Incidental Mutation 'IGL01724:Qrsl1'
ID |
105198 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Qrsl1
|
Ensembl Gene |
ENSMUSG00000019863 |
Gene Name |
glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1 |
Synonyms |
2700038P16Rik, GatA |
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.962)
|
Stock # |
IGL01724
|
Quality Score |
|
Status
|
|
Chromosome |
10 |
Chromosomal Location |
43750184-43777741 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 43750604 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Alanine
at position 485
(T485A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000020012
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000020012]
|
AlphaFold |
Q9CZN8 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000020012
AA Change: T485A
PolyPhen 2
Score 0.007 (Sensitivity: 0.96; Specificity: 0.75)
|
SMART Domains |
Protein: ENSMUSP00000020012 Gene: ENSMUSG00000019863 AA Change: T485A
Domain | Start | End | E-Value | Type |
Pfam:Amidase
|
22 |
484 |
6e-129 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000146937
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2200002D01Rik |
C |
T |
7: 28,947,321 (GRCm39) |
|
probably null |
Het |
Abcc9 |
A |
G |
6: 142,610,259 (GRCm39) |
V635A |
probably benign |
Het |
Adgre1 |
T |
A |
17: 57,751,064 (GRCm39) |
Y579* |
probably null |
Het |
Adgrg3 |
T |
C |
8: 95,766,053 (GRCm39) |
F295L |
probably benign |
Het |
Arhgap42 |
A |
T |
9: 8,998,254 (GRCm39) |
|
probably benign |
Het |
Brd2 |
T |
A |
17: 34,335,976 (GRCm39) |
Q79L |
probably damaging |
Het |
Brd2 |
C |
A |
17: 34,335,975 (GRCm39) |
Q79H |
probably damaging |
Het |
Capn15 |
A |
G |
17: 26,181,037 (GRCm39) |
S705P |
probably damaging |
Het |
Cebpz |
T |
A |
17: 79,243,342 (GRCm39) |
D104V |
probably benign |
Het |
Chl1 |
T |
C |
6: 103,626,534 (GRCm39) |
I94T |
probably damaging |
Het |
Csf2rb |
C |
T |
15: 78,220,614 (GRCm39) |
A52V |
probably damaging |
Het |
Ddx27 |
T |
C |
2: 166,870,309 (GRCm39) |
L459P |
probably damaging |
Het |
Dhtkd1 |
T |
C |
2: 5,919,651 (GRCm39) |
T577A |
probably benign |
Het |
Dync2h1 |
G |
A |
9: 7,081,077 (GRCm39) |
T2873I |
probably benign |
Het |
Emg1 |
A |
G |
6: 124,688,984 (GRCm39) |
F8S |
possibly damaging |
Het |
Fermt3 |
A |
G |
19: 6,979,143 (GRCm39) |
I553T |
probably damaging |
Het |
Gaa |
A |
G |
11: 119,165,947 (GRCm39) |
D419G |
possibly damaging |
Het |
Hdac10 |
T |
C |
15: 89,008,912 (GRCm39) |
|
probably benign |
Het |
Hsf1 |
T |
A |
15: 76,381,037 (GRCm39) |
V122E |
possibly damaging |
Het |
Lig3 |
C |
A |
11: 82,681,448 (GRCm39) |
T480K |
possibly damaging |
Het |
Magi1 |
T |
C |
6: 93,769,381 (GRCm39) |
|
probably null |
Het |
Mcm2 |
G |
T |
6: 88,863,044 (GRCm39) |
H683N |
probably damaging |
Het |
Ncapg2 |
G |
T |
12: 116,390,331 (GRCm39) |
A427S |
probably damaging |
Het |
Nkd1 |
T |
C |
8: 89,248,923 (GRCm39) |
F23L |
probably damaging |
Het |
Or9i2 |
G |
A |
19: 13,816,225 (GRCm39) |
T104M |
probably damaging |
Het |
Pcdhb5 |
T |
G |
18: 37,454,075 (GRCm39) |
S152A |
probably benign |
Het |
Pdx1 |
A |
T |
5: 147,211,217 (GRCm39) |
E146V |
probably damaging |
Het |
Slc17a4 |
A |
G |
13: 24,089,516 (GRCm39) |
Y134H |
probably benign |
Het |
Slc24a4 |
A |
T |
12: 102,185,219 (GRCm39) |
M110L |
possibly damaging |
Het |
Tent5a |
A |
G |
9: 85,207,103 (GRCm39) |
C232R |
probably damaging |
Het |
Tnni3k |
T |
A |
3: 154,645,263 (GRCm39) |
I541F |
possibly damaging |
Het |
Uhrf2 |
T |
C |
19: 30,052,652 (GRCm39) |
V382A |
probably benign |
Het |
Vac14 |
T |
A |
8: 111,345,523 (GRCm39) |
M1K |
probably null |
Het |
Virma |
A |
G |
4: 11,528,672 (GRCm39) |
E1303G |
probably damaging |
Het |
Xirp2 |
T |
C |
2: 67,356,411 (GRCm39) |
V3724A |
probably benign |
Het |
|
Other mutations in Qrsl1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00477:Qrsl1
|
APN |
10 |
43,752,488 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01896:Qrsl1
|
APN |
10 |
43,752,500 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02192:Qrsl1
|
APN |
10 |
43,761,010 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02239:Qrsl1
|
APN |
10 |
43,770,596 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02478:Qrsl1
|
APN |
10 |
43,758,158 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02756:Qrsl1
|
APN |
10 |
43,758,110 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03386:Qrsl1
|
APN |
10 |
43,752,546 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0277:Qrsl1
|
UTSW |
10 |
43,772,003 (GRCm39) |
critical splice donor site |
probably null |
|
R0323:Qrsl1
|
UTSW |
10 |
43,772,003 (GRCm39) |
critical splice donor site |
probably null |
|
R0674:Qrsl1
|
UTSW |
10 |
43,771,997 (GRCm39) |
splice site |
probably benign |
|
R1054:Qrsl1
|
UTSW |
10 |
43,758,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R1719:Qrsl1
|
UTSW |
10 |
43,772,026 (GRCm39) |
missense |
probably damaging |
0.97 |
R1743:Qrsl1
|
UTSW |
10 |
43,757,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R1854:Qrsl1
|
UTSW |
10 |
43,770,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R2233:Qrsl1
|
UTSW |
10 |
43,772,092 (GRCm39) |
missense |
probably benign |
0.00 |
R4176:Qrsl1
|
UTSW |
10 |
43,760,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R4452:Qrsl1
|
UTSW |
10 |
43,758,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R4732:Qrsl1
|
UTSW |
10 |
43,752,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R4733:Qrsl1
|
UTSW |
10 |
43,752,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R5626:Qrsl1
|
UTSW |
10 |
43,757,516 (GRCm39) |
missense |
probably benign |
0.00 |
R6159:Qrsl1
|
UTSW |
10 |
43,758,189 (GRCm39) |
missense |
probably benign |
0.00 |
R7563:Qrsl1
|
UTSW |
10 |
43,752,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R8050:Qrsl1
|
UTSW |
10 |
43,750,631 (GRCm39) |
missense |
probably damaging |
0.98 |
R8092:Qrsl1
|
UTSW |
10 |
43,760,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R8221:Qrsl1
|
UTSW |
10 |
43,758,080 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8331:Qrsl1
|
UTSW |
10 |
43,752,521 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Qrsl1
|
UTSW |
10 |
43,760,944 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Posted On |
2014-01-21 |