Mutagenetix > Incidental Mutation

Incidental Mutation 'R4785:Atrnl1'

367045

Institutional Source

Beutler Lab

Gene Symbol

Atrnl1

Ensembl Gene

ENSMUSG00000054843

Gene Name

attractin like 1

Synonyms

Alp

MMRRC Submission

042417-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.210) question?

Stock #

R4785 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

57611034-58133338 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 57629158 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Valine at position 122 (I122V)

Ref Sequence

ENSEMBL: ENSMUSP00000076514 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000077282]

AlphaFold

Q6A051

Predicted Effect

probably damaging
Transcript: ENSMUST00000077282
AA Change: I122V

PolyPhen 2 Score 0.974 (Sensitivity: 0.76; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000076514
Gene: ENSMUSG00000054843
AA Change: I122V

Domain	Start	End	E-Value	Type
low complexity region	25	32	N/A	INTRINSIC
EGF	61	90	5.71e-1	SMART
CUB	92	208	1.43e-11	SMART
EGF	209	244	1.95e1	SMART
Pfam:EGF_2	248	279	5.8e-7	PFAM
Pfam:Kelch_5	350	391	2.1e-9	PFAM
Pfam:Kelch_6	354	401	5.8e-8	PFAM
Pfam:Kelch_4	465	517	4.3e-7	PFAM
Pfam:Kelch_1	519	573	2.7e-6	PFAM
PSI	613	656	3.38e-1	SMART
PSI	665	708	2e-3	SMART
PSI	714	759	1.72e-2	SMART
CLECT	747	872	2.86e-20	SMART
PSI	888	938	6.26e-5	SMART
PSI	941	1011	1.73e-7	SMART
EGF_Lam	1013	1056	1.07e-5	SMART
low complexity region	1157	1173	N/A	INTRINSIC
transmembrane domain	1229	1251	N/A	INTRINSIC
low complexity region	1261	1272	N/A	INTRINSIC
low complexity region	1326	1339	N/A	INTRINSIC

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.9%
20x: 94.4%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice homozygous for a null allele exhibit normal coat coloring and normal brain morphology. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 145 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4921517D22Rik	T	C	13: 59,691,592 (GRCm38)	D13G	probably benign	Het
4930442H23Rik	C	T	10: 81,183,144 (GRCm38)		probably benign	Het
Adamts13	T	A	2: 26,983,042 (GRCm38)	S341T	probably damaging	Het
Adamts2	A	G	11: 50,792,722 (GRCm38)	I944V	probably benign	Het
Adcy3	A	G	12: 4,206,542 (GRCm38)	T783A	probably benign	Het
Ago3	A	T	4: 126,368,503 (GRCm38)	M418K	probably benign	Het
Alpk1	G	T	3: 127,687,592 (GRCm38)	N175K	possibly damaging	Het
Als2	A	G	1: 59,215,313 (GRCm38)	V295A	probably benign	Het
Anapc13	T	C	9: 102,629,821 (GRCm38)	I11T	probably benign	Het
Ankrd12	T	A	17: 65,982,999 (GRCm38)	N1813I	probably damaging	Het
Anks1b	A	T	10: 90,914,750 (GRCm38)	I176F	probably null	Het
Ap3d1	TTCTCTCTCTCTCTCTCT	TTCTCTCTCTCTCTCT	10: 80,712,778 (GRCm38)		probably null	Het
Arhgap32	A	G	9: 32,129,653 (GRCm38)	D67G	probably damaging	Het
Arhgap32	T	C	9: 32,260,780 (GRCm38)	C1619R	probably damaging	Het
Atp1a4	A	T	1: 172,254,110 (GRCm38)	Y158*	probably null	Het
Atp8b5	A	T	4: 43,356,980 (GRCm38)	D576V	probably damaging	Het
B430203G13Rik	A	T	12: 17,924,519 (GRCm38)		noncoding transcript	Het
Baz1b	T	G	5: 135,217,413 (GRCm38)	L572R	possibly damaging	Het
Ccn3	A	T	15: 54,752,207 (GRCm38)		probably null	Het
Ccnd2	T	C	6: 127,148,798 (GRCm38)	T92A	possibly damaging	Het
Ccndbp1	A	T	2: 121,008,522 (GRCm38)	T5S	probably benign	Het
Ccr2	G	A	9: 124,106,372 (GRCm38)	V230I	probably benign	Het
Cct4	T	A	11: 23,002,866 (GRCm38)	V514E	probably damaging	Het
Cep152	A	G	2: 125,586,329 (GRCm38)		probably null	Het
Cflar	C	T	1: 58,752,567 (GRCm38)	T343M	probably benign	Het
Chrm5	A	C	2: 112,479,585 (GRCm38)	N395K	probably benign	Het
Chrna10	G	A	7: 102,113,219 (GRCm38)	P255S	possibly damaging	Het
Chrna6	T	A	8: 27,407,106 (GRCm38)	I248F	probably damaging	Het
Clip1	T	C	5: 123,579,293 (GRCm38)	D1387G	probably damaging	Het
Clstn3	T	C	6: 124,437,372 (GRCm38)		probably null	Het
Cntnap5a	C	T	1: 116,101,565 (GRCm38)	R250W	probably benign	Het
Col12a1	C	A	9: 79,678,494 (GRCm38)	V1228F	possibly damaging	Het
Cxcr5	T	C	9: 44,513,341 (GRCm38)	T340A	probably benign	Het
Cyp2a4	G	A	7: 26,312,875 (GRCm38)	R361K	probably damaging	Het
Dnah1	T	A	14: 31,263,479 (GRCm38)	K3818N	probably damaging	Het
Dnah3	T	A	7: 119,967,824 (GRCm38)	K2393M	probably benign	Het
Dpy19l1	A	T	9: 24,424,823 (GRCm38)	L529Q	probably damaging	Het
Eif4g2	C	T	7: 111,076,796 (GRCm38)	R399H	probably damaging	Het
Elapor1	A	T	3: 108,458,227 (GRCm38)		probably benign	Het
Fam76a	A	T	4: 132,902,117 (GRCm38)		probably null	Het
Fam76a	A	G	4: 132,916,190 (GRCm38)	Y78H	probably damaging	Het
Fbn1	A	T	2: 125,324,919 (GRCm38)	C2026S	probably damaging	Het
Fbxo4	T	C	15: 3,969,041 (GRCm38)	T312A	probably benign	Het
Fbxw26	A	G	9: 109,724,800 (GRCm38)	V257A	possibly damaging	Het
Fhip1a	G	T	3: 85,688,570 (GRCm38)	T115K	probably damaging	Het
Flnb	A	T	14: 7,905,701 (GRCm38)	E1150D	probably benign	Het
Fndc3c1	A	T	X: 106,437,702 (GRCm38)	S661R	possibly damaging	Het
Gba2	A	C	4: 43,568,315 (GRCm38)	L684R	probably damaging	Het
Gbf1	G	T	19: 46,268,395 (GRCm38)	C812F	possibly damaging	Het
Glt8d2	A	T	10: 82,660,749 (GRCm38)	D158E	probably damaging	Het
Golga2	T	A	2: 32,297,156 (GRCm38)	N89K	probably damaging	Het
Got1	A	G	19: 43,502,937 (GRCm38)	I358T	possibly damaging	Het
Gpx6	C	T	13: 21,312,264 (GRCm38)	Q3*	probably null	Het
Grin1	T	A	2: 25,292,381 (GRCm38)	H956L	possibly damaging	Het
Grin2d	A	G	7: 45,856,781 (GRCm38)	V562A	probably damaging	Het
Grm6	A	G	11: 50,857,277 (GRCm38)	I405V	probably benign	Het
Hcar2	C	G	5: 123,864,450 (GRCm38)	G330A	probably benign	Het
Hcfc1	T	C	X: 73,965,946 (GRCm38)	K20E	probably damaging	Het
Iars1	T	A	13: 49,724,663 (GRCm38)	Y888N	probably damaging	Het
Ifi206	A	T	1: 173,480,866 (GRCm38)	H521Q	probably benign	Het
Impg1	A	G	9: 80,398,450 (GRCm38)	S112P	probably benign	Het
Incenp	T	A	19: 9,877,691 (GRCm38)	R619W	unknown	Het
Incenp	C	A	19: 9,877,690 (GRCm38)	R619M	unknown	Het
Kat2b	A	G	17: 53,653,203 (GRCm38)	E513G	possibly damaging	Het
Kbtbd12	G	T	6: 88,618,021 (GRCm38)	L276I	probably damaging	Het
Kctd9	T	A	14: 67,734,164 (GRCm38)	D229E	probably damaging	Het
Kdm1b	C	T	13: 47,063,077 (GRCm38)	R308W	probably damaging	Het
Kif2b	G	A	11: 91,576,428 (GRCm38)	P343L	probably benign	Het
Kntc1	T	G	5: 123,816,762 (GRCm38)	M2081R	possibly damaging	Het
Lamc1	T	C	1: 153,231,740 (GRCm38)	N1231S	probably damaging	Het
Lclat1	T	A	17: 73,240,070 (GRCm38)	Y327*	probably null	Het
Lgals3bp	G	A	11: 118,393,514 (GRCm38)	T413I	probably damaging	Het
Lin54	A	G	5: 100,459,738 (GRCm38)	I250T	probably damaging	Het
Lrp1	T	C	10: 127,558,133 (GRCm38)	N2621S	probably benign	Het
Lrrtm3	T	A	10: 64,088,002 (GRCm38)	H462L	probably benign	Het
Lysmd1	A	G	3: 95,134,986 (GRCm38)	Y57C	probably damaging	Het
Mccc1	C	A	3: 35,975,873 (GRCm38)	M429I	probably damaging	Het
Metrnl	A	G	11: 121,707,924 (GRCm38)	E40G	probably benign	Het
Mios	T	A	6: 8,222,464 (GRCm38)	M466K	probably benign	Het
Mrgpra1	A	G	7: 47,335,470 (GRCm38)	S154P	probably damaging	Het
Mrpl24	T	C	3: 87,922,050 (GRCm38)		probably null	Het
Myo1f	A	G	17: 33,598,191 (GRCm38)	N736S	possibly damaging	Het
Myo1h	A	G	5: 114,360,599 (GRCm38)	I919V	possibly damaging	Het
Nampt	T	C	12: 32,848,714 (GRCm38)	L443P	possibly damaging	Het
Ndufaf2	C	G	13: 108,052,780 (GRCm38)	A145P	probably damaging	Het
Nek10	A	T	14: 14,855,714 (GRCm38)	T403S	probably benign	Het
Nme8	C	A	13: 19,657,930 (GRCm38)	V219L	probably damaging	Het
Nps	T	A	7: 135,268,788 (GRCm38)	L13Q	probably damaging	Het
Nutm1	G	A	2: 112,248,936 (GRCm38)	A878V	probably benign	Het
Ogdh	T	C	11: 6,349,875 (GRCm38)	F794L	probably damaging	Het
Olfr721-ps1	A	C	14: 14,407,729 (GRCm38)	Y167S	possibly damaging	Het
Or14a259	C	A	7: 86,363,735 (GRCm38)	G201C	probably damaging	Het
Or14c39	T	C	7: 86,694,528 (GRCm38)	L24P	probably damaging	Het
Or4f56	A	T	2: 111,873,050 (GRCm38)	D268E	possibly damaging	Het
Or5a3	A	T	19: 12,422,977 (GRCm38)	I223F	probably damaging	Het
Or5g29	A	G	2: 85,590,938 (GRCm38)	T133A	probably benign	Het
Pik3cg	T	C	12: 32,205,199 (GRCm38)	E263G	probably damaging	Het
Pikfyve	A	G	1: 65,267,846 (GRCm38)	T1798A	probably benign	Het
Poldip3	T	C	15: 83,131,501 (GRCm38)	Y305C	probably damaging	Het
Prkdc	T	C	16: 15,648,976 (GRCm38)	I107T	probably benign	Het
Prmt2	A	G	10: 76,226,221 (GRCm38)	I50T	probably damaging	Het
Ptprd	T	C	4: 76,140,553 (GRCm38)	T168A	probably benign	Het
Pudp	A	G	18: 50,568,065 (GRCm38)	V199A	probably damaging	Het
Rab3c	T	C	13: 110,061,900 (GRCm38)	E198G	probably benign	Het
Rasl12	A	G	9: 65,413,448 (GRCm38)	Y156C	probably damaging	Het
Rbm12	T	C	2: 156,096,564 (GRCm38)	D596G	possibly damaging	Het
Rbm6	T	C	9: 107,787,352 (GRCm38)	E694G	probably benign	Het
Rif1	T	C	2: 52,112,747 (GRCm38)	V2071A	probably damaging	Het
Ripply2	A	T	9: 87,019,796 (GRCm38)	N125I	probably damaging	Het
Rps6kc1	A	T	1: 190,750,188 (GRCm38)	H284Q	probably benign	Het
Scara3	A	T	14: 65,953,501 (GRCm38)	M1K	probably null	Het
Sfswap	A	G	5: 129,513,083 (GRCm38)	T215A	probably damaging	Het
Shroom2	A	C	X: 152,660,907 (GRCm38)	F421V	probably benign	Het
Sipa1l3	A	G	7: 29,377,641 (GRCm38)	V902A	probably damaging	Het
Slamf8	G	T	1: 172,584,214 (GRCm38)	P238Q	probably damaging	Het
Slc44a3	T	C	3: 121,527,074 (GRCm38)	T93A	possibly damaging	Het
Slc5a7	A	T	17: 54,278,700 (GRCm38)	I363N	probably damaging	Het
Slc66a1	G	T	4: 139,300,001 (GRCm38)	H343Q	probably benign	Het
Slc7a2	T	A	8: 40,911,058 (GRCm38)	M436K	probably benign	Het
Spindoc	A	G	19: 7,374,091 (GRCm38)	S223P	probably benign	Het
Stk11ip	T	C	1: 75,530,281 (GRCm38)	F669L	possibly damaging	Het
Sun3	G	A	11: 9,038,266 (GRCm38)	L19F	probably benign	Het
Sycp1	C	A	3: 102,853,489 (GRCm38)	A703S	possibly damaging	Het
Tas2r139	T	G	6: 42,141,284 (GRCm38)	F117V	probably damaging	Het
Tdrd6	T	C	17: 43,625,576 (GRCm38)	Y1527C	probably damaging	Het
Tenm4	A	C	7: 96,774,046 (GRCm38)	K683Q	probably damaging	Het
Tfeb	T	A	17: 47,788,227 (GRCm38)		probably null	Het
Tmco4	T	C	4: 138,998,039 (GRCm38)	S121P	probably damaging	Het
Tmprss11d	C	T	5: 86,306,281 (GRCm38)	V222M	probably damaging	Het
Tnks1bp1	T	C	2: 85,063,034 (GRCm38)	W440R	probably damaging	Het
Trp53bp2	A	G	1: 182,448,997 (GRCm38)	T848A	probably benign	Het
Tssk1	G	A	16: 17,895,062 (GRCm38)	R237H	probably benign	Het
Ttll4	A	T	1: 74,679,007 (GRCm38)	T6S	possibly damaging	Het
Ttn	G	T	2: 76,721,797 (GRCm38)	Y29419*	probably null	Het
Ttn	A	G	2: 76,769,603 (GRCm38)	Y19076H	probably damaging	Het
Ubr3	T	A	2: 69,959,603 (GRCm38)	V867D	probably damaging	Het
Usp29	A	G	7: 6,961,391 (GRCm38)	T78A	probably damaging	Het
Utrn	T	G	10: 12,654,745 (GRCm38)	Q2108P	probably benign	Het
Vcan	T	C	13: 89,705,789 (GRCm38)	N351D	probably damaging	Het
Vmn1r61	A	T	7: 5,611,127 (GRCm38)	Y63N	probably benign	Het
Vmn1r61	A	T	7: 5,611,125 (GRCm38)	Y63*	probably null	Het
Vmn1r85	A	T	7: 13,084,861 (GRCm38)	W119R	probably damaging	Het
Zbtb21	A	C	16: 97,950,455 (GRCm38)	V190G	possibly damaging	Het
Zfp157	C	A	5: 138,444,789 (GRCm38)	T14N	probably damaging	Het
Zfp942	A	T	17: 21,929,419 (GRCm38)	H76Q	probably damaging	Het

Other mutations in Atrnl1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00323:Atrnl1	APN	19	57,691,817 (GRCm38)	missense	probably benign	0.02
IGL00707:Atrnl1	APN	19	57,673,265 (GRCm38)	missense	probably damaging	0.96
IGL00921:Atrnl1	APN	19	57,702,153 (GRCm38)	missense	probably damaging	1.00
IGL01410:Atrnl1	APN	19	58,131,104 (GRCm38)	missense	probably damaging	1.00
IGL01468:Atrnl1	APN	19	57,699,712 (GRCm38)	missense	probably benign	0.02
IGL01756:Atrnl1	APN	19	57,652,948 (GRCm38)	missense	probably benign
IGL01971:Atrnl1	APN	19	57,753,283 (GRCm38)	missense	probably damaging	1.00
IGL02019:Atrnl1	APN	19	57,691,763 (GRCm38)	splice site	probably benign
IGL02580:Atrnl1	APN	19	57,714,576 (GRCm38)	splice site	probably benign
IGL02649:Atrnl1	APN	19	57,650,441 (GRCm38)	splice site	probably benign
IGL02676:Atrnl1	APN	19	57,691,884 (GRCm38)	missense	probably damaging	1.00
IGL03276:Atrnl1	APN	19	57,652,927 (GRCm38)	missense	probably damaging	0.99
IGL03379:Atrnl1	APN	19	57,642,541 (GRCm38)	missense	probably benign	0.02
Magnetogorsk	UTSW	19	57,630,306 (GRCm38)	missense	probably damaging	1.00
polar	UTSW	19	57,652,950 (GRCm38)	missense	probably benign	0.00
PIT4812001:Atrnl1	UTSW	19	57,731,623 (GRCm38)	missense	probably benign	0.08
R0109:Atrnl1	UTSW	19	57,755,517 (GRCm38)	missense	possibly damaging	0.78
R0308:Atrnl1	UTSW	19	57,753,288 (GRCm38)	missense	probably benign	0.04
R0394:Atrnl1	UTSW	19	57,673,176 (GRCm38)	missense	probably benign	0.10
R0734:Atrnl1	UTSW	19	57,654,861 (GRCm38)	missense	probably damaging	1.00
R0811:Atrnl1	UTSW	19	57,673,141 (GRCm38)	missense	probably benign	0.07
R0812:Atrnl1	UTSW	19	57,673,141 (GRCm38)	missense	probably benign	0.07
R1183:Atrnl1	UTSW	19	57,650,293 (GRCm38)	missense	probably damaging	0.97
R1213:Atrnl1	UTSW	19	57,638,462 (GRCm38)	missense	probably benign	0.25
R1344:Atrnl1	UTSW	19	57,935,705 (GRCm38)	critical splice donor site	probably null
R1418:Atrnl1	UTSW	19	57,935,705 (GRCm38)	critical splice donor site	probably null
R1707:Atrnl1	UTSW	19	57,686,737 (GRCm38)	missense	probably benign	0.00
R1748:Atrnl1	UTSW	19	57,714,702 (GRCm38)	missense	probably damaging	0.99
R2051:Atrnl1	UTSW	19	57,691,849 (GRCm38)	missense	probably benign	0.01
R2113:Atrnl1	UTSW	19	57,755,616 (GRCm38)	nonsense	probably null
R2130:Atrnl1	UTSW	19	57,654,994 (GRCm38)	missense	probably damaging	1.00
R3710:Atrnl1	UTSW	19	57,657,114 (GRCm38)	missense	probably damaging	1.00
R3916:Atrnl1	UTSW	19	57,935,652 (GRCm38)	missense	possibly damaging	0.82
R4524:Atrnl1	UTSW	19	57,630,306 (GRCm38)	missense	probably damaging	1.00
R4707:Atrnl1	UTSW	19	57,629,158 (GRCm38)	missense	probably damaging	0.97
R4712:Atrnl1	UTSW	19	57,652,950 (GRCm38)	missense	probably benign	0.00
R4784:Atrnl1	UTSW	19	57,629,158 (GRCm38)	missense	probably damaging	0.97
R4798:Atrnl1	UTSW	19	58,042,361 (GRCm38)	missense	probably benign
R5172:Atrnl1	UTSW	19	57,685,513 (GRCm38)	nonsense	probably null
R5226:Atrnl1	UTSW	19	57,650,335 (GRCm38)	missense	probably benign
R5289:Atrnl1	UTSW	19	57,657,082 (GRCm38)	missense	probably damaging	1.00
R5372:Atrnl1	UTSW	19	57,755,536 (GRCm38)	missense	probably benign
R5737:Atrnl1	UTSW	19	57,777,888 (GRCm38)	missense	possibly damaging	0.84
R5782:Atrnl1	UTSW	19	57,753,286 (GRCm38)	missense	possibly damaging	0.95
R5826:Atrnl1	UTSW	19	57,630,292 (GRCm38)	nonsense	probably null
R6169:Atrnl1	UTSW	19	57,642,463 (GRCm38)	missense	probably benign	0.00
R6242:Atrnl1	UTSW	19	57,642,478 (GRCm38)	missense	probably benign	0.02
R6342:Atrnl1	UTSW	19	57,638,510 (GRCm38)	missense	probably damaging	1.00
R6372:Atrnl1	UTSW	19	57,650,332 (GRCm38)	missense	probably benign	0.01
R6811:Atrnl1	UTSW	19	57,654,961 (GRCm38)	missense	probably damaging	0.98
R6897:Atrnl1	UTSW	19	58,042,368 (GRCm38)	missense	probably benign	0.01
R7024:Atrnl1	UTSW	19	57,638,450 (GRCm38)	critical splice acceptor site	probably null
R7085:Atrnl1	UTSW	19	57,691,857 (GRCm38)	missense	probably damaging	1.00
R7144:Atrnl1	UTSW	19	58,042,352 (GRCm38)	missense	probably damaging	1.00
R7259:Atrnl1	UTSW	19	57,935,606 (GRCm38)	nonsense	probably null
R7289:Atrnl1	UTSW	19	57,650,414 (GRCm38)	missense	probably benign	0.13
R7310:Atrnl1	UTSW	19	57,642,424 (GRCm38)	missense	possibly damaging	0.69
R7372:Atrnl1	UTSW	19	57,935,646 (GRCm38)	missense	possibly damaging	0.47
R7432:Atrnl1	UTSW	19	57,755,524 (GRCm38)	missense	probably damaging	1.00
R7478:Atrnl1	UTSW	19	57,696,312 (GRCm38)	missense	possibly damaging	0.89
R7556:Atrnl1	UTSW	19	57,654,846 (GRCm38)	missense	probably benign
R7567:Atrnl1	UTSW	19	57,699,523 (GRCm38)	missense	probably damaging	0.98
R7608:Atrnl1	UTSW	19	57,714,687 (GRCm38)	missense	probably damaging	1.00
R7632:Atrnl1	UTSW	19	57,630,306 (GRCm38)	missense	probably damaging	1.00
R7655:Atrnl1	UTSW	19	57,611,379 (GRCm38)	nonsense	probably null
R7656:Atrnl1	UTSW	19	57,611,379 (GRCm38)	nonsense	probably null
R7718:Atrnl1	UTSW	19	57,740,183 (GRCm38)	nonsense	probably null
R7721:Atrnl1	UTSW	19	57,696,331 (GRCm38)	missense	probably benign	0.00
R7726:Atrnl1	UTSW	19	57,702,072 (GRCm38)	missense	probably damaging	1.00
R7733:Atrnl1	UTSW	19	57,701,988 (GRCm38)	missense	probably benign	0.00
R7774:Atrnl1	UTSW	19	57,699,671 (GRCm38)	missense	probably damaging	1.00
R8010:Atrnl1	UTSW	19	57,682,446 (GRCm38)	missense	probably benign	0.14
R8119:Atrnl1	UTSW	19	57,642,463 (GRCm38)	missense	probably benign	0.00
R9242:Atrnl1	UTSW	19	57,657,228 (GRCm38)	missense	probably benign	0.07
R9265:Atrnl1	UTSW	19	57,777,927 (GRCm38)	missense	probably benign	0.11
R9272:Atrnl1	UTSW	19	57,654,988 (GRCm38)	missense	probably benign	0.00
R9480:Atrnl1	UTSW	19	57,701,988 (GRCm38)	missense	possibly damaging	0.61
R9526:Atrnl1	UTSW	19	57,629,119 (GRCm38)	missense	probably damaging	0.99
R9672:Atrnl1	UTSW	19	57,630,263 (GRCm38)	missense	possibly damaging	0.87
R9673:Atrnl1	UTSW	19	57,611,354 (GRCm38)	start codon destroyed	probably null	0.04
RF021:Atrnl1	UTSW	19	57,642,473 (GRCm38)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- TGTCAGTTGAAACAGCCGTG -3'
(R):5'- TACCATTAAGGGAAGACACTATGG -3'

Sequencing Primer
(F):5'- CAGTTGAAACAGCCGTGCTTTATC -3'
(R):5'- CATTAAGGGAAGACACTATGGTTTAC -3'

Posted On

2015-12-29