Incidental Mutation 'R8818:Unc13d'
| ID |
672883 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Unc13d
|
| Ensembl Gene |
ENSMUSG00000057948 |
| Gene Name |
unc-13 homolog D |
| Synonyms |
Jinx, 2610108D09Rik, Munc13-4 |
| MMRRC Submission |
068651-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.120)
|
| Stock # |
R8818 (G1)
|
| Quality Score |
217.468 |
|
Status
|
Validated
|
| Chromosome |
11 |
| Chromosomal Location |
115952921-115968787 bp(-) (GRCm39) |
| Type of Mutation |
small insertion (3 aa in frame mutation) |
| DNA Base Change (assembly) |
AATGCCTCCCATGCC to AATGCCTCCCATGCCTCCCATGCC
at 115958998 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000134260
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000075036]
[ENSMUST00000106450]
[ENSMUST00000106451]
[ENSMUST00000173345]
[ENSMUST00000174822]
|
| AlphaFold |
B2RUP2 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000075036
|
| SMART Domains |
Protein: ENSMUSP00000074549
Gene: ENSMUSG00000057948
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
21 |
26 |
N/A |
INTRINSIC |
|
C2
|
111 |
261 |
5.31e-11 |
SMART |
|
PDB:3SWH|B
|
585 |
735 |
8e-6 |
PDB |
|
low complexity region
|
738 |
751 |
N/A |
INTRINSIC |
|
Pfam:Membr_traf_MHD
|
785 |
892 |
1.9e-25 |
PFAM |
|
C2
|
923 |
1031 |
7.93e-10 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000106450
|
| SMART Domains |
Protein: ENSMUSP00000102058
Gene: ENSMUSG00000057948
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
21 |
26 |
N/A |
INTRINSIC |
|
C2
|
111 |
261 |
5.31e-11 |
SMART |
|
PDB:3SWH|B
|
587 |
737 |
8e-6 |
PDB |
|
low complexity region
|
740 |
753 |
N/A |
INTRINSIC |
|
Pfam:Membr_traf_MHD
|
787 |
894 |
1.9e-25 |
PFAM |
|
C2
|
925 |
1033 |
7.93e-10 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000106451
|
| SMART Domains |
Protein: ENSMUSP00000102059
Gene: ENSMUSG00000057948
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
21 |
26 |
N/A |
INTRINSIC |
|
C2
|
111 |
261 |
5.31e-11 |
SMART |
|
PDB:3SWH|B
|
587 |
737 |
8e-6 |
PDB |
|
low complexity region
|
740 |
753 |
N/A |
INTRINSIC |
|
Pfam:Membr_traf_MHD
|
788 |
838 |
7.1e-10 |
PFAM |
|
Pfam:Membr_traf_MHD
|
830 |
893 |
1.4e-15 |
PFAM |
|
C2
|
925 |
1033 |
7.93e-10 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000173345
|
| SMART Domains |
Protein: ENSMUSP00000133679
Gene: ENSMUSG00000057948
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
21 |
26 |
N/A |
INTRINSIC |
|
C2
|
111 |
261 |
5.31e-11 |
SMART |
|
PDB:3SWH|B
|
587 |
737 |
5e-6 |
PDB |
|
low complexity region
|
740 |
753 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000174822
|
| SMART Domains |
Protein: ENSMUSP00000134260
Gene: ENSMUSG00000057948
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
21 |
26 |
N/A |
INTRINSIC |
|
C2
|
111 |
261 |
5.31e-11 |
SMART |
|
PDB:3SWH|B
|
585 |
735 |
8e-6 |
PDB |
|
low complexity region
|
738 |
751 |
N/A |
INTRINSIC |
|
Pfam:Membr_traf_MHD
|
785 |
892 |
1.9e-25 |
PFAM |
|
C2
|
923 |
1031 |
7.93e-10 |
SMART |
|
| Meta Mutation Damage Score |
0.0846 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 98.9%
|
| Validation Efficiency |
98% (55/56) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that is a member of the UNC13 family, containing similar domain structure as other family members but lacking an N-terminal phorbol ester-binding C1 domain present in other Munc13 proteins. The protein appears to play a role in vesicle maturation during exocytosis and is involved in regulation of cytolytic granules secretion. Mutations in this gene are associated with familial hemophagocytic lymphohistiocytosis type 3, a genetically heterogeneous, rare autosomal recessive disorder. [provided by RefSeq, Jul 2008]
PHENOTYPE: Targeted deletion of this gene leads to defective hemostasis, abrogated thrombus formation and protection of homozygotes from ischemic stroke in the absence of intracranial bleeding. Homozygous ENU mutant mice are sensitive to infection by mouse cytomegalovirus. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 55 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca14 |
G |
T |
7: 119,815,524 (GRCm39) |
M257I |
probably benign |
Het |
| Adam23 |
T |
C |
1: 63,584,627 (GRCm39) |
V345A |
probably damaging |
Het |
| Anxa6 |
T |
G |
11: 54,902,578 (GRCm39) |
N52T |
possibly damaging |
Het |
| Arhgef15 |
G |
A |
11: 68,841,938 (GRCm39) |
H496Y |
probably damaging |
Het |
| Atp2a3 |
A |
G |
11: 72,872,765 (GRCm39) |
E771G |
probably damaging |
Het |
| B3gnt5 |
A |
G |
16: 19,588,347 (GRCm39) |
T189A |
possibly damaging |
Het |
| Becn1 |
A |
T |
11: 101,186,230 (GRCm39) |
S125T |
probably damaging |
Het |
| Bltp1 |
T |
G |
3: 37,050,697 (GRCm39) |
M3011R |
possibly damaging |
Het |
| Ccdc180 |
A |
G |
4: 45,900,484 (GRCm39) |
M283V |
probably benign |
Het |
| Cdh17 |
T |
C |
4: 11,771,323 (GRCm39) |
F35S |
probably damaging |
Het |
| Clcn1 |
T |
A |
6: 42,282,477 (GRCm39) |
I515N |
probably damaging |
Het |
| Cyp4f17 |
A |
G |
17: 32,743,068 (GRCm39) |
Y247C |
probably damaging |
Het |
| Dcp1a |
T |
A |
14: 30,240,899 (GRCm39) |
H236Q |
possibly damaging |
Het |
| Dnah11 |
T |
A |
12: 117,874,764 (GRCm39) |
N4034Y |
probably damaging |
Het |
| Dsg1a |
A |
G |
18: 20,473,599 (GRCm39) |
I891V |
possibly damaging |
Het |
| Eid3 |
A |
G |
10: 82,703,441 (GRCm39) |
N301D |
probably damaging |
Het |
| Fbrs |
C |
A |
7: 127,078,694 (GRCm39) |
D108E |
unknown |
Het |
| Fbxw14 |
A |
C |
9: 109,116,071 (GRCm39) |
|
probably benign |
Het |
| Fzd8 |
A |
G |
18: 9,214,474 (GRCm39) |
T519A |
probably benign |
Het |
| Gldc |
C |
G |
19: 30,078,212 (GRCm39) |
M928I |
probably benign |
Het |
| Gpr3 |
C |
A |
4: 132,938,538 (GRCm39) |
V45L |
possibly damaging |
Het |
| Gramd1b |
A |
T |
9: 40,215,780 (GRCm39) |
I690K |
probably benign |
Het |
| Grhl2 |
T |
A |
15: 37,270,912 (GRCm39) |
D33E |
probably damaging |
Het |
| Kcnj4 |
C |
A |
15: 79,369,920 (GRCm39) |
R20L |
probably damaging |
Het |
| Klhl5 |
A |
G |
5: 65,305,989 (GRCm39) |
I319V |
probably benign |
Het |
| Lars2 |
A |
T |
9: 123,221,892 (GRCm39) |
E135D |
possibly damaging |
Het |
| Map9 |
T |
A |
3: 82,291,270 (GRCm39) |
Y602N |
possibly damaging |
Het |
| Mphosph9 |
A |
T |
5: 124,463,027 (GRCm39) |
L6* |
probably null |
Het |
| Naa35 |
C |
T |
13: 59,748,761 (GRCm39) |
T131M |
probably damaging |
Het |
| Nucb2 |
T |
A |
7: 116,121,136 (GRCm39) |
L22Q |
possibly damaging |
Het |
| Or8g26 |
A |
G |
9: 39,096,062 (GRCm39) |
Y193C |
probably damaging |
Het |
| Or8k28 |
C |
A |
2: 86,286,078 (GRCm39) |
C179F |
probably damaging |
Het |
| Pcdhb6 |
C |
T |
18: 37,468,837 (GRCm39) |
T586I |
probably benign |
Het |
| Ppcs |
A |
T |
4: 119,279,330 (GRCm39) |
L74Q |
probably damaging |
Het |
| Ppp6r3 |
A |
T |
19: 3,517,216 (GRCm39) |
V677D |
probably benign |
Het |
| Psg27 |
C |
T |
7: 18,294,337 (GRCm39) |
G357S |
probably damaging |
Het |
| Ptgdr2 |
A |
G |
19: 10,918,380 (GRCm39) |
N299S |
probably damaging |
Het |
| Relb |
T |
A |
7: 19,353,762 (GRCm39) |
I39F |
probably damaging |
Het |
| Ripor2 |
T |
A |
13: 24,901,651 (GRCm39) |
S907R |
possibly damaging |
Het |
| Rnf170 |
T |
G |
8: 26,629,043 (GRCm39) |
D172E |
probably benign |
Het |
| Rnf31 |
C |
A |
14: 55,832,396 (GRCm39) |
Q273K |
probably benign |
Het |
| Rrp36 |
A |
T |
17: 46,983,336 (GRCm39) |
S93T |
probably damaging |
Het |
| Rsad1 |
A |
T |
11: 94,439,100 (GRCm39) |
V120D |
probably benign |
Het |
| Ryr3 |
C |
T |
2: 112,661,441 (GRCm39) |
A1870T |
probably damaging |
Het |
| Serpina10 |
T |
G |
12: 103,595,063 (GRCm39) |
D52A |
probably benign |
Het |
| Slc47a1 |
A |
G |
11: 61,261,055 (GRCm39) |
I115T |
probably benign |
Het |
| Spag17 |
T |
A |
3: 99,920,543 (GRCm39) |
M426K |
probably benign |
Het |
| Sppl2b |
TGTCACAGGT |
TGT |
10: 80,701,903 (GRCm39) |
|
probably null |
Het |
| Sptbn4 |
T |
G |
7: 27,063,592 (GRCm39) |
E2283A |
possibly damaging |
Het |
| Top3a |
A |
G |
11: 60,633,877 (GRCm39) |
C740R |
probably damaging |
Het |
| Tpgs2 |
A |
T |
18: 25,291,365 (GRCm39) |
V33E |
probably damaging |
Het |
| Treh |
T |
C |
9: 44,592,823 (GRCm39) |
I116T |
probably damaging |
Het |
| Trpm3 |
A |
T |
19: 22,955,952 (GRCm39) |
N1138I |
possibly damaging |
Het |
| Vamp9 |
A |
T |
5: 100,089,094 (GRCm39) |
N120Y |
probably damaging |
Het |
| Zswim9 |
G |
T |
7: 12,994,456 (GRCm39) |
Q567K |
probably benign |
Het |
|
| Other mutations in Unc13d |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00711:Unc13d
|
APN |
11 |
115,965,229 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL00976:Unc13d
|
APN |
11 |
115,961,293 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01630:Unc13d
|
APN |
11 |
115,964,692 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01761:Unc13d
|
APN |
11 |
115,964,695 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01772:Unc13d
|
APN |
11 |
115,967,358 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
IGL01935:Unc13d
|
APN |
11 |
115,960,577 (GRCm39) |
missense |
probably benign |
|
|
IGL02486:Unc13d
|
APN |
11 |
115,960,632 (GRCm39) |
splice site |
probably benign |
|
|
IGL02503:Unc13d
|
APN |
11 |
115,959,628 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
IGL02519:Unc13d
|
APN |
11 |
115,961,359 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02524:Unc13d
|
APN |
11 |
115,961,145 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02634:Unc13d
|
APN |
11 |
115,961,382 (GRCm39) |
splice site |
probably benign |
|
|
IGL02636:Unc13d
|
APN |
11 |
115,964,444 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03243:Unc13d
|
APN |
11 |
115,958,670 (GRCm39) |
missense |
probably benign |
0.34 |
|
jinx
|
UTSW |
11 |
115,964,249 (GRCm39) |
unclassified |
probably benign |
|
|
R0033:Unc13d
|
UTSW |
11 |
115,959,991 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0084:Unc13d
|
UTSW |
11 |
115,954,657 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0122:Unc13d
|
UTSW |
11 |
115,956,308 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0422:Unc13d
|
UTSW |
11 |
115,960,846 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0666:Unc13d
|
UTSW |
11 |
115,960,318 (GRCm39) |
splice site |
probably benign |
|
|
R1019:Unc13d
|
UTSW |
11 |
115,958,900 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1333:Unc13d
|
UTSW |
11 |
115,964,381 (GRCm39) |
splice site |
probably benign |
|
|
R1484:Unc13d
|
UTSW |
11 |
115,964,701 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R1594:Unc13d
|
UTSW |
11 |
115,959,538 (GRCm39) |
missense |
probably benign |
0.04 |
|
R1597:Unc13d
|
UTSW |
11 |
115,965,262 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1603:Unc13d
|
UTSW |
11 |
115,964,481 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R1662:Unc13d
|
UTSW |
11 |
115,959,499 (GRCm39) |
missense |
probably null |
1.00 |
|
R1909:Unc13d
|
UTSW |
11 |
115,961,121 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2015:Unc13d
|
UTSW |
11 |
115,959,581 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2313:Unc13d
|
UTSW |
11 |
115,954,560 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2435:Unc13d
|
UTSW |
11 |
115,959,514 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4705:Unc13d
|
UTSW |
11 |
115,964,214 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R4732:Unc13d
|
UTSW |
11 |
115,964,408 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R4733:Unc13d
|
UTSW |
11 |
115,964,408 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R4792:Unc13d
|
UTSW |
11 |
115,961,108 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4843:Unc13d
|
UTSW |
11 |
115,965,085 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5496:Unc13d
|
UTSW |
11 |
115,957,534 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5571:Unc13d
|
UTSW |
11 |
115,954,480 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5589:Unc13d
|
UTSW |
11 |
115,960,579 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5838:Unc13d
|
UTSW |
11 |
115,955,451 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R6058:Unc13d
|
UTSW |
11 |
115,964,394 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6266:Unc13d
|
UTSW |
11 |
115,959,064 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6807:Unc13d
|
UTSW |
11 |
115,957,577 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7085:Unc13d
|
UTSW |
11 |
115,955,633 (GRCm39) |
missense |
probably benign |
0.07 |
|
R7098:Unc13d
|
UTSW |
11 |
115,954,552 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7269:Unc13d
|
UTSW |
11 |
115,959,056 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7291:Unc13d
|
UTSW |
11 |
115,964,876 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R7453:Unc13d
|
UTSW |
11 |
115,958,697 (GRCm39) |
missense |
probably benign |
|
|
R7486:Unc13d
|
UTSW |
11 |
115,965,259 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R7618:Unc13d
|
UTSW |
11 |
115,957,547 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7817:Unc13d
|
UTSW |
11 |
115,967,109 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8290:Unc13d
|
UTSW |
11 |
115,958,973 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R8442:Unc13d
|
UTSW |
11 |
115,958,657 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8817:Unc13d
|
UTSW |
11 |
115,958,998 (GRCm39) |
small insertion |
probably benign |
|
|
R8820:Unc13d
|
UTSW |
11 |
115,958,998 (GRCm39) |
small insertion |
probably benign |
|
|
R8821:Unc13d
|
UTSW |
11 |
115,958,998 (GRCm39) |
small insertion |
probably benign |
|
|
R8858:Unc13d
|
UTSW |
11 |
115,953,618 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9031:Unc13d
|
UTSW |
11 |
115,958,998 (GRCm39) |
small insertion |
probably benign |
|
|
R9066:Unc13d
|
UTSW |
11 |
115,957,561 (GRCm39) |
missense |
probably benign |
0.07 |
|
R9084:Unc13d
|
UTSW |
11 |
115,958,998 (GRCm39) |
small insertion |
probably benign |
|
|
R9085:Unc13d
|
UTSW |
11 |
115,958,998 (GRCm39) |
small insertion |
probably benign |
|
|
R9258:Unc13d
|
UTSW |
11 |
115,959,007 (GRCm39) |
small insertion |
probably benign |
|
|
R9258:Unc13d
|
UTSW |
11 |
115,958,998 (GRCm39) |
small insertion |
probably benign |
|
|
R9259:Unc13d
|
UTSW |
11 |
115,958,998 (GRCm39) |
small insertion |
probably benign |
|
|
R9260:Unc13d
|
UTSW |
11 |
115,958,998 (GRCm39) |
small insertion |
probably benign |
|
|
R9396:Unc13d
|
UTSW |
11 |
115,966,529 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9612:Unc13d
|
UTSW |
11 |
115,961,144 (GRCm39) |
nonsense |
probably null |
|
|
R9648:Unc13d
|
UTSW |
11 |
115,958,998 (GRCm39) |
small insertion |
probably benign |
|
|
R9649:Unc13d
|
UTSW |
11 |
115,958,998 (GRCm39) |
small insertion |
probably benign |
|
|
R9650:Unc13d
|
UTSW |
11 |
115,958,998 (GRCm39) |
small insertion |
probably benign |
|
|
X0027:Unc13d
|
UTSW |
11 |
115,960,582 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- TGGGATAGACATCAGCTCAGGTC -3'
(R):5'- AGCTGACATGGTAAGACCCAG -3'
Sequencing Primer
(F):5'- GATAGACATCAGCTCAGGTCCTACTG -3'
(R):5'- CTGACATGGTAAGACCCAGAGCTG -3'
|
| Posted On |
2021-04-30 |
Incidental Mutation