Mutagenetix > Incidental Mutation

Incidental Mutation 'R9366:Proser3'

708970

Institutional Source

Beutler Lab

Gene Symbol

Proser3

Ensembl Gene

ENSMUSG00000036864

Gene Name

proline and serine rich 3

Synonyms

BC053749

MMRRC Submission

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.056) question?

Stock #

R9366 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

30238559-30251724 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 30248478 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Leucine at position 72 (S72L)

Ref Sequence

ENSEMBL: ENSMUSP00000103800 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000044048] [ENSMUST00000062708] [ENSMUST00000108165] [ENSMUST00000153594] [ENSMUST00000215288]

AlphaFold

Q7TSA6

Predicted Effect

probably benign
Transcript: ENSMUST00000044048

SMART Domains

Protein: ENSMUSP00000039172
Gene: ENSMUSG00000036854

Domain	Start	End	E-Value	Type
Pfam:Crystallin	1	62	4.4e-24	PFAM
Pfam:HSP20	66	158	5.6e-21	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000062708
AA Change: S72L

PolyPhen 2 Score 0.958 (Sensitivity: 0.78; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000059135
Gene: ENSMUSG00000036864
AA Change: S72L

Domain	Start	End	E-Value	Type
low complexity region	33	56	N/A	INTRINSIC
low complexity region	128	140	N/A	INTRINSIC
low complexity region	152	163	N/A	INTRINSIC
low complexity region	179	202	N/A	INTRINSIC
low complexity region	351	365	N/A	INTRINSIC
low complexity region	369	383	N/A	INTRINSIC
low complexity region	388	407	N/A	INTRINSIC
low complexity region	599	614	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000108165
AA Change: S72L

PolyPhen 2 Score 0.958 (Sensitivity: 0.78; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000103800
Gene: ENSMUSG00000036864
AA Change: S72L

Domain	Start	End	E-Value	Type
low complexity region	33	56	N/A	INTRINSIC
low complexity region	128	140	N/A	INTRINSIC
low complexity region	152	163	N/A	INTRINSIC
low complexity region	179	202	N/A	INTRINSIC
low complexity region	351	365	N/A	INTRINSIC
low complexity region	369	383	N/A	INTRINSIC
low complexity region	388	407	N/A	INTRINSIC
low complexity region	599	614	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000153594
AA Change: S72L

PolyPhen 2 Score 0.958 (Sensitivity: 0.78; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000123095
Gene: ENSMUSG00000036864
AA Change: S72L

Domain	Start	End	E-Value	Type
low complexity region	33	56	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000215288
AA Change: S72L

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

Coding Region Coverage

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

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abhd8	C	T	8: 71,914,328 (GRCm39)	R100Q	probably benign	Het
Acp5	C	T	9: 22,039,224 (GRCm39)	C163Y	probably damaging	Het
Ankrd17	C	T	5: 90,416,508 (GRCm39)	R1108Q	probably damaging	Het
Atp2b4	C	A	1: 133,642,920 (GRCm39)	G1062C	probably damaging	Het
Bicral	A	T	17: 47,117,558 (GRCm39)	M788K	possibly damaging	Het
C1s2	C	A	6: 124,602,694 (GRCm39)	A506S	probably benign	Het
Capn9	C	G	8: 125,332,280 (GRCm39)	T417S	probably benign	Het
Cd109	T	G	9: 78,622,275 (GRCm39)	S1422A	probably benign	Het
Cd207	G	T	6: 83,648,779 (GRCm39)	N294K	probably damaging	Het
Cdc42bpa	A	G	1: 179,921,675 (GRCm39)	E605G	probably damaging	Het
Cdhr1	C	A	14: 36,811,463 (GRCm39)	G216V	possibly damaging	Het
Ckap2	A	T	8: 22,658,988 (GRCm39)	M585K	possibly damaging	Het
Clp1	G	T	2: 84,556,473 (GRCm39)	S2R	probably benign	Het
Cngb3	G	T	4: 19,395,983 (GRCm39)	V342F	probably benign	Het
Col18a1	T	C	10: 76,932,258 (GRCm39)	D65G	unknown	Het
Col3a1	C	T	1: 45,380,391 (GRCm39)	P972S	unknown	Het
Cxcr5	C	T	9: 44,424,730 (GRCm39)	C309Y	possibly damaging	Het
Cyp2t4	G	A	7: 26,854,717 (GRCm39)	V66M	possibly damaging	Het
Dcc	A	T	18: 71,708,281 (GRCm39)	N478K	probably damaging	Het
Emb	G	T	13: 117,357,096 (GRCm39)		probably benign	Het
Emsy	A	T	7: 98,290,860 (GRCm39)	N101K	probably benign	Het
Epb41l5	A	G	1: 119,548,448 (GRCm39)	Y137H	probably damaging	Het
Etfdh	C	T	3: 79,519,271 (GRCm39)	G354D	probably benign	Het
Fa2h	A	T	8: 112,076,006 (GRCm39)	Y206N	probably benign	Het
Gabrr2	T	C	4: 33,085,771 (GRCm39)	V217A		Het
Gimap4	A	G	6: 48,668,037 (GRCm39)	K264R	probably benign	Het
Gpr31b	C	A	17: 13,270,375 (GRCm39)	D265Y	probably damaging	Het
Irx4	A	G	13: 73,417,025 (GRCm39)	T474A	probably benign	Het
Kif21a	T	C	15: 90,843,951 (GRCm39)	E1096G	probably damaging	Het
Letm2	A	T	8: 26,084,165 (GRCm39)	V22E	probably damaging	Het
Lrrc45	A	G	11: 120,611,552 (GRCm39)	E642G	probably damaging	Het
Mark1	A	T	1: 184,653,792 (GRCm39)	V170E	probably damaging	Het
Mbd6	G	A	10: 127,122,304 (GRCm39)	Q175*	probably null	Het
Mrc1	T	A	2: 14,321,709 (GRCm39)	D1067E	probably damaging	Het
Muc5b	A	G	7: 141,417,041 (GRCm39)	H3329R	probably benign	Het
Myh1	A	T	11: 67,110,114 (GRCm39)	D1434V	probably damaging	Het
Myo5a	T	A	9: 75,124,800 (GRCm39)	L1785Q	probably damaging	Het
Myrfl	A	G	10: 116,670,358 (GRCm39)	I295T	possibly damaging	Het
Nav3	C	A	10: 109,659,364 (GRCm39)	R751L	probably damaging	Het
Neb	T	C	2: 52,172,699 (GRCm39)	K1536R	probably benign	Het
Nynrin	T	G	14: 56,100,587 (GRCm39)	S126A	probably damaging	Het
Or13p3	A	T	4: 118,566,831 (GRCm39)	T76S	probably damaging	Het
Or5m8	A	G	2: 85,822,731 (GRCm39)	D190G	possibly damaging	Het
Or6c69c	A	T	10: 129,911,067 (GRCm39)	K263*	probably null	Het
Parp14	A	C	16: 35,659,630 (GRCm39)		probably null	Het
Phldb1	G	T	9: 44,622,546 (GRCm39)	L36M	possibly damaging	Het
Pin1	C	A	9: 20,566,841 (GRCm39)	T81N	probably damaging	Het
Pkhd1l1	T	C	15: 44,410,308 (GRCm39)	I2605T	probably benign	Het
Plcb3	A	G	19: 6,937,658 (GRCm39)		probably null	Het
Pum2	T	A	12: 8,783,344 (GRCm39)	S598T	probably benign	Het
Pwp1	T	A	10: 85,717,870 (GRCm39)	N269K	probably damaging	Het
Qsox1	A	G	1: 155,665,162 (GRCm39)	S260P	probably benign	Het
Ric3	A	G	7: 108,653,644 (GRCm39)	L149P	probably damaging	Het
Rif1	A	G	2: 52,010,356 (GRCm39)	T707A		Het
Rnf213	A	C	11: 119,327,057 (GRCm39)	R1682S		Het
Rpgrip1l	G	T	8: 91,996,809 (GRCm39)	Y690*	probably null	Het
Slc29a2	A	G	19: 5,074,609 (GRCm39)	T34A	probably damaging	Het
Slc6a1	A	G	6: 114,280,974 (GRCm39)	N176S	possibly damaging	Het
Slco1b2	T	A	6: 141,602,552 (GRCm39)	Y168*	probably null	Het
Snca	C	A	6: 60,792,675 (GRCm39)	A78S	probably benign	Het
Snrnp200	T	A	2: 127,058,010 (GRCm39)	D257E	probably benign	Het
Srebf2	T	C	15: 82,083,837 (GRCm39)	V959A	probably benign	Het
Stk3	A	C	15: 35,072,634 (GRCm39)	I209S	probably damaging	Het
Thsd7a	A	T	6: 12,555,480 (GRCm39)	C135S		Het
Tlnrd1	G	T	7: 83,531,582 (GRCm39)	A283E	probably benign	Het
Tomm70a	A	T	16: 56,970,259 (GRCm39)	K546*	probably null	Het
Trak1	C	T	9: 121,301,578 (GRCm39)	T778I	probably damaging	Het
Trappc9	T	C	15: 72,808,937 (GRCm39)	I709V	probably benign	Het
Trgc3	A	G	13: 19,446,825 (GRCm39)	T115A	probably benign	Het
Trp53rkb	T	C	2: 166,637,700 (GRCm39)	S219P	possibly damaging	Het
Ubqlnl	G	C	7: 103,798,592 (GRCm39)	L302V	possibly damaging	Het
Uqcc1	C	A	2: 155,771,995 (GRCm39)		probably benign	Het
Vps13a	G	A	19: 16,672,894 (GRCm39)	R1293W	probably damaging	Het
Vps9d1	G	T	8: 123,974,486 (GRCm39)	S267*	probably null	Het
Vwa5b1	A	T	4: 138,318,229 (GRCm39)	I546N	probably damaging	Het
Zbtb8b	A	T	4: 129,326,151 (GRCm39)	M338K	probably benign	Het
Zfp652	C	T	11: 95,643,833 (GRCm39)	R344*	probably null	Het

Other mutations in Proser3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00533:Proser3	APN	7	30,240,096 (GRCm39)	missense	possibly damaging	0.62
IGL01346:Proser3	APN	7	30,249,071 (GRCm39)	missense	probably benign	0.21
IGL02465:Proser3	APN	7	30,242,958 (GRCm39)	missense	possibly damaging	0.87
IGL03178:Proser3	APN	7	30,243,034 (GRCm39)	missense	probably damaging	0.99
IGL03372:Proser3	APN	7	30,242,993 (GRCm39)	missense	probably damaging	1.00
K3955:Proser3	UTSW	7	30,242,924 (GRCm39)	missense	probably damaging	0.96
R0008:Proser3	UTSW	7	30,239,563 (GRCm39)	missense	probably damaging	0.99
R0008:Proser3	UTSW	7	30,239,563 (GRCm39)	missense	probably damaging	0.99
R0255:Proser3	UTSW	7	30,245,842 (GRCm39)	missense	probably damaging	1.00
R0627:Proser3	UTSW	7	30,240,208 (GRCm39)	missense	probably benign	0.04
R0702:Proser3	UTSW	7	30,238,955 (GRCm39)	missense	probably benign	0.00
R0883:Proser3	UTSW	7	30,240,124 (GRCm39)	missense	probably damaging	0.99
R1185:Proser3	UTSW	7	30,245,572 (GRCm39)	missense	probably benign	0.01
R1457:Proser3	UTSW	7	30,239,172 (GRCm39)	critical splice donor site	probably null
R1650:Proser3	UTSW	7	30,239,751 (GRCm39)	missense	probably damaging	0.99
R1697:Proser3	UTSW	7	30,239,446 (GRCm39)	missense	probably benign	0.00
R3121:Proser3	UTSW	7	30,239,796 (GRCm39)	missense	probably benign	0.10
R4210:Proser3	UTSW	7	30,245,525 (GRCm39)	intron	probably benign
R4375:Proser3	UTSW	7	30,240,096 (GRCm39)	missense	possibly damaging	0.62
R5364:Proser3	UTSW	7	30,245,573 (GRCm39)	missense	possibly damaging	0.60
R6225:Proser3	UTSW	7	30,243,153 (GRCm39)	missense	probably damaging	1.00
R6831:Proser3	UTSW	7	30,239,781 (GRCm39)	missense	probably benign
R7151:Proser3	UTSW	7	30,239,749 (GRCm39)	missense	possibly damaging	0.79
R7707:Proser3	UTSW	7	30,239,216 (GRCm39)	missense	probably benign	0.27
R7748:Proser3	UTSW	7	30,239,497 (GRCm39)	missense	possibly damaging	0.90
R7923:Proser3	UTSW	7	30,249,086 (GRCm39)	missense	possibly damaging	0.79
R8975:Proser3	UTSW	7	30,239,458 (GRCm39)	missense	possibly damaging	0.95
R9502:Proser3	UTSW	7	30,245,587 (GRCm39)	missense	possibly damaging	0.55
R9673:Proser3	UTSW	7	30,248,530 (GRCm39)	missense	probably damaging	0.99
X0028:Proser3	UTSW	7	30,240,187 (GRCm39)	missense	probably damaging	0.99
Z31818:Proser3	UTSW	7	30,245,790 (GRCm39)	missense	possibly damaging	0.85

Predicted Primers

PCR Primer
(F):5'- CAAGCAGGATTTGAACCCAGG -3'
(R):5'- GTTCATTCCCCTATGAGGTCAC -3'

Sequencing Primer
(F):5'- GGATTTGAACCCAGGCTCTACAG -3'
(R):5'- ATGAGGTCACCTTTCTGATCTG -3'

Posted On

2022-04-18