Incidental Mutation 'IGL01938:Nlrp4g'
| ID |
180746 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Nlrp4g
|
| Ensembl Gene |
ENSMUSG00000079741 |
| Gene Name |
NLR family, pyrin domain containing 4G |
| Synonyms |
nalp4g |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.074)
|
| Stock # |
IGL01938
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
9 |
| Chromosomal Location |
124117991-124126089 bp(-) (GRCm39) |
| Type of Mutation |
unclassified |
| DNA Base Change (assembly) |
G to A
at 124349068 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Gene Model |
predicted gene model for transcript(s):
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000067621
|
| SMART Domains |
Protein: ENSMUSP00000065508
Gene: ENSMUSG00000079741
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:NACHT
|
69 |
238 |
1.5e-39 |
PFAM |
|
Blast:LRR
|
555 |
582 |
9e-10 |
BLAST |
|
Blast:LRR
|
610 |
637 |
7e-10 |
BLAST |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000214229
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000215276
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000215602
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000216416
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000217178
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000217183
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 36 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2310003L06Rik |
C |
T |
5: 88,119,567 (GRCm39) |
T108I |
probably damaging |
Het |
| Adam34 |
A |
G |
8: 44,104,053 (GRCm39) |
Y531H |
probably damaging |
Het |
| Arhgef10 |
T |
A |
8: 15,041,062 (GRCm39) |
N1077K |
probably benign |
Het |
| BC034090 |
G |
T |
1: 155,108,338 (GRCm39) |
|
probably null |
Het |
| Cachd1 |
A |
G |
4: 100,831,325 (GRCm39) |
I706V |
possibly damaging |
Het |
| Cebpz |
A |
T |
17: 79,242,390 (GRCm39) |
C421* |
probably null |
Het |
| Celsr3 |
T |
C |
9: 108,705,614 (GRCm39) |
V699A |
probably benign |
Het |
| Col5a1 |
A |
G |
2: 27,886,885 (GRCm39) |
N935S |
unknown |
Het |
| Dnah1 |
C |
T |
14: 31,005,844 (GRCm39) |
V2312I |
probably benign |
Het |
| Ebf3 |
T |
C |
7: 136,911,047 (GRCm39) |
T156A |
probably damaging |
Het |
| Ern1 |
A |
G |
11: 106,302,483 (GRCm39) |
V457A |
probably benign |
Het |
| Flii |
T |
C |
11: 60,605,942 (GRCm39) |
Y1177C |
probably damaging |
Het |
| Fryl |
T |
A |
5: 73,279,707 (GRCm39) |
K197M |
probably damaging |
Het |
| Glb1l3 |
A |
G |
9: 26,729,825 (GRCm39) |
F515S |
probably damaging |
Het |
| Gm10718 |
A |
T |
9: 3,025,118 (GRCm39) |
Y194F |
probably benign |
Het |
| Kif26b |
T |
C |
1: 178,743,603 (GRCm39) |
I1233T |
probably damaging |
Het |
| Kptn |
A |
G |
7: 15,858,714 (GRCm39) |
Y286C |
probably damaging |
Het |
| Lyst |
A |
G |
13: 13,812,009 (GRCm39) |
N807S |
possibly damaging |
Het |
| Mki67 |
C |
T |
7: 135,296,059 (GRCm39) |
V2992M |
probably benign |
Het |
| Myocd |
A |
G |
11: 65,077,914 (GRCm39) |
L627P |
probably damaging |
Het |
| Neto2 |
A |
G |
8: 86,417,484 (GRCm39) |
I40T |
probably benign |
Het |
| Niban1 |
A |
G |
1: 151,565,365 (GRCm39) |
T232A |
probably benign |
Het |
| Nipsnap1 |
C |
T |
11: 4,843,134 (GRCm39) |
H269Y |
probably benign |
Het |
| Nup188 |
A |
T |
2: 30,219,371 (GRCm39) |
R862S |
probably benign |
Het |
| Or1e16 |
T |
A |
11: 73,286,471 (GRCm39) |
I126F |
probably damaging |
Het |
| Or4a80 |
G |
T |
2: 89,582,692 (GRCm39) |
A160D |
probably benign |
Het |
| Or6c33 |
T |
A |
10: 129,853,981 (GRCm39) |
Y250* |
probably null |
Het |
| Pde4c |
A |
T |
8: 71,202,027 (GRCm39) |
K549N |
probably damaging |
Het |
| Pkd1l3 |
A |
G |
8: 110,361,933 (GRCm39) |
T992A |
probably benign |
Het |
| Pramel32 |
A |
G |
4: 88,547,600 (GRCm39) |
S24P |
possibly damaging |
Het |
| Smyd2 |
A |
G |
1: 189,621,079 (GRCm39) |
V213A |
probably benign |
Het |
| Sult1c2 |
C |
T |
17: 54,138,954 (GRCm39) |
V208M |
probably damaging |
Het |
| Ush2a |
T |
C |
1: 188,530,042 (GRCm39) |
L3277P |
probably damaging |
Het |
| Wdr72 |
T |
C |
9: 74,056,056 (GRCm39) |
V304A |
probably benign |
Het |
| Xrra1 |
T |
C |
7: 99,528,676 (GRCm39) |
|
probably null |
Het |
| Zscan29 |
C |
T |
2: 120,996,690 (GRCm39) |
A344T |
probably benign |
Het |
|
| Other mutations in Nlrp4g |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01066:Nlrp4g
|
APN |
9 |
124,349,526 (GRCm38) |
unclassified |
noncoding transcript |
|
|
IGL01087:Nlrp4g
|
APN |
9 |
124,353,858 (GRCm38) |
critical splice acceptor site |
noncoding transcript |
|
|
IGL01106:Nlrp4g
|
APN |
9 |
124,350,452 (GRCm38) |
unclassified |
noncoding transcript |
|
|
IGL02088:Nlrp4g
|
APN |
9 |
124,350,453 (GRCm38) |
unclassified |
noncoding transcript |
|
|
IGL02170:Nlrp4g
|
APN |
9 |
124,348,980 (GRCm38) |
unclassified |
noncoding transcript |
|
|
IGL02582:Nlrp4g
|
APN |
9 |
124,349,764 (GRCm38) |
unclassified |
noncoding transcript |
|
|
IGL02588:Nlrp4g
|
APN |
9 |
124,348,843 (GRCm38) |
unclassified |
noncoding transcript |
|
|
IGL02931:Nlrp4g
|
APN |
9 |
124,348,940 (GRCm38) |
unclassified |
noncoding transcript |
|
|
IGL03111:Nlrp4g
|
APN |
9 |
124,353,978 (GRCm38) |
exon |
noncoding transcript |
|
|
IGL03373:Nlrp4g
|
APN |
9 |
124,349,853 (GRCm38) |
unclassified |
noncoding transcript |
|
|
R0617:Nlrp4g
|
UTSW |
9 |
124,349,540 (GRCm38) |
unclassified |
noncoding transcript |
|
|
R1419:Nlrp4g
|
UTSW |
9 |
124,349,434 (GRCm38) |
unclassified |
noncoding transcript |
|
|
R2060:Nlrp4g
|
UTSW |
9 |
124,349,693 (GRCm38) |
unclassified |
noncoding transcript |
|
|
R2152:Nlrp4g
|
UTSW |
9 |
124,353,339 (GRCm38) |
exon |
noncoding transcript |
|
|
R2356:Nlrp4g
|
UTSW |
9 |
124,349,306 (GRCm38) |
unclassified |
noncoding transcript |
|
|
R2384:Nlrp4g
|
UTSW |
9 |
124,349,707 (GRCm38) |
unclassified |
noncoding transcript |
|
|
R2698:Nlrp4g
|
UTSW |
9 |
124,349,630 (GRCm38) |
unclassified |
noncoding transcript |
|
|
R3878:Nlrp4g
|
UTSW |
9 |
124,349,362 (GRCm38) |
unclassified |
noncoding transcript |
|
|
R4640:Nlrp4g
|
UTSW |
9 |
124,349,153 (GRCm38) |
unclassified |
noncoding transcript |
|
|
R4745:Nlrp4g
|
UTSW |
9 |
124,349,515 (GRCm38) |
unclassified |
noncoding transcript |
|
|
R4754:Nlrp4g
|
UTSW |
9 |
124,349,788 (GRCm38) |
unclassified |
noncoding transcript |
|
|
R4937:Nlrp4g
|
UTSW |
9 |
124,354,005 (GRCm38) |
exon |
noncoding transcript |
|
|
R5024:Nlrp4g
|
UTSW |
9 |
124,350,155 (GRCm38) |
unclassified |
noncoding transcript |
|
|
R5162:Nlrp4g
|
UTSW |
9 |
124,350,394 (GRCm38) |
unclassified |
noncoding transcript |
|
|
R5407:Nlrp4g
|
UTSW |
9 |
124,349,930 (GRCm38) |
unclassified |
noncoding transcript |
|
|
R5521:Nlrp4g
|
UTSW |
9 |
124,350,020 (GRCm38) |
unclassified |
noncoding transcript |
|
|
R8224:Nlrp4g
|
UTSW |
9 |
124,353,374 (GRCm38) |
missense |
noncoding transcript |
|
|
R8259:Nlrp4g
|
UTSW |
9 |
124,353,392 (GRCm38) |
missense |
noncoding transcript |
|
|
Z1088:Nlrp4g
|
UTSW |
9 |
124,349,201 (GRCm38) |
unclassified |
noncoding transcript |
|
|
| Posted On |
2014-05-07 |
Incidental Mutation