Incidental Mutation 'IGL01087:Nlrp4g'
ID |
51890 |
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 # |
IGL01087
|
Quality Score |
|
Status
|
|
Chromosome |
9 |
Chromosomal Location |
124117991-124126089 bp(-) (GRCm39) |
Type of Mutation |
critical splice acceptor site |
DNA Base Change (assembly) |
A to G
at 124353858 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: ENSMUST00000215602
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700003E16Rik |
A |
T |
6: 83,139,770 (GRCm39) |
|
probably null |
Het |
Abca6 |
C |
A |
11: 110,082,476 (GRCm39) |
A1166S |
probably benign |
Het |
Arhgdib |
C |
A |
6: 136,910,622 (GRCm39) |
K46N |
probably damaging |
Het |
Ash1l |
T |
A |
3: 88,971,209 (GRCm39) |
V2507D |
probably damaging |
Het |
B4galnt1 |
A |
T |
10: 127,002,060 (GRCm39) |
I63F |
probably damaging |
Het |
Bclaf1 |
A |
G |
10: 20,201,056 (GRCm39) |
D394G |
probably damaging |
Het |
Btbd10 |
T |
C |
7: 112,915,763 (GRCm39) |
D442G |
probably damaging |
Het |
Cd44 |
A |
T |
2: 102,652,607 (GRCm39) |
L492H |
probably damaging |
Het |
Cfap206 |
C |
T |
4: 34,721,562 (GRCm39) |
S162N |
probably damaging |
Het |
Chsy1 |
T |
G |
7: 65,821,874 (GRCm39) |
V703G |
possibly damaging |
Het |
Clrn2 |
T |
C |
5: 45,621,311 (GRCm39) |
|
probably benign |
Het |
Crtc3 |
T |
C |
7: 80,248,487 (GRCm39) |
|
probably benign |
Het |
Cul1 |
A |
G |
6: 47,485,978 (GRCm39) |
T342A |
probably benign |
Het |
Dgki |
T |
C |
6: 36,989,846 (GRCm39) |
D631G |
probably damaging |
Het |
Eif3b |
T |
C |
5: 140,426,862 (GRCm39) |
I706T |
probably damaging |
Het |
Fam120a |
A |
G |
13: 49,055,549 (GRCm39) |
L713P |
probably damaging |
Het |
I830077J02Rik |
C |
A |
3: 105,836,049 (GRCm39) |
|
probably null |
Het |
Jmjd8 |
A |
C |
17: 26,048,145 (GRCm39) |
|
probably benign |
Het |
Kmt5a |
T |
C |
5: 124,589,443 (GRCm39) |
|
probably benign |
Het |
Krt87 |
C |
A |
15: 101,329,706 (GRCm39) |
C486F |
probably benign |
Het |
Lrp2 |
A |
T |
2: 69,354,417 (GRCm39) |
N470K |
probably damaging |
Het |
Med1 |
C |
A |
11: 98,071,111 (GRCm39) |
D79Y |
probably damaging |
Het |
Myo1d |
A |
G |
11: 80,573,261 (GRCm39) |
S189P |
probably damaging |
Het |
Myo9a |
T |
A |
9: 59,697,361 (GRCm39) |
Y381N |
possibly damaging |
Het |
Nipbl |
C |
A |
15: 8,379,981 (GRCm39) |
S937I |
possibly damaging |
Het |
Nutm2 |
A |
G |
13: 50,623,665 (GRCm39) |
T121A |
probably damaging |
Het |
Opa1 |
C |
T |
16: 29,405,815 (GRCm39) |
P127S |
probably damaging |
Het |
Or2h1b |
C |
T |
17: 37,462,332 (GRCm39) |
C177Y |
probably damaging |
Het |
Pcdh15 |
A |
T |
10: 74,178,464 (GRCm39) |
I574F |
possibly damaging |
Het |
Pcnx1 |
G |
A |
12: 82,042,113 (GRCm39) |
|
probably benign |
Het |
Prex2 |
A |
G |
1: 11,138,328 (GRCm39) |
T136A |
probably benign |
Het |
Prph2 |
A |
G |
17: 47,222,085 (GRCm39) |
T155A |
probably damaging |
Het |
Rsl1d1 |
T |
C |
16: 11,012,539 (GRCm39) |
K296E |
possibly damaging |
Het |
Syne1 |
A |
T |
10: 5,375,708 (GRCm39) |
I128N |
probably damaging |
Het |
Tlk1 |
A |
T |
2: 70,582,660 (GRCm39) |
N156K |
possibly damaging |
Het |
Trem2 |
C |
T |
17: 48,658,956 (GRCm39) |
T222I |
probably damaging |
Het |
Trip12 |
A |
T |
1: 84,735,580 (GRCm39) |
F872L |
probably damaging |
Het |
Trrap |
T |
A |
5: 144,783,349 (GRCm39) |
S3393T |
probably damaging |
Het |
Vwa8 |
T |
A |
14: 79,172,669 (GRCm39) |
S304T |
probably benign |
Het |
Zc3h7a |
T |
C |
16: 10,971,046 (GRCm39) |
T328A |
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 |
|
IGL01106:Nlrp4g
|
APN |
9 |
124,350,452 (GRCm38) |
unclassified |
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 |