Mutagenetix > Incidental Mutation

Incidental Mutation 'R2118:Abca13'

231217

Institutional Source

Beutler Lab

Gene Symbol

Abca13

Ensembl Gene

ENSMUSG00000004668

Gene Name

ATP-binding cassette, sub-family A (ABC1), member 13

Synonyms

A930002G16Rik

MMRRC Submission

040122-MU

Accession Numbers

NCBI RefSeq: NM_178259.3; MGI:2388707

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R2118 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

9191942-9684259 bp(+) (GRCm38)

Type of Mutation

splice site

DNA Base Change (assembly)

T to C at 9309013 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000040465 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000042740]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000042740

SMART Domains

Protein: ENSMUSP00000040465
Gene: ENSMUSG00000004668

Domain	Start	End	E-Value	Type
transmembrane domain	20	42	N/A	INTRINSIC
low complexity region	358	379	N/A	INTRINSIC
low complexity region	441	451	N/A	INTRINSIC
low complexity region	820	831	N/A	INTRINSIC
low complexity region	1382	1393	N/A	INTRINSIC
low complexity region	1721	1737	N/A	INTRINSIC
low complexity region	1859	1872	N/A	INTRINSIC
Pfam:ABC2_membrane_3	3288	3740	4.7e-21	PFAM
low complexity region	3796	3809	N/A	INTRINSIC
AAA	3835	4019	8.08e-12	SMART
transmembrane domain	4206	4228	N/A	INTRINSIC
Pfam:ABC2_membrane_3	4317	4646	1.6e-33	PFAM
AAA	4721	4909	8.86e-9	SMART

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.4%
20x: 95.6%

Validation Efficiency

100% (90/90)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] In human, the ATP-binding cassette (ABC) family of transmembrane transporters has at least 48 genes and 7 gene subfamilies. This gene is a member of ABC gene subfamily A (ABCA). Genes within the ABCA family typically encode several thousand amino acids. Like other ABC transmembrane transporter proteins, this protein has 12 or more transmembrane alpha-helix domains that likely arrange to form a single central chamber with multiple substrate binding sites. It is also predicted to have two large extracellular domains and two nucleotide binding domains as is typical for ABCA proteins. Alternative splice variants have been described but their biological validity has not been demonstrated.[provided by RefSeq, Mar 2009]

Allele List at MGI

All alleles(3) : Targeted(3)

Other mutations in this stock

Total: 87 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700020L24Rik	T	C	11: 83,440,364 (GRCm38)	S31P	possibly damaging	Het
4933430I17Rik	T	A	4: 62,538,872 (GRCm38)	L143M	possibly damaging	Het
Abcg5	T	A	17: 84,671,147 (GRCm38)	E294D	probably benign	Het
Abi3bp	T	C	16: 56,477,864 (GRCm38)		probably benign	Het
Adamts8	T	C	9: 30,943,063 (GRCm38)	F76S	probably damaging	Het
Agpat3	T	C	10: 78,278,084 (GRCm38)	R257G	probably damaging	Het
Ahctf1	C	A	1: 179,769,452 (GRCm38)	R43L	probably damaging	Het
AI593442	T	C	9: 52,677,693 (GRCm38)	T195A	probably benign	Het
Aipl1	A	T	11: 72,029,369 (GRCm38)	L291Q	possibly damaging	Het
Ambn	T	A	5: 88,460,758 (GRCm38)		probably benign	Het
Arap2	G	A	5: 62,706,685 (GRCm38)	T532I	probably damaging	Het
Arg1	T	C	10: 24,920,723 (GRCm38)	N69D	possibly damaging	Het
Arhgef10	A	G	8: 14,934,820 (GRCm38)	D200G	probably damaging	Het
Arhgef38	T	C	3: 133,160,753 (GRCm38)	K208E	probably benign	Het
Asb4	A	T	6: 5,390,687 (GRCm38)	T27S	probably benign	Het
Ash1l	C	G	3: 88,985,295 (GRCm38)	Q1494E	possibly damaging	Het
Car12	T	C	9: 66,713,892 (GRCm38)	V15A	probably benign	Het
Cdc20b	A	G	13: 113,078,698 (GRCm38)	I267V	probably benign	Het
Cdh1	A	G	8: 106,664,210 (GRCm38)	I653V	probably benign	Het
Cenpe	T	A	3: 135,246,884 (GRCm38)	M1445K	possibly damaging	Het
Cfap43	T	C	19: 47,770,438 (GRCm38)	E932G	probably damaging	Het
Cfhr1	G	C	1: 139,550,904 (GRCm38)	Q243E	probably benign	Het
Cnih2	C	A	19: 5,098,248 (GRCm38)	A6S	possibly damaging	Het
Cntnap1	G	T	11: 101,188,657 (GRCm38)	M1240I	probably benign	Het
Cntrl	T	C	2: 35,161,965 (GRCm38)	S1050P	probably benign	Het
Cyp2a12	A	G	7: 27,036,646 (GRCm38)	*493W	probably null	Het
Dbx2	A	C	15: 95,624,800 (GRCm38)	L342R	probably damaging	Het
Dmd	G	C	X: 84,312,483 (GRCm38)	A2257P	probably benign	Het
Dnajb2	T	C	1: 75,237,477 (GRCm38)	W30R	probably damaging	Het
Ecel1	A	G	1: 87,148,275 (GRCm38)	S727P	probably damaging	Het
Ednrb	T	A	14: 103,821,768 (GRCm38)	D274V	probably benign	Het
Fam78b	G	A	1: 167,078,709 (GRCm38)	V146M	probably damaging	Het
Fancd2	A	G	6: 113,560,074 (GRCm38)		probably benign	Het
Fbxw14	T	C	9: 109,274,624 (GRCm38)		probably benign	Het
Gimap4	G	T	6: 48,690,971 (GRCm38)	C92F	probably benign	Het
Gm5828	A	G	1: 16,769,975 (GRCm38)		noncoding transcript	Het
Gnpat	T	C	8: 124,876,941 (GRCm38)	V186A	probably damaging	Het
Gnptab	T	C	10: 88,436,398 (GRCm38)	S967P	probably benign	Het
Ikbkb	T	C	8: 22,667,217 (GRCm38)		probably benign	Het
Il1rap	A	T	16: 26,710,565 (GRCm38)	H379L	probably damaging	Het
Ints12	T	C	3: 133,109,160 (GRCm38)	V376A	probably damaging	Het
Kalrn	C	T	16: 34,332,230 (GRCm38)	S309N	possibly damaging	Het
Kel	T	A	6: 41,689,300 (GRCm38)	I471L	probably benign	Het
Klhl25	T	C	7: 75,866,732 (GRCm38)	V462A	probably damaging	Het
Ksr1	A	T	11: 79,045,193 (GRCm38)	M77K	probably benign	Het
Leo1	T	A	9: 75,445,812 (GRCm38)	N212K	probably damaging	Het
Ltbp1	T	A	17: 75,310,159 (GRCm38)	V1031E	possibly damaging	Het
Ltbr	A	G	6: 125,309,477 (GRCm38)	S249P	probably benign	Het
Mast4	A	G	13: 102,754,205 (GRCm38)	V855A	probably damaging	Het
Mdga2	T	A	12: 66,868,752 (GRCm38)	E43V	probably damaging	Het
Mmaa	A	T	8: 79,267,959 (GRCm38)	L406*	probably null	Het
Nlrp12	A	T	7: 3,241,449 (GRCm38)	N144K	probably damaging	Het
Nlrp6	T	C	7: 140,926,444 (GRCm38)	V766A	probably benign	Het
Olfr1314	C	A	2: 112,092,330 (GRCm38)	V124L	probably benign	Het
Olfr186	A	G	16: 59,027,815 (GRCm38)	F31L	possibly damaging	Het
Pabpc4l	T	C	3: 46,446,841 (GRCm38)	T123A	probably benign	Het
Pappa2	T	C	1: 158,857,266 (GRCm38)	T768A	probably damaging	Het
Pde6d	A	G	1: 86,545,802 (GRCm38)	F91L	probably benign	Het
Ppp1r13l	A	G	7: 19,371,421 (GRCm38)	M373V	possibly damaging	Het
Prss37	G	A	6: 40,515,360 (GRCm38)	R186*	probably null	Het
Psg16	C	A	7: 17,090,623 (GRCm38)	H111N	probably benign	Het
Psg20	T	A	7: 18,681,022 (GRCm38)	Y316F	probably benign	Het
Psmd1	T	A	1: 86,078,700 (GRCm38)	S263T	possibly damaging	Het
Rai14	A	G	15: 10,575,166 (GRCm38)	F569L	probably benign	Het
Rbpms2	T	A	9: 65,650,947 (GRCm38)	D116E	probably damaging	Het
Rgs20	A	G	1: 4,916,890 (GRCm38)		probably benign	Het
Rnf114	T	C	2: 167,510,883 (GRCm38)	L101P	probably damaging	Het
Rnf168	T	G	16: 32,278,218 (GRCm38)	L37R	probably damaging	Het
RP23-114B10.6	A	C	8: 69,372,290 (GRCm38)		noncoding transcript	Het
Rpe	T	C	1: 66,715,228 (GRCm38)	M153T	probably damaging	Het
Sap18	T	A	14: 57,798,554 (GRCm38)	S66T	probably damaging	Het
Slc2a13	A	G	15: 91,516,476 (GRCm38)	V181A	probably damaging	Het
Soga1	T	C	2: 157,033,325 (GRCm38)	E835G	probably damaging	Het
Spag17	A	G	3: 100,049,240 (GRCm38)	E884G	possibly damaging	Het
Sycn	T	C	7: 28,541,288 (GRCm38)	S127P	probably damaging	Het
Tas2r106	A	T	6: 131,678,354 (GRCm38)	L178H	probably damaging	Het
Tas2r117	T	A	6: 132,803,166 (GRCm38)	I89K	probably damaging	Het
Tep1	C	A	14: 50,855,572 (GRCm38)		probably null	Het
Tex14	T	C	11: 87,519,743 (GRCm38)		probably benign	Het
Tll1	T	C	8: 64,085,557 (GRCm38)	E351G	probably benign	Het
Tmem44	T	A	16: 30,547,444 (GRCm38)	K55*	probably null	Het
Trak1	T	A	9: 121,472,997 (GRCm38)	*940R	probably null	Het
Vmn1r200	C	T	13: 22,395,183 (GRCm38)	T43I	probably damaging	Het
Wars2	T	C	3: 99,216,567 (GRCm38)	V248A	probably benign	Het
Wfdc6b	C	T	2: 164,617,443 (GRCm38)	R142C	probably benign	Het
Zfp729a	A	T	13: 67,621,494 (GRCm38)		probably null	Het
Zfp759	C	A	13: 67,139,514 (GRCm38)		probably benign	Het

Other mutations in Abca13

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00094:Abca13	APN	11	9,297,443 (GRCm38)	missense	probably benign	0.24
IGL00481:Abca13	APN	11	9,290,969 (GRCm38)	missense	probably damaging	0.99
IGL00707:Abca13	APN	11	9,291,586 (GRCm38)	missense	probably damaging	0.99
IGL00755:Abca13	APN	11	9,542,102 (GRCm38)	missense	possibly damaging	0.87
IGL00771:Abca13	APN	11	9,290,870 (GRCm38)	missense	probably damaging	1.00
IGL00802:Abca13	APN	11	9,297,717 (GRCm38)	missense	probably damaging	0.96
IGL00807:Abca13	APN	11	9,378,285 (GRCm38)	missense	probably benign	0.10
IGL00977:Abca13	APN	11	9,399,284 (GRCm38)	missense	probably damaging	1.00
IGL01064:Abca13	APN	11	9,483,855 (GRCm38)	missense	probably benign	0.01
IGL01100:Abca13	APN	11	9,274,673 (GRCm38)	splice site	probably null
IGL01290:Abca13	APN	11	9,256,232 (GRCm38)	missense	probably damaging	1.00
IGL01299:Abca13	APN	11	9,298,743 (GRCm38)	missense	probably benign	0.22
IGL01302:Abca13	APN	11	9,399,470 (GRCm38)	splice site	probably benign
IGL01307:Abca13	APN	11	9,297,159 (GRCm38)	missense	possibly damaging	0.86
IGL01349:Abca13	APN	11	9,292,076 (GRCm38)	missense	probably benign	0.05
IGL01351:Abca13	APN	11	9,267,565 (GRCm38)	missense	probably benign	0.28
IGL01446:Abca13	APN	11	9,403,834 (GRCm38)	missense	probably damaging	0.97
IGL01453:Abca13	APN	11	9,403,834 (GRCm38)	missense	probably damaging	0.97
IGL01461:Abca13	APN	11	9,403,834 (GRCm38)	missense	probably damaging	0.97
IGL01476:Abca13	APN	11	9,403,834 (GRCm38)	missense	probably damaging	0.97
IGL01506:Abca13	APN	11	9,297,447 (GRCm38)	missense	probably benign	0.36
IGL01527:Abca13	APN	11	9,290,788 (GRCm38)	missense	possibly damaging	0.49
IGL01559:Abca13	APN	11	9,309,020 (GRCm38)	missense	possibly damaging	0.82
IGL01580:Abca13	APN	11	9,293,527 (GRCm38)	missense	probably benign	0.00
IGL01679:Abca13	APN	11	9,298,071 (GRCm38)	missense	probably benign	0.07
IGL01731:Abca13	APN	11	9,249,749 (GRCm38)	splice site	probably benign
IGL01762:Abca13	APN	11	9,315,423 (GRCm38)	missense	probably benign	0.18
IGL01781:Abca13	APN	11	9,399,280 (GRCm38)	missense	probably damaging	1.00
IGL01802:Abca13	APN	11	9,292,438 (GRCm38)	missense	probably benign	0.00
IGL01809:Abca13	APN	11	9,290,339 (GRCm38)	missense	probably damaging	0.96
IGL01906:Abca13	APN	11	9,216,225 (GRCm38)	missense	probably damaging	1.00
IGL01928:Abca13	APN	11	9,683,342 (GRCm38)	missense	probably benign	0.13
IGL01940:Abca13	APN	11	9,567,661 (GRCm38)	splice site	probably benign
IGL01993:Abca13	APN	11	9,258,452 (GRCm38)	unclassified	probably benign
IGL02039:Abca13	APN	11	9,297,193 (GRCm38)	nonsense	probably null
IGL02159:Abca13	APN	11	9,314,545 (GRCm38)	missense	probably benign	0.00
IGL02202:Abca13	APN	11	9,288,529 (GRCm38)	missense	possibly damaging	0.55
IGL02268:Abca13	APN	11	9,290,626 (GRCm38)	missense	probably benign	0.00
IGL02332:Abca13	APN	11	9,291,482 (GRCm38)	missense	probably damaging	0.98
IGL02380:Abca13	APN	11	9,291,599 (GRCm38)	missense	possibly damaging	0.73
IGL02466:Abca13	APN	11	9,297,527 (GRCm38)	missense	probably benign	0.00
IGL02505:Abca13	APN	11	9,581,498 (GRCm38)	missense	probably damaging	1.00
IGL02507:Abca13	APN	11	9,399,388 (GRCm38)	missense	probably damaging	1.00
IGL02558:Abca13	APN	11	9,399,387 (GRCm38)	missense	probably damaging	1.00
IGL02581:Abca13	APN	11	9,399,132 (GRCm38)	splice site	probably benign
IGL02586:Abca13	APN	11	9,293,983 (GRCm38)	missense	possibly damaging	0.56
IGL02598:Abca13	APN	11	9,431,898 (GRCm38)	missense	probably damaging	1.00
IGL02747:Abca13	APN	11	9,373,282 (GRCm38)	nonsense	probably null
IGL02893:Abca13	APN	11	9,290,543 (GRCm38)	missense	probably damaging	0.96
IGL02930:Abca13	APN	11	9,378,226 (GRCm38)	missense	possibly damaging	0.86
IGL02967:Abca13	APN	11	9,378,291 (GRCm38)	missense	probably damaging	0.99
IGL02983:Abca13	APN	11	9,290,663 (GRCm38)	missense	probably benign	0.40
IGL02999:Abca13	APN	11	9,581,757 (GRCm38)	splice site	probably benign
IGL03100:Abca13	APN	11	9,258,527 (GRCm38)	missense	probably benign	0.25
IGL03114:Abca13	APN	11	9,528,999 (GRCm38)	missense	probably benign	0.06
IGL03230:Abca13	APN	11	9,294,313 (GRCm38)	missense	probably benign	0.02
IGL03329:Abca13	APN	11	9,298,047 (GRCm38)	missense	probably benign	0.08
IGL03380:Abca13	APN	11	9,298,574 (GRCm38)	missense	probably benign	0.10
IGL02835:Abca13	UTSW	11	9,451,515 (GRCm38)	missense	probably damaging	1.00
PIT4366001:Abca13	UTSW	11	9,294,962 (GRCm38)	missense	probably benign
PIT4458001:Abca13	UTSW	11	9,298,304 (GRCm38)	missense	probably benign	0.05
R0017:Abca13	UTSW	11	9,292,775 (GRCm38)	missense	probably damaging	0.99
R0079:Abca13	UTSW	11	9,293,493 (GRCm38)	missense	probably benign	0.00
R0089:Abca13	UTSW	11	9,292,886 (GRCm38)	missense	possibly damaging	0.76
R0103:Abca13	UTSW	11	9,273,951 (GRCm38)	missense	probably damaging	1.00
R0103:Abca13	UTSW	11	9,273,951 (GRCm38)	missense	probably damaging	1.00
R0113:Abca13	UTSW	11	9,292,114 (GRCm38)	missense	possibly damaging	0.54
R0119:Abca13	UTSW	11	9,298,076 (GRCm38)	missense	probably benign	0.03
R0152:Abca13	UTSW	11	9,581,724 (GRCm38)	missense	probably damaging	0.98
R0255:Abca13	UTSW	11	9,581,545 (GRCm38)	missense	probably damaging	1.00
R0277:Abca13	UTSW	11	9,294,701 (GRCm38)	missense	probably benign	0.25
R0278:Abca13	UTSW	11	9,378,215 (GRCm38)	missense	probably damaging	1.00
R0294:Abca13	UTSW	11	9,269,122 (GRCm38)	splice site	probably null
R0299:Abca13	UTSW	11	9,298,076 (GRCm38)	missense	probably benign	0.03
R0310:Abca13	UTSW	11	9,293,810 (GRCm38)	missense	probably benign	0.36
R0317:Abca13	UTSW	11	9,293,459 (GRCm38)	missense	probably damaging	1.00
R0323:Abca13	UTSW	11	9,294,701 (GRCm38)	missense	probably benign	0.25
R0324:Abca13	UTSW	11	9,297,669 (GRCm38)	missense	possibly damaging	0.76
R0329:Abca13	UTSW	11	9,399,430 (GRCm38)	missense	probably damaging	0.97
R0336:Abca13	UTSW	11	9,298,481 (GRCm38)	missense	probably benign	0.04
R0346:Abca13	UTSW	11	9,566,278 (GRCm38)	missense	probably damaging	0.99
R0380:Abca13	UTSW	11	9,588,500 (GRCm38)	splice site	probably null
R0382:Abca13	UTSW	11	9,636,650 (GRCm38)	splice site	probably benign
R0482:Abca13	UTSW	11	9,328,207 (GRCm38)	missense	possibly damaging	0.88
R0487:Abca13	UTSW	11	9,331,687 (GRCm38)	missense	probably benign	0.07
R0491:Abca13	UTSW	11	9,298,235 (GRCm38)	missense	probably benign	0.02
R0496:Abca13	UTSW	11	9,291,701 (GRCm38)	missense	probably benign	0.01
R0505:Abca13	UTSW	11	9,291,058 (GRCm38)	missense	probably benign	0.00
R0511:Abca13	UTSW	11	9,294,559 (GRCm38)	missense	probably benign
R0525:Abca13	UTSW	11	9,293,371 (GRCm38)	missense	probably damaging	1.00
R0538:Abca13	UTSW	11	9,267,622 (GRCm38)	critical splice donor site	probably null
R0615:Abca13	UTSW	11	9,256,197 (GRCm38)	missense	probably damaging	0.96
R0634:Abca13	UTSW	11	9,314,491 (GRCm38)	missense	possibly damaging	0.59
R0699:Abca13	UTSW	11	9,588,508 (GRCm38)	splice site	probably benign
R0848:Abca13	UTSW	11	9,682,011 (GRCm38)	nonsense	probably null
R0883:Abca13	UTSW	11	9,291,238 (GRCm38)	nonsense	probably null
R0892:Abca13	UTSW	11	9,298,305 (GRCm38)	missense	probably benign	0.00
R0904:Abca13	UTSW	11	9,298,740 (GRCm38)	missense	probably benign	0.22
R0968:Abca13	UTSW	11	9,298,016 (GRCm38)	missense	probably benign	0.00
R1187:Abca13	UTSW	11	9,528,981 (GRCm38)	missense	probably benign	0.00
R1299:Abca13	UTSW	11	9,294,821 (GRCm38)	missense	possibly damaging	0.94
R1323:Abca13	UTSW	11	9,290,937 (GRCm38)	missense	possibly damaging	0.86
R1323:Abca13	UTSW	11	9,290,937 (GRCm38)	missense	possibly damaging	0.86
R1368:Abca13	UTSW	11	9,291,836 (GRCm38)	missense	probably benign
R1387:Abca13	UTSW	11	9,682,085 (GRCm38)	nonsense	probably null
R1436:Abca13	UTSW	11	9,292,646 (GRCm38)	missense	probably damaging	0.99
R1449:Abca13	UTSW	11	9,298,580 (GRCm38)	missense	probably damaging	1.00
R1450:Abca13	UTSW	11	9,430,531 (GRCm38)	splice site	probably benign
R1462:Abca13	UTSW	11	9,483,924 (GRCm38)	splice site	probably benign
R1465:Abca13	UTSW	11	9,399,303 (GRCm38)	missense	probably damaging	1.00
R1465:Abca13	UTSW	11	9,399,303 (GRCm38)	missense	probably damaging	1.00
R1466:Abca13	UTSW	11	9,570,536 (GRCm38)	splice site	probably benign
R1494:Abca13	UTSW	11	9,466,429 (GRCm38)	nonsense	probably null
R1559:Abca13	UTSW	11	9,399,180 (GRCm38)	missense	probably null	1.00
R1564:Abca13	UTSW	11	9,434,316 (GRCm38)	nonsense	probably null
R1698:Abca13	UTSW	11	9,314,507 (GRCm38)	missense	probably benign	0.13
R1728:Abca13	UTSW	11	9,249,680 (GRCm38)	missense	probably benign	0.02
R1734:Abca13	UTSW	11	9,585,460 (GRCm38)	missense	probably benign	0.03
R1781:Abca13	UTSW	11	9,269,194 (GRCm38)	missense	probably damaging	1.00
R1782:Abca13	UTSW	11	9,297,971 (GRCm38)	missense	probably benign	0.36
R1807:Abca13	UTSW	11	9,291,755 (GRCm38)	missense	probably damaging	0.98
R1830:Abca13	UTSW	11	9,290,350 (GRCm38)	missense	probably benign	0.04
R1869:Abca13	UTSW	11	9,292,134 (GRCm38)	missense	probably benign	0.19
R1870:Abca13	UTSW	11	9,292,134 (GRCm38)	missense	probably benign	0.19
R1871:Abca13	UTSW	11	9,292,134 (GRCm38)	missense	probably benign	0.19
R1903:Abca13	UTSW	11	9,466,411 (GRCm38)	missense	probably benign	0.13
R1916:Abca13	UTSW	11	9,534,456 (GRCm38)	missense	probably damaging	1.00
R1936:Abca13	UTSW	11	9,293,595 (GRCm38)	missense	probably benign	0.13
R1976:Abca13	UTSW	11	9,397,815 (GRCm38)	missense	probably damaging	1.00
R2001:Abca13	UTSW	11	9,273,967 (GRCm38)	missense	probably benign	0.01
R2007:Abca13	UTSW	11	9,191,987 (GRCm38)	missense	probably benign	0.19
R2016:Abca13	UTSW	11	9,290,619 (GRCm38)	missense	probably damaging	1.00
R2017:Abca13	UTSW	11	9,290,619 (GRCm38)	missense	probably damaging	1.00
R2034:Abca13	UTSW	11	9,292,628 (GRCm38)	missense	possibly damaging	0.83
R2051:Abca13	UTSW	11	9,328,098 (GRCm38)	missense	probably benign	0.04
R2075:Abca13	UTSW	11	9,522,382 (GRCm38)	missense	probably damaging	1.00
R2120:Abca13	UTSW	11	9,309,013 (GRCm38)	splice site	probably benign
R2124:Abca13	UTSW	11	9,309,013 (GRCm38)	splice site	probably benign
R2148:Abca13	UTSW	11	9,615,764 (GRCm38)	missense	probably damaging	1.00
R2149:Abca13	UTSW	11	9,267,508 (GRCm38)	missense	possibly damaging	0.68
R2157:Abca13	UTSW	11	9,577,170 (GRCm38)	missense	probably damaging	0.97
R2167:Abca13	UTSW	11	9,288,532 (GRCm38)	missense	probably benign	0.19
R2261:Abca13	UTSW	11	9,292,288 (GRCm38)	missense	probably benign
R2263:Abca13	UTSW	11	9,274,702 (GRCm38)	missense	probably benign	0.04
R2281:Abca13	UTSW	11	9,328,136 (GRCm38)	missense	probably damaging	0.98
R2340:Abca13	UTSW	11	9,399,165 (GRCm38)	missense	probably damaging	0.99
R2357:Abca13	UTSW	11	9,297,336 (GRCm38)	missense	probably damaging	1.00
R2370:Abca13	UTSW	11	9,256,185 (GRCm38)	missense	possibly damaging	0.85
R2384:Abca13	UTSW	11	9,267,450 (GRCm38)	splice site	probably benign
R2393:Abca13	UTSW	11	9,275,057 (GRCm38)	nonsense	probably null
R2432:Abca13	UTSW	11	9,451,333 (GRCm38)	splice site	probably benign
R2446:Abca13	UTSW	11	9,275,101 (GRCm38)	missense	probably benign
R2568:Abca13	UTSW	11	9,333,310 (GRCm38)	missense	probably benign	0.40
R2847:Abca13	UTSW	11	9,294,584 (GRCm38)	missense	possibly damaging	0.59
R2860:Abca13	UTSW	11	9,309,057 (GRCm38)	missense	probably damaging	0.99
R2861:Abca13	UTSW	11	9,309,057 (GRCm38)	missense	probably damaging	0.99
R2862:Abca13	UTSW	11	9,309,057 (GRCm38)	missense	probably damaging	0.99
R2877:Abca13	UTSW	11	9,291,889 (GRCm38)	missense	possibly damaging	0.91
R2878:Abca13	UTSW	11	9,291,889 (GRCm38)	missense	possibly damaging	0.91
R3748:Abca13	UTSW	11	9,316,119 (GRCm38)	splice site	probably benign
R3789:Abca13	UTSW	11	9,510,668 (GRCm38)	missense	probably damaging	0.97
R3933:Abca13	UTSW	11	9,354,856 (GRCm38)	missense	probably damaging	1.00
R3981:Abca13	UTSW	11	9,532,407 (GRCm38)	missense	probably benign
R4002:Abca13	UTSW	11	9,585,415 (GRCm38)	missense	probably benign	0.00
R4010:Abca13	UTSW	11	9,622,013 (GRCm38)	splice site	probably benign
R4011:Abca13	UTSW	11	9,622,013 (GRCm38)	splice site	probably benign
R4127:Abca13	UTSW	11	9,191,973 (GRCm38)	missense	probably benign	0.00
R4214:Abca13	UTSW	11	9,293,877 (GRCm38)	missense	probably damaging	0.96
R4236:Abca13	UTSW	11	9,256,205 (GRCm38)	missense	probably damaging	1.00
R4237:Abca13	UTSW	11	9,434,188 (GRCm38)	missense	probably benign	0.01
R4359:Abca13	UTSW	11	9,297,629 (GRCm38)	missense	probably benign	0.02
R4378:Abca13	UTSW	11	9,293,644 (GRCm38)	missense	probably benign	0.00
R4389:Abca13	UTSW	11	9,297,878 (GRCm38)	missense	probably damaging	0.98
R4392:Abca13	UTSW	11	9,309,034 (GRCm38)	missense	possibly damaging	0.94
R4623:Abca13	UTSW	11	9,309,130 (GRCm38)	missense	probably damaging	1.00
R4684:Abca13	UTSW	11	9,434,193 (GRCm38)	nonsense	probably null
R4691:Abca13	UTSW	11	9,434,195 (GRCm38)	missense	probably damaging	1.00
R4700:Abca13	UTSW	11	9,292,306 (GRCm38)	missense	possibly damaging	0.59
R4701:Abca13	UTSW	11	9,292,306 (GRCm38)	missense	possibly damaging	0.59
R4704:Abca13	UTSW	11	9,276,990 (GRCm38)	missense	possibly damaging	0.94
R4751:Abca13	UTSW	11	9,277,973 (GRCm38)	critical splice donor site	probably null
R4772:Abca13	UTSW	11	9,315,339 (GRCm38)	splice site	probably null
R4782:Abca13	UTSW	11	9,328,096 (GRCm38)	missense	probably damaging	0.96
R4801:Abca13	UTSW	11	9,522,341 (GRCm38)	missense	possibly damaging	0.94
R4802:Abca13	UTSW	11	9,522,341 (GRCm38)	missense	possibly damaging	0.94
R4819:Abca13	UTSW	11	9,290,421 (GRCm38)	missense	possibly damaging	0.88
R4831:Abca13	UTSW	11	9,542,077 (GRCm38)	nonsense	probably null
R4851:Abca13	UTSW	11	9,483,890 (GRCm38)	missense	probably benign	0.02
R4857:Abca13	UTSW	11	9,294,143 (GRCm38)	missense	probably benign	0.22
R4869:Abca13	UTSW	11	9,315,434 (GRCm38)	splice site	probably null
R4982:Abca13	UTSW	11	9,292,348 (GRCm38)	missense	possibly damaging	0.58
R5031:Abca13	UTSW	11	9,297,678 (GRCm38)	missense	probably damaging	0.99
R5044:Abca13	UTSW	11	9,373,323 (GRCm38)	missense	possibly damaging	0.80
R5092:Abca13	UTSW	11	9,258,535 (GRCm38)	missense	probably damaging	1.00
R5155:Abca13	UTSW	11	9,532,447 (GRCm38)	missense	probably damaging	0.98
R5173:Abca13	UTSW	11	9,682,032 (GRCm38)	frame shift	probably null
R5180:Abca13	UTSW	11	9,466,510 (GRCm38)	missense	probably benign	0.01
R5244:Abca13	UTSW	11	9,275,081 (GRCm38)	missense	probably benign	0.28
R5257:Abca13	UTSW	11	9,249,684 (GRCm38)	missense	possibly damaging	0.94
R5258:Abca13	UTSW	11	9,249,684 (GRCm38)	missense	possibly damaging	0.94
R5299:Abca13	UTSW	11	9,431,861 (GRCm38)	missense	probably damaging	1.00
R5363:Abca13	UTSW	11	9,277,035 (GRCm38)	missense	possibly damaging	0.75
R5365:Abca13	UTSW	11	9,628,629 (GRCm38)	missense	probably damaging	1.00
R5419:Abca13	UTSW	11	9,193,533 (GRCm38)	critical splice donor site	probably null
R5426:Abca13	UTSW	11	9,290,722 (GRCm38)	missense	probably damaging	1.00
R5468:Abca13	UTSW	11	9,294,062 (GRCm38)	missense	probably damaging	1.00
R5477:Abca13	UTSW	11	9,301,298 (GRCm38)	missense	possibly damaging	0.49
R5541:Abca13	UTSW	11	9,291,545 (GRCm38)	missense	probably benign	0.00
R5553:Abca13	UTSW	11	9,328,158 (GRCm38)	missense	probably damaging	1.00
R5556:Abca13	UTSW	11	9,258,546 (GRCm38)	missense	possibly damaging	0.91
R5566:Abca13	UTSW	11	9,294,615 (GRCm38)	nonsense	probably null
R5582:Abca13	UTSW	11	9,636,639 (GRCm38)	splice site	probably null
R5604:Abca13	UTSW	11	9,566,279 (GRCm38)	missense	probably damaging	0.97
R5609:Abca13	UTSW	11	9,403,874 (GRCm38)	missense	probably benign	0.01
R5617:Abca13	UTSW	11	9,277,891 (GRCm38)	missense	probably benign	0.00
R5693:Abca13	UTSW	11	9,316,233 (GRCm38)	missense	probably benign	0.29
R5707:Abca13	UTSW	11	9,510,620 (GRCm38)	missense	probably damaging	1.00
R5725:Abca13	UTSW	11	9,577,181 (GRCm38)	missense	probably benign	0.00
R5728:Abca13	UTSW	11	9,570,576 (GRCm38)	missense	probably damaging	1.00
R5738:Abca13	UTSW	11	9,621,917 (GRCm38)	missense	probably damaging	1.00
R5758:Abca13	UTSW	11	9,314,536 (GRCm38)	missense	probably damaging	0.97
R5762:Abca13	UTSW	11	9,581,665 (GRCm38)	missense	probably damaging	1.00
R5771:Abca13	UTSW	11	9,291,411 (GRCm38)	missense	probably damaging	1.00
R5809:Abca13	UTSW	11	9,293,692 (GRCm38)	missense	probably damaging	1.00
R5826:Abca13	UTSW	11	9,682,056 (GRCm38)	missense	probably damaging	0.99
R5831:Abca13	UTSW	11	9,567,777 (GRCm38)	nonsense	probably null
R5834:Abca13	UTSW	11	9,277,974 (GRCm38)	critical splice donor site	probably null
R5902:Abca13	UTSW	11	9,297,177 (GRCm38)	missense	probably damaging	1.00
R5933:Abca13	UTSW	11	9,249,658 (GRCm38)	missense	possibly damaging	0.63
R5945:Abca13	UTSW	11	9,293,398 (GRCm38)	missense	probably benign	0.04
R5969:Abca13	UTSW	11	9,292,214 (GRCm38)	nonsense	probably null
R5985:Abca13	UTSW	11	9,291,628 (GRCm38)	missense	probably benign	0.02
R5998:Abca13	UTSW	11	9,567,708 (GRCm38)	missense	probably damaging	0.97
R6021:Abca13	UTSW	11	9,290,465 (GRCm38)	nonsense	probably null
R6022:Abca13	UTSW	11	9,290,759 (GRCm38)	missense	probably damaging	1.00
R6032:Abca13	UTSW	11	9,297,752 (GRCm38)	missense	possibly damaging	0.52
R6032:Abca13	UTSW	11	9,297,752 (GRCm38)	missense	possibly damaging	0.52
R6105:Abca13	UTSW	11	9,397,812 (GRCm38)	missense	probably damaging	1.00
R6153:Abca13	UTSW	11	9,301,259 (GRCm38)	critical splice acceptor site	probably null
R6162:Abca13	UTSW	11	9,309,047 (GRCm38)	missense	probably damaging	1.00
R6187:Abca13	UTSW	11	9,309,085 (GRCm38)	missense	probably damaging	1.00
R6247:Abca13	UTSW	11	9,403,874 (GRCm38)	missense	probably benign	0.01
R6329:Abca13	UTSW	11	9,277,937 (GRCm38)	missense	probably damaging	1.00
R6352:Abca13	UTSW	11	9,309,139 (GRCm38)	splice site	probably null
R6367:Abca13	UTSW	11	9,216,248 (GRCm38)	missense	possibly damaging	0.85
R6423:Abca13	UTSW	11	9,298,778 (GRCm38)	missense	probably benign	0.01
R6424:Abca13	UTSW	11	9,510,542 (GRCm38)	missense	probably benign
R6456:Abca13	UTSW	11	9,290,474 (GRCm38)	missense	possibly damaging	0.94
R6490:Abca13	UTSW	11	9,298,661 (GRCm38)	missense	probably benign	0.00
R6547:Abca13	UTSW	11	9,274,757 (GRCm38)	missense	probably benign	0.04
R6594:Abca13	UTSW	11	9,294,632 (GRCm38)	missense	possibly damaging	0.52
R6604:Abca13	UTSW	11	9,378,384 (GRCm38)	missense	probably damaging	1.00
R6614:Abca13	UTSW	11	9,294,371 (GRCm38)	missense	probably benign	0.04
R6736:Abca13	UTSW	11	9,465,058 (GRCm38)	missense	probably damaging	1.00
R6742:Abca13	UTSW	11	9,328,168 (GRCm38)	missense	probably damaging	1.00
R6791:Abca13	UTSW	11	9,378,504 (GRCm38)	missense	probably damaging	1.00
R6834:Abca13	UTSW	11	9,275,110 (GRCm38)	missense	possibly damaging	0.48
R6936:Abca13	UTSW	11	9,298,568 (GRCm38)	missense	probably damaging	0.96
R6955:Abca13	UTSW	11	9,294,307 (GRCm38)	missense	probably benign	0.28
R7031:Abca13	UTSW	11	9,621,892 (GRCm38)	missense	probably damaging	1.00
R7065:Abca13	UTSW	11	9,292,595 (GRCm38)	missense	probably benign	0.02
R7067:Abca13	UTSW	11	9,291,845 (GRCm38)	missense	probably benign	0.14
R7070:Abca13	UTSW	11	9,290,701 (GRCm38)	missense	probably benign	0.06
R7094:Abca13	UTSW	11	9,298,610 (GRCm38)	missense	probably damaging	0.96
R7102:Abca13	UTSW	11	9,335,215 (GRCm38)	missense	probably damaging	1.00
R7105:Abca13	UTSW	11	9,397,842 (GRCm38)	missense	probably damaging	1.00
R7131:Abca13	UTSW	11	9,291,893 (GRCm38)	missense	probably benign	0.37
R7155:Abca13	UTSW	11	9,529,010 (GRCm38)	missense	probably benign
R7158:Abca13	UTSW	11	9,273,982 (GRCm38)	missense	probably benign
R7212:Abca13	UTSW	11	9,298,854 (GRCm38)	missense	probably benign	0.04
R7215:Abca13	UTSW	11	9,288,405 (GRCm38)	splice site	probably null
R7228:Abca13	UTSW	11	9,297,653 (GRCm38)	missense	probably benign
R7231:Abca13	UTSW	11	9,294,175 (GRCm38)	missense	probably benign	0.25
R7247:Abca13	UTSW	11	9,290,732 (GRCm38)	missense	probably benign	0.00
R7278:Abca13	UTSW	11	9,291,126 (GRCm38)	missense	possibly damaging	0.56
R7299:Abca13	UTSW	11	9,294,649 (GRCm38)	missense	probably damaging	0.98
R7304:Abca13	UTSW	11	9,297,203 (GRCm38)	missense	probably benign
R7328:Abca13	UTSW	11	9,291,545 (GRCm38)	missense	probably benign	0.14
R7374:Abca13	UTSW	11	9,292,136 (GRCm38)	missense	possibly damaging	0.46
R7376:Abca13	UTSW	11	9,291,118 (GRCm38)	missense	probably benign	0.00
R7384:Abca13	UTSW	11	9,333,257 (GRCm38)	missense	probably damaging	1.00
R7395:Abca13	UTSW	11	9,291,658 (GRCm38)	missense	probably benign	0.01
R7419:Abca13	UTSW	11	9,297,833 (GRCm38)	missense	probably damaging	1.00
R7419:Abca13	UTSW	11	9,276,959 (GRCm38)	missense	probably damaging	1.00
R7421:Abca13	UTSW	11	9,510,463 (GRCm38)	missense	probably benign
R7458:Abca13	UTSW	11	9,290,777 (GRCm38)	missense	possibly damaging	0.94
R7474:Abca13	UTSW	11	9,328,088 (GRCm38)	nonsense	probably null
R7492:Abca13	UTSW	11	9,293,167 (GRCm38)	missense	probably benign	0.08
R7660:Abca13	UTSW	11	9,290,678 (GRCm38)	missense	probably benign	0.00
R7677:Abca13	UTSW	11	9,298,349 (GRCm38)	nonsense	probably null
R7744:Abca13	UTSW	11	9,290,421 (GRCm38)	missense	possibly damaging	0.88
R7790:Abca13	UTSW	11	9,297,915 (GRCm38)	missense	probably damaging	1.00
R7798:Abca13	UTSW	11	9,291,664 (GRCm38)	missense	probably benign	0.04
R7811:Abca13	UTSW	11	9,577,141 (GRCm38)	splice site	probably null
R7831:Abca13	UTSW	11	9,297,404 (GRCm38)	missense	possibly damaging	0.46
R7867:Abca13	UTSW	11	9,262,139 (GRCm38)	critical splice donor site	probably null
R7910:Abca13	UTSW	11	9,581,590 (GRCm38)	missense	probably damaging	1.00
R7964:Abca13	UTSW	11	9,316,146 (GRCm38)	missense	probably benign	0.06
R8037:Abca13	UTSW	11	9,293,904 (GRCm38)	missense	probably damaging	1.00
R8049:Abca13	UTSW	11	9,291,867 (GRCm38)	missense	probably damaging	0.99
R8059:Abca13	UTSW	11	9,373,279 (GRCm38)	missense	probably benign	0.00
R8072:Abca13	UTSW	11	9,294,574 (GRCm38)	missense	probably benign	0.10
R8078:Abca13	UTSW	11	9,301,279 (GRCm38)	missense	probably benign	0.32
R8112:Abca13	UTSW	11	9,314,624 (GRCm38)	missense	probably benign	0.01
R8146:Abca13	UTSW	11	9,397,829 (GRCm38)	missense	probably damaging	1.00
R8164:Abca13	UTSW	11	9,615,799 (GRCm38)	missense	probably damaging	1.00
R8195:Abca13	UTSW	11	9,274,735 (GRCm38)	missense	probably benign	0.00
R8220:Abca13	UTSW	11	9,434,299 (GRCm38)	missense	possibly damaging	0.58
R8235:Abca13	UTSW	11	9,262,077 (GRCm38)	missense	probably damaging	0.99
R8307:Abca13	UTSW	11	9,277,922 (GRCm38)	nonsense	probably null
R8310:Abca13	UTSW	11	9,378,269 (GRCm38)	missense	possibly damaging	0.90
R8315:Abca13	UTSW	11	9,585,502 (GRCm38)	missense	probably benign	0.44
R8315:Abca13	UTSW	11	9,378,460 (GRCm38)	missense	probably null	1.00
R8324:Abca13	UTSW	11	9,290,395 (GRCm38)	missense	probably damaging	1.00
R8375:Abca13	UTSW	11	9,397,841 (GRCm38)	missense	probably damaging	1.00
R8375:Abca13	UTSW	11	9,315,416 (GRCm38)	missense	probably benign	0.00
R8400:Abca13	UTSW	11	9,298,218 (GRCm38)	missense	probably damaging	0.97
R8400:Abca13	UTSW	11	9,293,925 (GRCm38)	missense	probably benign	0.00
R8425:Abca13	UTSW	11	9,314,623 (GRCm38)	missense	possibly damaging	0.92
R8486:Abca13	UTSW	11	9,275,092 (GRCm38)	missense	probably benign	0.00
R8493:Abca13	UTSW	11	9,510,668 (GRCm38)	missense	probably damaging	0.97
R8502:Abca13	UTSW	11	9,269,282 (GRCm38)	missense	probably benign	0.02
R8716:Abca13	UTSW	11	9,293,774 (GRCm38)	missense	probably benign	0.09
R8787:Abca13	UTSW	11	9,275,053 (GRCm38)	missense	possibly damaging	0.92
R8829:Abca13	UTSW	11	9,621,881 (GRCm38)	missense	probably damaging	1.00
R8859:Abca13	UTSW	11	9,378,397 (GRCm38)	missense
R8871:Abca13	UTSW	11	9,298,071 (GRCm38)	missense	probably benign	0.07
R8883:Abca13	UTSW	11	9,333,168 (GRCm38)	missense	probably benign	0.00
R8919:Abca13	UTSW	11	9,291,653 (GRCm38)	missense	possibly damaging	0.84
R8966:Abca13	UTSW	11	9,628,588 (GRCm38)	missense	probably damaging	1.00
R8967:Abca13	UTSW	11	9,292,696 (GRCm38)	missense	probably benign	0.18
R8969:Abca13	UTSW	11	9,277,944 (GRCm38)	missense	probably benign
R8972:Abca13	UTSW	11	9,328,138 (GRCm38)	missense	probably damaging	1.00
R9002:Abca13	UTSW	11	9,291,926 (GRCm38)	missense	possibly damaging	0.94
R9046:Abca13	UTSW	11	9,293,525 (GRCm38)	missense	probably benign	0.04
R9051:Abca13	UTSW	11	9,335,232 (GRCm38)	missense	probably damaging	1.00
R9056:Abca13	UTSW	11	9,464,921 (GRCm38)	missense	probably damaging	1.00
R9061:Abca13	UTSW	11	9,277,847 (GRCm38)	missense	probably benign	0.02
R9072:Abca13	UTSW	11	9,290,834 (GRCm38)	missense	possibly damaging	0.93
R9090:Abca13	UTSW	11	9,291,698 (GRCm38)	missense	probably damaging	0.98
R9127:Abca13	UTSW	11	9,292,080 (GRCm38)	missense	probably benign	0.03
R9164:Abca13	UTSW	11	9,328,157 (GRCm38)	missense	probably damaging	1.00
R9175:Abca13	UTSW	11	9,581,593 (GRCm38)	missense	probably damaging	0.98
R9190:Abca13	UTSW	11	9,291,886 (GRCm38)	missense	probably damaging	0.96
R9244:Abca13	UTSW	11	9,291,577 (GRCm38)	missense	probably benign	0.01
R9255:Abca13	UTSW	11	9,328,213 (GRCm38)	missense	probably damaging	1.00
R9271:Abca13	UTSW	11	9,291,698 (GRCm38)	missense	probably damaging	0.98
R9321:Abca13	UTSW	11	9,510,475 (GRCm38)	missense	probably benign	0.00
R9356:Abca13	UTSW	11	9,256,305 (GRCm38)	missense	probably benign	0.11
R9369:Abca13	UTSW	11	9,378,444 (GRCm38)	missense	probably damaging	1.00
R9423:Abca13	UTSW	11	9,290,395 (GRCm38)	missense	probably damaging	1.00
R9432:Abca13	UTSW	11	9,294,559 (GRCm38)	missense	probably benign	0.00
R9455:Abca13	UTSW	11	9,403,897 (GRCm38)	missense	probably damaging	1.00
R9486:Abca13	UTSW	11	9,290,621 (GRCm38)	missense	possibly damaging	0.88
R9492:Abca13	UTSW	11	9,293,667 (GRCm38)	nonsense	probably null
R9511:Abca13	UTSW	11	9,328,130 (GRCm38)	missense	probably benign	0.16
R9545:Abca13	UTSW	11	9,466,538 (GRCm38)	missense	probably damaging	1.00
R9566:Abca13	UTSW	11	9,464,927 (GRCm38)	missense	probably damaging	1.00
R9609:Abca13	UTSW	11	9,258,549 (GRCm38)	missense	probably damaging	1.00
R9616:Abca13	UTSW	11	9,290,501 (GRCm38)	missense	probably benign	0.00
R9651:Abca13	UTSW	11	9,585,484 (GRCm38)	missense	probably benign
R9651:Abca13	UTSW	11	9,293,741 (GRCm38)	missense	probably benign	0.31
R9653:Abca13	UTSW	11	9,293,741 (GRCm38)	missense	probably benign	0.31
R9657:Abca13	UTSW	11	9,293,379 (GRCm38)	missense	probably benign	0.35
R9684:Abca13	UTSW	11	9,333,307 (GRCm38)	missense	probably damaging	1.00
X0013:Abca13	UTSW	11	9,273,899 (GRCm38)	missense	probably benign	0.02
X0057:Abca13	UTSW	11	9,294,744 (GRCm38)	missense	probably damaging	0.96
X0066:Abca13	UTSW	11	9,267,565 (GRCm38)	missense	probably damaging	0.96
Z1088:Abca13	UTSW	11	9,294,687 (GRCm38)	missense	probably damaging	0.99
Z1176:Abca13	UTSW	11	9,267,461 (GRCm38)	missense	probably damaging	1.00
Z1176:Abca13	UTSW	11	9,251,376 (GRCm38)	missense	possibly damaging	0.88
Z1176:Abca13	UTSW	11	9,335,182 (GRCm38)	missense	probably damaging	1.00
Z1176:Abca13	UTSW	11	9,335,181 (GRCm38)	missense	probably damaging	1.00
Z1176:Abca13	UTSW	11	9,294,342 (GRCm38)	missense	probably benign	0.01
Z1177:Abca13	UTSW	11	9,314,545 (GRCm38)	frame shift	probably null

Predicted Primers

PCR Primer
(F):5'- GCCCAGGTGAAACCAAAATATT -3'
(R):5'- TGACCACAGAGCAGAGTATCT -3'

Sequencing Primer
(F):5'- GCTTGTCCATCTTGGAGA -3'
(R):5'- ACCTTGCCTGAGCCAACTG -3'

Posted On

2014-09-18