Mutagenetix > Incidental Mutation

Incidental Mutation 'R5916:Ptprq'

461347

Institutional Source

Beutler Lab

Gene Symbol

Ptprq

Ensembl Gene

ENSMUSG00000035916

Gene Name

protein tyrosine phosphatase, receptor type, Q

Synonyms

MMRRC Submission

044113-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.203) question?

Stock #

R5916 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

107517049-107720051 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 107523513 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Lysine at position 2243 (M2243K)

Ref Sequence

ENSEMBL: ENSMUSP00000058572 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000050702]

AlphaFold

P0C5E4

Predicted Effect

probably damaging
Transcript: ENSMUST00000050702
AA Change: M2243K

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

SMART Domains

Protein: ENSMUSP00000058572
Gene: ENSMUSG00000035916
AA Change: M2243K

Domain	Start	End	E-Value	Type
FN3	57	141	3.17e-13	SMART
FN3	156	294	1.55e-7	SMART
FN3	307	384	4.45e-8	SMART
FN3	398	555	1.17e-7	SMART
FN3	569	648	7.06e-11	SMART
FN3	666	743	7.68e-12	SMART
FN3	760	839	1.88e-6	SMART
FN3	855	932	1.33e-6	SMART
FN3	949	1037	2.31e-6	SMART
FN3	1054	1135	1.24e-6	SMART
FN3	1151	1229	2.39e-8	SMART
FN3	1244	1325	6.29e-8	SMART
FN3	1341	1416	2.87e-11	SMART
FN3	1431	1524	2.82e-10	SMART
FN3	1540	1622	6.35e-4	SMART
FN3	1642	1732	7.93e-5	SMART
transmembrane domain	1907	1929	N/A	INTRINSIC
PTPc	2003	2262	1.14e-130	SMART

Coding Region Coverage

1x: 99.8%
3x: 99.3%
10x: 97.2%
20x: 92.4%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This locus encodes a member of the type III receptor-like protein-tyrosine phosphatase family. The encoded protein catalyzes the dephosphorylation of phosphotyrosine and phosphatidylinositol and plays roles in cellular proliferation and differentiation. Mutations at this locus have been linked to autosomal recessive deafness. [provided by RefSeq, Mar 2014]
PHENOTYPE: Homozygotes for targeted mutations show absence of shaft connectors from vestibular hair bundles, postnatal degeneration in cochlear hair-bundle structure, reduced transducer currents but otherwise normal adaptation properties, a progressive loss of basal-coil cochlear hair cells, and deafness. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 61 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2810474O19Rik	C	T	6: 149,326,578 (GRCm38)	T374I	probably damaging	Het
4930563D23Rik	T	A	16: 92,320,671 (GRCm38)	E243V	probably damaging	Het
Aadacl4	A	T	4: 144,622,980 (GRCm38)	N269I	possibly damaging	Het
Abcc1	G	T	16: 14,465,142 (GRCm38)	V1161F	possibly damaging	Het
Adam3	A	T	8: 24,684,539 (GRCm38)		probably null	Het
Agt	A	T	8: 124,563,858 (GRCm38)	S237T	possibly damaging	Het
Ano3	A	T	2: 110,681,836 (GRCm38)	F674L	probably benign	Het
Asb2	G	T	12: 103,323,876 (GRCm38)	A504E	probably damaging	Het
Atp13a1	T	A	8: 69,807,098 (GRCm38)	I1113N	probably damaging	Het
Atxn7l2	T	C	3: 108,205,662 (GRCm38)		probably null	Het
Bambi	A	G	18: 3,511,463 (GRCm38)	T95A	probably benign	Het
Ccdc173	A	T	2: 69,789,462 (GRCm38)	M1K	probably null	Het
Clrn1	T	C	3: 58,846,362 (GRCm38)	T193A	probably benign	Het
Colgalt2	T	A	1: 152,504,122 (GRCm38)	D437E	probably damaging	Het
Dchs1	C	A	7: 105,759,166 (GRCm38)	A1820S	probably damaging	Het
Dnah12	T	A	14: 26,706,918 (GRCm38)	I233N	possibly damaging	Het
Dsc3	T	C	18: 19,987,020 (GRCm38)	N194D	probably damaging	Het
Dync2h1	A	G	9: 7,102,309 (GRCm38)		probably null	Het
Erich3	A	T	3: 154,695,823 (GRCm38)	R36S	probably damaging	Het
Fmnl3	A	T	15: 99,321,828 (GRCm38)	C680S	probably damaging	Het
Focad	T	C	4: 88,357,541 (GRCm38)	L1129P	unknown	Het
Fzd3	G	A	14: 65,202,729 (GRCm38)	T664I	probably benign	Het
Glb1l3	T	C	9: 26,854,736 (GRCm38)	I129V	probably benign	Het
Heatr1	T	C	13: 12,434,471 (GRCm38)	F1950S	probably damaging	Het
Herc6	G	A	6: 57,646,203 (GRCm38)	G597E	probably benign	Het
Hmcn2	T	A	2: 31,396,139 (GRCm38)	V2101D	probably damaging	Het
Il17re	T	A	6: 113,470,123 (GRCm38)	C612S	probably damaging	Het
Il1f9	T	G	2: 24,192,794 (GRCm38)	*194E	probably null	Het
Junb	T	C	8: 84,977,876 (GRCm38)	Y185C	probably benign	Het
Lrriq1	G	A	10: 103,221,382 (GRCm38)	Q186*	probably null	Het
Lrrn2	T	A	1: 132,937,800 (GRCm38)	V201E	probably damaging	Het
Ly6l	A	T	15: 75,451,178 (GRCm38)	T68S	probably benign	Het
March1	G	T	8: 66,387,111 (GRCm38)	R182L	possibly damaging	Het
Megf6	A	G	4: 154,249,425 (GRCm38)		probably null	Het
Mga	T	A	2: 119,964,312 (GRCm38)	S2708T	probably benign	Het
Mx1	T	C	16: 97,451,733 (GRCm38)	T396A	probably benign	Het
Naip5	A	C	13: 100,222,701 (GRCm38)	S676A	probably benign	Het
Npepl1	G	T	2: 174,121,544 (GRCm38)	W456C	probably benign	Het
Ntrk2	A	G	13: 58,808,729 (GRCm38)	M1V	probably null	Het
Nufip1	T	C	14: 76,134,900 (GRCm38)	*485Q	probably null	Het
Ocln	T	G	13: 100,506,179 (GRCm38)	D216A	possibly damaging	Het
Olfr108	C	T	17: 37,445,679 (GRCm38)	L53F	probably benign	Het
Olfr1308	A	G	2: 111,960,830 (GRCm38)	M81T	probably damaging	Het
Olfr417	A	T	1: 174,369,132 (GRCm38)	T72S	probably damaging	Het
Olfr544	G	A	7: 102,484,379 (GRCm38)	S247F	probably damaging	Het
Papd4	T	C	13: 93,175,547 (GRCm38)	D215G	probably damaging	Het
Rad51b	C	T	12: 79,325,082 (GRCm38)	Q190*	probably null	Het
Rfx8	T	C	1: 39,688,619 (GRCm38)	Y182C	probably benign	Het
Rpgrip1l	C	A	8: 91,252,913 (GRCm38)	R967L	possibly damaging	Het
Scube2	A	G	7: 109,831,724 (GRCm38)	Y423H	possibly damaging	Het
Sipa1l2	A	T	8: 125,468,573 (GRCm38)	Y809N	probably damaging	Het
Slc35f1	C	A	10: 52,933,221 (GRCm38)	Y101*	probably null	Het
Tbc1d22a	A	G	15: 86,214,608 (GRCm38)	K12E	possibly damaging	Het
Tmcc2	C	T	1: 132,357,691 (GRCm38)	V646M	probably damaging	Het
Tpp1	A	T	7: 105,749,380 (GRCm38)	M243K	probably damaging	Het
Trappc12	A	G	12: 28,691,514 (GRCm38)	L732P	probably damaging	Het
U2af2	A	T	7: 5,079,180 (GRCm38)		probably null	Het
Utrn	T	A	10: 12,665,051 (GRCm38)	N1877Y	probably damaging	Het
Vsir	C	T	10: 60,358,037 (GRCm38)	T93I	probably damaging	Het
Zkscan5	T	A	5: 145,205,302 (GRCm38)	M3K	possibly damaging	Het
Zscan29	G	T	2: 121,164,037 (GRCm38)	T489N	probably damaging	Het

Other mutations in Ptprq

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00340:Ptprq	APN	10	107,576,929 (GRCm38)	missense	probably damaging	0.98
IGL00537:Ptprq	APN	10	107,710,522 (GRCm38)	missense	probably benign	0.07
IGL00547:Ptprq	APN	10	107,718,541 (GRCm38)	missense	probably damaging	0.99
IGL00586:Ptprq	APN	10	107,608,122 (GRCm38)	splice site	probably benign
IGL00648:Ptprq	APN	10	107,646,716 (GRCm38)	missense	probably benign	0.10
IGL01123:Ptprq	APN	10	107,686,218 (GRCm38)	missense	probably damaging	0.96
IGL01343:Ptprq	APN	10	107,638,839 (GRCm38)	missense	probably damaging	0.96
IGL01348:Ptprq	APN	10	107,711,904 (GRCm38)	missense	probably damaging	1.00
IGL01433:Ptprq	APN	10	107,576,880 (GRCm38)	missense	probably damaging	0.99
IGL01510:Ptprq	APN	10	107,712,048 (GRCm38)	missense	probably damaging	1.00
IGL01535:Ptprq	APN	10	107,699,596 (GRCm38)	missense	probably benign
IGL01631:Ptprq	APN	10	107,643,538 (GRCm38)	missense	probably benign	0.00
IGL01633:Ptprq	APN	10	107,699,723 (GRCm38)	splice site	probably benign
IGL01702:Ptprq	APN	10	107,517,866 (GRCm38)	missense	probably benign	0.00
IGL01733:Ptprq	APN	10	107,662,599 (GRCm38)	missense	probably benign	0.10
IGL01806:Ptprq	APN	10	107,699,608 (GRCm38)	missense	probably damaging	1.00
IGL01832:Ptprq	APN	10	107,565,839 (GRCm38)	critical splice donor site	probably null
IGL01961:Ptprq	APN	10	107,643,654 (GRCm38)	missense	probably damaging	1.00
IGL02108:Ptprq	APN	10	107,646,617 (GRCm38)	missense	probably damaging	1.00
IGL02120:Ptprq	APN	10	107,667,472 (GRCm38)	missense	probably damaging	1.00
IGL02160:Ptprq	APN	10	107,653,565 (GRCm38)	missense	probably benign	0.00
IGL02178:Ptprq	APN	10	107,686,319 (GRCm38)	missense	probably benign	0.03
IGL02249:Ptprq	APN	10	107,582,359 (GRCm38)	missense	probably damaging	1.00
IGL02267:Ptprq	APN	10	107,646,558 (GRCm38)	missense	probably damaging	1.00
IGL02527:Ptprq	APN	10	107,686,563 (GRCm38)	missense	probably benign	0.04
IGL02529:Ptprq	APN	10	107,635,365 (GRCm38)	missense	probably benign	0.03
IGL02542:Ptprq	APN	10	107,662,555 (GRCm38)	missense	probably damaging	1.00
IGL02582:Ptprq	APN	10	107,643,999 (GRCm38)	missense	probably benign	0.00
IGL02708:Ptprq	APN	10	107,652,700 (GRCm38)	missense	probably damaging	1.00
IGL02894:Ptprq	APN	10	107,667,424 (GRCm38)	missense	probably benign
IGL02903:Ptprq	APN	10	107,666,586 (GRCm38)	missense	possibly damaging	0.51
IGL02951:Ptprq	APN	10	107,667,460 (GRCm38)	missense	probably benign	0.03
IGL02982:Ptprq	APN	10	107,586,684 (GRCm38)	missense	probably damaging	1.00
IGL03000:Ptprq	APN	10	107,542,657 (GRCm38)	missense	probably damaging	1.00
IGL03024:Ptprq	APN	10	107,685,566 (GRCm38)	missense	possibly damaging	0.69
IGL03240:Ptprq	APN	10	107,688,507 (GRCm38)	missense	probably benign
P0043:Ptprq	UTSW	10	107,580,225 (GRCm38)	missense	probably benign	0.03
PIT4812001:Ptprq	UTSW	10	107,666,567 (GRCm38)	missense	probably damaging	1.00
R0200:Ptprq	UTSW	10	107,685,157 (GRCm38)	missense	probably benign
R0268:Ptprq	UTSW	10	107,705,548 (GRCm38)	missense	probably benign
R0276:Ptprq	UTSW	10	107,542,735 (GRCm38)	critical splice acceptor site	probably null
R0279:Ptprq	UTSW	10	107,608,417 (GRCm38)	missense	probably damaging	0.96
R0335:Ptprq	UTSW	10	107,708,728 (GRCm38)	missense	probably benign
R0344:Ptprq	UTSW	10	107,705,582 (GRCm38)	missense	probably benign
R0357:Ptprq	UTSW	10	107,686,199 (GRCm38)	splice site	probably benign
R0454:Ptprq	UTSW	10	107,582,530 (GRCm38)	nonsense	probably null
R0479:Ptprq	UTSW	10	107,643,994 (GRCm38)	nonsense	probably null
R0491:Ptprq	UTSW	10	107,608,175 (GRCm38)	missense	probably damaging	0.98
R0519:Ptprq	UTSW	10	107,538,920 (GRCm38)	splice site	probably benign
R0523:Ptprq	UTSW	10	107,580,220 (GRCm38)	missense	possibly damaging	0.54
R0553:Ptprq	UTSW	10	107,710,627 (GRCm38)	missense	probably benign	0.33
R0746:Ptprq	UTSW	10	107,517,831 (GRCm38)	missense	probably damaging	1.00
R0755:Ptprq	UTSW	10	107,582,539 (GRCm38)	missense	probably benign	0.09
R1434:Ptprq	UTSW	10	107,586,714 (GRCm38)	missense	probably damaging	1.00
R1445:Ptprq	UTSW	10	107,662,562 (GRCm38)	missense	probably damaging	1.00
R1470:Ptprq	UTSW	10	107,718,574 (GRCm38)	missense	probably damaging	0.97
R1470:Ptprq	UTSW	10	107,718,574 (GRCm38)	missense	probably damaging	0.97
R1558:Ptprq	UTSW	10	107,644,043 (GRCm38)	missense	probably damaging	1.00
R1567:Ptprq	UTSW	10	107,565,887 (GRCm38)	missense	probably benign	0.13
R1711:Ptprq	UTSW	10	107,534,699 (GRCm38)	nonsense	probably null
R1720:Ptprq	UTSW	10	107,686,294 (GRCm38)	missense	probably damaging	1.00
R1746:Ptprq	UTSW	10	107,638,830 (GRCm38)	missense	probably damaging	1.00
R1776:Ptprq	UTSW	10	107,685,089 (GRCm38)	missense	probably damaging	1.00
R1822:Ptprq	UTSW	10	107,718,478 (GRCm38)	missense	probably damaging	1.00
R1872:Ptprq	UTSW	10	107,643,999 (GRCm38)	missense	probably benign	0.19
R1944:Ptprq	UTSW	10	107,582,388 (GRCm38)	missense	probably benign	0.23
R1945:Ptprq	UTSW	10	107,582,388 (GRCm38)	missense	probably benign	0.23
R2006:Ptprq	UTSW	10	107,666,546 (GRCm38)	missense	probably damaging	1.00
R2014:Ptprq	UTSW	10	107,667,422 (GRCm38)	missense	probably damaging	0.96
R2015:Ptprq	UTSW	10	107,667,422 (GRCm38)	missense	probably damaging	0.96
R2097:Ptprq	UTSW	10	107,653,493 (GRCm38)	missense	probably benign	0.05
R2172:Ptprq	UTSW	10	107,590,994 (GRCm38)	nonsense	probably null
R2174:Ptprq	UTSW	10	107,705,553 (GRCm38)	missense	probably damaging	1.00
R2248:Ptprq	UTSW	10	107,643,070 (GRCm38)	splice site	probably null
R2404:Ptprq	UTSW	10	107,686,599 (GRCm38)	missense	probably damaging	1.00
R3423:Ptprq	UTSW	10	107,582,476 (GRCm38)	missense	probably damaging	0.99
R3683:Ptprq	UTSW	10	107,708,628 (GRCm38)	missense	probably benign	0.01
R3875:Ptprq	UTSW	10	107,685,104 (GRCm38)	missense	possibly damaging	0.88
R3945:Ptprq	UTSW	10	107,686,392 (GRCm38)	splice site	probably benign
R3946:Ptprq	UTSW	10	107,686,392 (GRCm38)	splice site	probably benign
R3974:Ptprq	UTSW	10	107,712,062 (GRCm38)	missense	possibly damaging	0.88
R3982:Ptprq	UTSW	10	107,543,396 (GRCm38)	missense	probably damaging	0.99
R4105:Ptprq	UTSW	10	107,572,967 (GRCm38)	missense	probably damaging	1.00
R4118:Ptprq	UTSW	10	107,711,920 (GRCm38)	missense	probably benign	0.37
R4175:Ptprq	UTSW	10	107,711,917 (GRCm38)	missense	probably benign
R4231:Ptprq	UTSW	10	107,686,283 (GRCm38)	nonsense	probably null
R4356:Ptprq	UTSW	10	107,608,364 (GRCm38)	missense	probably damaging	0.99
R4435:Ptprq	UTSW	10	107,685,055 (GRCm38)	missense	possibly damaging	0.89
R4678:Ptprq	UTSW	10	107,685,182 (GRCm38)	missense	probably benign	0.19
R4679:Ptprq	UTSW	10	107,685,182 (GRCm38)	missense	probably benign	0.19
R4745:Ptprq	UTSW	10	107,524,253 (GRCm38)	missense	probably damaging	1.00
R4771:Ptprq	UTSW	10	107,688,427 (GRCm38)	missense	probably benign
R4778:Ptprq	UTSW	10	107,591,022 (GRCm38)	missense	probably benign	0.15
R4808:Ptprq	UTSW	10	107,718,507 (GRCm38)	missense	probably damaging	1.00
R4809:Ptprq	UTSW	10	107,563,175 (GRCm38)	missense	probably damaging	1.00
R4818:Ptprq	UTSW	10	107,710,581 (GRCm38)	missense	possibly damaging	0.86
R4845:Ptprq	UTSW	10	107,653,532 (GRCm38)	missense	probably benign	0.00
R4901:Ptprq	UTSW	10	107,688,414 (GRCm38)	missense	probably benign	0.01
R4942:Ptprq	UTSW	10	107,688,429 (GRCm38)	missense	probably benign	0.01
R4946:Ptprq	UTSW	10	107,525,734 (GRCm38)	missense	probably benign
R4959:Ptprq	UTSW	10	107,686,555 (GRCm38)	missense	probably damaging	1.00
R4973:Ptprq	UTSW	10	107,686,555 (GRCm38)	missense	probably damaging	1.00
R5007:Ptprq	UTSW	10	107,608,276 (GRCm38)	missense	probably benign	0.00
R5053:Ptprq	UTSW	10	107,563,202 (GRCm38)	missense	probably damaging	1.00
R5055:Ptprq	UTSW	10	107,534,679 (GRCm38)	missense	probably benign	0.37
R5090:Ptprq	UTSW	10	107,526,089 (GRCm38)	missense	probably damaging	1.00
R5158:Ptprq	UTSW	10	107,534,704 (GRCm38)	missense	probably damaging	1.00
R5163:Ptprq	UTSW	10	107,524,331 (GRCm38)	missense	probably damaging	1.00
R5222:Ptprq	UTSW	10	107,662,564 (GRCm38)	missense	probably damaging	0.96
R5244:Ptprq	UTSW	10	107,586,695 (GRCm38)	missense	possibly damaging	0.62
R5249:Ptprq	UTSW	10	107,699,635 (GRCm38)	missense	probably damaging	0.99
R5503:Ptprq	UTSW	10	107,688,328 (GRCm38)	splice site	probably null
R5508:Ptprq	UTSW	10	107,686,231 (GRCm38)	missense	probably benign	0.00
R5601:Ptprq	UTSW	10	107,608,430 (GRCm38)	missense	probably benign
R5722:Ptprq	UTSW	10	107,686,365 (GRCm38)	missense	possibly damaging	0.72
R5819:Ptprq	UTSW	10	107,719,883 (GRCm38)	start gained	probably benign
R5862:Ptprq	UTSW	10	107,565,878 (GRCm38)	missense	probably benign	0.02
R5891:Ptprq	UTSW	10	107,576,895 (GRCm38)	missense	possibly damaging	0.94
R6054:Ptprq	UTSW	10	107,582,358 (GRCm38)	missense	probably damaging	1.00
R6058:Ptprq	UTSW	10	107,635,274 (GRCm38)	missense	probably benign	0.00
R6075:Ptprq	UTSW	10	107,525,760 (GRCm38)	missense	probably damaging	1.00
R6101:Ptprq	UTSW	10	107,580,266 (GRCm38)	missense	possibly damaging	0.93
R6189:Ptprq	UTSW	10	107,517,887 (GRCm38)	missense	probably damaging	1.00
R6235:Ptprq	UTSW	10	107,635,338 (GRCm38)	missense	possibly damaging	0.61
R6351:Ptprq	UTSW	10	107,708,668 (GRCm38)	missense	probably damaging	0.99
R6394:Ptprq	UTSW	10	107,642,943 (GRCm38)	nonsense	probably null
R6449:Ptprq	UTSW	10	107,705,583 (GRCm38)	missense	probably benign	0.00
R6526:Ptprq	UTSW	10	107,542,653 (GRCm38)	nonsense	probably null
R6544:Ptprq	UTSW	10	107,608,241 (GRCm38)	missense	probably damaging	1.00
R6609:Ptprq	UTSW	10	107,572,968 (GRCm38)	missense	probably damaging	0.99
R6862:Ptprq	UTSW	10	107,686,225 (GRCm38)	missense	probably damaging	0.96
R6874:Ptprq	UTSW	10	107,718,599 (GRCm38)	missense	possibly damaging	0.80
R6892:Ptprq	UTSW	10	107,576,004 (GRCm38)	missense	probably benign	0.00
R7082:Ptprq	UTSW	10	107,708,730 (GRCm38)	missense	probably benign	0.10
R7210:Ptprq	UTSW	10	107,685,171 (GRCm38)	missense	probably damaging	1.00
R7253:Ptprq	UTSW	10	107,608,273 (GRCm38)	missense	probably benign	0.30
R7293:Ptprq	UTSW	10	107,635,506 (GRCm38)	nonsense	probably null
R7445:Ptprq	UTSW	10	107,590,959 (GRCm38)	missense	probably damaging	1.00
R7632:Ptprq	UTSW	10	107,711,922 (GRCm38)	missense	probably benign	0.32
R7685:Ptprq	UTSW	10	107,643,978 (GRCm38)	missense	probably damaging	1.00
R7703:Ptprq	UTSW	10	107,644,146 (GRCm38)	missense	probably benign	0.01
R7774:Ptprq	UTSW	10	107,643,669 (GRCm38)	missense	probably damaging	0.96
R7897:Ptprq	UTSW	10	107,710,623 (GRCm38)	missense	probably benign	0.21
R7936:Ptprq	UTSW	10	107,652,711 (GRCm38)	missense	probably damaging	1.00
R7983:Ptprq	UTSW	10	107,608,411 (GRCm38)	nonsense	probably null
R8023:Ptprq	UTSW	10	107,652,616 (GRCm38)	nonsense	probably null
R8071:Ptprq	UTSW	10	107,644,035 (GRCm38)	missense	possibly damaging	0.62
R8084:Ptprq	UTSW	10	107,608,433 (GRCm38)	missense	probably benign
R8086:Ptprq	UTSW	10	107,646,639 (GRCm38)	nonsense	probably null
R8169:Ptprq	UTSW	10	107,582,490 (GRCm38)	missense	probably damaging	1.00
R8223:Ptprq	UTSW	10	107,699,638 (GRCm38)	missense	probably benign	0.00
R8235:Ptprq	UTSW	10	107,705,490 (GRCm38)	missense	probably benign	0.32
R8235:Ptprq	UTSW	10	107,582,541 (GRCm38)	missense	probably damaging	1.00
R8278:Ptprq	UTSW	10	107,686,378 (GRCm38)	missense	possibly damaging	0.87
R8710:Ptprq	UTSW	10	107,576,058 (GRCm38)	missense	possibly damaging	0.67
R8828:Ptprq	UTSW	10	107,646,652 (GRCm38)	missense	probably benign
R8830:Ptprq	UTSW	10	107,586,695 (GRCm38)	missense	possibly damaging	0.62
R8869:Ptprq	UTSW	10	107,699,608 (GRCm38)	missense	probably damaging	1.00
R9012:Ptprq	UTSW	10	107,653,550 (GRCm38)	missense	probably benign	0.09
R9072:Ptprq	UTSW	10	107,565,875 (GRCm38)	missense
R9153:Ptprq	UTSW	10	107,580,265 (GRCm38)	missense	probably damaging	0.98
R9202:Ptprq	UTSW	10	107,686,555 (GRCm38)	missense	probably damaging	1.00
R9252:Ptprq	UTSW	10	107,686,386 (GRCm38)	missense	probably benign	0.12
R9306:Ptprq	UTSW	10	107,586,738 (GRCm38)	missense	probably benign	0.00
R9492:Ptprq	UTSW	10	107,642,952 (GRCm38)	missense	probably damaging	1.00
R9519:Ptprq	UTSW	10	107,685,100 (GRCm38)	missense	probably damaging	1.00
R9581:Ptprq	UTSW	10	107,711,910 (GRCm38)	missense	possibly damaging	0.53
R9593:Ptprq	UTSW	10	107,688,393 (GRCm38)	missense	possibly damaging	0.92
R9621:Ptprq	UTSW	10	107,542,662 (GRCm38)	missense	probably damaging	1.00
R9732:Ptprq	UTSW	10	107,576,906 (GRCm38)	missense	probably damaging	1.00
R9743:Ptprq	UTSW	10	107,685,121 (GRCm38)	missense	probably damaging	1.00
R9771:Ptprq	UTSW	10	107,685,224 (GRCm38)	missense	probably damaging	0.99
R9788:Ptprq	UTSW	10	107,565,890 (GRCm38)	missense	probably benign	0.24
Z1088:Ptprq	UTSW	10	107,699,672 (GRCm38)	missense	possibly damaging	0.56
Z1176:Ptprq	UTSW	10	107,526,070 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CCCACCAATTCGGATGTACAGTC -3'
(R):5'- CATCAACATGACTCAGCCTTTGC -3'

Sequencing Primer
(F):5'- TGTACAGTCAGTGAAAGTACCC -3'
(R):5'- TGCTGACCAATGATCCCCG -3'

Posted On

2017-02-28