Incidental Mutation 'R3422:Mgat4d'
ID |
267084 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Mgat4d
|
Ensembl Gene |
ENSMUSG00000035057 |
Gene Name |
MGAT4 family, member C |
Synonyms |
4933434I20Rik |
MMRRC Submission |
040640-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R3422 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
8 |
Chromosomal Location |
84075101-84106031 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 84084772 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Proline
at position 172
(S172P)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000041629
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000038692]
|
AlphaFold |
Q9D4R2 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000038692
AA Change: S172P
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000041629 Gene: ENSMUSG00000035057 AA Change: S172P
Domain | Start | End | E-Value | Type |
transmembrane domain
|
7 |
29 |
N/A |
INTRINSIC |
Pfam:Glyco_transf_54
|
70 |
373 |
5.9e-120 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000139692
|
Meta Mutation Damage Score |
0.6467 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 97.2%
- 20x: 94.7%
|
Validation Efficiency |
100% (40/40) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agbl3 |
A |
G |
6: 34,770,900 (GRCm39) |
T132A |
probably benign |
Het |
Ahnak |
A |
G |
19: 8,983,072 (GRCm39) |
D1452G |
probably benign |
Het |
Ahnak |
A |
G |
19: 8,984,116 (GRCm39) |
D1800G |
probably benign |
Het |
Atp7b |
C |
T |
8: 22,518,686 (GRCm39) |
D51N |
probably damaging |
Het |
Brca2 |
A |
G |
5: 150,466,586 (GRCm39) |
T2117A |
possibly damaging |
Het |
Ccdc73 |
A |
T |
2: 104,782,292 (GRCm39) |
K216M |
probably null |
Het |
Ccdc73 |
G |
A |
2: 104,782,293 (GRCm39) |
|
probably null |
Het |
Ckap5 |
T |
A |
2: 91,400,597 (GRCm39) |
W650R |
probably damaging |
Het |
D930048N14Rik |
T |
C |
11: 51,545,785 (GRCm39) |
*226R |
probably null |
Het |
Grin1 |
C |
T |
2: 25,193,926 (GRCm39) |
G390D |
probably damaging |
Het |
Ifit1bl1 |
T |
G |
19: 34,571,350 (GRCm39) |
N369T |
probably benign |
Het |
Kcnip1 |
A |
G |
11: 33,595,594 (GRCm39) |
V43A |
probably damaging |
Het |
Kifap3 |
T |
A |
1: 163,621,595 (GRCm39) |
I81N |
probably damaging |
Het |
Me2 |
C |
T |
18: 73,924,265 (GRCm39) |
A316T |
probably damaging |
Het |
Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
Nmt2 |
A |
G |
2: 3,285,425 (GRCm39) |
E31G |
possibly damaging |
Het |
Nuak2 |
A |
G |
1: 132,259,818 (GRCm39) |
D532G |
probably benign |
Het |
Nwd2 |
G |
T |
5: 63,882,536 (GRCm39) |
V63L |
possibly damaging |
Het |
Odad2 |
T |
C |
18: 7,223,523 (GRCm39) |
|
probably benign |
Het |
Or1e1 |
A |
G |
11: 73,245,460 (GRCm39) |
N294D |
probably damaging |
Het |
Or4k15b |
T |
C |
14: 50,271,997 (GRCm39) |
T288A |
possibly damaging |
Het |
Otub1 |
C |
T |
19: 7,176,424 (GRCm39) |
D237N |
probably damaging |
Het |
Pik3cg |
A |
T |
12: 32,254,738 (GRCm39) |
F416L |
probably damaging |
Het |
Psmb2 |
T |
C |
4: 126,571,630 (GRCm39) |
M28T |
probably damaging |
Het |
Saysd1 |
T |
A |
14: 20,132,994 (GRCm39) |
K54N |
probably benign |
Het |
Slc5a4a |
T |
C |
10: 76,012,407 (GRCm39) |
V359A |
probably benign |
Het |
Slc7a3 |
T |
A |
X: 100,124,481 (GRCm39) |
|
probably benign |
Het |
Soat2 |
T |
C |
15: 102,065,244 (GRCm39) |
|
probably benign |
Het |
Spink5 |
A |
G |
18: 44,143,311 (GRCm39) |
K756R |
probably benign |
Het |
Tafa1 |
C |
A |
6: 96,626,099 (GRCm39) |
D112E |
probably damaging |
Het |
Tlr4 |
A |
G |
4: 66,757,773 (GRCm39) |
I189V |
probably benign |
Het |
Vsig2 |
G |
A |
9: 37,452,775 (GRCm39) |
V195I |
possibly damaging |
Het |
Zfp217 |
A |
G |
2: 169,961,937 (GRCm39) |
F130S |
possibly damaging |
Het |
Zfp91 |
G |
A |
19: 12,747,656 (GRCm39) |
A489V |
probably benign |
Het |
|
Other mutations in Mgat4d |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00542:Mgat4d
|
APN |
8 |
84,081,425 (GRCm39) |
missense |
probably benign |
0.21 |
IGL01634:Mgat4d
|
APN |
8 |
84,094,745 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01987:Mgat4d
|
APN |
8 |
84,094,731 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02084:Mgat4d
|
APN |
8 |
84,095,610 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0546:Mgat4d
|
UTSW |
8 |
84,082,350 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1322:Mgat4d
|
UTSW |
8 |
84,092,354 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1526:Mgat4d
|
UTSW |
8 |
84,095,666 (GRCm39) |
missense |
probably benign |
0.25 |
R1617:Mgat4d
|
UTSW |
8 |
84,092,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R2223:Mgat4d
|
UTSW |
8 |
84,082,301 (GRCm39) |
splice site |
probably benign |
|
R3157:Mgat4d
|
UTSW |
8 |
84,081,450 (GRCm39) |
missense |
probably benign |
|
R3421:Mgat4d
|
UTSW |
8 |
84,084,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R4387:Mgat4d
|
UTSW |
8 |
84,098,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R4796:Mgat4d
|
UTSW |
8 |
84,084,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R4805:Mgat4d
|
UTSW |
8 |
84,084,787 (GRCm39) |
splice site |
probably null |
|
R5054:Mgat4d
|
UTSW |
8 |
84,094,837 (GRCm39) |
splice site |
probably null |
|
R6366:Mgat4d
|
UTSW |
8 |
84,095,580 (GRCm39) |
splice site |
probably null |
|
R6927:Mgat4d
|
UTSW |
8 |
84,081,496 (GRCm39) |
missense |
probably benign |
0.03 |
R7053:Mgat4d
|
UTSW |
8 |
84,098,261 (GRCm39) |
missense |
probably damaging |
0.98 |
R7554:Mgat4d
|
UTSW |
8 |
84,082,402 (GRCm39) |
missense |
probably benign |
0.00 |
R7566:Mgat4d
|
UTSW |
8 |
84,084,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R7965:Mgat4d
|
UTSW |
8 |
84,084,722 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8111:Mgat4d
|
UTSW |
8 |
84,094,776 (GRCm39) |
missense |
probably damaging |
0.96 |
R8344:Mgat4d
|
UTSW |
8 |
84,094,762 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Mgat4d
|
UTSW |
8 |
84,094,741 (GRCm39) |
missense |
probably benign |
0.39 |
Z1176:Mgat4d
|
UTSW |
8 |
84,075,150 (GRCm39) |
missense |
probably benign |
0.04 |
|
Predicted Primers |
PCR Primer
(F):5'- AGCCCACGGTAAACACTTG -3'
(R):5'- ACAATCTGATGGCTCTCCTATAAG -3'
Sequencing Primer
(F):5'- AACACTTGTTTACCGATGGCTTG -3'
(R):5'- CTGATGGCTCTCCTATAAGATTCATG -3'
|
Posted On |
2015-02-18 |