Mutagenetix > Incidental Mutation

Incidental Mutation 'R6861:Bptf'

535547

Institutional Source

Beutler Lab

Gene Symbol

Bptf

Ensembl Gene

ENSMUSG00000040481

Gene Name

bromodomain PHD finger transcription factor

Synonyms

Falz, 9430093H17Rik

MMRRC Submission

044962-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R6861 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

106923907-107022953 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 106953391 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Methionine at position 2117 (T2117M)

Ref Sequence

ENSEMBL: ENSMUSP00000102374 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000057892] [ENSMUST00000106762] [ENSMUST00000106763] [ENSMUST00000149486]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000057892
AA Change: T2002M

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

SMART Domains

Protein: ENSMUSP00000052303
Gene: ENSMUSG00000040481
AA Change: T2002M

Domain	Start	End	E-Value	Type
low complexity region	12	44	N/A	INTRINSIC
low complexity region	49	62	N/A	INTRINSIC
low complexity region	77	119	N/A	INTRINSIC
low complexity region	137	197	N/A	INTRINSIC
low complexity region	202	215	N/A	INTRINSIC
DDT	252	312	2.02e-23	SMART
Pfam:WHIM1	351	400	4.7e-8	PFAM
PHD	404	447	2.23e-11	SMART
coiled coil region	864	894	N/A	INTRINSIC
low complexity region	961	973	N/A	INTRINSIC
low complexity region	987	998	N/A	INTRINSIC
low complexity region	1062	1072	N/A	INTRINSIC
low complexity region	1086	1098	N/A	INTRINSIC
low complexity region	1225	1238	N/A	INTRINSIC
low complexity region	1251	1265	N/A	INTRINSIC
low complexity region	1491	1503	N/A	INTRINSIC
low complexity region	1594	1613	N/A	INTRINSIC
low complexity region	1636	1645	N/A	INTRINSIC
low complexity region	1665	1683	N/A	INTRINSIC
low complexity region	1818	1834	N/A	INTRINSIC
coiled coil region	1908	1936	N/A	INTRINSIC
low complexity region	1941	1957	N/A	INTRINSIC
low complexity region	2051	2061	N/A	INTRINSIC
low complexity region	2092	2107	N/A	INTRINSIC
low complexity region	2115	2128	N/A	INTRINSIC
low complexity region	2175	2197	N/A	INTRINSIC
low complexity region	2227	2252	N/A	INTRINSIC
low complexity region	2275	2312	N/A	INTRINSIC
low complexity region	2336	2355	N/A	INTRINSIC
low complexity region	2361	2378	N/A	INTRINSIC
low complexity region	2390	2420	N/A	INTRINSIC
low complexity region	2430	2463	N/A	INTRINSIC
coiled coil region	2489	2527	N/A	INTRINSIC
coiled coil region	2576	2604	N/A	INTRINSIC
low complexity region	2663	2700	N/A	INTRINSIC
low complexity region	2713	2736	N/A	INTRINSIC
PHD	2744	2791	5.32e-9	SMART
BROMO	2800	2908	5.5e-37	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000106762
AA Change: T2054M

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

SMART Domains

Protein: ENSMUSP00000102373
Gene: ENSMUSG00000040481
AA Change: T2054M

Domain	Start	End	E-Value	Type
low complexity region	12	44	N/A	INTRINSIC
low complexity region	49	62	N/A	INTRINSIC
low complexity region	77	119	N/A	INTRINSIC
low complexity region	137	197	N/A	INTRINSIC
low complexity region	202	215	N/A	INTRINSIC
DDT	252	312	2.02e-23	SMART
Pfam:WHIM1	351	400	4.7e-8	PFAM
PHD	404	447	2.23e-11	SMART
internal_repeat_1	589	642	6.48e-5	PROSPERO
low complexity region	644	654	N/A	INTRINSIC
low complexity region	662	679	N/A	INTRINSIC
coiled coil region	926	956	N/A	INTRINSIC
low complexity region	1013	1025	N/A	INTRINSIC
low complexity region	1039	1050	N/A	INTRINSIC
low complexity region	1114	1124	N/A	INTRINSIC
low complexity region	1138	1150	N/A	INTRINSIC
low complexity region	1277	1290	N/A	INTRINSIC
low complexity region	1303	1317	N/A	INTRINSIC
internal_repeat_1	1387	1440	6.48e-5	PROSPERO
low complexity region	1543	1555	N/A	INTRINSIC
low complexity region	1646	1665	N/A	INTRINSIC
low complexity region	1688	1697	N/A	INTRINSIC
low complexity region	1717	1735	N/A	INTRINSIC
low complexity region	1870	1886	N/A	INTRINSIC
coiled coil region	1960	1988	N/A	INTRINSIC
low complexity region	1993	2009	N/A	INTRINSIC
low complexity region	2103	2113	N/A	INTRINSIC
low complexity region	2144	2159	N/A	INTRINSIC
low complexity region	2167	2180	N/A	INTRINSIC
low complexity region	2227	2249	N/A	INTRINSIC
low complexity region	2279	2304	N/A	INTRINSIC
low complexity region	2327	2364	N/A	INTRINSIC
low complexity region	2388	2407	N/A	INTRINSIC
low complexity region	2413	2430	N/A	INTRINSIC
low complexity region	2442	2472	N/A	INTRINSIC
low complexity region	2482	2515	N/A	INTRINSIC
coiled coil region	2541	2579	N/A	INTRINSIC
coiled coil region	2628	2656	N/A	INTRINSIC
low complexity region	2715	2752	N/A	INTRINSIC
low complexity region	2765	2788	N/A	INTRINSIC
PHD	2796	2843	5.32e-9	SMART
BROMO	2852	2960	5.5e-37	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000106763
AA Change: T2117M

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

SMART Domains

Protein: ENSMUSP00000102374
Gene: ENSMUSG00000040481
AA Change: T2117M

Domain	Start	End	E-Value	Type
low complexity region	12	44	N/A	INTRINSIC
low complexity region	49	62	N/A	INTRINSIC
low complexity region	77	119	N/A	INTRINSIC
low complexity region	137	197	N/A	INTRINSIC
low complexity region	202	215	N/A	INTRINSIC
DDT	252	312	2.02e-23	SMART
Pfam:WHIM1	351	400	4.9e-8	PFAM
PHD	404	447	2.23e-11	SMART
low complexity region	624	639	N/A	INTRINSIC
low complexity region	707	717	N/A	INTRINSIC
low complexity region	725	742	N/A	INTRINSIC
coiled coil region	989	1019	N/A	INTRINSIC
low complexity region	1076	1088	N/A	INTRINSIC
low complexity region	1102	1113	N/A	INTRINSIC
low complexity region	1177	1187	N/A	INTRINSIC
low complexity region	1201	1213	N/A	INTRINSIC
low complexity region	1340	1353	N/A	INTRINSIC
low complexity region	1366	1380	N/A	INTRINSIC
low complexity region	1606	1618	N/A	INTRINSIC
low complexity region	1709	1728	N/A	INTRINSIC
low complexity region	1751	1760	N/A	INTRINSIC
low complexity region	1780	1798	N/A	INTRINSIC
low complexity region	1933	1949	N/A	INTRINSIC
coiled coil region	2023	2051	N/A	INTRINSIC
low complexity region	2056	2072	N/A	INTRINSIC
low complexity region	2166	2176	N/A	INTRINSIC
low complexity region	2207	2222	N/A	INTRINSIC
low complexity region	2230	2243	N/A	INTRINSIC
low complexity region	2290	2312	N/A	INTRINSIC
low complexity region	2342	2367	N/A	INTRINSIC
low complexity region	2390	2427	N/A	INTRINSIC
low complexity region	2451	2470	N/A	INTRINSIC
low complexity region	2476	2493	N/A	INTRINSIC
low complexity region	2505	2535	N/A	INTRINSIC
low complexity region	2545	2578	N/A	INTRINSIC
coiled coil region	2604	2642	N/A	INTRINSIC
coiled coil region	2691	2719	N/A	INTRINSIC
low complexity region	2778	2815	N/A	INTRINSIC
low complexity region	2828	2851	N/A	INTRINSIC
PHD	2859	2906	5.32e-9	SMART
BROMO	2915	3023	5.5e-37	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000149486
AA Change: T164M

PolyPhen 2 Score 0.802 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000122575
Gene: ENSMUSG00000040481
AA Change: T164M

Domain	Start	End	E-Value	Type
coiled coil region	70	98	N/A	INTRINSIC
low complexity region	103	119	N/A	INTRINSIC
low complexity region	171	188	N/A	INTRINSIC
low complexity region	267	277	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.6%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene was identified by the reactivity of its encoded protein to a monoclonal antibody prepared against brain homogenates from patients with Alzheimer's disease. Analysis of the original protein (fetal Alz-50 reactive clone 1, or FAC1), identified as an 810 aa protein containing a DNA-binding domain and a zinc finger motif, suggested it might play a role in the regulation of transcription. High levels of FAC1 were detected in fetal brain and in patients with neurodegenerative diseases. The protein encoded by this gene is actually much larger than originally thought, and it also contains a C-terminal bromodomain characteristic of proteins that regulate transcription during proliferation. The encoded protein is highly similar to the largest subunit of the Drosophila NURF (nucleosome remodeling factor) complex. In Drosophila, the NURF complex, which catalyzes nucleosome sliding on DNA and interacts with sequence-specific transcription factors, is necessary for the chromatin remodeling required for transcription. Two alternative transcripts encoding different isoforms have been described completely. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a null mutation display embryonic lethality during organogenesis with embryonic growth arrest around early gastrulation and a greatly reduced ectoplacental cone. [provided by MGI curators]

Allele List at MGI

All alleles(58) : Targeted, knock-out(1) Targeted, other(1) Gene trapped(56)

Other mutations in this stock

Total: 86 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamtsl4	G	A	3: 95,588,194 (GRCm39)	R598C	probably damaging	Het
Adra2a	T	C	19: 54,034,818 (GRCm39)	L58P	probably damaging	Het
Ajm1	C	CTCTA	2: 25,469,733 (GRCm39)		probably null	Het
Alox5ap	A	G	5: 149,201,927 (GRCm39)	D2G	probably damaging	Het
Arid1b	G	A	17: 5,377,961 (GRCm39)	V1238M	possibly damaging	Het
Bank1	A	G	3: 135,960,764 (GRCm39)	V31A	probably benign	Het
Cadps	G	A	14: 12,522,401 (GRCm38)	R588*	probably null	Het
Cavin4	A	G	4: 48,672,214 (GRCm39)	I220V	probably benign	Het
Cep192	G	A	18: 67,974,699 (GRCm39)	M1267I	probably benign	Het
Cers5	G	A	15: 99,670,244 (GRCm39)		probably benign	Het
Cfap65	A	T	1: 74,964,274 (GRCm39)	I558N	probably damaging	Het
Cfh	A	T	1: 140,028,621 (GRCm39)	S1025T	probably benign	Het
Cftr	A	G	6: 18,268,107 (GRCm39)	I689V	probably benign	Het
Cgrrf1	T	C	14: 47,069,785 (GRCm39)	I18T	probably damaging	Het
CK137956	A	G	4: 127,864,519 (GRCm39)	S37P	probably damaging	Het
Clca4a	T	C	3: 144,676,416 (GRCm39)	D88G	probably benign	Het
Col11a1	G	A	3: 113,961,141 (GRCm39)	G1166D	probably damaging	Het
Col24a1	G	A	3: 145,166,589 (GRCm39)	G1075S	probably damaging	Het
Crispld2	C	T	8: 120,752,852 (GRCm39)	T299M	probably damaging	Het
Cyb561a3	T	A	19: 10,562,701 (GRCm39)	Y114N	probably damaging	Het
Cyp3a57	T	A	5: 145,307,773 (GRCm39)	W147R	possibly damaging	Het
Dnah2	C	A	11: 69,346,789 (GRCm39)	R2599L	possibly damaging	Het
Dock1	T	A	7: 134,373,207 (GRCm39)	S525T	probably benign	Het
Drc7	T	G	8: 95,789,025 (GRCm39)		probably null	Het
Efhd2	G	T	4: 141,587,192 (GRCm39)		probably null	Het
Epb41l1	A	T	2: 156,367,142 (GRCm39)	E658D	probably benign	Het
Evi5	C	T	5: 107,896,184 (GRCm39)	S753N	probably benign	Het
Exoc3	A	T	13: 74,337,319 (GRCm39)	D427E	probably benign	Het
Fbxw9	A	G	8: 85,792,740 (GRCm39)	D363G	probably damaging	Het
Fcer2a	T	C	8: 3,732,910 (GRCm39)	Y277C	probably damaging	Het
Fstl5	A	T	3: 76,229,523 (GRCm39)	Y108F	probably damaging	Het
Gcn1	A	G	5: 115,749,108 (GRCm39)	D1880G	probably benign	Het
Gm4924	T	A	10: 82,214,948 (GRCm39)	Y915*	probably null	Het
Gpr139	T	A	7: 118,743,875 (GRCm39)	I237F	probably benign	Het
Hao2	A	G	3: 98,784,498 (GRCm39)	L289S	probably damaging	Het
Hexim1	A	G	11: 103,007,793 (GRCm39)	S16G	probably benign	Het
Hmgcs1	T	A	13: 120,161,535 (GRCm39)	M109K	probably damaging	Het
Hs3st4	T	A	7: 123,996,052 (GRCm39)	N239K	possibly damaging	Het
Hsd3b5	T	A	3: 98,529,328 (GRCm39)	N101Y	probably damaging	Het
Idh2	G	A	7: 79,747,966 (GRCm39)	P245S	probably damaging	Het
Irx3	A	G	8: 92,525,530 (GRCm39)		probably benign	Het
Lilra5	A	T	7: 4,244,931 (GRCm39)	D234V	probably benign	Het
Lrfn5	G	A	12: 61,886,476 (GRCm39)	S88N	probably damaging	Het
Lrp2	A	T	2: 69,343,721 (GRCm39)	S879R	possibly damaging	Het
Lsm11	A	G	11: 45,824,781 (GRCm39)	S249P	probably benign	Het
Ltbp1	C	T	17: 75,534,187 (GRCm39)	A543V	possibly damaging	Het
Mbd1	GTCTGCATCTGCGTCTTCGTCTGCATCTGCATCTGCGTCTTCGTCTGCATCTGCATCTGC	GTCTGCATCTGCGTCTTCGTCTGCATCTGCATCTGC	18: 74,406,645 (GRCm39)			Het
Mier2	C	T	10: 79,376,990 (GRCm39)		probably benign	Het
Mup6	G	C	4: 60,004,093 (GRCm39)	G70A	probably benign	Het
Neb	A	G	2: 52,085,732 (GRCm39)	L5258P	probably damaging	Het
Nlrc5	G	A	8: 95,247,857 (GRCm39)		probably benign	Het
Nr6a1	A	T	2: 38,630,597 (GRCm39)	F207I	possibly damaging	Het
Or2y1	A	T	11: 49,385,632 (GRCm39)	T91S	probably benign	Het
Or5k17	A	T	16: 58,746,867 (GRCm39)	D22E	probably benign	Het
Or8b43	T	C	9: 38,360,731 (GRCm39)	C188R	probably damaging	Het
Osbp2	A	G	11: 3,665,191 (GRCm39)	V51A	possibly damaging	Het
Papln	G	T	12: 83,821,723 (GRCm39)	C317F	probably damaging	Het
Pdcd7	T	C	9: 65,265,904 (GRCm39)	S454P	probably damaging	Het
Pde4a	C	T	9: 21,116,597 (GRCm39)	T473I	probably damaging	Het
Peg10	CC	CCCCATCAGGC	6: 4,756,350 (GRCm39)		probably benign	Het
Peg10	C	CCCATCAGGA	6: 4,756,351 (GRCm39)		probably benign	Het
Peg3	G	T	7: 6,714,385 (GRCm39)	S279*	probably null	Het
Rbl1	A	G	2: 156,994,887 (GRCm39)	Y929H	probably damaging	Het
Rsf1	G	GACGGCGGCA	7: 97,229,116 (GRCm39)		probably benign	Het
Sall3	C	A	18: 81,017,590 (GRCm39)	E113*	probably null	Het
Scn5a	A	C	9: 119,359,089 (GRCm39)	F653V	probably damaging	Het
Selenok	T	A	14: 29,692,005 (GRCm39)	N14K	possibly damaging	Het
Slc22a20	T	C	19: 6,021,838 (GRCm39)	T426A	probably benign	Het
Slc4a2	T	A	5: 24,640,007 (GRCm39)	S563T	probably damaging	Het
Sspo	T	A	6: 48,464,889 (GRCm39)	S3798T	probably benign	Het
Stag3	G	T	5: 138,302,969 (GRCm39)	R63L	possibly damaging	Het
Stard9	A	T	2: 120,535,667 (GRCm39)	M3975L	probably benign	Het
Syne2	C	A	12: 75,956,040 (GRCm39)	T582K	probably damaging	Het
Synj1	G	A	16: 90,760,768 (GRCm39)	Q748*	probably null	Het
Tas2r109	T	C	6: 132,957,048 (GRCm39)	D294G	probably benign	Het
Tbl1xr1	C	T	3: 22,245,603 (GRCm39)	T203M	possibly damaging	Het
Tbl1xr1	T	A	3: 22,245,703 (GRCm39)		probably null	Het
Tcf7l2	A	G	19: 55,730,955 (GRCm39)	D19G	probably damaging	Het
Tecta	A	G	9: 42,248,633 (GRCm39)	V1923A	possibly damaging	Het
Tg	T	A	15: 66,560,740 (GRCm39)	M1034K	probably benign	Het
Ttf2	T	C	3: 100,876,941 (GRCm39)	E8G	possibly damaging	Het
Vps13b	T	A	15: 35,576,541 (GRCm39)	V983E	probably damaging	Het
Vps35l	A	G	7: 118,342,898 (GRCm39)	H32R	probably damaging	Het
Vwa2	T	C	19: 56,890,025 (GRCm39)	V210A	probably benign	Het
Xkr6	T	A	14: 64,057,093 (GRCm39)	Y335N	probably benign	Het
Zfp97	A	G	17: 17,365,437 (GRCm39)	H312R	probably damaging	Het

Other mutations in Bptf

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00553:Bptf	APN	11	106,946,105 (GRCm39)	missense	possibly damaging	0.88
IGL00664:Bptf	APN	11	106,968,491 (GRCm39)	missense	possibly damaging	0.78
IGL00705:Bptf	APN	11	106,986,534 (GRCm39)	splice site	probably benign
IGL00796:Bptf	APN	11	106,945,376 (GRCm39)	missense	probably damaging	1.00
IGL00834:Bptf	APN	11	106,964,754 (GRCm39)	missense	possibly damaging	0.59
IGL01155:Bptf	APN	11	106,971,553 (GRCm39)	missense	probably damaging	1.00
IGL01314:Bptf	APN	11	106,945,679 (GRCm39)	missense	probably damaging	1.00
IGL01371:Bptf	APN	11	106,946,733 (GRCm39)	missense	probably benign	0.00
IGL01567:Bptf	APN	11	106,949,600 (GRCm39)	missense	probably damaging	1.00
IGL01794:Bptf	APN	11	106,944,047 (GRCm39)	critical splice donor site	probably null
IGL02108:Bptf	APN	11	106,965,814 (GRCm39)	missense	probably benign	0.45
IGL02367:Bptf	APN	11	106,964,178 (GRCm39)	missense	probably benign
IGL02437:Bptf	APN	11	106,965,521 (GRCm39)	missense	probably benign	0.00
IGL02589:Bptf	APN	11	107,002,357 (GRCm39)	missense	possibly damaging	0.92
IGL02897:Bptf	APN	11	106,937,947 (GRCm39)	missense	probably damaging	1.00
IGL02935:Bptf	APN	11	106,971,625 (GRCm39)	missense	probably damaging	1.00
IGL02954:Bptf	APN	11	106,945,575 (GRCm39)	missense	possibly damaging	0.89
IGL02982:Bptf	APN	11	106,967,500 (GRCm39)	missense	probably damaging	1.00
IGL03109:Bptf	APN	11	106,952,527 (GRCm39)	missense	possibly damaging	0.53
IGL03265:Bptf	APN	11	106,945,454 (GRCm39)	missense	probably benign	0.00
IGL03403:Bptf	APN	11	106,990,559 (GRCm39)	missense	possibly damaging	0.51
Anodyne	UTSW	11	106,934,457 (GRCm39)	critical splice donor site	probably null
Arroyo	UTSW	11	106,933,516 (GRCm39)	missense	probably benign	0.32
mojado	UTSW	11	106,935,466 (GRCm39)	missense	probably benign	0.03
IGL03097:Bptf	UTSW	11	106,968,506 (GRCm39)	missense	probably damaging	1.00
PIT4486001:Bptf	UTSW	11	106,945,614 (GRCm39)	missense	probably damaging	0.98
R0066:Bptf	UTSW	11	106,952,962 (GRCm39)	missense	possibly damaging	0.90
R0157:Bptf	UTSW	11	106,965,484 (GRCm39)	missense	possibly damaging	0.89
R0320:Bptf	UTSW	11	106,963,645 (GRCm39)	missense	probably damaging	1.00
R0328:Bptf	UTSW	11	106,937,953 (GRCm39)	missense	probably damaging	1.00
R0402:Bptf	UTSW	11	106,964,940 (GRCm39)	missense	probably damaging	1.00
R0482:Bptf	UTSW	11	106,972,088 (GRCm39)	missense	probably benign	0.13
R0574:Bptf	UTSW	11	106,967,353 (GRCm39)	missense	probably damaging	1.00
R0598:Bptf	UTSW	11	106,963,791 (GRCm39)	missense	probably damaging	0.99
R0599:Bptf	UTSW	11	106,959,208 (GRCm39)	missense	probably damaging	1.00
R0601:Bptf	UTSW	11	106,952,518 (GRCm39)	missense	probably benign	0.04
R0744:Bptf	UTSW	11	107,001,638 (GRCm39)	critical splice donor site	probably null
R0836:Bptf	UTSW	11	107,001,638 (GRCm39)	critical splice donor site	probably null
R0885:Bptf	UTSW	11	106,934,617 (GRCm39)	missense	probably damaging	1.00
R1070:Bptf	UTSW	11	106,945,881 (GRCm39)	missense	possibly damaging	0.92
R1252:Bptf	UTSW	11	106,964,077 (GRCm39)	missense	probably benign	0.00
R1370:Bptf	UTSW	11	106,937,920 (GRCm39)	missense	probably damaging	0.99
R1428:Bptf	UTSW	11	106,963,873 (GRCm39)	missense	probably damaging	0.99
R1467:Bptf	UTSW	11	106,945,881 (GRCm39)	missense	possibly damaging	0.92
R1467:Bptf	UTSW	11	106,945,881 (GRCm39)	missense	possibly damaging	0.92
R1742:Bptf	UTSW	11	107,001,777 (GRCm39)	missense	probably damaging	1.00
R1816:Bptf	UTSW	11	106,951,405 (GRCm39)	missense	probably damaging	1.00
R1858:Bptf	UTSW	11	106,964,127 (GRCm39)	missense	probably benign	0.00
R1989:Bptf	UTSW	11	106,965,652 (GRCm39)	missense	probably damaging	1.00
R2253:Bptf	UTSW	11	107,002,148 (GRCm39)	missense	probably damaging	1.00
R2392:Bptf	UTSW	11	106,963,573 (GRCm39)	missense	probably damaging	1.00
R2431:Bptf	UTSW	11	106,938,066 (GRCm39)	missense	possibly damaging	0.48
R3022:Bptf	UTSW	11	107,002,463 (GRCm39)	critical splice acceptor site	probably null
R3161:Bptf	UTSW	11	106,965,302 (GRCm39)	missense	probably damaging	1.00
R3686:Bptf	UTSW	11	106,965,024 (GRCm39)	missense	probably benign	0.25
R3687:Bptf	UTSW	11	106,965,024 (GRCm39)	missense	probably benign	0.25
R3688:Bptf	UTSW	11	106,965,024 (GRCm39)	missense	probably benign	0.25
R3787:Bptf	UTSW	11	106,964,653 (GRCm39)	missense	probably damaging	1.00
R3834:Bptf	UTSW	11	106,964,683 (GRCm39)	missense	probably benign	0.05
R3885:Bptf	UTSW	11	106,965,339 (GRCm39)	missense	probably damaging	0.97
R4090:Bptf	UTSW	11	106,972,349 (GRCm39)	missense	probably damaging	0.99
R4398:Bptf	UTSW	11	107,001,670 (GRCm39)	missense	probably damaging	1.00
R4437:Bptf	UTSW	11	106,965,300 (GRCm39)	missense	possibly damaging	0.59
R4514:Bptf	UTSW	11	106,968,518 (GRCm39)	missense	probably damaging	1.00
R4565:Bptf	UTSW	11	106,963,836 (GRCm39)	missense	probably damaging	1.00
R4715:Bptf	UTSW	11	106,938,007 (GRCm39)	missense	probably damaging	1.00
R4748:Bptf	UTSW	11	106,986,706 (GRCm39)	missense	probably damaging	0.96
R4764:Bptf	UTSW	11	106,934,520 (GRCm39)	missense	probably damaging	1.00
R4885:Bptf	UTSW	11	106,965,474 (GRCm39)	missense	probably benign	0.39
R4901:Bptf	UTSW	11	107,001,686 (GRCm39)	nonsense	probably null
R4995:Bptf	UTSW	11	106,945,391 (GRCm39)	missense	probably damaging	0.98
R5057:Bptf	UTSW	11	106,973,354 (GRCm39)	missense	probably damaging	0.98
R5120:Bptf	UTSW	11	106,964,211 (GRCm39)	missense	probably damaging	0.99
R5320:Bptf	UTSW	11	106,972,193 (GRCm39)	nonsense	probably null
R5329:Bptf	UTSW	11	106,964,121 (GRCm39)	missense	probably benign	0.06
R5418:Bptf	UTSW	11	107,002,120 (GRCm39)	missense	probably damaging	1.00
R5461:Bptf	UTSW	11	106,952,590 (GRCm39)	missense	probably damaging	1.00
R5664:Bptf	UTSW	11	106,964,525 (GRCm39)	missense	probably benign	0.01
R5718:Bptf	UTSW	11	107,002,260 (GRCm39)	missense	probably damaging	1.00
R5774:Bptf	UTSW	11	107,001,963 (GRCm39)	missense	probably damaging	1.00
R5851:Bptf	UTSW	11	107,001,688 (GRCm39)	missense	probably damaging	1.00
R5930:Bptf	UTSW	11	106,964,022 (GRCm39)	missense	probably damaging	1.00
R5949:Bptf	UTSW	11	107,001,915 (GRCm39)	missense	probably damaging	0.99
R5975:Bptf	UTSW	11	106,926,690 (GRCm39)	utr 3 prime	probably benign
R6027:Bptf	UTSW	11	106,965,771 (GRCm39)	missense	probably damaging	1.00
R6128:Bptf	UTSW	11	106,965,516 (GRCm39)	missense	possibly damaging	0.87
R6337:Bptf	UTSW	11	106,949,605 (GRCm39)	missense	possibly damaging	0.89
R6407:Bptf	UTSW	11	107,001,952 (GRCm39)	missense	probably damaging	1.00
R6470:Bptf	UTSW	11	106,963,593 (GRCm39)	missense	probably damaging	1.00
R6487:Bptf	UTSW	11	106,968,552 (GRCm39)	missense	probably damaging	0.99
R6501:Bptf	UTSW	11	106,968,509 (GRCm39)	missense	probably null	1.00
R6755:Bptf	UTSW	11	106,938,082 (GRCm39)	missense	probably benign	0.27
R6866:Bptf	UTSW	11	106,964,406 (GRCm39)	missense	probably damaging	1.00
R6879:Bptf	UTSW	11	106,933,516 (GRCm39)	missense	probably benign	0.32
R6927:Bptf	UTSW	11	106,945,421 (GRCm39)	missense	probably damaging	1.00
R6944:Bptf	UTSW	11	106,971,649 (GRCm39)	missense	probably damaging	1.00
R7082:Bptf	UTSW	11	106,977,573 (GRCm39)	missense	probably benign	0.00
R7136:Bptf	UTSW	11	106,990,541 (GRCm39)	missense	probably damaging	1.00
R7162:Bptf	UTSW	11	106,934,457 (GRCm39)	critical splice donor site	probably null
R7171:Bptf	UTSW	11	107,022,233 (GRCm39)	missense	unknown
R7193:Bptf	UTSW	11	106,945,635 (GRCm39)	nonsense	probably null
R7210:Bptf	UTSW	11	106,945,290 (GRCm39)	nonsense	probably null
R7221:Bptf	UTSW	11	106,945,658 (GRCm39)	missense	probably damaging	1.00
R7316:Bptf	UTSW	11	107,001,740 (GRCm39)	nonsense	probably null
R7316:Bptf	UTSW	11	106,963,935 (GRCm39)	missense	probably damaging	1.00
R7422:Bptf	UTSW	11	106,951,384 (GRCm39)	missense	probably damaging	1.00
R7454:Bptf	UTSW	11	106,935,466 (GRCm39)	missense	probably benign	0.03
R7657:Bptf	UTSW	11	106,965,555 (GRCm39)	missense	probably damaging	1.00
R7718:Bptf	UTSW	11	106,972,282 (GRCm39)	missense	possibly damaging	0.65
R7827:Bptf	UTSW	11	106,938,013 (GRCm39)	missense	probably benign	0.01
R7844:Bptf	UTSW	11	106,964,887 (GRCm39)	missense	probably damaging	0.97
R7992:Bptf	UTSW	11	107,001,709 (GRCm39)	missense	probably benign	0.00
R8001:Bptf	UTSW	11	106,938,166 (GRCm39)	nonsense	probably null
R8037:Bptf	UTSW	11	106,946,776 (GRCm39)	missense	probably damaging	1.00
R8122:Bptf	UTSW	11	106,927,417 (GRCm39)	critical splice acceptor site	probably null
R8235:Bptf	UTSW	11	106,967,458 (GRCm39)	missense	probably benign	0.04
R8308:Bptf	UTSW	11	106,943,815 (GRCm39)	missense	probably damaging	0.99
R8409:Bptf	UTSW	11	106,953,495 (GRCm39)	missense	probably damaging	1.00
R8464:Bptf	UTSW	11	107,022,168 (GRCm39)	missense	probably benign	0.01
R8477:Bptf	UTSW	11	106,943,679 (GRCm39)	missense	probably damaging	0.98
R8482:Bptf	UTSW	11	106,934,524 (GRCm39)	missense	probably benign	0.19
R8515:Bptf	UTSW	11	106,946,064 (GRCm39)	missense	possibly damaging	0.85
R8519:Bptf	UTSW	11	106,952,590 (GRCm39)	missense	probably damaging	1.00
R8708:Bptf	UTSW	11	106,964,140 (GRCm39)	missense	probably damaging	1.00
R8708:Bptf	UTSW	11	106,964,139 (GRCm39)	missense	probably damaging	0.99
R8722:Bptf	UTSW	11	107,022,295 (GRCm39)	missense	unknown
R8732:Bptf	UTSW	11	106,931,206 (GRCm39)	missense	probably damaging	1.00
R8783:Bptf	UTSW	11	107,022,357 (GRCm39)	missense	unknown
R8828:Bptf	UTSW	11	106,945,836 (GRCm39)	missense	probably damaging	0.98
R9004:Bptf	UTSW	11	106,945,713 (GRCm39)	missense	probably damaging	1.00
R9010:Bptf	UTSW	11	106,964,576 (GRCm39)	missense	probably damaging	1.00
R9035:Bptf	UTSW	11	106,963,842 (GRCm39)	missense	probably damaging	1.00
R9083:Bptf	UTSW	11	106,959,176 (GRCm39)	missense	probably damaging	1.00
R9211:Bptf	UTSW	11	106,946,124 (GRCm39)	missense	probably damaging	1.00
R9345:Bptf	UTSW	11	106,971,588 (GRCm39)	missense	possibly damaging	0.77
R9393:Bptf	UTSW	11	106,965,134 (GRCm39)	missense	probably benign	0.00
R9451:Bptf	UTSW	11	106,935,411 (GRCm39)	missense	probably damaging	1.00
R9561:Bptf	UTSW	11	106,964,954 (GRCm39)	nonsense	probably null
R9632:Bptf	UTSW	11	106,952,545 (GRCm39)	missense	probably damaging	1.00
R9648:Bptf	UTSW	11	106,943,720 (GRCm39)	missense	probably damaging	0.99
R9650:Bptf	UTSW	11	106,935,412 (GRCm39)	missense	probably benign	0.15
R9658:Bptf	UTSW	11	107,002,170 (GRCm39)	missense	probably damaging	1.00
R9775:Bptf	UTSW	11	106,934,502 (GRCm39)	missense	probably benign	0.04
R9776:Bptf	UTSW	11	106,969,396 (GRCm39)	missense	probably damaging	1.00
Z1088:Bptf	UTSW	11	106,965,408 (GRCm39)	missense	probably benign	0.00
Z1176:Bptf	UTSW	11	106,949,510 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GCACAAAGAGCAGCTATGAC -3'
(R):5'- TCAGAAACGTTTGGAGCAGC -3'

Sequencing Primer
(F):5'- AGCAGCTATGACAACGACTG -3'
(R):5'- AGAAGCCTGCAGTCATCG -3'

Posted On

2018-09-12