Mutagenetix > Incidental Mutation

Incidental Mutation 'R8934:Prss30'

680541

Institutional Source

Beutler Lab

Gene Symbol

Prss30

Ensembl Gene

ENSMUSG00000024124

Gene Name

serine protease 30

Synonyms

Disp, Tmprss8, Disp1, 2010015P21Rik

MMRRC Submission

068777-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.052) question?

Stock #

R8934 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

24191100-24199540 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 24192628 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Tyrosine at position 147 (C147Y)

Ref Sequence

ENSEMBL: ENSMUSP00000024936 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000024936] [ENSMUST00000135549] [ENSMUST00000147626] [ENSMUST00000151448]

AlphaFold

Q9QYZ9

Predicted Effect

probably damaging
Transcript: ENSMUST00000024936
AA Change: C147Y

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000024936
Gene: ENSMUSG00000024124
AA Change: C147Y

Domain	Start	End	E-Value	Type
signal peptide	1	21	N/A	INTRINSIC
Tryp_SPc	36	272	2.07e-90	SMART
low complexity region	281	294	N/A	INTRINSIC
low complexity region	297	307	N/A	INTRINSIC

Predicted Effect

SMART Domains

Protein: ENSMUSP00000114293
Gene: ENSMUSG00000024124
AA Change: C184Y

Domain	Start	End	E-Value	Type
low complexity region	14	23	N/A	INTRINSIC
Tryp_SPc	73	272	5.43e-53	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000147626

SMART Domains

Protein: ENSMUSP00000118063
Gene: ENSMUSG00000024124

Domain	Start	End	E-Value	Type
signal peptide	1	21	N/A	INTRINSIC
SCOP:g1h8d.1	27	60	2e-6	SMART
Blast:Tryp_SPc	27	61	3e-17	BLAST

Predicted Effect

probably damaging
Transcript: ENSMUST00000151448
AA Change: C184Y

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000117647
Gene: ENSMUSG00000024124
AA Change: C184Y

Domain	Start	End	E-Value	Type
low complexity region	14	23	N/A	INTRINSIC
Tryp_SPc	73	212	9.69e-9	SMART

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.1%

Validation Efficiency

100% (55/55)

Allele List at MGI

Other mutations in this stock

Total: 56 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3425401B19Rik	G	A	14: 32,382,614 (GRCm39)	S1117L	possibly damaging	Het
Abce1	A	G	8: 80,429,661 (GRCm39)	Y87H	probably damaging	Het
Adad2	G	A	8: 120,341,535 (GRCm39)		probably benign	Het
Adamts12	A	G	15: 11,300,015 (GRCm39)	T901A	probably damaging	Het
Adamts18	T	A	8: 114,463,510 (GRCm39)	I779F	possibly damaging	Het
Bod1l	T	C	5: 41,976,944 (GRCm39)	T1457A	probably benign	Het
Brat1	T	C	5: 140,696,004 (GRCm39)	V125A	probably benign	Het
C4b	G	A	17: 34,951,958 (GRCm39)	R1296C	possibly damaging	Het
C5ar1	A	T	7: 15,982,402 (GRCm39)	L206Q	probably damaging	Het
Cfap126	A	G	1: 170,953,690 (GRCm39)	T87A	probably benign	Het
Cnot1	A	T	8: 96,491,695 (GRCm39)	N376K	probably benign	Het
Cyp3a44	A	T	5: 145,731,786 (GRCm39)	I120K	possibly damaging	Het
Ddx17	T	C	15: 79,420,217 (GRCm39)	E384G	possibly damaging	Het
Dipk1b	G	A	2: 26,524,866 (GRCm39)	V89M	possibly damaging	Het
Dnah14	T	C	1: 181,450,288 (GRCm39)	S634P	possibly damaging	Het
Dusp16	A	T	6: 134,718,639 (GRCm39)		probably benign	Het
Eml2	G	A	7: 18,913,738 (GRCm39)	R185H	probably damaging	Het
Epdr1	T	C	13: 19,777,350 (GRCm39)	E216G	possibly damaging	Het
Erv3	T	C	2: 131,698,101 (GRCm39)	H86R	probably benign	Het
Gm5114	A	G	7: 39,060,553 (GRCm39)	W99R	probably benign	Het
Grid1	G	A	14: 35,043,664 (GRCm39)	D340N	probably damaging	Het
Hjv	T	G	3: 96,433,909 (GRCm39)	C27G	probably damaging	Het
Ifrd2	T	C	9: 107,469,469 (GRCm39)		probably benign	Het
Ikbkb	T	C	8: 23,150,407 (GRCm39)	*758W	probably null	Het
Il1rap	T	C	16: 26,495,734 (GRCm39)	C114R	probably damaging	Het
Irf6	T	C	1: 192,845,033 (GRCm39)	I168T	probably benign	Het
Kmt2d	T	C	15: 98,759,767 (GRCm39)	I1164V	unknown	Het
Lamb3	T	C	1: 193,021,168 (GRCm39)	L915P	probably damaging	Het
Lca5	T	C	9: 83,273,909 (GRCm39)		probably benign	Het
Lhx3	C	A	2: 26,092,258 (GRCm39)	R211L	probably damaging	Het
Mettl8	T	C	2: 70,882,062 (GRCm39)		probably benign	Het
Mroh1	T	C	15: 76,334,386 (GRCm39)	S1297P	probably benign	Het
Myh14	T	A	7: 44,306,852 (GRCm39)	T232S	probably benign	Het
Nemp2	T	A	1: 52,688,868 (GRCm39)	F377L	probably damaging	Het
Obscn	A	G	11: 58,889,085 (GRCm39)		probably null	Het
Or4b1b	T	A	2: 90,112,356 (GRCm39)	T188S	probably benign	Het
Or51ah3	T	C	7: 103,210,290 (GRCm39)	V202A	probably benign	Het
Pgbd5	A	C	8: 125,110,998 (GRCm39)	V231G	possibly damaging	Het
Pitrm1	T	C	13: 6,606,666 (GRCm39)	L240P	probably benign	Het
Pkhd1	A	G	1: 20,462,234 (GRCm39)		probably null	Het
Ppp2r5a	T	A	1: 191,100,835 (GRCm39)		probably benign	Het
Pramel31	C	T	4: 144,090,345 (GRCm39)	L462F	possibly damaging	Het
Ptpru	C	T	4: 131,546,297 (GRCm39)	V318M	probably damaging	Het
Rpap1	C	T	2: 119,599,730 (GRCm39)		probably null	Het
Rptn	A	G	3: 93,303,219 (GRCm39)	Q184R	probably benign	Het
Rufy1	T	A	11: 50,298,705 (GRCm39)	Q362L	probably benign	Het
Rundc1	A	G	11: 101,322,327 (GRCm39)	K274E	probably damaging	Het
Shroom3	T	A	5: 93,089,584 (GRCm39)	I778K	probably damaging	Het
Slamf6	C	T	1: 171,745,338 (GRCm39)	L22F	possibly damaging	Het
St7l	A	G	3: 104,796,634 (GRCm39)	E249G	probably damaging	Het
Tmem237	T	C	1: 59,153,338 (GRCm39)	N61S	probably benign	Het
Tyk2	T	C	9: 21,038,416 (GRCm39)		probably benign	Het
Ubtf	G	T	11: 102,204,855 (GRCm39)	P115T	probably damaging	Het
Vmn2r70	T	A	7: 85,211,188 (GRCm39)	I508F	possibly damaging	Het
Zfp609	C	T	9: 65,610,561 (GRCm39)	A801T	possibly damaging	Het
Zfp663	A	T	2: 165,194,714 (GRCm39)	C502S	probably damaging	Het

Other mutations in Prss30

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00336:Prss30	APN	17	24,192,695 (GRCm39)	missense	probably benign	0.05
IGL01687:Prss30	APN	17	24,194,106 (GRCm39)	missense	probably benign	0.00
R1444:Prss30	UTSW	17	24,192,712 (GRCm39)	missense	probably damaging	1.00
R1662:Prss30	UTSW	17	24,191,806 (GRCm39)	missense	possibly damaging	0.68
R2061:Prss30	UTSW	17	24,193,642 (GRCm39)	start gained	probably benign
R4485:Prss30	UTSW	17	24,192,130 (GRCm39)	missense	probably damaging	1.00
R4849:Prss30	UTSW	17	24,191,769 (GRCm39)	missense	probably benign	0.00
R5305:Prss30	UTSW	17	24,191,750 (GRCm39)	missense	probably benign	0.00
R5853:Prss30	UTSW	17	24,191,820 (GRCm39)	missense	probably damaging	1.00
X0057:Prss30	UTSW	17	24,192,987 (GRCm39)	missense	probably benign	0.00
Z1176:Prss30	UTSW	17	24,193,560 (GRCm39)	missense	unknown
Z1176:Prss30	UTSW	17	24,193,558 (GRCm39)	missense	unknown

Predicted Primers

PCR Primer
(F):5'- TGGGTGGGCTTCTCCAAATC -3'
(R):5'- GGTCTCTGAACCCTAGCTTC -3'

Sequencing Primer
(F):5'- TCTCCAAATCCATCATGAGTGGG -3'
(R):5'- TGAACCCTAGCTTCTACCATGTGAAG -3'

Posted On

2021-08-31