Mutagenetix > Incidental Mutation

Incidental Mutation 'R1854:Zdbf2'

205865

Institutional Source

Beutler Lab

Gene Symbol

Zdbf2

Ensembl Gene

ENSMUSG00000027520

Gene Name

zinc finger, DBF-type containing 2

Synonyms

4930431J08Rik, 9330107J05Rik

MMRRC Submission

039878-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.119) question?

Stock #

R1854 (G1)

Quality Score

101

Status

Not validated

Chromosome

Chromosomal Location

63273265-63314576 bp(+) (GRCm38)

Type of Mutation

frame shift

DNA Base Change (assembly)

GAAAAA to GAAAAAA at 63305542 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000109767 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000029025] [ENSMUST00000114132]

AlphaFold

Q5SS00

Predicted Effect

probably null
Transcript: ENSMUST00000029025

SMART Domains

Protein: ENSMUSP00000029025
Gene: ENSMUSG00000027520

Domain	Start	End	E-Value	Type
low complexity region	79	99	N/A	INTRINSIC
low complexity region	150	164	N/A	INTRINSIC
low complexity region	378	405	N/A	INTRINSIC
internal_repeat_6	407	565	7.68e-5	PROSPERO
internal_repeat_5	418	768	5.53e-5	PROSPERO
internal_repeat_1	618	873	3.17e-15	PROSPERO
internal_repeat_4	621	885	2.09e-6	PROSPERO
internal_repeat_3	642	886	1.52e-7	PROSPERO
internal_repeat_2	650	912	5.87e-11	PROSPERO
internal_repeat_6	722	891	7.68e-5	PROSPERO
low complexity region	965	982	N/A	INTRINSIC
internal_repeat_4	1061	1328	2.09e-6	PROSPERO
internal_repeat_2	1215	1484	5.87e-11	PROSPERO
internal_repeat_3	1287	1507	1.52e-7	PROSPERO
internal_repeat_1	1307	1536	3.17e-15	PROSPERO
internal_repeat_5	1388	1758	5.53e-5	PROSPERO
low complexity region	1767	1778	N/A	INTRINSIC
low complexity region	2211	2235	N/A	INTRINSIC
low complexity region	2240	2399	N/A	INTRINSIC
low complexity region	2402	2420	N/A	INTRINSIC
low complexity region	2446	2458	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000114132

SMART Domains

Protein: ENSMUSP00000109767
Gene: ENSMUSG00000027520

Domain	Start	End	E-Value	Type
low complexity region	79	99	N/A	INTRINSIC
low complexity region	150	164	N/A	INTRINSIC
low complexity region	378	405	N/A	INTRINSIC
internal_repeat_6	407	565	7.68e-5	PROSPERO
internal_repeat_5	418	768	5.53e-5	PROSPERO
internal_repeat_1	618	873	3.17e-15	PROSPERO
internal_repeat_4	621	885	2.09e-6	PROSPERO
internal_repeat_3	642	886	1.52e-7	PROSPERO
internal_repeat_2	650	912	5.87e-11	PROSPERO
internal_repeat_6	722	891	7.68e-5	PROSPERO
low complexity region	965	982	N/A	INTRINSIC
internal_repeat_4	1061	1328	2.09e-6	PROSPERO
internal_repeat_2	1215	1484	5.87e-11	PROSPERO
internal_repeat_3	1287	1507	1.52e-7	PROSPERO
internal_repeat_1	1307	1536	3.17e-15	PROSPERO
internal_repeat_5	1388	1758	5.53e-5	PROSPERO
low complexity region	1767	1778	N/A	INTRINSIC
low complexity region	2211	2235	N/A	INTRINSIC
low complexity region	2240	2399	N/A	INTRINSIC
low complexity region	2402	2420	N/A	INTRINSIC
low complexity region	2446	2458	N/A	INTRINSIC

Coding Region Coverage

1x: 97.5%
3x: 96.9%
10x: 95.3%
20x: 92.5%

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 containing DBF4-type zinc finger domains. This gene is imprinted and paternally expressed in lymphocytes but is more stochastically expressed in the placenta. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2015]

Allele List at MGI

Other mutations in this stock

Total: 113 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310061N02Rik	C	T	16: 88,707,780 (GRCm38)	R43K	possibly damaging	Het
Acp1	A	G	12: 30,897,805 (GRCm38)	I78T	possibly damaging	Het
Afap1l1	G	T	18: 61,743,294 (GRCm38)	D417E	probably benign	Het
Agap2	G	A	10: 127,080,516 (GRCm38)	V299I	unknown	Het
Ahnak	C	T	19: 9,013,832 (GRCm38)	A4160V	possibly damaging	Het
Anapc1	T	C	2: 128,675,890 (GRCm38)	E278G	probably damaging	Het
Atad2	G	A	15: 58,097,289 (GRCm38)	P971L	possibly damaging	Het
Atg2a	A	G	19: 6,252,431 (GRCm38)	E928G	probably benign	Het
Atp2b2	A	C	6: 113,842,283 (GRCm38)	N16K	probably damaging	Het
Atp6ap1l	T	C	13: 90,883,588 (GRCm38)	E325G	probably damaging	Het
Bfsp2	C	T	9: 103,449,831 (GRCm38)	G236S	probably benign	Het
Ccar1	A	T	10: 62,764,517 (GRCm38)	I545N	probably damaging	Het
Ccser2	A	G	14: 36,918,591 (GRCm38)	C11R	possibly damaging	Het
Cdc42bpg	A	T	19: 6,320,807 (GRCm38)	H1310L	possibly damaging	Het
Ces1h	T	C	8: 93,358,822 (GRCm38)	K339E	probably benign	Het
Cfap91	T	C	16: 38,324,297 (GRCm38)		probably null	Het
Cit	A	G	5: 115,873,901 (GRCm38)	Y189C	probably damaging	Het
Cnih3	C	A	1: 181,454,621 (GRCm38)	S140*	probably null	Het
Cntrl	A	G	2: 35,122,684 (GRCm38)	D278G	probably damaging	Het
Col24a1	G	A	3: 145,459,140 (GRCm38)	G1033D	probably damaging	Het
Col6a1	T	G	10: 76,721,949 (GRCm38)	Y151S	probably damaging	Het
Col6a2	T	A	10: 76,614,812 (GRCm38)	Q95L	probably damaging	Het
Cpd	G	T	11: 76,786,338 (GRCm38)	P1185Q	probably damaging	Het
Cycs	T	A	6: 50,565,329 (GRCm38)	I76F	possibly damaging	Het
Cyp4f16	T	A	17: 32,537,099 (GRCm38)	I34N	probably damaging	Het
Ddx1	A	C	12: 13,229,331 (GRCm38)	S436A	probably benign	Het
Defa30	A	G	8: 21,135,484 (GRCm38)	Y88C	probably damaging	Het
Dhx30	G	A	9: 110,088,672 (GRCm38)	L317F	probably damaging	Het
Dll3	C	A	7: 28,296,410 (GRCm38)	G322V	probably damaging	Het
Dnah10	G	A	5: 124,804,689 (GRCm38)	D2843N	probably damaging	Het
Dnaja3	C	T	16: 4,697,269 (GRCm38)	T266I	probably damaging	Het
Dpp9	T	C	17: 56,202,885 (GRCm38)	I314V	probably benign	Het
E030025P04Rik	A	G	11: 109,143,918 (GRCm38)	V48A	unknown	Het
Enpp2	C	T	15: 54,845,823 (GRCm38)	E803K	probably damaging	Het
Eri3	G	A	4: 117,649,365 (GRCm38)	G297D	probably benign	Het
Esp34	A	G	17: 38,559,533 (GRCm38)	E38G	possibly damaging	Het
Fabp3	C	T	4: 130,312,387 (GRCm38)	T57I	probably benign	Het
Frzb	A	G	2: 80,446,380 (GRCm38)	V154A	possibly damaging	Het
Fsip2	G	T	2: 82,993,257 (GRCm38)	A6445S	possibly damaging	Het
Gm11938	G	A	11: 99,603,017 (GRCm38)	T84I	possibly damaging	Het
Gm4787	T	A	12: 81,378,334 (GRCm38)	H350L	probably damaging	Het
Gpa33	A	G	1: 166,165,190 (GRCm38)	I291V	probably benign	Het
Gpr158	A	G	2: 21,369,124 (GRCm38)	Y290C	probably damaging	Het
Gpsm1	G	T	2: 26,344,713 (GRCm38)	G84W	probably damaging	Het
Hormad1	A	G	3: 95,580,006 (GRCm38)	N267S	probably benign	Het
Htr2a	A	T	14: 74,705,753 (GRCm38)	I258F	probably damaging	Het
Htra4	T	C	8: 25,033,581 (GRCm38)	T323A	probably damaging	Het
Ift140	T	A	17: 25,035,839 (GRCm38)	F162Y	probably benign	Het
Islr2	T	C	9: 58,199,816 (GRCm38)	T54A	probably damaging	Het
Kcna4	T	G	2: 107,296,484 (GRCm38)	V521G	probably damaging	Het
Kdr	C	T	5: 75,952,905 (GRCm38)	G768S	possibly damaging	Het
Kif6	G	T	17: 49,901,771 (GRCm38)	A740S	probably benign	Het
Lad1	T	A	1: 135,827,730 (GRCm38)	V248E	probably damaging	Het
Lamb1	T	G	12: 31,318,272 (GRCm38)	C1134G	probably damaging	Het
Lamc1	A	G	1: 153,249,872 (GRCm38)	Y552H	probably damaging	Het
Mctp1	A	T	13: 76,825,741 (GRCm38)	T706S	probably damaging	Het
Med12l	A	G	3: 59,260,772 (GRCm38)	Y1541C	probably damaging	Het
Mnx1	C	T	5: 29,477,782 (GRCm38)	S165N	unknown	Het
Morn3	A	T	5: 123,046,629 (GRCm38)		probably null	Het
Nalcn	C	T	14: 123,460,412 (GRCm38)	R484Q	probably damaging	Het
Nr4a1	T	C	15: 101,271,764 (GRCm38)	I305T	probably benign	Het
Or1j11	C	T	2: 36,421,874 (GRCm38)	H159Y	probably damaging	Het
Or2z2	G	A	11: 58,455,431 (GRCm38)	R173W	probably damaging	Het
Pabir2	T	A	X: 53,254,056 (GRCm38)	Q201H	probably benign	Het
Pcdhb5	T	C	18: 37,322,340 (GRCm38)	V591A	possibly damaging	Het
Pdia3	T	C	2: 121,431,663 (GRCm38)	I205T	probably benign	Het
Pdia4	A	T	6: 47,813,227 (GRCm38)	D26E	unknown	Het
Phactr3	C	A	2: 178,283,147 (GRCm38)	L292M	probably damaging	Het
Phf21b	T	A	15: 84,854,762 (GRCm38)	I21F	probably benign	Het
Pign	A	G	1: 105,554,498 (GRCm38)	V791A	probably damaging	Het
Pitpna	A	G	11: 75,609,103 (GRCm38)		probably null	Het
Piwil1	G	T	5: 128,747,839 (GRCm38)	E534*	probably null	Het
Plcz1	T	A	6: 139,993,049 (GRCm38)	I526F	probably benign	Het
Pms2	A	T	5: 143,925,896 (GRCm38)	K607I	probably benign	Het
Pnn	T	A	12: 59,071,613 (GRCm38)	N327K	probably damaging	Het
Pogz	C	T	3: 94,878,849 (GRCm38)	T863I	probably benign	Het
Polq	C	T	16: 37,062,109 (GRCm38)	T1545I	probably benign	Het
Psd4	G	A	2: 24,397,456 (GRCm38)	E467K	probably benign	Het
Pstpip2	T	A	18: 77,871,799 (GRCm38)	L198Q	probably damaging	Het
Pzp	T	C	6: 128,502,225 (GRCm38)	Y655C	probably damaging	Het
Qrsl1	C	T	10: 43,894,545 (GRCm38)	G117E	probably damaging	Het
Rad54b	G	A	4: 11,601,669 (GRCm38)	C408Y	probably damaging	Het
Ralb	T	A	1: 119,476,067 (GRCm38)	Q110L	possibly damaging	Het
Rrm2	A	G	12: 24,713,152 (GRCm38)	K218E	probably damaging	Het
Siglece	A	G	7: 43,659,936 (GRCm38)	F66S	probably benign	Het
Slc17a8	A	T	10: 89,606,765 (GRCm38)	C69S	unknown	Het
Slc1a6	T	A	10: 78,812,924 (GRCm38)	V493E	probably damaging	Het
Slc38a11	A	T	2: 65,363,516 (GRCm38)		probably null	Het
Smarcal1	G	A	1: 72,586,099 (GRCm38)	G135D	possibly damaging	Het
Snrnp70	T	A	7: 45,377,220 (GRCm38)	R242*	probably null	Het
St3gal5	T	C	6: 72,132,093 (GRCm38)	L55P	probably damaging	Het
Sulf1	A	G	1: 12,838,437 (GRCm38)	N558S	probably benign	Het
Supt6	T	C	11: 78,232,540 (GRCm38)	I104V	possibly damaging	Het
Tas2r113	T	A	6: 132,893,329 (GRCm38)	Y107N	probably damaging	Het
Tcf7	A	G	11: 52,257,064 (GRCm38)	V187A	probably benign	Het
Tdrd9	G	A	12: 112,044,812 (GRCm38)	G1152R	probably damaging	Het
Tfpi	A	G	2: 84,458,107 (GRCm38)	Y9H	probably benign	Het
Tnk2	G	A	16: 32,680,142 (GRCm38)	V758I	probably damaging	Het
Trim72	A	G	7: 128,009,082 (GRCm38)	I251V	probably benign	Het
Trip12	T	A	1: 84,728,145 (GRCm38)	N655Y	probably damaging	Het
Ttn	A	G	2: 76,751,429 (GRCm38)	V23040A	probably damaging	Het
Tulp2	T	A	7: 45,517,943 (GRCm38)	N188K	probably damaging	Het
Ube2c	C	T	2: 164,771,362 (GRCm38)	H67Y	probably damaging	Het
Unc80	C	A	1: 66,631,414 (GRCm38)	P1899T	possibly damaging	Het
Usp34	C	T	11: 23,426,153 (GRCm38)	A1879V	probably benign	Het
Vmn2r118	G	A	17: 55,611,556 (GRCm38)	S112L	possibly damaging	Het
Wdfy3	A	T	5: 101,888,186 (GRCm38)	V2122E	probably benign	Het
Zcchc4	A	G	5: 52,815,826 (GRCm38)	Y344C	probably damaging	Het
Zdhhc25	A	T	15: 88,600,486 (GRCm38)	H8L	probably benign	Het
Zfp455	A	T	13: 67,207,817 (GRCm38)	H383L	probably damaging	Het
Zfp663	A	G	2: 165,353,291 (GRCm38)	I336T	probably benign	Het
Zfp738	T	A	13: 67,670,357 (GRCm38)	H505L	probably damaging	Het
Zfp84	T	G	7: 29,775,371 (GRCm38)	F23V	possibly damaging	Het

Other mutations in Zdbf2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00790:Zdbf2	APN	1	63,306,514 (GRCm38)	missense	possibly damaging	0.92
IGL00796:Zdbf2	APN	1	63,307,205 (GRCm38)	missense	probably benign	0.04
IGL00801:Zdbf2	APN	1	63,303,038 (GRCm38)	missense	possibly damaging	0.66
IGL02803:Zdbf2	APN	1	63,303,077 (GRCm38)	missense	possibly damaging	0.46
R0143:Zdbf2	UTSW	1	63,308,074 (GRCm38)	missense	probably benign	0.01
R0147:Zdbf2	UTSW	1	63,304,006 (GRCm38)	nonsense	probably null
R0148:Zdbf2	UTSW	1	63,304,006 (GRCm38)	nonsense	probably null
R0433:Zdbf2	UTSW	1	63,306,143 (GRCm38)	missense	possibly damaging	0.46
R0502:Zdbf2	UTSW	1	63,305,290 (GRCm38)	missense	possibly damaging	0.66
R0645:Zdbf2	UTSW	1	63,304,950 (GRCm38)	missense	possibly damaging	0.81
R0765:Zdbf2	UTSW	1	63,305,723 (GRCm38)	missense	possibly damaging	0.46
R1068:Zdbf2	UTSW	1	63,303,430 (GRCm38)	missense	possibly damaging	0.94
R1216:Zdbf2	UTSW	1	63,303,002 (GRCm38)	missense	possibly damaging	0.83
R1235:Zdbf2	UTSW	1	63,309,073 (GRCm38)	missense	possibly damaging	0.66
R1352:Zdbf2	UTSW	1	63,303,053 (GRCm38)	missense	probably damaging	0.96
R1402:Zdbf2	UTSW	1	63,303,627 (GRCm38)	missense	possibly damaging	0.46
R1402:Zdbf2	UTSW	1	63,303,627 (GRCm38)	missense	possibly damaging	0.46
R1435:Zdbf2	UTSW	1	63,303,040 (GRCm38)	missense	possibly damaging	0.66
R1562:Zdbf2	UTSW	1	63,303,588 (GRCm38)	missense	possibly damaging	0.83
R1624:Zdbf2	UTSW	1	63,303,859 (GRCm38)	missense	possibly damaging	0.66
R1635:Zdbf2	UTSW	1	63,304,334 (GRCm38)	missense	possibly damaging	0.92
R1644:Zdbf2	UTSW	1	63,308,972 (GRCm38)	missense	possibly damaging	0.66
R1662:Zdbf2	UTSW	1	63,304,249 (GRCm38)	nonsense	probably null
R1700:Zdbf2	UTSW	1	63,302,741 (GRCm38)	missense	unknown
R1720:Zdbf2	UTSW	1	63,303,277 (GRCm38)	missense	possibly damaging	0.46
R1853:Zdbf2	UTSW	1	63,305,542 (GRCm38)	frame shift	probably null
R1973:Zdbf2	UTSW	1	63,309,701 (GRCm38)	missense	unknown
R2336:Zdbf2	UTSW	1	63,303,464 (GRCm38)	missense	probably benign	0.00
R2428:Zdbf2	UTSW	1	63,305,615 (GRCm38)	missense	probably benign	0.04
R3010:Zdbf2	UTSW	1	63,303,065 (GRCm38)	missense	possibly damaging	0.92
R3034:Zdbf2	UTSW	1	63,304,205 (GRCm38)	missense	probably damaging	0.96
R3079:Zdbf2	UTSW	1	63,307,477 (GRCm38)	missense	probably benign	0.05
R3196:Zdbf2	UTSW	1	63,308,420 (GRCm38)	missense	possibly damaging	0.46
R3711:Zdbf2	UTSW	1	63,308,671 (GRCm38)	missense	possibly damaging	0.83
R3845:Zdbf2	UTSW	1	63,308,324 (GRCm38)	missense	possibly damaging	0.66
R4093:Zdbf2	UTSW	1	63,309,781 (GRCm38)	missense	possibly damaging	0.83
R4250:Zdbf2	UTSW	1	63,302,861 (GRCm38)	missense	possibly damaging	0.46
R4592:Zdbf2	UTSW	1	63,306,591 (GRCm38)	missense	possibly damaging	0.82
R4721:Zdbf2	UTSW	1	63,308,792 (GRCm38)	missense	possibly damaging	0.46
R4779:Zdbf2	UTSW	1	63,303,238 (GRCm38)	missense	possibly damaging	0.66
R4928:Zdbf2	UTSW	1	63,308,814 (GRCm38)	missense	possibly damaging	0.81
R4943:Zdbf2	UTSW	1	63,302,914 (GRCm38)	missense	possibly damaging	0.92
R5025:Zdbf2	UTSW	1	63,303,650 (GRCm38)	missense	possibly damaging	0.82
R5095:Zdbf2	UTSW	1	63,309,073 (GRCm38)	missense	possibly damaging	0.66
R5149:Zdbf2	UTSW	1	63,304,903 (GRCm38)	missense	possibly damaging	0.83
R5326:Zdbf2	UTSW	1	63,304,411 (GRCm38)	missense	possibly damaging	0.66
R5341:Zdbf2	UTSW	1	63,307,933 (GRCm38)	missense	probably benign	0.27
R5511:Zdbf2	UTSW	1	63,305,677 (GRCm38)	missense	probably benign	0.03
R5809:Zdbf2	UTSW	1	63,305,876 (GRCm38)	missense	possibly damaging	0.90
R5902:Zdbf2	UTSW	1	63,306,526 (GRCm38)	missense	possibly damaging	0.83
R6162:Zdbf2	UTSW	1	63,280,818 (GRCm38)	start gained	probably benign
R6245:Zdbf2	UTSW	1	63,304,433 (GRCm38)	missense	possibly damaging	0.46
R6332:Zdbf2	UTSW	1	63,307,822 (GRCm38)	missense	possibly damaging	0.66
R6361:Zdbf2	UTSW	1	63,303,321 (GRCm38)	missense	possibly damaging	0.66
R6489:Zdbf2	UTSW	1	63,307,478 (GRCm38)	missense	possibly damaging	0.46
R6517:Zdbf2	UTSW	1	63,305,520 (GRCm38)	missense	possibly damaging	0.81
R6624:Zdbf2	UTSW	1	63,303,914 (GRCm38)	missense	possibly damaging	0.46
R6643:Zdbf2	UTSW	1	63,304,508 (GRCm38)	missense	possibly damaging	0.82
R6786:Zdbf2	UTSW	1	63,304,520 (GRCm38)	missense	possibly damaging	0.46
R6808:Zdbf2	UTSW	1	63,308,528 (GRCm38)	missense	possibly damaging	0.66
R6896:Zdbf2	UTSW	1	63,308,872 (GRCm38)	missense	probably damaging	0.98
R6997:Zdbf2	UTSW	1	63,290,766 (GRCm38)	missense	probably benign	0.09
R7011:Zdbf2	UTSW	1	63,306,766 (GRCm38)	missense	possibly damaging	0.66
R7058:Zdbf2	UTSW	1	63,307,404 (GRCm38)	missense	possibly damaging	0.66
R7066:Zdbf2	UTSW	1	63,307,559 (GRCm38)	missense	probably benign
R7177:Zdbf2	UTSW	1	63,294,961 (GRCm38)	missense	possibly damaging	0.94
R7184:Zdbf2	UTSW	1	63,306,505 (GRCm38)	missense	possibly damaging	0.92
R7273:Zdbf2	UTSW	1	63,303,404 (GRCm38)	missense	possibly damaging	0.90
R7387:Zdbf2	UTSW	1	63,304,039 (GRCm38)	missense	possibly damaging	0.46
R7468:Zdbf2	UTSW	1	63,307,510 (GRCm38)	missense	probably benign
R7695:Zdbf2	UTSW	1	63,307,370 (GRCm38)	missense	possibly damaging	0.83
R7712:Zdbf2	UTSW	1	63,305,371 (GRCm38)	missense	possibly damaging	0.83
R7735:Zdbf2	UTSW	1	63,304,105 (GRCm38)	missense	possibly damaging	0.66
R7736:Zdbf2	UTSW	1	63,308,007 (GRCm38)	nonsense	probably null
R7759:Zdbf2	UTSW	1	63,308,376 (GRCm38)	missense	possibly damaging	0.46
R7796:Zdbf2	UTSW	1	63,303,424 (GRCm38)	missense	possibly damaging	0.90
R7908:Zdbf2	UTSW	1	63,306,827 (GRCm38)	missense	possibly damaging	0.46
R7970:Zdbf2	UTSW	1	63,304,171 (GRCm38)	missense	possibly damaging	0.92
R8076:Zdbf2	UTSW	1	63,306,101 (GRCm38)	missense	possibly damaging	0.92
R8152:Zdbf2	UTSW	1	63,306,413 (GRCm38)	missense	possibly damaging	0.92
R8195:Zdbf2	UTSW	1	63,304,066 (GRCm38)	missense	possibly damaging	0.83
R8272:Zdbf2	UTSW	1	63,305,983 (GRCm38)	missense	probably benign
R8306:Zdbf2	UTSW	1	63,304,075 (GRCm38)	missense	possibly damaging	0.66
R8309:Zdbf2	UTSW	1	63,306,591 (GRCm38)	missense	possibly damaging	0.82
R8323:Zdbf2	UTSW	1	63,302,914 (GRCm38)	missense	possibly damaging	0.46
R8400:Zdbf2	UTSW	1	63,304,976 (GRCm38)	missense	possibly damaging	0.92
R8443:Zdbf2	UTSW	1	63,306,007 (GRCm38)	missense	possibly damaging	0.83
R8460:Zdbf2	UTSW	1	63,309,570 (GRCm38)	small deletion	probably benign
R8528:Zdbf2	UTSW	1	63,303,386 (GRCm38)	missense	possibly damaging	0.82
R8812:Zdbf2	UTSW	1	63,308,113 (GRCm38)	missense	probably benign	0.00
R8962:Zdbf2	UTSW	1	63,308,003 (GRCm38)	missense	probably benign	0.00
R9061:Zdbf2	UTSW	1	63,307,137 (GRCm38)	missense
R9072:Zdbf2	UTSW	1	63,305,764 (GRCm38)	missense	possibly damaging	0.83
R9232:Zdbf2	UTSW	1	63,308,009 (GRCm38)	missense	possibly damaging	0.66
R9257:Zdbf2	UTSW	1	63,306,241 (GRCm38)	missense	probably damaging	1.00
R9411:Zdbf2	UTSW	1	63,304,129 (GRCm38)	missense	probably damaging	0.97
R9470:Zdbf2	UTSW	1	63,305,625 (GRCm38)	missense	possibly damaging	0.82
R9606:Zdbf2	UTSW	1	63,303,377 (GRCm38)	missense	possibly damaging	0.92
R9621:Zdbf2	UTSW	1	63,303,476 (GRCm38)	missense	possibly damaging	0.66
RF021:Zdbf2	UTSW	1	63,302,652 (GRCm38)	missense	possibly damaging	0.82
X0018:Zdbf2	UTSW	1	63,305,351 (GRCm38)	missense	possibly damaging	0.92
X0027:Zdbf2	UTSW	1	63,308,007 (GRCm38)	nonsense	probably null
X0057:Zdbf2	UTSW	1	63,305,390 (GRCm38)	missense	possibly damaging	0.66
X0063:Zdbf2	UTSW	1	63,305,537 (GRCm38)	missense	probably benign	0.04
Z1176:Zdbf2	UTSW	1	63,304,245 (GRCm38)	missense	possibly damaging	0.83
Z1177:Zdbf2	UTSW	1	63,309,203 (GRCm38)	missense	unknown
Z1177:Zdbf2	UTSW	1	63,304,086 (GRCm38)	frame shift	probably null

Predicted Primers

PCR Primer
(F):5'- GCATGCTGAGTTAACAAGTAAAAGC -3'
(R):5'- ACTTGCTTTAGAGTCACTGGG -3'

Sequencing Primer
(F):5'- GCACGGAATCTCATTCTGAAG -3'
(R):5'- AGAGTCACTGGGTTTGCCATC -3'

Posted On

2014-06-23