Incidental Mutation 'R5002:Ms4a14'
| ID |
390017 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ms4a14
|
| Ensembl Gene |
ENSMUSG00000099398 |
| Gene Name |
membrane-spanning 4-domains, subfamily A, member 14 |
| Synonyms |
LOC383435 |
| MMRRC Submission |
042596-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.162)
|
| Stock # |
R5002 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
19 |
| Chromosomal Location |
11278613-11291818 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 11281653 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Valine
at position 302
(I302V)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000140996
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000187467]
|
| AlphaFold |
A0A087WSD2 |
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000181137
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000187467
AA Change: I302V
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000140996
Gene: ENSMUSG00000099398
AA Change: I302V
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:CD20
|
44 |
182 |
2.9e-27 |
PFAM |
|
internal_repeat_2
|
356 |
466 |
2.78e-10 |
PROSPERO |
|
internal_repeat_1
|
390 |
506 |
1.75e-17 |
PROSPERO |
|
low complexity region
|
522 |
540 |
N/A |
INTRINSIC |
|
low complexity region
|
625 |
640 |
N/A |
INTRINSIC |
|
low complexity region
|
642 |
660 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
665 |
786 |
1.75e-17 |
PROSPERO |
|
internal_repeat_2
|
700 |
811 |
2.78e-10 |
PROSPERO |
|
low complexity region
|
911 |
936 |
N/A |
INTRINSIC |
|
low complexity region
|
975 |
992 |
N/A |
INTRINSIC |
|
low complexity region
|
1079 |
1092 |
N/A |
INTRINSIC |
|
| Meta Mutation Damage Score |
0.0898 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.4%
- 10x: 96.7%
- 20x: 93.7%
|
| Validation Efficiency |
94% (44/47) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 40 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca8b |
G |
A |
11: 109,852,623 (GRCm39) |
P736S |
probably damaging |
Het |
| Apbb2 |
A |
G |
5: 66,470,668 (GRCm39) |
I523T |
possibly damaging |
Het |
| Casq1 |
T |
A |
1: 172,040,945 (GRCm39) |
D281V |
possibly damaging |
Het |
| Catsperb |
T |
C |
12: 101,486,813 (GRCm39) |
F447L |
probably benign |
Het |
| Cenpe |
A |
T |
3: 134,952,842 (GRCm39) |
M1511L |
probably benign |
Het |
| Cep128 |
T |
C |
12: 91,222,497 (GRCm39) |
|
probably null |
Het |
| Col6a6 |
T |
C |
9: 105,663,292 (GRCm39) |
T82A |
probably benign |
Het |
| Dna2 |
A |
G |
10: 62,786,621 (GRCm39) |
D123G |
probably damaging |
Het |
| Ergic2 |
A |
G |
6: 148,085,656 (GRCm39) |
I281T |
probably benign |
Het |
| Fcgbp |
T |
A |
7: 27,785,528 (GRCm39) |
|
probably null |
Het |
| Filip1l |
T |
C |
16: 57,391,466 (GRCm39) |
Y447H |
probably benign |
Het |
| Flnb |
T |
A |
14: 7,945,882 (GRCm38) |
M2429K |
probably damaging |
Het |
| Fn1 |
T |
A |
1: 71,668,887 (GRCm39) |
Q686L |
possibly damaging |
Het |
| Gm10644 |
T |
C |
8: 84,660,216 (GRCm39) |
D43G |
possibly damaging |
Het |
| Gm10717 |
A |
G |
9: 3,025,532 (GRCm39) |
Y39C |
probably benign |
Het |
| Gpx6 |
A |
G |
13: 21,497,858 (GRCm39) |
Y43C |
probably damaging |
Het |
| Hhat |
A |
T |
1: 192,225,498 (GRCm39) |
F494I |
probably benign |
Het |
| Itga9 |
C |
A |
9: 118,492,966 (GRCm39) |
S287* |
probably null |
Het |
| Lrrk1 |
C |
A |
7: 65,982,111 (GRCm39) |
G177W |
probably damaging |
Het |
| Ltbp4 |
GT |
G |
7: 27,027,110 (GRCm39) |
|
probably null |
Het |
| Nepn |
A |
C |
10: 52,267,850 (GRCm39) |
M39L |
probably benign |
Het |
| Nfil3 |
C |
A |
13: 53,122,712 (GRCm39) |
R64L |
probably damaging |
Het |
| Ociad1 |
T |
C |
5: 73,467,659 (GRCm39) |
V199A |
possibly damaging |
Het |
| Or2r3 |
C |
A |
6: 42,448,906 (GRCm39) |
V69L |
probably benign |
Het |
| Or8k3b |
C |
A |
2: 86,520,429 (GRCm39) |
V297L |
possibly damaging |
Het |
| Polk |
A |
G |
13: 96,625,752 (GRCm39) |
Y431H |
probably damaging |
Het |
| Prss33 |
C |
T |
17: 24,054,332 (GRCm39) |
|
probably benign |
Het |
| Semp2l2b |
G |
C |
10: 21,943,716 (GRCm39) |
P88R |
probably damaging |
Het |
| Slc12a7 |
A |
G |
13: 73,911,896 (GRCm39) |
N4S |
possibly damaging |
Het |
| Slc29a4 |
A |
T |
5: 142,704,501 (GRCm39) |
I348F |
probably damaging |
Het |
| Smarce1 |
T |
C |
11: 99,115,889 (GRCm39) |
N44S |
probably damaging |
Het |
| Spast |
C |
T |
17: 74,676,221 (GRCm39) |
Q344* |
probably null |
Het |
| Stk11ip |
C |
A |
1: 75,509,187 (GRCm39) |
|
probably benign |
Het |
| Tas2r131 |
T |
C |
6: 132,934,114 (GRCm39) |
I232V |
probably benign |
Het |
| Tesk1 |
T |
C |
4: 43,444,573 (GRCm39) |
Y126H |
probably damaging |
Het |
| Tmpo |
A |
G |
10: 90,999,976 (GRCm39) |
V164A |
possibly damaging |
Het |
| Ttc23l |
G |
T |
15: 10,551,636 (GRCm39) |
T30K |
possibly damaging |
Het |
| Vwc2l |
T |
G |
1: 70,768,205 (GRCm39) |
C43G |
probably damaging |
Het |
| Wnk1 |
G |
A |
6: 119,914,924 (GRCm39) |
T1626I |
probably benign |
Het |
| Zpld2 |
T |
A |
4: 133,924,231 (GRCm39) |
N438I |
probably benign |
Het |
|
| Other mutations in Ms4a14 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00594:Ms4a14
|
APN |
19 |
11,278,983 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
IGL03131:Ms4a14
|
APN |
19 |
11,285,056 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL03136:Ms4a14
|
APN |
19 |
11,281,775 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
IGL03173:Ms4a14
|
APN |
19 |
11,281,560 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
IGL03210:Ms4a14
|
APN |
19 |
11,279,325 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R0054:Ms4a14
|
UTSW |
19 |
11,281,303 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2895:Ms4a14
|
UTSW |
19 |
11,281,595 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R4455:Ms4a14
|
UTSW |
19 |
11,280,990 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R4574:Ms4a14
|
UTSW |
19 |
11,281,335 (GRCm39) |
missense |
probably benign |
|
|
R4804:Ms4a14
|
UTSW |
19 |
11,281,404 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R4815:Ms4a14
|
UTSW |
19 |
11,291,641 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4854:Ms4a14
|
UTSW |
19 |
11,287,733 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
R4858:Ms4a14
|
UTSW |
19 |
11,278,976 (GRCm39) |
missense |
probably benign |
0.33 |
|
R5382:Ms4a14
|
UTSW |
19 |
11,280,421 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R5580:Ms4a14
|
UTSW |
19 |
11,280,590 (GRCm39) |
missense |
probably benign |
0.33 |
|
R5626:Ms4a14
|
UTSW |
19 |
11,281,419 (GRCm39) |
missense |
probably benign |
|
|
R5767:Ms4a14
|
UTSW |
19 |
11,279,391 (GRCm39) |
missense |
probably benign |
0.18 |
|
R5801:Ms4a14
|
UTSW |
19 |
11,279,246 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R5801:Ms4a14
|
UTSW |
19 |
11,279,150 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R5865:Ms4a14
|
UTSW |
19 |
11,281,581 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R5919:Ms4a14
|
UTSW |
19 |
11,291,661 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R6261:Ms4a14
|
UTSW |
19 |
11,281,384 (GRCm39) |
missense |
probably benign |
0.33 |
|
R6585:Ms4a14
|
UTSW |
19 |
11,281,009 (GRCm39) |
missense |
unknown |
|
|
R6974:Ms4a14
|
UTSW |
19 |
11,279,499 (GRCm39) |
missense |
probably benign |
|
|
R7401:Ms4a14
|
UTSW |
19 |
11,279,594 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R7445:Ms4a14
|
UTSW |
19 |
11,280,336 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7489:Ms4a14
|
UTSW |
19 |
11,279,395 (GRCm39) |
missense |
probably benign |
0.07 |
|
R7524:Ms4a14
|
UTSW |
19 |
11,281,200 (GRCm39) |
missense |
unknown |
|
|
R7532:Ms4a14
|
UTSW |
19 |
11,281,323 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R7689:Ms4a14
|
UTSW |
19 |
11,279,906 (GRCm39) |
missense |
probably benign |
0.33 |
|
R7732:Ms4a14
|
UTSW |
19 |
11,279,047 (GRCm39) |
missense |
probably benign |
|
|
R7737:Ms4a14
|
UTSW |
19 |
11,280,150 (GRCm39) |
nonsense |
probably null |
|
|
R7860:Ms4a14
|
UTSW |
19 |
11,280,308 (GRCm39) |
missense |
probably benign |
|
|
R8098:Ms4a14
|
UTSW |
19 |
11,281,979 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R8924:Ms4a14
|
UTSW |
19 |
11,281,113 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R9014:Ms4a14
|
UTSW |
19 |
11,278,871 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R9133:Ms4a14
|
UTSW |
19 |
11,281,038 (GRCm39) |
missense |
|
|
|
R9240:Ms4a14
|
UTSW |
19 |
11,281,864 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R9679:Ms4a14
|
UTSW |
19 |
11,280,048 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R9725:Ms4a14
|
UTSW |
19 |
11,280,729 (GRCm39) |
missense |
probably benign |
0.05 |
|
| Predicted Primers |
PCR Primer
(F):5'- TGTGTTGACAGAGATGCCATTAATG -3'
(R):5'- AGGCGGTTATGCTTTCTTCAAG -3'
Sequencing Primer
(F):5'- GATGCCATTAATGATTGGGATGAC -3'
(R):5'- CGGTTATGCTTTCTTCAAGTTAAGAG -3'
|
| Posted On |
2016-06-06 |
Incidental Mutation