Mutagenetix > Incidental Mutation

Incidental Mutation 'R1565:Cpxm2'

175198

Institutional Source

Beutler Lab

Gene Symbol

Cpxm2

Ensembl Gene

ENSMUSG00000030862

Gene Name

carboxypeptidase X, M14 family member 2

Synonyms

4632435C11Rik

MMRRC Submission

039604-MU

Accession Numbers

Essential gene?

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

Stock #

R1565 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

131634416-131756468 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 131663874 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Asparagine at position 350 (Y350N)

Ref Sequence

ENSEMBL: ENSMUSP00000033149 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000033149
AA Change: Y350N

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

SMART Domains

Protein: ENSMUSP00000033149
Gene: ENSMUSG00000030862
AA Change: Y350N

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

0.9554

Coding Region Coverage

1x: 99.0%
3x: 98.1%
10x: 95.5%
20x: 90.0%

Validation Efficiency

96% (82/85)

Allele List at MGI

Other mutations in this stock

Total: 74 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2810021J22Rik	G	A	11: 58,771,327 (GRCm39)	G270S	probably benign	Het
Abtb1	T	C	6: 88,813,536 (GRCm39)	T401A	probably benign	Het
Adamts14	A	T	10: 61,106,676 (GRCm39)	M148K	probably damaging	Het
Adcy5	A	G	16: 35,089,327 (GRCm39)	E508G	probably damaging	Het
Ankfy1	T	A	11: 72,648,144 (GRCm39)	L875H	probably damaging	Het
Cacng3	A	T	7: 122,367,624 (GRCm39)	D168V	probably damaging	Het
Clpb	G	A	7: 101,434,668 (GRCm39)	R488Q	probably benign	Het
Cltrn	A	G	X: 162,901,230 (GRCm39)	D184G	possibly damaging	Het
D130040H23Rik	T	A	8: 69,755,812 (GRCm39)	*406R	probably null	Het
Dnah10	T	A	5: 124,906,678 (GRCm39)	D4236E	probably damaging	Het
Dpf3	T	A	12: 83,417,391 (GRCm39)	Y27F	probably damaging	Het
Esp4	T	C	17: 40,913,486 (GRCm39)	*118Q	probably null	Het
Fam222b	T	C	11: 78,045,488 (GRCm39)	S222P	possibly damaging	Het
Flnc	T	C	6: 29,455,170 (GRCm39)	V1933A	probably damaging	Het
Gem	T	C	4: 11,713,709 (GRCm39)	F282L	possibly damaging	Het
Gli2	T	C	1: 118,769,660 (GRCm39)	T631A	possibly damaging	Het
Gpld1	T	A	13: 25,140,051 (GRCm39)	V116E	probably damaging	Het
Gpr176	A	G	2: 118,110,695 (GRCm39)	M188T	probably benign	Het
Grk5	T	C	19: 61,078,410 (GRCm39)	V489A	probably damaging	Het
Hpdl	T	C	4: 116,678,080 (GRCm39)	N127S	probably damaging	Het
Hsd17b8	C	T	17: 34,246,469 (GRCm39)	V105I	possibly damaging	Het
Id4	G	T	13: 48,415,770 (GRCm39)	V151L	possibly damaging	Het
Kcnh8	G	T	17: 53,263,909 (GRCm39)	G802V	probably benign	Het
Lamc1	C	A	1: 153,118,489 (GRCm39)	S894I	probably benign	Het
Larp1b	A	G	3: 40,926,819 (GRCm39)	N184S	probably damaging	Het
Lhx1	A	T	11: 84,410,647 (GRCm39)	S226T	probably benign	Het
Lmo7	A	T	14: 102,124,957 (GRCm39)	Q472L	probably damaging	Het
Mog	G	C	17: 37,328,474 (GRCm39)	N152K	possibly damaging	Het
Mttp	A	G	3: 137,822,166 (GRCm39)		probably null	Het
Mycbp2	A	G	14: 103,489,945 (GRCm39)	V953A	possibly damaging	Het
Myo3a	A	T	2: 22,345,091 (GRCm39)	Y509F	probably damaging	Het
Myo9b	A	G	8: 71,767,836 (GRCm39)	N303S	possibly damaging	Het
Nek3	T	C	8: 22,622,217 (GRCm39)		probably null	Het
Nlrc4	A	T	17: 74,748,926 (GRCm39)	D771E	probably benign	Het
Nup160	A	T	2: 90,552,405 (GRCm39)	N1127I	possibly damaging	Het
Oas1h	A	T	5: 121,000,663 (GRCm39)	N91I	probably damaging	Het
Or13p4	T	A	4: 118,547,389 (GRCm39)	N87Y	probably damaging	Het
Or4c120	A	T	2: 89,000,971 (GRCm39)	V195D	probably benign	Het
Or4c121	G	T	2: 89,024,227 (GRCm39)	S50R	probably damaging	Het
Parp4	T	C	14: 56,827,329 (GRCm39)		probably benign	Het
Pi4ka	G	A	16: 17,099,764 (GRCm39)	C96Y	probably null	Het
Pira2	A	T	7: 3,847,548 (GRCm39)	F47Y	probably damaging	Het
Pkhd1	C	A	1: 20,417,681 (GRCm39)	G2490V	probably damaging	Het
Plekhg1	C	T	10: 3,890,526 (GRCm39)	T394I	probably damaging	Het
Pramel22	G	A	4: 143,382,187 (GRCm39)	Q170*	probably null	Het
Psmd1	T	C	1: 86,019,719 (GRCm39)		probably benign	Het
Rab3ip	A	T	10: 116,775,128 (GRCm39)	C77S	probably benign	Het
Reln	A	T	5: 22,130,211 (GRCm39)	M2700K	probably benign	Het
Rfx1	A	G	8: 84,800,575 (GRCm39)	T59A	probably benign	Het
Ric8b	G	T	10: 84,815,963 (GRCm39)	V405L	probably benign	Het
Rufy3	G	T	5: 88,788,491 (GRCm39)	A479S	probably damaging	Het
Sardh	A	T	2: 27,132,731 (GRCm39)	Y166N	probably damaging	Het
Slamf6	T	G	1: 171,761,975 (GRCm39)	V132G	possibly damaging	Het
Slc12a3	T	G	8: 95,072,505 (GRCm39)	H674Q	possibly damaging	Het
Sned1	G	A	1: 93,209,376 (GRCm39)	V830M	possibly damaging	Het
Srsf9	A	G	5: 115,465,429 (GRCm39)	N21S	possibly damaging	Het
Stkld1	A	T	2: 26,840,102 (GRCm39)	T391S	probably benign	Het
Sumf2	C	A	5: 129,888,755 (GRCm39)	N230K	probably damaging	Het
Tbc1d22a	T	C	15: 86,119,770 (GRCm39)	V22A	possibly damaging	Het
Thsd7b	T	A	1: 129,523,778 (GRCm39)	S194T	possibly damaging	Het
Tnn	T	A	1: 159,924,835 (GRCm39)	Y1173F	probably damaging	Het
Top2a	A	G	11: 98,891,880 (GRCm39)	F1122L	probably damaging	Het
Trappc9	G	A	15: 72,897,816 (GRCm39)	R377W	probably damaging	Het
Trim39	G	A	17: 36,579,746 (GRCm39)	R70W	probably damaging	Het
Ttn	G	A	2: 76,624,605 (GRCm39)	T15289I	probably damaging	Het
Ugt2b38	A	T	5: 87,559,773 (GRCm39)	V373E	probably damaging	Het
Usp54	A	G	14: 20,657,227 (GRCm39)	S24P	probably damaging	Het
Vmn2r27	C	T	6: 124,208,593 (GRCm39)	G51S	probably benign	Het
Xylt2	C	T	11: 94,558,420 (GRCm39)	A579T	probably benign	Het
Zbtb21	A	G	16: 97,753,627 (GRCm39)	S247P	probably benign	Het
Zc3h7b	C	T	15: 81,661,289 (GRCm39)	P376L	probably benign	Het
Zfp251	T	A	15: 76,737,238 (GRCm39)	R613S	probably damaging	Het
Zfp251	C	T	15: 76,737,239 (GRCm39)	R613K	possibly damaging	Het
Zfp91	T	C	19: 12,756,439 (GRCm39)	D135G	probably benign	Het

Other mutations in Cpxm2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01862:Cpxm2	APN	7	131,661,540 (GRCm39)	missense	probably benign	0.01
IGL02039:Cpxm2	APN	7	131,649,482 (GRCm39)	missense	probably damaging	1.00
IGL03011:Cpxm2	APN	7	131,650,807 (GRCm39)	missense	possibly damaging	0.46
R0033:Cpxm2	UTSW	7	131,663,886 (GRCm39)	missense	possibly damaging	0.55
R0100:Cpxm2	UTSW	7	131,656,600 (GRCm39)	missense	possibly damaging	0.90
R0100:Cpxm2	UTSW	7	131,656,600 (GRCm39)	missense	possibly damaging	0.90
R0453:Cpxm2	UTSW	7	131,730,134 (GRCm39)	missense	probably damaging	1.00
R0555:Cpxm2	UTSW	7	131,645,772 (GRCm39)	nonsense	probably null
R0655:Cpxm2	UTSW	7	131,656,549 (GRCm39)	missense	possibly damaging	0.87
R0834:Cpxm2	UTSW	7	131,756,342 (GRCm39)	intron	probably benign
R1145:Cpxm2	UTSW	7	131,659,377 (GRCm39)	missense	probably damaging	0.99
R1145:Cpxm2	UTSW	7	131,659,377 (GRCm39)	missense	probably damaging	0.99
R1249:Cpxm2	UTSW	7	131,730,079 (GRCm39)	critical splice donor site	probably null
R1563:Cpxm2	UTSW	7	131,745,411 (GRCm39)	missense	probably benign	0.00
R1709:Cpxm2	UTSW	7	131,661,563 (GRCm39)	missense	probably damaging	1.00
R1863:Cpxm2	UTSW	7	131,745,392 (GRCm39)	splice site	probably null
R1874:Cpxm2	UTSW	7	131,661,563 (GRCm39)	missense	probably damaging	1.00
R1958:Cpxm2	UTSW	7	131,663,876 (GRCm39)	missense	probably damaging	1.00
R2273:Cpxm2	UTSW	7	131,661,581 (GRCm39)	intron	probably benign
R3806:Cpxm2	UTSW	7	131,681,820 (GRCm39)	missense	probably benign	0.12
R3861:Cpxm2	UTSW	7	131,656,648 (GRCm39)	missense	probably benign	0.00
R4570:Cpxm2	UTSW	7	131,745,435 (GRCm39)	missense	probably benign	0.11
R4642:Cpxm2	UTSW	7	131,672,610 (GRCm39)	missense	probably benign	0.11
R4684:Cpxm2	UTSW	7	131,650,767 (GRCm39)	missense	possibly damaging	0.92
R4717:Cpxm2	UTSW	7	131,656,574 (GRCm39)	missense	possibly damaging	0.61
R4863:Cpxm2	UTSW	7	131,661,476 (GRCm39)	missense	probably benign	0.13
R5079:Cpxm2	UTSW	7	131,756,014 (GRCm39)	critical splice donor site	probably null
R5341:Cpxm2	UTSW	7	131,756,342 (GRCm39)	intron	probably benign
R5626:Cpxm2	UTSW	7	131,661,581 (GRCm39)	intron	probably benign
R5666:Cpxm2	UTSW	7	131,656,625 (GRCm39)	missense	probably benign	0.44
R5815:Cpxm2	UTSW	7	131,645,839 (GRCm39)	missense	probably damaging	1.00
R6114:Cpxm2	UTSW	7	131,756,035 (GRCm39)	missense	probably benign
R6133:Cpxm2	UTSW	7	131,730,182 (GRCm39)	missense	probably damaging	1.00
R6224:Cpxm2	UTSW	7	131,745,460 (GRCm39)	missense	probably benign
R6468:Cpxm2	UTSW	7	131,672,589 (GRCm39)	missense	probably damaging	1.00
R6657:Cpxm2	UTSW	7	131,650,806 (GRCm39)	missense	probably damaging	1.00
R7058:Cpxm2	UTSW	7	131,745,408 (GRCm39)	missense	probably benign	0.32
R7100:Cpxm2	UTSW	7	131,656,544 (GRCm39)	missense	probably benign	0.06
R7198:Cpxm2	UTSW	7	131,681,813 (GRCm39)	missense	probably damaging	1.00
R7712:Cpxm2	UTSW	7	131,756,107 (GRCm39)	missense	possibly damaging	0.69
R7855:Cpxm2	UTSW	7	131,659,424 (GRCm39)	missense	possibly damaging	0.56
R7867:Cpxm2	UTSW	7	131,650,800 (GRCm39)	missense	probably damaging	1.00
R8513:Cpxm2	UTSW	7	131,745,431 (GRCm39)	missense	probably benign	0.01
R8694:Cpxm2	UTSW	7	131,681,783 (GRCm39)	missense	probably benign	0.03
R8874:Cpxm2	UTSW	7	131,708,010 (GRCm39)	critical splice donor site	probably null
R8967:Cpxm2	UTSW	7	131,661,564 (GRCm39)	missense	probably damaging	1.00
R9680:Cpxm2	UTSW	7	131,661,651 (GRCm39)	missense	probably damaging	1.00
R9759:Cpxm2	UTSW	7	131,756,242 (GRCm39)	missense	probably benign	0.03
RF014:Cpxm2	UTSW	7	131,672,592 (GRCm39)	missense	possibly damaging	0.85
Z1177:Cpxm2	UTSW	7	131,656,730 (GRCm39)	missense	probably benign	0.01

Predicted Primers

PCR Primer
(F):5'- AGGGTATGAACACTGTCATGTGGGG -3'
(R):5'- ATTCTGGACAGGTATAGCAGTGGGGC -3'

Sequencing Primer
(F):5'- gcaataagcagactcctccc -3'
(R):5'- AGTGGGGCTGTGGGGAG -3'

Posted On

2014-04-24