Mutagenetix > Incidental Mutation

Incidental Mutation 'R1761:Zfp808'

192797

Institutional Source

Beutler Lab

Gene Symbol

Zfp808

Ensembl Gene

ENSMUSG00000074867

Gene Name

zinc finger protein 808

Synonyms

Gm7036

MMRRC Submission

039793-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.068) question?

Stock #

R1761 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

62277674-62321752 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 62319460 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Serine at position 230 (C230S)

Ref Sequence

ENSEMBL: ENSMUSP00000097048 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000099449] [ENSMUST00000221772]

AlphaFold

B8JJZ4

Predicted Effect

possibly damaging
Transcript: ENSMUST00000099449
AA Change: C230S

PolyPhen 2 Score 0.711 (Sensitivity: 0.86; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000097048
Gene: ENSMUSG00000074867
AA Change: C230S

Domain	Start	End	E-Value	Type
KRAB	4	66	2.1e-17	SMART
ZnF_C2H2	133	155	2.4e-3	SMART
ZnF_C2H2	161	183	8.34e-3	SMART
ZnF_C2H2	189	211	2.75e-3	SMART
ZnF_C2H2	217	239	1.98e-4	SMART
ZnF_C2H2	245	267	3.21e-4	SMART
ZnF_C2H2	273	295	2.43e-4	SMART
ZnF_C2H2	301	323	8.6e-5	SMART
ZnF_C2H2	329	351	4.54e-4	SMART
ZnF_C2H2	357	379	9.22e-5	SMART
ZnF_C2H2	385	407	8.22e-2	SMART
ZnF_C2H2	413	435	1.56e-2	SMART
ZnF_C2H2	441	463	5.99e-4	SMART
ZnF_C2H2	469	491	2.79e-4	SMART
ZnF_C2H2	497	519	4.54e-4	SMART
ZnF_C2H2	525	547	1.95e-3	SMART
ZnF_C2H2	553	575	4.24e-4	SMART
ZnF_C2H2	581	603	2.27e-4	SMART
ZnF_C2H2	609	631	2.27e-4	SMART
ZnF_C2H2	637	659	9.08e-4	SMART
ZnF_C2H2	665	687	1.4e-4	SMART
ZnF_C2H2	693	715	4.24e-4	SMART
ZnF_C2H2	721	743	1.26e-2	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000221542

Predicted Effect

probably benign
Transcript: ENSMUST00000221772

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000222809

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000222947

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000223094

Coding Region Coverage

1x: 97.5%
3x: 96.9%
10x: 95.4%
20x: 92.9%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abi3bp	C	T	16: 56,488,672 (GRCm39)	H1268Y	possibly damaging	Het
Acan	T	A	7: 78,743,833 (GRCm39)	Y621*	probably null	Het
Aig1	T	C	10: 13,566,328 (GRCm39)	Y152C	probably damaging	Het
Arhgap33	C	T	7: 30,232,488 (GRCm39)		probably null	Het
Bcl6	G	T	16: 23,796,292 (GRCm39)	A45D	probably damaging	Het
Cbx5	T	C	15: 103,121,607 (GRCm39)	D10G	possibly damaging	Het
Ccdc191	A	G	16: 43,763,873 (GRCm39)	I445V	probably benign	Het
Cdk4	T	A	10: 126,900,546 (GRCm39)		probably benign	Het
Chil6	A	G	3: 106,301,654 (GRCm39)	F149L	probably damaging	Het
Cntn5	T	C	9: 10,172,059 (GRCm39)	T42A	probably benign	Het
Cpn2	A	T	16: 30,079,014 (GRCm39)	I229N	probably damaging	Het
Cpne8	A	G	15: 90,532,821 (GRCm39)	V62A	probably damaging	Het
Cr2	A	G	1: 194,837,431 (GRCm39)		probably null	Het
Crnn	A	T	3: 93,055,958 (GRCm39)	H248L	probably benign	Het
Csn1s1	A	G	5: 87,826,894 (GRCm39)	S254G	probably benign	Het
Cubn	A	G	2: 13,494,128 (GRCm39)		probably null	Het
Dnah8	A	G	17: 30,998,890 (GRCm39)	N3525S	probably damaging	Het
Dpp3	A	G	19: 4,971,177 (GRCm39)	L220P	probably benign	Het
Fam110a	T	C	2: 151,812,125 (GRCm39)	E215G	probably benign	Het
Fam20a	A	T	11: 109,568,664 (GRCm39)	N287K	probably damaging	Het
Fat4	T	C	3: 38,941,638 (GRCm39)	V177A	possibly damaging	Het
Fzd8	C	T	18: 9,213,643 (GRCm39)	R242C	probably damaging	Het
Gimap5	A	T	6: 48,730,195 (GRCm39)	Q255L	probably damaging	Het
Gm4787	A	G	12: 81,423,950 (GRCm39)	L736S	probably benign	Het
Gmeb1	G	A	4: 131,962,198 (GRCm39)	Q154*	probably null	Het
Gpr156	T	C	16: 37,807,929 (GRCm39)	L192P	probably damaging	Het
Gpr179	A	C	11: 97,225,932 (GRCm39)	S2074R	probably benign	Het
Hddc2	G	T	10: 31,202,135 (GRCm39)	D161Y	probably damaging	Het
Hlcs	T	C	16: 94,068,866 (GRCm39)	D265G	probably benign	Het
Hspg2	A	T	4: 137,241,984 (GRCm39)	I573F	possibly damaging	Het
Il1b	T	C	2: 129,207,101 (GRCm39)	K220E	probably damaging	Het
Il5	T	C	11: 53,614,557 (GRCm39)	I66T	probably damaging	Het
Irf6	G	A	1: 192,851,609 (GRCm39)	R400H	probably damaging	Het
Klra1	A	T	6: 130,349,836 (GRCm39)	Y201N	probably damaging	Het
Lmf2	A	G	15: 89,236,916 (GRCm39)	V442A	possibly damaging	Het
Mcm2	T	C	6: 88,866,770 (GRCm39)	I412M	possibly damaging	Het
Mlkl	T	A	8: 112,060,355 (GRCm39)	L18F	possibly damaging	Het
Mug2	C	A	6: 122,051,664 (GRCm39)	H949N	probably benign	Het
Nf1	T	C	11: 79,275,091 (GRCm39)	F51L	probably damaging	Het
Or52j3	T	G	7: 102,836,325 (GRCm39)	C172W	probably damaging	Het
Or7d10	A	T	9: 19,832,445 (GRCm39)	*313C	probably null	Het
Or8k18	T	G	2: 86,085,383 (GRCm39)	Y218S	probably damaging	Het
P3h2	T	C	16: 25,803,800 (GRCm39)	E322G	probably damaging	Het
Pramel21	T	C	4: 143,342,438 (GRCm39)	Y182H	probably benign	Het
Psmg2	CTTCAGTT	CTTCAGTTCAGTT	18: 67,779,095 (GRCm39)		probably null	Het
Ptdss1	T	C	13: 67,104,476 (GRCm39)	V116A	possibly damaging	Het
Ranbp2	T	C	10: 58,321,563 (GRCm39)	V2620A	probably benign	Het
Robo2	A	G	16: 73,831,912 (GRCm39)	V256A	probably damaging	Het
Scg3	T	A	9: 75,584,040 (GRCm39)	I154F	probably damaging	Het
Scgn	A	T	13: 24,143,689 (GRCm39)	F225Y	probably damaging	Het
Sec61b	T	C	4: 47,480,137 (GRCm39)	C58R	possibly damaging	Het
Slc25a46	G	T	18: 31,740,315 (GRCm39)	Q96K	possibly damaging	Het
Spmip6	G	A	4: 41,507,223 (GRCm39)	P109L	probably damaging	Het
Sptb	A	G	12: 76,659,382 (GRCm39)	F1173L	probably damaging	Het
Srcap	T	A	7: 127,134,017 (GRCm39)	C893S	probably damaging	Het
Tet3	T	C	6: 83,380,641 (GRCm39)	E509G	probably damaging	Het
Timm10b	C	T	7: 105,332,915 (GRCm39)	R897*	probably null	Het
Tln2	C	T	9: 67,193,796 (GRCm39)	A1773T	probably benign	Het
Tom1	T	C	8: 75,778,179 (GRCm39)	V87A	probably benign	Het
Tti1	T	C	2: 157,849,617 (GRCm39)	I541V	probably benign	Het
Ttn	A	T	2: 76,641,587 (GRCm39)	L5176Q	possibly damaging	Het
Tubb1	A	G	2: 174,298,689 (GRCm39)	S124G	probably benign	Het
Vgll3	A	T	16: 65,636,614 (GRCm39)	D310V	probably damaging	Het
Vmac	A	G	17: 57,022,788 (GRCm39)	L74P	probably damaging	Het
Zbtb1	A	T	12: 76,432,595 (GRCm39)	K194*	probably null	Het
Zfp429	A	G	13: 67,544,195 (GRCm39)	M76T	probably benign	Het
Zfp980	A	G	4: 145,428,612 (GRCm39)	Y447C	probably damaging	Het
Zfp985	A	G	4: 147,668,502 (GRCm39)	T457A	probably benign	Het

Other mutations in Zfp808

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01609:Zfp808	APN	13	62,321,023 (GRCm39)	missense	probably damaging	0.96
IGL02517:Zfp808	APN	13	62,321,032 (GRCm39)	makesense	probably null
IGL02809:Zfp808	APN	13	62,320,994 (GRCm39)	missense	probably benign	0.00
IGL02882:Zfp808	APN	13	62,320,994 (GRCm39)	missense	probably benign	0.00
IGL02941:Zfp808	APN	13	62,320,944 (GRCm39)	missense	possibly damaging	0.82
IGL03184:Zfp808	APN	13	62,317,381 (GRCm39)	missense	possibly damaging	0.90
LCD18:Zfp808	UTSW	13	62,314,465 (GRCm39)	intron	probably benign
R0387:Zfp808	UTSW	13	62,317,292 (GRCm39)	missense	probably damaging	1.00
R0472:Zfp808	UTSW	13	62,320,120 (GRCm39)	missense	probably damaging	1.00
R0544:Zfp808	UTSW	13	62,317,248 (GRCm39)	splice site	probably benign
R0635:Zfp808	UTSW	13	62,320,233 (GRCm39)	missense	probably damaging	1.00
R0981:Zfp808	UTSW	13	62,319,487 (GRCm39)	missense	possibly damaging	0.47
R1446:Zfp808	UTSW	13	62,320,821 (GRCm39)	missense	probably damaging	1.00
R1569:Zfp808	UTSW	13	62,320,714 (GRCm39)	nonsense	probably null
R1573:Zfp808	UTSW	13	62,319,311 (GRCm39)	missense	possibly damaging	0.52
R1796:Zfp808	UTSW	13	62,319,670 (GRCm39)	missense	probably damaging	1.00
R1993:Zfp808	UTSW	13	62,320,721 (GRCm39)	missense	probably benign	0.10
R2656:Zfp808	UTSW	13	62,320,666 (GRCm39)	missense	possibly damaging	0.63
R2938:Zfp808	UTSW	13	62,319,032 (GRCm39)	missense	probably benign
R3027:Zfp808	UTSW	13	62,319,404 (GRCm39)	missense	probably benign	0.33
R3777:Zfp808	UTSW	13	62,319,717 (GRCm39)	missense	probably damaging	0.97
R3779:Zfp808	UTSW	13	62,319,717 (GRCm39)	missense	probably damaging	0.97
R3801:Zfp808	UTSW	13	62,319,897 (GRCm39)	missense	probably damaging	1.00
R3802:Zfp808	UTSW	13	62,319,897 (GRCm39)	missense	probably damaging	1.00
R3804:Zfp808	UTSW	13	62,319,897 (GRCm39)	missense	probably damaging	1.00
R4024:Zfp808	UTSW	13	62,319,544 (GRCm39)	missense	possibly damaging	0.71
R4741:Zfp808	UTSW	13	62,319,763 (GRCm39)	missense	probably damaging	1.00
R4791:Zfp808	UTSW	13	62,319,045 (GRCm39)	missense	probably damaging	0.97
R4809:Zfp808	UTSW	13	62,319,106 (GRCm39)	nonsense	probably null
R4907:Zfp808	UTSW	13	62,319,287 (GRCm39)	missense	possibly damaging	0.71
R5056:Zfp808	UTSW	13	62,320,444 (GRCm39)	missense	probably damaging	1.00
R5760:Zfp808	UTSW	13	62,319,740 (GRCm39)	missense	probably damaging	1.00
R5869:Zfp808	UTSW	13	62,319,069 (GRCm39)	missense	probably damaging	1.00
R6230:Zfp808	UTSW	13	62,320,136 (GRCm39)	missense	probably benign	0.19
R6372:Zfp808	UTSW	13	62,320,291 (GRCm39)	missense	probably damaging	1.00
R6545:Zfp808	UTSW	13	62,319,709 (GRCm39)	missense	probably benign	0.02
R6620:Zfp808	UTSW	13	62,320,638 (GRCm39)	missense	probably benign	0.08
R6622:Zfp808	UTSW	13	62,319,646 (GRCm39)	missense	possibly damaging	0.90
R6813:Zfp808	UTSW	13	62,320,849 (GRCm39)	missense	probably damaging	0.99
R6920:Zfp808	UTSW	13	62,320,982 (GRCm39)	missense	probably benign	0.05
R7511:Zfp808	UTSW	13	62,320,637 (GRCm39)	missense	probably benign
R7666:Zfp808	UTSW	13	62,319,225 (GRCm39)	missense	probably benign
R7747:Zfp808	UTSW	13	62,319,319 (GRCm39)	missense	probably benign	0.39
R7763:Zfp808	UTSW	13	62,320,478 (GRCm39)	missense	probably benign	0.28
R7779:Zfp808	UTSW	13	62,320,571 (GRCm39)	missense	possibly damaging	0.68
R8147:Zfp808	UTSW	13	62,320,934 (GRCm39)	missense	probably damaging	1.00
R8182:Zfp808	UTSW	13	62,319,521 (GRCm39)	missense	probably damaging	0.96
R8260:Zfp808	UTSW	13	62,320,552 (GRCm39)	missense	probably benign	0.01
R8434:Zfp808	UTSW	13	62,319,926 (GRCm39)	missense	probably damaging	1.00
R8822:Zfp808	UTSW	13	62,320,869 (GRCm39)	missense	probably damaging	1.00
R9330:Zfp808	UTSW	13	62,319,974 (GRCm39)	missense	probably benign	0.00
R9564:Zfp808	UTSW	13	62,320,661 (GRCm39)	missense	possibly damaging	0.49
RF005:Zfp808	UTSW	13	62,319,113 (GRCm39)	missense	probably benign	0.14
RF024:Zfp808	UTSW	13	62,319,113 (GRCm39)	missense	probably benign	0.14

Predicted Primers

Posted On

2014-05-23