Mutagenetix > Incidental Mutation

Incidental Mutation 'R7650:Prex2'

590727

Institutional Source

Beutler Lab

Gene Symbol

Prex2

Ensembl Gene

ENSMUSG00000048960

Gene Name

phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 2

Synonyms

C030045D06Rik, 6230420N16Rik, Depdc2

MMRRC Submission

045727-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.220) question?

Stock #

R7650 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

10993465-11303681 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 11149854 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Threonine at position 683 (I683T)

Ref Sequence

ENSEMBL: ENSMUSP00000027056 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000027056]

AlphaFold

Q3LAC4

Predicted Effect

possibly damaging
Transcript: ENSMUST00000027056
AA Change: I683T

PolyPhen 2 Score 0.665 (Sensitivity: 0.86; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000027056
Gene: ENSMUSG00000048960
AA Change: I683T

Domain	Start	End	E-Value	Type
RhoGEF	19	205	8.61e-45	SMART
PH	238	355	2.43e-12	SMART
DEP	383	456	4.46e-26	SMART
DEP	484	557	6.57e-15	SMART
PDZ	593	666	9.62e-2	SMART
PDZ	677	744	6.37e-8	SMART
low complexity region	1112	1127	N/A	INTRINSIC
low complexity region	1498	1507	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.9%

Validation Efficiency

100% (80/80)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs to the phosphatidylinositol 3,4,5-trisphosphate (PIP3)-dependent Rac exchanger (PREX) family, which are Dbl-type guanine-nucleotide exchange factors for Rac family small G proteins. Structural domains of this protein include the catalytic diffuse B-cell lymphoma homology and pleckstrin homology (DHPH) domain, two disheveled, EGL-10, and pleckstrin homology (DEP) domains, two PDZ domains, and a C-terminal inositol polyphosphate-4 phosphatase (IP4P) domain that is found in one of the isoforms. This protein facilitates the exchange of GDP for GTP on Rac1, allowing the GTP-bound Rac1 to activate downstream effectors. Studies also show that the pleckstrin homology domain of this protein interacts with the phosphatase and tensin homolog (PTEN) gene product to inhibit PTEN phosphatase activity, thus activating the phosphoinositide-3 kinase (PI3K) signaling pathway. Conversely, the PTEN gene product has also been shown to inhibit the GEF activity of this protein. This gene plays a role in insulin-signaling pathways, and either mutations or overexpression of this gene have been observed in some cancers. [provided by RefSeq, Apr 2016]
PHENOTYPE: Mice homozygous for gene trapped alleles may exhibit abnormal Purkinje cell dendrite morphology, a mild motor coordination defect that progressively worsens with age, hypoactivity, impaired glucose tolerance and/or insulin resistance. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 81 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2200002J24Rik	G	A	7: 30,699,789 (GRCm38)	V3I	probably benign	Het
Adam33	T	C	2: 131,061,147 (GRCm38)	E59G	probably damaging	Het
Akap13	T	A	7: 75,643,454 (GRCm38)	V45E	probably benign	Het
Ap1s1	A	G	5: 137,045,533 (GRCm38)	S28P	probably benign	Het
Btnl2	T	C	17: 34,358,129 (GRCm38)	L86P	probably damaging	Het
Carm1	G	A	9: 21,580,372 (GRCm38)	V246I	probably benign	Het
Cdk5rap1	C	T	2: 154,354,116 (GRCm38)	D283N	probably benign	Het
Cfap58	C	A	19: 47,986,528 (GRCm38)	N709K	possibly damaging	Het
Col24a1	A	G	3: 145,314,453 (GRCm38)	D195G	probably benign	Het
Dcaf1	A	G	9: 106,838,344 (GRCm38)	D220G	probably benign	Het
Ddias	C	T	7: 92,858,935 (GRCm38)	G591R	probably benign	Het
Defb22	A	T	2: 152,486,103 (GRCm38)	I54K	probably benign	Het
Dennd4b	G	A	3: 90,268,749 (GRCm38)	W202*	probably null	Het
F2	T	C	2: 91,628,396 (GRCm38)	N523S	possibly damaging	Het
Fam186a	A	G	15: 99,939,907 (GRCm38)	Y2819H	unknown	Het
Fanca	A	T	8: 123,268,564 (GRCm38)		probably null	Het
Fezf2	T	C	14: 12,342,653 (GRCm38)	H404R	probably damaging	Het
Fry	A	G	5: 150,413,418 (GRCm38)	N1418S	probably damaging	Het
Gak	A	G	5: 108,584,295 (GRCm38)	S776P	probably benign	Het
Gbf1	A	G	19: 46,272,539 (GRCm38)	H1181R	probably damaging	Het
Gdf9	G	A	11: 53,437,098 (GRCm38)	E294K	probably benign	Het
Gje1	G	A	10: 14,716,424 (GRCm38)	R205*	probably null	Het
Gm8206	T	C	14: 6,055,211 (GRCm38)		probably null	Het
Gpr162	T	A	6: 124,861,843 (GRCm38)		probably benign	Het
Gxylt1	C	T	15: 93,245,658 (GRCm38)	R363H	probably benign	Het
Hnrnph1	A	T	11: 50,383,899 (GRCm38)	M396L	probably benign	Het
Ice1	T	A	13: 70,605,483 (GRCm38)	Q828L	probably damaging	Het
Ice1	A	G	13: 70,589,797 (GRCm38)	V2177A	possibly damaging	Het
Ift56	T	A	6: 38,395,040 (GRCm38)	N188K	probably benign	Het
Il10	A	T	1: 131,021,455 (GRCm38)	T118S	probably benign	Het
Itpr2	C	T	6: 146,233,994 (GRCm38)	R1813Q	probably benign	Het
Kbtbd12	T	A	6: 88,618,548 (GRCm38)	Q100L	probably damaging	Het
Kin	A	G	2: 10,092,168 (GRCm38)	D276G	possibly damaging	Het
Klhl1	T	C	14: 96,346,943 (GRCm38)	T284A	probably damaging	Het
Kmt2d	C	T	15: 98,850,870 (GRCm38)	A2858T	unknown	Het
Krt8	G	A	15: 102,004,163 (GRCm38)	T26M	probably benign	Het
Lama3	T	A	18: 12,537,838 (GRCm38)	M827K	probably benign	Het
Lingo3	T	C	10: 80,835,763 (GRCm38)	N111S	probably damaging	Het
Megf10	GGCAGCAACAGCACCAGCAGCAACAGCACCAGCAGCA	GGCAGCAACAGCACCAGCAGCA	18: 57,293,999 (GRCm38)		probably benign	Het
Metap1	A	G	3: 138,466,367 (GRCm38)	V263A	probably damaging	Het
Msantd5	G	A	11: 51,234,786 (GRCm38)	E179K	possibly damaging	Het
Muc5ac	A	G	7: 141,809,422 (GRCm38)	T2157A	unknown	Het
Myo1d	G	T	11: 80,601,684 (GRCm38)	H748Q	probably benign	Het
Nfkbiz	A	T	16: 55,817,839 (GRCm38)	N419K	probably benign	Het
Nol10	T	C	12: 17,362,682 (GRCm38)		probably null	Het
Nrcam	T	C	12: 44,547,322 (GRCm38)	L284P	probably damaging	Het
Nrp1	T	A	8: 128,498,014 (GRCm38)	W753R	possibly damaging	Het
Obscn	A	G	11: 59,060,994 (GRCm38)	S3978P	probably benign	Het
Opa3	C	A	7: 19,244,971 (GRCm38)	N120K	probably benign	Het
Or5k17	T	A	16: 58,926,053 (GRCm38)	R173*	probably null	Het
Or8g53	A	T	9: 39,771,873 (GRCm38)	F309Y	probably benign	Het
Pabpc1l	T	C	2: 164,049,590 (GRCm38)	L576S	probably benign	Het
Panx3	A	G	9: 37,661,405 (GRCm38)	L283S	probably damaging	Het
Pcdhb4	T	A	18: 37,309,614 (GRCm38)	V659E	probably damaging	Het
Pde4dip	A	T	3: 97,699,107 (GRCm38)		probably null	Het
Pkd1l3	T	C	8: 109,672,585 (GRCm38)	V2200A	probably benign	Het
Pkp3	G	A	7: 141,082,370 (GRCm38)	M112I	probably benign	Het
Psg22	C	A	7: 18,726,759 (GRCm38)	Q438K	possibly damaging	Het
Ptgir	T	C	7: 16,906,951 (GRCm38)	V56A	possibly damaging	Het
Pus7	G	T	5: 23,760,246 (GRCm38)	T304K	probably damaging	Het
Rab38	T	C	7: 88,430,429 (GRCm38)	Y10H	possibly damaging	Het
Ros1	C	T	10: 52,046,209 (GRCm38)	G2277D	probably benign	Het
Rpain	A	T	11: 70,970,445 (GRCm38)		probably benign	Het
Shh	C	A	5: 28,458,306 (GRCm38)	S288I	probably benign	Het
Slc26a5	C	T	5: 21,834,330 (GRCm38)	V259M	possibly damaging	Het
Slc4a7	G	A	14: 14,773,348 (GRCm38)	E773K	probably benign	Het
Slit1	T	A	19: 41,629,924 (GRCm38)	N771I	probably damaging	Het
Stim1	T	A	7: 102,428,827 (GRCm38)	S179T		Het
Syk	A	G	13: 52,611,095 (GRCm38)	D86G	probably benign	Het
Tmem132b	T	G	5: 125,787,010 (GRCm38)	S727A	probably benign	Het
Trim42	T	A	9: 97,363,148 (GRCm38)	Y533F	probably benign	Het
Trpm6	A	T	19: 18,876,013 (GRCm38)	D1799V	possibly damaging	Het
Ube4a	A	T	9: 44,933,436 (GRCm38)	I839N	probably damaging	Het
Ugt2b36	A	G	5: 87,080,972 (GRCm38)	I404T	probably damaging	Het
Ushbp1	T	A	8: 71,390,924 (GRCm38)	Q290L	possibly damaging	Het
Vcl	T	A	14: 20,995,046 (GRCm38)	I273K	probably damaging	Het
Vmn2r73	T	A	7: 85,871,939 (GRCm38)	I274L	probably benign	Het
Zc3h7b	A	G	15: 81,793,650 (GRCm38)	D945G	possibly damaging	Het
Zfp454	A	G	11: 50,883,753 (GRCm38)	L31P	probably damaging	Het
Zfp536	C	A	7: 37,569,692 (GRCm38)	V100L	probably damaging	Het
Zfp942	A	T	17: 21,928,837 (GRCm38)	S270R	probably benign	Het

Other mutations in Prex2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00497:Prex2	APN	1	11,186,652 (GRCm38)	missense	possibly damaging	0.51
IGL00948:Prex2	APN	1	11,170,614 (GRCm38)	missense	probably damaging	0.98
IGL01087:Prex2	APN	1	11,068,104 (GRCm38)	missense	probably benign	0.00
IGL01490:Prex2	APN	1	11,184,545 (GRCm38)	splice site	probably null
IGL01533:Prex2	APN	1	11,186,741 (GRCm38)	nonsense	probably null
IGL01661:Prex2	APN	1	11,208,614 (GRCm38)	missense	probably benign	0.01
IGL01668:Prex2	APN	1	11,153,645 (GRCm38)	missense	probably benign	0.00
IGL01674:Prex2	APN	1	11,170,741 (GRCm38)	missense	probably damaging	1.00
IGL01716:Prex2	APN	1	11,266,054 (GRCm38)	missense	probably benign	0.04
IGL01867:Prex2	APN	1	11,098,503 (GRCm38)	missense	probably benign	0.11
IGL01954:Prex2	APN	1	11,140,011 (GRCm38)	missense	possibly damaging	0.75
IGL01990:Prex2	APN	1	11,123,233 (GRCm38)	splice site	probably benign
IGL02022:Prex2	APN	1	11,297,739 (GRCm38)	missense	probably benign	0.04
IGL02130:Prex2	APN	1	11,160,162 (GRCm38)	missense	probably damaging	1.00
IGL02130:Prex2	APN	1	11,112,799 (GRCm38)	missense	probably damaging	1.00
IGL02221:Prex2	APN	1	11,061,345 (GRCm38)	missense	probably benign	0.00
IGL02369:Prex2	APN	1	11,101,169 (GRCm38)	critical splice donor site	probably null
IGL02440:Prex2	APN	1	11,153,657 (GRCm38)	missense	possibly damaging	0.94
IGL02477:Prex2	APN	1	11,204,154 (GRCm38)	missense	probably benign
IGL02492:Prex2	APN	1	11,123,845 (GRCm38)	missense	possibly damaging	0.93
IGL03051:Prex2	APN	1	11,142,665 (GRCm38)	missense	probably damaging	1.00
IGL03154:Prex2	APN	1	11,153,633 (GRCm38)	missense	possibly damaging	0.63
IGL03158:Prex2	APN	1	11,266,067 (GRCm38)	missense	possibly damaging	0.89
IGL03308:Prex2	APN	1	11,185,175 (GRCm38)	missense	possibly damaging	0.89
IGL03338:Prex2	APN	1	11,140,265 (GRCm38)	missense	probably benign	0.01
R0042:Prex2	UTSW	1	11,080,081 (GRCm38)	missense	probably damaging	1.00
R0052:Prex2	UTSW	1	11,160,156 (GRCm38)	missense	probably damaging	1.00
R0052:Prex2	UTSW	1	11,160,156 (GRCm38)	missense	probably damaging	1.00
R0138:Prex2	UTSW	1	11,285,043 (GRCm38)	splice site	probably benign
R0206:Prex2	UTSW	1	11,285,144 (GRCm38)	missense	probably damaging	1.00
R0206:Prex2	UTSW	1	11,285,144 (GRCm38)	missense	probably damaging	1.00
R0208:Prex2	UTSW	1	11,285,144 (GRCm38)	missense	probably damaging	1.00
R0325:Prex2	UTSW	1	11,200,057 (GRCm38)	splice site	probably null
R0326:Prex2	UTSW	1	11,285,065 (GRCm38)	missense	probably damaging	1.00
R0390:Prex2	UTSW	1	11,089,706 (GRCm38)	splice site	probably null
R0492:Prex2	UTSW	1	11,186,633 (GRCm38)	splice site	probably benign
R0512:Prex2	UTSW	1	11,199,933 (GRCm38)	missense	probably benign
R0515:Prex2	UTSW	1	11,199,874 (GRCm38)	missense	probably damaging	0.99
R0894:Prex2	UTSW	1	11,181,898 (GRCm38)	missense	probably benign
R1259:Prex2	UTSW	1	11,289,270 (GRCm38)	missense	probably damaging	1.00
R1332:Prex2	UTSW	1	11,204,091 (GRCm38)	missense	probably damaging	1.00
R1356:Prex2	UTSW	1	11,080,092 (GRCm38)	nonsense	probably null
R1451:Prex2	UTSW	1	11,156,259 (GRCm38)	missense	probably benign	0.01
R1488:Prex2	UTSW	1	11,193,528 (GRCm38)	missense	probably benign	0.05
R1512:Prex2	UTSW	1	11,061,330 (GRCm38)	missense	possibly damaging	0.64
R1641:Prex2	UTSW	1	11,231,772 (GRCm38)	missense	probably damaging	0.99
R1667:Prex2	UTSW	1	11,186,757 (GRCm38)	missense	probably benign
R1678:Prex2	UTSW	1	11,285,089 (GRCm38)	missense	possibly damaging	0.51
R1736:Prex2	UTSW	1	11,089,884 (GRCm38)	splice site	probably benign
R1781:Prex2	UTSW	1	11,199,955 (GRCm38)	missense	probably benign	0.17
R1804:Prex2	UTSW	1	11,132,342 (GRCm38)	missense	probably damaging	1.00
R1836:Prex2	UTSW	1	11,136,780 (GRCm38)	missense	probably damaging	1.00
R1899:Prex2	UTSW	1	11,162,366 (GRCm38)	nonsense	probably null
R1900:Prex2	UTSW	1	11,162,366 (GRCm38)	nonsense	probably null
R2020:Prex2	UTSW	1	11,162,312 (GRCm38)	missense	probably damaging	0.98
R2114:Prex2	UTSW	1	11,186,713 (GRCm38)	missense	probably damaging	1.00
R2117:Prex2	UTSW	1	11,186,713 (GRCm38)	missense	probably damaging	1.00
R2436:Prex2	UTSW	1	11,266,152 (GRCm38)	missense	possibly damaging	0.90
R2902:Prex2	UTSW	1	11,208,614 (GRCm38)	missense	possibly damaging	0.77
R2915:Prex2	UTSW	1	11,169,853 (GRCm38)	missense	probably damaging	1.00
R2924:Prex2	UTSW	1	11,098,487 (GRCm38)	missense	probably damaging	1.00
R2981:Prex2	UTSW	1	11,181,962 (GRCm38)	missense	probably damaging	1.00
R3430:Prex2	UTSW	1	11,149,854 (GRCm38)	missense	possibly damaging	0.88
R3832:Prex2	UTSW	1	11,156,364 (GRCm38)	splice site	probably benign
R3870:Prex2	UTSW	1	11,160,192 (GRCm38)	missense	possibly damaging	0.86
R3963:Prex2	UTSW	1	11,110,357 (GRCm38)	missense	possibly damaging	0.93
R4012:Prex2	UTSW	1	11,184,516 (GRCm38)	missense	probably benign
R4030:Prex2	UTSW	1	11,208,568 (GRCm38)	missense	probably benign	0.06
R4214:Prex2	UTSW	1	11,101,159 (GRCm38)	missense	probably damaging	1.00
R4214:Prex2	UTSW	1	11,285,061 (GRCm38)	missense	probably damaging	1.00
R4242:Prex2	UTSW	1	11,156,304 (GRCm38)	missense	probably benign	0.06
R4490:Prex2	UTSW	1	11,162,263 (GRCm38)	missense	probably benign	0.05
R4491:Prex2	UTSW	1	11,162,263 (GRCm38)	missense	probably benign	0.05
R4492:Prex2	UTSW	1	11,162,263 (GRCm38)	missense	probably benign	0.05
R4561:Prex2	UTSW	1	11,184,545 (GRCm38)	splice site	probably null
R4624:Prex2	UTSW	1	11,289,265 (GRCm38)	nonsense	probably null
R4647:Prex2	UTSW	1	11,162,285 (GRCm38)	missense	probably damaging	1.00
R4657:Prex2	UTSW	1	11,065,825 (GRCm38)	missense	probably benign	0.00
R4706:Prex2	UTSW	1	11,199,988 (GRCm38)	missense	probably damaging	1.00
R4806:Prex2	UTSW	1	11,068,020 (GRCm38)	missense	probably damaging	1.00
R4900:Prex2	UTSW	1	11,149,905 (GRCm38)	splice site	probably benign
R4922:Prex2	UTSW	1	11,169,940 (GRCm38)	missense	probably damaging	1.00
R4961:Prex2	UTSW	1	11,098,481 (GRCm38)	missense	possibly damaging	0.75
R5284:Prex2	UTSW	1	11,266,090 (GRCm38)	nonsense	probably null
R5305:Prex2	UTSW	1	11,107,678 (GRCm38)	missense	probably damaging	1.00
R5307:Prex2	UTSW	1	11,200,032 (GRCm38)	missense	probably damaging	0.99
R5331:Prex2	UTSW	1	11,140,011 (GRCm38)	missense	possibly damaging	0.75
R5385:Prex2	UTSW	1	11,139,980 (GRCm38)	missense	probably damaging	0.99
R5574:Prex2	UTSW	1	11,140,058 (GRCm38)	missense	probably damaging	1.00
R5979:Prex2	UTSW	1	11,132,372 (GRCm38)	missense	probably damaging	1.00
R6076:Prex2	UTSW	1	11,185,950 (GRCm38)	missense	probably benign	0.09
R6160:Prex2	UTSW	1	10,993,851 (GRCm38)	missense	probably damaging	1.00
R6177:Prex2	UTSW	1	11,136,777 (GRCm38)	missense	possibly damaging	0.49
R6221:Prex2	UTSW	1	11,266,012 (GRCm38)	missense	probably benign	0.01
R6293:Prex2	UTSW	1	11,162,298 (GRCm38)	missense	probably benign
R6335:Prex2	UTSW	1	11,110,320 (GRCm38)	missense	probably benign	0.13
R6401:Prex2	UTSW	1	11,186,727 (GRCm38)	missense	probably benign	0.00
R6427:Prex2	UTSW	1	11,182,031 (GRCm38)	missense	probably damaging	1.00
R6467:Prex2	UTSW	1	11,266,035 (GRCm38)	missense	probably damaging	1.00
R6564:Prex2	UTSW	1	11,101,061 (GRCm38)	splice site	probably null
R6734:Prex2	UTSW	1	11,080,059 (GRCm38)	missense	probably damaging	1.00
R6753:Prex2	UTSW	1	11,184,456 (GRCm38)	missense	probably damaging	0.98
R6880:Prex2	UTSW	1	11,132,384 (GRCm38)	missense	probably damaging	1.00
R6973:Prex2	UTSW	1	11,112,743 (GRCm38)	missense	probably damaging	1.00
R6980:Prex2	UTSW	1	11,162,263 (GRCm38)	missense	probably benign	0.05
R6987:Prex2	UTSW	1	11,170,752 (GRCm38)	missense	probably damaging	0.99
R7085:Prex2	UTSW	1	11,098,588 (GRCm38)	missense	possibly damaging	0.73
R7101:Prex2	UTSW	1	11,153,609 (GRCm38)	missense	possibly damaging	0.86
R7106:Prex2	UTSW	1	11,136,793 (GRCm38)	missense	probably benign	0.33
R7319:Prex2	UTSW	1	11,162,308 (GRCm38)	missense	probably benign	0.10
R7342:Prex2	UTSW	1	11,162,325 (GRCm38)	missense	probably benign	0.00
R7469:Prex2	UTSW	1	11,285,069 (GRCm38)	missense	probably damaging	1.00
R7528:Prex2	UTSW	1	11,204,092 (GRCm38)	missense	probably damaging	1.00
R7592:Prex2	UTSW	1	11,123,213 (GRCm38)	missense	probably damaging	1.00
R7695:Prex2	UTSW	1	11,162,273 (GRCm38)	missense	probably benign	0.00
R7720:Prex2	UTSW	1	11,181,937 (GRCm38)	missense	possibly damaging	0.47
R7733:Prex2	UTSW	1	11,181,959 (GRCm38)	missense	probably benign	0.31
R7859:Prex2	UTSW	1	11,080,050 (GRCm38)	missense	probably damaging	1.00
R8247:Prex2	UTSW	1	11,199,970 (GRCm38)	missense	probably benign
R8300:Prex2	UTSW	1	11,231,718 (GRCm38)	missense	possibly damaging	0.49
R8345:Prex2	UTSW	1	11,199,894 (GRCm38)	missense	possibly damaging	0.65
R8352:Prex2	UTSW	1	11,285,140 (GRCm38)	missense	probably benign
R8352:Prex2	UTSW	1	11,285,139 (GRCm38)	missense	probably benign
R8410:Prex2	UTSW	1	11,153,657 (GRCm38)	missense	possibly damaging	0.94
R8452:Prex2	UTSW	1	11,285,140 (GRCm38)	missense	probably benign
R8452:Prex2	UTSW	1	11,285,139 (GRCm38)	missense	probably benign
R8885:Prex2	UTSW	1	11,170,575 (GRCm38)	splice site	probably benign
R8926:Prex2	UTSW	1	11,089,706 (GRCm38)	splice site	probably null
R8968:Prex2	UTSW	1	11,110,338 (GRCm38)	nonsense	probably null
R9049:Prex2	UTSW	1	11,185,906 (GRCm38)	missense	probably damaging	0.98
R9398:Prex2	UTSW	1	11,136,804 (GRCm38)	missense	probably benign	0.00
R9452:Prex2	UTSW	1	11,185,927 (GRCm38)	missense	probably benign	0.01
R9549:Prex2	UTSW	1	11,186,691 (GRCm38)	missense	probably damaging	1.00
RF005:Prex2	UTSW	1	11,185,166 (GRCm38)	missense	possibly damaging	0.47
Z1177:Prex2	UTSW	1	11,289,252 (GRCm38)	critical splice acceptor site	probably null

Predicted Primers

PCR Primer
(F):5'- TTTACATCCTGTTGAGGGCCC -3'
(R):5'- CCAAAGATTTTCCTGGAGTACACC -3'

Sequencing Primer
(F):5'- TTGAGGGCCCTGAGCTGTC -3'
(R):5'- AGAAAGGTCTCACTCTTGCCTGAG -3'

Posted On

2019-10-24