Mutagenetix > Incidental Mutation

Incidental Mutation 'R5069:Birc6'

388588

Institutional Source

Beutler Lab

Gene Symbol

Birc6

Ensembl Gene

ENSMUSG00000024073

Gene Name

baculoviral IAP repeat-containing 6

Synonyms

D630005A10Rik, A430032G04Rik, apollon, Bruce, A430040A19Rik

MMRRC Submission

042659-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R5069 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

74835290-75010351 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 74872967 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Cysteine at position 409 (R409C)

Ref Sequence

ENSEMBL: ENSMUSP00000138333 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000180037
AA Change: R409C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000136329
Gene: ENSMUSG00000024073
AA Change: R409C

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

noncoding transcript
Transcript: ENSMUST00000182108

Predicted Effect

probably damaging
Transcript: ENSMUST00000182133
AA Change: R409C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000138693
Gene: ENSMUSG00000024073
AA Change: R409C

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

noncoding transcript
Transcript: ENSMUST00000182257

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000182362

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000182382

Predicted Effect

probably damaging
Transcript: ENSMUST00000182597
AA Change: R409C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000138333
Gene: ENSMUSG00000024073
AA Change: R409C

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 damaging
Transcript: ENSMUST00000183224
AA Change: R381C

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000138270
Gene: ENSMUSG00000024073
AA Change: R381C

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 damaging
Transcript: ENSMUST00000182944
AA Change: R409C

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000138732
Gene: ENSMUSG00000024073
AA Change: R409C

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

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.7%
20x: 93.5%

Validation Efficiency

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: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3425401B19Rik	A	G	14: 32,383,749 (GRCm39)	S739P	possibly damaging	Het
AAdacl4fm3	T	A	4: 144,430,437 (GRCm39)	D184V	probably damaging	Het
Actn2	A	G	13: 12,303,408 (GRCm39)	I464T	possibly damaging	Het
Adcy7	T	C	8: 89,054,325 (GRCm39)	L1060P	probably damaging	Het
Aff3	A	G	1: 38,220,694 (GRCm39)		probably null	Het
Ankar	T	C	1: 72,719,369 (GRCm39)		probably null	Het
Ankrd27	A	T	7: 35,327,860 (GRCm39)	K793N	probably damaging	Het
Arhgef28	T	C	13: 98,211,714 (GRCm39)	T90A	probably damaging	Het
Armc9	A	T	1: 86,184,959 (GRCm39)	H670L	probably benign	Het
Arvcf	A	G	16: 18,217,736 (GRCm39)	Y412C	probably damaging	Het
Ass1	C	T	2: 31,400,185 (GRCm39)	T301M	probably damaging	Het
Baiap3	A	T	17: 25,468,082 (GRCm39)	C283S	probably damaging	Het
Calcoco1	A	G	15: 102,619,527 (GRCm39)	L354P	probably damaging	Het
Cdh3	A	G	8: 107,263,458 (GRCm39)	N126S	probably benign	Het
Cfap54	A	C	10: 92,773,636 (GRCm39)	F135L	probably benign	Het
Dlg1	G	T	16: 31,503,113 (GRCm39)		probably null	Het
Dnah3	T	C	7: 119,632,013 (GRCm39)	H1314R	probably benign	Het
Dsp	A	C	13: 38,381,099 (GRCm39)	T2615P	possibly damaging	Het
Elapor2	T	A	5: 9,490,897 (GRCm39)	C636S	probably damaging	Het
Enpp2	T	C	15: 54,727,450 (GRCm39)	Y513C	probably damaging	Het
Ercc6	T	C	14: 32,292,020 (GRCm39)	V1128A	probably benign	Het
Firrm	T	C	1: 163,815,243 (GRCm39)	T93A	possibly damaging	Het
Gipc2	A	G	3: 151,799,885 (GRCm39)	F282L	probably benign	Het
Gm1043	T	G	5: 37,344,580 (GRCm39)	L231R	probably damaging	Het
Gpr153	T	A	4: 152,364,340 (GRCm39)	M132K	probably damaging	Het
Hbs1l	T	A	10: 21,230,546 (GRCm39)	S496T	probably damaging	Het
Inpp5f	A	G	7: 128,278,451 (GRCm39)		probably null	Het
Kat6a	G	A	8: 23,393,149 (GRCm39)	C209Y	probably damaging	Het
Kcna2	T	A	3: 107,011,953 (GRCm39)	V178D	probably damaging	Het
Krt75	A	G	15: 101,474,673 (GRCm39)		probably null	Het
Letm2	G	A	8: 26,083,980 (GRCm39)	Q84*	probably null	Het
Mib1	A	G	18: 10,793,002 (GRCm39)	E646G	probably damaging	Het
Mmp14	T	A	14: 54,676,570 (GRCm39)	Y372N	probably damaging	Het
Muc6	A	G	7: 141,237,564 (GRCm39)	C218R	probably damaging	Het
Myof	A	T	19: 37,893,773 (GRCm39)	I1130N	possibly damaging	Het
Neil3	A	G	8: 54,054,076 (GRCm39)	S318P	possibly damaging	Het
Nhlh1	A	G	1: 171,881,467 (GRCm39)	V133A	probably benign	Het
Nup153	A	C	13: 46,863,268 (GRCm39)	S331A	probably benign	Het
Nup98	T	C	7: 101,794,862 (GRCm39)	T882A	probably benign	Het
Or11g2	T	A	14: 50,856,197 (GRCm39)	C173S	probably damaging	Het
Or11h4	C	A	14: 50,974,531 (GRCm39)	L29F	probably benign	Het
Or52ab4	A	T	7: 102,987,229 (GRCm39)		probably null	Het
Or9s23	T	A	1: 92,501,135 (GRCm39)	S81T	probably damaging	Het
Otx1	C	A	11: 21,947,037 (GRCm39)	A91S	probably damaging	Het
Pald1	A	T	10: 61,177,025 (GRCm39)	M675K	possibly damaging	Het
Pex5	A	G	6: 124,390,555 (GRCm39)	S97P	probably benign	Het
Pitpnm1	C	T	19: 4,161,140 (GRCm39)	A897V	probably benign	Het
Plxnd1	A	T	6: 115,942,862 (GRCm39)	V1274E	probably damaging	Het
Polr2a	T	C	11: 69,627,561 (GRCm39)		probably null	Het
Ppfia1	G	A	7: 144,068,210 (GRCm39)	Q446*	probably null	Het
Psma2	G	A	13: 14,790,613 (GRCm39)	V20I	probably benign	Het
Pwwp4a	T	C	X: 72,171,577 (GRCm39)	I323T	probably damaging	Het
Rhbdl2	T	A	4: 123,711,710 (GRCm39)	L149*	probably null	Het
Rnf17	T	C	14: 56,743,385 (GRCm39)	V1317A	probably damaging	Het
Rtel1	G	A	2: 180,997,285 (GRCm39)	V1042M	probably benign	Het
Sidt2	A	T	9: 45,850,759 (GRCm39)		probably null	Het
Slc11a1	G	A	1: 74,424,343 (GRCm39)	A434T	probably damaging	Het
Slc28a2b	A	T	2: 122,324,854 (GRCm39)	N142I	possibly damaging	Het
Slc4a10	G	A	2: 62,097,915 (GRCm39)	R508H	probably benign	Het
Slc5a8	A	T	10: 88,722,460 (GRCm39)	I98F	possibly damaging	Het
Slf2	T	A	19: 44,923,692 (GRCm39)	S169T	possibly damaging	Het
Snx33	A	T	9: 56,833,475 (GRCm39)	I198N	probably damaging	Het
Spock3	A	G	8: 63,808,299 (GRCm39)	T396A	probably benign	Het
Sva	A	T	6: 42,015,351 (GRCm39)		probably benign	Het
Syt7	A	G	19: 10,416,601 (GRCm39)	N261S	probably benign	Het
Taar7b	T	G	10: 23,876,359 (GRCm39)	S175A	probably benign	Het
Thoc2	C	T	X: 40,895,570 (GRCm39)	E1491K	probably damaging	Het
Tlr1	T	C	5: 65,083,743 (GRCm39)	Y278C	probably benign	Het
Tph2	T	A	10: 114,987,079 (GRCm39)	Y237F	probably benign	Het
Trim35	C	T	14: 66,546,421 (GRCm39)		probably benign	Het
Trpm4	T	G	7: 44,959,893 (GRCm39)	Y667S	probably damaging	Het
Ttc27	T	A	17: 75,106,337 (GRCm39)	H541Q	probably damaging	Het
Ube4a	T	C	9: 44,851,387 (GRCm39)	H709R	probably damaging	Het
Vwa7	G	A	17: 35,243,166 (GRCm39)	V615I	probably benign	Het
Wars2	A	G	3: 99,094,849 (GRCm39)	H48R	probably damaging	Het
Xlr4c	T	A	X: 72,282,290 (GRCm39)	K121M	probably damaging	Het
Zfc3h1	T	A	10: 115,254,688 (GRCm39)	C1427*	probably null	Het

Other mutations in Birc6

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00402:Birc6	APN	17	74,880,558 (GRCm39)	splice site	probably benign
IGL00542:Birc6	APN	17	74,930,766 (GRCm39)	splice site	probably null
IGL00659:Birc6	APN	17	74,967,648 (GRCm39)	missense	probably damaging	1.00
IGL00710:Birc6	APN	17	74,916,084 (GRCm39)	missense	probably benign	0.37
IGL00806:Birc6	APN	17	74,918,524 (GRCm39)	missense	possibly damaging	0.85
IGL00848:Birc6	APN	17	75,003,388 (GRCm39)	nonsense	probably null
IGL01071:Birc6	APN	17	74,873,127 (GRCm39)	missense	possibly damaging	0.84
IGL01071:Birc6	APN	17	74,938,696 (GRCm39)	missense	probably damaging	1.00
IGL01121:Birc6	APN	17	74,938,033 (GRCm39)	missense	probably benign	0.08
IGL01132:Birc6	APN	17	74,910,055 (GRCm39)	missense	probably damaging	1.00
IGL01323:Birc6	APN	17	74,929,920 (GRCm39)	missense	probably damaging	1.00
IGL01444:Birc6	APN	17	74,938,682 (GRCm39)	missense	probably damaging	1.00
IGL01511:Birc6	APN	17	74,933,998 (GRCm39)	nonsense	probably null
IGL01576:Birc6	APN	17	74,984,365 (GRCm39)	missense	possibly damaging	0.80
IGL01578:Birc6	APN	17	74,955,192 (GRCm39)	missense	probably benign	0.08
IGL01649:Birc6	APN	17	74,911,541 (GRCm39)	missense	probably benign	0.03
IGL01657:Birc6	APN	17	74,967,606 (GRCm39)	missense	probably damaging	1.00
IGL01739:Birc6	APN	17	74,966,216 (GRCm39)	missense	probably benign
IGL01756:Birc6	APN	17	74,947,203 (GRCm39)	missense	probably benign	0.00
IGL01807:Birc6	APN	17	74,938,032 (GRCm39)	missense	probably benign
IGL01885:Birc6	APN	17	74,911,511 (GRCm39)	missense	possibly damaging	0.51
IGL01906:Birc6	APN	17	74,945,353 (GRCm39)	missense	probably damaging	1.00
IGL01915:Birc6	APN	17	74,938,715 (GRCm39)	missense	probably benign	0.34
IGL01998:Birc6	APN	17	74,886,880 (GRCm39)	missense	probably benign	0.06
IGL02084:Birc6	APN	17	74,915,277 (GRCm39)	missense	probably benign	0.45
IGL02086:Birc6	APN	17	74,946,822 (GRCm39)	missense	probably damaging	1.00
IGL02161:Birc6	APN	17	74,855,832 (GRCm39)	missense	probably damaging	0.99
IGL02195:Birc6	APN	17	75,004,376 (GRCm39)	splice site	probably benign
IGL02283:Birc6	APN	17	74,906,935 (GRCm39)	missense	probably benign
IGL02476:Birc6	APN	17	75,003,386 (GRCm39)	missense	possibly damaging	0.81
IGL02493:Birc6	APN	17	74,959,054 (GRCm39)	unclassified	probably benign
IGL02547:Birc6	APN	17	74,886,640 (GRCm39)	missense	probably benign	0.21
IGL02678:Birc6	APN	17	74,956,898 (GRCm39)	missense	probably damaging	1.00
IGL02713:Birc6	APN	17	74,886,319 (GRCm39)	missense	probably benign
IGL02851:Birc6	APN	17	74,916,184 (GRCm39)	missense	probably damaging	1.00
IGL02875:Birc6	APN	17	74,896,713 (GRCm39)	missense	probably damaging	1.00
IGL02985:Birc6	APN	17	74,947,185 (GRCm39)	missense	probably benign	0.00
IGL03004:Birc6	APN	17	74,919,180 (GRCm39)	missense	probably benign	0.10
IGL03053:Birc6	APN	17	74,872,967 (GRCm39)	missense	probably damaging	1.00
IGL03085:Birc6	APN	17	74,903,945 (GRCm39)	missense	probably damaging	0.97
IGL03109:Birc6	APN	17	74,886,329 (GRCm39)	missense	possibly damaging	0.71
IGL03143:Birc6	APN	17	74,905,994 (GRCm39)	missense	possibly damaging	0.89
IGL03180:Birc6	APN	17	74,966,226 (GRCm39)	missense	probably benign
IGL03221:Birc6	APN	17	74,934,002 (GRCm39)	missense	probably benign	0.00
IGL03230:Birc6	APN	17	74,918,065 (GRCm39)	missense	probably damaging	1.00
IGL03294:Birc6	APN	17	74,956,881 (GRCm39)	missense	probably benign	0.02
IGL03399:Birc6	APN	17	74,901,368 (GRCm39)	missense	probably benign	0.01
Badlands	UTSW	17	74,910,031 (GRCm39)	missense	probably damaging	1.00
Big_sky	UTSW	17	74,835,533 (GRCm39)	missense	probably null	0.33
bitterroot	UTSW	17	74,956,691 (GRCm39)	missense	probably damaging	1.00
Black_hills	UTSW	17	74,999,327 (GRCm39)	missense	probably damaging	1.00
bottomlands	UTSW	17	74,916,654 (GRCm39)	missense	probably damaging	1.00
Chai	UTSW	17	74,977,369 (GRCm39)	missense	probably damaging	1.00
Dakota	UTSW	17	74,932,099 (GRCm39)	critical splice acceptor site	probably null
Sempervirens	UTSW	17	74,949,499 (GRCm39)	missense	probably damaging	1.00
E0370:Birc6	UTSW	17	74,984,352 (GRCm39)	missense	probably damaging	1.00
G1citation:Birc6	UTSW	17	74,905,039 (GRCm39)	missense	probably damaging	1.00
G1citation:Birc6	UTSW	17	74,887,377 (GRCm39)	missense	possibly damaging	0.82
PIT4494001:Birc6	UTSW	17	74,933,975 (GRCm39)	missense	probably damaging	1.00
R0081:Birc6	UTSW	17	74,950,436 (GRCm39)	missense	probably benign	0.01
R0086:Birc6	UTSW	17	74,900,161 (GRCm39)	missense	possibly damaging	0.54
R0089:Birc6	UTSW	17	74,945,371 (GRCm39)	missense	possibly damaging	0.90
R0116:Birc6	UTSW	17	74,930,741 (GRCm39)	splice site	probably benign
R0129:Birc6	UTSW	17	74,835,755 (GRCm39)	missense	probably benign	0.05
R0196:Birc6	UTSW	17	74,887,282 (GRCm39)	missense	possibly damaging	0.57
R0201:Birc6	UTSW	17	74,916,322 (GRCm39)	missense	possibly damaging	0.92
R0207:Birc6	UTSW	17	74,969,827 (GRCm39)	splice site	probably benign
R0295:Birc6	UTSW	17	74,920,357 (GRCm39)	intron	probably benign
R0386:Birc6	UTSW	17	74,906,335 (GRCm39)	missense	probably damaging	0.99
R0423:Birc6	UTSW	17	75,003,292 (GRCm39)	missense	probably damaging	1.00
R0449:Birc6	UTSW	17	74,999,290 (GRCm39)	missense	probably damaging	1.00
R0453:Birc6	UTSW	17	74,956,749 (GRCm39)	missense	probably damaging	1.00
R0457:Birc6	UTSW	17	74,969,620 (GRCm39)	missense	probably damaging	1.00
R0457:Birc6	UTSW	17	74,959,023 (GRCm39)	missense	probably benign
R0564:Birc6	UTSW	17	74,932,238 (GRCm39)	splice site	probably benign
R0575:Birc6	UTSW	17	74,996,232 (GRCm39)	missense	probably damaging	1.00
R0582:Birc6	UTSW	17	74,950,332 (GRCm39)	missense	probably damaging	1.00
R0624:Birc6	UTSW	17	74,887,344 (GRCm39)	missense	probably benign	0.20
R0973:Birc6	UTSW	17	74,872,856 (GRCm39)	missense	probably damaging	0.99
R1061:Birc6	UTSW	17	74,996,307 (GRCm39)	missense	probably damaging	1.00
R1378:Birc6	UTSW	17	74,967,450 (GRCm39)	missense	probably damaging	1.00
R1402:Birc6	UTSW	17	75,004,528 (GRCm39)	splice site	probably benign
R1436:Birc6	UTSW	17	74,959,700 (GRCm39)	missense	probably damaging	1.00
R1456:Birc6	UTSW	17	74,916,285 (GRCm39)	missense	probably benign	0.35
R1465:Birc6	UTSW	17	74,930,853 (GRCm39)	missense	probably benign	0.03
R1465:Birc6	UTSW	17	74,930,853 (GRCm39)	missense	probably benign	0.03
R1474:Birc6	UTSW	17	74,886,673 (GRCm39)	missense	probably damaging	0.98
R1479:Birc6	UTSW	17	74,941,848 (GRCm39)	missense	probably damaging	1.00
R1486:Birc6	UTSW	17	74,946,815 (GRCm39)	missense	probably damaging	1.00
R1499:Birc6	UTSW	17	74,919,314 (GRCm39)	missense	probably damaging	1.00
R1515:Birc6	UTSW	17	74,835,631 (GRCm39)	nonsense	probably null
R1549:Birc6	UTSW	17	74,969,737 (GRCm39)	missense	probably damaging	1.00
R1559:Birc6	UTSW	17	74,999,232 (GRCm39)	missense	probably damaging	1.00
R1573:Birc6	UTSW	17	74,967,685 (GRCm39)	splice site	probably benign
R1615:Birc6	UTSW	17	74,916,404 (GRCm39)	splice site	probably null
R1621:Birc6	UTSW	17	74,977,245 (GRCm39)	missense	probably benign
R1680:Birc6	UTSW	17	74,855,741 (GRCm39)	missense	probably benign	0.01
R1743:Birc6	UTSW	17	74,886,751 (GRCm39)	missense	possibly damaging	0.95
R1774:Birc6	UTSW	17	74,947,008 (GRCm39)	missense	probably damaging	1.00
R1775:Birc6	UTSW	17	74,919,281 (GRCm39)	missense	probably damaging	1.00
R1818:Birc6	UTSW	17	74,956,844 (GRCm39)	missense	probably damaging	1.00
R1836:Birc6	UTSW	17	74,921,385 (GRCm39)	missense	probably benign	0.41
R1931:Birc6	UTSW	17	74,872,977 (GRCm39)	missense	probably damaging	0.99
R1939:Birc6	UTSW	17	74,977,332 (GRCm39)	missense	probably damaging	1.00
R1964:Birc6	UTSW	17	74,941,880 (GRCm39)	missense	possibly damaging	0.94
R1994:Birc6	UTSW	17	74,905,057 (GRCm39)	missense	probably benign	0.01
R2000:Birc6	UTSW	17	74,911,614 (GRCm39)	missense	possibly damaging	0.46
R2042:Birc6	UTSW	17	74,916,654 (GRCm39)	missense	probably damaging	1.00
R2090:Birc6	UTSW	17	74,969,791 (GRCm39)	missense	probably benign
R2130:Birc6	UTSW	17	74,966,149 (GRCm39)	splice site	probably benign
R2144:Birc6	UTSW	17	74,967,408 (GRCm39)	missense	possibly damaging	0.71
R2145:Birc6	UTSW	17	74,967,408 (GRCm39)	missense	possibly damaging	0.71
R2166:Birc6	UTSW	17	74,942,790 (GRCm39)	missense	probably benign	0.02
R2180:Birc6	UTSW	17	74,919,146 (GRCm39)	missense	probably benign	0.03
R2271:Birc6	UTSW	17	74,909,966 (GRCm39)	missense	probably benign	0.06
R2272:Birc6	UTSW	17	74,909,966 (GRCm39)	missense	probably benign	0.06
R2416:Birc6	UTSW	17	74,915,214 (GRCm39)	missense	possibly damaging	0.83
R2420:Birc6	UTSW	17	74,967,609 (GRCm39)	missense	probably damaging	1.00
R2421:Birc6	UTSW	17	74,967,609 (GRCm39)	missense	probably damaging	1.00
R2422:Birc6	UTSW	17	74,967,609 (GRCm39)	missense	probably damaging	1.00
R2513:Birc6	UTSW	17	74,954,724 (GRCm39)	missense	probably damaging	0.97
R2912:Birc6	UTSW	17	74,999,201 (GRCm39)	missense	probably damaging	1.00
R3024:Birc6	UTSW	17	74,915,214 (GRCm39)	missense	possibly damaging	0.83
R3771:Birc6	UTSW	17	74,925,424 (GRCm39)	splice site	probably benign
R3772:Birc6	UTSW	17	74,925,424 (GRCm39)	splice site	probably benign
R3829:Birc6	UTSW	17	74,962,173 (GRCm39)	missense	probably damaging	1.00
R3913:Birc6	UTSW	17	74,880,608 (GRCm39)	nonsense	probably null
R3915:Birc6	UTSW	17	74,886,603 (GRCm39)	missense	probably benign	0.12
R3921:Birc6	UTSW	17	74,934,014 (GRCm39)	missense	probably damaging	0.98
R3928:Birc6	UTSW	17	74,945,404 (GRCm39)	missense	probably damaging	1.00
R3928:Birc6	UTSW	17	74,918,170 (GRCm39)	missense	possibly damaging	0.91
R4111:Birc6	UTSW	17	74,873,010 (GRCm39)	missense	probably damaging	1.00
R4155:Birc6	UTSW	17	74,903,934 (GRCm39)	missense	probably benign	0.00
R4163:Birc6	UTSW	17	74,933,975 (GRCm39)	missense	probably damaging	1.00
R4226:Birc6	UTSW	17	74,926,835 (GRCm39)	critical splice donor site	probably null
R4227:Birc6	UTSW	17	74,926,835 (GRCm39)	critical splice donor site	probably null
R4358:Birc6	UTSW	17	74,926,663 (GRCm39)	splice site	probably null
R4524:Birc6	UTSW	17	74,948,772 (GRCm39)	missense	probably damaging	1.00
R4605:Birc6	UTSW	17	74,946,929 (GRCm39)	missense	probably damaging	1.00
R4619:Birc6	UTSW	17	74,947,145 (GRCm39)	missense	probably benign	0.18
R4620:Birc6	UTSW	17	74,947,145 (GRCm39)	missense	probably benign	0.18
R4762:Birc6	UTSW	17	74,936,484 (GRCm39)	missense	probably damaging	1.00
R4814:Birc6	UTSW	17	74,956,667 (GRCm39)	missense	probably damaging	1.00
R4849:Birc6	UTSW	17	74,954,383 (GRCm39)	missense	probably damaging	0.99
R4869:Birc6	UTSW	17	74,893,007 (GRCm39)	missense	probably benign	0.05
R4912:Birc6	UTSW	17	74,872,900 (GRCm39)	missense	probably damaging	1.00
R4921:Birc6	UTSW	17	74,957,094 (GRCm39)	missense	probably damaging	1.00
R4942:Birc6	UTSW	17	74,930,045 (GRCm39)	missense	probably damaging	1.00
R4954:Birc6	UTSW	17	74,919,026 (GRCm39)	missense	probably damaging	1.00
R4992:Birc6	UTSW	17	74,996,251 (GRCm39)	missense	probably benign	0.44
R4994:Birc6	UTSW	17	74,901,319 (GRCm39)	intron	probably benign
R5018:Birc6	UTSW	17	74,947,054 (GRCm39)	missense	probably damaging	1.00
R5022:Birc6	UTSW	17	74,999,327 (GRCm39)	missense	probably damaging	1.00
R5054:Birc6	UTSW	17	74,962,320 (GRCm39)	missense	probably damaging	1.00
R5068:Birc6	UTSW	17	74,872,967 (GRCm39)	missense	probably damaging	1.00
R5070:Birc6	UTSW	17	74,872,967 (GRCm39)	missense	probably damaging	1.00
R5196:Birc6	UTSW	17	74,913,136 (GRCm39)	splice site	probably benign
R5209:Birc6	UTSW	17	74,977,369 (GRCm39)	missense	probably damaging	1.00
R5212:Birc6	UTSW	17	74,977,369 (GRCm39)	missense	probably damaging	1.00
R5216:Birc6	UTSW	17	74,920,465 (GRCm39)	missense	probably damaging	1.00
R5279:Birc6	UTSW	17	74,957,042 (GRCm39)	missense	probably damaging	0.98
R5286:Birc6	UTSW	17	74,977,242 (GRCm39)	missense	probably damaging	1.00
R5399:Birc6	UTSW	17	74,911,573 (GRCm39)	missense	possibly damaging	0.75
R5482:Birc6	UTSW	17	74,969,685 (GRCm39)	missense	probably damaging	1.00
R5482:Birc6	UTSW	17	74,948,777 (GRCm39)	missense	possibly damaging	0.86
R5492:Birc6	UTSW	17	74,977,369 (GRCm39)	missense	probably damaging	1.00
R5504:Birc6	UTSW	17	74,962,208 (GRCm39)	missense	probably damaging	1.00
R5519:Birc6	UTSW	17	74,887,173 (GRCm39)	missense	probably benign
R5544:Birc6	UTSW	17	74,977,369 (GRCm39)	missense	probably damaging	1.00
R5608:Birc6	UTSW	17	74,920,539 (GRCm39)	missense	probably damaging	0.99
R5623:Birc6	UTSW	17	74,835,651 (GRCm39)	missense	probably damaging	0.99
R5701:Birc6	UTSW	17	75,004,420 (GRCm39)	missense	possibly damaging	0.59
R5707:Birc6	UTSW	17	75,003,399 (GRCm39)	missense	probably damaging	1.00
R5715:Birc6	UTSW	17	74,938,615 (GRCm39)	missense	probably damaging	1.00
R5734:Birc6	UTSW	17	74,925,419 (GRCm39)	splice site	probably benign
R5792:Birc6	UTSW	17	74,938,048 (GRCm39)	missense	probably benign	0.05
R5809:Birc6	UTSW	17	74,977,369 (GRCm39)	missense	probably damaging	1.00
R5810:Birc6	UTSW	17	74,977,369 (GRCm39)	missense	probably damaging	1.00
R5813:Birc6	UTSW	17	74,953,497 (GRCm39)	missense	probably damaging	1.00
R5933:Birc6	UTSW	17	74,906,232 (GRCm39)	missense	probably damaging	1.00
R5933:Birc6	UTSW	17	74,906,233 (GRCm39)	missense	probably damaging	0.98
R5960:Birc6	UTSW	17	74,835,760 (GRCm39)	missense	probably damaging	0.97
R5961:Birc6	UTSW	17	74,953,596 (GRCm39)	missense	probably damaging	1.00
R5967:Birc6	UTSW	17	74,967,434 (GRCm39)	missense	probably damaging	0.99
R5970:Birc6	UTSW	17	74,925,497 (GRCm39)	missense	possibly damaging	0.95
R5977:Birc6	UTSW	17	74,910,031 (GRCm39)	missense	probably damaging	1.00
R5982:Birc6	UTSW	17	74,955,153 (GRCm39)	missense	probably benign
R6023:Birc6	UTSW	17	74,961,372 (GRCm39)	missense	probably benign	0.24
R6034:Birc6	UTSW	17	74,922,278 (GRCm39)	missense	probably damaging	1.00
R6034:Birc6	UTSW	17	74,922,278 (GRCm39)	missense	probably damaging	1.00
R6243:Birc6	UTSW	17	74,916,382 (GRCm39)	missense	probably damaging	0.96
R6294:Birc6	UTSW	17	74,996,252 (GRCm39)	missense	probably benign	0.00
R6327:Birc6	UTSW	17	74,969,774 (GRCm39)	missense	probably damaging	1.00
R6501:Birc6	UTSW	17	74,886,276 (GRCm39)	missense	probably damaging	1.00
R6810:Birc6	UTSW	17	74,919,215 (GRCm39)	missense	possibly damaging	0.63
R6822:Birc6	UTSW	17	74,905,039 (GRCm39)	missense	probably damaging	1.00
R6822:Birc6	UTSW	17	74,887,377 (GRCm39)	missense	possibly damaging	0.82
R6835:Birc6	UTSW	17	74,949,499 (GRCm39)	missense	probably damaging	1.00
R6945:Birc6	UTSW	17	74,886,526 (GRCm39)	missense	probably benign	0.04
R6957:Birc6	UTSW	17	74,886,486 (GRCm39)	missense	probably benign
R6989:Birc6	UTSW	17	74,937,984 (GRCm39)	missense	probably benign	0.18
R6991:Birc6	UTSW	17	74,869,090 (GRCm39)	missense	probably damaging	1.00
R7019:Birc6	UTSW	17	74,916,340 (GRCm39)	missense	probably benign	0.01
R7092:Birc6	UTSW	17	74,953,740 (GRCm39)	missense	probably damaging	1.00
R7158:Birc6	UTSW	17	74,901,371 (GRCm39)	missense	probably benign	0.25
R7204:Birc6	UTSW	17	74,947,103 (GRCm39)	missense	probably damaging	1.00
R7267:Birc6	UTSW	17	74,892,980 (GRCm39)	missense	probably benign	0.00
R7316:Birc6	UTSW	17	74,911,489 (GRCm39)	missense	probably damaging	0.99
R7341:Birc6	UTSW	17	74,919,069 (GRCm39)	missense	probably damaging	1.00
R7404:Birc6	UTSW	17	74,946,789 (GRCm39)	missense	possibly damaging	0.73
R7449:Birc6	UTSW	17	75,009,336 (GRCm39)	missense	probably benign
R7498:Birc6	UTSW	17	74,967,465 (GRCm39)	missense	probably damaging	1.00
R7539:Birc6	UTSW	17	74,956,691 (GRCm39)	missense	probably damaging	1.00
R7569:Birc6	UTSW	17	74,905,077 (GRCm39)	missense	possibly damaging	0.71
R7574:Birc6	UTSW	17	74,886,879 (GRCm39)	missense	probably benign
R7611:Birc6	UTSW	17	74,969,713 (GRCm39)	missense	probably damaging	0.98
R7653:Birc6	UTSW	17	74,954,729 (GRCm39)	missense	possibly damaging	0.91
R7716:Birc6	UTSW	17	74,869,056 (GRCm39)	missense	probably damaging	0.99
R7728:Birc6	UTSW	17	74,929,100 (GRCm39)	missense	probably benign	0.01
R7810:Birc6	UTSW	17	74,855,815 (GRCm39)	missense	probably damaging	0.98
R7828:Birc6	UTSW	17	74,886,501 (GRCm39)	missense	probably damaging	0.97
R7881:Birc6	UTSW	17	74,948,666 (GRCm39)	missense	probably damaging	0.99
R7896:Birc6	UTSW	17	74,929,077 (GRCm39)	missense	probably damaging	0.99
R7950:Birc6	UTSW	17	74,900,095 (GRCm39)	missense	probably damaging	1.00
R7988:Birc6	UTSW	17	74,906,368 (GRCm39)	splice site	probably null
R8073:Birc6	UTSW	17	74,910,080 (GRCm39)	missense	probably damaging	1.00
R8128:Birc6	UTSW	17	74,916,253 (GRCm39)	missense	probably damaging	1.00
R8167:Birc6	UTSW	17	74,950,389 (GRCm39)	missense	probably damaging	1.00
R8236:Birc6	UTSW	17	74,918,126 (GRCm39)	missense	probably damaging	1.00
R8237:Birc6	UTSW	17	74,918,126 (GRCm39)	missense	probably damaging	1.00
R8255:Birc6	UTSW	17	74,969,775 (GRCm39)	missense	probably damaging	0.99
R8259:Birc6	UTSW	17	74,905,073 (GRCm39)	missense	probably benign	0.01
R8297:Birc6	UTSW	17	74,932,099 (GRCm39)	critical splice acceptor site	probably null
R8376:Birc6	UTSW	17	74,896,635 (GRCm39)	missense	probably benign	0.18
R8413:Birc6	UTSW	17	74,853,388 (GRCm39)	missense	possibly damaging	0.54
R8503:Birc6	UTSW	17	74,999,239 (GRCm39)	missense	probably damaging	1.00
R8504:Birc6	UTSW	17	74,959,000 (GRCm39)	missense	probably damaging	0.98
R8543:Birc6	UTSW	17	74,872,860 (GRCm39)	missense	probably damaging	1.00
R8550:Birc6	UTSW	17	74,864,949 (GRCm39)	missense	probably benign	0.37
R8551:Birc6	UTSW	17	74,864,949 (GRCm39)	missense	probably benign	0.37
R8556:Birc6	UTSW	17	74,864,949 (GRCm39)	missense	probably benign	0.37
R8683:Birc6	UTSW	17	74,916,114 (GRCm39)	missense	possibly damaging	0.74
R8751:Birc6	UTSW	17	74,955,135 (GRCm39)	missense	probably damaging	0.98
R8803:Birc6	UTSW	17	74,959,033 (GRCm39)	missense	probably damaging	0.99
R8806:Birc6	UTSW	17	74,949,311 (GRCm39)	missense	probably damaging	1.00
R8825:Birc6	UTSW	17	74,920,500 (GRCm39)	missense	probably damaging	0.99
R8888:Birc6	UTSW	17	74,835,533 (GRCm39)	missense	probably null	0.33
R8972:Birc6	UTSW	17	75,009,313 (GRCm39)	missense	probably benign	0.05
R9069:Birc6	UTSW	17	74,868,260 (GRCm39)	splice site	probably benign
R9111:Birc6	UTSW	17	74,966,340 (GRCm39)	missense	probably damaging	0.99
R9130:Birc6	UTSW	17	74,919,146 (GRCm39)	missense
R9352:Birc6	UTSW	17	74,965,347 (GRCm39)	critical splice donor site	probably null
R9354:Birc6	UTSW	17	74,921,401 (GRCm39)	missense	probably benign
R9432:Birc6	UTSW	17	74,966,216 (GRCm39)	missense	probably benign
R9446:Birc6	UTSW	17	74,925,491 (GRCm39)	missense	probably damaging	1.00
R9485:Birc6	UTSW	17	74,945,398 (GRCm39)	missense	probably damaging	1.00
R9499:Birc6	UTSW	17	74,916,064 (GRCm39)	missense	probably benign	0.05
R9551:Birc6	UTSW	17	74,916,064 (GRCm39)	missense	probably benign	0.05
R9552:Birc6	UTSW	17	74,916,064 (GRCm39)	missense	probably benign	0.05
R9585:Birc6	UTSW	17	74,916,265 (GRCm39)	missense	probably damaging	1.00
R9647:Birc6	UTSW	17	74,999,305 (GRCm39)	missense	probably damaging	1.00
R9648:Birc6	UTSW	17	74,938,696 (GRCm39)	missense	probably damaging	1.00
R9667:Birc6	UTSW	17	75,004,420 (GRCm39)	missense	possibly damaging	0.59
R9696:Birc6	UTSW	17	74,947,292 (GRCm39)	missense	probably damaging	0.99
RF016:Birc6	UTSW	17	74,996,319 (GRCm39)	missense	probably damaging	1.00
Z1088:Birc6	UTSW	17	74,918,537 (GRCm39)	missense	probably damaging	0.99
Z1177:Birc6	UTSW	17	74,954,275 (GRCm39)	missense	probably benign	0.10

Predicted Primers

PCR Primer
(F):5'- AGGCAATCTTCTAGTTTCTGCTTTG -3'
(R):5'- AGAAGAGTCTTCCAGCCATGC -3'

Sequencing Primer
(F):5'- CCTCTAAAGGTCCGAACATGAGAG -3'
(R):5'- GCCAAAGTGGGTCTCCTTGAATC -3'

Posted On

2016-06-06