Mutagenetix > Incidental Mutation

Incidental Mutation 'R6019:Stab2'

478805

Institutional Source

Beutler Lab

Gene Symbol

Stab2

Ensembl Gene

ENSMUSG00000035459

Gene Name

stabilin 2

Synonyms

STAB-2, FEEL-2

MMRRC Submission

044193-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R6019 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

86841198-87008025 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 87003022 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 60 (V60A)

Ref Sequence

ENSEMBL: ENSMUSP00000048309 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000035288]

AlphaFold

Q8R4U0

Predicted Effect

probably benign
Transcript: ENSMUST00000035288
AA Change: V60A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000048309
Gene: ENSMUSG00000035459
AA Change: V60A

Domain	Start	End	E-Value	Type
signal peptide	1	27	N/A	INTRINSIC
EGF	119	156	1.85e0	SMART
EGF	167	201	2.43e1	SMART
EGF	206	244	1.43e-1	SMART
EGF	248	284	3.82e-2	SMART
EGF	333	370	2.02e-1	SMART
FAS1	414	515	1.06e-8	SMART
FAS1	561	662	3.54e-19	SMART
EGF	746	783	6.76e-3	SMART
EGF	836	873	1.31e0	SMART
EGF	877	917	2.99e-4	SMART
EGF	921	960	3.51e-1	SMART
EGF	964	1002	1.99e0	SMART
FAS1	1038	1138	1.73e-13	SMART
FAS1	1181	1276	1.83e-12	SMART
EGF	1354	1391	6.92e0	SMART
EGF	1401	1435	1.11e1	SMART
EGF	1442	1477	3.01e0	SMART
EGF	1481	1519	1.64e-1	SMART
EGF	1523	1561	1.14e0	SMART
EGF	1565	1603	5.62e0	SMART
FAS1	1638	1734	2.23e-25	SMART
FAS1	1785	1891	6.92e-22	SMART
EGF	1966	2006	1.95e1	SMART
EGF_like	1977	2017	2.46e-1	SMART
EGF	2016	2050	1.14e0	SMART
EGF	2058	2089	1.56e1	SMART
EGF	2093	2130	1.36e1	SMART
EGF	2134	2173	2.13e0	SMART
LINK	2204	2298	2.08e-29	SMART
FAS1	2363	2455	3.19e-12	SMART
transmembrane domain	2467	2489	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000099390

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000160532

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000162837

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000163045

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000218366

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000219280

Meta Mutation Damage Score

0.1322

Coding Region Coverage

1x: 99.9%
3x: 99.4%
10x: 97.2%
20x: 91.1%

Validation Efficiency

96% (81/84)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a large, transmembrane receptor protein which may function in angiogenesis, lymphocyte homing, cell adhesion, or receptor scavenging. The protein contains 7 fasciclin, 15 epidermal growth factor (EGF)-like, and 2 laminin-type EGF-like domains as well as a C-type lectin-like hyaluronan-binding Link module. The protein is primarily expressed on sinusoidal endothelial cells of liver, spleen, and lymph node. The receptor has been shown to bind and endocytose ligands such as hyaluronan, low density lipoprotein, Gram-positive and Gram-negative bacteria, and advanced glycosylation end products. Supporting its possible role as a scavenger receptor, the protein has been shown to cycle between the plasma membrane and lysosomes. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for knock-out alleles exhibit no gross abnormaities. Mice homozygous for one null allele display elevated serum hyaluronic acid levels and decreased metastasis. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 83 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcf3	C	T	16: 20,552,451 (GRCm38)	H436Y	possibly damaging	Het
Acad10	A	T	5: 121,634,801 (GRCm38)	H472Q	possibly damaging	Het
Ano8	G	A	8: 71,482,380 (GRCm38)	R393C	probably damaging	Het
Arhgap18	T	A	10: 26,860,650 (GRCm38)	V163E	probably damaging	Het
AW209491	C	T	13: 14,637,780 (GRCm38)	A406V	probably benign	Het
Brix1	C	T	15: 10,476,589 (GRCm38)	R267H	probably benign	Het
Cacng5	T	C	11: 107,884,388 (GRCm38)	M52V	probably benign	Het
Casz1	T	C	4: 148,947,038 (GRCm38)	C1249R	probably damaging	Het
Cenpj	C	T	14: 56,534,815 (GRCm38)	S1086N	probably benign	Het
Chil1	T	C	1: 134,189,572 (GRCm38)	F367S	probably benign	Het
Copg2	A	T	6: 30,810,933 (GRCm38)	I610N	possibly damaging	Het
Cpa6	T	C	1: 10,595,643 (GRCm38)	K57E	possibly damaging	Het
D5Ertd579e	C	T	5: 36,629,692 (GRCm38)	A111T	possibly damaging	Het
Dgat2	A	G	7: 99,154,631 (GRCm38)	M361T	probably benign	Het
Dnm3	G	T	1: 162,134,501 (GRCm38)	F46L	probably damaging	Het
Dph7	T	A	2: 24,963,540 (GRCm38)	C122*	probably null	Het
Dspp	A	T	5: 104,178,039 (GRCm38)	D756V	unknown	Het
Ep300	T	A	15: 81,641,382 (GRCm38)	M1469K	unknown	Het
Fsip2	T	C	2: 82,987,939 (GRCm38)	I4672T	possibly damaging	Het
Gapdh	A	T	6: 125,163,033 (GRCm38)	L67*	probably null	Het
Gm11639	T	C	11: 105,042,902 (GRCm38)		probably null	Het
Gm14025	T	C	2: 129,037,690 (GRCm38)	Q772R	probably benign	Het
Gm21994	T	A	2: 150,255,212 (GRCm38)	H99L	probably damaging	Het
Gm3259	G	A	5: 95,340,213 (GRCm38)	S2N	probably damaging	Het
Gm9495	A	T	8: 69,429,314 (GRCm38)	C337S	probably benign	Het
Gpr75	A	G	11: 30,891,640 (GRCm38)	R182G	probably benign	Het
Gsr	G	T	8: 33,693,807 (GRCm38)	A366S	probably damaging	Het
Gypc	A	G	18: 32,530,195 (GRCm38)	I33T	probably damaging	Het
Hapln1	A	G	13: 89,608,100 (GRCm38)	D341G	probably benign	Het
Hnrnpd	A	G	5: 99,967,236 (GRCm38)	S148P	probably benign	Het
Hydin	A	T	8: 110,566,620 (GRCm38)	T3450S	probably benign	Het
Kif20b	T	C	19: 34,950,464 (GRCm38)	V1002A	probably benign	Het
Kif5c	T	C	2: 49,735,509 (GRCm38)	V597A	probably benign	Het
Kntc1	A	G	5: 123,762,516 (GRCm38)	T226A	probably benign	Het
Krt75	C	A	15: 101,573,723 (GRCm38)	V37L	probably benign	Het
L3mbtl2	A	G	15: 81,686,942 (GRCm38)	I668V	probably benign	Het
Lrp1b	G	A	2: 41,302,970 (GRCm38)	A480V	probably damaging	Het
Lrp1b	T	A	2: 41,476,809 (GRCm38)	D485V	probably damaging	Het
Lrrc37a	T	C	11: 103,456,596 (GRCm38)	H3091R	unknown	Het
Msi1	A	G	5: 115,451,491 (GRCm38)	Y361C	probably damaging	Het
Mtus1	G	T	8: 41,083,040 (GRCm38)	N546K	probably benign	Het
Mup17	T	A	4: 61,593,699 (GRCm38)	T113S	probably benign	Het
Myh11	T	A	16: 14,206,074 (GRCm38)	D1479V	probably damaging	Het
Ncor1	C	T	11: 62,373,161 (GRCm38)	E198K	probably benign	Het
Nrde2	A	G	12: 100,132,242 (GRCm38)	V722A	probably benign	Het
Olfr206	C	T	16: 59,345,435 (GRCm38)	D89N	possibly damaging	Het
Olfr564	C	T	7: 102,804,284 (GRCm38)	R269*	probably null	Het
Olfr61	T	C	7: 140,638,012 (GRCm38)	F104L	probably benign	Het
Otog	A	G	7: 46,288,950 (GRCm38)	M2028V	probably benign	Het
Paox	T	A	7: 140,131,742 (GRCm38)	V169E	probably damaging	Het
Pcsk9	T	G	4: 106,456,876 (GRCm38)	D174A	probably benign	Het
Pde4b	A	G	4: 102,570,769 (GRCm38)	E41G	possibly damaging	Het
Pip4k2c	A	G	10: 127,199,074 (GRCm38)	I419T	probably damaging	Het
Plekhg3	G	T	12: 76,577,941 (GRCm38)	E1186*	probably null	Het
Pole	C	T	5: 110,324,515 (GRCm38)	P1548L	probably benign	Het
Pole	C	A	5: 110,324,514 (GRCm38)	P1548T	probably benign	Het
Polq	A	G	16: 37,061,764 (GRCm38)	E1430G	probably damaging	Het
Ptgr2	T	C	12: 84,298,146 (GRCm38)	S98P	probably damaging	Het
Ralgapa1	A	G	12: 55,684,042 (GRCm38)	Y1903H	possibly damaging	Het
Rasgrp1	T	C	2: 117,291,895 (GRCm38)	D338G	probably damaging	Het
Rif1	C	G	2: 52,095,844 (GRCm38)	L614V	probably damaging	Het
Rnase13	C	T	14: 51,922,403 (GRCm38)	C93Y	probably damaging	Het
Rnd2	C	T	11: 101,468,999 (GRCm38)	L57F	probably damaging	Het
S100z	T	A	13: 95,477,426 (GRCm38)	M59L	probably benign	Het
Ska1	T	A	18: 74,199,921 (GRCm38)	D142V	probably benign	Het
Slc16a3	T	C	11: 120,957,105 (GRCm38)		probably null	Het
Snd1	T	C	6: 28,880,234 (GRCm38)	V669A	probably benign	Het
Snrpd3	A	T	10: 75,532,195 (GRCm38)	T49S	probably damaging	Het
Sort1	T	C	3: 108,357,233 (GRCm38)	L856P	possibly damaging	Het
Srek1ip1	T	A	13: 104,834,322 (GRCm38)		probably null	Het
Ssrp1	T	C	2: 85,045,452 (GRCm38)	S552P	probably damaging	Het
Stard9	GCCC	GCC	2: 120,693,715 (GRCm38)		probably null	Het
Tll1	A	C	8: 64,041,491 (GRCm38)	H743Q	possibly damaging	Het
Tpo	G	T	12: 30,094,981 (GRCm38)	R590S	possibly damaging	Het
Trbv12-1	A	T	6: 41,113,846 (GRCm38)	T51S	probably benign	Het
Trbv30	C	T	6: 41,281,774 (GRCm38)	A40V	probably benign	Het
Tulp4	T	A	17: 6,233,215 (GRCm38)	V1173E	possibly damaging	Het
Upk1a	A	T	7: 30,612,385 (GRCm38)		probably null	Het
Vmn1r199	A	G	13: 22,382,599 (GRCm38)	D21G	possibly damaging	Het
Vmn2r7	T	C	3: 64,716,222 (GRCm38)	T317A	probably damaging	Het
Wdfy3	A	G	5: 101,849,423 (GRCm38)	V3112A	probably damaging	Het
Zbtb8os	T	C	4: 129,340,749 (GRCm38)	V40A	possibly damaging	Het
Zwint	A	G	10: 72,656,853 (GRCm38)	K108E	possibly damaging	Het

Other mutations in Stab2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00091:Stab2	APN	10	86,869,206 (GRCm38)	splice site	probably null
IGL00809:Stab2	APN	10	86,848,174 (GRCm38)	splice site	probably benign
IGL00911:Stab2	APN	10	86,969,753 (GRCm38)	missense	probably damaging	1.00
IGL01347:Stab2	APN	10	86,901,703 (GRCm38)	splice site	probably null
IGL01411:Stab2	APN	10	86,980,008 (GRCm38)	splice site	probably benign
IGL01503:Stab2	APN	10	86,940,613 (GRCm38)	splice site	probably benign
IGL01599:Stab2	APN	10	86,922,895 (GRCm38)	missense	probably damaging	1.00
IGL01635:Stab2	APN	10	86,981,128 (GRCm38)	missense	probably benign	0.04
IGL01640:Stab2	APN	10	86,954,171 (GRCm38)	missense	probably benign	0.09
IGL01671:Stab2	APN	10	86,969,277 (GRCm38)	missense	possibly damaging	0.80
IGL02023:Stab2	APN	10	86,871,831 (GRCm38)	missense	possibly damaging	0.67
IGL02075:Stab2	APN	10	86,967,650 (GRCm38)	missense	possibly damaging	0.71
IGL02174:Stab2	APN	10	86,859,742 (GRCm38)	splice site	probably null
IGL02600:Stab2	APN	10	86,954,259 (GRCm38)	missense	probably damaging	1.00
IGL02666:Stab2	APN	10	86,850,902 (GRCm38)	missense	possibly damaging	0.67
IGL02668:Stab2	APN	10	86,846,163 (GRCm38)	splice site	probably benign
IGL02709:Stab2	APN	10	86,846,165 (GRCm38)	splice site	probably benign
IGL02728:Stab2	APN	10	86,856,556 (GRCm38)	missense	possibly damaging	0.95
IGL02803:Stab2	APN	10	86,950,269 (GRCm38)	splice site	probably benign
IGL02938:Stab2	APN	10	86,871,921 (GRCm38)	missense	possibly damaging	0.77
IGL03033:Stab2	APN	10	86,996,803 (GRCm38)	critical splice donor site	probably null
IGL03238:Stab2	APN	10	86,855,121 (GRCm38)	missense	probably damaging	1.00
IGL03402:Stab2	APN	10	86,969,301 (GRCm38)	missense	probably benign	0.03
prospector	UTSW	10	86,901,567 (GRCm38)	splice site	probably null
songbird	UTSW	10	86,858,152 (GRCm38)	missense	probably damaging	1.00
3-1:Stab2	UTSW	10	86,869,177 (GRCm38)	missense	probably damaging	0.96
F6893:Stab2	UTSW	10	86,855,171 (GRCm38)	missense	probably damaging	1.00
K7371:Stab2	UTSW	10	86,943,289 (GRCm38)	critical splice donor site	probably null
PIT4142001:Stab2	UTSW	10	86,867,175 (GRCm38)	missense	possibly damaging	0.94
PIT4362001:Stab2	UTSW	10	86,861,435 (GRCm38)	nonsense	probably null
R0015:Stab2	UTSW	10	86,843,617 (GRCm38)	missense	probably benign
R0254:Stab2	UTSW	10	86,897,960 (GRCm38)	missense	probably benign
R0310:Stab2	UTSW	10	86,967,613 (GRCm38)	splice site	probably benign
R0333:Stab2	UTSW	10	86,841,627 (GRCm38)	missense	probably benign
R0391:Stab2	UTSW	10	86,947,144 (GRCm38)	missense	probably benign	0.27
R0400:Stab2	UTSW	10	86,872,610 (GRCm38)	missense	probably damaging	1.00
R0433:Stab2	UTSW	10	86,843,491 (GRCm38)	splice site	probably benign
R0440:Stab2	UTSW	10	86,949,928 (GRCm38)	missense	probably benign	0.23
R0743:Stab2	UTSW	10	86,887,895 (GRCm38)	missense	probably damaging	1.00
R0847:Stab2	UTSW	10	86,969,871 (GRCm38)	missense	probably benign	0.00
R0883:Stab2	UTSW	10	86,924,450 (GRCm38)	splice site	probably benign
R1078:Stab2	UTSW	10	86,907,133 (GRCm38)	splice site	probably null
R1118:Stab2	UTSW	10	86,885,718 (GRCm38)	splice site	probably null
R1119:Stab2	UTSW	10	86,859,755 (GRCm38)	missense	possibly damaging	0.51
R1179:Stab2	UTSW	10	86,950,301 (GRCm38)	missense	probably damaging	0.98
R1440:Stab2	UTSW	10	86,861,367 (GRCm38)	splice site	probably null
R1550:Stab2	UTSW	10	86,878,926 (GRCm38)	missense	probably benign	0.01
R1616:Stab2	UTSW	10	86,885,718 (GRCm38)	splice site	probably null
R1728:Stab2	UTSW	10	86,938,039 (GRCm38)	missense	probably benign	0.41
R1768:Stab2	UTSW	10	87,003,008 (GRCm38)	missense	probably damaging	1.00
R1772:Stab2	UTSW	10	86,954,234 (GRCm38)	missense	probably benign	0.06
R1776:Stab2	UTSW	10	86,957,816 (GRCm38)	missense	possibly damaging	0.92
R1784:Stab2	UTSW	10	86,938,039 (GRCm38)	missense	probably benign	0.41
R1892:Stab2	UTSW	10	86,938,049 (GRCm38)	missense	probably damaging	0.99
R1957:Stab2	UTSW	10	86,861,470 (GRCm38)	missense	probably benign	0.13
R1972:Stab2	UTSW	10	86,960,316 (GRCm38)	missense	probably damaging	0.99
R1975:Stab2	UTSW	10	86,896,496 (GRCm38)	critical splice donor site	probably null
R1976:Stab2	UTSW	10	86,896,496 (GRCm38)	critical splice donor site	probably null
R1996:Stab2	UTSW	10	87,003,031 (GRCm38)	missense	probably damaging	1.00
R2085:Stab2	UTSW	10	86,954,159 (GRCm38)	missense	probably damaging	1.00
R2149:Stab2	UTSW	10	86,865,040 (GRCm38)	nonsense	probably null
R2169:Stab2	UTSW	10	86,887,862 (GRCm38)	missense	probably damaging	1.00
R2201:Stab2	UTSW	10	86,940,639 (GRCm38)	missense	probably benign	0.22
R2296:Stab2	UTSW	10	86,954,474 (GRCm38)	critical splice acceptor site	probably null
R2297:Stab2	UTSW	10	86,954,474 (GRCm38)	critical splice acceptor site	probably null
R2298:Stab2	UTSW	10	86,954,474 (GRCm38)	critical splice acceptor site	probably null
R2326:Stab2	UTSW	10	86,954,474 (GRCm38)	critical splice acceptor site	probably null
R2434:Stab2	UTSW	10	86,969,319 (GRCm38)	missense	possibly damaging	0.78
R2519:Stab2	UTSW	10	86,934,840 (GRCm38)	splice site	probably benign
R2696:Stab2	UTSW	10	86,861,499 (GRCm38)	missense	probably benign	0.45
R2883:Stab2	UTSW	10	86,967,686 (GRCm38)	missense	possibly damaging	0.92
R2923:Stab2	UTSW	10	86,861,461 (GRCm38)	missense	probably damaging	1.00
R3711:Stab2	UTSW	10	86,866,708 (GRCm38)	missense	probably damaging	1.00
R3787:Stab2	UTSW	10	86,969,277 (GRCm38)	missense	possibly damaging	0.50
R3834:Stab2	UTSW	10	86,949,912 (GRCm38)	missense	possibly damaging	0.87
R3970:Stab2	UTSW	10	86,878,886 (GRCm38)	missense	probably damaging	0.97
R3979:Stab2	UTSW	10	86,863,456 (GRCm38)	missense	possibly damaging	0.56
R4003:Stab2	UTSW	10	86,858,124 (GRCm38)	missense	probably damaging	1.00
R4088:Stab2	UTSW	10	86,922,185 (GRCm38)	missense	probably damaging	1.00
R4151:Stab2	UTSW	10	87,002,983 (GRCm38)	missense	probably benign	0.12
R4190:Stab2	UTSW	10	86,878,944 (GRCm38)	missense	probably damaging	0.98
R4556:Stab2	UTSW	10	86,967,679 (GRCm38)	missense	possibly damaging	0.95
R4773:Stab2	UTSW	10	86,907,371 (GRCm38)	nonsense	probably null
R4825:Stab2	UTSW	10	86,947,147 (GRCm38)	missense	probably benign	0.08
R4865:Stab2	UTSW	10	86,843,500 (GRCm38)	splice site	probably null
R4871:Stab2	UTSW	10	86,942,235 (GRCm38)	missense	probably damaging	0.99
R4943:Stab2	UTSW	10	86,954,162 (GRCm38)	missense	probably damaging	0.99
R4981:Stab2	UTSW	10	86,960,223 (GRCm38)	missense	probably benign
R4994:Stab2	UTSW	10	86,949,907 (GRCm38)	missense	probably benign
R4999:Stab2	UTSW	10	86,937,909 (GRCm38)	missense	probably damaging	0.97
R5061:Stab2	UTSW	10	86,907,385 (GRCm38)	missense	probably damaging	1.00
R5072:Stab2	UTSW	10	86,863,558 (GRCm38)	missense	probably benign	0.23
R5073:Stab2	UTSW	10	86,863,558 (GRCm38)	missense	probably benign	0.23
R5074:Stab2	UTSW	10	86,863,558 (GRCm38)	missense	probably benign	0.23
R5134:Stab2	UTSW	10	86,871,810 (GRCm38)	splice site	probably null
R5213:Stab2	UTSW	10	86,907,197 (GRCm38)	missense	probably damaging	0.99
R5508:Stab2	UTSW	10	86,960,279 (GRCm38)	missense	probably benign	0.01
R5530:Stab2	UTSW	10	86,947,162 (GRCm38)	missense	probably benign	0.04
R5540:Stab2	UTSW	10	86,848,125 (GRCm38)	missense	probably benign	0.30
R5839:Stab2	UTSW	10	86,872,691 (GRCm38)	missense	probably damaging	0.97
R5949:Stab2	UTSW	10	86,969,849 (GRCm38)	missense	possibly damaging	0.87
R6015:Stab2	UTSW	10	86,938,042 (GRCm38)	missense	probably damaging	0.99
R6116:Stab2	UTSW	10	86,907,190 (GRCm38)	missense	probably damaging	1.00
R6131:Stab2	UTSW	10	86,883,778 (GRCm38)	splice site	probably null
R6209:Stab2	UTSW	10	86,923,003 (GRCm38)	missense	possibly damaging	0.94
R6243:Stab2	UTSW	10	86,907,161 (GRCm38)	missense	probably damaging	1.00
R6433:Stab2	UTSW	10	86,901,567 (GRCm38)	splice site	probably null
R6787:Stab2	UTSW	10	86,919,084 (GRCm38)	missense	probably benign	0.07
R6841:Stab2	UTSW	10	86,942,190 (GRCm38)	missense	probably damaging	1.00
R6873:Stab2	UTSW	10	86,861,366 (GRCm38)	critical splice donor site	probably null
R7025:Stab2	UTSW	10	86,850,837 (GRCm38)	missense	probably damaging	1.00
R7043:Stab2	UTSW	10	86,870,246 (GRCm38)	missense	probably damaging	0.99
R7047:Stab2	UTSW	10	86,858,152 (GRCm38)	missense	probably damaging	1.00
R7107:Stab2	UTSW	10	86,905,592 (GRCm38)	missense	possibly damaging	0.96
R7214:Stab2	UTSW	10	86,899,841 (GRCm38)	missense	probably damaging	0.99
R7271:Stab2	UTSW	10	87,003,108 (GRCm38)	splice site	probably null
R7291:Stab2	UTSW	10	86,946,220 (GRCm38)	missense	probably damaging	0.96
R7336:Stab2	UTSW	10	86,969,185 (GRCm38)	nonsense	probably null
R7432:Stab2	UTSW	10	86,885,683 (GRCm38)	missense	probably damaging	0.99
R7580:Stab2	UTSW	10	86,869,164 (GRCm38)	missense	probably benign	0.00
R7622:Stab2	UTSW	10	86,873,902 (GRCm38)	missense	possibly damaging	0.65
R7629:Stab2	UTSW	10	86,883,782 (GRCm38)	critical splice donor site	probably null
R7658:Stab2	UTSW	10	86,981,135 (GRCm38)	missense	probably benign	0.12
R7798:Stab2	UTSW	10	86,957,912 (GRCm38)	missense	probably damaging	0.98
R7835:Stab2	UTSW	10	86,872,619 (GRCm38)	missense	probably benign	0.06
R7845:Stab2	UTSW	10	86,996,894 (GRCm38)	missense	probably benign	0.09
R7863:Stab2	UTSW	10	86,972,881 (GRCm38)	missense	probably benign	0.30
R7885:Stab2	UTSW	10	86,878,912 (GRCm38)	missense	probably benign	0.03
R7904:Stab2	UTSW	10	86,954,192 (GRCm38)	nonsense	probably null
R7947:Stab2	UTSW	10	86,846,033 (GRCm38)	missense	probably benign	0.31
R7963:Stab2	UTSW	10	86,848,023 (GRCm38)	critical splice donor site	probably null
R8014:Stab2	UTSW	10	86,850,903 (GRCm38)	missense	possibly damaging	0.78
R8021:Stab2	UTSW	10	86,905,539 (GRCm38)	missense	possibly damaging	0.69
R8024:Stab2	UTSW	10	86,846,052 (GRCm38)	missense	probably benign	0.34
R8097:Stab2	UTSW	10	86,869,095 (GRCm38)	missense	possibly damaging	0.86
R8281:Stab2	UTSW	10	86,873,864 (GRCm38)	missense	probably damaging	0.98
R8462:Stab2	UTSW	10	86,967,734 (GRCm38)	missense	possibly damaging	0.79
R8670:Stab2	UTSW	10	86,940,723 (GRCm38)	missense	probably damaging	1.00
R8692:Stab2	UTSW	10	86,972,930 (GRCm38)	missense	probably damaging	0.99
R8744:Stab2	UTSW	10	86,969,349 (GRCm38)	missense	probably benign	0.32
R8745:Stab2	UTSW	10	86,969,349 (GRCm38)	missense	probably benign	0.32
R8782:Stab2	UTSW	10	86,899,821 (GRCm38)	missense	probably benign	0.00
R8875:Stab2	UTSW	10	86,996,864 (GRCm38)	missense	probably damaging	1.00
R8978:Stab2	UTSW	10	86,949,918 (GRCm38)	missense	possibly damaging	0.64
R9141:Stab2	UTSW	10	86,869,047 (GRCm38)	missense	probably damaging	1.00
R9248:Stab2	UTSW	10	86,891,617 (GRCm38)	missense	probably damaging	0.98
R9326:Stab2	UTSW	10	86,955,146 (GRCm38)	missense	probably damaging	1.00
R9426:Stab2	UTSW	10	86,869,047 (GRCm38)	missense	probably damaging	1.00
R9568:Stab2	UTSW	10	86,863,556 (GRCm38)	missense	probably damaging	1.00
R9627:Stab2	UTSW	10	86,957,840 (GRCm38)	missense	probably damaging	0.98
R9635:Stab2	UTSW	10	86,850,787 (GRCm38)	nonsense	probably null
R9648:Stab2	UTSW	10	86,856,697 (GRCm38)	frame shift	probably null
R9649:Stab2	UTSW	10	86,856,697 (GRCm38)	frame shift	probably null
R9650:Stab2	UTSW	10	86,856,697 (GRCm38)	frame shift	probably null
R9726:Stab2	UTSW	10	86,954,231 (GRCm38)	missense	probably benign	0.00
R9756:Stab2	UTSW	10	86,967,689 (GRCm38)	missense	possibly damaging	0.50
R9786:Stab2	UTSW	10	86,922,133 (GRCm38)	missense	probably benign	0.03
RF061:Stab2	UTSW	10	86,866,758 (GRCm38)	critical splice acceptor site	probably benign
X0023:Stab2	UTSW	10	86,922,198 (GRCm38)	critical splice acceptor site	probably null
X0025:Stab2	UTSW	10	86,887,816 (GRCm38)	missense	probably damaging	1.00
Z1176:Stab2	UTSW	10	86,949,914 (GRCm38)	missense	probably damaging	0.99
Z1177:Stab2	UTSW	10	86,896,596 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TCAAATGACACAAGACTCCAAGTTG -3'
(R):5'- CCATGGCAGACATTACTTGCTC -3'

Sequencing Primer
(F):5'- GGAAGAGAGTGTTTATGTGCAAC -3'
(R):5'- ATGGCAGACATTACTTGCTCATCAC -3'

Posted On

2017-06-26