Mutagenetix > Incidental Mutation

Incidental Mutation 'R4992:Birc6'

386308

Institutional Source

Beutler Lab

Gene Symbol

Birc6

Ensembl Gene

ENSMUSG00000024073

Gene Name

baculoviral IAP repeat-containing 6

Synonyms

D630005A10Rik, apollon, Bruce, A430032G04Rik, A430040A19Rik

MMRRC Submission

042586-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R4992 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

74528295-74703356 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 74689256 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 4475 (D4475G)

Ref Sequence

ENSEMBL: ENSMUSP00000138693 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000180037] [ENSMUST00000182133] [ENSMUST00000182597] [ENSMUST00000182944] [ENSMUST00000183224]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000180037
AA Change: D4481G

PolyPhen 2 Score 0.439 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000136329
Gene: ENSMUSG00000024073
AA Change: D4481G

Domain	Start	End	E-Value	Type
low complexity region	24	54	N/A	INTRINSIC
BIR	287	363	2.87e-24	SMART
low complexity region	472	493	N/A	INTRINSIC
low complexity region	624	635	N/A	INTRINSIC
low complexity region	674	685	N/A	INTRINSIC
low complexity region	769	781	N/A	INTRINSIC
low complexity region	1054	1071	N/A	INTRINSIC
low complexity region	1369	1380	N/A	INTRINSIC
coiled coil region	1620	1675	N/A	INTRINSIC
low complexity region	1709	1726	N/A	INTRINSIC
low complexity region	1993	1998	N/A	INTRINSIC
low complexity region	2044	2059	N/A	INTRINSIC
low complexity region	2142	2163	N/A	INTRINSIC
low complexity region	2253	2266	N/A	INTRINSIC
low complexity region	2491	2505	N/A	INTRINSIC
low complexity region	2671	2688	N/A	INTRINSIC
low complexity region	2893	2905	N/A	INTRINSIC
low complexity region	2958	2970	N/A	INTRINSIC
Pfam:DUF3643	3477	3632	1e-69	PFAM
low complexity region	3747	3772	N/A	INTRINSIC
low complexity region	3900	3919	N/A	INTRINSIC
low complexity region	3940	3958	N/A	INTRINSIC
low complexity region	3963	3972	N/A	INTRINSIC
low complexity region	4146	4157	N/A	INTRINSIC
low complexity region	4307	4318	N/A	INTRINSIC
low complexity region	4433	4444	N/A	INTRINSIC
UBCc	4592	4756	1.04e-25	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000182133
AA Change: D4475G

PolyPhen 2 Score 0.439 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000138693
Gene: ENSMUSG00000024073
AA Change: D4475G

Domain	Start	End	E-Value	Type
low complexity region	24	54	N/A	INTRINSIC
BIR	287	363	2.87e-24	SMART
low complexity region	472	493	N/A	INTRINSIC
low complexity region	624	635	N/A	INTRINSIC
low complexity region	674	685	N/A	INTRINSIC
low complexity region	769	781	N/A	INTRINSIC
low complexity region	1054	1071	N/A	INTRINSIC
low complexity region	1369	1380	N/A	INTRINSIC
coiled coil region	1620	1675	N/A	INTRINSIC
low complexity region	1709	1726	N/A	INTRINSIC
low complexity region	1993	1998	N/A	INTRINSIC
low complexity region	2044	2055	N/A	INTRINSIC
low complexity region	2136	2157	N/A	INTRINSIC
low complexity region	2247	2260	N/A	INTRINSIC
low complexity region	2485	2499	N/A	INTRINSIC
low complexity region	2665	2682	N/A	INTRINSIC
low complexity region	2887	2899	N/A	INTRINSIC
low complexity region	2952	2964	N/A	INTRINSIC
Pfam:DUF3643	3470	3626	2.1e-71	PFAM
low complexity region	3741	3766	N/A	INTRINSIC
low complexity region	3894	3913	N/A	INTRINSIC
low complexity region	3934	3952	N/A	INTRINSIC
low complexity region	3957	3966	N/A	INTRINSIC
low complexity region	4140	4151	N/A	INTRINSIC
low complexity region	4301	4312	N/A	INTRINSIC
low complexity region	4427	4438	N/A	INTRINSIC
UBCc	4586	4750	1.04e-25	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000182597
AA Change: D4490G

PolyPhen 2 Score 0.312 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000138333
Gene: ENSMUSG00000024073
AA Change: D4490G

Domain	Start	End	E-Value	Type
low complexity region	24	54	N/A	INTRINSIC
BIR	287	363	2.87e-24	SMART
low complexity region	472	493	N/A	INTRINSIC
low complexity region	624	635	N/A	INTRINSIC
low complexity region	674	685	N/A	INTRINSIC
low complexity region	769	781	N/A	INTRINSIC
low complexity region	1054	1071	N/A	INTRINSIC
low complexity region	1369	1380	N/A	INTRINSIC
coiled coil region	1620	1675	N/A	INTRINSIC
low complexity region	1709	1726	N/A	INTRINSIC
low complexity region	1993	1998	N/A	INTRINSIC
low complexity region	2044	2059	N/A	INTRINSIC
low complexity region	2142	2163	N/A	INTRINSIC
low complexity region	2262	2275	N/A	INTRINSIC
low complexity region	2500	2514	N/A	INTRINSIC
low complexity region	2680	2697	N/A	INTRINSIC
low complexity region	2902	2914	N/A	INTRINSIC
low complexity region	2967	2979	N/A	INTRINSIC
Pfam:DUF3643	3485	3641	2.2e-71	PFAM
low complexity region	3756	3781	N/A	INTRINSIC
low complexity region	3909	3928	N/A	INTRINSIC
low complexity region	3949	3967	N/A	INTRINSIC
low complexity region	3972	3981	N/A	INTRINSIC
low complexity region	4155	4166	N/A	INTRINSIC
low complexity region	4316	4327	N/A	INTRINSIC
low complexity region	4442	4453	N/A	INTRINSIC
UBCc	4601	4765	1.04e-25	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000182944
AA Change: D4477G

PolyPhen 2 Score 0.055 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000138732
Gene: ENSMUSG00000024073
AA Change: D4477G

Domain	Start	End	E-Value	Type
low complexity region	24	54	N/A	INTRINSIC
BIR	287	363	2.87e-24	SMART
low complexity region	472	493	N/A	INTRINSIC
low complexity region	624	635	N/A	INTRINSIC
low complexity region	674	685	N/A	INTRINSIC
low complexity region	769	781	N/A	INTRINSIC
low complexity region	1054	1071	N/A	INTRINSIC
low complexity region	1369	1380	N/A	INTRINSIC
coiled coil region	1616	1671	N/A	INTRINSIC
low complexity region	1705	1722	N/A	INTRINSIC
low complexity region	1989	1994	N/A	INTRINSIC
low complexity region	2040	2055	N/A	INTRINSIC
low complexity region	2138	2159	N/A	INTRINSIC
low complexity region	2249	2262	N/A	INTRINSIC
low complexity region	2487	2501	N/A	INTRINSIC
low complexity region	2667	2684	N/A	INTRINSIC
low complexity region	2889	2901	N/A	INTRINSIC
low complexity region	2954	2966	N/A	INTRINSIC
Pfam:DUF3643	3472	3628	3.2e-71	PFAM
low complexity region	3743	3768	N/A	INTRINSIC
low complexity region	3896	3915	N/A	INTRINSIC
low complexity region	3936	3954	N/A	INTRINSIC
low complexity region	3959	3968	N/A	INTRINSIC
low complexity region	4142	4153	N/A	INTRINSIC
low complexity region	4303	4314	N/A	INTRINSIC
low complexity region	4429	4440	N/A	INTRINSIC
UBCc	4588	4752	1.04e-25	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000183224
AA Change: D4461G

PolyPhen 2 Score 0.415 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000138270
Gene: ENSMUSG00000024073
AA Change: D4461G

Domain	Start	End	E-Value	Type
low complexity region	2	26	N/A	INTRINSIC
BIR	259	335	2.87e-24	SMART
low complexity region	444	465	N/A	INTRINSIC
low complexity region	596	607	N/A	INTRINSIC
low complexity region	646	657	N/A	INTRINSIC
low complexity region	741	753	N/A	INTRINSIC
low complexity region	1026	1043	N/A	INTRINSIC
low complexity region	1355	1366	N/A	INTRINSIC
coiled coil region	1606	1661	N/A	INTRINSIC
low complexity region	1695	1712	N/A	INTRINSIC
low complexity region	1979	1984	N/A	INTRINSIC
low complexity region	2030	2041	N/A	INTRINSIC
low complexity region	2122	2143	N/A	INTRINSIC
low complexity region	2233	2246	N/A	INTRINSIC
low complexity region	2471	2485	N/A	INTRINSIC
low complexity region	2651	2668	N/A	INTRINSIC
low complexity region	2873	2885	N/A	INTRINSIC
low complexity region	2938	2950	N/A	INTRINSIC
Pfam:DUF3643	3456	3612	3.2e-71	PFAM
low complexity region	3727	3752	N/A	INTRINSIC
low complexity region	3880	3899	N/A	INTRINSIC
low complexity region	3920	3938	N/A	INTRINSIC
low complexity region	3943	3952	N/A	INTRINSIC
low complexity region	4126	4137	N/A	INTRINSIC
low complexity region	4287	4298	N/A	INTRINSIC
low complexity region	4413	4424	N/A	INTRINSIC
UBCc	4572	4736	1.04e-25	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000183249

Meta Mutation Damage Score

0.1219

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.8%
20x: 93.7%

Validation Efficiency

98% (84/86)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein with a BIR (baculoviral inhibition of apoptosis protein repeat) domain and a UBCc (ubiquitin-conjugating enzyme E2, catalytic) domain. This protein inhibits apoptosis by facilitating the degradation of apoptotic proteins by ubiquitination. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous mice exhibit perinatal lethality and exhibit placental defects. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 81 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930407I10Rik	G	A	15: 82,064,002 (GRCm38)	R700Q	possibly damaging	Het
4930444P10Rik	T	A	1: 16,080,877 (GRCm38)	E27V	probably damaging	Het
Acsm4	T	A	7: 119,711,417 (GRCm38)	I509N	probably benign	Het
Asb18	T	C	1: 89,952,863 (GRCm38)	M143V	probably benign	Het
Bsn	A	T	9: 108,115,548 (GRCm38)	S1002T	probably damaging	Het
Bub3	T	C	7: 131,560,806 (GRCm38)	S33P	probably damaging	Het
Ccna1	T	A	3: 55,049,890 (GRCm38)	R35S	probably damaging	Het
Cdc23	T	A	18: 34,646,919 (GRCm38)	M119L	probably benign	Het
Ces1a	A	G	8: 93,045,022 (GRCm38)	V49A	probably benign	Het
Chil1	A	T	1: 134,188,626 (GRCm38)	E282D	probably benign	Het
Crocc	G	A	4: 141,046,666 (GRCm38)	A220V	probably damaging	Het
Cstf1	A	G	2: 172,377,800 (GRCm38)	Y277C	probably damaging	Het
D930020B18Rik	C	T	10: 121,654,762 (GRCm38)	P89L	probably damaging	Het
D930020B18Rik	C	G	10: 121,654,761 (GRCm38)	P89A	probably damaging	Het
Dennd5a	A	G	7: 109,894,712 (GRCm38)	S1262P	probably damaging	Het
Dnajb5	G	A	4: 42,953,386 (GRCm38)		probably null	Het
E330034G19Rik	A	G	14: 24,306,996 (GRCm38)	K200R	unknown	Het
Ect2l	A	G	10: 18,172,729 (GRCm38)	F156S	probably benign	Het
Egf	T	C	3: 129,711,530 (GRCm38)		probably null	Het
Elmo1	T	C	13: 20,342,519 (GRCm38)	F413S	probably damaging	Het
Elmo3	T	A	8: 105,309,501 (GRCm38)	Y607*	probably null	Het
Eno3	A	G	11: 70,658,647 (GRCm38)	D98G	probably damaging	Het
Ephb2	A	G	4: 136,660,839 (GRCm38)	V651A	probably damaging	Het
Fbp1	C	T	13: 62,865,074 (GRCm38)	V102I	probably benign	Het
Gcn1l1	T	C	5: 115,599,166 (GRCm38)	V1321A	probably benign	Het
Gimd1	A	T	3: 132,634,957 (GRCm38)	Y78F	probably benign	Het
Glmn	T	G	5: 107,557,301 (GRCm38)	D483A	probably damaging	Het
Gsr	C	T	8: 33,693,913 (GRCm38)	T401I	probably damaging	Het
Htr3b	G	A	9: 48,959,218 (GRCm38)	H62Y	possibly damaging	Het
Ifna6	T	C	4: 88,827,540 (GRCm38)	V42A	probably benign	Het
Igkv4-80	A	C	6: 69,016,665 (GRCm38)	S81A	probably benign	Het
Inpp4b	A	T	8: 82,033,208 (GRCm38)	R627S	probably damaging	Het
Kif13a	C	T	13: 46,777,163 (GRCm38)	V142M	probably damaging	Het
Lims1	A	C	10: 58,410,241 (GRCm38)		probably benign	Het
Ltn1	T	C	16: 87,405,587 (GRCm38)	T1059A	possibly damaging	Het
Lyst	T	C	13: 13,661,163 (GRCm38)	L1810P	probably damaging	Het
Mboat1	T	G	13: 30,202,360 (GRCm38)	I119R	possibly damaging	Het
Mgat3	T	A	15: 80,212,542 (GRCm38)	D523E	probably benign	Het
Mphosph9	T	C	5: 124,304,190 (GRCm38)	E395G	probably damaging	Het
Mtcl1	G	T	17: 66,342,839 (GRCm38)	P1877Q	probably damaging	Het
Myo6	T	C	9: 80,283,510 (GRCm38)	V781A	possibly damaging	Het
Ncoa3	T	A	2: 166,069,939 (GRCm38)	M1395K	probably benign	Het
Nhlrc2	T	A	19: 56,570,534 (GRCm38)	D150E	probably benign	Het
Nlrp9a	T	C	7: 26,557,386 (GRCm38)	V54A	probably benign	Het
Olfr392	G	A	11: 73,814,320 (GRCm38)	T254I	probably damaging	Het
Olfr411	A	G	11: 74,347,197 (GRCm38)	I129T	probably damaging	Het
Parp14	A	T	16: 35,841,142 (GRCm38)	C1479S	probably benign	Het
Pdcd1lg2	T	C	19: 29,446,084 (GRCm38)	V176A	probably damaging	Het
Pibf1	T	A	14: 99,150,667 (GRCm38)	N416K	probably damaging	Het
Polb	A	T	8: 22,645,071 (GRCm38)	V115E	probably damaging	Het
Polq	T	A	16: 37,061,162 (GRCm38)	N1229K	possibly damaging	Het
Ppp1r21	A	T	17: 88,569,080 (GRCm38)	D440V	probably benign	Het
Ppp2ca	T	A	11: 52,113,206 (GRCm38)	H63Q	possibly damaging	Het
Prl7a1	C	T	13: 27,635,686 (GRCm38)		probably null	Het
Rgs1	C	A	1: 144,246,322 (GRCm38)	K77N	probably damaging	Het
Rnf112	T	A	11: 61,452,711 (GRCm38)	I100F	possibly damaging	Het
Rnf139	G	T	15: 58,898,476 (GRCm38)	E117*	probably null	Het
Robo1	G	A	16: 72,979,868 (GRCm38)	V743I	probably damaging	Het
Scarf1	T	C	11: 75,526,015 (GRCm38)	V761A	probably benign	Het
Scarf1	T	C	11: 75,522,230 (GRCm38)	L434P	probably damaging	Het
Sgsm1	A	T	5: 113,282,620 (GRCm38)	S300T	possibly damaging	Het
Slc26a7	T	G	4: 14,565,508 (GRCm38)	T192P	probably damaging	Het
Smarcc2	A	G	10: 128,474,710 (GRCm38)	K403E	probably damaging	Het
Snai3	G	A	8: 122,456,332 (GRCm38)	T158M	possibly damaging	Het
Spata31d1a	T	C	13: 59,703,151 (GRCm38)	N388D	probably benign	Het
Sptlc3	G	A	2: 139,596,003 (GRCm38)	V406I	probably benign	Het
Tgds	A	C	14: 118,117,763 (GRCm38)	Y197D	probably damaging	Het
Tll1	G	T	8: 64,093,944 (GRCm38)	R323S	probably damaging	Het
Tmem55b	A	G	14: 50,929,233 (GRCm38)	V179A	probably damaging	Het
Trim14	A	G	4: 46,507,110 (GRCm38)	Y369H	probably damaging	Het
Ube2nl	C	T	7: 61,549,364 (GRCm38)		noncoding transcript	Het
Ube3a	T	A	7: 59,284,820 (GRCm38)	D560E	possibly damaging	Het
Vmn2r10	A	G	5: 108,997,726 (GRCm38)	V505A	possibly damaging	Het
Vmn2r114	T	G	17: 23,291,791 (GRCm38)	I572L	probably benign	Het
Vmn2r26	A	T	6: 124,026,111 (GRCm38)	Q160L	probably benign	Het
Vmn2r75	A	C	7: 86,166,167 (GRCm38)		probably null	Het
Vps8	A	G	16: 21,461,408 (GRCm38)	K336E	possibly damaging	Het
Zfp324	T	C	7: 12,969,373 (GRCm38)	S32P	probably benign	Het
Zfp366	T	C	13: 99,229,495 (GRCm38)	I388T	possibly damaging	Het
Zfp68	A	T	5: 138,607,337 (GRCm38)	N203K	possibly damaging	Het
Zhx2	A	T	15: 57,823,587 (GRCm38)	N784I	probably damaging	Het

Other mutations in Birc6

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00402:Birc6	APN	17	74,573,563 (GRCm38)	splice site	probably benign
IGL00542:Birc6	APN	17	74,623,771 (GRCm38)	splice site	probably null
IGL00659:Birc6	APN	17	74,660,653 (GRCm38)	missense	probably damaging	1.00
IGL00710:Birc6	APN	17	74,609,089 (GRCm38)	missense	probably benign	0.37
IGL00806:Birc6	APN	17	74,611,529 (GRCm38)	missense	possibly damaging	0.85
IGL00848:Birc6	APN	17	74,696,393 (GRCm38)	nonsense	probably null
IGL01071:Birc6	APN	17	74,566,132 (GRCm38)	missense	possibly damaging	0.84
IGL01071:Birc6	APN	17	74,631,701 (GRCm38)	missense	probably damaging	1.00
IGL01121:Birc6	APN	17	74,631,038 (GRCm38)	missense	probably benign	0.08
IGL01132:Birc6	APN	17	74,603,060 (GRCm38)	missense	probably damaging	1.00
IGL01323:Birc6	APN	17	74,622,925 (GRCm38)	missense	probably damaging	1.00
IGL01444:Birc6	APN	17	74,631,687 (GRCm38)	missense	probably damaging	1.00
IGL01511:Birc6	APN	17	74,627,003 (GRCm38)	nonsense	probably null
IGL01576:Birc6	APN	17	74,677,370 (GRCm38)	missense	possibly damaging	0.80
IGL01578:Birc6	APN	17	74,648,197 (GRCm38)	missense	probably benign	0.08
IGL01649:Birc6	APN	17	74,604,546 (GRCm38)	missense	probably benign	0.03
IGL01657:Birc6	APN	17	74,660,611 (GRCm38)	missense	probably damaging	1.00
IGL01739:Birc6	APN	17	74,659,221 (GRCm38)	missense	probably benign
IGL01756:Birc6	APN	17	74,640,208 (GRCm38)	missense	probably benign	0.00
IGL01807:Birc6	APN	17	74,631,037 (GRCm38)	missense	probably benign
IGL01885:Birc6	APN	17	74,604,516 (GRCm38)	missense	possibly damaging	0.51
IGL01906:Birc6	APN	17	74,638,358 (GRCm38)	missense	probably damaging	1.00
IGL01915:Birc6	APN	17	74,631,720 (GRCm38)	missense	probably benign	0.34
IGL01998:Birc6	APN	17	74,579,885 (GRCm38)	missense	probably benign	0.06
IGL02084:Birc6	APN	17	74,608,282 (GRCm38)	missense	probably benign	0.45
IGL02086:Birc6	APN	17	74,639,827 (GRCm38)	missense	probably damaging	1.00
IGL02161:Birc6	APN	17	74,548,837 (GRCm38)	missense	probably damaging	0.99
IGL02195:Birc6	APN	17	74,697,381 (GRCm38)	splice site	probably benign
IGL02283:Birc6	APN	17	74,599,940 (GRCm38)	missense	probably benign
IGL02476:Birc6	APN	17	74,696,391 (GRCm38)	missense	possibly damaging	0.81
IGL02493:Birc6	APN	17	74,652,059 (GRCm38)	unclassified	probably benign
IGL02547:Birc6	APN	17	74,579,645 (GRCm38)	missense	probably benign	0.21
IGL02678:Birc6	APN	17	74,649,903 (GRCm38)	missense	probably damaging	1.00
IGL02713:Birc6	APN	17	74,579,324 (GRCm38)	missense	probably benign
IGL02851:Birc6	APN	17	74,609,189 (GRCm38)	missense	probably damaging	1.00
IGL02875:Birc6	APN	17	74,589,718 (GRCm38)	missense	probably damaging	1.00
IGL02985:Birc6	APN	17	74,640,190 (GRCm38)	missense	probably benign	0.00
IGL03004:Birc6	APN	17	74,612,185 (GRCm38)	missense	probably benign	0.10
IGL03053:Birc6	APN	17	74,565,972 (GRCm38)	missense	probably damaging	1.00
IGL03085:Birc6	APN	17	74,596,950 (GRCm38)	missense	probably damaging	0.97
IGL03109:Birc6	APN	17	74,579,334 (GRCm38)	missense	possibly damaging	0.71
IGL03143:Birc6	APN	17	74,598,999 (GRCm38)	missense	possibly damaging	0.89
IGL03180:Birc6	APN	17	74,659,231 (GRCm38)	missense	probably benign
IGL03221:Birc6	APN	17	74,627,007 (GRCm38)	missense	probably benign	0.00
IGL03230:Birc6	APN	17	74,611,070 (GRCm38)	missense	probably damaging	1.00
IGL03294:Birc6	APN	17	74,649,886 (GRCm38)	missense	probably benign	0.02
IGL03399:Birc6	APN	17	74,594,373 (GRCm38)	missense	probably benign	0.01
Badlands	UTSW	17	74,603,036 (GRCm38)	missense	probably damaging	1.00
Big_sky	UTSW	17	74,528,538 (GRCm38)	missense	probably null	0.33
bitterroot	UTSW	17	74,649,696 (GRCm38)	missense	probably damaging	1.00
Black_hills	UTSW	17	74,692,332 (GRCm38)	missense	probably damaging	1.00
bottomlands	UTSW	17	74,609,659 (GRCm38)	missense	probably damaging	1.00
Chai	UTSW	17	74,670,374 (GRCm38)	missense	probably damaging	1.00
Dakota	UTSW	17	74,625,104 (GRCm38)	critical splice acceptor site	probably null
Sempervirens	UTSW	17	74,642,504 (GRCm38)	missense	probably damaging	1.00
E0370:Birc6	UTSW	17	74,677,357 (GRCm38)	missense	probably damaging	1.00
G1citation:Birc6	UTSW	17	74,598,044 (GRCm38)	missense	probably damaging	1.00
G1citation:Birc6	UTSW	17	74,580,382 (GRCm38)	missense	possibly damaging	0.82
PIT4494001:Birc6	UTSW	17	74,626,980 (GRCm38)	missense	probably damaging	1.00
R0081:Birc6	UTSW	17	74,643,441 (GRCm38)	missense	probably benign	0.01
R0086:Birc6	UTSW	17	74,593,166 (GRCm38)	missense	possibly damaging	0.54
R0089:Birc6	UTSW	17	74,638,376 (GRCm38)	missense	possibly damaging	0.90
R0116:Birc6	UTSW	17	74,623,746 (GRCm38)	splice site	probably benign
R0129:Birc6	UTSW	17	74,528,760 (GRCm38)	missense	probably benign	0.05
R0196:Birc6	UTSW	17	74,580,287 (GRCm38)	missense	possibly damaging	0.57
R0201:Birc6	UTSW	17	74,609,327 (GRCm38)	missense	possibly damaging	0.92
R0207:Birc6	UTSW	17	74,662,832 (GRCm38)	splice site	probably benign
R0295:Birc6	UTSW	17	74,613,362 (GRCm38)	intron	probably benign
R0386:Birc6	UTSW	17	74,599,340 (GRCm38)	missense	probably damaging	0.99
R0423:Birc6	UTSW	17	74,696,297 (GRCm38)	missense	probably damaging	1.00
R0449:Birc6	UTSW	17	74,692,295 (GRCm38)	missense	probably damaging	1.00
R0453:Birc6	UTSW	17	74,649,754 (GRCm38)	missense	probably damaging	1.00
R0457:Birc6	UTSW	17	74,662,625 (GRCm38)	missense	probably damaging	1.00
R0457:Birc6	UTSW	17	74,652,028 (GRCm38)	missense	probably benign
R0564:Birc6	UTSW	17	74,625,243 (GRCm38)	splice site	probably benign
R0575:Birc6	UTSW	17	74,689,237 (GRCm38)	missense	probably damaging	1.00
R0582:Birc6	UTSW	17	74,643,337 (GRCm38)	missense	probably damaging	1.00
R0624:Birc6	UTSW	17	74,580,349 (GRCm38)	missense	probably benign	0.20
R0973:Birc6	UTSW	17	74,565,861 (GRCm38)	missense	probably damaging	0.99
R1061:Birc6	UTSW	17	74,689,312 (GRCm38)	missense	probably damaging	1.00
R1378:Birc6	UTSW	17	74,660,455 (GRCm38)	missense	probably damaging	1.00
R1402:Birc6	UTSW	17	74,697,533 (GRCm38)	splice site	probably benign
R1436:Birc6	UTSW	17	74,652,705 (GRCm38)	missense	probably damaging	1.00
R1456:Birc6	UTSW	17	74,609,290 (GRCm38)	missense	probably benign	0.35
R1465:Birc6	UTSW	17	74,623,858 (GRCm38)	missense	probably benign	0.03
R1465:Birc6	UTSW	17	74,623,858 (GRCm38)	missense	probably benign	0.03
R1474:Birc6	UTSW	17	74,579,678 (GRCm38)	missense	probably damaging	0.98
R1479:Birc6	UTSW	17	74,634,853 (GRCm38)	missense	probably damaging	1.00
R1486:Birc6	UTSW	17	74,639,820 (GRCm38)	missense	probably damaging	1.00
R1499:Birc6	UTSW	17	74,612,319 (GRCm38)	missense	probably damaging	1.00
R1515:Birc6	UTSW	17	74,528,636 (GRCm38)	nonsense	probably null
R1549:Birc6	UTSW	17	74,662,742 (GRCm38)	missense	probably damaging	1.00
R1559:Birc6	UTSW	17	74,692,237 (GRCm38)	missense	probably damaging	1.00
R1573:Birc6	UTSW	17	74,660,690 (GRCm38)	splice site	probably benign
R1615:Birc6	UTSW	17	74,609,409 (GRCm38)	splice site	probably null
R1621:Birc6	UTSW	17	74,670,250 (GRCm38)	missense	probably benign
R1680:Birc6	UTSW	17	74,548,746 (GRCm38)	missense	probably benign	0.01
R1743:Birc6	UTSW	17	74,579,756 (GRCm38)	missense	possibly damaging	0.95
R1774:Birc6	UTSW	17	74,640,013 (GRCm38)	missense	probably damaging	1.00
R1775:Birc6	UTSW	17	74,612,286 (GRCm38)	missense	probably damaging	1.00
R1818:Birc6	UTSW	17	74,649,849 (GRCm38)	missense	probably damaging	1.00
R1836:Birc6	UTSW	17	74,614,390 (GRCm38)	missense	probably benign	0.41
R1931:Birc6	UTSW	17	74,565,982 (GRCm38)	missense	probably damaging	0.99
R1939:Birc6	UTSW	17	74,670,337 (GRCm38)	missense	probably damaging	1.00
R1964:Birc6	UTSW	17	74,634,885 (GRCm38)	missense	possibly damaging	0.94
R1994:Birc6	UTSW	17	74,598,062 (GRCm38)	missense	probably benign	0.01
R2000:Birc6	UTSW	17	74,604,619 (GRCm38)	missense	possibly damaging	0.46
R2042:Birc6	UTSW	17	74,609,659 (GRCm38)	missense	probably damaging	1.00
R2090:Birc6	UTSW	17	74,662,796 (GRCm38)	missense	probably benign
R2130:Birc6	UTSW	17	74,659,154 (GRCm38)	splice site	probably benign
R2144:Birc6	UTSW	17	74,660,413 (GRCm38)	missense	possibly damaging	0.71
R2145:Birc6	UTSW	17	74,660,413 (GRCm38)	missense	possibly damaging	0.71
R2166:Birc6	UTSW	17	74,635,795 (GRCm38)	missense	probably benign	0.02
R2180:Birc6	UTSW	17	74,612,151 (GRCm38)	missense	probably benign	0.03
R2271:Birc6	UTSW	17	74,602,971 (GRCm38)	missense	probably benign	0.06
R2272:Birc6	UTSW	17	74,602,971 (GRCm38)	missense	probably benign	0.06
R2416:Birc6	UTSW	17	74,608,219 (GRCm38)	missense	possibly damaging	0.83
R2420:Birc6	UTSW	17	74,660,614 (GRCm38)	missense	probably damaging	1.00
R2421:Birc6	UTSW	17	74,660,614 (GRCm38)	missense	probably damaging	1.00
R2422:Birc6	UTSW	17	74,660,614 (GRCm38)	missense	probably damaging	1.00
R2513:Birc6	UTSW	17	74,647,729 (GRCm38)	missense	probably damaging	0.97
R2912:Birc6	UTSW	17	74,692,206 (GRCm38)	missense	probably damaging	1.00
R3024:Birc6	UTSW	17	74,608,219 (GRCm38)	missense	possibly damaging	0.83
R3771:Birc6	UTSW	17	74,618,429 (GRCm38)	splice site	probably benign
R3772:Birc6	UTSW	17	74,618,429 (GRCm38)	splice site	probably benign
R3829:Birc6	UTSW	17	74,655,178 (GRCm38)	missense	probably damaging	1.00
R3913:Birc6	UTSW	17	74,573,613 (GRCm38)	nonsense	probably null
R3915:Birc6	UTSW	17	74,579,608 (GRCm38)	missense	probably benign	0.12
R3921:Birc6	UTSW	17	74,627,019 (GRCm38)	missense	probably damaging	0.98
R3928:Birc6	UTSW	17	74,638,409 (GRCm38)	missense	probably damaging	1.00
R3928:Birc6	UTSW	17	74,611,175 (GRCm38)	missense	possibly damaging	0.91
R4111:Birc6	UTSW	17	74,566,015 (GRCm38)	missense	probably damaging	1.00
R4155:Birc6	UTSW	17	74,596,939 (GRCm38)	missense	probably benign	0.00
R4163:Birc6	UTSW	17	74,626,980 (GRCm38)	missense	probably damaging	1.00
R4226:Birc6	UTSW	17	74,619,840 (GRCm38)	critical splice donor site	probably null
R4227:Birc6	UTSW	17	74,619,840 (GRCm38)	critical splice donor site	probably null
R4358:Birc6	UTSW	17	74,619,668 (GRCm38)	splice site	probably null
R4524:Birc6	UTSW	17	74,641,777 (GRCm38)	missense	probably damaging	1.00
R4605:Birc6	UTSW	17	74,639,934 (GRCm38)	missense	probably damaging	1.00
R4619:Birc6	UTSW	17	74,640,150 (GRCm38)	missense	probably benign	0.18
R4620:Birc6	UTSW	17	74,640,150 (GRCm38)	missense	probably benign	0.18
R4762:Birc6	UTSW	17	74,629,489 (GRCm38)	missense	probably damaging	1.00
R4814:Birc6	UTSW	17	74,649,672 (GRCm38)	missense	probably damaging	1.00
R4849:Birc6	UTSW	17	74,647,388 (GRCm38)	missense	probably damaging	0.99
R4869:Birc6	UTSW	17	74,586,012 (GRCm38)	missense	probably benign	0.05
R4912:Birc6	UTSW	17	74,565,905 (GRCm38)	missense	probably damaging	1.00
R4921:Birc6	UTSW	17	74,650,099 (GRCm38)	missense	probably damaging	1.00
R4942:Birc6	UTSW	17	74,623,050 (GRCm38)	missense	probably damaging	1.00
R4954:Birc6	UTSW	17	74,612,031 (GRCm38)	missense	probably damaging	1.00
R4994:Birc6	UTSW	17	74,594,324 (GRCm38)	intron	probably benign
R5018:Birc6	UTSW	17	74,640,059 (GRCm38)	missense	probably damaging	1.00
R5022:Birc6	UTSW	17	74,692,332 (GRCm38)	missense	probably damaging	1.00
R5054:Birc6	UTSW	17	74,655,325 (GRCm38)	missense	probably damaging	1.00
R5068:Birc6	UTSW	17	74,565,972 (GRCm38)	missense	probably damaging	1.00
R5069:Birc6	UTSW	17	74,565,972 (GRCm38)	missense	probably damaging	1.00
R5070:Birc6	UTSW	17	74,565,972 (GRCm38)	missense	probably damaging	1.00
R5196:Birc6	UTSW	17	74,606,141 (GRCm38)	splice site	probably benign
R5209:Birc6	UTSW	17	74,670,374 (GRCm38)	missense	probably damaging	1.00
R5212:Birc6	UTSW	17	74,670,374 (GRCm38)	missense	probably damaging	1.00
R5216:Birc6	UTSW	17	74,613,470 (GRCm38)	missense	probably damaging	1.00
R5279:Birc6	UTSW	17	74,650,047 (GRCm38)	missense	probably damaging	0.98
R5286:Birc6	UTSW	17	74,670,247 (GRCm38)	missense	probably damaging	1.00
R5399:Birc6	UTSW	17	74,604,578 (GRCm38)	missense	possibly damaging	0.75
R5482:Birc6	UTSW	17	74,662,690 (GRCm38)	missense	probably damaging	1.00
R5482:Birc6	UTSW	17	74,641,782 (GRCm38)	missense	possibly damaging	0.86
R5492:Birc6	UTSW	17	74,670,374 (GRCm38)	missense	probably damaging	1.00
R5504:Birc6	UTSW	17	74,655,213 (GRCm38)	missense	probably damaging	1.00
R5519:Birc6	UTSW	17	74,580,178 (GRCm38)	missense	probably benign
R5544:Birc6	UTSW	17	74,670,374 (GRCm38)	missense	probably damaging	1.00
R5608:Birc6	UTSW	17	74,613,544 (GRCm38)	missense	probably damaging	0.99
R5623:Birc6	UTSW	17	74,528,656 (GRCm38)	missense	probably damaging	0.99
R5701:Birc6	UTSW	17	74,697,425 (GRCm38)	missense	possibly damaging	0.59
R5707:Birc6	UTSW	17	74,696,404 (GRCm38)	missense	probably damaging	1.00
R5715:Birc6	UTSW	17	74,631,620 (GRCm38)	missense	probably damaging	1.00
R5734:Birc6	UTSW	17	74,618,424 (GRCm38)	splice site	probably benign
R5792:Birc6	UTSW	17	74,631,053 (GRCm38)	missense	probably benign	0.05
R5809:Birc6	UTSW	17	74,670,374 (GRCm38)	missense	probably damaging	1.00
R5810:Birc6	UTSW	17	74,670,374 (GRCm38)	missense	probably damaging	1.00
R5813:Birc6	UTSW	17	74,646,502 (GRCm38)	missense	probably damaging	1.00
R5933:Birc6	UTSW	17	74,599,237 (GRCm38)	missense	probably damaging	1.00
R5933:Birc6	UTSW	17	74,599,238 (GRCm38)	missense	probably damaging	0.98
R5960:Birc6	UTSW	17	74,528,765 (GRCm38)	missense	probably damaging	0.97
R5961:Birc6	UTSW	17	74,646,601 (GRCm38)	missense	probably damaging	1.00
R5967:Birc6	UTSW	17	74,660,439 (GRCm38)	missense	probably damaging	0.99
R5970:Birc6	UTSW	17	74,618,502 (GRCm38)	missense	possibly damaging	0.95
R5977:Birc6	UTSW	17	74,603,036 (GRCm38)	missense	probably damaging	1.00
R5982:Birc6	UTSW	17	74,648,158 (GRCm38)	missense	probably benign
R6023:Birc6	UTSW	17	74,654,377 (GRCm38)	missense	probably benign	0.24
R6034:Birc6	UTSW	17	74,615,283 (GRCm38)	missense	probably damaging	1.00
R6034:Birc6	UTSW	17	74,615,283 (GRCm38)	missense	probably damaging	1.00
R6243:Birc6	UTSW	17	74,609,387 (GRCm38)	missense	probably damaging	0.96
R6294:Birc6	UTSW	17	74,689,257 (GRCm38)	missense	probably benign	0.00
R6327:Birc6	UTSW	17	74,662,779 (GRCm38)	missense	probably damaging	1.00
R6501:Birc6	UTSW	17	74,579,281 (GRCm38)	missense	probably damaging	1.00
R6810:Birc6	UTSW	17	74,612,220 (GRCm38)	missense	possibly damaging	0.63
R6822:Birc6	UTSW	17	74,598,044 (GRCm38)	missense	probably damaging	1.00
R6822:Birc6	UTSW	17	74,580,382 (GRCm38)	missense	possibly damaging	0.82
R6835:Birc6	UTSW	17	74,642,504 (GRCm38)	missense	probably damaging	1.00
R6945:Birc6	UTSW	17	74,579,531 (GRCm38)	missense	probably benign	0.04
R6957:Birc6	UTSW	17	74,579,491 (GRCm38)	missense	probably benign
R6989:Birc6	UTSW	17	74,630,989 (GRCm38)	missense	probably benign	0.18
R6991:Birc6	UTSW	17	74,562,095 (GRCm38)	missense	probably damaging	1.00
R7019:Birc6	UTSW	17	74,609,345 (GRCm38)	missense	probably benign	0.01
R7092:Birc6	UTSW	17	74,646,745 (GRCm38)	missense	probably damaging	1.00
R7158:Birc6	UTSW	17	74,594,376 (GRCm38)	missense	probably benign	0.25
R7204:Birc6	UTSW	17	74,640,108 (GRCm38)	missense	probably damaging	1.00
R7267:Birc6	UTSW	17	74,585,985 (GRCm38)	missense	probably benign	0.00
R7316:Birc6	UTSW	17	74,604,494 (GRCm38)	missense	probably damaging	0.99
R7341:Birc6	UTSW	17	74,612,074 (GRCm38)	missense	probably damaging	1.00
R7404:Birc6	UTSW	17	74,639,794 (GRCm38)	missense	possibly damaging	0.73
R7449:Birc6	UTSW	17	74,702,341 (GRCm38)	missense	probably benign
R7498:Birc6	UTSW	17	74,660,470 (GRCm38)	missense	probably damaging	1.00
R7539:Birc6	UTSW	17	74,649,696 (GRCm38)	missense	probably damaging	1.00
R7569:Birc6	UTSW	17	74,598,082 (GRCm38)	missense	possibly damaging	0.71
R7574:Birc6	UTSW	17	74,579,884 (GRCm38)	missense	probably benign
R7611:Birc6	UTSW	17	74,662,718 (GRCm38)	missense	probably damaging	0.98
R7653:Birc6	UTSW	17	74,647,734 (GRCm38)	missense	possibly damaging	0.91
R7716:Birc6	UTSW	17	74,562,061 (GRCm38)	missense	probably damaging	0.99
R7728:Birc6	UTSW	17	74,622,105 (GRCm38)	missense	probably benign	0.01
R7810:Birc6	UTSW	17	74,548,820 (GRCm38)	missense	probably damaging	0.98
R7828:Birc6	UTSW	17	74,579,506 (GRCm38)	missense	probably damaging	0.97
R7881:Birc6	UTSW	17	74,641,671 (GRCm38)	missense	probably damaging	0.99
R7896:Birc6	UTSW	17	74,622,082 (GRCm38)	missense	probably damaging	0.99
R7950:Birc6	UTSW	17	74,593,100 (GRCm38)	missense	probably damaging	1.00
R7988:Birc6	UTSW	17	74,599,373 (GRCm38)	splice site	probably null
R8073:Birc6	UTSW	17	74,603,085 (GRCm38)	missense	probably damaging	1.00
R8128:Birc6	UTSW	17	74,609,258 (GRCm38)	missense	probably damaging	1.00
R8167:Birc6	UTSW	17	74,643,394 (GRCm38)	missense	probably damaging	1.00
R8236:Birc6	UTSW	17	74,611,131 (GRCm38)	missense	probably damaging	1.00
R8237:Birc6	UTSW	17	74,611,131 (GRCm38)	missense	probably damaging	1.00
R8255:Birc6	UTSW	17	74,662,780 (GRCm38)	missense	probably damaging	0.99
R8259:Birc6	UTSW	17	74,598,078 (GRCm38)	missense	probably benign	0.01
R8297:Birc6	UTSW	17	74,625,104 (GRCm38)	critical splice acceptor site	probably null
R8376:Birc6	UTSW	17	74,589,640 (GRCm38)	missense	probably benign	0.18
R8413:Birc6	UTSW	17	74,546,393 (GRCm38)	missense	possibly damaging	0.54
R8503:Birc6	UTSW	17	74,692,244 (GRCm38)	missense	probably damaging	1.00
R8504:Birc6	UTSW	17	74,652,005 (GRCm38)	missense	probably damaging	0.98
R8543:Birc6	UTSW	17	74,565,865 (GRCm38)	missense	probably damaging	1.00
R8550:Birc6	UTSW	17	74,557,954 (GRCm38)	missense	probably benign	0.37
R8551:Birc6	UTSW	17	74,557,954 (GRCm38)	missense	probably benign	0.37
R8556:Birc6	UTSW	17	74,557,954 (GRCm38)	missense	probably benign	0.37
R8683:Birc6	UTSW	17	74,609,119 (GRCm38)	missense	possibly damaging	0.74
R8751:Birc6	UTSW	17	74,648,140 (GRCm38)	missense	probably damaging	0.98
R8803:Birc6	UTSW	17	74,652,038 (GRCm38)	missense	probably damaging	0.99
R8806:Birc6	UTSW	17	74,642,316 (GRCm38)	missense	probably damaging	1.00
R8825:Birc6	UTSW	17	74,613,505 (GRCm38)	missense	probably damaging	0.99
R8888:Birc6	UTSW	17	74,528,538 (GRCm38)	missense	probably null	0.33
R8972:Birc6	UTSW	17	74,702,318 (GRCm38)	missense	probably benign	0.05
R9069:Birc6	UTSW	17	74,561,265 (GRCm38)	splice site	probably benign
R9111:Birc6	UTSW	17	74,659,345 (GRCm38)	missense	probably damaging	0.99
R9130:Birc6	UTSW	17	74,612,151 (GRCm38)	missense
R9352:Birc6	UTSW	17	74,658,352 (GRCm38)	critical splice donor site	probably null
R9354:Birc6	UTSW	17	74,614,406 (GRCm38)	missense	probably benign
R9432:Birc6	UTSW	17	74,659,221 (GRCm38)	missense	probably benign
R9446:Birc6	UTSW	17	74,618,496 (GRCm38)	missense	probably damaging	1.00
R9485:Birc6	UTSW	17	74,638,403 (GRCm38)	missense	probably damaging	1.00
R9499:Birc6	UTSW	17	74,609,069 (GRCm38)	missense	probably benign	0.05
R9551:Birc6	UTSW	17	74,609,069 (GRCm38)	missense	probably benign	0.05
R9552:Birc6	UTSW	17	74,609,069 (GRCm38)	missense	probably benign	0.05
R9585:Birc6	UTSW	17	74,609,270 (GRCm38)	missense	probably damaging	1.00
R9647:Birc6	UTSW	17	74,692,310 (GRCm38)	missense	probably damaging	1.00
R9648:Birc6	UTSW	17	74,631,701 (GRCm38)	missense	probably damaging	1.00
R9667:Birc6	UTSW	17	74,697,425 (GRCm38)	missense	possibly damaging	0.59
R9696:Birc6	UTSW	17	74,640,297 (GRCm38)	missense	probably damaging	0.99
RF016:Birc6	UTSW	17	74,689,324 (GRCm38)	missense	probably damaging	1.00
Z1088:Birc6	UTSW	17	74,611,542 (GRCm38)	missense	probably damaging	0.99
Z1177:Birc6	UTSW	17	74,647,280 (GRCm38)	missense	probably benign	0.10

Predicted Primers

PCR Primer
(F):5'- AATGACTGTGACTAGCCTCCC -3'
(R):5'- ACCTACCAGACAATGAATTCGTAAG -3'

Sequencing Primer
(F):5'- CCTGCTCATCACATGGGAC -3'
(R):5'- CAGACAGTTCTCAATTACGTTTGTTG -3'

Posted On

2016-05-10