Mutagenetix > Incidental Mutation

Incidental Mutation 'R7148:Zfp748'

553969

Institutional Source

Beutler Lab

Gene Symbol

Zfp748

Ensembl Gene

ENSMUSG00000095432

Gene Name

zinc finger protein 748

Synonyms

2610014M12Rik, mszf54, Zfp208, KRAB-O

MMRRC Submission

045225-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.093) question?

Stock #

R7148 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

67538641-67553830 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 67542239 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Methionine at position 301 (V301M)

Ref Sequence

ENSEMBL: ENSMUSP00000137928 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000181892]

AlphaFold

Q7TPL6

Predicted Effect

possibly damaging
Transcript: ENSMUST00000181892
AA Change: V301M

PolyPhen 2 Score 0.956 (Sensitivity: 0.79; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000137928
Gene: ENSMUSG00000095432
AA Change: V301M

Domain	Start	End	E-Value	Type
KRAB	5	65	3.39e-35	SMART
ZnF_C2H2	81	101	1.59e1	SMART
low complexity region	133	144	N/A	INTRINSIC
ZnF_C2H2	165	187	5.14e-3	SMART
ZnF_C2H2	193	215	2.71e-2	SMART
ZnF_C2H2	277	298	7.37e1	SMART
ZnF_C2H2	304	326	1.95e-3	SMART
ZnF_C2H2	332	354	8.94e-3	SMART
ZnF_C2H2	360	382	2.61e-4	SMART
ZnF_C2H2	388	410	5.9e-3	SMART
ZnF_C2H2	416	438	3.44e-4	SMART
ZnF_C2H2	444	466	3.89e-3	SMART
ZnF_C2H2	472	494	4.79e-3	SMART
ZnF_C2H2	500	522	1.6e-4	SMART
ZnF_C2H2	528	550	1.18e-2	SMART
ZnF_C2H2	556	578	1.12e-3	SMART
ZnF_C2H2	584	606	3.89e-3	SMART
ZnF_C2H2	612	634	2.95e-3	SMART
ZnF_C2H2	640	662	1.6e-4	SMART
ZnF_C2H2	668	690	2.95e-3	SMART
ZnF_C2H2	696	718	2.12e-4	SMART
ZnF_C2H2	724	746	4.47e-3	SMART
ZnF_C2H2	752	774	1.12e-3	SMART
ZnF_C2H2	780	802	3.89e-3	SMART
ZnF_C2H2	808	830	1.47e-3	SMART
ZnF_C2H2	836	858	4.87e-4	SMART
ZnF_C2H2	864	886	7.9e-4	SMART

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.2%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700024G13Rik	T	A	14: 32,388,312	Y14F	probably damaging	Het
2410131K14Rik	A	G	5: 118,255,694	N46D	probably benign	Het
4930563D23Rik	T	C	16: 92,320,987	K138E	probably benign	Het
Acly	A	G	11: 100,483,782	V805A	possibly damaging	Het
AF366264	T	A	8: 13,837,996	I32L	probably benign	Het
Apcdd1	T	C	18: 62,951,845	V371A	probably damaging	Het
Cacna1g	A	T	11: 94,465,930	F127I	probably benign	Het
Ccdc129	T	C	6: 55,897,686	I207T	probably damaging	Het
Ccdc138	T	C	10: 58,538,280	L374P	probably damaging	Het
Ces2b	A	G	8: 104,838,296	Y504C	probably damaging	Het
Ces5a	C	T	8: 93,502,322	G427S	probably damaging	Het
Chd1l	C	T	3: 97,591,316	V256M	probably damaging	Het
Col24a1	C	T	3: 145,315,299	T477M	probably damaging	Het
Dmbt1	T	A	7: 131,066,734	C573*	probably null	Het
Emcn	A	T	3: 137,417,094	Y188F	possibly damaging	Het
Eva1a	T	G	6: 82,071,144	M1R	probably null	Het
Fam83h	C	A	15: 76,005,167	D194Y	probably damaging	Het
Flywch1	T	C	17: 23,755,675	K664E	probably benign	Het
Fzd9	A	G	5: 135,249,690	V447A	probably benign	Het
Gm21964	G	T	8: 110,109,416	R119I	probably benign	Het
Heatr5b	T	C	17: 78,831,434	D93G	probably damaging	Het
Hmcn1	T	C	1: 150,686,854	I2318V	probably benign	Het
Hyal5	T	A	6: 24,876,902	L258Q	probably damaging	Het
Kmo	T	A	1: 175,651,602	C235S	probably damaging	Het
Lamc2	G	A	1: 153,185,984	P2S	probably benign	Het
Lman2	G	A	13: 55,352,949	P146S	probably benign	Het
Mars2	T	C	1: 55,237,514	I92T	probably damaging	Het
Msh3	A	G	13: 92,354,822	F27L	probably benign	Het
Myom2	T	C	8: 15,084,577	V460A	possibly damaging	Het
Nicn1	T	A	9: 108,295,107	*214R	probably null	Het
Nsd2	T	C	5: 33,885,511	F1040L	possibly damaging	Het
Olfr374	T	A	8: 72,110,157	I197N	possibly damaging	Het
Osm	T	A	11: 4,239,936	I240N	probably benign	Het
Pard3b	T	A	1: 62,440,032	D884E	probably benign	Het
Pex5	T	G	6: 124,405,272	D150A	probably benign	Het
Pfkfb4	T	C	9: 109,027,608	V394A	probably damaging	Het
Pjvk	A	G	2: 76,658,487	K334R	possibly damaging	Het
Pkd1l2	T	C	8: 117,080,786	D171G	probably benign	Het
Prpf4b	T	G	13: 34,894,472	N688K	probably benign	Het
R3hcc1	T	C	14: 69,705,552	E192G	possibly damaging	Het
Rad54l2	C	A	9: 106,719,119	G207*	probably null	Het
Rhobtb3	G	T	13: 75,910,887	T264K	probably benign	Het
Rpl27	A	G	11: 101,442,406		probably benign	Het
Rxfp3	C	T	15: 11,036,777	V170I	possibly damaging	Het
Samd4	T	A	14: 47,016,683	S201R	probably benign	Het
Sell	A	G	1: 164,065,607	I131V	possibly damaging	Het
Sirpb1c	A	T	3: 15,833,059	Y205*	probably null	Het
Smc3	A	T	19: 53,641,895	E1111V	possibly damaging	Het
Sowaha	C	A	11: 53,479,355	V185L	probably benign	Het
Spata4	A	C	8: 54,602,550	I159L	probably benign	Het
Tekt2	A	G	4: 126,322,381	I373T	probably benign	Het
Tomm20l	T	C	12: 71,117,539	V65A	probably benign	Het
Trabd2b	A	G	4: 114,409,350	D187G	probably damaging	Het
Trrap	A	G	5: 144,821,803	I2147V	possibly damaging	Het
Tsc22d2	T	A	3: 58,417,008	C440*	probably null	Het
Ube3b	A	C	5: 114,406,252	N570T	probably damaging	Het
Uevld	A	G	7: 46,950,976	I70T	probably damaging	Het
Usp10	C	T	8: 119,936,550	T37I	possibly damaging	Het
Vmn2r23	T	A	6: 123,713,022	F286I	probably benign	Het
Vmn2r62	A	G	7: 42,765,216	V601A	probably benign	Het
Wdr81	G	C	11: 75,446,002	N401K		Het
Ythdc2	G	T	18: 44,833,122	V142F	probably benign	Het
Zfp346	T	C	13: 55,105,450	F36S	possibly damaging	Het
Zim1	T	C	7: 6,678,221	K148E	possibly damaging	Het

Other mutations in Zfp748

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02366:Zfp748	APN	13	67545427	splice site	probably benign
R0440:Zfp748	UTSW	13	67553025	splice site	probably null
R0790:Zfp748	UTSW	13	67545362	missense	probably benign	0.03
R1760:Zfp748	UTSW	13	67545421	critical splice acceptor site	probably null
R2520:Zfp748	UTSW	13	67546662	missense	possibly damaging	0.84
R3711:Zfp748	UTSW	13	67540796	missense	probably damaging	1.00
R4157:Zfp748	UTSW	13	67542106	missense	possibly damaging	0.80
R4288:Zfp748	UTSW	13	67541083	missense	probably damaging	1.00
R4289:Zfp748	UTSW	13	67541083	missense	probably damaging	1.00
R5091:Zfp748	UTSW	13	67541519	missense	probably damaging	1.00
R5441:Zfp748	UTSW	13	67540618	missense	probably damaging	1.00
R5686:Zfp748	UTSW	13	67542528	nonsense	probably null
R5907:Zfp748	UTSW	13	67541173	missense	possibly damaging	0.87
R6210:Zfp748	UTSW	13	67540804	missense	possibly damaging	0.85
R6268:Zfp748	UTSW	13	67542586	missense	possibly damaging	0.77
R6639:Zfp748	UTSW	13	67542905	missense	probably damaging	1.00
R6810:Zfp748	UTSW	13	67541725	missense	probably damaging	1.00
R7464:Zfp748	UTSW	13	67541972	missense	probably damaging	1.00
R7593:Zfp748	UTSW	13	67542519	missense	probably benign	0.20
R7644:Zfp748	UTSW	13	67541449	missense	probably damaging	0.99
R7799:Zfp748	UTSW	13	67541489	missense	probably benign	0.02
R8872:Zfp748	UTSW	13	67541795	missense	probably damaging	1.00
R9140:Zfp748	UTSW	13	67540954	missense	probably damaging	1.00
R9402:Zfp748	UTSW	13	67545392	missense	probably benign	0.33
R9649:Zfp748	UTSW	13	67542528	nonsense	probably null
R9687:Zfp748	UTSW	13	67542352	missense	probably benign	0.00
R9749:Zfp748	UTSW	13	67542454	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- ACACTTGTAGGGTTTCTCTTGAGAATG -3'
(R):5'- AGGTCTTTTGTGCTCCCATAGAAC -3'

Sequencing Primer
(F):5'- CTTGAGAATGAGTTATTTGATGTTGC -3'
(R):5'- GTGCTCCCATAGAACTTTCTAAAGAC -3'

Posted On

2019-05-15