Mutagenetix > Incidental Mutation

Incidental Mutation 'R2421:Birc6'

249335

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

040383-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R2421 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

74835290-75010351 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 74967609 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Glutamine at position 301 (L301Q)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000180037] [ENSMUST00000182133] [ENSMUST00000182597] [ENSMUST00000182817] [ENSMUST00000182944] [ENSMUST00000183224]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000180037
AA Change: L4190Q

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

SMART Domains

Protein: ENSMUSP00000136329
Gene: ENSMUSG00000024073
AA Change: L4190Q

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 damaging
Transcript: ENSMUST00000182133
AA Change: L4184Q

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

SMART Domains

Protein: ENSMUSP00000138693
Gene: ENSMUSG00000024073
AA Change: L4184Q

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: ENSMUST00000182147

Predicted Effect

probably damaging
Transcript: ENSMUST00000182597
AA Change: L4199Q

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

SMART Domains

Protein: ENSMUSP00000138333
Gene: ENSMUSG00000024073
AA Change: L4199Q

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: ENSMUST00000182817

SMART Domains

Protein: ENSMUSP00000138349
Gene: ENSMUSG00000024073

Domain	Start	End	E-Value	Type
low complexity region	63	82	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000182944
AA Change: L4186Q

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

SMART Domains

Protein: ENSMUSP00000138732
Gene: ENSMUSG00000024073
AA Change: L4186Q

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 damaging
Transcript: ENSMUST00000183224
AA Change: L4170Q

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

SMART Domains

Protein: ENSMUSP00000138270
Gene: ENSMUSG00000024073
AA Change: L4170Q

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: ENSMUST00000183249
AA Change: L301Q

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

Meta Mutation Damage Score

0.6104

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 97.0%
20x: 94.2%

Validation Efficiency

96% (81/84)

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: 84 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abraxas1	C	T	5: 100,960,040 (GRCm39)	R104H	possibly damaging	Het
Adamts3	A	G	5: 89,831,034 (GRCm39)	S1007P	probably damaging	Het
Adcy10	T	A	1: 165,386,166 (GRCm39)	L1118Q	probably damaging	Het
Adgre4	A	G	17: 56,085,872 (GRCm39)	E57G	probably benign	Het
Alpk2	T	C	18: 65,439,687 (GRCm39)	S1036G	probably benign	Het
Ank3	T	C	10: 69,818,034 (GRCm39)		probably benign	Het
Ankfy1	T	A	11: 72,646,722 (GRCm39)		probably benign	Het
Antxrl	A	G	14: 33,793,646 (GRCm39)		probably benign	Het
Apaf1	A	T	10: 90,856,585 (GRCm39)	V874D	probably damaging	Het
Arhgap39	T	A	15: 76,609,346 (GRCm39)	T1025S	probably damaging	Het
Arhgef12	A	T	9: 42,912,302 (GRCm39)	C519S	probably damaging	Het
Aspm	G	A	1: 139,416,225 (GRCm39)	V1512M	possibly damaging	Het
Atp13a3	T	C	16: 30,168,643 (GRCm39)	T449A	probably benign	Het
Atxn2	A	T	5: 121,940,142 (GRCm39)		probably null	Het
Camk2d	A	G	3: 126,574,064 (GRCm39)	D157G	probably damaging	Het
Ccdc122	T	C	14: 77,329,103 (GRCm39)		probably benign	Het
Ccdc137	G	A	11: 120,353,090 (GRCm39)		probably null	Het
Ccdc18	A	C	5: 108,376,454 (GRCm39)	E1298D	probably damaging	Het
Col4a3	G	A	1: 82,647,996 (GRCm39)		probably benign	Het
Coq10b	G	A	1: 55,092,136 (GRCm39)	A35T	probably benign	Het
Cracdl	C	A	1: 37,652,556 (GRCm39)	V1084L	probably benign	Het
Creb3l3	T	C	10: 80,927,652 (GRCm39)	I47V	probably benign	Het
Csgalnact1	A	T	8: 68,914,160 (GRCm39)	I15N	probably benign	Het
Dcp1b	A	G	6: 119,192,227 (GRCm39)	Q381R	probably benign	Het
Dnajc21	A	G	15: 10,462,021 (GRCm39)	S127P	probably benign	Het
Dnal1	C	T	12: 84,183,480 (GRCm39)	Q80*	probably null	Het
Dtd2	A	G	12: 52,046,638 (GRCm39)	V67A	probably benign	Het
Gart	A	G	16: 91,439,928 (GRCm39)		probably null	Het
Gm17421	T	A	12: 113,333,107 (GRCm39)		noncoding transcript	Het
Gm6327	T	C	16: 12,577,958 (GRCm39)		noncoding transcript	Het
Gm8674	T	C	13: 50,054,699 (GRCm39)		noncoding transcript	Het
Gpr107	G	A	2: 31,075,541 (GRCm39)	G351S	probably damaging	Het
H2-M10.5	A	G	17: 37,085,891 (GRCm39)	I308V	probably benign	Het
Krt13	A	T	11: 100,010,877 (GRCm39)	L159Q	probably benign	Het
Krt78	T	C	15: 101,855,699 (GRCm39)	E704G	probably damaging	Het
Lama1	A	T	17: 68,057,548 (GRCm39)	M541L	probably benign	Het
Lenep	G	A	3: 89,309,881 (GRCm39)		probably null	Het
Lrp1b	T	C	2: 40,772,145 (GRCm39)		probably benign	Het
Ly6g6e	G	A	17: 35,297,122 (GRCm39)	R121Q	probably benign	Het
Lyn	C	T	4: 3,748,787 (GRCm39)	A255V	possibly damaging	Het
Mdn1	T	A	4: 32,723,621 (GRCm39)	I2519K	probably damaging	Het
Mmaa	T	A	8: 80,008,061 (GRCm39)	R59W	probably damaging	Het
Ms4a4b	A	G	19: 11,432,061 (GRCm39)	I61V	possibly damaging	Het
Ndufaf1	T	C	2: 119,486,218 (GRCm39)	E298G	probably damaging	Het
Or10d5	A	G	9: 39,861,824 (GRCm39)	L81P	possibly damaging	Het
Or13a1	T	A	6: 116,470,674 (GRCm39)	C35S	probably benign	Het
Or4c114	T	C	2: 88,905,336 (GRCm39)	Y33C	possibly damaging	Het
Or5k15	T	C	16: 58,710,328 (GRCm39)	E85G	probably benign	Het
Or5k8	T	C	16: 58,644,709 (GRCm39)	D121G	probably damaging	Het
Pef1	C	A	4: 130,021,110 (GRCm39)	C221*	probably null	Het
Plekhg1	G	A	10: 3,908,048 (GRCm39)	M988I	probably benign	Het
Pnliprp1	T	A	19: 58,732,517 (GRCm39)	I460N	probably benign	Het
Ppfia4	T	C	1: 134,255,138 (GRCm39)	N239S	probably benign	Het
Ppp4r3a	A	G	12: 101,008,912 (GRCm39)		probably benign	Het
Prlr	T	A	15: 10,319,343 (GRCm39)	W91R	probably damaging	Het
Psmd2	T	A	16: 20,478,856 (GRCm39)		probably null	Het
Ptprt	T	A	2: 162,119,960 (GRCm39)		probably benign	Het
Pttg1ip2	T	C	5: 5,505,912 (GRCm39)	Y123C	probably benign	Het
Rbm12b2	T	C	4: 12,095,127 (GRCm39)	F662S	possibly damaging	Het
Rgs6	C	A	12: 83,163,057 (GRCm39)	T421K	possibly damaging	Het
Ryr2	T	G	13: 11,606,123 (GRCm39)	Q4486H	probably damaging	Het
Scn7a	A	T	2: 66,556,646 (GRCm39)		probably benign	Het
Smc1a	A	G	X: 150,830,971 (GRCm39)		probably benign	Het
Synrg	A	G	11: 83,900,050 (GRCm39)	E674G	probably damaging	Het
Syt9	G	A	7: 107,035,988 (GRCm39)	R335K	probably benign	Het
Taar7a	T	C	10: 23,868,415 (GRCm39)	N322S	probably damaging	Het
Tfb2m	C	A	1: 179,361,231 (GRCm39)	W252C	possibly damaging	Het
Tmub2	T	A	11: 102,178,581 (GRCm39)	D161E	probably benign	Het
Ttc23l	G	A	15: 10,537,652 (GRCm39)	S206L	probably benign	Het
Tyw1	A	T	5: 130,298,101 (GRCm39)	H214L	probably damaging	Het
Tyw5	A	G	1: 57,435,907 (GRCm39)	I82T	possibly damaging	Het
Uba6	A	G	5: 86,280,475 (GRCm39)		probably null	Het
Unc13c	T	C	9: 73,838,829 (GRCm39)	Y674C	probably damaging	Het
Vangl2	T	C	1: 171,835,526 (GRCm39)	Y382C	probably damaging	Het
Vmn2r105	T	A	17: 20,448,097 (GRCm39)	R242S	probably benign	Het
Vmn2r12	A	G	5: 109,234,398 (GRCm39)	Y605H	probably benign	Het
Vps13a	T	G	19: 16,737,035 (GRCm39)	I101L	probably benign	Het
Washc4	T	A	10: 83,415,385 (GRCm39)	F792I	probably damaging	Het
Wdhd1	G	A	14: 47,496,041 (GRCm39)	H608Y	probably benign	Het
Wdr48	T	A	9: 119,731,470 (GRCm39)	I56K	probably damaging	Het
Xpo4	T	C	14: 57,866,960 (GRCm39)	D194G	probably benign	Het
Zfp644	A	G	5: 106,785,110 (GRCm39)	M479T	possibly damaging	Het
Zfp821	T	A	8: 110,436,165 (GRCm39)		probably null	Het
Zswim8	A	G	14: 20,769,525 (GRCm39)	Y1237C	probably damaging	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
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
R5069: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'- TGATCGCTTCCACCACTCAG -3'
(R):5'- TCACACGATTCCAATGTCACTTAC -3'

Sequencing Primer
(F):5'- GCCAAAGGATAGTGATCAGTTTG -3'
(R):5'- CACCCTGTTTGTGTAGTGT -3'

Posted On

2014-11-12