Incidental Mutation 'R6867:F3'
| ID |
535964 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
F3
|
| Ensembl Gene |
ENSMUSG00000028128 |
| Gene Name |
coagulation factor III |
| Synonyms |
Cf-3, tissue factor, TF, Cf3, CD142 |
| MMRRC Submission |
045028-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.067)
|
| Stock # |
R6867 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
3 |
| Chromosomal Location |
121517186-121528697 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 121523020 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Proline
at position 77
(S77P)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000029771
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000029771]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000029771
AA Change: S77P
PolyPhen 2
Score 0.928 (Sensitivity: 0.81; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000029771
Gene: ENSMUSG00000028128
AA Change: S77P
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Tissue_fac
|
12 |
110 |
1.1e-26 |
PFAM |
|
Pfam:Interfer-bind
|
138 |
245 |
5.1e-26 |
PFAM |
|
transmembrane domain
|
253 |
275 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000199997
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.4%
- 20x: 98.0%
|
| Validation Efficiency |
100% (43/43) |
| MGI Phenotype |
FUNCTION: This gene encodes a membrane-bound glycoprotein that forms the primary physiological initiator of the blood coagulation process following vascular damage. The encoded protein binds to coagulation factor VIIa and the ensuing complex catalyzes the proteolytic activation of coagulation factors IX and X. Mice lacking encoded protein die in utero resulting from massive hemorrhaging in both extraembryonic and embryonic vessels. A severe deficiency of the encoded protein in mice results in impaired uterine homeostasis, shorter life spans due to spontaneous fatal hemorrhages and cardiac fibrosis. [provided by RefSeq, Aug 2015]
PHENOTYPE: Homozygotes for targeted null mutations exhibit impaired blood vessel development, retarded growth, and, in most cases, midgestational lethality. On a mixed background, some mutants survive to birth and appear to be normal. [provided by MGI curators]
|
| Allele List at MGI |
All alleles(7) : Targeted, knock-out(5) Targeted, other(2) |
| Other mutations in this stock |
Total: 42 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Apold1 |
T |
C |
6: 134,961,019 (GRCm39) |
S158P |
possibly damaging |
Het |
| Cep162 |
A |
T |
9: 87,099,134 (GRCm39) |
L788* |
probably null |
Het |
| Cyp7b1 |
T |
C |
3: 18,151,394 (GRCm39) |
Y273C |
probably damaging |
Het |
| Dlx1 |
C |
A |
2: 71,361,353 (GRCm39) |
N122K |
probably damaging |
Het |
| Dock10 |
A |
T |
1: 80,508,976 (GRCm39) |
I1605K |
probably damaging |
Het |
| Enox1 |
T |
C |
14: 77,936,739 (GRCm39) |
|
probably null |
Het |
| Fam186a |
T |
A |
15: 99,843,731 (GRCm39) |
I838L |
unknown |
Het |
| Flrt2 |
T |
C |
12: 95,746,156 (GRCm39) |
F165L |
probably damaging |
Het |
| Gcgr |
T |
A |
11: 120,427,295 (GRCm39) |
V135E |
possibly damaging |
Het |
| Gm6741 |
T |
C |
17: 91,544,339 (GRCm39) |
L34P |
probably benign |
Het |
| Gna13 |
T |
C |
11: 109,286,948 (GRCm39) |
M257T |
possibly damaging |
Het |
| Hsd11b2 |
G |
A |
8: 106,248,949 (GRCm39) |
R147H |
probably benign |
Het |
| Hydin |
A |
G |
8: 111,266,434 (GRCm39) |
Y2865C |
probably benign |
Het |
| Igdcc3 |
A |
G |
9: 65,090,320 (GRCm39) |
N610D |
probably damaging |
Het |
| Ipp |
T |
A |
4: 116,367,606 (GRCm39) |
|
probably null |
Het |
| Kdm5d |
A |
G |
Y: 927,425 (GRCm39) |
T682A |
probably benign |
Het |
| Megf8 |
A |
G |
7: 25,030,460 (GRCm39) |
Y471C |
probably benign |
Het |
| Mprip |
T |
C |
11: 59,640,456 (GRCm39) |
|
probably null |
Het |
| Mtres1 |
ACTGCACCACCT |
ACT |
10: 43,408,721 (GRCm39) |
|
probably benign |
Het |
| Myrfl |
T |
A |
10: 116,684,187 (GRCm39) |
R179* |
probably null |
Het |
| Nek1 |
C |
A |
8: 61,525,364 (GRCm39) |
Q601K |
possibly damaging |
Het |
| Neurod4 |
C |
G |
10: 130,106,583 (GRCm39) |
K230N |
probably damaging |
Het |
| Or1ab2 |
C |
T |
8: 72,863,707 (GRCm39) |
T99I |
possibly damaging |
Het |
| Or8u10 |
A |
G |
2: 85,916,082 (GRCm39) |
I13T |
possibly damaging |
Het |
| Orc3 |
A |
G |
4: 34,605,539 (GRCm39) |
L114P |
probably damaging |
Het |
| Rag1 |
T |
C |
2: 101,472,292 (GRCm39) |
D950G |
probably damaging |
Het |
| Rasgrp2 |
G |
A |
19: 6,463,213 (GRCm39) |
S504N |
probably benign |
Het |
| Rgl2 |
A |
G |
17: 34,151,661 (GRCm39) |
D235G |
probably benign |
Het |
| Slc35e2 |
A |
G |
4: 155,703,157 (GRCm39) |
E390G |
probably benign |
Het |
| Slc39a1 |
T |
A |
3: 90,156,759 (GRCm39) |
V105E |
probably damaging |
Het |
| Tesk2 |
T |
A |
4: 116,658,995 (GRCm39) |
C291S |
probably damaging |
Het |
| Tmco3 |
T |
A |
8: 13,363,927 (GRCm39) |
F83Y |
probably damaging |
Het |
| Trim25 |
T |
C |
11: 88,901,713 (GRCm39) |
I336T |
probably benign |
Het |
| Ush2a |
A |
G |
1: 188,643,170 (GRCm39) |
I4177M |
probably damaging |
Het |
| Veph1 |
T |
A |
3: 66,162,458 (GRCm39) |
T67S |
probably damaging |
Het |
| Vmn2r43 |
A |
G |
7: 8,258,125 (GRCm39) |
F363L |
probably benign |
Het |
| Vps28 |
A |
T |
15: 76,506,871 (GRCm39) |
I109N |
probably damaging |
Het |
| Vps50 |
A |
G |
6: 3,517,835 (GRCm39) |
D91G |
probably benign |
Het |
| Wdr20 |
T |
C |
12: 110,760,133 (GRCm39) |
F340L |
probably benign |
Het |
| Wdr95 |
A |
G |
5: 149,504,388 (GRCm39) |
|
probably null |
Het |
| Zfand6 |
A |
G |
7: 84,265,122 (GRCm39) |
V193A |
probably damaging |
Het |
| Zfp703 |
C |
A |
8: 27,468,668 (GRCm39) |
P111T |
probably damaging |
Het |
|
| Other mutations in F3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02506:F3
|
APN |
3 |
121,525,323 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
G5030:F3
|
UTSW |
3 |
121,518,648 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0020:F3
|
UTSW |
3 |
121,525,265 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0020:F3
|
UTSW |
3 |
121,525,265 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0622:F3
|
UTSW |
3 |
121,518,668 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1367:F3
|
UTSW |
3 |
121,523,023 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1371:F3
|
UTSW |
3 |
121,526,159 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1925:F3
|
UTSW |
3 |
121,523,032 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2100:F3
|
UTSW |
3 |
121,526,082 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R2366:F3
|
UTSW |
3 |
121,526,194 (GRCm39) |
splice site |
probably null |
|
|
R2471:F3
|
UTSW |
3 |
121,518,689 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4577:F3
|
UTSW |
3 |
121,527,763 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5752:F3
|
UTSW |
3 |
121,526,053 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6440:F3
|
UTSW |
3 |
121,518,686 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6713:F3
|
UTSW |
3 |
121,525,323 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R6845:F3
|
UTSW |
3 |
121,526,124 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7145:F3
|
UTSW |
3 |
121,525,235 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7511:F3
|
UTSW |
3 |
121,525,206 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8865:F3
|
UTSW |
3 |
121,523,060 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9455:F3
|
UTSW |
3 |
121,527,866 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9563:F3
|
UTSW |
3 |
121,527,822 (GRCm39) |
missense |
|
|
|
| Predicted Primers |
PCR Primer
(F):5'- AGAGCTAACCTGGTTACTGGG -3'
(R):5'- GTGAAGGCATTACAAACCAAGC -3'
Sequencing Primer
(F):5'- AGCTAACCTGGTTACTGGGTGAAC -3'
(R):5'- AACCAAGCTACTTACTGTCTCGG -3'
|
| Posted On |
2018-10-18 |
Incidental Mutation