Mutagenetix > Incidental Mutation

Incidental Mutation 'R2165:Stab1'

235456

Institutional Source

Beutler Lab

Gene Symbol

Stab1

Ensembl Gene

ENSMUSG00000042286

Gene Name

stabilin 1

Synonyms

MS-1

MMRRC Submission

040168-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R2165 (G1)

Quality Score

176

Status

Validated

Chromosome

Chromosomal Location

31139013-31168641 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 31168435 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Threonine at position 20 (S20T)

Ref Sequence

ENSEMBL: ENSMUSP00000046199 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000022469] [ENSMUST00000036618] [ENSMUST00000167449] [ENSMUST00000168206] [ENSMUST00000169628]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000022469

SMART Domains

Protein: ENSMUSP00000022469
Gene: ENSMUSG00000021910

Domain	Start	End	E-Value	Type
PX	15	119	2.17e-26	SMART
PDB:4PQ8\|A	287	420	9e-8	PDB
SCOP:d1h6ta2	291	421	6e-29	SMART
Blast:LRR	311	332	5e-6	BLAST
Blast:LRR	333	355	6e-6	BLAST
Blast:LRR	378	403	5e-7	BLAST
Blast:LRR	403	429	6e-7	BLAST
low complexity region	489	501	N/A	INTRINSIC
low complexity region	517	534	N/A	INTRINSIC
coiled coil region	625	650	N/A	INTRINSIC
low complexity region	662	695	N/A	INTRINSIC
low complexity region	1038	1069	N/A	INTRINSIC
low complexity region	1081	1193	N/A	INTRINSIC
low complexity region	1491	1509	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000036618
AA Change: S20T

PolyPhen 2 Score 0.196 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000046199
Gene: ENSMUSG00000042286
AA Change: S20T

Domain	Start	End	E-Value	Type
signal peptide	1	25	N/A	INTRINSIC
EGF	112	149	6.65e-2	SMART
EGF	160	194	2.28e0	SMART
EGF	199	232	1.4e0	SMART
EGF	236	272	4.97e-1	SMART
EGF	276	319	1.95e1	SMART
EGF_like	321	357	5.03e1	SMART
low complexity region	400	413	N/A	INTRINSIC
Blast:FAS1	414	501	2e-52	BLAST
FAS1	543	645	1.35e-24	SMART
EGF_like	780	817	5.45e1	SMART
EGF	822	861	1.08e-1	SMART
EGF	865	904	3.15e-3	SMART
EGF	908	947	1.3e1	SMART
EGF	951	989	1.47e1	SMART
FAS1	1023	1122	1.3e-17	SMART
FAS1	1165	1257	2.94e0	SMART
EGF	1332	1369	1.4e0	SMART
EGF	1379	1413	1.88e-1	SMART
EGF	1420	1455	6.02e0	SMART
EGF	1459	1497	3.82e-2	SMART
EGF	1501	1540	2.05e-2	SMART
EGF	1544	1583	2.25e1	SMART
FAS1	1616	1712	1.61e-22	SMART
FAS1	1763	1868	2.12e-17	SMART
EGF	1970	2007	1.26e-2	SMART
EGF	2017	2051	1.61e0	SMART
EGF	2059	2090	2.45e0	SMART
EGF	2094	2131	3.46e0	SMART
EGF	2135	2174	3.82e-2	SMART
LINK	2206	2301	8.55e-49	SMART
FAS1	2367	2462	2.06e-6	SMART
transmembrane domain	2476	2498	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000159532

Predicted Effect

probably benign
Transcript: ENSMUST00000167449

Predicted Effect

probably benign
Transcript: ENSMUST00000168206

SMART Domains

Protein: ENSMUSP00000132842
Gene: ENSMUSG00000021910

Domain	Start	End	E-Value	Type
Pfam:LRR_8	44	101	3.9e-9	PFAM
Pfam:LRR_1	45	66	2.6e-2	PFAM
Pfam:LRR_6	88	109	1.1e-2	PFAM
Pfam:LRR_4	89	132	6.5e-8	PFAM
Pfam:LRR_1	90	109	6.9e-2	PFAM
Blast:LRR	133	158	4e-7	BLAST
Blast:LRR	158	184	6e-7	BLAST
low complexity region	244	256	N/A	INTRINSIC
low complexity region	272	289	N/A	INTRINSIC
coiled coil region	380	405	N/A	INTRINSIC
low complexity region	417	450	N/A	INTRINSIC
low complexity region	793	824	N/A	INTRINSIC
low complexity region	836	948	N/A	INTRINSIC
low complexity region	1246	1264	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000169628

SMART Domains

Protein: ENSMUSP00000131465
Gene: ENSMUSG00000021910

Domain	Start	End	E-Value	Type
low complexity region	231	249	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000170253

SMART Domains

Protein: ENSMUSP00000129547
Gene: ENSMUSG00000021910

Domain	Start	End	E-Value	Type
SCOP:d1dcea3	2	86	3e-11	SMART
Blast:LRR	13	34	1e-5	BLAST
Blast:LRR	35	60	1e-7	BLAST
Blast:LRR	60	86	2e-8	BLAST

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.7%
10x: 97.6%
20x: 96.0%

Validation Efficiency

99% (71/72)

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, 16 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 endocytose ligands such as low density lipoprotein, Gram-positive and Gram-negative bacteria, and advanced glycosylation end products. Supporting its possible role as a scavenger receptor, the protein rapidly cycles between the plasma membrane and early endosomes. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit no physical or behavioral abnormalities. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 73 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca4	A	G	3: 122,112,399 (GRCm38)	T806A	possibly damaging	Het
Adgre1	T	G	17: 57,419,338 (GRCm38)	L403R	probably damaging	Het
Alox12	A	T	11: 70,242,572 (GRCm38)		probably null	Het
Ankib1	A	T	5: 3,713,210 (GRCm38)	D506E	possibly damaging	Het
Ascc3	T	G	10: 50,721,839 (GRCm38)	Y1268D	probably damaging	Het
Bik	A	G	15: 83,541,423 (GRCm38)	M42V	probably benign	Het
Bola1	A	T	3: 96,197,201 (GRCm38)	S26T	probably benign	Het
Bub1	T	C	2: 127,801,281 (GRCm38)	I1048V	probably benign	Het
Cad	A	G	5: 31,062,220 (GRCm38)	N621S	probably damaging	Het
Camkv	C	A	9: 107,945,600 (GRCm38)	N69K	possibly damaging	Het
Ccdc110	T	C	8: 45,942,839 (GRCm38)	M589T	probably benign	Het
Ccdc154	T	A	17: 25,170,890 (GRCm38)	V498E	probably damaging	Het
Ccr1l1	A	G	9: 123,977,654 (GRCm38)	L252P	probably damaging	Het
Cdh1	T	C	8: 106,664,321 (GRCm38)	C690R	probably damaging	Het
Cfap157	T	G	2: 32,778,163 (GRCm38)		probably null	Het
Cux2	A	G	5: 121,887,477 (GRCm38)	S43P	possibly damaging	Het
Cyb5rl	C	T	4: 107,068,683 (GRCm38)	P21S	probably damaging	Het
Cyp51	T	G	5: 4,086,594 (GRCm38)	Q400P	probably damaging	Het
Dnah7b	T	C	1: 46,097,992 (GRCm38)		probably benign	Het
Ephb4	A	G	5: 137,354,426 (GRCm38)	I90M	probably benign	Het
Fam13c	A	G	10: 70,542,693 (GRCm38)	N269S	probably damaging	Het
Fam83c	T	A	2: 155,831,524 (GRCm38)	Y248F	possibly damaging	Het
Fat2	A	G	11: 55,303,716 (GRCm38)	F1166L	probably benign	Het
Fem1a	A	G	17: 56,257,686 (GRCm38)	N260D	probably benign	Het
Fnbp4	T	A	2: 90,767,399 (GRCm38)		probably null	Het
Fut9	T	A	4: 25,619,733 (GRCm38)	*360Y	probably null	Het
Fut9	T	A	4: 25,619,734 (GRCm38)	*360L	probably null	Het
Gm11639	G	A	11: 104,751,862 (GRCm38)	V1104I	possibly damaging	Het
Gm3727	T	A	14: 7,264,625 (GRCm38)	Q10L	probably damaging	Het
Gpat2	G	A	2: 127,428,291 (GRCm38)	V75M	probably damaging	Het
Haspin	A	C	11: 73,136,630 (GRCm38)	N544K	probably damaging	Het
Havcr1	A	G	11: 46,778,552 (GRCm38)	N286S	probably benign	Het
Lrp6	A	C	6: 134,459,283 (GRCm38)	C1307G	probably damaging	Het
Lrrc2	A	C	9: 110,979,577 (GRCm38)	H294P	possibly damaging	Het
Mettl25b	A	T	3: 87,927,053 (GRCm38)		probably null	Het
Mon2	A	C	10: 123,042,364 (GRCm38)		probably null	Het
Mrc2	G	A	11: 105,348,431 (GRCm38)		probably null	Het
Mrgprb1	T	C	7: 48,447,322 (GRCm38)	I281V	probably benign	Het
Muc4	A	G	16: 32,750,476 (GRCm38)	E118G	probably damaging	Het
Nefh	T	C	11: 4,943,872 (GRCm38)	D394G	probably damaging	Het
Neurl4	A	G	11: 69,903,221 (GRCm38)	T168A	probably benign	Het
Or10s1	A	G	9: 40,074,915 (GRCm38)	N207D	possibly damaging	Het
Or1j18	T	A	2: 36,734,701 (GRCm38)	C127S	probably damaging	Het
Or51a10	T	C	7: 104,049,638 (GRCm38)	T239A	probably benign	Het
Or5ak4	A	T	2: 85,331,102 (GRCm38)	N265K	probably benign	Het
Oxsr1	A	C	9: 119,294,432 (GRCm38)	M92R	probably damaging	Het
Pde8a	T	C	7: 81,295,768 (GRCm38)		probably null	Het
Pex5l	T	A	3: 32,953,132 (GRCm38)		probably null	Het
Pik3r4	T	A	9: 105,672,785 (GRCm38)	M1025K	probably benign	Het
Plch1	C	T	3: 63,698,482 (GRCm38)	E1325K	probably benign	Het
Plin2	A	T	4: 86,668,432 (GRCm38)	V54E	probably damaging	Het
Prss47	A	T	13: 65,045,073 (GRCm38)	I298N	probably damaging	Het
Prune2	A	G	19: 17,120,182 (GRCm38)	R1017G	probably benign	Het
Psg19	T	A	7: 18,796,986 (GRCm38)	Y81F	possibly damaging	Het
Ptch1	T	G	13: 63,524,959 (GRCm38)	E944A	probably benign	Het
Serpinb1a	T	C	13: 32,850,414 (GRCm38)		probably benign	Het
Sh3pxd2a	A	T	19: 47,278,355 (GRCm38)	V265E	probably damaging	Het
Slc22a17	A	T	14: 54,908,825 (GRCm38)	Y337*	probably null	Het
Slc25a27	A	G	17: 43,657,772 (GRCm38)	V138A	probably benign	Het
Slc4a2	A	G	5: 24,431,316 (GRCm38)	Y220C	probably damaging	Het
Slc66a3	G	A	12: 16,989,839 (GRCm38)	L192F	probably damaging	Het
Tcstv2a	A	T	13: 120,264,097 (GRCm38)	Q99L	probably damaging	Het
Thsd1	G	T	8: 22,238,522 (GRCm38)		probably benign	Het
Tmem204	G	A	17: 25,080,592 (GRCm38)		probably benign	Het
Tom1l1	A	G	11: 90,649,895 (GRCm38)		probably benign	Het
Toporsl	T	A	4: 52,612,072 (GRCm38)	F655Y	possibly damaging	Het
Vmn2r98	A	G	17: 19,081,291 (GRCm38)	K852E	unknown	Het
Wdpcp	T	G	11: 21,691,884 (GRCm38)	L174R	probably damaging	Het
Zbbx	G	A	3: 75,112,107 (GRCm38)	P99S	probably damaging	Het
Zfhx4	C	T	3: 5,403,358 (GRCm38)	P2859S	probably benign	Het
Zfp600	A	T	4: 146,196,918 (GRCm38)	R719*	probably null	Het
Zfp697	C	A	3: 98,428,014 (GRCm38)	A365E	unknown	Het
Zfp957	A	C	14: 79,213,613 (GRCm38)	S249A	probably benign	Het

Other mutations in Stab1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00087:Stab1	APN	14	31,161,357 (GRCm38)	missense	probably benign	0.01
IGL00323:Stab1	APN	14	31,139,306 (GRCm38)	missense	probably benign	0.04
IGL00515:Stab1	APN	14	31,159,729 (GRCm38)	missense	probably benign	0.20
IGL00844:Stab1	APN	14	31,147,066 (GRCm38)	missense	probably damaging	1.00
IGL01374:Stab1	APN	14	31,147,075 (GRCm38)	missense	probably damaging	1.00
IGL01384:Stab1	APN	14	31,150,408 (GRCm38)	missense	probably benign
IGL01431:Stab1	APN	14	31,148,995 (GRCm38)	missense	probably benign	0.06
IGL01787:Stab1	APN	14	31,139,808 (GRCm38)	missense	probably damaging	1.00
IGL02128:Stab1	APN	14	31,150,441 (GRCm38)	missense	probably damaging	1.00
IGL02138:Stab1	APN	14	31,143,513 (GRCm38)	critical splice donor site	probably null
IGL02256:Stab1	APN	14	31,141,592 (GRCm38)	missense	probably damaging	1.00
IGL02340:Stab1	APN	14	31,140,410 (GRCm38)	missense	probably damaging	0.96
IGL02507:Stab1	APN	14	31,139,210 (GRCm38)	unclassified	probably benign
IGL02695:Stab1	APN	14	31,159,271 (GRCm38)	missense	probably damaging	1.00
IGL02755:Stab1	APN	14	31,139,638 (GRCm38)	missense	probably benign	0.01
IGL02870:Stab1	APN	14	31,139,397 (GRCm38)	missense	probably benign	0.00
IGL02884:Stab1	APN	14	31,150,143 (GRCm38)	splice site	probably null
IGL03035:Stab1	APN	14	31,147,769 (GRCm38)	missense	probably benign	0.00
IGL03267:Stab1	APN	14	31,142,729 (GRCm38)	missense	probably damaging	1.00
IGL03286:Stab1	APN	14	31,159,326 (GRCm38)	splice site	probably benign
IGL03366:Stab1	APN	14	31,150,263 (GRCm38)	missense	possibly damaging	0.58
IGL03412:Stab1	APN	14	31,154,407 (GRCm38)	missense	probably benign	0.42
R0906_Stab1_335	UTSW	14	31,145,249 (GRCm38)	missense	probably benign	0.19
R5086_Stab1_467	UTSW	14	31,159,304 (GRCm38)	missense	probably damaging	1.00
IGL02835:Stab1	UTSW	14	31,146,024 (GRCm38)	critical splice donor site	probably null
K7371:Stab1	UTSW	14	31,150,249 (GRCm38)	missense	probably damaging	1.00
R0053:Stab1	UTSW	14	31,140,687 (GRCm38)	missense	possibly damaging	0.57
R0053:Stab1	UTSW	14	31,140,687 (GRCm38)	missense	possibly damaging	0.57
R0066:Stab1	UTSW	14	31,157,070 (GRCm38)	splice site	probably benign
R0066:Stab1	UTSW	14	31,157,070 (GRCm38)	splice site	probably benign
R0363:Stab1	UTSW	14	31,159,008 (GRCm38)	splice site	probably benign
R0387:Stab1	UTSW	14	31,148,101 (GRCm38)	missense	probably benign	0.00
R0391:Stab1	UTSW	14	31,143,418 (GRCm38)	missense	probably benign	0.21
R0513:Stab1	UTSW	14	31,148,945 (GRCm38)	missense	probably benign	0.08
R0546:Stab1	UTSW	14	31,139,550 (GRCm38)	missense	possibly damaging	0.92
R0825:Stab1	UTSW	14	31,152,600 (GRCm38)	missense	probably benign	0.16
R0906:Stab1	UTSW	14	31,145,249 (GRCm38)	missense	probably benign	0.19
R0963:Stab1	UTSW	14	31,147,274 (GRCm38)	missense	probably damaging	0.97
R1219:Stab1	UTSW	14	31,140,621 (GRCm38)	splice site	probably null
R1234:Stab1	UTSW	14	31,150,236 (GRCm38)	missense	probably damaging	1.00
R1260:Stab1	UTSW	14	31,151,889 (GRCm38)	missense	probably damaging	1.00
R1400:Stab1	UTSW	14	31,139,830 (GRCm38)	missense	possibly damaging	0.92
R1405:Stab1	UTSW	14	31,149,001 (GRCm38)	missense	probably benign	0.19
R1405:Stab1	UTSW	14	31,149,001 (GRCm38)	missense	probably benign	0.19
R1440:Stab1	UTSW	14	31,151,690 (GRCm38)	nonsense	probably null
R1472:Stab1	UTSW	14	31,141,586 (GRCm38)	missense	probably benign	0.01
R1474:Stab1	UTSW	14	31,149,861 (GRCm38)	missense	probably benign	0.45
R1475:Stab1	UTSW	14	31,163,828 (GRCm38)	missense	probably benign
R1509:Stab1	UTSW	14	31,151,584 (GRCm38)	splice site	probably benign
R1551:Stab1	UTSW	14	31,160,499 (GRCm38)	missense	probably benign	0.00
R1572:Stab1	UTSW	14	31,150,823 (GRCm38)	missense	probably damaging	1.00
R1633:Stab1	UTSW	14	31,150,380 (GRCm38)	splice site	probably null
R1719:Stab1	UTSW	14	31,146,028 (GRCm38)	nonsense	probably null
R1733:Stab1	UTSW	14	31,145,303 (GRCm38)	missense	probably damaging	1.00
R1763:Stab1	UTSW	14	31,168,416 (GRCm38)	missense	probably benign	0.04
R1808:Stab1	UTSW	14	31,141,144 (GRCm38)	missense	possibly damaging	0.80
R1816:Stab1	UTSW	14	31,157,465 (GRCm38)	missense	probably benign	0.03
R1853:Stab1	UTSW	14	31,140,463 (GRCm38)	missense	probably damaging	1.00
R1891:Stab1	UTSW	14	31,141,330 (GRCm38)	missense	probably benign	0.07
R1984:Stab1	UTSW	14	31,150,648 (GRCm38)	missense	probably benign	0.20
R1998:Stab1	UTSW	14	31,162,153 (GRCm38)	nonsense	probably null
R2191:Stab1	UTSW	14	31,159,270 (GRCm38)	missense	probably damaging	1.00
R2191:Stab1	UTSW	14	31,142,800 (GRCm38)	missense	probably benign	0.03
R2233:Stab1	UTSW	14	31,161,880 (GRCm38)	missense	probably benign	0.08
R2303:Stab1	UTSW	14	31,146,070 (GRCm38)	missense	probably damaging	1.00
R2496:Stab1	UTSW	14	31,161,463 (GRCm38)	missense	probably damaging	1.00
R2504:Stab1	UTSW	14	31,163,040 (GRCm38)	critical splice donor site	probably null
R2519:Stab1	UTSW	14	31,154,872 (GRCm38)	missense	probably damaging	1.00
R2926:Stab1	UTSW	14	31,161,799 (GRCm38)	missense	probably damaging	1.00
R4025:Stab1	UTSW	14	31,154,952 (GRCm38)	missense	possibly damaging	0.46
R4113:Stab1	UTSW	14	31,168,479 (GRCm38)	missense	probably damaging	0.98
R4258:Stab1	UTSW	14	31,154,672 (GRCm38)	missense	possibly damaging	0.92
R4588:Stab1	UTSW	14	31,157,445 (GRCm38)	missense	probably benign	0.01
R4644:Stab1	UTSW	14	31,140,487 (GRCm38)	unclassified	probably benign
R4660:Stab1	UTSW	14	31,154,915 (GRCm38)	missense	possibly damaging	0.91
R4801:Stab1	UTSW	14	31,141,371 (GRCm38)	nonsense	probably null
R4802:Stab1	UTSW	14	31,141,371 (GRCm38)	nonsense	probably null
R4870:Stab1	UTSW	14	31,142,043 (GRCm38)	missense	probably benign	0.13
R4872:Stab1	UTSW	14	31,140,393 (GRCm38)	missense	probably damaging	1.00
R4881:Stab1	UTSW	14	31,143,672 (GRCm38)	missense	probably benign	0.32
R4941:Stab1	UTSW	14	31,151,571 (GRCm38)	missense	probably benign	0.00
R5061:Stab1	UTSW	14	31,163,099 (GRCm38)	missense	probably damaging	1.00
R5086:Stab1	UTSW	14	31,159,304 (GRCm38)	missense	probably damaging	1.00
R5086:Stab1	UTSW	14	31,143,624 (GRCm38)	missense	probably damaging	1.00
R5087:Stab1	UTSW	14	31,159,304 (GRCm38)	missense	probably damaging	1.00
R5092:Stab1	UTSW	14	31,145,855 (GRCm38)	missense	probably benign	0.01
R5102:Stab1	UTSW	14	31,148,017 (GRCm38)	critical splice donor site	probably null
R5107:Stab1	UTSW	14	31,163,795 (GRCm38)	splice site	probably null
R5195:Stab1	UTSW	14	31,140,521 (GRCm38)	unclassified	probably benign
R5217:Stab1	UTSW	14	31,159,519 (GRCm38)	missense	probably benign	0.25
R5285:Stab1	UTSW	14	31,143,476 (GRCm38)	unclassified	probably benign
R5327:Stab1	UTSW	14	31,161,836 (GRCm38)	nonsense	probably null
R5647:Stab1	UTSW	14	31,157,440 (GRCm38)	nonsense	probably null
R5696:Stab1	UTSW	14	31,160,221 (GRCm38)	missense	probably benign
R5996:Stab1	UTSW	14	31,139,551 (GRCm38)	missense	probably benign	0.39
R6016:Stab1	UTSW	14	31,158,993 (GRCm38)	missense	probably damaging	1.00
R6017:Stab1	UTSW	14	31,141,544 (GRCm38)	missense	probably benign	0.00
R6174:Stab1	UTSW	14	31,162,519 (GRCm38)	nonsense	probably null
R6366:Stab1	UTSW	14	31,141,438 (GRCm38)	missense	probably benign	0.10
R6754:Stab1	UTSW	14	31,141,081 (GRCm38)	missense	probably benign
R6788:Stab1	UTSW	14	31,139,160 (GRCm38)	missense	probably damaging	1.00
R6898:Stab1	UTSW	14	31,158,963 (GRCm38)	missense	probably benign	0.00
R7124:Stab1	UTSW	14	31,160,867 (GRCm38)	missense	possibly damaging	0.94
R7145:Stab1	UTSW	14	31,145,073 (GRCm38)	critical splice donor site	probably null
R7153:Stab1	UTSW	14	31,160,584 (GRCm38)	missense	probably benign	0.16
R7213:Stab1	UTSW	14	31,143,673 (GRCm38)	missense	probably benign
R7215:Stab1	UTSW	14	31,160,797 (GRCm38)	missense	possibly damaging	0.93
R7319:Stab1	UTSW	14	31,140,826 (GRCm38)	missense	probably damaging	1.00
R7389:Stab1	UTSW	14	31,147,239 (GRCm38)	missense	probably benign	0.00
R7400:Stab1	UTSW	14	31,157,384 (GRCm38)	missense	probably null	1.00
R7427:Stab1	UTSW	14	31,159,259 (GRCm38)	missense	probably benign	0.00
R7428:Stab1	UTSW	14	31,159,259 (GRCm38)	missense	probably benign	0.00
R7484:Stab1	UTSW	14	31,160,317 (GRCm38)	missense	probably benign	0.00
R7568:Stab1	UTSW	14	31,152,595 (GRCm38)	missense	probably damaging	1.00
R7574:Stab1	UTSW	14	31,154,665 (GRCm38)	missense	probably benign
R7619:Stab1	UTSW	14	31,145,237 (GRCm38)	missense	probably benign
R7623:Stab1	UTSW	14	31,140,621 (GRCm38)	missense	probably benign	0.03
R7721:Stab1	UTSW	14	31,141,456 (GRCm38)	missense	possibly damaging	0.48
R7869:Stab1	UTSW	14	31,154,472 (GRCm38)	missense	probably benign	0.01
R7936:Stab1	UTSW	14	31,157,415 (GRCm38)	missense	possibly damaging	0.88
R7956:Stab1	UTSW	14	31,160,024 (GRCm38)	missense	probably benign	0.02
R7973:Stab1	UTSW	14	31,159,633 (GRCm38)	critical splice donor site	probably null
R8059:Stab1	UTSW	14	31,160,241 (GRCm38)	missense	probably benign	0.02
R8116:Stab1	UTSW	14	31,158,953 (GRCm38)	missense	possibly damaging	0.80
R8304:Stab1	UTSW	14	31,148,954 (GRCm38)	missense	probably benign	0.14
R8368:Stab1	UTSW	14	31,148,411 (GRCm38)	missense	possibly damaging	0.91
R8495:Stab1	UTSW	14	31,155,833 (GRCm38)	missense	probably damaging	1.00
R8513:Stab1	UTSW	14	31,149,790 (GRCm38)	critical splice donor site	probably null
R8544:Stab1	UTSW	14	31,163,051 (GRCm38)	nonsense	probably null
R8671:Stab1	UTSW	14	31,157,408 (GRCm38)	missense	probably damaging	1.00
R8885:Stab1	UTSW	14	31,161,814 (GRCm38)	missense	possibly damaging	0.79
R8974:Stab1	UTSW	14	31,160,822 (GRCm38)	missense	probably benign
R9022:Stab1	UTSW	14	31,160,269 (GRCm38)	missense	probably benign	0.01
R9059:Stab1	UTSW	14	31,154,848 (GRCm38)	missense	probably benign	0.01
R9226:Stab1	UTSW	14	31,145,855 (GRCm38)	missense	probably benign	0.00
R9272:Stab1	UTSW	14	31,145,341 (GRCm38)	missense	probably benign	0.05
R9388:Stab1	UTSW	14	31,154,355 (GRCm38)	missense	probably damaging	1.00
R9401:Stab1	UTSW	14	31,161,112 (GRCm38)	missense	probably benign
R9433:Stab1	UTSW	14	31,143,574 (GRCm38)	missense	probably benign	0.00
R9450:Stab1	UTSW	14	31,162,939 (GRCm38)	missense	possibly damaging	0.62
R9505:Stab1	UTSW	14	31,155,765 (GRCm38)	missense	probably damaging	1.00
R9570:Stab1	UTSW	14	31,142,681 (GRCm38)	missense	probably benign	0.01
R9624:Stab1	UTSW	14	31,141,388 (GRCm38)	missense
R9694:Stab1	UTSW	14	31,154,944 (GRCm38)	missense	probably benign	0.06
R9723:Stab1	UTSW	14	31,163,891 (GRCm38)	missense	probably benign	0.10
X0026:Stab1	UTSW	14	31,162,191 (GRCm38)	missense	possibly damaging	0.91
Z1176:Stab1	UTSW	14	31,150,660 (GRCm38)	missense	probably benign	0.00
Z1176:Stab1	UTSW	14	31,142,038 (GRCm38)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- AGGTAGAACAGCCGTAGACTTC -3'
(R):5'- GTGAGCTGACGGATAGCTTTTAAAG -3'

Sequencing Primer
(F):5'- ACAGCCGTAGACTTCAGCCTG -3'
(R):5'- GCTGCTCACCCACCCTG -3'

Posted On

2014-10-01