Incidental Mutation 'IGL02337:Gna15'
ID |
288900 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Gna15
|
Ensembl Gene |
ENSMUSG00000034792 |
Gene Name |
guanine nucleotide binding protein, alpha 15 |
Synonyms |
Galpha15, G[a]15 |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.211)
|
Stock # |
IGL02337
|
Quality Score |
|
Status
|
|
Chromosome |
10 |
Chromosomal Location |
81338140-81360059 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 81350244 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Glycine
at position 53
(S53G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000049175
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000043709]
|
AlphaFold |
P30678 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000043709
AA Change: S53G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000049175 Gene: ENSMUSG00000034792 AA Change: S53G
Domain | Start | End | E-Value | Type |
G_alpha
|
22 |
373 |
1.22e-188 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000150586
|
Coding Region Coverage |
|
Validation Efficiency |
|
MGI Phenotype |
PHENOTYPE: Mice homozygous for a targeted null mutation exhibit normal hematopoiesis and normal response to inflammatory challenges. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aaas |
A |
G |
15: 102,247,662 (GRCm39) |
V403A |
probably benign |
Het |
Afm |
A |
G |
5: 90,695,770 (GRCm39) |
T426A |
probably benign |
Het |
Atp8a2 |
T |
C |
14: 60,235,451 (GRCm39) |
D697G |
probably benign |
Het |
Barhl1 |
G |
T |
2: 28,801,431 (GRCm39) |
S204R |
probably damaging |
Het |
Ceacam11 |
T |
A |
7: 17,707,550 (GRCm39) |
S111R |
probably benign |
Het |
Cenpe |
A |
G |
3: 134,926,037 (GRCm39) |
|
probably benign |
Het |
Cnot11 |
G |
A |
1: 39,583,964 (GRCm39) |
|
probably benign |
Het |
Ctc1 |
A |
G |
11: 68,916,957 (GRCm39) |
T284A |
probably damaging |
Het |
Ephb3 |
A |
G |
16: 21,040,253 (GRCm39) |
|
probably null |
Het |
Fsip1 |
T |
A |
2: 118,082,195 (GRCm39) |
K80* |
probably null |
Het |
Gaa |
G |
T |
11: 119,168,429 (GRCm39) |
G220C |
probably damaging |
Het |
Hfm1 |
A |
T |
5: 107,052,133 (GRCm39) |
M321K |
possibly damaging |
Het |
Hgfac |
C |
A |
5: 35,199,722 (GRCm39) |
T68K |
probably benign |
Het |
Hmgxb4 |
C |
T |
8: 75,726,259 (GRCm39) |
R35W |
probably damaging |
Het |
Itfg2 |
T |
C |
6: 128,390,533 (GRCm39) |
D184G |
probably benign |
Het |
Kirrel1 |
G |
A |
3: 86,996,519 (GRCm39) |
T360I |
possibly damaging |
Het |
Lrp1 |
T |
C |
10: 127,412,756 (GRCm39) |
Q1240R |
possibly damaging |
Het |
Lrrk1 |
G |
T |
7: 65,929,164 (GRCm39) |
T1156N |
possibly damaging |
Het |
Olfm1 |
A |
G |
2: 28,119,697 (GRCm39) |
Y429C |
probably damaging |
Het |
Or4k77 |
T |
G |
2: 111,199,496 (GRCm39) |
V173G |
probably benign |
Het |
Or5t5 |
T |
A |
2: 86,616,518 (GRCm39) |
M148K |
probably damaging |
Het |
Pafah1b2 |
C |
T |
9: 45,884,287 (GRCm39) |
V122I |
probably benign |
Het |
Pdcd1 |
T |
C |
1: 93,968,582 (GRCm39) |
T151A |
probably benign |
Het |
Pkd1l1 |
T |
C |
11: 8,892,079 (GRCm39) |
S697G |
probably damaging |
Het |
Rgs12 |
T |
A |
5: 35,177,697 (GRCm39) |
F96I |
probably damaging |
Het |
Sptbn4 |
T |
C |
7: 27,127,672 (GRCm39) |
D176G |
probably benign |
Het |
Tarbp2 |
C |
A |
15: 102,430,428 (GRCm39) |
Q148K |
probably damaging |
Het |
Txk |
T |
C |
5: 72,864,889 (GRCm39) |
R329G |
possibly damaging |
Het |
Unc79 |
T |
A |
12: 103,122,705 (GRCm39) |
|
probably benign |
Het |
Vmn1r73 |
C |
A |
7: 11,490,640 (GRCm39) |
P153T |
possibly damaging |
Het |
Zeb2 |
G |
A |
2: 44,887,242 (GRCm39) |
T605I |
probably damaging |
Het |
Zfp654 |
A |
G |
16: 64,605,512 (GRCm39) |
S897P |
probably benign |
Het |
|
Other mutations in Gna15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03346:Gna15
|
APN |
10 |
81,338,879 (GRCm39) |
missense |
probably damaging |
0.99 |
R0062:Gna15
|
UTSW |
10 |
81,348,239 (GRCm39) |
splice site |
probably null |
|
R0062:Gna15
|
UTSW |
10 |
81,348,239 (GRCm39) |
splice site |
probably null |
|
R0464:Gna15
|
UTSW |
10 |
81,348,338 (GRCm39) |
missense |
probably benign |
0.15 |
R0732:Gna15
|
UTSW |
10 |
81,348,390 (GRCm39) |
missense |
probably damaging |
0.97 |
R1529:Gna15
|
UTSW |
10 |
81,345,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R1768:Gna15
|
UTSW |
10 |
81,347,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R2151:Gna15
|
UTSW |
10 |
81,338,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R2153:Gna15
|
UTSW |
10 |
81,338,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R5575:Gna15
|
UTSW |
10 |
81,359,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R5750:Gna15
|
UTSW |
10 |
81,345,230 (GRCm39) |
nonsense |
probably null |
|
R5790:Gna15
|
UTSW |
10 |
81,345,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R6123:Gna15
|
UTSW |
10 |
81,345,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R6222:Gna15
|
UTSW |
10 |
81,347,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R6750:Gna15
|
UTSW |
10 |
81,350,117 (GRCm39) |
missense |
probably benign |
|
R7138:Gna15
|
UTSW |
10 |
81,343,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R7426:Gna15
|
UTSW |
10 |
81,338,831 (GRCm39) |
missense |
probably benign |
0.03 |
R7542:Gna15
|
UTSW |
10 |
81,350,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R7802:Gna15
|
UTSW |
10 |
81,350,175 (GRCm39) |
missense |
probably benign |
0.28 |
R7942:Gna15
|
UTSW |
10 |
81,359,745 (GRCm39) |
missense |
probably damaging |
0.98 |
R9168:Gna15
|
UTSW |
10 |
81,350,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R9188:Gna15
|
UTSW |
10 |
81,343,798 (GRCm39) |
missense |
probably benign |
0.43 |
R9206:Gna15
|
UTSW |
10 |
81,345,224 (GRCm39) |
missense |
probably benign |
0.25 |
R9208:Gna15
|
UTSW |
10 |
81,345,224 (GRCm39) |
missense |
probably benign |
0.25 |
R9237:Gna15
|
UTSW |
10 |
81,359,683 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9695:Gna15
|
UTSW |
10 |
81,359,752 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Posted On |
2015-04-16 |