Mutagenetix > Incidental Mutations

Incidental Mutation 'IGL02088:Nlrp4g'

279337

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

Is this an essential gene?

Probably non essential (E-score: 0.071) question?

Stock #

IGL02088

Quality Score

Status

Chromosome

Chromosomal Location

124348831-124354028 bp(+) (GRCm38)

Type of Mutation

unclassified

DNA Base Change (assembly)

T to C at 124350453 bp

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s):

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: 38 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ackr4	T	C	9: 104,098,881	E289G	probably damaging	Het
Aldh1l1	A	T	6: 90,580,590		probably benign	Het
Ampd3	T	A	7: 110,793,686	D220E	probably benign	Het
Ank3	T	C	10: 69,999,373	V136A	probably damaging	Het
Atg14	T	C	14: 47,542,859	K486R	probably benign	Het
Axin1	A	G	17: 26,188,695	I637V	probably benign	Het
Axin2	T	A	11: 108,923,616	F110Y	probably damaging	Het
Cdh12	A	T	15: 21,480,339	K214*	probably null	Het
Cfap44	A	C	16: 44,451,628	E1248A	possibly damaging	Het
Cryba4	A	G	5: 112,251,009		probably benign	Het
Cyp2c68	A	G	19: 39,703,521		probably benign	Het
Dnah5	G	T	15: 28,459,118		probably null	Het
Dok3	A	T	13: 55,524,370	V165E	probably damaging	Het
Etl4	A	T	2: 20,806,548	R1147S	probably damaging	Het
Fam212a	A	G	9: 107,984,457	F220S	probably damaging	Het
Fbxl6	G	T	15: 76,535,906	C502*	probably null	Het
Gp2	A	T	7: 119,454,469	Y90N	probably damaging	Het
H1fnt	G	T	15: 98,257,178	T30K	probably damaging	Het
Itfg2	A	G	6: 128,411,606	V306A	probably benign	Het
Lrig2	T	C	3: 104,467,108	Y219C	probably damaging	Het
Mccc1	A	T	3: 35,974,202	I485N	probably damaging	Het
Mettl25	A	G	10: 105,823,250	F391L	probably damaging	Het
Muc19	C	T	15: 91,891,168		noncoding transcript	Het
Muc2	T	C	7: 141,751,504	C182R	probably damaging	Het
Nms	A	G	1: 38,939,277		probably benign	Het
Nr3c1	T	C	18: 39,424,391	N503S	probably damaging	Het
Olfr1495	T	C	19: 13,768,666	F108S	probably damaging	Het
Olfr186	A	G	16: 59,027,052	L285P	probably damaging	Het
Olfr828	C	T	9: 18,815,923	V124I	probably benign	Het
Pcdhb5	G	A	18: 37,321,959	S464N	probably benign	Het
Pcgf6	T	C	19: 47,050,804	T6A	unknown	Het
Rdx	A	G	9: 52,060,883		probably benign	Het
Shmt1	T	C	11: 60,789,653	T403A	probably damaging	Het
Slc35d1	A	G	4: 103,211,325	F148L	probably benign	Het
Tk1	A	G	11: 117,824,665		probably benign	Het
Tnks	T	A	8: 34,839,994	I1134F	possibly damaging	Het
Ttn	A	G	2: 76,726,691	V29990A	probably damaging	Het
Zcchc11	A	G	4: 108,512,218		probably benign	Het

Other mutations in Nlrp4g

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01066:Nlrp4g	APN	9	124349526	unclassified	noncoding transcript
IGL01087:Nlrp4g	APN	9	124353858	critical splice acceptor site	noncoding transcript
IGL01106:Nlrp4g	APN	9	124350452	unclassified	noncoding transcript
IGL01938:Nlrp4g	APN	9	124349068	unclassified	noncoding transcript
IGL02170:Nlrp4g	APN	9	124348980	unclassified	noncoding transcript
IGL02582:Nlrp4g	APN	9	124349764	unclassified	noncoding transcript
IGL02588:Nlrp4g	APN	9	124348843	unclassified	noncoding transcript
IGL02931:Nlrp4g	APN	9	124348940	unclassified	noncoding transcript
IGL03111:Nlrp4g	APN	9	124353978	exon	noncoding transcript
IGL03373:Nlrp4g	APN	9	124349853	unclassified	noncoding transcript
R0617:Nlrp4g	UTSW	9	124349540	unclassified	noncoding transcript
R1419:Nlrp4g	UTSW	9	124349434	unclassified	noncoding transcript
R2060:Nlrp4g	UTSW	9	124349693	unclassified	noncoding transcript
R2152:Nlrp4g	UTSW	9	124353339	exon	noncoding transcript
R2356:Nlrp4g	UTSW	9	124349306	unclassified	noncoding transcript
R2384:Nlrp4g	UTSW	9	124349707	unclassified	noncoding transcript
R2698:Nlrp4g	UTSW	9	124349630	unclassified	noncoding transcript
R3878:Nlrp4g	UTSW	9	124349362	unclassified	noncoding transcript
R4640:Nlrp4g	UTSW	9	124349153	unclassified	noncoding transcript
R4745:Nlrp4g	UTSW	9	124349515	unclassified	noncoding transcript
R4754:Nlrp4g	UTSW	9	124349788	unclassified	noncoding transcript
R4937:Nlrp4g	UTSW	9	124354005	exon	noncoding transcript
R5024:Nlrp4g	UTSW	9	124350155	unclassified	noncoding transcript
R5162:Nlrp4g	UTSW	9	124350394	unclassified	noncoding transcript
R5407:Nlrp4g	UTSW	9	124349930	unclassified	noncoding transcript
R5521:Nlrp4g	UTSW	9	124350020	unclassified	noncoding transcript
R8224:Nlrp4g	UTSW	9	124353374	missense	noncoding transcript
R8259:Nlrp4g	UTSW	9	124353392	missense	noncoding transcript
Z1088:Nlrp4g	UTSW	9	124349201	unclassified	noncoding transcript

Posted On

2015-04-16