Mutagenetix > Incidental Mutations

Incidental Mutation 'R5240:Zfp672'

400745

Institutional Source

Beutler Lab

Gene Symbol

Zfp672

Ensembl Gene

ENSMUSG00000049755

Gene Name

zinc finger protein 672

Synonyms

4930511N19Rik, 4930488P06Rik

MMRRC Submission

042811-MU

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.100) question?

Stock #

R5240 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

58315114-58330339 bp(-) (GRCm38)

Type of Mutation

intron

DNA Base Change (assembly)

A to G at 58329701 bp

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000140236 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000065533] [ENSMUST00000073128] [ENSMUST00000116376] [ENSMUST00000186859]

Predicted Effect

unknown
Transcript: ENSMUST00000065533
AA Change: V24A

Predicted Effect

probably benign
Transcript: ENSMUST00000073128

SMART Domains

Protein: ENSMUSP00000072872
Gene: ENSMUSG00000013646

Domain	Start	End	E-Value	Type
low complexity region	34	45	N/A	INTRINSIC
Pfam:SH3BP5	52	289	1.3e-103	PFAM
low complexity region	296	337	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000116376

SMART Domains

Protein: ENSMUSP00000112077
Gene: ENSMUSG00000013646

Domain	Start	End	E-Value	Type
low complexity region	34	45	N/A	INTRINSIC
Pfam:SH3BP5	54	280	2.5e-97	PFAM
low complexity region	296	337	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000149701

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000154278

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000185661

Predicted Effect

probably benign
Transcript: ENSMUST00000186859

SMART Domains

Protein: ENSMUSP00000140236
Gene: ENSMUSG00000049755

Domain	Start	End	E-Value	Type
ZnF_C2H2	15	37	1.8e-5	SMART
ZnF_C2H2	43	65	3.6e-2	SMART
ZnF_C2H2	71	90	6.1e-1	SMART

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.1%
20x: 95.1%

Validation Efficiency

100% (69/69)

Allele List at MGI

Other mutations in this stock

Total: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Cdc42bpg	T	G	19: 6,315,899	L786R	probably damaging	Het
Cfap73	C	T	5: 120,629,707	V260I	probably damaging	Het
Chchd10	A	T	10: 75,937,449	N131I	probably damaging	Het
Chn2	T	C	6: 54,220,695	V190A	probably benign	Het
Clec2l	C	T	6: 38,673,452	T64I	probably damaging	Het
Cpeb3	T	A	19: 37,174,515	T154S	probably damaging	Het
D130043K22Rik	A	G	13: 24,877,977	E643G	probably damaging	Het
Ddx31	A	G	2: 28,846,030	M127V	probably benign	Het
Dennd1b	A	G	1: 139,062,877	Y193C	probably damaging	Het
Dgke	T	A	11: 89,050,685	D288V	probably damaging	Het
Dst	T	A	1: 34,208,558	L1683*	probably null	Het
Dupd1	G	A	14: 21,677,023	R186W	probably benign	Het
E130116L18Rik	G	T	5: 25,223,020		probably benign	Het
Eif2b5	G	A	16: 20,501,398	V115I	possibly damaging	Het
Fchsd1	C	T	18: 37,959,873		probably benign	Het
Fgfr3	A	T	5: 33,730,038	T234S	probably damaging	Het
Gipc2	A	T	3: 152,102,662	D251E	possibly damaging	Het
Gm11787	A	C	4: 3,511,810		noncoding transcript	Het
Gm5538	A	C	3: 59,752,028	T301P	probably damaging	Het
Haus6	A	G	4: 86,583,178	Y819H	possibly damaging	Het
Homez	G	A	14: 54,858,074	A59V	probably damaging	Het
Iffo1	T	C	6: 125,152,460	V363A	probably benign	Het
Ifit2	T	A	19: 34,574,396	D445E	probably benign	Het
Ipo9	A	C	1: 135,389,606		probably benign	Het
Kcnv1	C	T	15: 45,113,244	G216R	probably damaging	Het
Kdm6b	A	C	11: 69,401,904		probably benign	Het
Mplkip	T	C	13: 17,695,719	S79P	probably damaging	Het
Nae1	T	C	8: 104,523,144		probably benign	Het
Nfe2l2	A	T	2: 75,676,009	N582K	possibly damaging	Het
Nsmce4a	G	A	7: 130,537,024	R297C	probably damaging	Het
Olfr397	T	C	11: 73,964,806	L66P	probably damaging	Het
Olfr411	T	A	11: 74,347,242	D114V	probably damaging	Het
Olfr495	A	T	7: 108,395,702	D194V	probably damaging	Het
Osbp	T	A	19: 11,978,290	F357I	probably damaging	Het
Pcdhb4	A	G	18: 37,309,926	D763G	possibly damaging	Het
Pcdhgb2	A	C	18: 37,691,050	I365L	possibly damaging	Het
Pde6g	A	G	11: 120,448,086		probably benign	Het
Pigo	C	A	4: 43,020,675	V756L	possibly damaging	Het
Pkhd1	G	T	1: 20,275,641	T2721K	probably benign	Het
Pls1	A	T	9: 95,776,622		probably null	Het
Prim2	A	G	1: 33,480,316		probably benign	Het
Prkd2	T	A	7: 16,855,786	I471N	probably benign	Het
Prrc2b	C	T	2: 32,206,396	T593I	probably benign	Het
Ptch2	C	A	4: 117,106,138		probably benign	Het
Pth	A	T	7: 113,385,844	D107E	probably damaging	Het
Pycr2	A	C	1: 180,907,623	Q315P	probably benign	Het
Rbpj	A	T	5: 53,649,440	Y209F	probably damaging	Het
Ripk4	C	A	16: 97,743,767	R560L	probably damaging	Het
Sdr42e1	T	C	8: 117,663,282	R207G	probably benign	Het
Sipa1l1	A	G	12: 82,341,588	Y196C	possibly damaging	Het
Smarcc2	T	C	10: 128,481,006		probably null	Het
Stom	T	A	2: 35,336,877	I15F	probably benign	Het
Sugp2	G	T	8: 70,243,275	L299F	probably benign	Het
Tbrg4	A	T	11: 6,617,516		probably null	Het
Tkt	G	T	14: 30,565,678	G210C	probably damaging	Het
Tmem163	G	A	1: 127,491,552		probably benign	Het
Trip12	A	G	1: 84,794,133	I98T	probably benign	Het
Unc5b	A	G	10: 60,774,640	I466T	probably damaging	Het
Unc79	T	A	12: 103,070,751	F599L	probably damaging	Het
Vav1	G	A	17: 57,297,122	E151K	probably damaging	Het
Vcan	T	G	13: 89,692,532	D1631A	probably benign	Het
Vmn2r4	A	C	3: 64,406,937	S208A	possibly damaging	Het
Zfp619	A	G	7: 39,537,218	T891A	possibly damaging	Het
Znhit1	T	A	5: 136,982,381		probably null	Het

Other mutations in Zfp672

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01391:Zfp672	APN	11	58317366	missense	probably damaging	1.00
R0326:Zfp672	UTSW	11	58316347	missense	possibly damaging	0.86
R1485:Zfp672	UTSW	11	58329569	intron	probably benign
R1664:Zfp672	UTSW	11	58317312	missense	probably damaging	0.99
R1667:Zfp672	UTSW	11	58316095	missense	possibly damaging	0.53
R1853:Zfp672	UTSW	11	58316964	missense	probably benign
R2074:Zfp672	UTSW	11	58316636	missense	possibly damaging	0.71
R3817:Zfp672	UTSW	11	58316636	missense	possibly damaging	0.71
R4623:Zfp672	UTSW	11	58316455	missense	probably benign	0.34
R4745:Zfp672	UTSW	11	58329498	intron	probably benign
R5157:Zfp672	UTSW	11	58316851	missense	possibly damaging	0.86
R5510:Zfp672	UTSW	11	58316630	nonsense	probably null
R6207:Zfp672	UTSW	11	58317523	start gained	probably benign
R6279:Zfp672	UTSW	11	58317268	missense	probably damaging	0.99
R6300:Zfp672	UTSW	11	58317268	missense	probably damaging	0.99
R6432:Zfp672	UTSW	11	58316932	missense	possibly damaging	0.53
R6438:Zfp672	UTSW	11	58316737	missense	probably benign	0.07
R7777:Zfp672	UTSW	11	58317255	missense	possibly damaging	0.71
R8401:Zfp672	UTSW	11	58316802	missense	probably benign	0.28
R8489:Zfp672	UTSW	11	58329855	intron	probably benign
RF012:Zfp672	UTSW	11	58316112	missense	probably benign
Z1186:Zfp672	UTSW	11	58329626	missense	unknown
Z1186:Zfp672	UTSW	11	58329960	intron	probably benign
Z1187:Zfp672	UTSW	11	58329626	missense	unknown
Z1188:Zfp672	UTSW	11	58329626	missense	unknown
Z1189:Zfp672	UTSW	11	58329626	missense	unknown
Z1190:Zfp672	UTSW	11	58329626	missense	unknown
Z1191:Zfp672	UTSW	11	58329626	missense	unknown
Z1191:Zfp672	UTSW	11	58329960	intron	probably benign
Z1192:Zfp672	UTSW	11	58329626	missense	unknown

Predicted Primers

PCR Primer
(F):5'- ACAGTTGAAGCCTGTTCCCC -3'
(R):5'- TTCTGTTGAACATAGCCCGTG -3'

Sequencing Primer
(F):5'- CCATATATCCCGGTATGTTCAGAGG -3'
(R):5'- CATAGCCCGTGTTTAGTAAATCGG -3'

Posted On

2016-07-06