11: 94,863,129 (GRCm39) |
W75R |
probably damaging |
Het |
| Sirt7 |
A |
T |
11: 120,511,042 (GRCm39) |
D318E |
probably benign |
Het |
| Smr2l |
A |
T |
5: 88,424,976 (GRCm39) |
I14L |
probably benign |
Het |
| Snta1 |
C |
T |
2: 154,222,959 (GRCm39) |
A255T |
probably benign |
Het |
| Sycp1 |
T |
A |
3: 102,726,134 (GRCm39) |
|
probably benign |
Het |
| Tenm2 |
A |
G |
11: 35,917,997 (GRCm39) |
V1922A |
possibly damaging |
Het |
| Ttc7b |
A |
T |
12: 100,369,674 (GRCm39) |
V365D |
probably damaging |
Het |
| Upk3b |
A |
G |
5: 136,067,995 (GRCm39) |
E62G |
probably benign |
Het |
| Wdr36 |
T |
C |
18: 32,980,372 (GRCm39) |
|
probably null |
Het |
| Yars2 |
T |
C |
16: 16,121,410 (GRCm39) |
F188S |
probably damaging |
Het |
|
| Other mutations in Stxbp2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00160:Stxbp2
|
APN |
8 |
3,686,354 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
IGL00466:Stxbp2
|
APN |
8 |
3,684,065 (GRCm39) |
missense |
probably benign |
0.29 |
|
IGL02315:Stxbp2
|
APN |
8 |
3,685,607 (GRCm39) |
unclassified |
probably benign |
|
|
IGL02508:Stxbp2
|
APN |
8 |
3,682,531 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02811:Stxbp2
|
APN |
8 |
3,691,971 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL02833:Stxbp2
|
APN |
8 |
3,691,971 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL02868:Stxbp2
|
APN |
8 |
3,691,971 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL02869:Stxbp2
|
APN |
8 |
3,691,971 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL02896:Stxbp2
|
APN |
8 |
3,691,971 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL02926:Stxbp2
|
APN |
8 |
3,685,629 (GRCm39) |
missense |
probably benign |
0.31 |
|
IGL02927:Stxbp2
|
APN |
8 |
3,692,685 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL02943:Stxbp2
|
APN |
8 |
3,691,971 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL02945:Stxbp2
|
APN |
8 |
3,691,971 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL02948:Stxbp2
|
APN |
8 |
3,691,971 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL02951:Stxbp2
|
APN |
8 |
3,691,971 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL02972:Stxbp2
|
APN |
8 |
3,691,971 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL02976:Stxbp2
|
APN |
8 |
3,691,971 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL02977:Stxbp2
|
APN |
8 |
3,691,971 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL02983:Stxbp2
|
APN |
8 |
3,691,971 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL02993:Stxbp2
|
APN |
8 |
3,691,971 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL03008:Stxbp2
|
APN |
8 |
3,691,971 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL03009:Stxbp2
|
APN |
8 |
3,691,971 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL03038:Stxbp2
|
APN |
8 |
3,691,971 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL03051:Stxbp2
|
APN |
8 |
3,691,971 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL03061:Stxbp2
|
APN |
8 |
3,691,971 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL03072:Stxbp2
|
APN |
8 |
3,691,971 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL03110:Stxbp2
|
APN |
8 |
3,683,342 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02988:Stxbp2
|
UTSW |
8 |
3,683,267 (GRCm39) |
intron |
probably benign |
|
|
R0463:Stxbp2
|
UTSW |
8 |
3,682,559 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0608:Stxbp2
|
UTSW |
8 |
3,682,559 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0755:Stxbp2
|
UTSW |
8 |
3,692,019 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1328:Stxbp2
|
UTSW |
8 |
3,692,657 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R1771:Stxbp2
|
UTSW |
8 |
3,684,064 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1962:Stxbp2
|
UTSW |
8 |
3,692,672 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2195:Stxbp2
|
UTSW |
8 |
3,684,615 (GRCm39) |
splice site |
probably null |
|
|
R2319:Stxbp2
|
UTSW |
8 |
3,683,834 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R3614:Stxbp2
|
UTSW |
8 |
3,681,196 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R3870:Stxbp2
|
UTSW |
8 |
3,684,079 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3876:Stxbp2
|
UTSW |
8 |
3,683,369 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4703:Stxbp2
|
UTSW |
8 |
3,682,521 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6533:Stxbp2
|
UTSW |
8 |
3,692,683 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6623:Stxbp2
|
UTSW |
8 |
3,682,561 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6665:Stxbp2
|
UTSW |
8 |
3,691,998 (GRCm39) |
missense |
probably benign |
0.41 |
|
R6798:Stxbp2
|
UTSW |
8 |
3,691,180 (GRCm39) |
missense |
probably benign |
|
|
R7152:Stxbp2
|
UTSW |
8 |
3,682,583 (GRCm39) |
missense |
probably benign |
0.33 |
|
R7326:Stxbp2
|
UTSW |
8 |
3,691,151 (GRCm39) |
missense |
|
|
|
R8237:Stxbp2
|
UTSW |
8 |
3,685,695 (GRCm39) |
missense |
|
|
|
R8268:Stxbp2
|
UTSW |
8 |
3,682,234 (GRCm39) |
missense |
|
|
|
R8709:Stxbp2
|
UTSW |
8 |
3,683,914 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R8811:Stxbp2
|
UTSW |
8 |
3,689,541 (GRCm39) |
missense |
|
|
|
R9018:Stxbp2
|
UTSW |
8 |
3,692,627 (GRCm39) |
intron |
probably benign |
|
|
R9043:Stxbp2
|
UTSW |
8 |
3,684,478 (GRCm39) |
missense |
|
|
|
R9048:Stxbp2
|
UTSW |
8 |
3,687,218 (GRCm39) |
missense |
|
|
|
R9212:Stxbp2
|
UTSW |
8 |
3,686,220 (GRCm39) |
missense |
|
|
|
R9421:Stxbp2
|
UTSW |
8 |
3,682,264 (GRCm39) |
missense |
|
|
|
R9643:Stxbp2
|
UTSW |
8 |
3,686,392 (GRCm39) |
missense |
|
|
|
Z1177:Stxbp2
|
UTSW |
8 |
3,691,123 (GRCm39) |
missense |
probably benign |
|
|
| Posted On |
2015-12-18 |
Incidental Mutation