Mutagenetix > Incidental Mutation

Incidental Mutation 'R7153:Stab1'

554274

Institutional Source

Beutler Lab

Gene Symbol

Stab1

Ensembl Gene

ENSMUSG00000042286

Gene Name

stabilin 1

Synonyms

MS-1

MMRRC Submission

045255-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7153 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

31139013-31168641 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to G at 31160584 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Alanine at position 432 (E432A)

Ref Sequence

ENSEMBL: ENSMUSP00000046199 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000036618]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000036618
AA Change: E432A

PolyPhen 2 Score 0.164 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000046199
Gene: ENSMUSG00000042286
AA Change: E432A

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

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.8%

Validation Efficiency

100% (75/75)

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: 75 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ano2	A	G	6: 125,992,943 (GRCm38)	T741A	possibly damaging	Het
Aox4	T	C	1: 58,250,219 (GRCm38)	M767T	probably damaging	Het
Arhgap39	C	A	15: 76,765,491 (GRCm38)	S27I	probably benign	Het
AU018091	T	A	7: 3,159,513 (GRCm38)	M296L	probably benign	Het
Axin1	A	G	17: 26,187,968 (GRCm38)	T512A	probably benign	Het
B4galnt3	A	T	6: 120,214,968 (GRCm38)	D602E	probably benign	Het
Bcl6	G	A	16: 23,966,226 (GRCm38)	R675*	probably null	Het
Bsnd	A	T	4: 106,492,033 (GRCm38)	D3E	probably benign	Het
Btbd18	C	T	2: 84,666,428 (GRCm38)	R137*	probably null	Het
C2cd5	A	G	6: 143,019,409 (GRCm38)	S871P	probably benign	Het
Cobl	G	T	11: 12,254,128 (GRCm38)	P858Q	probably damaging	Het
Col6a1	C	T	10: 76,710,341 (GRCm38)		probably null	Het
Crb2	A	T	2: 37,787,408 (GRCm38)	H304L	probably benign	Het
Crybg1	T	A	10: 43,964,666 (GRCm38)	Y1812F	possibly damaging	Het
Ddx60	A	T	8: 61,988,108 (GRCm38)	K1070N	possibly damaging	Het
Defb22	T	C	2: 152,485,920 (GRCm38)	K115R	unknown	Het
Dhx8	C	T	11: 101,740,175 (GRCm38)		probably null	Het
Dnah5	T	A	15: 28,365,522 (GRCm38)		probably null	Het
Dnah7b	T	A	1: 46,126,804 (GRCm38)	F543Y	probably benign	Het
Ehhadh	A	G	16: 21,766,321 (GRCm38)	F270S	probably damaging	Het
Esyt2	A	G	12: 116,346,508 (GRCm38)	M397V	probably benign	Het
Fanca	A	T	8: 123,316,425 (GRCm38)	L74H	probably damaging	Het
Fbxl17	C	A	17: 63,060,351 (GRCm38)	V676F	probably benign	Het
Fndc1	A	G	17: 7,801,645 (GRCm38)	V102A	probably damaging	Het
Gpalpp1	T	C	14: 76,095,011 (GRCm38)	Y273C	probably damaging	Het
Gpatch8	TTCCTCCTCCTCCTCTTCCTCCTCCTC	TTCCTCCTCCTCCTCCTCTTCCTCCTCCTC	11: 102,480,188 (GRCm38)		probably benign	Het
Grik2	T	C	10: 49,535,367 (GRCm38)	H225R	probably benign	Het
Helz2	A	T	2: 181,231,285 (GRCm38)	S2411T	probably benign	Het
Hnmt	C	T	2: 24,014,341 (GRCm38)	A103T	probably damaging	Het
Ighv15-2	G	T	12: 114,564,590 (GRCm38)	Y114*	probably null	Het
Irak2	A	G	6: 113,678,709 (GRCm38)	H357R	probably benign	Het
Kcp	T	C	6: 29,499,015 (GRCm38)	E320G	probably damaging	Het
Kpna4	A	G	3: 69,089,798 (GRCm38)	L352S	probably damaging	Het
Krt36	G	A	11: 100,105,146 (GRCm38)	Q151*	probably null	Het
Krt77	G	A	15: 101,865,496 (GRCm38)	T241M	probably benign	Het
Lca5l	T	A	16: 96,173,809 (GRCm38)	N305I	probably damaging	Het
Lefty1	T	A	1: 180,937,767 (GRCm38)	L300Q	probably benign	Het
Mertk	A	G	2: 128,736,649 (GRCm38)	Y185C	probably damaging	Het
Mmp14	T	C	14: 54,436,251 (GRCm38)	I124T	possibly damaging	Het
Nlrc4	T	C	17: 74,447,103 (GRCm38)	E95G	possibly damaging	Het
Npc1	A	G	18: 12,213,291 (GRCm38)	F283L	possibly damaging	Het
Olfr1180	A	C	2: 88,412,118 (GRCm38)	L180W	probably damaging	Het
Olfr1282	A	T	2: 111,335,901 (GRCm38)	M59K	probably damaging	Het
Pcdha11	T	C	18: 37,011,225 (GRCm38)	V123A	probably damaging	Het
Pcdhga2	T	C	18: 37,669,208 (GRCm38)	V35A	probably damaging	Het
Pgd	G	T	4: 149,161,678 (GRCm38)	T94K	probably benign	Het
Pik3c2a	T	C	7: 116,342,252 (GRCm38)	N1593S	probably damaging	Het
Pkd1l3	GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA	GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA	8: 109,624,195 (GRCm38)		probably benign	Het
Plcb3	A	G	19: 6,958,084 (GRCm38)		probably null	Het
Prkd3	C	T	17: 78,966,355 (GRCm38)	D491N	probably benign	Het
Ptprf	T	C	4: 118,231,543 (GRCm38)	T688A	probably damaging	Het
Pycr2	T	A	1: 180,906,682 (GRCm38)	L210M	probably damaging	Het
Rpl36	T	C	17: 56,614,137 (GRCm38)	I81T	probably benign	Het
Rraga	C	T	4: 86,576,016 (GRCm38)	A33V	probably damaging	Het
Slc29a1	G	A	17: 45,585,762 (GRCm38)	A429V	probably damaging	Het
Synj1	C	T	16: 90,948,090 (GRCm38)	G1189R	probably benign	Het
Synpo2	A	G	3: 123,112,404 (GRCm38)	*1088Q	probably null	Het
Tbc1d21	T	C	9: 58,363,093 (GRCm38)	D133G	probably damaging	Het
Tenm2	A	G	11: 36,024,182 (GRCm38)	V2176A	probably damaging	Het
Tff1	A	G	17: 31,162,798 (GRCm38)	I35T	probably benign	Het
Thnsl1	T	C	2: 21,212,953 (GRCm38)	V506A	possibly damaging	Het
Timm10b	A	G	7: 105,640,880 (GRCm38)	Q50R	unknown	Het
Tjp2	A	T	19: 24,101,981 (GRCm38)	N843K	probably benign	Het
Tle1	A	T	4: 72,139,061 (GRCm38)	F101I	probably benign	Het
Tmem225	T	C	9: 40,148,368 (GRCm38)	F15L	probably benign	Het
Trav12-3	T	C	14: 53,622,161 (GRCm38)	L88P	probably benign	Het
Ttc7b	A	T	12: 100,355,034 (GRCm38)	W613R	probably damaging	Het
Ttn	T	C	2: 76,945,316 (GRCm38)	D1840G	unknown	Het
Ttn	T	A	2: 76,778,504 (GRCm38)	M17723L	probably benign	Het
Tubgcp2	T	C	7: 140,001,036 (GRCm38)	H668R	probably benign	Het
Ush2a	C	A	1: 188,728,484 (GRCm38)	N2647K	possibly damaging	Het
Vmn1r14	C	T	6: 57,233,866 (GRCm38)	S143F	probably benign	Het
Vmn2r70	A	G	7: 85,565,054 (GRCm38)	S297P	probably damaging	Het
Ywhab	T	C	2: 164,014,060 (GRCm38)	F119L	probably damaging	Het
Zmym2	T	A	14: 56,950,202 (GRCm38)	D1108E	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
R2165:Stab1	UTSW	14	31,168,435 (GRCm38)	missense	probably benign	0.20
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
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'- GCCTTGTGGATGCTGAACTG -3'
(R):5'- CCTTCCCTTTGAGACTGTGG -3'

Sequencing Primer
(F):5'- TCTCTGATGAGATAGACACTGGAC -3'
(R):5'- ACTGTGGTCGGCAAAGC -3'

Posted On

2019-05-15