Mutagenetix > Incidental Mutation

Incidental Mutation 'R9041:Gsdmc4'

687746

Institutional Source

Beutler Lab

Gene Symbol

Gsdmc4

Ensembl Gene

ENSMUSG00000055748

Gene Name

gasdermin C4

Synonyms

9030605I04Rik

MMRRC Submission

068868-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.074) question?

Stock #

R9041 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

63763113-63784146 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 63774586 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Serine at position 65 (N65S)

Ref Sequence

ENSEMBL: ENSMUSP00000140269 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000063530] [ENSMUST00000188108]

AlphaFold

Q3TR54

Predicted Effect

probably benign
Transcript: ENSMUST00000063530
AA Change: N65S

PolyPhen 2 Score 0.105 (Sensitivity: 0.93; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000066072
Gene: ENSMUSG00000055748
AA Change: N65S

Domain	Start	End	E-Value	Type
Pfam:Gasdermin	4	443	1.2e-162	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000188108
AA Change: N65S

PolyPhen 2 Score 0.105 (Sensitivity: 0.93; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000140269
Gene: ENSMUSG00000055748
AA Change: N65S

Domain	Start	End	E-Value	Type
Pfam:Gasdermin	4	443	3.8e-153	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.8%

Validation Efficiency

100% (60/60)

Allele List at MGI

Other mutations in this stock

Total: 61 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700113H08Rik	T	C	10: 87,062,054 (GRCm39)	I168T	probably benign	Het
Acvr2b	G	T	9: 119,257,052 (GRCm39)	E94*	probably null	Het
Adcy8	A	T	15: 64,609,287 (GRCm39)	I874N	probably benign	Het
Ahcyl	T	G	16: 45,974,468 (GRCm39)	D303A	possibly damaging	Het
Angptl1	G	T	1: 156,685,999 (GRCm39)	D362Y	probably damaging	Het
Arc	A	G	15: 74,543,896 (GRCm39)	V109A	probably damaging	Het
Asphd2	T	A	5: 112,539,768 (GRCm39)	T22S	probably benign	Het
Caprin2	A	T	6: 148,771,030 (GRCm39)	N321K	probably benign	Het
Carmil1	T	C	13: 24,282,793 (GRCm39)	D547G	possibly damaging	Het
Cd38	G	A	5: 44,058,899 (GRCm39)		probably null	Het
Cd3g	A	G	9: 44,884,818 (GRCm39)	V142A	possibly damaging	Het
Chrna6	A	T	8: 27,896,923 (GRCm39)	I318N	probably damaging	Het
Cmah	T	C	13: 24,641,004 (GRCm39)		probably null	Het
Cmklr1	G	C	5: 113,752,043 (GRCm39)	H319Q	probably benign	Het
Cplx4	T	C	18: 66,103,097 (GRCm39)	M8V	probably damaging	Het
Dnajc19	T	C	3: 34,134,282 (GRCm39)	K27R	probably damaging	Het
E2f3	C	A	13: 30,093,939 (GRCm39)	D441Y	probably damaging	Het
Erap1	A	G	13: 74,822,818 (GRCm39)	K777R	probably benign	Het
Fastkd1	C	T	2: 69,532,715 (GRCm39)	V551I	probably benign	Het
Fgd5	A	G	6: 91,964,427 (GRCm39)	E220G	probably benign	Het
Gal3st2	T	C	1: 93,800,206 (GRCm39)	V19A	possibly damaging	Het
Ghr	T	C	15: 3,357,530 (GRCm39)	E246G	probably benign	Het
Gm10228	A	T	16: 88,838,113 (GRCm39)	Y64N	unknown	Het
Heatr5b	C	A	17: 79,103,861 (GRCm39)	A1105S	probably benign	Het
Hipk2	A	T	6: 38,724,909 (GRCm39)	L376*	probably null	Het
Il6st	A	G	13: 112,611,631 (GRCm39)	T18A	probably benign	Het
Kif3b	T	C	2: 153,159,468 (GRCm39)	I423T	probably benign	Het
Klf17	T	C	4: 117,617,556 (GRCm39)	Y267C	probably damaging	Het
Kntc1	A	G	5: 123,927,093 (GRCm39)	T1183A	probably benign	Het
Lrrc71	A	G	3: 87,650,660 (GRCm39)	S201P	probably damaging	Het
Mrgprb5	A	T	7: 47,818,509 (GRCm39)	D75E	probably damaging	Het
Myef2l	T	C	3: 10,157,353 (GRCm39)	*499Q	probably null	Het
Myf6	A	G	10: 107,329,225 (GRCm39)	V240A	probably benign	Het
Ncoa6	T	C	2: 155,257,450 (GRCm39)	M698V	possibly damaging	Het
Nox4	G	A	7: 87,025,448 (GRCm39)	R525Q	probably benign	Het
Nynrin	T	C	14: 56,108,753 (GRCm39)	S1287P	possibly damaging	Het
Or10ab5	A	G	7: 108,245,589 (GRCm39)	S65P	probably damaging	Het
Otud4	T	A	8: 80,400,441 (GRCm39)	S1052T	probably damaging	Het
Pcsk5	A	T	19: 17,538,132 (GRCm39)	C898*	probably null	Het
Pdcd1	T	C	1: 93,969,091 (GRCm39)	T76A	probably benign	Het
Plin2	T	A	4: 86,578,504 (GRCm39)	M198L	probably benign	Het
Prmt7	T	A	8: 106,963,460 (GRCm39)	V180D	possibly damaging	Het
R3hdm2	T	C	10: 127,320,405 (GRCm39)	Y549H	probably damaging	Het
Rad54l2	A	G	9: 106,600,018 (GRCm39)	S80P	possibly damaging	Het
Ryr3	T	A	2: 112,787,546 (GRCm39)	E235D	probably damaging	Het
Scart1	T	C	7: 139,808,503 (GRCm39)	C805R	probably damaging	Het
Serpina9	A	T	12: 103,967,737 (GRCm39)	S219R		Het
Sesn2	G	A	4: 132,225,272 (GRCm39)	T298I	probably benign	Het
Sf3b2	A	T	19: 5,324,872 (GRCm39)	V838E	possibly damaging	Het
Sfpq	C	A	4: 126,915,296 (GRCm39)	H29Q	unknown	Het
Smchd1	A	G	17: 71,701,710 (GRCm39)		probably null	Het
Sprr1b	A	G	3: 92,344,477 (GRCm39)	V133A	probably benign	Het
Srgap3	T	C	6: 112,754,054 (GRCm39)	Y243C	probably damaging	Het
Thop1	C	T	10: 80,917,228 (GRCm39)	A577V	possibly damaging	Het
Tmprss3	T	A	17: 31,410,014 (GRCm39)	D200V	probably benign	Het
Treh	A	T	9: 44,596,677 (GRCm39)	K512M	probably damaging	Het
Trip11	A	G	12: 101,845,127 (GRCm39)	V1537A	probably benign	Het
Trp63	A	G	16: 25,582,083 (GRCm39)	T44A	probably benign	Het
Vmn1r225	T	A	17: 20,722,577 (GRCm39)	M6K	possibly damaging	Het
Vmn2r90	A	C	17: 17,954,286 (GRCm39)	M817L	probably benign	Het
Zfp68	A	T	5: 138,604,699 (GRCm39)	Y541*	probably null	Het

Other mutations in Gsdmc4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00730:Gsdmc4	APN	15	63,769,653 (GRCm39)	missense	probably damaging	1.00
IGL02301:Gsdmc4	APN	15	63,767,113 (GRCm39)	missense	probably benign	0.00
IGL02586:Gsdmc4	APN	15	63,765,641 (GRCm39)	missense	probably damaging	0.98
IGL02747:Gsdmc4	APN	15	63,765,720 (GRCm39)	missense	probably benign	0.04
IGL02829:Gsdmc4	APN	15	63,764,497 (GRCm39)	missense	probably benign	0.01
IGL03233:Gsdmc4	APN	15	63,774,709 (GRCm39)	missense	probably damaging	1.00
R0835:Gsdmc4	UTSW	15	63,765,649 (GRCm39)	missense	probably damaging	1.00
R0981:Gsdmc4	UTSW	15	63,763,922 (GRCm39)	missense	probably damaging	1.00
R1946:Gsdmc4	UTSW	15	63,774,629 (GRCm39)	missense	probably benign	0.19
R2350:Gsdmc4	UTSW	15	63,765,014 (GRCm39)	missense	probably benign
R2967:Gsdmc4	UTSW	15	63,773,909 (GRCm39)	missense	probably benign	0.19
R3409:Gsdmc4	UTSW	15	63,763,895 (GRCm39)	missense	probably benign	0.09
R3410:Gsdmc4	UTSW	15	63,763,895 (GRCm39)	missense	probably benign	0.09
R4067:Gsdmc4	UTSW	15	63,765,736 (GRCm39)	splice site	probably null
R4840:Gsdmc4	UTSW	15	63,765,596 (GRCm39)	missense	probably benign	0.24
R5182:Gsdmc4	UTSW	15	63,765,653 (GRCm39)	missense	probably damaging	1.00
R5624:Gsdmc4	UTSW	15	63,764,503 (GRCm39)	missense	possibly damaging	0.91
R5910:Gsdmc4	UTSW	15	63,767,101 (GRCm39)	missense	possibly damaging	0.77
R6533:Gsdmc4	UTSW	15	63,763,909 (GRCm39)	missense	probably damaging	1.00
R6698:Gsdmc4	UTSW	15	63,765,613 (GRCm39)	missense	probably benign	0.10
R7291:Gsdmc4	UTSW	15	63,774,689 (GRCm39)	missense	possibly damaging	0.81
R7598:Gsdmc4	UTSW	15	63,772,235 (GRCm39)	missense	probably damaging	1.00
R7691:Gsdmc4	UTSW	15	63,765,640 (GRCm39)	missense	probably damaging	1.00
R7851:Gsdmc4	UTSW	15	63,774,595 (GRCm39)	nonsense	probably null
R7881:Gsdmc4	UTSW	15	63,769,568 (GRCm39)	missense	possibly damaging	0.91
R8300:Gsdmc4	UTSW	15	63,766,790 (GRCm39)	missense	probably damaging	0.97
R8512:Gsdmc4	UTSW	15	63,763,808 (GRCm39)	missense	probably damaging	1.00
R9357:Gsdmc4	UTSW	15	63,772,196 (GRCm39)	missense	probably benign	0.06
R9680:Gsdmc4	UTSW	15	63,774,706 (GRCm39)	missense	possibly damaging	0.61

Predicted Primers

PCR Primer
(F):5'- TGGGTATCATAGCTCTACTTAAAGAGG -3'
(R):5'- GTTTTGACCGGGCTAGCAAG -3'

Sequencing Primer
(F):5'- CTACTTAAAGAGGCTCTTACTCGGG -3'
(R):5'- TAGCAAGGATGTGGTTAAAAAGCTTC -3'

Posted On

2021-11-19