Mutagenetix > Incidental Mutation

Incidental Mutation 'R5964:Nlrp1a'

471966

Institutional Source

Beutler Lab

Gene Symbol

Nlrp1a

Ensembl Gene

ENSMUSG00000069830

Gene Name

NLR family, pyrin domain containing 1A

Synonyms

Nalp1

MMRRC Submission

044149-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.096) question?

Stock #

R5964 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

71092236-71144704 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 71123020 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Leucine at position 468 (Q468L)

Ref Sequence

ENSEMBL: ENSMUSP00000104158 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000048514] [ENSMUST00000108518]

AlphaFold

Q2LKU9

Predicted Effect

probably benign
Transcript: ENSMUST00000048514
AA Change: Q468L

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000038186
Gene: ENSMUSG00000069830
AA Change: Q468L

Domain	Start	End	E-Value	Type
low complexity region	2	11	N/A	INTRINSIC
Pfam:NACHT	133	302	4.6e-41	PFAM
low complexity region	482	494	N/A	INTRINSIC
LRR	632	659	4.53e-1	SMART
LRR	742	769	3.04e-5	SMART
low complexity region	856	870	N/A	INTRINSIC
Pfam:FIIND	921	1173	1.6e-102	PFAM
Pfam:CARD	1209	1292	2.3e-20	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000108518
AA Change: Q468L

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000104158
Gene: ENSMUSG00000069830
AA Change: Q468L

Domain	Start	End	E-Value	Type
low complexity region	2	11	N/A	INTRINSIC
Pfam:NACHT	133	302	1.1e-40	PFAM
low complexity region	482	494	N/A	INTRINSIC
LRR	632	659	4.53e-1	SMART
LRR	661	688	2.85e1	SMART
LRR	689	716	3.04e-5	SMART
Pfam:FIIND	819	1073	3e-136	PFAM
Pfam:CARD	1091	1174	8.2e-20	PFAM

Meta Mutation Damage Score

0.4564

Coding Region Coverage

1x: 99.9%
3x: 99.5%
10x: 97.5%
20x: 92.2%

Validation Efficiency

96% (87/91)

MGI Phenotype

PHENOTYPE: Mice heterozygous for an ENU-induced allele develop a multi-organ neutrophilic inflammatory disease. Homozygotes for the same ENU-induced allele develop a similar but lethal condition and exhibit neutrophilia, lymphopenia, splenomegaly, loss of peritoneal macrophages, and premature death. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 71 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam15	G	A	3: 89,343,567 (GRCm38)	Q581*	probably null	Het
Agl	A	G	3: 116,793,774 (GRCm38)	V44A	probably damaging	Het
Alpk3	T	A	7: 81,092,260 (GRCm38)	D608E	possibly damaging	Het
Aspm	C	A	1: 139,455,227 (GRCm38)		probably benign	Het
Bbs2	T	C	8: 94,068,367 (GRCm38)	N692S	probably benign	Het
Bend4	A	G	5: 67,417,818 (GRCm38)	I240T	probably benign	Het
Casp8	G	T	1: 58,833,736 (GRCm38)	R277L	possibly damaging	Het
Ccdc61	A	T	7: 18,900,940 (GRCm38)	I123N	probably damaging	Het
Ccr9	T	G	9: 123,779,434 (GRCm38)	I60M	probably benign	Het
Cd163	T	A	6: 124,326,572 (GRCm38)	W1066R	probably benign	Het
Cd226	A	T	18: 89,207,183 (GRCm38)	H68L	probably benign	Het
Cdkn3	T	A	14: 46,767,217 (GRCm38)	C79S	probably null	Het
Cnnm1	A	T	19: 43,469,723 (GRCm38)	E658V	probably benign	Het
Cog7	T	C	7: 121,956,029 (GRCm38)	R304G	probably damaging	Het
Cpt1a	T	A	19: 3,365,760 (GRCm38)	V286E	possibly damaging	Het
Creg2	C	A	1: 39,624,954 (GRCm38)	R212L	probably benign	Het
Cyp26a1	T	G	19: 37,699,962 (GRCm38)	S311A	probably damaging	Het
Cyp2b10	T	C	7: 25,926,223 (GRCm38)	Y484H	probably benign	Het
Cyp3a44	T	A	5: 145,788,467 (GRCm38)	Y308F	possibly damaging	Het
Dlg5	A	G	14: 24,164,089 (GRCm38)	V744A	probably benign	Het
Dlgap2	T	A	8: 14,727,128 (GRCm38)	Y124*	probably null	Het
Dnah3	T	C	7: 119,922,880 (GRCm38)	D4030G	probably benign	Het
Dnah5	A	G	15: 28,458,584 (GRCm38)	T4456A	possibly damaging	Het
Dtx2	T	A	5: 136,023,699 (GRCm38)	V347D	probably benign	Het
Gigyf2	C	T	1: 87,407,167 (GRCm38)	T294M	probably damaging	Het
Gli3	C	G	13: 15,726,162 (GRCm38)	S1378*	probably null	Het
Gm884	A	G	11: 103,542,120 (GRCm38)	S1232P	possibly damaging	Het
Gnao1	G	A	8: 93,966,999 (GRCm38)	D337N	probably benign	Het
Gp2	T	A	7: 119,449,129 (GRCm38)	Q422L	probably benign	Het
Ifit1	T	A	19: 34,648,469 (GRCm38)	M335K	possibly damaging	Het
Ism1	T	C	2: 139,678,757 (GRCm38)	S30P	probably benign	Het
Itgax	A	G	7: 128,140,447 (GRCm38)	D677G	probably damaging	Het
Kansl1l	G	A	1: 66,725,922 (GRCm38)	A442V	probably damaging	Het
Kif13a	T	C	13: 46,771,524 (GRCm38)	I311M	probably damaging	Het
Lsm14b	T	A	2: 180,031,425 (GRCm38)	S84R	probably benign	Het
Lzts3	A	G	2: 130,636,288 (GRCm38)	Y297H	probably damaging	Het
Map4k3	A	G	17: 80,644,762 (GRCm38)	I205T	probably damaging	Het
Matn2	A	T	15: 34,410,165 (GRCm38)	N501I	probably damaging	Het
Mctp2	T	C	7: 72,103,177 (GRCm38)	E776G	probably damaging	Het
Mex3d	A	T	10: 80,382,587 (GRCm38)	N265K	probably damaging	Het
Myo5a	A	G	9: 75,203,833 (GRCm38)	T1534A	probably benign	Het
Ncoa7	T	C	10: 30,704,636 (GRCm38)	M35V	probably damaging	Het
Nek4	G	A	14: 30,957,079 (GRCm38)		probably null	Het
Ngrn	T	C	7: 80,261,933 (GRCm38)		probably null	Het
Olfr1450	A	C	19: 12,954,531 (GRCm38)	Q314P	probably benign	Het
Olfr743	T	A	14: 50,534,198 (GRCm38)	M262K	probably damaging	Het
Phtf2	T	C	5: 20,775,934 (GRCm38)	D433G	probably damaging	Het
Prdm13	G	A	4: 21,683,852 (GRCm38)	Q140*	probably null	Het
Prtg	G	A	9: 72,892,254 (GRCm38)	G778E	probably benign	Het
Pum3	T	C	19: 27,420,051 (GRCm38)	E308G	probably damaging	Het
Pwp1	T	G	10: 85,882,886 (GRCm38)	F306V	probably damaging	Het
Rab24	A	T	13: 55,321,576 (GRCm38)	Y27N	probably damaging	Het
Rnf215	T	C	11: 4,135,898 (GRCm38)	F126L	probably benign	Het
Samd13	A	T	3: 146,680,696 (GRCm38)		probably benign	Het
Serac1	T	A	17: 6,065,049 (GRCm38)	H213L	probably benign	Het
Slc45a3	A	G	1: 131,978,073 (GRCm38)	E278G	probably damaging	Het
Slit3	C	T	11: 35,700,236 (GRCm38)	R1292C	probably damaging	Het
Slx4	A	T	16: 4,000,951 (GRCm38)		probably null	Het
Smarca4	C	A	9: 21,647,430 (GRCm38)	T631K	probably benign	Het
Snx16	C	T	3: 10,434,481 (GRCm38)	R163Q	possibly damaging	Het
Stk40	T	C	4: 126,128,895 (GRCm38)	V140A	probably damaging	Het
Tcf12	A	T	9: 71,868,240 (GRCm38)	D409E	probably damaging	Het
Tgfbr2	G	T	9: 116,110,255 (GRCm38)	T168K	possibly damaging	Het
Ticam1	G	T	17: 56,271,703 (GRCm38)	H131N	probably damaging	Het
Ttn	C	A	2: 76,829,888 (GRCm38)	R7458I	possibly damaging	Het
Ttn	C	A	2: 76,713,511 (GRCm38)	E31298*	probably null	Het
Usp7	A	G	16: 8,712,102 (GRCm38)	V133A	possibly damaging	Het
Wbp1l	C	T	19: 46,654,180 (GRCm38)	R191*	probably null	Het
Wdfy4	T	C	14: 33,106,011 (GRCm38)	E1118G	probably damaging	Het
Zfp81	G	C	17: 33,336,845 (GRCm38)	P3A	probably damaging	Het
Znhit6	A	G	3: 145,576,933 (GRCm38)	K21R	possibly damaging	Het

Other mutations in Nlrp1a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00648:Nlrp1a	APN	11	71,092,957 (GRCm38)	missense	probably benign	0.00
IGL00771:Nlrp1a	APN	11	71,122,741 (GRCm38)	nonsense	probably null
IGL01408:Nlrp1a	APN	11	71,122,916 (GRCm38)	missense	probably benign	0.04
IGL01886:Nlrp1a	APN	11	71,123,501 (GRCm38)	missense	probably benign
IGL02221:Nlrp1a	APN	11	71,123,118 (GRCm38)	missense	possibly damaging	0.88
IGL02291:Nlrp1a	APN	11	71,122,589 (GRCm38)	critical splice donor site	probably null
IGL02375:Nlrp1a	APN	11	71,113,513 (GRCm38)	nonsense	probably null
IGL02408:Nlrp1a	APN	11	71,122,630 (GRCm38)	missense	probably benign	0.00
IGL02516:Nlrp1a	APN	11	71,114,460 (GRCm38)	missense	probably damaging	1.00
IGL02583:Nlrp1a	APN	11	71,123,401 (GRCm38)	missense	probably benign	0.03
IGL02622:Nlrp1a	APN	11	71,123,000 (GRCm38)	missense	possibly damaging	0.88
IGL02642:Nlrp1a	APN	11	71,123,532 (GRCm38)	missense	probably benign	0.12
IGL02823:Nlrp1a	APN	11	71,092,423 (GRCm38)	missense	probably damaging	0.96
IGL02859:Nlrp1a	APN	11	71,106,086 (GRCm38)	missense	possibly damaging	0.57
IGL02997:Nlrp1a	APN	11	71,123,665 (GRCm38)	missense	probably damaging	1.00
IGL03342:Nlrp1a	APN	11	71,122,791 (GRCm38)	missense	probably benign	0.19
Ants	UTSW	11	71,142,338 (GRCm38)	missense	probably benign	0.01
dreary	UTSW	11	71,113,640 (GRCm38)	critical splice acceptor site	probably null
picnic	UTSW	11	71,122,747 (GRCm38)	missense	possibly damaging	0.87
seedless	UTSW	11	71,123,552 (GRCm38)	missense	probably benign	0.44
watermelon	UTSW	11	71,122,705 (GRCm38)	missense	probably benign	0.08
R0022:Nlrp1a	UTSW	11	71,123,381 (GRCm38)	missense	probably damaging	0.99
R0345:Nlrp1a	UTSW	11	71,123,675 (GRCm38)	missense	probably damaging	1.00
R0360:Nlrp1a	UTSW	11	71,114,004 (GRCm38)	intron	probably benign
R0364:Nlrp1a	UTSW	11	71,114,004 (GRCm38)	intron	probably benign
R0566:Nlrp1a	UTSW	11	71,122,942 (GRCm38)	missense	probably benign	0.00
R1177:Nlrp1a	UTSW	11	71,107,721 (GRCm38)	missense	probably damaging	1.00
R1240:Nlrp1a	UTSW	11	71,113,466 (GRCm38)	critical splice donor site	probably null
R1263:Nlrp1a	UTSW	11	71,097,122 (GRCm38)	missense	probably benign	0.01
R1681:Nlrp1a	UTSW	11	71,142,358 (GRCm38)	missense	unknown
R1743:Nlrp1a	UTSW	11	71,124,206 (GRCm38)	missense	probably benign	0.04
R1826:Nlrp1a	UTSW	11	71,122,747 (GRCm38)	missense	possibly damaging	0.87
R1826:Nlrp1a	UTSW	11	71,107,980 (GRCm38)	intron	probably benign
R1981:Nlrp1a	UTSW	11	71,098,938 (GRCm38)	missense	probably damaging	1.00
R2083:Nlrp1a	UTSW	11	71,124,220 (GRCm38)	missense	possibly damaging	0.59
R2116:Nlrp1a	UTSW	11	71,114,500 (GRCm38)	nonsense	probably null
R2134:Nlrp1a	UTSW	11	71,124,188 (GRCm38)	missense	probably benign	0.00
R2148:Nlrp1a	UTSW	11	71,122,907 (GRCm38)	nonsense	probably null
R2301:Nlrp1a	UTSW	11	71,106,101 (GRCm38)	missense	possibly damaging	0.94
R3029:Nlrp1a	UTSW	11	71,123,630 (GRCm38)	missense	probably damaging	1.00
R3113:Nlrp1a	UTSW	11	71,123,665 (GRCm38)	missense	probably damaging	1.00
R3801:Nlrp1a	UTSW	11	71,122,703 (GRCm38)	missense	probably benign	0.08
R3898:Nlrp1a	UTSW	11	71,122,874 (GRCm38)	missense	probably benign	0.00
R4254:Nlrp1a	UTSW	11	71,123,028 (GRCm38)	nonsense	probably null
R4397:Nlrp1a	UTSW	11	71,097,204 (GRCm38)	missense	probably benign	0.00
R4647:Nlrp1a	UTSW	11	71,097,126 (GRCm38)	splice site	probably null
R4740:Nlrp1a	UTSW	11	71,113,640 (GRCm38)	critical splice acceptor site	probably null
R4965:Nlrp1a	UTSW	11	71,092,315 (GRCm38)	missense	possibly damaging	0.94
R5009:Nlrp1a	UTSW	11	71,122,705 (GRCm38)	missense	probably benign	0.08
R5103:Nlrp1a	UTSW	11	71,099,526 (GRCm38)	missense	probably damaging	0.99
R5355:Nlrp1a	UTSW	11	71,124,251 (GRCm38)	missense	probably benign	0.00
R5577:Nlrp1a	UTSW	11	71,099,574 (GRCm38)	missense	probably damaging	1.00
R5892:Nlrp1a	UTSW	11	71,099,645 (GRCm38)	missense	probably damaging	1.00
R5949:Nlrp1a	UTSW	11	71,098,989 (GRCm38)	missense	probably damaging	1.00
R6220:Nlrp1a	UTSW	11	71,142,338 (GRCm38)	missense	probably benign	0.01
R6564:Nlrp1a	UTSW	11	71,123,572 (GRCm38)	missense	probably damaging	1.00
R6586:Nlrp1a	UTSW	11	71,106,073 (GRCm38)	missense	probably benign	0.00
R6925:Nlrp1a	UTSW	11	71,092,513 (GRCm38)	missense	probably null	0.99
R7013:Nlrp1a	UTSW	11	71,123,552 (GRCm38)	missense	probably benign	0.44
R7155:Nlrp1a	UTSW	11	71,124,079 (GRCm38)	missense	possibly damaging	0.93
R7214:Nlrp1a	UTSW	11	71,123,293 (GRCm38)	missense	probably damaging	1.00
R7268:Nlrp1a	UTSW	11	71,124,242 (GRCm38)	missense	probably benign	0.00
R7388:Nlrp1a	UTSW	11	71,123,197 (GRCm38)	missense	probably damaging	1.00
R7404:Nlrp1a	UTSW	11	71,097,093 (GRCm38)	nonsense	probably null
R7409:Nlrp1a	UTSW	11	71,122,808 (GRCm38)	missense	probably benign	0.03
R7410:Nlrp1a	UTSW	11	71,123,857 (GRCm38)	missense	probably damaging	0.99
R7440:Nlrp1a	UTSW	11	71,092,324 (GRCm38)	missense	probably damaging	0.99
R7447:Nlrp1a	UTSW	11	71,092,411 (GRCm38)	missense	probably damaging	1.00
R7450:Nlrp1a	UTSW	11	71,107,658 (GRCm38)	missense	probably damaging	1.00
R7569:Nlrp1a	UTSW	11	71,109,043 (GRCm38)	missense	probably benign	0.00
R7600:Nlrp1a	UTSW	11	71,098,914 (GRCm38)	missense	probably damaging	0.96
R7634:Nlrp1a	UTSW	11	71,099,528 (GRCm38)	missense	probably benign	0.19
R7734:Nlrp1a	UTSW	11	71,108,000 (GRCm38)	missense	unknown
R7747:Nlrp1a	UTSW	11	71,123,408 (GRCm38)	missense	possibly damaging	0.85
R8471:Nlrp1a	UTSW	11	71,123,059 (GRCm38)	missense	possibly damaging	0.68
R8482:Nlrp1a	UTSW	11	71,109,075 (GRCm38)	splice site	probably null
R9008:Nlrp1a	UTSW	11	71,123,909 (GRCm38)	missense	possibly damaging	0.89
R9028:Nlrp1a	UTSW	11	71,122,993 (GRCm38)	missense	probably benign	0.27
R9441:Nlrp1a	UTSW	11	71,123,108 (GRCm38)	missense	probably damaging	1.00
R9516:Nlrp1a	UTSW	11	71,107,662 (GRCm38)	missense	probably benign	0.05
R9701:Nlrp1a	UTSW	11	71,097,120 (GRCm38)	missense	probably benign	0.08
X0026:Nlrp1a	UTSW	11	71,142,316 (GRCm38)	missense	probably benign	0.18
Z1177:Nlrp1a	UTSW	11	71,123,169 (GRCm38)	missense	probably benign	0.27
Z1186:Nlrp1a	UTSW	11	71,124,088 (GRCm38)	missense	probably benign
Z1186:Nlrp1a	UTSW	11	71,142,529 (GRCm38)	critical splice acceptor site	probably null
Z1186:Nlrp1a	UTSW	11	71,092,243 (GRCm38)	missense	probably benign
Z1186:Nlrp1a	UTSW	11	71,097,251 (GRCm38)	missense	probably damaging	0.96
Z1186:Nlrp1a	UTSW	11	71,099,616 (GRCm38)	missense	probably benign
Z1187:Nlrp1a	UTSW	11	71,099,616 (GRCm38)	missense	probably benign
Z1187:Nlrp1a	UTSW	11	71,097,251 (GRCm38)	missense	probably damaging	0.96
Z1187:Nlrp1a	UTSW	11	71,092,243 (GRCm38)	missense	probably benign
Z1187:Nlrp1a	UTSW	11	71,142,529 (GRCm38)	critical splice acceptor site	probably null
Z1187:Nlrp1a	UTSW	11	71,124,088 (GRCm38)	missense	probably benign
Z1188:Nlrp1a	UTSW	11	71,099,616 (GRCm38)	missense	probably benign
Z1188:Nlrp1a	UTSW	11	71,097,251 (GRCm38)	missense	probably damaging	0.96
Z1188:Nlrp1a	UTSW	11	71,092,243 (GRCm38)	missense	probably benign
Z1188:Nlrp1a	UTSW	11	71,142,529 (GRCm38)	critical splice acceptor site	probably null
Z1188:Nlrp1a	UTSW	11	71,124,088 (GRCm38)	missense	probably benign
Z1189:Nlrp1a	UTSW	11	71,099,616 (GRCm38)	missense	probably benign
Z1189:Nlrp1a	UTSW	11	71,097,251 (GRCm38)	missense	probably damaging	0.96
Z1189:Nlrp1a	UTSW	11	71,092,243 (GRCm38)	missense	probably benign
Z1189:Nlrp1a	UTSW	11	71,142,529 (GRCm38)	critical splice acceptor site	probably null
Z1189:Nlrp1a	UTSW	11	71,124,088 (GRCm38)	missense	probably benign
Z1190:Nlrp1a	UTSW	11	71,099,616 (GRCm38)	missense	probably benign
Z1190:Nlrp1a	UTSW	11	71,097,251 (GRCm38)	missense	probably damaging	0.96
Z1190:Nlrp1a	UTSW	11	71,092,243 (GRCm38)	missense	probably benign
Z1190:Nlrp1a	UTSW	11	71,142,529 (GRCm38)	critical splice acceptor site	probably null
Z1190:Nlrp1a	UTSW	11	71,124,088 (GRCm38)	missense	probably benign
Z1191:Nlrp1a	UTSW	11	71,099,616 (GRCm38)	missense	probably benign
Z1191:Nlrp1a	UTSW	11	71,097,251 (GRCm38)	missense	probably damaging	0.96
Z1191:Nlrp1a	UTSW	11	71,092,243 (GRCm38)	missense	probably benign
Z1191:Nlrp1a	UTSW	11	71,142,529 (GRCm38)	critical splice acceptor site	probably null
Z1191:Nlrp1a	UTSW	11	71,124,088 (GRCm38)	missense	probably benign
Z1192:Nlrp1a	UTSW	11	71,099,616 (GRCm38)	missense	probably benign
Z1192:Nlrp1a	UTSW	11	71,097,251 (GRCm38)	missense	probably damaging	0.96
Z1192:Nlrp1a	UTSW	11	71,092,243 (GRCm38)	missense	probably benign
Z1192:Nlrp1a	UTSW	11	71,142,529 (GRCm38)	critical splice acceptor site	probably null
Z1192:Nlrp1a	UTSW	11	71,124,088 (GRCm38)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- TCATGCATCACGTGTGTCAG -3'
(R):5'- AGATTGGTGTCCTTCAAAAGCAG -3'

Sequencing Primer
(F):5'- ACGTGTGTCAGGAGCTCCATATC -3'
(R):5'- GTGTCCTTCAAAAGCAGGCCAG -3'

Posted On

2017-03-31