Mutagenetix > Incidental Mutation

Incidental Mutation 'R6522:Prss51'

521414

Institutional Source

Beutler Lab

Gene Symbol

Prss51

Ensembl Gene

ENSMUSG00000052099

Gene Name

serine protease 51

Synonyms

1700007N14Rik

MMRRC Submission

044648-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.394) question?

Stock #

R6522 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

64323683-64335127 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 64334855 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 137 (T137A)

Ref Sequence

ENSEMBL: ENSMUSP00000066111 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000063785] [ENSMUST00000165710] [ENSMUST00000170709] [ENSMUST00000224112]

AlphaFold

A0A286YDY8

Predicted Effect

possibly damaging
Transcript: ENSMUST00000063785
AA Change: T137A

PolyPhen 2 Score 0.904 (Sensitivity: 0.82; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000066111
Gene: ENSMUSG00000052099
AA Change: T137A

Domain	Start	End	E-Value	Type
Tryp_SPc	5	171	3.93e-9	SMART
low complexity region	181	195	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000165710
AA Change: T155A

PolyPhen 2 Score 0.841 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000132814
Gene: ENSMUSG00000052099
AA Change: T155A

Domain	Start	End	E-Value	Type
Tryp_SPc	9	189	2.09e-13	SMART
low complexity region	199	213	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000166038

Predicted Effect

probably benign
Transcript: ENSMUST00000170709

SMART Domains

Protein: ENSMUSP00000126778
Gene: ENSMUSG00000052099

Domain	Start	End	E-Value	Type
Pfam:Trypsin	2	94	2e-12	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000224112
AA Change: T234A

PolyPhen 2 Score 0.809 (Sensitivity: 0.84; Specificity: 0.93)

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 97.8%
20x: 93.3%

Validation Efficiency

100% (56/56)

Allele List at MGI

Other mutations in this stock

Total: 57 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgb	C	A	10: 10,253,636 (GRCm39)	E1209*	probably null	Het
Adgrg5	G	T	8: 95,668,696 (GRCm39)	R503L	probably benign	Het
Anks1b	C	T	10: 90,733,189 (GRCm39)		probably benign	Het
Anxa5	A	T	3: 36,519,451 (GRCm39)	F13I	probably damaging	Het
Bicd1	A	G	6: 149,385,503 (GRCm39)	I79V	probably benign	Het
Bnip1	A	G	17: 27,008,719 (GRCm39)	D107G	probably damaging	Het
Ccdc42	A	G	11: 68,479,046 (GRCm39)	E78G	probably damaging	Het
Ccnk	A	G	12: 108,153,446 (GRCm39)	D69G	probably damaging	Het
Clec2i	G	T	6: 128,870,692 (GRCm39)	V77F	probably damaging	Het
Clec4g	A	C	8: 3,768,803 (GRCm39)	V62G	probably benign	Het
Col4a4	G	A	1: 82,465,304 (GRCm39)	A957V	unknown	Het
Csnk1d	A	G	11: 120,862,449 (GRCm39)	F277L	probably damaging	Het
Dip2c	G	A	13: 9,625,264 (GRCm39)		probably null	Het
Dpf2	T	A	19: 5,955,560 (GRCm39)	K108*	probably null	Het
Dync1h1	G	A	12: 110,583,171 (GRCm39)	D423N	probably damaging	Het
Fbxl13	T	C	5: 21,766,554 (GRCm39)		probably null	Homo
Flad1	T	C	3: 89,310,490 (GRCm39)	R488G	probably damaging	Het
Galnt6	A	C	15: 100,591,236 (GRCm39)	*623E	probably null	Het
Gtf2e1	T	C	16: 37,331,816 (GRCm39)	T420A	possibly damaging	Het
Hspg2	T	C	4: 137,282,586 (GRCm39)	V3442A	probably damaging	Het
Itpr1	A	G	6: 108,365,237 (GRCm39)	D55G	probably damaging	Het
Kdm2a	C	A	19: 4,374,854 (GRCm39)	R759L	possibly damaging	Het
Kif19a	A	G	11: 114,676,605 (GRCm39)	E478G	probably damaging	Het
Lamb3	G	A	1: 193,017,761 (GRCm39)	V881I	probably benign	Het
Map3k6	T	C	4: 132,977,335 (GRCm39)	L894P	possibly damaging	Het
Mast4	A	G	13: 102,897,801 (GRCm39)		probably null	Het
Mst1r	G	A	9: 107,790,438 (GRCm39)	V684M	probably benign	Het
Naa15	T	C	3: 51,378,935 (GRCm39)	S727P	probably damaging	Het
Nap1l1	T	C	10: 111,330,084 (GRCm39)	L330S	probably damaging	Het
Nav2	A	G	7: 49,247,281 (GRCm39)	T2205A	probably damaging	Het
Ncf2	T	C	1: 152,703,214 (GRCm39)		probably null	Het
Opa1	T	A	16: 29,444,332 (GRCm39)	N839K	probably benign	Het
Or4c104	T	C	2: 88,586,452 (GRCm39)	D189G	probably damaging	Het
Or52a33	T	C	7: 103,288,504 (GRCm39)	Y281C	probably damaging	Het
Or52n4b	G	A	7: 108,144,202 (GRCm39)	V155I	probably benign	Het
Pcdha7	T	C	18: 37,106,995 (GRCm39)	Y7H	possibly damaging	Het
Pcdhb15	T	C	18: 37,607,314 (GRCm39)	V182A	probably benign	Het
Phf10	A	T	17: 15,176,269 (GRCm39)	I128N	probably damaging	Het
Plce1	T	A	19: 38,736,965 (GRCm39)		probably null	Het
Plxnb2	T	C	15: 89,048,629 (GRCm39)	N626S	probably benign	Het
Prh1	G	A	6: 132,548,996 (GRCm39)	G168R	unknown	Het
Ptprcap	C	T	19: 4,206,183 (GRCm39)	R89C	possibly damaging	Het
Scfd1	A	G	12: 51,478,324 (GRCm39)	K512R	probably benign	Het
Serpina1b	A	C	12: 103,701,296 (GRCm39)		probably null	Het
Setbp1	T	C	18: 78,900,605 (GRCm39)	T1021A	probably damaging	Het
Slco1b2	G	A	6: 141,601,145 (GRCm39)		probably null	Het
Snrnp200	C	T	2: 127,063,747 (GRCm39)	T642I	probably benign	Het
Tenm4	A	C	7: 96,492,251 (GRCm39)	I1063L	possibly damaging	Het
Tfb2m	G	A	1: 179,373,611 (GRCm39)	A29V	probably benign	Het
Tfeb	T	C	17: 48,100,627 (GRCm39)	V140A	probably damaging	Het
Tmem104	A	T	11: 115,134,579 (GRCm39)	I372F	probably damaging	Het
Tmem132d	G	T	5: 127,860,832 (GRCm39)	H1096Q	probably benign	Het
Trim12c	A	T	7: 103,997,531 (GRCm39)	N8K	probably benign	Het
Tti2	A	G	8: 31,643,631 (GRCm39)	I249V	probably null	Het
Vps8	T	A	16: 21,261,129 (GRCm39)	L90I	probably damaging	Het
Vwf	A	T	6: 125,639,926 (GRCm39)		probably null	Het
Wdfy4	A	G	14: 32,868,901 (GRCm39)	S376P	probably damaging	Het

Other mutations in Prss51

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01108:Prss51	APN	14	64,333,433 (GRCm39)	missense	probably damaging	1.00
PIT4354001:Prss51	UTSW	14	64,334,546 (GRCm39)	missense	probably damaging	0.99
R0453:Prss51	UTSW	14	64,334,588 (GRCm39)	missense	probably damaging	1.00
R1335:Prss51	UTSW	14	64,333,620 (GRCm39)	critical splice donor site	probably null
R1479:Prss51	UTSW	14	64,333,619 (GRCm39)	critical splice donor site	probably null
R3753:Prss51	UTSW	14	64,333,624 (GRCm39)	splice site	probably benign
R5384:Prss51	UTSW	14	64,334,543 (GRCm39)	missense	probably damaging	0.99
R5385:Prss51	UTSW	14	64,334,543 (GRCm39)	missense	probably damaging	0.99
R5386:Prss51	UTSW	14	64,334,543 (GRCm39)	missense	probably damaging	0.99
R6722:Prss51	UTSW	14	64,332,508 (GRCm39)	missense	probably damaging	0.99
R6908:Prss51	UTSW	14	64,333,601 (GRCm39)	missense	probably benign	0.00
R6919:Prss51	UTSW	14	64,334,937 (GRCm39)	missense	probably damaging	1.00
R7220:Prss51	UTSW	14	64,333,444 (GRCm39)	nonsense	probably null
R7510:Prss51	UTSW	14	64,333,489 (GRCm39)	missense	probably damaging	1.00
R7711:Prss51	UTSW	14	64,334,937 (GRCm39)	missense	probably damaging	1.00
R7753:Prss51	UTSW	14	64,333,376 (GRCm39)	missense	possibly damaging	0.86
R9000:Prss51	UTSW	14	64,332,420 (GRCm39)	missense	possibly damaging	0.95
R9164:Prss51	UTSW	14	64,334,958 (GRCm39)	missense	probably damaging	1.00
R9613:Prss51	UTSW	14	64,332,461 (GRCm39)	missense	possibly damaging	0.65
X0024:Prss51	UTSW	14	64,334,915 (GRCm39)	missense	probably damaging	1.00
Z1177:Prss51	UTSW	14	64,332,390 (GRCm39)	missense	possibly damaging	0.92

Predicted Primers

PCR Primer
(F):5'- CACAATTCTTAGGTTCCCAGAAGG -3'
(R):5'- GCAAGCAGTATTTGAGAGCCC -3'

Sequencing Primer
(F):5'- TCCCAGAAGGAGTCGGG -3'
(R):5'- CCATGCTTAGCAATATGGGATG -3'

Posted On

2018-06-06