Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02623:Ptprt'

300977

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Ptprt

Ensembl Gene

ENSMUSG00000053141

Gene Name

protein tyrosine phosphatase, receptor type, T

Synonyms

RPTPrho

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.087) question?

Stock #

IGL02623

Quality Score

Status

Chromosome

Chromosomal Location

161521990-162661147 bp(-) (GRCm38)

Type of Mutation

splice site

DNA Base Change (assembly)

C to A at 161607452 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000105071 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000109441] [ENSMUST00000109442] [ENSMUST00000109443] [ENSMUST00000109445]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000109441

SMART Domains

Protein: ENSMUSP00000105067
Gene: ENSMUSG00000053141

Domain	Start	End	E-Value	Type
signal peptide	1	20	N/A	INTRINSIC
MAM	31	195	2.21e-71	SMART
IG	202	290	3.94e-2	SMART
FN3	292	375	3.35e-3	SMART
FN3	388	477	4.06e-2	SMART
FN3	489	579	1.2e-4	SMART
transmembrane domain	753	772	N/A	INTRINSIC
PTPc	882	1159	3.64e-129	SMART
PTPc	1188	1453	4.24e-98	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000109442

SMART Domains

Protein: ENSMUSP00000105068
Gene: ENSMUSG00000053141

Domain	Start	End	E-Value	Type
signal peptide	1	20	N/A	INTRINSIC
MAM	31	195	2.21e-71	SMART
IG	202	290	3.94e-2	SMART
FN3	292	375	3.35e-3	SMART
FN3	388	477	4.06e-2	SMART
FN3	489	579	1.2e-4	SMART
low complexity region	738	749	N/A	INTRINSIC
transmembrane domain	772	791	N/A	INTRINSIC
PTPc	901	1158	5.56e-134	SMART
PTPc	1187	1452	4.24e-98	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000109443

SMART Domains

Protein: ENSMUSP00000105069
Gene: ENSMUSG00000053141

Domain	Start	End	E-Value	Type
signal peptide	1	20	N/A	INTRINSIC
MAM	31	195	2.21e-71	SMART
IG	202	290	3.94e-2	SMART
FN3	292	375	3.35e-3	SMART
FN3	388	477	4.06e-2	SMART
FN3	489	579	1.2e-4	SMART
low complexity region	778	792	N/A	INTRINSIC
PTPc	892	1149	5.56e-134	SMART
PTPc	1178	1443	4.24e-98	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000109445

SMART Domains

Protein: ENSMUSP00000105071
Gene: ENSMUSG00000053141

Domain	Start	End	E-Value	Type
signal peptide	1	20	N/A	INTRINSIC
MAM	31	195	2.21e-71	SMART
IG	202	290	3.94e-2	SMART
FN3	292	375	3.35e-3	SMART
FN3	388	477	4.06e-2	SMART
FN3	489	579	1.2e-4	SMART
transmembrane domain	753	772	N/A	INTRINSIC
PTPc	882	1139	5.56e-134	SMART
PTPc	1168	1433	4.24e-98	SMART

Coding Region Coverage

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic transformation. This PTP possesses an extracellular region, a single transmembrane region, and two tandem intracellular catalytic domains, and thus represents a receptor-type PTP. The extracellular region contains a meprin-A5 antigen-PTP (MAM) domain, Ig-like and fibronectin type III-like repeats. The protein domain structure and the expression pattern of the mouse counterpart of this PTP suggest its roles in both signal transduction and cellular adhesion in the central nervous system. Two alternatively spliced transcript variants of this gene, which encode distinct proteins, have been reported. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele are highly susceptible to carcinogen azoxymethane-induced colon tumors. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 43 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4932438H23Rik	T	A	16: 91,056,144 (GRCm38)	I35F	probably benign	Het
Acad10	A	G	5: 121,629,930 (GRCm38)	V819A	possibly damaging	Het
Adgrd1	A	T	5: 129,132,745 (GRCm38)	N279Y	probably damaging	Het
Aplp2	C	A	9: 31,178,083 (GRCm38)		probably benign	Het
Armc8	T	C	9: 99,527,069 (GRCm38)		probably benign	Het
B3gnt5	A	G	16: 19,769,610 (GRCm38)	D193G	probably damaging	Het
Cacng1	A	G	11: 107,704,319 (GRCm38)	F144S	probably damaging	Het
Dnm3	T	A	1: 162,355,432 (GRCm38)	T105S	probably damaging	Het
Efcab6	T	A	15: 83,879,448 (GRCm38)	I1228F	probably damaging	Het
Erc2	A	G	14: 27,776,980 (GRCm38)	D271G	probably damaging	Het
Fat3	T	C	9: 15,997,137 (GRCm38)	Y2523C	probably damaging	Het
Fhl4	A	G	10: 85,098,171 (GRCm38)	F249L	probably damaging	Het
Gm17782	T	C	17: 36,162,066 (GRCm38)		probably benign	Het
Gm4787	A	G	12: 81,378,728 (GRCm38)	Y219H	probably damaging	Het
Hk1	A	G	10: 62,292,359 (GRCm38)	L328P	probably benign	Het
Hspa12a	T	A	19: 58,809,551 (GRCm38)	Y245F	probably benign	Het
Kbtbd12	T	C	6: 88,618,389 (GRCm38)	Y153C	probably damaging	Het
Kcnd2	A	T	6: 21,726,195 (GRCm38)	R562S	probably benign	Het
Lct	T	C	1: 128,308,251 (GRCm38)	S340G	probably benign	Het
Maats1	T	A	16: 38,333,778 (GRCm38)	D135V	possibly damaging	Het
Mettl25	C	A	10: 105,826,324 (GRCm38)	G262W	probably damaging	Het
Mindy3	G	A	2: 12,364,483 (GRCm38)	Q142*	probably null	Het
Olfr1045	A	T	2: 86,198,019 (GRCm38)	H244Q	probably damaging	Het
Optn	T	C	2: 5,035,022 (GRCm38)	E318G	probably damaging	Het
Pan2	T	C	10: 128,312,899 (GRCm38)	S443P	probably benign	Het
Parva	A	G	7: 112,576,439 (GRCm38)	D259G	probably damaging	Het
Pkhd1l1	T	A	15: 44,584,873 (GRCm38)	L3816Q	probably damaging	Het
Polq	T	C	16: 37,060,375 (GRCm38)	F967S	probably benign	Het
Prdm16	T	C	4: 154,340,877 (GRCm38)	N817S	probably damaging	Het
Rbbp8nl	T	A	2: 180,281,443 (GRCm38)	S154C	probably damaging	Het
Ror2	C	T	13: 53,110,728 (GRCm38)	S764N	probably damaging	Het
Slit1	T	C	19: 41,651,683 (GRCm38)	I169V	probably damaging	Het
Smyd4	G	T	11: 75,390,064 (GRCm38)		probably benign	Het
Tial1	A	G	7: 128,443,883 (GRCm38)	Y326H	probably benign	Het
Tmem198b	A	G	10: 128,802,451 (GRCm38)	L81P	probably damaging	Het
Tmem94	T	A	11: 115,796,401 (GRCm38)	C1115*	probably null	Het
Tns3	A	G	11: 8,437,141 (GRCm38)	S1349P	probably damaging	Het
Wdr38	A	T	2: 38,998,412 (GRCm38)	N7I	probably damaging	Het
Zfp106	A	T	2: 120,545,914 (GRCm38)		probably null	Het
Zfp119b	T	C	17: 55,939,793 (GRCm38)	E99G	probably damaging	Het
Zfp462	T	A	4: 55,012,986 (GRCm38)	C503S	probably damaging	Het
Zfyve19	G	A	2: 119,212,015 (GRCm38)		probably null	Het
Zxdc	G	T	6: 90,382,370 (GRCm38)	K661N	probably damaging	Het

Other mutations in Ptprt

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00231:Ptprt	APN	2	161,810,624 (GRCm38)	missense	probably benign	0.00
IGL00565:Ptprt	APN	2	161,560,191 (GRCm38)	missense	probably damaging	1.00
IGL00925:Ptprt	APN	2	161,656,163 (GRCm38)	missense	possibly damaging	0.52
IGL01344:Ptprt	APN	2	161,551,817 (GRCm38)	missense	probably damaging	1.00
IGL01432:Ptprt	APN	2	162,268,079 (GRCm38)	splice site	probably benign
IGL02008:Ptprt	APN	2	161,927,673 (GRCm38)	missense	probably benign	0.02
IGL02040:Ptprt	APN	2	162,238,072 (GRCm38)	missense	probably damaging	1.00
IGL02172:Ptprt	APN	2	161,555,502 (GRCm38)	missense	probably damaging	1.00
IGL02231:Ptprt	APN	2	162,278,046 (GRCm38)	critical splice donor site	probably null
IGL02231:Ptprt	APN	2	162,238,060 (GRCm38)	missense	probably damaging	1.00
IGL02232:Ptprt	APN	2	161,530,517 (GRCm38)	missense	probably damaging	0.96
IGL02277:Ptprt	APN	2	161,547,381 (GRCm38)	missense	probably damaging	1.00
IGL02447:Ptprt	APN	2	162,278,107 (GRCm38)	missense	probably benign	0.01
IGL02601:Ptprt	APN	2	161,766,307 (GRCm38)	missense	probably benign	0.10
IGL03379:Ptprt	APN	2	161,555,459 (GRCm38)	nonsense	probably null
Poverina	UTSW	2	161,901,497 (GRCm38)	missense	possibly damaging	0.70
IGL03055:Ptprt	UTSW	2	161,533,613 (GRCm38)	missense	probably damaging	0.96
R0064:Ptprt	UTSW	2	161,927,791 (GRCm38)	splice site	probably benign
R0129:Ptprt	UTSW	2	162,278,070 (GRCm38)	missense	probably benign	0.35
R0131:Ptprt	UTSW	2	162,278,110 (GRCm38)	missense	probably benign	0.00
R0131:Ptprt	UTSW	2	162,278,110 (GRCm38)	missense	probably benign	0.00
R0132:Ptprt	UTSW	2	162,278,110 (GRCm38)	missense	probably benign	0.00
R0316:Ptprt	UTSW	2	161,607,319 (GRCm38)	missense	probably damaging	1.00
R0454:Ptprt	UTSW	2	161,553,822 (GRCm38)	missense	probably damaging	0.96
R0488:Ptprt	UTSW	2	161,553,825 (GRCm38)	missense	probably damaging	0.99
R0573:Ptprt	UTSW	2	161,551,748 (GRCm38)	missense	probably damaging	1.00
R0614:Ptprt	UTSW	2	161,812,120 (GRCm38)	missense	possibly damaging	0.59
R0834:Ptprt	UTSW	2	161,812,139 (GRCm38)	splice site	probably null
R1023:Ptprt	UTSW	2	161,558,943 (GRCm38)	missense	probably damaging	1.00
R1184:Ptprt	UTSW	2	161,927,772 (GRCm38)	missense	possibly damaging	0.82
R1253:Ptprt	UTSW	2	162,278,226 (GRCm38)	missense	probably damaging	1.00
R1476:Ptprt	UTSW	2	161,927,484 (GRCm38)	missense	probably damaging	1.00
R1515:Ptprt	UTSW	2	162,238,034 (GRCm38)	missense	probably damaging	1.00
R1595:Ptprt	UTSW	2	161,810,549 (GRCm38)	critical splice donor site	probably null
R1939:Ptprt	UTSW	2	161,927,640 (GRCm38)	missense	probably benign	0.45
R1987:Ptprt	UTSW	2	161,766,321 (GRCm38)	missense	possibly damaging	0.48
R1987:Ptprt	UTSW	2	161,558,898 (GRCm38)	missense	probably damaging	1.00
R2049:Ptprt	UTSW	2	161,534,545 (GRCm38)	missense	probably damaging	1.00
R2140:Ptprt	UTSW	2	161,811,988 (GRCm38)	missense	probably damaging	1.00
R2421:Ptprt	UTSW	2	162,278,040 (GRCm38)	splice site	probably benign
R3432:Ptprt	UTSW	2	161,927,529 (GRCm38)	missense	probably damaging	1.00
R3619:Ptprt	UTSW	2	161,566,157 (GRCm38)	missense	probably damaging	1.00
R3757:Ptprt	UTSW	2	161,812,030 (GRCm38)	missense	probably damaging	1.00
R3758:Ptprt	UTSW	2	161,812,030 (GRCm38)	missense	probably damaging	1.00
R3834:Ptprt	UTSW	2	161,547,387 (GRCm38)	missense	probably damaging	1.00
R3835:Ptprt	UTSW	2	161,547,387 (GRCm38)	missense	probably damaging	1.00
R3915:Ptprt	UTSW	2	161,555,555 (GRCm38)	splice site	probably benign
R4003:Ptprt	UTSW	2	161,566,117 (GRCm38)	splice site	probably benign
R4387:Ptprt	UTSW	2	161,927,650 (GRCm38)	missense	probably damaging	1.00
R4519:Ptprt	UTSW	2	161,564,689 (GRCm38)	missense	probably damaging	1.00
R4618:Ptprt	UTSW	2	161,553,845 (GRCm38)	missense	probably damaging	1.00
R4677:Ptprt	UTSW	2	161,901,446 (GRCm38)	critical splice donor site	probably null
R4866:Ptprt	UTSW	2	161,560,239 (GRCm38)	missense	probably damaging	1.00
R5088:Ptprt	UTSW	2	162,238,175 (GRCm38)	missense	probably benign	0.01
R5173:Ptprt	UTSW	2	161,927,756 (GRCm38)	missense	probably benign	0.01
R5215:Ptprt	UTSW	2	162,278,164 (GRCm38)	missense	probably damaging	1.00
R5383:Ptprt	UTSW	2	161,698,049 (GRCm38)	missense	probably damaging	1.00
R5398:Ptprt	UTSW	2	161,927,592 (GRCm38)	missense	probably damaging	1.00
R5518:Ptprt	UTSW	2	162,278,223 (GRCm38)	missense	probably damaging	0.99
R5711:Ptprt	UTSW	2	161,810,604 (GRCm38)	missense	probably damaging	0.98
R5735:Ptprt	UTSW	2	161,534,564 (GRCm38)	missense	probably damaging	0.98
R5834:Ptprt	UTSW	2	161,560,269 (GRCm38)	missense	probably damaging	1.00
R5872:Ptprt	UTSW	2	162,135,218 (GRCm38)	missense	probably damaging	1.00
R5926:Ptprt	UTSW	2	161,564,686 (GRCm38)	missense	probably benign	0.00
R6210:Ptprt	UTSW	2	162,268,029 (GRCm38)	missense	probably damaging	1.00
R6285:Ptprt	UTSW	2	161,901,497 (GRCm38)	missense	possibly damaging	0.70
R6298:Ptprt	UTSW	2	161,553,859 (GRCm38)	missense	probably damaging	1.00
R6406:Ptprt	UTSW	2	161,553,783 (GRCm38)	missense	probably damaging	0.98
R6499:Ptprt	UTSW	2	161,534,587 (GRCm38)	missense	probably benign	0.32
R6613:Ptprt	UTSW	2	161,530,447 (GRCm38)	missense	probably damaging	1.00
R6622:Ptprt	UTSW	2	161,553,840 (GRCm38)	missense	probably damaging	1.00
R7218:Ptprt	UTSW	2	161,547,364 (GRCm38)	missense	probably damaging	1.00
R7247:Ptprt	UTSW	2	161,533,523 (GRCm38)	missense	probably benign	0.15
R7576:Ptprt	UTSW	2	161,607,305 (GRCm38)	missense	possibly damaging	0.88
R7733:Ptprt	UTSW	2	161,575,787 (GRCm38)	missense	probably damaging	1.00
R7735:Ptprt	UTSW	2	161,575,741 (GRCm38)	missense	probably damaging	1.00
R7813:Ptprt	UTSW	2	161,530,493 (GRCm38)	missense	probably damaging	1.00
R8031:Ptprt	UTSW	2	162,135,457 (GRCm38)	missense	probably damaging	1.00
R8074:Ptprt	UTSW	2	161,927,661 (GRCm38)	missense	possibly damaging	0.77
R8151:Ptprt	UTSW	2	162,278,085 (GRCm38)	missense	probably damaging	1.00
R8236:Ptprt	UTSW	2	161,687,068 (GRCm38)	critical splice donor site	probably null
R8308:Ptprt	UTSW	2	161,927,646 (GRCm38)	missense	probably benign	0.00
R8348:Ptprt	UTSW	2	161,558,886 (GRCm38)	missense	probably damaging	1.00
R8362:Ptprt	UTSW	2	161,551,747 (GRCm38)	missense	probably damaging	1.00
R8365:Ptprt	UTSW	2	161,901,531 (GRCm38)	missense	probably benign	0.05
R8448:Ptprt	UTSW	2	161,558,886 (GRCm38)	missense	probably damaging	1.00
R8512:Ptprt	UTSW	2	161,558,863 (GRCm38)	missense	probably benign	0.00
R8715:Ptprt	UTSW	2	161,530,543 (GRCm38)	missense	probably damaging	1.00
R9004:Ptprt	UTSW	2	161,766,394 (GRCm38)	missense	probably benign	0.04
R9046:Ptprt	UTSW	2	161,530,441 (GRCm38)	missense	possibly damaging	0.58
R9222:Ptprt	UTSW	2	161,560,186 (GRCm38)	missense	probably damaging	1.00
R9297:Ptprt	UTSW	2	161,575,778 (GRCm38)	missense	probably benign
R9318:Ptprt	UTSW	2	161,575,778 (GRCm38)	missense	probably benign
R9476:Ptprt	UTSW	2	161,555,461 (GRCm38)	missense	probably damaging	1.00
R9510:Ptprt	UTSW	2	161,555,461 (GRCm38)	missense	probably damaging	1.00
R9571:Ptprt	UTSW	2	161,553,812 (GRCm38)	missense	probably benign	0.10
X0064:Ptprt	UTSW	2	161,927,483 (GRCm38)	missense	probably damaging	1.00
Z1088:Ptprt	UTSW	2	162,238,121 (GRCm38)	missense	possibly damaging	0.86
Z1177:Ptprt	UTSW	2	162,362,948 (GRCm38)	missense	possibly damaging	0.77
Z1177:Ptprt	UTSW	2	161,732,887 (GRCm38)	missense	probably damaging	1.00

Posted On

2015-04-16