Mutagenetix > Incidental Mutation

Incidental Mutation 'R5629:Prss23'

441983

Institutional Source

Beutler Lab

Gene Symbol

Prss23

Ensembl Gene

ENSMUSG00000039405

Gene Name

serine protease 23

Synonyms

2310046G15Rik

MMRRC Submission

043280-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.061) question?

Stock #

R5629 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

89156991-89176395 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 89159400 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Glycine at position 223 (V223G)

Ref Sequence

ENSEMBL: ENSMUSP00000147183 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000041761] [ENSMUST00000207538] [ENSMUST00000207636] [ENSMUST00000207932] [ENSMUST00000208402] [ENSMUST00000208888] [ENSMUST00000208903]

AlphaFold

Q9D6X6

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000032858

Predicted Effect

probably damaging
Transcript: ENSMUST00000041761
AA Change: V223G

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000045191
Gene: ENSMUSG00000039405
AA Change: V223G

Domain	Start	End	E-Value	Type
signal peptide	1	22	N/A	INTRINSIC
low complexity region	48	57	N/A	INTRINSIC
Tryp_SPc	137	372	2.87e-2	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000179361

Predicted Effect

probably benign
Transcript: ENSMUST00000207538

Predicted Effect

probably benign
Transcript: ENSMUST00000207636

Predicted Effect

probably damaging
Transcript: ENSMUST00000207932
AA Change: V223G

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)

Predicted Effect

probably benign
Transcript: ENSMUST00000208402

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000209064

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000208814

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000209118

Predicted Effect

probably benign
Transcript: ENSMUST00000208888

Predicted Effect

probably benign
Transcript: ENSMUST00000208903

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.2%
20x: 95.1%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a conserved member of the trypsin family of serine proteases. Mouse studies found a decrease of mRNA levels of this gene after ovulation was induced. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]

Allele List at MGI

Other mutations in this stock

Total: 71 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ablim2	G	A	5: 36,014,507 (GRCm39)	D189N	probably benign	Het
Adamts9	A	T	6: 92,775,114 (GRCm39)	V1052D	probably damaging	Het
Apob	T	C	12: 8,057,847 (GRCm39)	Y2077H	probably damaging	Het
Apol7e	A	T	15: 77,602,276 (GRCm39)	K291N	probably benign	Het
Arsk	A	T	13: 76,242,027 (GRCm39)	I82N	probably damaging	Het
Art1	A	G	7: 101,756,286 (GRCm39)	Q159R	probably benign	Het
Atp2a2	A	G	5: 122,598,159 (GRCm39)	V733A	probably damaging	Het
Btn2a2	A	T	13: 23,666,130 (GRCm39)		probably null	Het
Catsper1	C	T	19: 5,386,165 (GRCm39)	P133S	probably benign	Het
Celsr3	A	G	9: 108,726,266 (GRCm39)	D3165G	probably benign	Het
Cldn19	T	A	4: 119,114,116 (GRCm39)	V86E	probably damaging	Het
Ctnna1	T	A	18: 35,382,802 (GRCm39)	D649E	probably benign	Het
Cttnbp2	A	G	6: 18,405,217 (GRCm39)	I1094T	probably damaging	Het
Ddx24	T	C	12: 103,391,806 (GRCm39)		probably benign	Het
Ern2	T	A	7: 121,769,389 (GRCm39)	H879L	probably damaging	Het
Etv4	T	A	11: 101,662,751 (GRCm39)	H277L	probably damaging	Het
Faap100	G	T	11: 120,267,837 (GRCm39)	A312D	probably damaging	Het
Glipr1l1	G	A	10: 111,914,308 (GRCm39)	C223Y	possibly damaging	Het
Gna14	T	C	19: 16,414,097 (GRCm39)	S14P	possibly damaging	Het
Hapln1	A	G	13: 89,749,634 (GRCm39)	T60A	probably damaging	Het
Hars2	T	A	18: 36,921,719 (GRCm39)	Y273*	probably null	Het
Ighv5-6	A	T	12: 113,589,242 (GRCm39)	Y79*	probably null	Het
Iqgap2	T	A	13: 95,768,682 (GRCm39)	N1406I	probably damaging	Het
Kalrn	T	C	16: 33,860,304 (GRCm39)	T215A	possibly damaging	Het
Krtap13-1	T	A	16: 88,526,047 (GRCm39)	S90R	probably benign	Het
Mettl8	T	C	2: 70,795,913 (GRCm39)	I372V	probably benign	Het
Mfn1	A	T	3: 32,615,659 (GRCm39)	T341S	possibly damaging	Het
Mocos	T	A	18: 24,797,142 (GRCm39)		probably null	Het
Muc5b	T	C	7: 141,415,036 (GRCm39)	S2661P	possibly damaging	Het
Myo15a	C	T	11: 60,370,578 (GRCm39)	P1113S	probably benign	Het
Myo5a	A	T	9: 75,111,127 (GRCm39)	I1540F	possibly damaging	Het
Myoc	T	C	1: 162,476,156 (GRCm39)	Y287H	probably damaging	Het
Napepld	A	G	5: 21,880,901 (GRCm39)	F165L	probably benign	Het
Ndufb10	T	C	17: 24,941,656 (GRCm39)	E102G	probably damaging	Het
Nrros	T	A	16: 31,963,223 (GRCm39)	I265F	probably damaging	Het
Nrxn1	A	T	17: 90,897,460 (GRCm39)	F891I	possibly damaging	Het
Nsfl1c	T	C	2: 151,346,085 (GRCm39)	Y169H	probably damaging	Het
Oas2	G	A	5: 120,876,516 (GRCm39)	Q476*	probably null	Het
Or51f5	A	T	7: 102,423,847 (GRCm39)	I39F	possibly damaging	Het
Pcnx2	C	A	8: 126,624,780 (GRCm39)	W14L	probably damaging	Het
Pip4p1	T	C	14: 51,165,373 (GRCm39)	H278R	probably benign	Het
Piwil2	C	T	14: 70,660,416 (GRCm39)	V70M	probably damaging	Het
Rarres2	A	T	6: 48,547,194 (GRCm39)	L122Q	probably benign	Het
Robo1	T	C	16: 72,780,598 (GRCm39)	V776A	probably benign	Het
Robo3	G	A	9: 37,330,507 (GRCm39)	Q1008*	probably null	Het
Robo4	G	A	9: 37,319,658 (GRCm39)	C636Y	probably damaging	Het
Sacm1l	A	G	9: 123,395,464 (GRCm39)	M196V	probably benign	Het
Septin7	T	A	9: 25,199,589 (GRCm39)	Y163N	probably damaging	Het
Skint6	G	A	4: 112,870,176 (GRCm39)	T594I	possibly damaging	Het
Slc23a1	T	C	18: 35,759,545 (GRCm39)	H13R	probably benign	Het
Slc25a39	A	C	11: 102,295,719 (GRCm39)	Y109*	probably null	Het
Slc8a3	G	A	12: 81,246,405 (GRCm39)	R883C	probably damaging	Het
Spag17	A	T	3: 99,987,435 (GRCm39)	Y1575F	probably benign	Het
Spdye4c	T	A	2: 128,438,705 (GRCm39)	I321N	probably damaging	Het
Stk32b	G	A	5: 37,614,576 (GRCm39)	P311S	probably damaging	Het
Svs3a	T	A	2: 164,132,040 (GRCm39)	S203T	probably benign	Het
Taf3	A	T	2: 9,922,989 (GRCm39)	I45N	probably damaging	Het
Taf7	T	C	18: 37,776,555 (GRCm39)	N4S	probably benign	Het
Tial1	T	A	7: 128,046,421 (GRCm39)	D87V	probably damaging	Het
Tmem120a	T	A	5: 135,770,904 (GRCm39)	E78V	probably benign	Het
Tmem19	A	G	10: 115,183,165 (GRCm39)	F137L	probably benign	Het
Tns2	C	T	15: 102,017,369 (GRCm39)	R281C	probably damaging	Het
Trim30d	T	C	7: 104,137,136 (GRCm39)	K23E	possibly damaging	Het
Ubxn7	C	A	16: 32,151,117 (GRCm39)	H4Q	unknown	Het
Usp40	C	T	1: 87,908,731 (GRCm39)	R590H	probably benign	Het
Vmn1r90	A	G	7: 14,296,011 (GRCm39)	M22T	possibly damaging	Het
Vmn2r1	G	A	3: 64,012,538 (GRCm39)	V800M	possibly damaging	Het
Vps11	A	T	9: 44,267,673 (GRCm39)	I313N	probably damaging	Het
Zhx1	A	G	15: 57,918,207 (GRCm39)	V13A	probably damaging	Het
Zic4	G	A	9: 91,260,805 (GRCm39)	R20H	probably benign	Het
Zp3r	C	T	1: 130,510,616 (GRCm39)	V369M	probably damaging	Het

Other mutations in Prss23

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01296:Prss23	APN	7	89,159,095 (GRCm39)	missense	possibly damaging	0.83
IGL03308:Prss23	APN	7	89,158,938 (GRCm39)	missense	probably benign	0.09
IGL03349:Prss23	APN	7	89,159,065 (GRCm39)	missense	probably benign	0.09
IGL03378:Prss23	APN	7	89,159,352 (GRCm39)	missense	probably damaging	0.99
R0394:Prss23	UTSW	7	89,159,055 (GRCm39)	missense	probably damaging	1.00
R1026:Prss23	UTSW	7	89,159,166 (GRCm39)	missense	probably benign	0.01
R1417:Prss23	UTSW	7	89,159,392 (GRCm39)	missense	probably damaging	1.00
R1467:Prss23	UTSW	7	89,159,217 (GRCm39)	missense	probably damaging	1.00
R1467:Prss23	UTSW	7	89,159,217 (GRCm39)	missense	probably damaging	1.00
R1691:Prss23	UTSW	7	89,159,922 (GRCm39)	missense	probably benign	0.18
R1806:Prss23	UTSW	7	89,159,599 (GRCm39)	missense	probably damaging	1.00
R2153:Prss23	UTSW	7	89,159,119 (GRCm39)	missense	probably damaging	1.00
R3420:Prss23	UTSW	7	89,159,107 (GRCm39)	missense	possibly damaging	0.91
R3849:Prss23	UTSW	7	89,158,959 (GRCm39)	missense	probably damaging	1.00
R4567:Prss23	UTSW	7	89,160,074 (GRCm39)	utr 5 prime	probably benign
R4828:Prss23	UTSW	7	89,159,108 (GRCm39)	nonsense	probably null
R5010:Prss23	UTSW	7	89,159,422 (GRCm39)	missense	probably benign	0.25
R5251:Prss23	UTSW	7	89,159,530 (GRCm39)	missense	probably damaging	1.00
R5399:Prss23	UTSW	7	89,159,174 (GRCm39)	missense	probably benign	0.02
R5697:Prss23	UTSW	7	89,159,190 (GRCm39)	missense	probably damaging	0.99
R6378:Prss23	UTSW	7	89,159,241 (GRCm39)	missense	probably damaging	1.00
R6716:Prss23	UTSW	7	89,159,055 (GRCm39)	missense	probably damaging	1.00
R6880:Prss23	UTSW	7	89,160,033 (GRCm39)	missense	probably benign	0.03
R7097:Prss23	UTSW	7	89,159,392 (GRCm39)	missense	probably damaging	1.00
R7362:Prss23	UTSW	7	89,158,972 (GRCm39)	missense	probably damaging	1.00
R7563:Prss23	UTSW	7	89,159,038 (GRCm39)	missense	probably damaging	1.00
R7637:Prss23	UTSW	7	89,159,454 (GRCm39)	missense	probably benign	0.00
R7815:Prss23	UTSW	7	89,159,253 (GRCm39)	missense	probably damaging	0.99
R8047:Prss23	UTSW	7	89,159,136 (GRCm39)	missense	probably damaging	1.00
R8548:Prss23	UTSW	7	89,159,416 (GRCm39)	missense	probably benign	0.21
R8869:Prss23	UTSW	7	89,159,887 (GRCm39)	missense	probably benign	0.00
R8914:Prss23	UTSW	7	89,159,854 (GRCm39)	missense	probably benign
R9310:Prss23	UTSW	7	89,159,142 (GRCm39)	missense	probably damaging	1.00
R9729:Prss23	UTSW	7	89,159,931 (GRCm39)	missense	probably benign
R9762:Prss23	UTSW	7	89,159,683 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ATCTTTGACATCACAGAAGCGG -3'
(R):5'- AGAGAAGCACGTCCTCACTG -3'

Sequencing Primer
(F):5'- GCCGGTCATTGTCATAACCAGAG -3'
(R):5'- TCACTGCTGCCCACTGC -3'

Posted On

2016-11-08