Incidental Mutation 'IGL01106:Nlrp4g'
| ID |
51931 |
| 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: 0.078)
|
| Stock # |
IGL01106
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
9 |
| Chromosomal Location |
124117991-124126089 bp(-) (GRCm39) |
| Type of Mutation |
unclassified |
| DNA Base Change (assembly) |
A to T
at 124350452 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: 29 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Atg13 |
T |
C |
2: 91,526,297 (GRCm39) |
D12G |
probably damaging |
Het |
| Cmya5 |
A |
G |
13: 93,221,120 (GRCm39) |
L3163P |
probably damaging |
Het |
| Cntn2 |
A |
G |
1: 132,449,622 (GRCm39) |
|
probably benign |
Het |
| Ddx23 |
C |
T |
15: 98,548,821 (GRCm39) |
R327Q |
probably benign |
Het |
| Dlec1 |
G |
A |
9: 118,931,853 (GRCm39) |
E91K |
probably benign |
Het |
| Fam13c |
T |
C |
10: 70,284,646 (GRCm39) |
|
probably null |
Het |
| Fbn1 |
T |
C |
2: 125,193,626 (GRCm39) |
T1398A |
possibly damaging |
Het |
| Frem1 |
T |
C |
4: 82,840,494 (GRCm39) |
T1793A |
probably benign |
Het |
| Gprc5b |
T |
C |
7: 118,583,084 (GRCm39) |
K262E |
probably benign |
Het |
| Hadh |
A |
T |
3: 131,034,619 (GRCm39) |
Y226N |
possibly damaging |
Het |
| Herc1 |
T |
A |
9: 66,383,720 (GRCm39) |
|
probably benign |
Het |
| Ikbke |
A |
G |
1: 131,187,792 (GRCm39) |
|
probably benign |
Het |
| Iqcg |
T |
A |
16: 32,855,970 (GRCm39) |
I202L |
possibly damaging |
Het |
| Kank3 |
G |
A |
17: 34,036,375 (GRCm39) |
G81E |
probably damaging |
Het |
| Kcna3 |
A |
G |
3: 106,945,180 (GRCm39) |
E481G |
possibly damaging |
Het |
| Kdm1a |
A |
G |
4: 136,299,639 (GRCm39) |
|
probably benign |
Het |
| Klhdc8a |
A |
T |
1: 132,232,438 (GRCm39) |
S321C |
probably benign |
Het |
| Kntc1 |
A |
G |
5: 123,900,666 (GRCm39) |
K255E |
probably benign |
Het |
| Lhfpl4 |
T |
A |
6: 113,170,824 (GRCm39) |
T121S |
probably benign |
Het |
| Lsm11 |
G |
A |
11: 45,824,490 (GRCm39) |
Q346* |
probably null |
Het |
| Mcoln3 |
A |
G |
3: 145,843,019 (GRCm39) |
T368A |
probably benign |
Het |
| Nol8 |
A |
G |
13: 49,807,957 (GRCm39) |
I58V |
possibly damaging |
Het |
| Or5al6 |
C |
T |
2: 85,976,560 (GRCm39) |
V173M |
probably benign |
Het |
| Phactr4 |
A |
G |
4: 132,098,116 (GRCm39) |
F384S |
probably benign |
Het |
| Prkg1 |
T |
A |
19: 30,562,678 (GRCm39) |
I509L |
probably benign |
Het |
| Rims1 |
T |
A |
1: 22,449,671 (GRCm39) |
D1019V |
probably damaging |
Het |
| Sclt1 |
T |
C |
3: 41,629,754 (GRCm39) |
|
probably benign |
Het |
| Sntg2 |
T |
A |
12: 30,307,987 (GRCm39) |
K233* |
probably null |
Het |
| Syt5 |
T |
C |
7: 4,544,156 (GRCm39) |
T295A |
probably damaging |
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 |
|
|
IGL01938:Nlrp4g
|
APN |
9 |
124,349,068 (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 |
2013-06-21 |
Incidental Mutation