Mutagenetix > Incidental Mutation

Incidental Mutation 'R2130:Ptpro'

227949

Institutional Source

Beutler Lab

Gene Symbol

Ptpro

Ensembl Gene

ENSMUSG00000030223

Gene Name

protein tyrosine phosphatase, receptor type, O

Synonyms

Ptpn15, PTP-oc, GLEPP1, PTP-U2, PTP-BK, PTP-phi, D28, PTPROt

MMRRC Submission

040133-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R2130 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

137252319-137463233 bp(+) (GRCm38)

Type of Mutation

splice site (3 bp from exon)

DNA Base Change (assembly)

A to G at 137411116 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000144870 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000077115] [ENSMUST00000167002] [ENSMUST00000167679] [ENSMUST00000203914]

AlphaFold

E9Q612

Predicted Effect

probably null
Transcript: ENSMUST00000077115

SMART Domains

Protein: ENSMUSP00000076364
Gene: ENSMUSG00000030223

Domain	Start	End	E-Value	Type
signal peptide	1	29	N/A	INTRINSIC
low complexity region	269	291	N/A	INTRINSIC
FN3	443	528	1.07e-1	SMART
FN3	540	626	7.07e-2	SMART
FN3	642	722	4.47e1	SMART
FN3	733	812	5.92e-4	SMART
transmembrane domain	831	853	N/A	INTRINSIC
transmembrane domain	890	912	N/A	INTRINSIC
PTPc	947	1207	1.43e-127	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000167002

SMART Domains

Protein: ENSMUSP00000131764
Gene: ENSMUSG00000030223

Domain	Start	End	E-Value	Type
transmembrane domain	10	32	N/A	INTRINSIC
transmembrane domain	69	91	N/A	INTRINSIC
PTPc	126	386	1.43e-127	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000167679

SMART Domains

Protein: ENSMUSP00000127112
Gene: ENSMUSG00000030223

Domain	Start	End	E-Value	Type
signal peptide	1	29	N/A	INTRINSIC
low complexity region	269	291	N/A	INTRINSIC
FN3	443	528	1.07e-1	SMART
FN3	540	626	7.07e-2	SMART
FN3	642	722	4.47e1	SMART
FN3	733	812	5.92e-4	SMART
transmembrane domain	831	853	N/A	INTRINSIC
PTPc	919	1179	1.43e-127	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000203914

SMART Domains

Protein: ENSMUSP00000144870
Gene: ENSMUSG00000030223

Domain	Start	End	E-Value	Type
signal peptide	1	33	N/A	INTRINSIC
PTPc	98	358	6.1e-130	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000204780

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.2%
3x: 98.7%
10x: 97.5%
20x: 95.9%

Validation Efficiency

94% (94/100)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the R3 subtype family of receptor-type protein tyrosine phosphatases. These proteins are localized to the apical surface of polarized cells and may have tissue-specific functions through activation of Src family kinases. This gene contains two distinct promoters, and alternatively spliced transcript variants encoding multiple isoforms have been observed. The encoded proteins may have multiple isoform-specific and tissue-specific functions, including the regulation of osteoclast production and activity, inhibition of cell proliferation and facilitation of apoptosis. This gene is a candidate tumor suppressor, and decreased expression of this gene has been observed in several types of cancer. [provided by RefSeq, May 2011]
PHENOTYPE: Mice homozygous for one allele display impaired glomerular filtration due to podocyte structural anomalies and a predisposition for hypertension. Mice homozygous for a second allele exhibit susceptibility to pharmacologically induced seizures. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 97 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2010111I01Rik	T	A	13: 63,210,149 (GRCm38)	C656S	probably benign	Het
9030624J02Rik	T	C	7: 118,794,575 (GRCm38)	Y516H	probably damaging	Het
A2ml1	T	A	6: 128,576,260 (GRCm38)	N178I	probably damaging	Het
Adgrl2	T	C	3: 148,890,488 (GRCm38)	I71V	probably damaging	Het
Adgrv1	T	C	13: 81,581,727 (GRCm38)	T212A	possibly damaging	Het
Aox3	A	G	1: 58,169,843 (GRCm38)	H845R	probably damaging	Het
Apaf1	A	T	10: 91,060,165 (GRCm38)	Y348*	probably null	Het
Apobr	A	G	7: 126,587,206 (GRCm38)	T630A	probably benign	Het
Arhgap23	A	G	11: 97,451,561 (GRCm38)	D223G	possibly damaging	Het
Asic1	A	T	15: 99,671,875 (GRCm38)	T26S	possibly damaging	Het
Atp13a2	T	A	4: 141,005,016 (GRCm38)	M864K	probably damaging	Het
Atrnl1	G	A	19: 57,654,994 (GRCm38)	G438D	probably damaging	Het
Bbc3	T	C	7: 16,312,343 (GRCm38)	V68A	possibly damaging	Het
Birc6	T	C	17: 74,659,154 (GRCm38)		probably benign	Het
Btnl9	A	G	11: 49,180,696 (GRCm38)	F100S	probably damaging	Het
Ccpg1	A	G	9: 73,013,158 (GRCm38)	N685S	probably damaging	Het
Ces3b	T	A	8: 105,092,975 (GRCm38)		probably null	Het
Cfhr2	T	G	1: 139,831,155 (GRCm38)	R52S	probably benign	Het
Clhc1	A	G	11: 29,557,663 (GRCm38)	I126V	probably benign	Het
Crocc	T	C	4: 141,029,102 (GRCm38)	I1071V	probably benign	Het
Dbt	T	A	3: 116,539,124 (GRCm38)	D16E	probably damaging	Het
Dnajc8	T	C	4: 132,544,059 (GRCm38)	S62P	possibly damaging	Het
Dpyd	T	C	3: 118,674,568 (GRCm38)	V77A	probably benign	Het
Dram2	T	A	3: 106,570,760 (GRCm38)	M136K	possibly damaging	Het
Dtx2	T	A	5: 136,012,040 (GRCm38)	F100I	probably damaging	Het
Dync2h1	A	T	9: 7,011,253 (GRCm38)	W3654R	probably damaging	Het
Fam129b	A	G	2: 32,923,647 (GRCm38)	K624R	probably benign	Het
Fam208a	A	G	14: 27,476,614 (GRCm38)	N1301S	possibly damaging	Het
Fam208a	T	A	14: 27,446,388 (GRCm38)	Y296N	probably damaging	Het
Fbxw10	T	A	11: 62,859,857 (GRCm38)	I422N	probably damaging	Het
Fgf17	T	C	14: 70,638,487 (GRCm38)	R102G	probably damaging	Het
Gatsl2	G	A	5: 134,136,153 (GRCm38)	C187Y	probably damaging	Het
Gm28040	AGTG	AGTGGCACCTTTGGTG	1: 133,327,321 (GRCm38)		probably benign	Het
Gm6578	C	A	6: 12,100,187 (GRCm38)		noncoding transcript	Het
Gm8298	T	C	3: 59,865,348 (GRCm38)	V91A	probably damaging	Het
Gm8374	T	C	14: 7,364,194 (GRCm38)	T49A	probably damaging	Het
Gm9797	G	T	10: 11,609,369 (GRCm38)		noncoding transcript	Het
Golga3	T	C	5: 110,202,939 (GRCm38)		probably null	Het
Golim4	A	T	3: 75,908,149 (GRCm38)	V116D	probably damaging	Het
Igfn1	AGGG	AGG	1: 135,974,852 (GRCm38)		probably benign	Het
Insrr	G	A	3: 87,810,572 (GRCm38)		probably null	Het
Ipo9	A	G	1: 135,402,250 (GRCm38)	V484A	probably benign	Het
Ipo9	ATCCTCCTCCTCCTCCTC	ATCCTCCTCCTCCTCCTCCTC	1: 135,386,268 (GRCm38)		probably benign	Het
Isoc2b	A	T	7: 4,851,439 (GRCm38)	I31N	probably damaging	Het
Kif5c	T	A	2: 49,758,805 (GRCm38)		probably benign	Het
Krtap16-1	A	T	11: 99,985,776 (GRCm38)	C267*	probably null	Het
Lamc2	T	A	1: 153,127,124 (GRCm38)	D1037V	probably damaging	Het
Lhfpl2	A	G	13: 94,192,049 (GRCm38)	D206G	possibly damaging	Het
Lmtk2	C	T	5: 144,174,988 (GRCm38)	T842I	possibly damaging	Het
Mgat2	T	C	12: 69,185,294 (GRCm38)	F214S	probably damaging	Het
Mki67	T	A	7: 135,704,241 (GRCm38)		probably null	Het
Mpo	A	G	11: 87,797,361 (GRCm38)	D282G	possibly damaging	Het
Myh10	A	G	11: 68,807,289 (GRCm38)		probably benign	Het
Myo15b	G	A	11: 115,871,643 (GRCm38)	V1229I	probably benign	Het
Nfatc2ip	A	G	7: 126,390,462 (GRCm38)	V250A	probably benign	Het
Nrp1	A	T	8: 128,498,516 (GRCm38)	E782D	probably damaging	Het
Olfml3	T	A	3: 103,735,869 (GRCm38)	M399L	probably benign	Het
Olfr341	A	G	2: 36,480,047 (GRCm38)	S28P	possibly damaging	Het
Olfr453	C	A	6: 42,744,135 (GRCm38)	L33M	possibly damaging	Het
Olfr683	T	A	7: 105,143,550 (GRCm38)	I254F	probably benign	Het
Optc	A	T	1: 133,903,796 (GRCm38)		probably null	Het
Plekha6	C	A	1: 133,279,365 (GRCm38)		probably null	Het
Prelp	C	T	1: 133,915,131 (GRCm38)	R92K	probably benign	Het
Psph	T	A	5: 129,787,539 (GRCm38)		probably null	Het
Pzp	T	C	6: 128,491,161 (GRCm38)		probably null	Het
Qrich2	C	T	11: 116,448,417 (GRCm38)		probably benign	Het
Ren1	C	G	1: 133,350,778 (GRCm38)		probably null	Het
Rfwd3	A	T	8: 111,297,402 (GRCm38)	V96E	probably benign	Het
Rnf17	T	C	14: 56,493,354 (GRCm38)	V1205A	probably damaging	Het
Senp1	T	A	15: 98,075,967 (GRCm38)	T132S	probably benign	Het
Sgo2b	T	C	8: 63,927,147 (GRCm38)	R884G	probably benign	Het
Slc10a5	G	T	3: 10,335,218 (GRCm38)	D127E	probably benign	Het
Slc25a35	T	G	11: 68,968,965 (GRCm38)	S101R	possibly damaging	Het
Slc6a13	T	C	6: 121,325,041 (GRCm38)	L194P	possibly damaging	Het
Snw1	T	G	12: 87,452,703 (GRCm38)		probably benign	Het
Sort1	T	A	3: 108,351,686 (GRCm38)	F678Y	probably benign	Het
Srsf12	C	T	4: 33,225,764 (GRCm38)		probably benign	Het
Ssxa1	T	A	X: 21,119,342 (GRCm38)		probably benign	Het
Stard13	T	C	5: 151,045,168 (GRCm38)	Y879C	probably damaging	Het
Syt2	ACTCTCTCT	ACTCTCTCTCT	1: 134,746,741 (GRCm38)		probably benign	Het
Tacr3	T	C	3: 134,932,180 (GRCm38)	V366A	probably benign	Het
Tecpr1	T	A	5: 144,208,645 (GRCm38)	T595S	probably benign	Het
Tjp3	T	A	10: 81,278,054 (GRCm38)	M457L	possibly damaging	Het
Tkfc	A	G	19: 10,596,041 (GRCm38)	I279T	probably damaging	Het
Tmem98	A	G	11: 80,817,522 (GRCm38)	E106G	probably damaging	Het
Tnnt2	TG	TGG	1: 135,846,761 (GRCm38)		probably benign	Het
Trim41	C	A	11: 48,807,592 (GRCm38)	G516W	probably damaging	Het
Trove2	T	C	1: 143,760,034 (GRCm38)	D458G	probably benign	Het
Ttn	T	C	2: 76,742,517 (GRCm38)	T24265A	possibly damaging	Het
Usp37	A	G	1: 74,461,656 (GRCm38)	V582A	probably damaging	Het
Vps13b	T	A	15: 35,671,400 (GRCm38)	I1683N	probably benign	Het
Vps13d	C	T	4: 145,156,101 (GRCm38)	R968H	probably benign	Het
Vwf	C	T	6: 125,657,057 (GRCm38)	T166I	probably damaging	Het
Zfp280d	T	C	9: 72,308,005 (GRCm38)	F133L	probably damaging	Het
Zfp459	A	T	13: 67,408,276 (GRCm38)	H229Q	probably benign	Het
Zfyve26	T	A	12: 79,268,434 (GRCm38)	I1423F	possibly damaging	Het
Zmynd19	T	A	2: 24,952,636 (GRCm38)	Y15*	probably null	Het

Other mutations in Ptpro

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00334:Ptpro	APN	6	137,394,909 (GRCm38)	critical splice donor site	probably null
IGL00844:Ptpro	APN	6	137,414,239 (GRCm38)	missense	probably damaging	1.00
IGL00983:Ptpro	APN	6	137,418,248 (GRCm38)	missense	probably benign	0.01
IGL01073:Ptpro	APN	6	137,377,088 (GRCm38)	missense	probably damaging	1.00
IGL01832:Ptpro	APN	6	137,393,668 (GRCm38)	missense	possibly damaging	0.93
IGL02308:Ptpro	APN	6	137,454,700 (GRCm38)	missense	probably benign	0.37
IGL02387:Ptpro	APN	6	137,410,980 (GRCm38)	missense	probably damaging	0.96
IGL02605:Ptpro	APN	6	137,380,318 (GRCm38)	missense	probably benign	0.02
IGL02666:Ptpro	APN	6	137,378,059 (GRCm38)	missense	probably damaging	0.96
IGL03275:Ptpro	APN	6	137,450,006 (GRCm38)	missense	probably damaging	1.00
Brau	UTSW	6	137,454,598 (GRCm38)	missense	probably damaging	1.00
court	UTSW	6	137,393,675 (GRCm38)	nonsense	probably null
Hoff	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
Jester	UTSW	6	137,449,917 (GRCm38)	missense	probably damaging	1.00
mann	UTSW	6	137,411,116 (GRCm38)	splice site	probably null
R0017:Ptpro	UTSW	6	137,416,827 (GRCm38)	missense	probably benign	0.03
R0017:Ptpro	UTSW	6	137,416,827 (GRCm38)	missense	probably benign	0.03
R0020:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R0022:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R0023:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R0024:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R0094:Ptpro	UTSW	6	137,386,352 (GRCm38)	missense	probably benign	0.08
R0094:Ptpro	UTSW	6	137,386,352 (GRCm38)	missense	probably benign	0.08
R0103:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R0106:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R0316:Ptpro	UTSW	6	137,376,989 (GRCm38)	missense	possibly damaging	0.81
R0427:Ptpro	UTSW	6	137,368,296 (GRCm38)	missense	possibly damaging	0.81
R0456:Ptpro	UTSW	6	137,414,230 (GRCm38)	missense	probably benign	0.04
R0536:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R0537:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R0552:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R0555:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R0664:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R0708:Ptpro	UTSW	6	137,386,253 (GRCm38)	missense	probably benign	0.26
R0730:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R0735:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R0738:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R0786:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R0811:Ptpro	UTSW	6	137,368,079 (GRCm38)	missense	probably benign	0.00
R0812:Ptpro	UTSW	6	137,368,079 (GRCm38)	missense	probably benign	0.00
R0881:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R0973:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R1145:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R1145:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R1146:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R1146:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R1147:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R1147:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R1259:Ptpro	UTSW	6	137,392,741 (GRCm38)	missense	probably damaging	0.98
R1340:Ptpro	UTSW	6	137,441,081 (GRCm38)	missense	possibly damaging	0.95
R1381:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R1382:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R1385:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R1396:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R1401:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R1416:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R1422:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R1448:Ptpro	UTSW	6	137,441,116 (GRCm38)	missense	probably damaging	1.00
R1513:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R1518:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R1526:Ptpro	UTSW	6	137,461,726 (GRCm38)	missense	probably damaging	1.00
R1540:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R1571:Ptpro	UTSW	6	137,378,130 (GRCm38)	missense	probably benign
R1573:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R1587:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R1588:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R1649:Ptpro	UTSW	6	137,444,017 (GRCm38)	nonsense	probably null
R1700:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R1701:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R1745:Ptpro	UTSW	6	137,400,645 (GRCm38)	missense	probably benign	0.03
R1772:Ptpro	UTSW	6	137,430,743 (GRCm38)	missense	probably damaging	1.00
R1911:Ptpro	UTSW	6	137,400,619 (GRCm38)	splice site	probably benign
R1958:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R1967:Ptpro	UTSW	6	137,416,865 (GRCm38)	missense	probably benign	0.38
R2025:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R2026:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R2040:Ptpro	UTSW	6	137,386,164 (GRCm38)	splice site	probably benign
R2115:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R2117:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R2161:Ptpro	UTSW	6	137,449,887 (GRCm38)	missense	probably benign	0.01
R2431:Ptpro	UTSW	6	137,443,585 (GRCm38)	nonsense	probably null
R2915:Ptpro	UTSW	6	137,414,241 (GRCm38)	start gained	probably benign
R2988:Ptpro	UTSW	6	137,443,599 (GRCm38)	nonsense	probably null
R3772:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R3773:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R3795:Ptpro	UTSW	6	137,380,309 (GRCm38)	missense	probably benign
R3885:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R3886:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R3887:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R3888:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R3893:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R4032:Ptpro	UTSW	6	137,461,742 (GRCm38)	missense	probably damaging	1.00
R4133:Ptpro	UTSW	6	137,420,372 (GRCm38)	missense	probably damaging	1.00
R4377:Ptpro	UTSW	6	137,380,266 (GRCm38)	missense	probably benign	0.26
R4455:Ptpro	UTSW	6	137,393,659 (GRCm38)	missense	probably damaging	1.00
R4613:Ptpro	UTSW	6	137,416,836 (GRCm38)	nonsense	probably null
R4827:Ptpro	UTSW	6	137,442,710 (GRCm38)	missense	probably damaging	1.00
R4863:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R4870:Ptpro	UTSW	6	137,377,132 (GRCm38)	missense	probably damaging	0.96
R4910:Ptpro	UTSW	6	137,368,338 (GRCm38)	missense	probably damaging	0.99
R4932:Ptpro	UTSW	6	137,411,105 (GRCm38)	nonsense	probably null
R4941:Ptpro	UTSW	6	137,392,765 (GRCm38)	missense	probably damaging	1.00
R4989:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R5009:Ptpro	UTSW	6	137,377,132 (GRCm38)	missense	probably damaging	0.96
R5032:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R5033:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R5162:Ptpro	UTSW	6	137,443,594 (GRCm38)	missense	probably damaging	1.00
R5393:Ptpro	UTSW	6	137,380,224 (GRCm38)	missense	probably benign	0.04
R5423:Ptpro	UTSW	6	137,442,707 (GRCm38)	missense	probably damaging	1.00
R5782:Ptpro	UTSW	6	137,399,498 (GRCm38)	missense	possibly damaging	0.80
R6103:Ptpro	UTSW	6	137,400,706 (GRCm38)	missense	possibly damaging	0.76
R6239:Ptpro	UTSW	6	137,380,608 (GRCm38)	missense	probably benign	0.28
R6488:Ptpro	UTSW	6	137,393,675 (GRCm38)	nonsense	probably null
R6494:Ptpro	UTSW	6	137,382,642 (GRCm38)	missense	probably benign	0.20
R6746:Ptpro	UTSW	6	137,394,823 (GRCm38)	missense	probably damaging	1.00
R6763:Ptpro	UTSW	6	137,418,281 (GRCm38)	splice site	probably null
R6888:Ptpro	UTSW	6	137,380,200 (GRCm38)	missense	probably benign	0.30
R6983:Ptpro	UTSW	6	137,449,917 (GRCm38)	missense	probably damaging	1.00
R7019:Ptpro	UTSW	6	137,380,478 (GRCm38)	missense	probably benign
R7218:Ptpro	UTSW	6	137,454,598 (GRCm38)	missense	probably damaging	1.00
R7236:Ptpro	UTSW	6	137,368,337 (GRCm38)	missense	probably damaging	1.00
R7299:Ptpro	UTSW	6	137,441,144 (GRCm38)	critical splice donor site	probably null
R7381:Ptpro	UTSW	6	137,399,561 (GRCm38)	missense	possibly damaging	0.93
R7493:Ptpro	UTSW	6	137,382,649 (GRCm38)	missense	probably benign	0.01
R7733:Ptpro	UTSW	6	137,414,286 (GRCm38)	nonsense	probably null
R7793:Ptpro	UTSW	6	137,416,820 (GRCm38)	missense	probably damaging	0.99
R7804:Ptpro	UTSW	6	137,399,601 (GRCm38)	splice site	probably null
R7833:Ptpro	UTSW	6	137,416,863 (GRCm38)	nonsense	probably null
R7859:Ptpro	UTSW	6	137,392,807 (GRCm38)	critical splice donor site	probably null
R7873:Ptpro	UTSW	6	137,430,739 (GRCm38)	missense	probably benign	0.44
R8042:Ptpro	UTSW	6	137,416,883 (GRCm38)	missense	possibly damaging	0.71
R8859:Ptpro	UTSW	6	137,426,784 (GRCm38)	nonsense	probably null
R8979:Ptpro	UTSW	6	137,368,142 (GRCm38)	missense	probably benign
R9138:Ptpro	UTSW	6	137,411,115 (GRCm38)	critical splice donor site	probably null
R9309:Ptpro	UTSW	6	137,454,658 (GRCm38)	missense	probably damaging	1.00
R9420:Ptpro	UTSW	6	137,443,935 (GRCm38)	missense	probably benign	0.08
R9612:Ptpro	UTSW	6	137,414,320 (GRCm38)	missense	probably benign	0.31
R9625:Ptpro	UTSW	6	137,394,875 (GRCm38)	missense	probably damaging	1.00
R9697:Ptpro	UTSW	6	137,386,290 (GRCm38)	missense	probably damaging	1.00
R9715:Ptpro	UTSW	6	137,368,110 (GRCm38)	missense	probably damaging	0.96
Z1177:Ptpro	UTSW	6	137,378,140 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GTTACTAGTAAAAGAGTGTGTGCAC -3'
(R):5'- TCGTCATGGGCATGTCTCAC -3'

Sequencing Primer
(F):5'- ACAGGGCGTGTGTGTGTG -3'
(R):5'- ATGGGCATGTCTCACAACTACTG -3'

Posted On

2014-09-17