Incidental Mutation 'IGL00325:Gm4553'
ID |
332259 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Gm4553
|
Ensembl Gene |
ENSMUSG00000090471 |
Gene Name |
predicted gene 4553 |
Synonyms |
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.110)
|
Stock # |
IGL00325
|
Quality Score |
|
Status
|
|
Chromosome |
7 |
Chromosomal Location |
141718433-141719476 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 141718964 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Glycine
at position 155
(S155G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000147863
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000168049]
[ENSMUST00000210925]
|
AlphaFold |
A0A1B0GSA9 |
Predicted Effect |
unknown
Transcript: ENSMUST00000168049
AA Change: S171G
|
SMART Domains |
Protein: ENSMUSP00000131778 Gene: ENSMUSG00000090471 AA Change: S171G
Domain | Start | End | E-Value | Type |
low complexity region
|
18 |
238 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000210925
AA Change: S155G
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acap1 |
A |
G |
11: 69,773,517 (GRCm39) |
S431P |
possibly damaging |
Het |
Arid1b |
C |
A |
17: 5,387,385 (GRCm39) |
R1613S |
possibly damaging |
Het |
Atxn2l |
T |
C |
7: 126,097,460 (GRCm39) |
D196G |
possibly damaging |
Het |
Bag3 |
C |
A |
7: 128,148,065 (GRCm39) |
T560K |
probably benign |
Het |
BC051076 |
A |
G |
5: 88,112,354 (GRCm39) |
|
probably benign |
Het |
Becn1 |
A |
T |
11: 101,186,448 (GRCm39) |
M18K |
probably benign |
Het |
C130050O18Rik |
G |
A |
5: 139,400,493 (GRCm39) |
C182Y |
probably damaging |
Het |
Cfap43 |
A |
G |
19: 47,811,627 (GRCm39) |
|
probably benign |
Het |
Cfap97 |
C |
T |
8: 46,623,222 (GRCm39) |
S204L |
probably damaging |
Het |
Gaa |
A |
G |
11: 119,165,786 (GRCm39) |
T100A |
probably benign |
Het |
Gab2 |
C |
T |
7: 96,948,465 (GRCm39) |
P352S |
probably damaging |
Het |
Gckr |
T |
A |
5: 31,465,111 (GRCm39) |
I360N |
possibly damaging |
Het |
Gulo |
G |
T |
14: 66,243,398 (GRCm39) |
A40D |
probably damaging |
Het |
Irs1 |
T |
C |
1: 82,266,204 (GRCm39) |
I671V |
probably benign |
Het |
Itgax |
T |
C |
7: 127,747,481 (GRCm39) |
V1028A |
possibly damaging |
Het |
Lamb3 |
T |
C |
1: 193,002,755 (GRCm39) |
C67R |
probably damaging |
Het |
Mpdz |
A |
T |
4: 81,235,868 (GRCm39) |
V1237E |
probably damaging |
Het |
Nat8 |
C |
T |
6: 85,807,579 (GRCm39) |
V185M |
probably benign |
Het |
Ninj2 |
A |
C |
6: 120,175,023 (GRCm39) |
T65P |
probably benign |
Het |
Nrg2 |
T |
C |
18: 36,154,271 (GRCm39) |
M549V |
probably benign |
Het |
Nwd2 |
A |
G |
5: 63,962,818 (GRCm39) |
M801V |
probably benign |
Het |
Pde8b |
T |
C |
13: 95,170,875 (GRCm39) |
D589G |
probably damaging |
Het |
Ppp1r35 |
T |
A |
5: 137,777,799 (GRCm39) |
V155E |
probably damaging |
Het |
Prss36 |
T |
A |
7: 127,544,099 (GRCm39) |
|
probably benign |
Het |
Raver2 |
A |
G |
4: 100,960,065 (GRCm39) |
K182E |
probably damaging |
Het |
Ring1 |
T |
G |
17: 34,241,983 (GRCm39) |
E142A |
possibly damaging |
Het |
Sidt2 |
T |
A |
9: 45,853,534 (GRCm39) |
M689L |
possibly damaging |
Het |
Slc45a4 |
A |
G |
15: 73,459,504 (GRCm39) |
V95A |
probably damaging |
Het |
Ssc5d |
T |
C |
7: 4,947,480 (GRCm39) |
V1278A |
possibly damaging |
Het |
Stk36 |
A |
T |
1: 74,673,861 (GRCm39) |
K1251N |
possibly damaging |
Het |
Utp14b |
T |
A |
1: 78,642,262 (GRCm39) |
S53R |
probably damaging |
Het |
Vmn2r17 |
A |
T |
5: 109,575,858 (GRCm39) |
E243V |
probably benign |
Het |
|
Other mutations in Gm4553 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00323:Gm4553
|
APN |
7 |
141,718,964 (GRCm39) |
missense |
unknown |
|
IGL00324:Gm4553
|
APN |
7 |
141,718,964 (GRCm39) |
missense |
unknown |
|
IGL00329:Gm4553
|
APN |
7 |
141,718,964 (GRCm39) |
missense |
unknown |
|
IGL00332:Gm4553
|
APN |
7 |
141,718,964 (GRCm39) |
missense |
unknown |
|
IGL00336:Gm4553
|
APN |
7 |
141,718,964 (GRCm39) |
missense |
unknown |
|
IGL00337:Gm4553
|
APN |
7 |
141,718,964 (GRCm39) |
missense |
unknown |
|
IGL00338:Gm4553
|
APN |
7 |
141,718,964 (GRCm39) |
missense |
unknown |
|
IGL00339:Gm4553
|
APN |
7 |
141,718,964 (GRCm39) |
missense |
unknown |
|
IGL00340:Gm4553
|
APN |
7 |
141,718,964 (GRCm39) |
missense |
unknown |
|
IGL01348:Gm4553
|
APN |
7 |
141,718,909 (GRCm39) |
missense |
unknown |
|
R0468:Gm4553
|
UTSW |
7 |
141,719,362 (GRCm39) |
missense |
unknown |
|
R0568:Gm4553
|
UTSW |
7 |
141,719,357 (GRCm39) |
missense |
unknown |
|
R0932:Gm4553
|
UTSW |
7 |
141,719,423 (GRCm39) |
missense |
unknown |
|
R4988:Gm4553
|
UTSW |
7 |
141,718,729 (GRCm39) |
unclassified |
probably benign |
|
R5050:Gm4553
|
UTSW |
7 |
141,718,773 (GRCm39) |
missense |
unknown |
|
R7317:Gm4553
|
UTSW |
7 |
141,719,157 (GRCm39) |
small deletion |
probably benign |
|
R7372:Gm4553
|
UTSW |
7 |
141,719,157 (GRCm39) |
small deletion |
probably benign |
|
R7709:Gm4553
|
UTSW |
7 |
141,719,384 (GRCm39) |
missense |
unknown |
|
R7901:Gm4553
|
UTSW |
7 |
141,718,602 (GRCm39) |
small deletion |
probably benign |
|
R8179:Gm4553
|
UTSW |
7 |
141,718,594 (GRCm39) |
missense |
unknown |
|
R8296:Gm4553
|
UTSW |
7 |
141,719,458 (GRCm39) |
missense |
unknown |
|
R8510:Gm4553
|
UTSW |
7 |
141,719,025 (GRCm39) |
small deletion |
probably benign |
|
R8549:Gm4553
|
UTSW |
7 |
141,719,157 (GRCm39) |
small deletion |
probably benign |
|
R9288:Gm4553
|
UTSW |
7 |
141,719,025 (GRCm39) |
small deletion |
probably benign |
|
R9335:Gm4553
|
UTSW |
7 |
141,719,157 (GRCm39) |
small deletion |
probably benign |
|
R9497:Gm4553
|
UTSW |
7 |
141,719,298 (GRCm39) |
nonsense |
probably null |
|
|
Posted On |
2015-08-05 |