Mutagenetix > Incidental Mutation

Incidental Mutation 'R9264:Zfp760'

702450

Institutional Source

Beutler Lab

Gene Symbol

Zfp760

Ensembl Gene

ENSMUSG00000067928

Gene Name

zinc finger protein 760

Synonyms

MMRRC Submission

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.091) question?

Stock #

R9264 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

21707741-21725636 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 21723682 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 613 (S613P)

Ref Sequence

ENSEMBL: ENSMUSP00000073038 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000073312]

AlphaFold

E9QAF5

Predicted Effect

possibly damaging
Transcript: ENSMUST00000073312
AA Change: S613P

PolyPhen 2 Score 0.804 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000073038
Gene: ENSMUSG00000067928
AA Change: S613P

Domain	Start	End	E-Value	Type
KRAB	8	69	3.62e-21	SMART
ZnF_C2H2	183	202	1.78e2	SMART
ZnF_C2H2	208	230	1.69e-3	SMART
ZnF_C2H2	236	258	4.54e-4	SMART
ZnF_C2H2	264	286	2.79e-4	SMART
ZnF_C2H2	292	314	1.1e-2	SMART
ZnF_C2H2	320	342	2.71e-2	SMART
ZnF_C2H2	348	370	7.9e-4	SMART
ZnF_C2H2	376	398	1.72e-4	SMART
ZnF_C2H2	404	426	1.14e0	SMART
ZnF_C2H2	432	454	4.05e-1	SMART
ZnF_C2H2	460	482	5.14e-3	SMART
ZnF_C2H2	488	510	1.18e-2	SMART
ZnF_C2H2	516	538	1.95e-3	SMART
ZnF_C2H2	544	566	1.82e-3	SMART
ZnF_C2H2	572	594	4.17e-3	SMART
ZnF_C2H2	600	622	1.04e-3	SMART
ZnF_C2H2	628	650	1.28e-3	SMART

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.1%

Validation Efficiency

100% (58/58)

Allele List at MGI

Other mutations in this stock

Total: 57 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700017D01Rik	T	A	19: 11,116,466	M1L	probably benign	Het
Abca15	A	T	7: 120,401,833	I1531L	probably benign	Het
Adam28	T	C	14: 68,607,465	Y791C	probably benign	Het
Ankrd40	T	A	11: 94,338,361	I262N	probably damaging	Het
BC067074	G	A	13: 113,319,480	V687M		Het
Catsperg2	A	T	7: 29,698,188	N1033K	possibly damaging	Het
Cdh10	A	T	15: 18,963,995	D81V	probably damaging	Het
Cep290	T	C	10: 100,498,016	V310A	possibly damaging	Het
Cep78	T	C	19: 15,974,466	Y325C	probably damaging	Het
Clstn3	T	A	6: 124,459,768	D197V	probably damaging	Het
Col11a1	T	C	3: 114,212,160	I1647T	unknown	Het
Col5a1	G	A	2: 27,964,111	R569K	unknown	Het
Cyp4a10	T	C	4: 115,524,278	S180P	probably benign	Het
D630045J12Rik	T	C	6: 38,158,238	I1336V	probably benign	Het
Dchs2	G	A	3: 83,270,477	V946M	probably damaging	Het
Dnah10	A	G	5: 124,736,836	R347G	probably damaging	Het
Dnah11	T	A	12: 118,027,527	D2368V	probably damaging	Het
Ganab	T	C	19: 8,912,864	I719T	possibly damaging	Het
Gm10944	C	A	10: 10,681,839	A11D	unknown	Het
Gmcl1	T	C	6: 86,714,213	M267V	probably benign	Het
Inhbe	T	A	10: 127,350,558	D251V	probably damaging	Het
Kcnj1	G	A	9: 32,396,358	R26Q	probably benign	Het
Lama5	A	G	2: 180,196,478		probably benign	Het
Lin9	T	A	1: 180,667,347	D251E	probably damaging	Het
Magel2	T	A	7: 62,378,596	I416N	possibly damaging	Het
Mdga2	T	C	12: 66,513,283	N772S	probably damaging	Het
Msh3	G	T	13: 92,349,304	Q171K	probably benign	Het
Mslnl	T	G	17: 25,742,532		probably benign	Het
Mtpn	A	G	6: 35,512,241	L116P	possibly damaging	Het
Myh7	T	C	14: 54,975,997	T1351A	probably benign	Het
Nectin3	A	T	16: 46,454,635	I353N	probably damaging	Het
Nprl3	A	T	11: 32,233,948	N500K	probably benign	Het
Nup93	T	A	8: 94,292,720	I181N	probably benign	Het
Olfr1198	T	C	2: 88,746,432	H152R	probably damaging	Het
Olfr362	G	A	2: 37,104,789	T287I	probably damaging	Het
Optc	T	C	1: 133,905,240	I41V	probably benign	Het
Pcdh7	C	A	5: 58,129,321	N1246K	probably benign	Het
Pcdhb3	T	A	18: 37,302,113	D377E	probably benign	Het
Pnpla6	C	T	8: 3,523,294	P386L	probably benign	Het
Polr3a	T	C	14: 24,470,831	T587A	probably benign	Het
Pramel1	T	G	4: 143,398,529	L341R	probably damaging	Het
Rhot2	A	T	17: 25,841,766	N210K	probably damaging	Het
Slc37a1	A	G	17: 31,300,485	I12V	probably benign	Het
Spata48	T	A	11: 11,464,678	D141E		Het
Sstr3	G	T	15: 78,539,592	N318K	probably damaging	Het
Ssx2ip	T	C	3: 146,437,200	V511A	probably benign	Het
Stfa1	G	A	16: 36,280,568	V57I	unknown	Het
Syne1	T	G	10: 5,262,793	R3265S	probably damaging	Het
Tacc2	G	T	7: 130,626,803	K1739N	probably damaging	Het
Tas2r143	A	T	6: 42,400,739	M168L	probably benign	Het
Tm4sf1	A	T	3: 57,294,610		probably null	Het
Ttc16	A	G	2: 32,763,005	I604T	possibly damaging	Het
Ugt1a10	T	A	1: 88,055,671	W64R	possibly damaging	Het
Usp34	A	T	11: 23,489,064	H3561L		Het
Vasp	C	T	7: 19,259,451	V276I	unknown	Het
Vwa3a	A	G	7: 120,775,464	N333S	probably benign	Het
Wipf3	A	G	6: 54,483,881	N105D	probably benign	Het

Other mutations in Zfp760

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00472:Zfp760	APN	17	21723476	missense	possibly damaging	0.75
IGL00862:Zfp760	APN	17	21722284	missense	probably benign	0.00
IGL02198:Zfp760	APN	17	21722212	missense	probably benign	0.00
R0478:Zfp760	UTSW	17	21722014	nonsense	probably null
R0835:Zfp760	UTSW	17	21723578	missense	possibly damaging	0.63
R1191:Zfp760	UTSW	17	21723305	missense	probably damaging	1.00
R1760:Zfp760	UTSW	17	21722330	missense	probably damaging	1.00
R2698:Zfp760	UTSW	17	21720954	missense	probably damaging	0.99
R3722:Zfp760	UTSW	17	21722162	missense	probably damaging	1.00
R4561:Zfp760	UTSW	17	21723667	missense	probably benign	0.00
R4700:Zfp760	UTSW	17	21722407	missense	probably benign	0.01
R4859:Zfp760	UTSW	17	21723530	missense	probably damaging	0.97
R4859:Zfp760	UTSW	17	21723535	nonsense	probably null
R4897:Zfp760	UTSW	17	21723248	missense	probably benign	0.02
R6675:Zfp760	UTSW	17	21723010	missense	possibly damaging	0.92
R7286:Zfp760	UTSW	17	21722779	missense	probably benign	0.04
R7336:Zfp760	UTSW	17	21723833	missense	unknown
R7356:Zfp760	UTSW	17	21722620	missense	probably benign
R7369:Zfp760	UTSW	17	21723233	missense	probably benign	0.00
R7504:Zfp760	UTSW	17	21722674	missense	probably damaging	0.97
R7553:Zfp760	UTSW	17	21722891	missense	possibly damaging	0.82
R7577:Zfp760	UTSW	17	21722261	nonsense	probably null
R7579:Zfp760	UTSW	17	21722926	missense	possibly damaging	0.93
R7608:Zfp760	UTSW	17	21722816	missense	probably benign	0.00
R7973:Zfp760	UTSW	17	21722103	missense	probably benign	0.00
R8078:Zfp760	UTSW	17	21723455	missense	probably benign	0.27
R8332:Zfp760	UTSW	17	21723320	missense	probably damaging	0.99
R8750:Zfp760	UTSW	17	21722375	missense	possibly damaging	0.56
R9094:Zfp760	UTSW	17	21722951	missense	possibly damaging	0.86
R9372:Zfp760	UTSW	17	21722054	missense	probably benign	0.00
R9520:Zfp760	UTSW	17	21722055	missense	probably benign	0.00
R9564:Zfp760	UTSW	17	21723291	missense	possibly damaging	0.94
R9743:Zfp760	UTSW	17	21723357	missense	probably benign
X0057:Zfp760	UTSW	17	21723682	missense	possibly damaging	0.80

Predicted Primers

PCR Primer
(F):5'- AGGAATGTGGTAAGTTCTTCCATTG -3'
(R):5'- GACAGTGAACATTCTTCTGGTTTAG -3'

Sequencing Primer
(F):5'- AGTTCTTCCATTGGTTGTCAAAC -3'
(R):5'- AGTTCTGGTTTGAATTTCTGACTAC -3'

Posted On

2022-03-25