Mutagenetix > Incidental Mutation

Incidental Mutation 'R1583:Prss3'

177245

Institutional Source

Beutler Lab

Gene Symbol

Prss3

Ensembl Gene

ENSMUSG00000071519

Gene Name

protease, serine 3

Synonyms

TRY4, Tb, MTG, mesotrypsin, Try3

MMRRC Submission

039620-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.081) question?

Stock #

R1583 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

41373814-41377678 bp(-) (GRCm38)

Type of Mutation

start gained

DNA Base Change (assembly)

A to C at 41377627 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000093702 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000096003]

AlphaFold

Q792Z0

Predicted Effect

probably benign
Transcript: ENSMUST00000096003

SMART Domains

Protein: ENSMUSP00000093702
Gene: ENSMUSG00000071519

Domain	Start	End	E-Value	Type
low complexity region	3	15	N/A	INTRINSIC
Tryp_SPc	23	239	1.4e-105	SMART

Coding Region Coverage

1x: 99.0%
3x: 98.0%
10x: 95.2%
20x: 88.8%

Validation Efficiency

99% (79/80)

Allele List at MGI

Other mutations in this stock

Total: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aasdh	A	G	5: 76,882,681 (GRCm38)	S691P	probably benign	Het
Adgrb3	T	C	1: 25,226,831 (GRCm38)		probably null	Het
Ankar	A	G	1: 72,679,555 (GRCm38)		probably benign	Het
Aplf	A	T	6: 87,646,033 (GRCm38)	Y355N	probably damaging	Het
Bms1	A	G	6: 118,389,389 (GRCm38)		probably benign	Het
Catsperb	T	C	12: 101,463,114 (GRCm38)	I182T	probably damaging	Het
Cd300ld2	T	C	11: 115,013,777 (GRCm38)	D88G	probably benign	Het
Cebpz	T	C	17: 78,934,752 (GRCm38)	N491S	probably damaging	Het
Crybg2	T	C	4: 134,081,459 (GRCm38)	S1415P	probably damaging	Het
Ddc	A	G	11: 11,829,131 (GRCm38)	V331A	probably benign	Het
Decr2	T	C	17: 26,083,024 (GRCm38)	E244G	probably damaging	Het
Dhrs11	A	G	11: 84,823,117 (GRCm38)	M136T	probably damaging	Het
Eapp	G	A	12: 54,685,948 (GRCm38)	Q126*	probably null	Het
Fam111a	T	A	19: 12,587,778 (GRCm38)	V297D	probably damaging	Het
Fam84a	G	A	12: 14,150,408 (GRCm38)	A106V	probably benign	Het
Fbxo10	A	C	4: 45,062,118 (GRCm38)	L136R	probably damaging	Het
Fbxo30	T	A	10: 11,291,374 (GRCm38)	H613Q	possibly damaging	Het
Frk	A	T	10: 34,591,810 (GRCm38)		probably null	Het
Gm10392	T	A	11: 77,517,481 (GRCm38)	D104V	probably benign	Het
Gm960	T	A	19: 4,652,171 (GRCm38)	K282N	probably damaging	Het
Gpn1	A	G	5: 31,497,338 (GRCm38)	E78G	possibly damaging	Het
Hhip	T	C	8: 79,990,276 (GRCm38)	Y506C	probably damaging	Het
Hid1	G	A	11: 115,356,750 (GRCm38)	S274L	possibly damaging	Het
Immp2l	G	T	12: 41,703,765 (GRCm38)		probably benign	Het
Klhl21	T	C	4: 152,009,624 (GRCm38)	F228L	possibly damaging	Het
Lamc1	T	A	1: 153,243,478 (GRCm38)		probably null	Het
Lars	G	A	18: 42,210,050 (GRCm38)	R1101C	probably damaging	Het
Magi2	T	C	5: 19,227,332 (GRCm38)	V15A	probably benign	Het
Map2k7	T	C	8: 4,243,621 (GRCm38)		probably null	Het
Mga	T	A	2: 119,963,960 (GRCm38)	H2590Q	possibly damaging	Het
Mlxip	T	C	5: 123,450,223 (GRCm38)	I238T	possibly damaging	Het
Mylk	T	A	16: 34,875,586 (GRCm38)	D230E	probably benign	Het
Nacad	T	A	11: 6,601,185 (GRCm38)	T669S	probably benign	Het
Nin	C	T	12: 70,031,738 (GRCm38)	M1691I	probably benign	Het
Nlrp4d	C	T	7: 10,382,237 (GRCm38)	A203T	probably damaging	Het
Olfr1204	T	G	2: 88,852,262 (GRCm38)	F104C	probably damaging	Het
Olfr1301	A	T	2: 111,754,425 (GRCm38)	M59L	probably damaging	Het
Olfr1495	A	T	19: 13,768,510 (GRCm38)	H56L	probably benign	Het
Olfr201	A	G	16: 59,269,031 (GRCm38)	V212A	probably benign	Het
Olfr433	T	C	1: 174,042,480 (GRCm38)	F177L	probably benign	Het
Olfr729	C	A	14: 50,148,774 (GRCm38)	M33I	probably benign	Het
Osbp	C	A	19: 11,977,829 (GRCm38)	Q282K	probably benign	Het
Osbpl2	A	G	2: 180,148,463 (GRCm38)	S177G	probably damaging	Het
Pax1	A	G	2: 147,366,255 (GRCm38)	H261R	possibly damaging	Het
Pcif1	A	T	2: 164,886,727 (GRCm38)	L274F	probably damaging	Het
Pkhd1	A	G	1: 20,117,825 (GRCm38)	S3420P	probably benign	Het
Ptk2b	T	C	14: 66,163,114 (GRCm38)	T751A	possibly damaging	Het
Pus10	T	C	11: 23,673,239 (GRCm38)	V126A	probably damaging	Het
Rai14	A	C	15: 10,587,916 (GRCm38)	D258E	probably damaging	Het
Rbp3	T	C	14: 33,954,524 (GRCm38)	V143A	possibly damaging	Het
Sarm1	G	A	11: 78,483,327 (GRCm38)	Q625*	probably null	Het
Scgb1b21	T	G	7: 33,527,667 (GRCm38)		noncoding transcript	Het
Scrn1	A	T	6: 54,520,769 (GRCm38)	V279E	probably damaging	Het
Sipa1l2	T	C	8: 125,421,895 (GRCm38)	T1670A	probably damaging	Het
Slc9a4	A	T	1: 40,600,962 (GRCm38)	I305F	probably benign	Het
Smarcc1	A	G	9: 110,213,617 (GRCm38)	T918A	probably damaging	Het
Tas2r109	A	T	6: 132,980,426 (GRCm38)	H180Q	probably benign	Het
Tas2r121	G	A	6: 132,700,230 (GRCm38)	R260*	probably null	Het
Tenm3	T	C	8: 48,279,074 (GRCm38)	D1249G	probably benign	Het
Tgtp1	C	G	11: 48,987,530 (GRCm38)	G116A	probably damaging	Het
Tial1	A	G	7: 128,443,910 (GRCm38)	Y317H	probably damaging	Het
Trim66	A	T	7: 109,455,080 (GRCm38)	W1308R	probably damaging	Het
Ulk2	T	G	11: 61,783,545 (GRCm38)	K878N	possibly damaging	Het
Zfp41	T	A	15: 75,618,291 (GRCm38)	S31T	possibly damaging	Het

Other mutations in Prss3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0535:Prss3	UTSW	6	41,374,969 (GRCm38)	missense	probably benign	0.26
R4324:Prss3	UTSW	6	41,373,845 (GRCm38)	missense	probably benign	0.00
R4859:Prss3	UTSW	6	41,373,923 (GRCm38)	missense	probably damaging	0.96
R5004:Prss3	UTSW	6	41,373,902 (GRCm38)	missense	probably damaging	1.00
R5361:Prss3	UTSW	6	41,373,846 (GRCm38)	missense	probably benign	0.00
R5929:Prss3	UTSW	6	41,376,804 (GRCm38)	splice site	probably null
R6026:Prss3	UTSW	6	41,377,554 (GRCm38)	splice site	probably null
R6179:Prss3	UTSW	6	41,375,126 (GRCm38)	missense	probably benign	0.11
R7510:Prss3	UTSW	6	41,375,110 (GRCm38)	nonsense	probably null
R7514:Prss3	UTSW	6	41,373,914 (GRCm38)	missense	probably damaging	1.00
R8323:Prss3	UTSW	6	41,374,324 (GRCm38)	missense	probably damaging	1.00
R8463:Prss3	UTSW	6	41,375,125 (GRCm38)	missense	probably benign	0.02
R8734:Prss3	UTSW	6	41,373,893 (GRCm38)	missense	probably damaging	1.00
R8885:Prss3	UTSW	6	41,377,578 (GRCm38)	missense	probably damaging	0.99
R8972:Prss3	UTSW	6	41,376,938 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CTGAGGAAATTGCCTTCTGGTCTCC -3'
(R):5'- TGTTGGTGTTGTTCAAAGAGCCCC -3'

Sequencing Primer
(F):5'- GTGTATTGACAGAAACTGGTGTAAC -3'
(R):5'- ACCAGAATTGGGCATTCTTCAC -3'

Posted On

2014-04-24