Mutagenetix > Incidental Mutations

Incidental Mutation 'R4392:Zfp759'

326431

Institutional Source

Beutler Lab

Gene Symbol

Zfp759

Ensembl Gene

ENSMUSG00000057396

Gene Name

zinc finger protein 759

Synonyms

Rslcan-8

MMRRC Submission

041127-MU

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.055) question?

Stock #

R4392 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

67121660-67141787 bp(+) (GRCm38)

Type of Mutation

nonsense

DNA Base Change (assembly)

T to A at 67139643 bp

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Stop codon at position 419 (C419*)

Ref Sequence

ENSEMBL: ENSMUSP00000049650 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000052716] [ENSMUST00000224346]

Predicted Effect

probably null
Transcript: ENSMUST00000052716
AA Change: C419*

SMART Domains

Protein: ENSMUSP00000049650
Gene: ENSMUSG00000057396
AA Change: C419*

Domain	Start	End	E-Value	Type
KRAB	5	65	1.6e-22	SMART
ZnF_C2H2	106	128	5.54e1	SMART
ZnF_C2H2	162	184	3.83e-2	SMART
ZnF_C2H2	190	212	1.82e-3	SMART
ZnF_C2H2	218	240	1.64e-1	SMART
ZnF_C2H2	246	268	1.67e-2	SMART
ZnF_C2H2	274	296	1.95e-3	SMART
ZnF_C2H2	302	324	1.84e-4	SMART
ZnF_C2H2	330	352	7.78e-3	SMART
ZnF_C2H2	358	380	1.6e-4	SMART
ZnF_C2H2	386	408	1.67e-2	SMART
ZnF_C2H2	414	436	4.87e-4	SMART
ZnF_C2H2	442	464	3.39e-3	SMART
ZnF_C2H2	498	520	2.57e-3	SMART
ZnF_C2H2	526	548	8.47e-4	SMART
ZnF_C2H2	554	576	2.02e-1	SMART
ZnF_C2H2	582	604	2.53e-2	SMART
ZnF_C2H2	610	632	4.79e-3	SMART
ZnF_C2H2	638	660	1.84e-4	SMART
ZnF_C2H2	666	688	1.36e-2	SMART
ZnF_C2H2	694	716	4.17e-3	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000223605

Predicted Effect

probably benign
Transcript: ENSMUST00000224346

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000224426

Meta Mutation Damage Score

0.9716

Coding Region Coverage

1x: 99.5%
3x: 98.5%
10x: 96.1%
20x: 90.5%

Validation Efficiency

95% (69/73)

Allele List at MGI

Other mutations in this stock

Total: 60 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4931414P19Rik	C	T	14: 54,584,978		probably null	Het
Abca13	A	C	11: 9,309,034	K2920T	possibly damaging	Het
Amy2b	T	G	3: 113,149,408		noncoding transcript	Het
Anapc1	T	C	2: 128,676,249		probably null	Het
Bmp7	T	G	2: 172,916,542	D178A	probably benign	Het
Brsk1	T	A	7: 4,698,750	I170N	probably damaging	Het
Bub3	C	T	7: 131,566,335	A187V	probably benign	Het
Cacna2d2	A	G	9: 107,400,280	H71R	possibly damaging	Het
Cdrt4	A	T	11: 62,951,353	K20N	probably benign	Het
Clec12a	A	T	6: 129,353,464		probably benign	Het
Col12a1	T	A	9: 79,662,488	Y1600F	probably damaging	Het
Cyp2a12	T	A	7: 27,029,275	I57N	probably damaging	Het
Dip2b	T	C	15: 100,162,036	L223P	probably damaging	Het
Dnah5	G	A	15: 28,289,229	R1188H	probably benign	Het
Dopey1	T	C	9: 86,503,143		probably benign	Het
Efcab5	T	A	11: 77,090,458	N1354I	probably damaging	Het
Eif4b	T	A	15: 102,086,641		probably null	Het
Elmsan1	A	T	12: 84,173,111	D356E	probably benign	Het
Erlec1	A	G	11: 30,943,697		probably null	Het
Esp24	T	C	17: 39,040,077		probably benign	Het
Esp34	T	C	17: 38,559,491	V24A	possibly damaging	Het
Fbxw15	T	A	9: 109,568,232		probably benign	Het
Foxc2	T	C	8: 121,117,452	S280P	probably damaging	Het
Gm21738	G	C	14: 19,417,178	L117V	probably benign	Het
Grk3	A	G	5: 112,920,136	F467S	probably damaging	Het
Grwd1	C	T	7: 45,827,780	G228S	probably damaging	Het
Gtf2i	T	C	5: 134,260,629	E399G	probably damaging	Het
Hjurp	GT	GTT	1: 88,266,524		probably null	Het
Homer3	G	A	8: 70,290,143		probably null	Het
Lhx4	A	G	1: 155,710,134	Y83H	probably damaging	Het
Mdga1	T	C	17: 29,850,656	T413A	probably damaging	Het
Mmrn2	T	A	14: 34,397,616	L184H	probably damaging	Het
Mroh2a	C	T	1: 88,259,589	R133C	probably damaging	Het
Myh13	A	C	11: 67,344,881		probably null	Het
Nkain3	C	A	4: 20,282,985	R116L	possibly damaging	Het
Nxph2	A	C	2: 23,400,272	Q212P	probably damaging	Het
Olfr268-ps1	T	C	2: 111,844,345		noncoding transcript	Het
Olfr726	A	G	14: 50,084,603	F26S	probably benign	Het
Otog	T	C	7: 46,285,124	Y1369H	probably damaging	Het
Prl	A	G	13: 27,064,351	I131V	possibly damaging	Het
Ptprg	A	T	14: 12,142,467	I373F	possibly damaging	Het
Rad18	A	T	6: 112,693,529	C25S	probably damaging	Het
Rgs12	A	G	5: 35,032,311	T678A	probably damaging	Het
Scaper	T	A	9: 55,858,115	E557V	probably damaging	Het
Scube3	C	T	17: 28,164,788	P511L	probably null	Het
Sgpl1	A	G	10: 61,104,452		probably benign	Het
Slc10a1	C	A	12: 80,967,804	E47D	probably damaging	Het
Sptbn4	T	C	7: 27,418,471	N369S	probably damaging	Het
Sstr5	T	C	17: 25,491,224	T344A	probably benign	Het
Tgm4	C	T	9: 123,066,752	T631I	probably benign	Het
Tmprss15	A	G	16: 79,024,438	Y457H	probably damaging	Het
Trpm7	A	T	2: 126,795,509		probably null	Het
Trpm7	A	T	2: 126,848,538	W207R	probably damaging	Het
Ttc26	A	G	6: 38,381,557		probably benign	Het
Ugt1a1	CAGAGAGAGAGAGA	CAGAGAGAGAGA	1: 88,211,984		probably benign	Het
Ugt1a10	C	T	1: 88,215,123	P113L	probably damaging	Het
Usp2	A	T	9: 44,091,259	H384L	probably damaging	Het
Vmn2r27	C	T	6: 124,230,176	V169I	probably benign	Het
Vopp1	A	C	6: 57,762,476	F29C	probably damaging	Het
Wrn	T	C	8: 33,251,832	D953G	probably damaging	Het

Other mutations in Zfp759

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01509:Zfp759	APN	13	67139594	missense	probably benign	0.25
IGL03131:Zfp759	APN	13	67138664	missense	probably damaging	1.00
IGL03218:Zfp759	APN	13	67139416	missense	probably benign	0.00
R0243:Zfp759	UTSW	13	67138813	missense	possibly damaging	0.66
R0319:Zfp759	UTSW	13	67140292	missense	probably benign	0.00
R0520:Zfp759	UTSW	13	67137355	missense	probably benign	0.29
R0961:Zfp759	UTSW	13	67139863	missense	probably benign	0.32
R1435:Zfp759	UTSW	13	67138766	missense	possibly damaging	0.73
R1649:Zfp759	UTSW	13	67139604	missense	probably benign	0.00
R1880:Zfp759	UTSW	13	67139212	missense	probably damaging	1.00
R2118:Zfp759	UTSW	13	67139514	unclassified	probably benign
R2170:Zfp759	UTSW	13	67136748	missense	possibly damaging	0.88
R3154:Zfp759	UTSW	13	67138655	missense	probably benign	0.20
R3551:Zfp759	UTSW	13	67138967	missense	probably benign	0.24
R4495:Zfp759	UTSW	13	67138925	splice site	probably null
R4736:Zfp759	UTSW	13	67139344	missense	probably damaging	1.00
R4882:Zfp759	UTSW	13	67139290	missense	probably damaging	1.00
R5717:Zfp759	UTSW	13	67138708	missense	probably damaging	1.00
R5921:Zfp759	UTSW	13	67140494	missense	probably damaging	1.00
R6247:Zfp759	UTSW	13	67140460	missense	probably benign	0.00
R6381:Zfp759	UTSW	13	67138905	nonsense	probably null
R6427:Zfp759	UTSW	13	67139098	splice site	probably null
R6567:Zfp759	UTSW	13	67139086	missense	probably benign	0.34
R7140:Zfp759	UTSW	13	67140113	missense	possibly damaging	0.92
R7731:Zfp759	UTSW	13	67139626	missense	possibly damaging	0.82
R8504:Zfp759	UTSW	13	67138883	missense	probably benign	0.00
R8770:Zfp759	UTSW	13	67140353	missense	probably damaging	1.00
Z1176:Zfp759	UTSW	13	67136808	missense	probably damaging	0.98
Z1177:Zfp759	UTSW	13	67140148	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CAAGGCCTTCCGTTATTCATCA -3'
(R):5'- CAGAAGGCATTTCCACACACTTTA -3'

Sequencing Primer
(F):5'- CACCATACAAGTGTAAAGTGTGTG -3'
(R):5'- TGATGGAGACCAGAAGACCTTTCTAC -3'

Posted On

2015-07-06