Mutagenetix > Incidental Mutation

Incidental Mutation 'R4791:Zfp808'

368613

Institutional Source

Beutler Lab

Gene Symbol

Zfp808

Ensembl Gene

ENSMUSG00000074867

Gene Name

zinc finger protein 808

Synonyms

Gm7036

MMRRC Submission

041976-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.074) question?

Stock #

R4791 (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 62319045 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Glutamine at position 91 (H91Q)

Ref Sequence

ENSEMBL: ENSMUSP00000097048 (fasta)

Gene Model

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

AlphaFold

B8JJZ4

Predicted Effect

probably damaging
Transcript: ENSMUST00000099449
AA Change: H91Q

PolyPhen 2 Score 0.973 (Sensitivity: 0.76; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000097048
Gene: ENSMUSG00000074867
AA Change: H91Q

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
AA Change: M71K

PolyPhen 2 Score 0.317 (Sensitivity: 0.90; Specificity: 0.89)

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000222809

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000222947

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000223094

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.9%
20x: 94.3%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 97 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc6	C	T	7: 45,631,584 (GRCm39)	V1231M	probably benign	Het
Agl	A	G	3: 116,580,177 (GRCm39)		probably null	Het
Ak7	T	C	12: 105,676,404 (GRCm39)	F35L	probably benign	Het
Aldh1a1	A	G	19: 20,597,349 (GRCm39)	N110S	probably damaging	Het
Arhgef5	C	T	6: 43,260,117 (GRCm39)	L1368F	probably damaging	Het
Atp5mf	T	C	5: 145,121,365 (GRCm39)	Y72C	possibly damaging	Het
Atp6v0a2	T	G	5: 124,784,667 (GRCm39)	F317V	probably benign	Het
Bank1	A	T	3: 135,960,690 (GRCm39)	S56T	probably benign	Het
Cachd1	T	A	4: 100,775,282 (GRCm39)	C166S	probably damaging	Het
Cand1	A	G	10: 119,046,607 (GRCm39)	I961T	probably benign	Het
Ccdc73	G	A	2: 104,811,450 (GRCm39)		probably null	Het
Cct6b	A	T	11: 82,632,830 (GRCm39)		probably null	Het
Chd2	A	C	7: 73,118,325 (GRCm39)	S1098A	probably benign	Het
Col6a4	A	T	9: 105,957,401 (GRCm39)	V141E	possibly damaging	Het
Col6a5	T	C	9: 105,807,983 (GRCm39)	T1022A	unknown	Het
Cr2	A	T	1: 194,838,243 (GRCm39)	C698S	probably damaging	Het
Dnaaf5	C	A	5: 139,170,405 (GRCm39)	Q786K	possibly damaging	Het
Dnah6	T	C	6: 73,072,057 (GRCm39)	D2423G	probably benign	Het
Dnhd1	T	C	7: 105,370,324 (GRCm39)	F4583S	probably damaging	Het
Duoxa2	A	T	2: 122,131,679 (GRCm39)	T123S	probably damaging	Het
Edem1	T	G	6: 108,818,595 (GRCm39)	V201G	probably damaging	Het
Eef1d	C	T	15: 75,775,531 (GRCm39)	A43T	possibly damaging	Het
Elavl3	T	C	9: 21,935,974 (GRCm39)	K249E	probably damaging	Het
Epg5	G	T	18: 77,992,211 (GRCm39)	E303*	probably null	Het
Fam83h	T	C	15: 75,874,217 (GRCm39)	D1040G	probably damaging	Het
Fndc7	A	T	3: 108,783,975 (GRCm39)	F211L	probably benign	Het
Fsip2	A	G	2: 82,812,452 (GRCm39)	T2924A	possibly damaging	Het
Gm5616	T	C	9: 48,361,983 (GRCm39)		noncoding transcript	Het
Gpr135	T	A	12: 72,116,642 (GRCm39)	D375V	probably benign	Het
Hgd	A	G	16: 37,452,187 (GRCm39)	*446W	probably null	Het
Hivep2	C	A	10: 14,004,713 (GRCm39)	T437K	probably benign	Het
Htra2	A	G	6: 83,028,798 (GRCm39)	L379P	probably damaging	Het
Hypk	G	T	2: 121,288,136 (GRCm39)		probably null	Het
Ica1l	A	G	1: 60,049,360 (GRCm39)	F198L	probably damaging	Het
Igsf11	G	A	16: 38,845,226 (GRCm39)	S319N	probably damaging	Het
Il12rb1	T	C	8: 71,266,012 (GRCm39)	S213P	possibly damaging	Het
Katnal1	C	T	5: 148,841,460 (GRCm39)	V135M	probably damaging	Het
Kcnc4	G	A	3: 107,354,859 (GRCm39)	P530S	probably benign	Het
Kcnu1	T	C	8: 26,403,780 (GRCm39)	Y24H	probably damaging	Het
Kdm5b	A	G	1: 134,558,538 (GRCm39)	E1515G	possibly damaging	Het
Kif18a	A	T	2: 109,118,220 (GRCm39)	M12L	probably benign	Het
Klre1	T	C	6: 129,561,118 (GRCm39)	S160P	probably damaging	Het
Lama2	A	T	10: 27,343,267 (GRCm39)	H68Q	probably damaging	Het
Lgals8	T	C	13: 12,468,203 (GRCm39)	K49R	possibly damaging	Het
Lmf1	G	A	17: 25,873,445 (GRCm39)	V317M	probably damaging	Het
Lsr	T	C	7: 30,657,977 (GRCm39)	T328A	probably damaging	Het
Mark4	C	T	7: 19,185,582 (GRCm39)	E51K	probably benign	Het
Mindy2	T	C	9: 70,541,283 (GRCm39)		probably null	Het
Mkks	G	A	2: 136,718,082 (GRCm39)	T400I	probably benign	Het
Mon2	T	A	10: 122,841,962 (GRCm39)	M1544L	probably benign	Het
Mrc2	G	A	11: 105,239,257 (GRCm39)		probably null	Het
Myo5c	T	G	9: 75,198,198 (GRCm39)	L1341R	probably damaging	Het
Nin	T	C	12: 70,090,581 (GRCm39)	R945G	possibly damaging	Het
Nox4	T	C	7: 86,954,055 (GRCm39)	V120A	probably benign	Het
Or1s2	T	A	19: 13,758,706 (GRCm39)	C243*	probably null	Het
Or2aj4	G	T	16: 19,385,413 (GRCm39)	H73Q	possibly damaging	Het
Or2z2	A	T	11: 58,346,370 (GRCm39)	V135E	possibly damaging	Het
Or4a66	C	T	2: 88,531,242 (GRCm39)	V144I	probably benign	Het
Or7g29	T	C	9: 19,287,105 (GRCm39)	E24G	probably benign	Het
Plekha2	T	A	8: 25,532,778 (GRCm39)	R398W	probably damaging	Het
Pradc1	A	G	6: 85,424,173 (GRCm39)	W58R	probably damaging	Het
Pramel20	A	G	4: 143,297,559 (GRCm39)		probably benign	Het
Prrc2b	A	G	2: 32,107,351 (GRCm39)		probably null	Het
Psg19	T	A	7: 18,528,071 (GRCm39)	N224I	probably damaging	Het
Ranbp17	A	C	11: 33,437,746 (GRCm39)	V164G	probably benign	Het
Rasgrp3	A	G	17: 75,807,168 (GRCm39)	S211G	probably benign	Het
Rcc1l	G	A	5: 134,192,615 (GRCm39)	P270S	possibly damaging	Het
Rfx6	T	A	10: 51,596,040 (GRCm39)		probably null	Het
Rnf222	A	T	11: 68,783,845 (GRCm39)	E137D	probably damaging	Het
Selenof	T	G	3: 144,302,584 (GRCm39)	Y120D	probably damaging	Het
Sema3b	G	T	9: 107,481,012 (GRCm39)	D108E	probably damaging	Het
Shank3	T	A	15: 89,384,557 (GRCm39)	L143Q	probably damaging	Het
Shtn1	G	C	19: 59,039,305 (GRCm39)	R45G	probably damaging	Het
Sirt4	T	C	5: 115,618,373 (GRCm39)	T234A	possibly damaging	Het
Slc25a30	C	A	14: 76,000,806 (GRCm39)	W266L	probably benign	Het
Spata20	A	T	11: 94,375,412 (GRCm39)	N127K	probably damaging	Het
Spmip4	G	T	6: 50,572,817 (GRCm39)	P32Q	probably damaging	Het
St14	C	T	9: 31,006,918 (GRCm39)	G636D	probably benign	Het
Stat5a	G	A	11: 100,756,289 (GRCm39)	E170K	probably damaging	Het
Sugp2	C	T	8: 70,695,440 (GRCm39)	R138C	probably damaging	Het
Sult1e1	C	A	5: 87,734,589 (GRCm39)	W119L	possibly damaging	Het
Sv2a	T	C	3: 96,099,874 (GRCm39)	V608A	possibly damaging	Het
Syne2	T	C	12: 75,956,018 (GRCm39)	Y575H	possibly damaging	Het
Taok2	G	A	7: 126,467,304 (GRCm39)	S167L	possibly damaging	Het
Thoc6	T	C	17: 23,889,041 (GRCm39)	H151R	possibly damaging	Het
Tm9sf2	T	C	14: 122,377,062 (GRCm39)	S197P	probably benign	Het
Tmem260	CAGGGACCGGCATAG	CAG	14: 48,749,451 (GRCm39)		probably benign	Het
Tmx2	G	A	2: 84,508,340 (GRCm39)	P15L	probably damaging	Het
Top1mt	C	T	15: 75,540,474 (GRCm39)		probably null	Het
Trpm6	T	A	19: 18,845,345 (GRCm39)	S1682T	probably benign	Het
Trrap	C	T	5: 144,740,087 (GRCm39)	R1171W	probably damaging	Het
Ugt3a1	A	G	15: 9,361,665 (GRCm39)	D147G	probably damaging	Het
Utp25	G	A	1: 192,810,575 (GRCm39)	H143Y	probably benign	Het
Vnn3	A	G	10: 23,740,519 (GRCm39)	H274R	probably benign	Het
Vwf	C	A	6: 125,620,326 (GRCm39)	T1668K		Het
Zfp568	T	C	7: 29,714,608 (GRCm39)	S162P	probably damaging	Het
Zfp658	T	A	7: 43,223,890 (GRCm39)	C722S	possibly damaging	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
R1761:Zfp808	UTSW	13	62,319,460 (GRCm39)	missense	possibly damaging	0.71
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
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

PCR Primer
(F):5'- ACTTCAGAGATGGCTCAGCAG -3'
(R):5'- TGAAGGGTTTCTCTCCAGTATGT -3'

Sequencing Primer
(F):5'- GACAGGACAGCTACAGTGTACTTAC -3'
(R):5'- ACATATGAAGGGTTGCTCTACG -3'

Posted On

2016-02-04