Mutagenetix > Incidental Mutation

Incidental Mutation 'R8988:Prickle2'

684213

Institutional Source

Beutler Lab

Gene Symbol

Prickle2

Ensembl Gene

ENSMUSG00000030020

Gene Name

prickle planar cell polarity protein 2

Synonyms

6230400G14Rik, mpk2, 6720451F06Rik

MMRRC Submission

068820-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.491) question?

Stock #

R8988 (G1)

Quality Score

104.008

Status

Validated

Chromosome

Chromosomal Location

92370908-92706155 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 92458639 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Glutamic Acid at position 50 (K50E)

Ref Sequence

ENSEMBL: ENSMUSP00000032093 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000032093] [ENSMUST00000113445] [ENSMUST00000113446] [ENSMUST00000113447]

AlphaFold

Q80Y24

Predicted Effect

possibly damaging
Transcript: ENSMUST00000032093
AA Change: K50E

PolyPhen 2 Score 0.916 (Sensitivity: 0.81; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000032093
Gene: ENSMUSG00000030020
AA Change: K50E

Domain	Start	End	E-Value	Type
low complexity region	3	15	N/A	INTRINSIC
Pfam:PET	76	176	1.2e-45	PFAM
LIM	185	242	3.05e-10	SMART
LIM	250	302	5.43e-16	SMART
LIM	310	365	2.92e-7	SMART
low complexity region	465	477	N/A	INTRINSIC
low complexity region	534	546	N/A	INTRINSIC
low complexity region	725	753	N/A	INTRINSIC
low complexity region	832	841	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000113445

SMART Domains

Protein: ENSMUSP00000109072
Gene: ENSMUSG00000030020

Domain	Start	End	E-Value	Type
Pfam:PET	17	122	8.9e-47	PFAM
LIM	129	186	3.05e-10	SMART
LIM	194	246	5.43e-16	SMART
LIM	254	309	2.92e-7	SMART
low complexity region	409	421	N/A	INTRINSIC
low complexity region	478	490	N/A	INTRINSIC
low complexity region	669	697	N/A	INTRINSIC
low complexity region	776	785	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000113446

SMART Domains

Protein: ENSMUSP00000109073
Gene: ENSMUSG00000030020

Domain	Start	End	E-Value	Type
Pfam:PET	17	122	8.9e-47	PFAM
LIM	129	186	3.05e-10	SMART
LIM	194	246	5.43e-16	SMART
LIM	254	309	2.92e-7	SMART
low complexity region	409	421	N/A	INTRINSIC
low complexity region	478	490	N/A	INTRINSIC
low complexity region	669	697	N/A	INTRINSIC
low complexity region	776	785	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000113447

SMART Domains

Protein: ENSMUSP00000109074
Gene: ENSMUSG00000030020

Domain	Start	End	E-Value	Type
Pfam:PET	17	122	8.9e-47	PFAM
LIM	129	186	3.05e-10	SMART
LIM	194	246	5.43e-16	SMART
LIM	254	309	2.92e-7	SMART
low complexity region	409	421	N/A	INTRINSIC
low complexity region	478	490	N/A	INTRINSIC
low complexity region	669	697	N/A	INTRINSIC
low complexity region	776	785	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.5%
20x: 98.3%

Validation Efficiency

96% (81/84)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a homolog of Drosophila prickle. The exact function of this gene is not known, however, studies in mice suggest that it may be involved in seizure prevention. Mutations in this gene are associated with progressive myoclonic epilepsy type 5. [provided by RefSeq, Dec 2011]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit increased susceptibility to electroconvulsive or PTZ-induced seizures. Mice heterozygous for a knock-out allele exhibit increased susceptibility to electroconvulsive seizures. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 84 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2810403A07Rik	A	G	3: 88,699,979 (GRCm38)	N330S	probably benign	Het
Abi2	C	T	1: 60,450,092 (GRCm38)	T291I	probably benign	Het
Aox1	A	C	1: 58,049,466 (GRCm38)	D137A	possibly damaging	Het
Apbb2	T	C	5: 66,452,101 (GRCm38)	K68E	probably damaging	Het
Arf3	A	T	15: 98,741,052 (GRCm38)	M108K	probably benign	Het
Atg2b	T	A	12: 105,617,129 (GRCm38)	I2058F	probably damaging	Het
Bhlhe40	C	T	6: 108,662,557 (GRCm38)	L99F	probably damaging	Het
Cyp2b10	G	A	7: 25,926,245 (GRCm38)	R500H	probably damaging	Het
Dlc1	C	T	8: 36,572,843 (GRCm38)	E937K	probably damaging	Het
Dll3	A	T	7: 28,296,368 (GRCm38)	V336D	possibly damaging	Het
Dync2h1	A	G	9: 7,037,727 (GRCm38)	F3377L	probably benign	Het
Eef1d	A	G	15: 75,896,311 (GRCm38)	Y561H	probably damaging	Het
Epb41l1	C	A	2: 156,521,671 (GRCm38)	T700K	probably benign	Het
Epha8	G	T	4: 136,938,586 (GRCm38)	L420M	probably damaging	Het
Ephb2	C	A	4: 136,675,458 (GRCm38)	G501C	probably benign	Het
Erbb3	T	C	10: 128,570,161 (GRCm38)	Y1129C	probably damaging	Het
Fbn1	C	T	2: 125,370,806 (GRCm38)	V799M	possibly damaging	Het
Fbxo9	G	A	9: 78,084,651 (GRCm38)	P353S	probably benign	Het
Ggt1	T	G	10: 75,576,222 (GRCm38)	V100G	probably benign	Het
Gm11639	T	G	11: 105,020,526 (GRCm38)	V4544G	probably benign	Het
Gm45861	T	C	8: 27,542,503 (GRCm38)	M885T	unknown	Het
Gm609	T	C	16: 45,417,908 (GRCm38)	H294R	probably benign	Het
Grin2d	A	T	7: 45,834,001 (GRCm38)	Y917*	probably null	Het
Hectd4	T	A	5: 121,277,756 (GRCm38)	V540D	possibly damaging	Het
Helz	T	A	11: 107,604,253 (GRCm38)	I351K	probably damaging	Het
Ighv2-6-8	A	G	12: 113,796,360 (GRCm38)	V43A	probably damaging	Het
Igkv9-129	T	A	6: 67,840,122 (GRCm38)	I70N	probably damaging	Het
Il18	A	T	9: 50,577,878 (GRCm38)	D69V	probably damaging	Het
Kcnh7	T	A	2: 62,721,865 (GRCm38)	E927D		Het
Kcnt2	T	A	1: 140,428,849 (GRCm38)	V342E	probably benign	Het
Krt1	AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC	AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC	15: 101,850,378 (GRCm38)		probably benign	Het
Krt18	C	G	15: 102,029,527 (GRCm38)	A153G	probably damaging	Het
Lmntd2	A	T	7: 141,212,064 (GRCm38)		probably benign	Het
Lrrc26	G	T	2: 25,290,274 (GRCm38)	A96S	probably benign	Het
Map3k11	A	T	19: 5,702,138 (GRCm38)	S783C	probably damaging	Het
Mib2	G	A	4: 155,656,272 (GRCm38)	L632F	possibly damaging	Het
Mical2	A	C	7: 112,311,454 (GRCm38)	D277A	possibly damaging	Het
Mtr	A	T	13: 12,235,479 (GRCm38)	F339L	probably benign	Het
Musk	T	C	4: 58,354,032 (GRCm38)	F362L	probably benign	Het
Ncor1	G	A	11: 62,343,045 (GRCm38)	Q444*	probably null	Het
Nek4	T	C	14: 30,963,967 (GRCm38)	S279P		Het
Nell1	C	T	7: 50,560,795 (GRCm38)	T348I	unknown	Het
Nicn1	C	T	9: 108,294,509 (GRCm38)	R163C	possibly damaging	Het
Nrip1	T	C	16: 76,292,014 (GRCm38)	H885R	probably damaging	Het
Olfr1382	C	A	11: 49,535,201 (GRCm38)	N5K	probably damaging	Het
Olfr214	A	G	6: 116,557,294 (GRCm38)	T290A	possibly damaging	Het
Olfr448	T	A	6: 42,897,267 (GRCm38)	V272D		Het
Olfr525	G	A	7: 140,323,025 (GRCm38)	G109R	possibly damaging	Het
Olfr784	T	C	10: 129,388,371 (GRCm38)	V246A	probably damaging	Het
Olfr822	T	A	10: 130,074,653 (GRCm38)	V81D	possibly damaging	Het
Otog	A	G	7: 46,310,147 (GRCm38)	D720G	probably damaging	Het
P3h3	C	A	6: 124,857,601 (GRCm38)	Q29H	possibly damaging	Het
Parn	A	G	16: 13,648,417 (GRCm38)		probably null	Het
Pcnt	C	A	10: 76,409,573 (GRCm38)	E1077*	probably null	Het
Peg10	CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG	CCACATCAGGATCCACATCAGGATGCACATCAG	6: 4,756,398 (GRCm38)		probably benign	Het
Pigb	A	G	9: 73,022,294 (GRCm38)	W336R	probably damaging	Het
Pkdrej	A	T	15: 85,816,337 (GRCm38)	S1799R	probably damaging	Het
Pnpla6	G	T	8: 3,517,401 (GRCm38)	M86I	possibly damaging	Het
Psg21	A	G	7: 18,652,464 (GRCm38)	V199A	probably benign	Het
Reep3	T	C	10: 67,036,007 (GRCm38)		probably null	Het
Reln	T	C	5: 21,899,157 (GRCm38)	D3272G	probably damaging	Het
Rps6ka4	A	G	19: 6,831,299 (GRCm38)	V526A	possibly damaging	Het
Sel1l3	T	C	5: 53,123,429 (GRCm38)	E911G	probably damaging	Het
Serpinb6b	C	A	13: 32,978,142 (GRCm38)	A308E	probably benign	Het
Slc26a4	A	G	12: 31,522,524 (GRCm38)	V746A	probably benign	Het
Slc4a3	T	G	1: 75,551,313 (GRCm38)	M402R	probably damaging	Het
Slc9b1	A	T	3: 135,373,139 (GRCm38)	T186S	possibly damaging	Het
Slk	A	G	19: 47,620,273 (GRCm38)	Q555R	probably benign	Het
Smc2	T	A	4: 52,475,100 (GRCm38)	D925E	probably benign	Het
Stat5a	A	T	11: 100,883,938 (GRCm38)	T758S	unknown	Het
Sulf1	A	G	1: 12,836,275 (GRCm38)	S514G	probably benign	Het
Tcp11l1	T	A	2: 104,706,508 (GRCm38)	N4I	probably damaging	Het
Tex2	A	T	11: 106,511,905 (GRCm38)	I1047K	unknown	Het
Tmem184b	A	G	15: 79,377,064 (GRCm38)	V114A	possibly damaging	Het
Trmt11	A	G	10: 30,591,031 (GRCm38)	V95A	probably benign	Het
Trp53bp2	A	G	1: 182,440,868 (GRCm38)	D169G	possibly damaging	Het
Ttc41	T	A	10: 86,713,735 (GRCm38)	N264K	possibly damaging	Het
Uba2	A	C	7: 34,154,562 (GRCm38)	S318R	probably benign	Het
Wapl	T	A	14: 34,729,182 (GRCm38)	N724K	probably damaging	Het
Wfdc9	T	A	2: 164,651,751 (GRCm38)	I5F	probably damaging	Het
Zan	C	T	5: 137,408,301 (GRCm38)	D3686N	unknown	Het
Zfp618	A	T	4: 63,094,471 (GRCm38)	Y140F	probably benign	Het
Zfp790	A	G	7: 29,828,168 (GRCm38)	T93A	probably benign	Het
Zfp979	A	C	4: 147,613,527 (GRCm38)	F242V	probably benign	Het

Other mutations in Prickle2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02962:Prickle2	APN	6	92,376,422 (GRCm38)	missense	probably benign	0.00
R0028:Prickle2	UTSW	6	92,422,342 (GRCm38)	missense	probably benign	0.12
R0122:Prickle2	UTSW	6	92,411,345 (GRCm38)	nonsense	probably null
R0555:Prickle2	UTSW	6	92,458,565 (GRCm38)	missense	probably benign	0.02
R0940:Prickle2	UTSW	6	92,411,003 (GRCm38)	missense	probably benign	0.02
R1394:Prickle2	UTSW	6	92,376,382 (GRCm38)	missense	possibly damaging	0.87
R1470:Prickle2	UTSW	6	92,458,602 (GRCm38)	missense	probably damaging	0.96
R1470:Prickle2	UTSW	6	92,458,602 (GRCm38)	missense	probably damaging	0.96
R1599:Prickle2	UTSW	6	92,410,874 (GRCm38)	missense	probably benign
R1745:Prickle2	UTSW	6	92,376,593 (GRCm38)	missense	probably damaging	1.00
R1801:Prickle2	UTSW	6	92,416,904 (GRCm38)	missense	probably damaging	0.98
R1985:Prickle2	UTSW	6	92,411,452 (GRCm38)	missense	probably damaging	1.00
R2085:Prickle2	UTSW	6	92,376,364 (GRCm38)	missense	probably damaging	0.96
R2147:Prickle2	UTSW	6	92,425,671 (GRCm38)	missense	probably damaging	0.99
R2148:Prickle2	UTSW	6	92,425,671 (GRCm38)	missense	probably damaging	0.99
R2571:Prickle2	UTSW	6	92,705,400 (GRCm38)	missense	probably benign	0.09
R3547:Prickle2	UTSW	6	92,411,137 (GRCm38)	missense	probably damaging	1.00
R4356:Prickle2	UTSW	6	92,411,509 (GRCm38)	missense	probably damaging	1.00
R4569:Prickle2	UTSW	6	92,422,342 (GRCm38)	missense	probably benign	0.12
R4896:Prickle2	UTSW	6	92,416,755 (GRCm38)	missense	probably benign	0.26
R5004:Prickle2	UTSW	6	92,416,755 (GRCm38)	missense	probably benign	0.26
R5045:Prickle2	UTSW	6	92,376,394 (GRCm38)	missense	probably damaging	0.96
R5219:Prickle2	UTSW	6	92,376,530 (GRCm38)	missense	probably benign
R5247:Prickle2	UTSW	6	92,375,969 (GRCm38)	missense	probably damaging	1.00
R5280:Prickle2	UTSW	6	92,376,210 (GRCm38)	missense	probably damaging	1.00
R5334:Prickle2	UTSW	6	92,425,684 (GRCm38)	missense	probably damaging	1.00
R5780:Prickle2	UTSW	6	92,458,612 (GRCm38)	missense	probably benign	0.06
R5960:Prickle2	UTSW	6	92,376,305 (GRCm38)	missense	probably benign	0.08
R6084:Prickle2	UTSW	6	92,416,848 (GRCm38)	nonsense	probably null
R6362:Prickle2	UTSW	6	92,458,615 (GRCm38)	missense	possibly damaging	0.77
R6368:Prickle2	UTSW	6	92,420,237 (GRCm38)	missense	probably damaging	1.00
R6852:Prickle2	UTSW	6	92,376,544 (GRCm38)	missense	probably benign
R7041:Prickle2	UTSW	6	92,376,305 (GRCm38)	missense	probably benign	0.08
R7203:Prickle2	UTSW	6	92,410,978 (GRCm38)	missense	possibly damaging	0.61
R7352:Prickle2	UTSW	6	92,410,890 (GRCm38)	missense	probably benign	0.00
R7405:Prickle2	UTSW	6	92,458,543 (GRCm38)	missense	probably damaging	0.96
R7510:Prickle2	UTSW	6	92,376,470 (GRCm38)	missense	possibly damaging	0.58
R7562:Prickle2	UTSW	6	92,375,948 (GRCm38)	makesense	probably null
R7578:Prickle2	UTSW	6	92,411,290 (GRCm38)	missense	probably benign	0.32
R7614:Prickle2	UTSW	6	92,425,650 (GRCm38)	missense	possibly damaging	0.46
R7732:Prickle2	UTSW	6	92,411,224 (GRCm38)	missense	probably damaging	1.00
R7948:Prickle2	UTSW	6	92,416,922 (GRCm38)	missense	possibly damaging	0.84
R7984:Prickle2	UTSW	6	92,410,874 (GRCm38)	missense	probably benign
R8350:Prickle2	UTSW	6	92,376,502 (GRCm38)	missense	probably benign
R8404:Prickle2	UTSW	6	92,420,321 (GRCm38)	missense	probably damaging	0.96
R9184:Prickle2	UTSW	6	92,411,524 (GRCm38)	missense	possibly damaging	0.46
R9348:Prickle2	UTSW	6	92,420,262 (GRCm38)	missense	probably benign	0.00
R9532:Prickle2	UTSW	6	92,706,115 (GRCm38)	missense	probably benign	0.00
R9755:Prickle2	UTSW	6	92,422,338 (GRCm38)	missense	probably damaging	1.00
X0020:Prickle2	UTSW	6	92,416,853 (GRCm38)	missense	probably damaging	0.98
X0026:Prickle2	UTSW	6	92,411,426 (GRCm38)	nonsense	probably null
X0066:Prickle2	UTSW	6	92,376,433 (GRCm38)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- ATTAAAGACACGGGAAGACTCC -3'
(R):5'- TCACCTAAGTGGCTTCCATATGG -3'

Sequencing Primer
(F):5'- ACTCCGGGCAGATGGCTAC -3'
(R):5'- TATGGGTTGGAATCCAGG -3'

Posted On

2021-10-11