Mutagenetix > Incidental Mutation

Incidental Mutation 'R7548:Prr5'

584342

Institutional Source

Beutler Lab

Gene Symbol

Prr5

Ensembl Gene

ENSMUSG00000036106

Gene Name

proline rich 5 (renal)

Synonyms

Protor-1, C030017C09Rik

MMRRC Submission

045619-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.106) question?

Stock #

R7548 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

84553821-84587874 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 84641259 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Proline to Glutamine at position 175 (P175Q)

Ref Sequence

ENSEMBL: ENSMUSP00000130977 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000006029] [ENSMUST00000168811] [ENSMUST00000172307]

AlphaFold

Q812A5

Predicted Effect

possibly damaging
Transcript: ENSMUST00000006029
AA Change: P175Q

PolyPhen 2 Score 0.765 (Sensitivity: 0.85; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000006029
Gene: ENSMUSG00000078954
AA Change: P175Q

Domain	Start	End	E-Value	Type
SEC14	14	165	1.48e-26	SMART
low complexity region	174	192	N/A	INTRINSIC
RhoGAP	207	378	2.93e-55	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000168811
AA Change: P175Q

PolyPhen 2 Score 0.765 (Sensitivity: 0.85; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000130977
Gene: ENSMUSG00000078954
AA Change: P175Q

Domain	Start	End	E-Value	Type
SEC14	14	165	1.48e-26	SMART
low complexity region	174	192	N/A	INTRINSIC
RhoGAP	207	378	2.93e-55	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000172307
AA Change: P175Q

PolyPhen 2 Score 0.765 (Sensitivity: 0.85; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000132008
Gene: ENSMUSG00000078954
AA Change: P175Q

Domain	Start	End	E-Value	Type
SEC14	14	165	1.48e-26	SMART
low complexity region	174	192	N/A	INTRINSIC
RhoGAP	207	378	2.93e-55	SMART

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.2%

Validation Efficiency

100% (71/71)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein with a proline-rich domain. This gene is located in a region of chromosome 22 reported to contain a tumor suppressor gene that may be involved in breast and colorectal tumorigenesis. The protein is a component of the mammalian target of rapamycin complex 2 (mTORC2), and it regulates platelet-derived growth factor (PDGF) receptor beta expression and PDGF signaling to Akt and S6K1. Alternative splicing and the use of alternative promoters results in transcripts encoding different isoforms. Read-through transcripts from this gene into the downstream Rho GTPase activating protein 8 (ARHGAP8) gene also exist, which led to the original description of PRR5 and ARHGAP8 being a single gene. [provided by RefSeq, Nov 2010]

Allele List at MGI

Other mutations in this stock

Total: 72 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930519G04Rik	G	A	5: 115,016,059 (GRCm39)	S146N	possibly damaging	Het
Acr	T	C	15: 89,458,596 (GRCm39)	S426P	possibly damaging	Het
Arl6ip1	A	T	7: 117,725,733 (GRCm39)	I59N	probably damaging	Het
Atp2b4	A	T	1: 133,629,379 (GRCm39)	*81K	probably null	Het
Atp8a1	T	A	5: 67,973,071 (GRCm39)	R26*	probably null	Het
Atp8b4	T	A	2: 126,231,262 (GRCm39)	Q453L	probably benign	Het
B4galt4	A	G	16: 38,574,428 (GRCm39)	E134G	probably damaging	Het
Bcl9	G	A	3: 97,113,209 (GRCm39)	T1082I	probably damaging	Het
Catsperg2	A	G	7: 29,409,251 (GRCm39)	F617L	probably benign	Het
Ccdc15	T	C	9: 37,188,723 (GRCm39)	N800S	probably benign	Het
Cd300ld	T	C	11: 114,878,248 (GRCm39)	D88G	probably benign	Het
Ceacam2	A	T	7: 25,229,958 (GRCm39)	V216E	probably benign	Het
Cecr2	T	A	6: 120,738,675 (GRCm39)	M356K		Het
Cenpm	T	C	15: 82,128,880 (GRCm39)	M1V	probably null	Het
Ces2e	A	G	8: 105,658,538 (GRCm39)	E401G	probably benign	Het
Cib3	C	A	8: 72,961,041 (GRCm39)	L65F	probably damaging	Het
Clip4	C	G	17: 72,096,963 (GRCm39)	T29R	probably benign	Het
Cnot7	A	G	8: 40,953,874 (GRCm39)	I131T	probably damaging	Het
Cntn5	A	T	9: 9,673,415 (GRCm39)		probably null	Het
Col11a1	A	C	3: 113,917,409 (GRCm39)	H732P	unknown	Het
Coq4	A	T	2: 29,685,420 (GRCm39)	T145S	possibly damaging	Het
Cwf19l1	T	C	19: 44,098,989 (GRCm39)	D527G	probably benign	Het
Cyp3a25	T	C	5: 145,923,735 (GRCm39)	I303V	probably damaging	Het
Dab2	C	T	15: 6,459,399 (GRCm39)	T437I	possibly damaging	Het
Dlc1	A	G	8: 37,051,809 (GRCm39)	S190P	probably benign	Het
Dnah6	G	A	6: 73,004,423 (GRCm39)	L3847F	probably damaging	Het
Dnmbp	T	C	19: 43,877,838 (GRCm39)	E411G	probably benign	Het
Dpp8	T	C	9: 64,944,517 (GRCm39)	Y95H	probably damaging	Het
Emb	T	A	13: 117,408,590 (GRCm39)	D310E	possibly damaging	Het
Eml4	C	A	17: 83,732,766 (GRCm39)	Q140K	probably benign	Het
Epb41l3	T	C	17: 69,517,271 (GRCm39)	S100P	probably damaging	Het
Fat4	A	T	3: 39,035,263 (GRCm39)	T2972S	probably benign	Het
Fignl2	T	C	15: 100,951,079 (GRCm39)	E401G	unknown	Het
Fryl	T	A	5: 73,349,105 (GRCm39)	D19V	unknown	Het
Gck	C	T	11: 5,852,040 (GRCm39)	G16R		Het
Gm3371	T	C	14: 44,648,145 (GRCm39)	M1V	probably null	Het
Hlcs	T	A	16: 93,933,876 (GRCm39)	K661*	probably null	Het
Il17re	C	G	6: 113,443,348 (GRCm39)	P363A	probably damaging	Het
Kif24	C	T	4: 41,423,601 (GRCm39)	E217K	possibly damaging	Het
Klhdc7b	T	C	15: 89,272,907 (GRCm39)	I605T	probably damaging	Het
Krt31	T	C	11: 99,940,346 (GRCm39)	T170A	probably damaging	Het
Lgals3bp	T	C	11: 118,287,669 (GRCm39)	D126G	probably benign	Het
Lig1	T	A	7: 13,035,344 (GRCm39)	F601Y	possibly damaging	Het
Lrp6	A	G	6: 134,484,471 (GRCm39)	I384T	probably damaging	Het
Mfap5	A	T	6: 122,502,993 (GRCm39)	T102S	probably benign	Het
Mfsd6	A	G	1: 52,702,446 (GRCm39)	F600S	possibly damaging	Het
Nlrp4a	G	A	7: 26,149,604 (GRCm39)	E404K	probably damaging	Het
Nme3	T	C	17: 25,115,522 (GRCm39)	L12P	probably damaging	Het
Nxpe5	A	T	5: 138,249,493 (GRCm39)	T428S	probably benign	Het
Or1e26	G	A	11: 73,479,802 (GRCm39)	T254I	possibly damaging	Het
Or4c122	T	C	2: 89,079,430 (GRCm39)	T191A	probably benign	Het
Psmc6	T	C	14: 45,572,375 (GRCm39)	Y110H	probably benign	Het
Pthlh	T	A	6: 147,158,653 (GRCm39)	R102S	possibly damaging	Het
Ric8b	G	T	10: 84,783,736 (GRCm39)	S198I	probably damaging	Het
Rrp7a	C	A	15: 83,001,871 (GRCm39)	R212S	possibly damaging	Het
Rubcnl	T	C	14: 75,279,792 (GRCm39)	Y392H	probably benign	Het
Sag	G	A	1: 87,772,638 (GRCm39)	V369I	probably benign	Het
Sar1b	A	G	11: 51,680,094 (GRCm39)	E140G	probably benign	Het
Sema3d	T	A	5: 12,627,783 (GRCm39)	M658K	unknown	Het
Skor2	C	T	18: 76,948,600 (GRCm39)	S774F	possibly damaging	Het
Slc1a6	G	T	10: 78,650,265 (GRCm39)	R501L	probably damaging	Het
Spata31d1b	A	G	13: 59,864,468 (GRCm39)	M539V	probably benign	Het
Spocd1	T	C	4: 129,823,602 (GRCm39)	L133P		Het
Sptlc1	A	T	13: 53,521,968 (GRCm39)	N96K	possibly damaging	Het
Stox1	A	T	10: 62,501,946 (GRCm39)	S205T	probably damaging	Het
Tec	T	C	5: 72,917,693 (GRCm39)	M509V	probably damaging	Het
Tmem161b	C	A	13: 84,370,537 (GRCm39)		probably benign	Het
Ttc34	T	A	4: 154,940,816 (GRCm39)	L499Q	probably damaging	Het
Uqcc1	A	G	2: 155,751,309 (GRCm39)	C120R	probably damaging	Het
Usp39	C	T	6: 72,321,996 (GRCm39)	S46N	possibly damaging	Het
Zbtb5	T	C	4: 44,994,724 (GRCm39)	E220G	probably benign	Het
Zfp287	A	T	11: 62,604,701 (GRCm39)	C735*	probably null	Het

Other mutations in Prr5

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01023:Prr5	APN	15	84,583,856 (GRCm39)	missense	possibly damaging	0.47
IGL01790:Prr5	APN	15	84,651,415 (GRCm39)	missense	possibly damaging	0.87
IGL01950:Prr5	APN	15	84,650,550 (GRCm39)	missense	probably benign	0.33
IGL02156:Prr5	APN	15	84,654,236 (GRCm39)	missense	possibly damaging	0.87
IGL02656:Prr5	APN	15	84,583,337 (GRCm39)	missense	probably damaging	1.00
IGL03102:Prr5	APN	15	84,650,508 (GRCm39)	splice site	probably benign
R0234:Prr5	UTSW	15	84,587,322 (GRCm39)	missense	probably damaging	1.00
R0234:Prr5	UTSW	15	84,587,322 (GRCm39)	missense	probably damaging	1.00
R0389:Prr5	UTSW	15	84,587,152 (GRCm39)	missense	probably benign	0.00
R0514:Prr5	UTSW	15	84,586,967 (GRCm39)	missense	probably benign	0.19
R1414:Prr5	UTSW	15	84,583,912 (GRCm39)	nonsense	probably null
R2027:Prr5	UTSW	15	84,585,580 (GRCm39)	missense	probably damaging	0.99
R2230:Prr5	UTSW	15	84,586,981 (GRCm39)	missense	probably benign	0.15
R2231:Prr5	UTSW	15	84,586,981 (GRCm39)	missense	probably benign	0.15
R2232:Prr5	UTSW	15	84,586,981 (GRCm39)	missense	probably benign	0.15
R3003:Prr5	UTSW	15	84,656,031 (GRCm39)	missense	probably damaging	0.99
R3498:Prr5	UTSW	15	84,587,345 (GRCm39)	missense	probably benign	0.12
R3791:Prr5	UTSW	15	84,565,417 (GRCm39)	missense	probably damaging	1.00
R3910:Prr5	UTSW	15	84,587,345 (GRCm39)	missense	probably benign	0.12
R4562:Prr5	UTSW	15	84,626,114 (GRCm39)	missense	probably damaging	0.99
R4866:Prr5	UTSW	15	84,626,105 (GRCm39)	missense	probably damaging	1.00
R4867:Prr5	UTSW	15	84,624,967 (GRCm39)	missense	probably benign	0.17
R5514:Prr5	UTSW	15	84,587,096 (GRCm39)	missense	probably benign	0.01
R5620:Prr5	UTSW	15	84,640,570 (GRCm39)	missense	probably benign	0.09
R5793:Prr5	UTSW	15	84,656,223 (GRCm39)	missense	probably benign
R5905:Prr5	UTSW	15	84,626,178 (GRCm39)	missense	possibly damaging	0.53
R5911:Prr5	UTSW	15	84,585,635 (GRCm39)	nonsense	probably null
R6033:Prr5	UTSW	15	84,626,126 (GRCm39)	missense	probably damaging	1.00
R6033:Prr5	UTSW	15	84,626,126 (GRCm39)	missense	probably damaging	1.00
R6085:Prr5	UTSW	15	84,572,106 (GRCm39)	missense	probably damaging	1.00
R6187:Prr5	UTSW	15	84,577,973 (GRCm39)	missense	probably damaging	1.00
R6394:Prr5	UTSW	15	84,583,925 (GRCm39)	missense	probably damaging	0.99
R6422:Prr5	UTSW	15	84,578,005 (GRCm39)	missense	probably damaging	1.00
R6631:Prr5	UTSW	15	84,586,978 (GRCm39)	missense	probably damaging	0.99
R7212:Prr5	UTSW	15	84,629,993 (GRCm39)	missense	probably null	0.99
R7614:Prr5	UTSW	15	84,641,276 (GRCm39)	missense	probably benign	0.44
R7822:Prr5	UTSW	15	84,649,933 (GRCm39)	missense	probably damaging	1.00
R8113:Prr5	UTSW	15	84,577,993 (GRCm39)	missense	probably damaging	1.00
R8268:Prr5	UTSW	15	84,587,192 (GRCm39)	missense	probably benign	0.02
R8328:Prr5	UTSW	15	84,587,387 (GRCm39)	makesense	probably null
R8488:Prr5	UTSW	15	84,578,005 (GRCm39)	missense	probably damaging	1.00
R8874:Prr5	UTSW	15	84,583,916 (GRCm39)	missense	probably damaging	1.00
R9058:Prr5	UTSW	15	84,641,241 (GRCm39)	missense	probably benign	0.00
R9317:Prr5	UTSW	15	84,583,324 (GRCm39)	nonsense	probably null
R9456:Prr5	UTSW	15	84,585,682 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- TCACTTCTCTCTGAGGATGCG -3'
(R):5'- GGGACTTGAACCTTTATCTCTCCTG -3'

Sequencing Primer
(F):5'- CCGGGATGCCTGAAACTTACAG -3'
(R):5'- GAACCTTTATCTCTCCTGTAGGCAG -3'

Posted On

2019-10-17