Mutagenetix > Incidental Mutation

Incidental Mutation 'R2915:Prss1'

254839

Institutional Source

Beutler Lab

Gene Symbol

Prss1

Ensembl Gene

ENSMUSG00000062751

Gene Name

protease, serine 1 (trypsin 1)

Synonyms

Try-1, PRSS1, Trygn16, Try1

MMRRC Submission

040502-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R2915 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

41458932-41463786 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 41462611 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Phenylalanine at position 93 (I93F)

Ref Sequence

ENSEMBL: ENSMUSP00000031910 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000031910]

AlphaFold

Q9Z1R9

Predicted Effect

probably benign
Transcript: ENSMUST00000031910
AA Change: I93F

PolyPhen 2 Score 0.110 (Sensitivity: 0.93; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000031910
Gene: ENSMUSG00000062751
AA Change: I93F

Domain	Start	End	E-Value	Type
low complexity region	3	16	N/A	INTRINSIC
Tryp_SPc	23	239	9.87e-106	SMART

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.4%
20x: 95.4%

Validation Efficiency

98% (50/51)

Allele List at MGI

Other mutations in this stock

Total: 49 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aif1	G	A	17: 35,172,151	P44L	probably benign	Het
Arhgap11a	A	G	2: 113,833,508	V810A	probably damaging	Het
B3gnt6	T	C	7: 98,193,593	N387D	probably benign	Het
Col5a2	C	G	1: 45,413,496	G358R	probably damaging	Het
Cracr2a	A	G	6: 127,611,505	K209R	probably damaging	Het
Dmkn	A	G	7: 30,765,316	N32S	unknown	Het
Dusp13	T	A	14: 21,740,137	N47I	probably damaging	Het
Elmo2	A	G	2: 165,297,653		probably benign	Het
Ephb6	T	C	6: 41,614,238	F110L	probably damaging	Het
Gabrb2	T	A	11: 42,591,907	N197K	probably benign	Het
Gdnf	T	A	15: 7,815,649	V41E	possibly damaging	Het
Gm21915	A	G	9: 40,670,787	I59V	possibly damaging	Het
Gprin2	C	T	14: 34,195,081	G244D	possibly damaging	Het
Grin2d	T	C	7: 45,833,357		probably benign	Het
Ice2	A	G	9: 69,410,840	D241G	probably benign	Het
Mios	C	T	6: 8,214,935	R44C	possibly damaging	Het
Nlrp5-ps	T	C	7: 14,586,711		noncoding transcript	Het
Nyap2	C	T	1: 81,087,471	R67*	probably null	Het
Olfr1031	T	A	2: 85,992,045	V76E	probably damaging	Het
Olfr1094	T	C	2: 86,829,226	I158T	probably benign	Het
Olfr1306	G	T	2: 111,912,719	D70E	probably damaging	Het
Olfr1428	G	A	19: 12,108,625	P81L	probably benign	Het
Olfr27	G	T	9: 39,144,466	R122L	possibly damaging	Het
Otop2	G	A	11: 115,329,146	A271T	probably benign	Het
Otulin	A	G	15: 27,619,630		probably benign	Het
Pax1	A	G	2: 147,368,428	Y361C	probably damaging	Het
Pcdhb12	A	T	18: 37,437,640	N613I	probably damaging	Het
Plekha5	A	G	6: 140,589,199	K173E	probably damaging	Het
Plin4	T	A	17: 56,104,389	T881S	probably damaging	Het
Poli	A	G	18: 70,522,700		probably null	Het
Prex2	T	A	1: 11,169,853	F898I	probably damaging	Het
Prr14l	A	T	5: 32,829,768	H794Q	probably benign	Het
Ptpro	C	T	6: 137,414,241		probably benign	Het
Rad1	T	C	15: 10,486,642	C42R	probably damaging	Het
Rnf20	A	G	4: 49,638,769	E197G	probably benign	Het
Setx	A	G	2: 29,172,324	E2260G	probably damaging	Het
Sgk1	C	T	10: 21,996,601	R171W	probably damaging	Het
Six2	A	G	17: 85,685,188	S296P	probably damaging	Het
Smg1	T	A	7: 118,210,879		probably benign	Het
Spred2	T	C	11: 19,998,215	V41A	probably damaging	Het
Ssu2	A	T	6: 112,377,605	C219*	probably null	Het
Tbc1d9b	T	A	11: 50,149,736	V360D	possibly damaging	Het
Tdrd9	G	A	12: 112,040,461	D920N	probably damaging	Het
Tyrp1	A	G	4: 80,837,455	T154A	possibly damaging	Het
Vrk3	C	T	7: 44,775,442	T427M	probably benign	Het
Wac	A	C	18: 7,926,131	M596L	possibly damaging	Het
Zfhx2	G	T	14: 55,064,557	P1990Q	probably damaging	Het
Zfp853	T	C	5: 143,289,577	E96G	unknown	Het
Zzef1	G	A	11: 72,910,326		probably null	Het

Other mutations in Prss1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00577:Prss1	APN	6	41462711	missense	possibly damaging	0.87
IGL00661:Prss1	APN	6	41462619	missense	possibly damaging	0.90
IGL01780:Prss1	APN	6	41463205	missense	probably damaging	0.96
IGL02350:Prss1	APN	6	41463205	missense	probably damaging	0.96
IGL02357:Prss1	APN	6	41463205	missense	probably damaging	0.96
R0090:Prss1	UTSW	6	41461232	missense	probably benign	0.00
R0137:Prss1	UTSW	6	41462561	missense	probably damaging	1.00
R0143:Prss1	UTSW	6	41463588	missense	probably damaging	1.00
R0422:Prss1	UTSW	6	41463312	missense	probably damaging	1.00
R0792:Prss1	UTSW	6	41458944	start codon destroyed	probably null
R0939:Prss1	UTSW	6	41463588	missense	probably damaging	1.00
R2762:Prss1	UTSW	6	41463281	missense	possibly damaging	0.93
R2896:Prss1	UTSW	6	41463705	nonsense	probably null
R2959:Prss1	UTSW	6	41463238	missense	probably damaging	0.99
R5123:Prss1	UTSW	6	41463197	missense	possibly damaging	0.84
R5587:Prss1	UTSW	6	41463265	missense	possibly damaging	0.57
R5610:Prss1	UTSW	6	41461213	missense	probably benign	0.07
R6521:Prss1	UTSW	6	41463681	missense	probably damaging	1.00
R6788:Prss1	UTSW	6	41463720	missense	possibly damaging	0.46
R7199:Prss1	UTSW	6	41462756	missense	probably damaging	1.00
R7552:Prss1	UTSW	6	41462573	missense	probably benign	0.05
R8812:Prss1	UTSW	6	41462586	missense	probably benign	0.01
R9136:Prss1	UTSW	6	41461346	splice site	probably benign
R9255:Prss1	UTSW	6	41461249	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ACAGCAGTCATTCACCTCTGAAG -3'
(R):5'- CCAAAGCTAAGAGTGTTGCCCC -3'

Sequencing Primer
(F):5'- GTCATTCACCTCTGAAGAAAAGG -3'
(R):5'- TAAGAGTGTTGCCCCAGCCAG -3'

Posted On

2014-12-29