Mutagenetix > Incidental Mutation

Incidental Mutation 'R4863:Cpxm2'

374658

Institutional Source

Beutler Lab

Gene Symbol

Cpxm2

Ensembl Gene

ENSMUSG00000030862

Gene Name

carboxypeptidase X 2 (M14 family)

Synonyms

4632435C11Rik

MMRRC Submission

042473-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.078) question?

Stock #

R4863 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

132032687-132154739 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 132059747 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Methionine at position 437 (K437M)

Ref Sequence

ENSEMBL: ENSMUSP00000033149 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000033149] [ENSMUST00000124096]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000033149
AA Change: K437M

PolyPhen 2 Score 0.129 (Sensitivity: 0.93; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000033149
Gene: ENSMUSG00000030862
AA Change: K437M

Domain	Start	End	E-Value	Type
signal peptide	1	27	N/A	INTRINSIC
low complexity region	52	59	N/A	INTRINSIC
low complexity region	72	82	N/A	INTRINSIC
low complexity region	87	98	N/A	INTRINSIC
FA58C	143	301	2.18e-46	SMART
Zn_pept	448	736	9.21e-58	SMART
low complexity region	751	764	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000122681

Predicted Effect

probably benign
Transcript: ENSMUST00000124096

SMART Domains

Protein: ENSMUSP00000130971
Gene: ENSMUSG00000030849

Domain	Start	End	E-Value	Type
Pfam:Pkinase	1	118	4.8e-19	PFAM
Pfam:Pkinase_Tyr	1	118	1.7e-50	PFAM
low complexity region	146	160	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000127039

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000150405

Meta Mutation Damage Score

0.1665

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.3%
20x: 95.2%

Validation Efficiency

99% (105/106)

Allele List at MGI

Other mutations in this stock

Total: 98 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2210407C18Rik	A	T	11: 58,612,512 (GRCm38)		probably null	Het
4930578I06Rik	C	T	14: 63,973,209 (GRCm38)	R190H	probably benign	Het
A530032D15Rik	C	T	1: 85,088,800 (GRCm38)		probably benign	Het
Abcc12	T	A	8: 86,538,376 (GRCm38)	I647F	probably damaging	Het
Acnat2	C	A	4: 49,380,172 (GRCm38)	W384L	probably damaging	Het
Acvr1	A	G	2: 58,477,711 (GRCm38)	L146P	possibly damaging	Het
Ankrd16	T	A	2: 11,784,316 (GRCm38)	M238K	probably benign	Het
BC005561	A	T	5: 104,517,750 (GRCm38)	D46V	possibly damaging	Het
Cd3eap	T	A	7: 19,357,759 (GRCm38)	Q141L	probably damaging	Het
Clmn	A	T	12: 104,797,094 (GRCm38)	I91N	probably damaging	Het
Cog8	A	T	8: 107,050,174 (GRCm38)	L523H	probably damaging	Het
Dhx57	A	T	17: 80,253,111 (GRCm38)	V999E	probably damaging	Het
Dnpep	T	C	1: 75,309,230 (GRCm38)		probably benign	Het
Dok3	G	A	13: 55,523,457 (GRCm38)	R434W	probably damaging	Het
Dpysl5	C	T	5: 30,784,343 (GRCm38)	H275Y	probably benign	Het
Ednra	A	T	8: 77,667,383 (GRCm38)	N361K	probably damaging	Het
Ei24	A	T	9: 36,784,565 (GRCm38)	S210R	probably damaging	Het
Erich3	T	A	3: 154,764,804 (GRCm38)	V158E	unknown	Het
Fam193a	T	A	5: 34,466,205 (GRCm38)	V1379E	possibly damaging	Het
Fasn	A	G	11: 120,808,828 (GRCm38)	V2304A	probably damaging	Het
Fcgbp	A	C	7: 28,086,344 (GRCm38)	D402A	probably benign	Het
Fkbp14	T	C	6: 54,585,945 (GRCm38)		probably benign	Het
Fnip1	G	A	11: 54,515,556 (GRCm38)	V1160I	possibly damaging	Het
Fsd2	T	C	7: 81,552,964 (GRCm38)	K289R	probably null	Het
Fuca2	A	T	10: 13,505,907 (GRCm38)	D188V	probably damaging	Het
Gfpt2	T	C	11: 49,810,970 (GRCm38)	V116A	probably benign	Het
Gm10770	T	A	2: 150,178,896 (GRCm38)	K234*	probably null	Het
Gm9887	A	G	12: 69,371,989 (GRCm38)		probably benign	Het
Gtf3c2	A	G	5: 31,159,233 (GRCm38)		probably benign	Het
H2-M10.3	T	C	17: 36,366,636 (GRCm38)	D250G	probably damaging	Het
Hapln4	G	A	8: 70,084,492 (GRCm38)	V26M	possibly damaging	Het
Hook3	G	A	8: 26,038,029 (GRCm38)	A611V	probably damaging	Het
Hr	T	C	14: 70,571,972 (GRCm38)	L1141P	probably damaging	Het
Ifngr1	T	C	10: 19,609,416 (GRCm38)	S388P	probably damaging	Het
Itga3	T	A	11: 95,061,967 (GRCm38)	Q326L	probably damaging	Het
Itgb3	T	A	11: 104,665,520 (GRCm38)	I729N	probably damaging	Het
Kcnab2	A	G	4: 152,401,946 (GRCm38)	S132P	probably damaging	Het
Lama3	T	C	18: 12,498,678 (GRCm38)		probably benign	Het
Lama3	C	T	18: 12,539,793 (GRCm38)	A2481V	probably damaging	Het
Lce1e	A	T	3: 92,707,871 (GRCm38)	C56*	probably null	Het
Lmcd1	T	C	6: 112,287,871 (GRCm38)		probably benign	Het
Lrrc14	T	A	15: 76,713,362 (GRCm38)		probably null	Het
Map4k5	G	A	12: 69,818,438 (GRCm38)	P591L	probably benign	Het
Mapk13	C	A	17: 28,776,310 (GRCm38)	D168E	probably damaging	Het
Marf1	A	C	16: 14,132,665 (GRCm38)	H952Q	possibly damaging	Het
Megf6	T	C	4: 154,254,281 (GRCm38)		probably null	Het
Mical3	T	C	6: 121,033,787 (GRCm38)	I411M	probably damaging	Het
Myo5a	A	T	9: 75,217,507 (GRCm38)	K1781N	probably damaging	Het
N4bp2	T	C	5: 65,808,130 (GRCm38)	V1174A	probably benign	Het
Ncdn	A	T	4: 126,750,423 (GRCm38)	L202Q	probably damaging	Het
Ncor1	T	A	11: 62,392,638 (GRCm38)	M408L	possibly damaging	Het
Nf1	T	C	11: 79,409,409 (GRCm38)	L249P	probably damaging	Het
Nlrp9b	T	A	7: 20,049,596 (GRCm38)		probably null	Het
Nxpe3	A	T	16: 55,849,633 (GRCm38)	Y370N	probably damaging	Het
P2rx2	T	A	5: 110,341,568 (GRCm38)	T167S	probably benign	Het
Pcdhb19	G	T	18: 37,499,108 (GRCm38)	R652L	probably benign	Het
Pcdhga12	T	C	18: 37,768,281 (GRCm38)	L722P	probably benign	Het
Pde6a	A	T	18: 61,245,592 (GRCm38)	I329F	probably damaging	Het
Pdpr	T	A	8: 111,101,951 (GRCm38)	S29T	probably benign	Het
Pfkfb3	T	C	2: 11,486,312 (GRCm38)	D173G	probably benign	Het
Plcd4	A	G	1: 74,565,802 (GRCm38)		probably null	Het
Pou2f2	A	G	7: 25,097,108 (GRCm38)		probably benign	Het
Ppp1r14c	TGGCGGCGGCGGCGGCGG	TGGCGGCGGCGGCGG	10: 3,366,702 (GRCm38)		probably benign	Het
Ppp1r42	T	C	1: 10,003,386 (GRCm38)		probably benign	Het
Ptpre	C	T	7: 135,669,132 (GRCm38)	H346Y	probably benign	Het
Ptpro	T	A	6: 137,443,594 (GRCm38)	V1007D	probably damaging	Het
Rab12	A	T	17: 66,498,108 (GRCm38)	Y142N	probably damaging	Het
Rai14	A	C	15: 10,572,470 (GRCm38)	M857R	probably damaging	Het
Ranbp2	A	G	10: 58,492,421 (GRCm38)	K2753R	probably damaging	Het
Rasa4	A	T	5: 136,103,911 (GRCm38)	K6*	probably null	Het
Rasgef1a	A	G	6: 118,089,139 (GRCm38)	M438V	probably benign	Het
Recql	T	G	6: 142,359,006 (GRCm38)		probably benign	Het
Rftn2	A	G	1: 55,172,039 (GRCm38)	V425A	probably benign	Het
Ror1	A	G	4: 100,409,804 (GRCm38)	Y234C	probably damaging	Het
Sap30l	T	A	11: 57,806,054 (GRCm38)	L70Q	probably damaging	Het
Scn4a	T	C	11: 106,320,002 (GRCm38)	R1730G	probably damaging	Het
Serinc5	T	G	13: 92,690,980 (GRCm38)	I268R	probably damaging	Het
Sin3b	G	A	8: 72,744,948 (GRCm38)	V432I	possibly damaging	Het
Slc30a6	T	C	17: 74,412,654 (GRCm38)	M203T	possibly damaging	Het
Soat1	T	C	1: 156,432,328 (GRCm38)	N481S	probably damaging	Het
Sos2	G	A	12: 69,640,154 (GRCm38)	T206I	probably benign	Het
Sp100	G	T	1: 85,705,003 (GRCm38)	A132S	probably benign	Het
Spata31d1c	T	A	13: 65,035,790 (GRCm38)	L382*	probably null	Het
Stard9	T	A	2: 120,700,860 (GRCm38)	W2533R	probably benign	Het
Tas2r126	A	G	6: 42,435,390 (GRCm38)	T286A	probably benign	Het
Tedc2	T	A	17: 24,217,936 (GRCm38)	K275M	probably damaging	Het
Ten1	A	T	11: 116,218,231 (GRCm38)	K242N	probably benign	Het
Tial1	C	T	7: 128,455,028 (GRCm38)	V1I	probably damaging	Het
Tle2	G	A	10: 81,588,891 (GRCm38)	R649H	possibly damaging	Het
Tmem178	A	G	17: 80,944,945 (GRCm38)	D86G	probably benign	Het
Trim29	T	A	9: 43,329,575 (GRCm38)	D528E	possibly damaging	Het
Vmn2r61	A	T	7: 42,300,708 (GRCm38)	T851S	probably benign	Het
Vmn2r72	T	A	7: 85,750,598 (GRCm38)	Q414H	possibly damaging	Het
Yars	A	T	4: 129,189,882 (GRCm38)		probably benign	Het
Yipf4	A	G	17: 74,494,092 (GRCm38)	Q135R	probably damaging	Het
Zfp341	G	A	2: 154,645,866 (GRCm38)		probably benign	Het
Zfp426	T	C	9: 20,470,038 (GRCm38)	Y536C	probably damaging	Het
Zp2	T	G	7: 120,135,772 (GRCm38)	Y430S	probably damaging	Het

Other mutations in Cpxm2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01862:Cpxm2	APN	7	132,059,811 (GRCm38)	missense	probably benign	0.01
IGL02039:Cpxm2	APN	7	132,047,753 (GRCm38)	missense	probably damaging	1.00
IGL03011:Cpxm2	APN	7	132,049,078 (GRCm38)	missense	possibly damaging	0.46
R0033:Cpxm2	UTSW	7	132,062,157 (GRCm38)	missense	possibly damaging	0.55
R0100:Cpxm2	UTSW	7	132,054,871 (GRCm38)	missense	possibly damaging	0.90
R0100:Cpxm2	UTSW	7	132,054,871 (GRCm38)	missense	possibly damaging	0.90
R0453:Cpxm2	UTSW	7	132,128,405 (GRCm38)	missense	probably damaging	1.00
R0555:Cpxm2	UTSW	7	132,044,043 (GRCm38)	nonsense	probably null
R0655:Cpxm2	UTSW	7	132,054,820 (GRCm38)	missense	possibly damaging	0.87
R0834:Cpxm2	UTSW	7	132,154,613 (GRCm38)	intron	probably benign
R1145:Cpxm2	UTSW	7	132,057,648 (GRCm38)	missense	probably damaging	0.99
R1145:Cpxm2	UTSW	7	132,057,648 (GRCm38)	missense	probably damaging	0.99
R1249:Cpxm2	UTSW	7	132,128,350 (GRCm38)	critical splice donor site	probably null
R1563:Cpxm2	UTSW	7	132,143,682 (GRCm38)	missense	probably benign	0.00
R1565:Cpxm2	UTSW	7	132,062,145 (GRCm38)	missense	probably damaging	1.00
R1709:Cpxm2	UTSW	7	132,059,834 (GRCm38)	missense	probably damaging	1.00
R1863:Cpxm2	UTSW	7	132,143,663 (GRCm38)	splice site	probably null
R1874:Cpxm2	UTSW	7	132,059,834 (GRCm38)	missense	probably damaging	1.00
R1958:Cpxm2	UTSW	7	132,062,147 (GRCm38)	missense	probably damaging	1.00
R2273:Cpxm2	UTSW	7	132,059,852 (GRCm38)	intron	probably benign
R3806:Cpxm2	UTSW	7	132,080,091 (GRCm38)	missense	probably benign	0.12
R3861:Cpxm2	UTSW	7	132,054,919 (GRCm38)	missense	probably benign	0.00
R4570:Cpxm2	UTSW	7	132,143,706 (GRCm38)	missense	probably benign	0.11
R4642:Cpxm2	UTSW	7	132,070,881 (GRCm38)	missense	probably benign	0.11
R4684:Cpxm2	UTSW	7	132,049,038 (GRCm38)	missense	possibly damaging	0.92
R4717:Cpxm2	UTSW	7	132,054,845 (GRCm38)	missense	possibly damaging	0.61
R5079:Cpxm2	UTSW	7	132,154,285 (GRCm38)	critical splice donor site	probably null
R5341:Cpxm2	UTSW	7	132,154,613 (GRCm38)	intron	probably benign
R5626:Cpxm2	UTSW	7	132,059,852 (GRCm38)	intron	probably benign
R5666:Cpxm2	UTSW	7	132,054,896 (GRCm38)	missense	probably benign	0.44
R5815:Cpxm2	UTSW	7	132,044,110 (GRCm38)	missense	probably damaging	1.00
R6114:Cpxm2	UTSW	7	132,154,306 (GRCm38)	missense	probably benign
R6133:Cpxm2	UTSW	7	132,128,453 (GRCm38)	missense	probably damaging	1.00
R6224:Cpxm2	UTSW	7	132,143,731 (GRCm38)	missense	probably benign
R6468:Cpxm2	UTSW	7	132,070,860 (GRCm38)	missense	probably damaging	1.00
R6657:Cpxm2	UTSW	7	132,049,077 (GRCm38)	missense	probably damaging	1.00
R7058:Cpxm2	UTSW	7	132,143,679 (GRCm38)	missense	probably benign	0.32
R7100:Cpxm2	UTSW	7	132,054,815 (GRCm38)	missense	probably benign	0.06
R7198:Cpxm2	UTSW	7	132,080,084 (GRCm38)	missense	probably damaging	1.00
R7712:Cpxm2	UTSW	7	132,154,378 (GRCm38)	missense	possibly damaging	0.69
R7855:Cpxm2	UTSW	7	132,057,695 (GRCm38)	missense	possibly damaging	0.56
R7867:Cpxm2	UTSW	7	132,049,071 (GRCm38)	missense	probably damaging	1.00
R8513:Cpxm2	UTSW	7	132,143,702 (GRCm38)	missense	probably benign	0.01
R8694:Cpxm2	UTSW	7	132,080,054 (GRCm38)	missense	probably benign	0.03
R8874:Cpxm2	UTSW	7	132,106,281 (GRCm38)	critical splice donor site	probably null
R8967:Cpxm2	UTSW	7	132,059,835 (GRCm38)	missense	probably damaging	1.00
R9680:Cpxm2	UTSW	7	132,059,922 (GRCm38)	missense	probably damaging	1.00
R9759:Cpxm2	UTSW	7	132,154,513 (GRCm38)	missense	probably benign	0.03
RF014:Cpxm2	UTSW	7	132,070,863 (GRCm38)	missense	possibly damaging	0.85
Z1177:Cpxm2	UTSW	7	132,055,001 (GRCm38)	missense	probably benign	0.01

Predicted Primers

PCR Primer
(F):5'- CAGCTTCAGCAATGAGATGC -3'
(R):5'- GAGTTCCACTACATCGCAGG -3'

Sequencing Primer
(F):5'- CATAATGGCCTAGTCGAATCAGTGC -3'
(R):5'- ACTACATCGCAGGGGCCC -3'

Posted On

2016-03-17