Mutagenetix > Incidental Mutation

Incidental Mutation 'R7263:Pp2d1'

564779

Institutional Source

Beutler Lab

Gene Symbol

Pp2d1

Ensembl Gene

ENSMUSG00000044957

Gene Name

protein phosphatase 2C-like domain containing 1

Synonyms

4921523A10Rik

MMRRC Submission

045388-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.070) question?

Stock #

R7263 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

53814488-53846479 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 53822358 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Threonine at position 236 (I236T)

Ref Sequence

ENSEMBL: ENSMUSP00000056682 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000056198]

AlphaFold

Q8BVT6

Predicted Effect

probably benign
Transcript: ENSMUST00000056198
AA Change: I236T

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)

SMART Domains

Protein: ENSMUSP00000056682
Gene: ENSMUSG00000044957
AA Change: I236T

Domain	Start	End	E-Value	Type
PP2Cc	173	609	4.04e-18	SMART

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.5%
20x: 98.4%

Validation Efficiency

96% (67/70)

Allele List at MGI

Other mutations in this stock

Total: 67 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca4	C	A	3: 121,847,843 (GRCm39)	H55N	probably damaging	Het
Acan	G	T	7: 78,742,066 (GRCm39)	V488L	probably damaging	Het
Adam12	T	C	7: 133,521,240 (GRCm39)	E638G	possibly damaging	Het
Adamts20	T	A	15: 94,220,772 (GRCm39)	Q1387L	possibly damaging	Het
Adamts3	G	T	5: 89,825,601 (GRCm39)	D1079E	probably benign	Het
Barx1	G	T	13: 48,818,555 (GRCm39)	G93C	probably damaging	Het
Carmil2	C	T	8: 106,419,677 (GRCm39)	R828C	probably damaging	Het
Catsper4	TTCTC	TTC	4: 133,954,423 (GRCm39)		probably null	Het
Ccdc159	T	C	9: 21,843,007 (GRCm39)	M148T	probably benign	Het
Cdk5rap1	T	A	2: 154,202,652 (GRCm39)	N193Y	probably benign	Het
Csnk1g2	G	A	10: 80,470,332 (GRCm39)	G15D	probably damaging	Het
Dach1	T	C	14: 98,406,295 (GRCm39)	S151G	probably benign	Het
Elf5	C	A	2: 103,269,645 (GRCm39)	N75K	probably benign	Het
Elp3	T	C	14: 65,802,782 (GRCm39)	D272G	probably damaging	Het
Epb41l1	T	A	2: 156,337,043 (GRCm39)		probably null	Het
Epha6	A	G	16: 59,596,028 (GRCm39)	Y888H	probably damaging	Het
Fibcd1	T	C	2: 31,707,222 (GRCm39)	Y345C	probably damaging	Het
Gjd3	C	T	11: 102,690,963 (GRCm39)	E347K	possibly damaging	Het
Gse1	A	G	8: 121,300,910 (GRCm39)	D892G	unknown	Het
Gtpbp6	A	T	5: 110,251,915 (GRCm39)	I506N	probably benign	Het
Hivep1	T	A	13: 42,311,668 (GRCm39)	F1303I	possibly damaging	Het
Il21r	A	G	7: 125,232,077 (GRCm39)	T502A	probably benign	Het
Ints1	T	C	5: 139,749,834 (GRCm39)	T997A	possibly damaging	Het
Invs	C	A	4: 48,396,381 (GRCm39)	N351K	probably damaging	Het
Iqcm	A	G	8: 76,489,701 (GRCm39)	T390A	probably benign	Het
Iqcn	A	G	8: 71,163,425 (GRCm39)	N873D	possibly damaging	Het
Kcnh4	C	T	11: 100,632,643 (GRCm39)	G948D	probably benign	Het
Kcnh7	T	A	2: 62,566,314 (GRCm39)		probably null	Het
Lrrc72	A	G	12: 36,258,611 (GRCm39)	V82A	probably damaging	Het
Macf1	A	T	4: 123,271,943 (GRCm39)	L6535Q	probably damaging	Het
Ncor2	G	C	5: 125,109,196 (GRCm39)	L585V		Het
Nipal2	G	C	15: 34,578,904 (GRCm39)	Y298*	probably null	Het
Nipsnap1	C	T	11: 4,832,960 (GRCm39)		probably benign	Het
Or12e1	T	A	2: 87,022,476 (GRCm39)	C148*	probably null	Het
Or4x12-ps1	T	C	2: 89,916,332 (GRCm39)	I158V	not run	Het
Or51g1	A	T	7: 102,633,524 (GRCm39)	Y282*	probably null	Het
Pcdhga4	C	T	18: 37,819,873 (GRCm39)	T474I	probably benign	Het
Pdp1	G	T	4: 11,960,821 (GRCm39)	Q516K	possibly damaging	Het
Pik3c2b	C	T	1: 133,017,940 (GRCm39)	P934L	probably damaging	Het
Pygm	G	A	19: 6,438,357 (GRCm39)	R278H	probably damaging	Het
Rb1	A	T	14: 73,520,363 (GRCm39)	C215*	probably null	Het
Rgs22	A	G	15: 36,015,789 (GRCm39)	S1156P	possibly damaging	Het
Rgs9bp	T	C	7: 35,284,126 (GRCm39)	T174A	probably damaging	Het
Rnf133	A	T	6: 23,649,667 (GRCm39)	Y130*	probably null	Het
Sctr	G	A	1: 119,949,955 (GRCm39)	R48Q	probably benign	Het
Serpinb6e	A	T	13: 34,022,923 (GRCm39)	F153L	probably benign	Het
Slc22a1	A	T	17: 12,885,587 (GRCm39)	Y200N	probably damaging	Het
Slc22a22	C	A	15: 57,113,107 (GRCm39)	M377I	probably benign	Het
Slc36a4	A	G	9: 15,633,452 (GRCm39)		probably null	Het
Slc39a6	A	G	18: 24,734,260 (GRCm39)	V143A	probably benign	Het
Slf2	G	A	19: 44,926,863 (GRCm39)		probably null	Het
Sowaha	T	C	11: 53,370,485 (GRCm39)	K84E	probably benign	Het
Spef2	T	G	15: 9,653,098 (GRCm39)		probably null	Het
Sphkap	A	T	1: 83,254,399 (GRCm39)	F1117I	probably damaging	Het
Tas2r113	T	C	6: 132,870,539 (GRCm39)	I189T	possibly damaging	Het
Tescl	T	C	7: 24,033,247 (GRCm39)	E26G	possibly damaging	Het
Trpm6	A	T	19: 18,854,150 (GRCm39)	I1847F	probably damaging	Het
Uba1y	T	A	Y: 822,200 (GRCm39)	C178S	possibly damaging	Het
Ush2a	T	A	1: 188,175,526 (GRCm39)	V1208D	possibly damaging	Het
Usp13	G	C	3: 32,949,000 (GRCm39)	A446P	probably damaging	Het
Usp7	A	T	16: 8,514,588 (GRCm39)	C722S	possibly damaging	Het
Vmn1r52	A	G	6: 90,156,535 (GRCm39)	S280G	probably benign	Het
Vmn2r84	T	C	10: 130,225,077 (GRCm39)	K478E	probably damaging	Het
Zfp112	C	A	7: 23,824,952 (GRCm39)	L311I	probably benign	Het
Zfp180	G	T	7: 23,805,125 (GRCm39)	E515*	probably null	Het
Zfp518b	A	G	5: 38,829,671 (GRCm39)	I778T	probably damaging	Het
Zfp800	A	T	6: 28,243,662 (GRCm39)	H434Q	probably benign	Het

Other mutations in Pp2d1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00949:Pp2d1	APN	17	53,822,667 (GRCm39)	missense	probably benign	0.00
IGL01939:Pp2d1	APN	17	53,822,167 (GRCm39)	missense	probably damaging	1.00
IGL02031:Pp2d1	APN	17	53,815,468 (GRCm39)	missense	probably damaging	1.00
IGL02039:Pp2d1	APN	17	53,823,022 (GRCm39)	nonsense	probably null
IGL02108:Pp2d1	APN	17	53,822,433 (GRCm39)	missense	probably damaging	1.00
IGL02121:Pp2d1	APN	17	53,814,949 (GRCm39)	missense	probably damaging	1.00
IGL03034:Pp2d1	APN	17	53,815,081 (GRCm39)	missense	possibly damaging	0.88
R0483:Pp2d1	UTSW	17	53,814,999 (GRCm39)	missense	probably benign	0.29
R0562:Pp2d1	UTSW	17	53,846,196 (GRCm39)	splice site	probably benign
R1416:Pp2d1	UTSW	17	53,822,835 (GRCm39)	missense	probably benign	0.07
R1464:Pp2d1	UTSW	17	53,823,015 (GRCm39)	missense	possibly damaging	0.94
R1464:Pp2d1	UTSW	17	53,823,015 (GRCm39)	missense	possibly damaging	0.94
R1479:Pp2d1	UTSW	17	53,814,883 (GRCm39)	missense	probably benign	0.05
R1659:Pp2d1	UTSW	17	53,822,406 (GRCm39)	missense	possibly damaging	0.50
R1711:Pp2d1	UTSW	17	53,822,338 (GRCm39)	missense	possibly damaging	0.47
R2214:Pp2d1	UTSW	17	53,822,424 (GRCm39)	missense	probably benign	0.01
R2217:Pp2d1	UTSW	17	53,822,482 (GRCm39)	missense	probably benign	0.02
R2218:Pp2d1	UTSW	17	53,822,482 (GRCm39)	missense	probably benign	0.02
R4463:Pp2d1	UTSW	17	53,822,886 (GRCm39)	missense	probably benign
R4644:Pp2d1	UTSW	17	53,823,015 (GRCm39)	missense	probably benign	0.00
R4901:Pp2d1	UTSW	17	53,822,037 (GRCm39)	missense	probably benign	0.20
R5164:Pp2d1	UTSW	17	53,815,098 (GRCm39)	missense	probably benign	0.11
R5169:Pp2d1	UTSW	17	53,814,930 (GRCm39)	missense	possibly damaging	0.78
R5186:Pp2d1	UTSW	17	53,815,168 (GRCm39)	missense	probably benign
R5223:Pp2d1	UTSW	17	53,814,873 (GRCm39)	missense	probably benign	0.12
R6550:Pp2d1	UTSW	17	53,822,604 (GRCm39)	missense	probably damaging	0.98
R6918:Pp2d1	UTSW	17	53,822,487 (GRCm39)	missense	probably damaging	0.99
R7623:Pp2d1	UTSW	17	53,822,907 (GRCm39)	missense	probably benign	0.00
R7712:Pp2d1	UTSW	17	53,815,318 (GRCm39)	missense	possibly damaging	0.63
R8062:Pp2d1	UTSW	17	53,822,798 (GRCm39)	missense	probably benign	0.01
R8165:Pp2d1	UTSW	17	53,822,257 (GRCm39)	missense	probably damaging	1.00
R8694:Pp2d1	UTSW	17	53,815,191 (GRCm39)	missense	probably benign	0.01
R8815:Pp2d1	UTSW	17	53,814,897 (GRCm39)	missense	probably benign	0.41
R9704:Pp2d1	UTSW	17	53,822,907 (GRCm39)	missense	probably benign	0.00
X0019:Pp2d1	UTSW	17	53,822,575 (GRCm39)	missense	probably benign	0.19

Predicted Primers

PCR Primer
(F):5'- ATATACAAGTGAGTGCCGAGC -3'
(R):5'- AATTCAGCCTGGAAAGCGG -3'

Sequencing Primer
(F):5'- GAACCCGGGAAGTCTCATTC -3'
(R):5'- GAGCCGAACTGTAAATTCACGGTC -3'

Posted On

2019-06-26