Incidental Mutation 'IGL01503:Nos2'
| ID |
88965 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Nos2
|
| Ensembl Gene |
ENSMUSG00000020826 |
| Gene Name |
nitric oxide synthase 2, inducible |
| Synonyms |
Nos2a, NOS-II, Nos-2, iNOS |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL01503
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
11 |
| Chromosomal Location |
78811613-78851052 bp(+) (GRCm39) |
| Type of Mutation |
splice site |
| DNA Base Change (assembly) |
A to G
at 78836689 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000150558
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000018610]
[ENSMUST00000214397]
|
| AlphaFold |
P29477 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000018610
|
| SMART Domains |
Protein: ENSMUSP00000018610
Gene: ENSMUSG00000020826
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:NO_synthase
|
129 |
491 |
6.7e-189 |
PFAM |
|
Pfam:Flavodoxin_1
|
535 |
666 |
5.5e-43 |
PFAM |
|
Pfam:FAD_binding_1
|
719 |
941 |
8.8e-79 |
PFAM |
|
Pfam:NAD_binding_1
|
973 |
1087 |
4.1e-24 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000214397
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: Nitric oxide is a reactive free radical which acts as a biologic mediator in several processes, including neurotransmission and antimicrobial and antitumoral activities. This gene encodes a nitric oxide synthase that is inducible by a combination of lipopolysaccharide and certain cytokines. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Sep 2015]
PHENOTYPE: Homozygous deletion of this gene alters susceptibility to infection, response to injury, sepsis and sensory stimuli, cardiac function, osteoclast, platelet and mammary gland physiology, tumor growth, testis and uterus morphology, diet-induced atherosclerosis, and blood, urine and glucose metabolism. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 39 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1110057P08Rik |
T |
A |
16: 88,971,757 (GRCm39) |
Y26* |
probably null |
Het |
| Aadacl4fm4 |
T |
A |
4: 144,401,137 (GRCm39) |
I116F |
probably damaging |
Het |
| Arpc1a |
T |
C |
5: 145,032,964 (GRCm39) |
V91A |
probably damaging |
Het |
| Atp2a1 |
T |
A |
7: 126,047,750 (GRCm39) |
I687F |
probably damaging |
Het |
| B3gnt5 |
A |
C |
16: 19,588,531 (GRCm39) |
Y250S |
probably damaging |
Het |
| Brip1 |
A |
G |
11: 85,952,703 (GRCm39) |
V1026A |
probably benign |
Het |
| C1s2 |
T |
C |
6: 124,602,612 (GRCm39) |
D527G |
probably damaging |
Het |
| Chrna5 |
T |
A |
9: 54,905,455 (GRCm39) |
|
probably benign |
Het |
| Cltc |
C |
A |
11: 86,586,526 (GRCm39) |
|
probably benign |
Het |
| Dgkh |
T |
G |
14: 78,853,710 (GRCm39) |
I439L |
possibly damaging |
Het |
| Dnajc16 |
G |
A |
4: 141,491,008 (GRCm39) |
T714I |
possibly damaging |
Het |
| Fam13a |
A |
T |
6: 58,933,065 (GRCm39) |
I349N |
probably damaging |
Het |
| Fig4 |
C |
T |
10: 41,132,514 (GRCm39) |
D431N |
probably benign |
Het |
| Gabra4 |
A |
T |
5: 71,798,429 (GRCm39) |
N183K |
possibly damaging |
Het |
| Ggt5 |
C |
T |
10: 75,445,944 (GRCm39) |
|
probably benign |
Het |
| Hdac6 |
A |
G |
X: 7,798,418 (GRCm39) |
L798P |
probably damaging |
Het |
| Hectd4 |
T |
C |
5: 121,456,714 (GRCm39) |
V2030A |
probably benign |
Het |
| Hecw2 |
A |
G |
1: 53,866,120 (GRCm39) |
Y1514H |
probably damaging |
Het |
| Hmcn1 |
T |
C |
1: 150,480,823 (GRCm39) |
D4451G |
probably benign |
Het |
| Krtcap3 |
T |
C |
5: 31,409,167 (GRCm39) |
|
probably benign |
Het |
| Ltn1 |
A |
T |
16: 87,217,695 (GRCm39) |
|
probably benign |
Het |
| Mapkapk2 |
T |
C |
1: 130,986,499 (GRCm39) |
M1V |
probably null |
Het |
| Mical3 |
A |
T |
6: 120,935,537 (GRCm39) |
I1663N |
probably benign |
Het |
| Mvp |
G |
T |
7: 126,601,133 (GRCm39) |
|
probably benign |
Het |
| Myo5c |
A |
G |
9: 75,170,324 (GRCm39) |
I485V |
probably damaging |
Het |
| N4bp2 |
T |
A |
5: 65,960,890 (GRCm39) |
C520* |
probably null |
Het |
| Ogdh |
G |
A |
11: 6,305,069 (GRCm39) |
V925M |
probably damaging |
Het |
| Pde2a |
T |
A |
7: 101,151,143 (GRCm39) |
|
probably benign |
Het |
| Plpp6 |
A |
G |
19: 28,942,279 (GRCm39) |
*293W |
probably null |
Het |
| Pole |
T |
A |
5: 110,451,750 (GRCm39) |
I864K |
probably damaging |
Het |
| Rexo4 |
A |
T |
2: 26,850,645 (GRCm39) |
I239N |
probably benign |
Het |
| Scn1a |
T |
A |
2: 66,152,687 (GRCm39) |
I748F |
probably damaging |
Het |
| Sfmbt2 |
A |
T |
2: 10,584,165 (GRCm39) |
R841* |
probably null |
Het |
| Sh3bp5l |
A |
G |
11: 58,228,827 (GRCm39) |
N100S |
probably damaging |
Het |
| Spic |
T |
A |
10: 88,511,623 (GRCm39) |
D211V |
probably damaging |
Het |
| Stab2 |
A |
G |
10: 86,776,477 (GRCm39) |
|
probably benign |
Het |
| Tshr |
A |
G |
12: 91,478,708 (GRCm39) |
Y83C |
probably damaging |
Het |
| Vsir |
A |
G |
10: 60,204,373 (GRCm39) |
E172G |
probably damaging |
Het |
| Wwp2 |
T |
C |
8: 108,276,413 (GRCm39) |
S508P |
probably damaging |
Het |
|
| Other mutations in Nos2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01388:Nos2
|
APN |
11 |
78,848,278 (GRCm39) |
missense |
probably damaging |
0.96 |
|
IGL01789:Nos2
|
APN |
11 |
78,835,483 (GRCm39) |
splice site |
probably benign |
|
|
IGL02797:Nos2
|
APN |
11 |
78,831,170 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02968:Nos2
|
APN |
11 |
78,828,463 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6762_Nos2_754
|
UTSW |
11 |
78,850,574 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R0035:Nos2
|
UTSW |
11 |
78,836,553 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0265:Nos2
|
UTSW |
11 |
78,828,428 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0441:Nos2
|
UTSW |
11 |
78,819,409 (GRCm39) |
missense |
probably benign |
0.10 |
|
R0504:Nos2
|
UTSW |
11 |
78,830,903 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0570:Nos2
|
UTSW |
11 |
78,826,187 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R1356:Nos2
|
UTSW |
11 |
78,843,629 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1538:Nos2
|
UTSW |
11 |
78,847,396 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3414:Nos2
|
UTSW |
11 |
78,848,414 (GRCm39) |
missense |
probably benign |
0.14 |
|
R3418:Nos2
|
UTSW |
11 |
78,850,521 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R4279:Nos2
|
UTSW |
11 |
78,820,602 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4492:Nos2
|
UTSW |
11 |
78,840,921 (GRCm39) |
missense |
probably benign |
|
|
R4632:Nos2
|
UTSW |
11 |
78,848,417 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4686:Nos2
|
UTSW |
11 |
78,819,456 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R5038:Nos2
|
UTSW |
11 |
78,813,140 (GRCm39) |
missense |
probably benign |
|
|
R5214:Nos2
|
UTSW |
11 |
78,846,267 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5377:Nos2
|
UTSW |
11 |
78,848,317 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5777:Nos2
|
UTSW |
11 |
78,830,978 (GRCm39) |
missense |
probably null |
1.00 |
|
R5834:Nos2
|
UTSW |
11 |
78,819,405 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5930:Nos2
|
UTSW |
11 |
78,828,741 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6511:Nos2
|
UTSW |
11 |
78,846,290 (GRCm39) |
splice site |
probably null |
|
|
R6706:Nos2
|
UTSW |
11 |
78,835,549 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R6747:Nos2
|
UTSW |
11 |
78,843,780 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6762:Nos2
|
UTSW |
11 |
78,850,574 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R6817:Nos2
|
UTSW |
11 |
78,836,092 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R6868:Nos2
|
UTSW |
11 |
78,848,332 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6917:Nos2
|
UTSW |
11 |
78,842,053 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R7082:Nos2
|
UTSW |
11 |
78,819,405 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7286:Nos2
|
UTSW |
11 |
78,820,680 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7367:Nos2
|
UTSW |
11 |
78,840,916 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R7398:Nos2
|
UTSW |
11 |
78,827,297 (GRCm39) |
nonsense |
probably null |
|
|
R7411:Nos2
|
UTSW |
11 |
78,835,681 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7469:Nos2
|
UTSW |
11 |
78,843,797 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R7736:Nos2
|
UTSW |
11 |
78,813,192 (GRCm39) |
nonsense |
probably null |
|
|
R8694:Nos2
|
UTSW |
11 |
78,836,515 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R8832:Nos2
|
UTSW |
11 |
78,846,290 (GRCm39) |
splice site |
probably null |
|
|
R8872:Nos2
|
UTSW |
11 |
78,839,949 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8952:Nos2
|
UTSW |
11 |
78,836,089 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9433:Nos2
|
UTSW |
11 |
78,850,490 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9580:Nos2
|
UTSW |
11 |
78,828,457 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9612:Nos2
|
UTSW |
11 |
78,839,984 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9727:Nos2
|
UTSW |
11 |
78,843,825 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
R9747:Nos2
|
UTSW |
11 |
78,822,472 (GRCm39) |
missense |
probably damaging |
0.96 |
|
X0063:Nos2
|
UTSW |
11 |
78,813,193 (GRCm39) |
missense |
probably benign |
0.01 |
|
Z1177:Nos2
|
UTSW |
11 |
78,822,498 (GRCm39) |
missense |
probably benign |
|
|
| Posted On |
2013-12-03 |
Incidental Mutation