Mutagenetix > Incidental Mutation

Incidental Mutation 'R5445:Zfp7'

427426

Institutional Source

Beutler Lab

Gene Symbol

Zfp7

Ensembl Gene

ENSMUSG00000033669

Gene Name

zinc finger protein 7

Synonyms

Zfp86-rs1, Zfp-7, Zfp65, Krox-2, KRAB20, Zfp80, mszf73-2, KRAB7

MMRRC Submission

043010-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5445 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

76763459-76776595 bp(+) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

T to A at 76775054 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Stop codon at position 365 (C365*)

Ref Sequence

ENSEMBL: ENSMUSP00000155599 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000023179] [ENSMUST00000229831] [ENSMUST00000229990] [ENSMUST00000230106] [ENSMUST00000230214]

AlphaFold

Q3TFZ4

Predicted Effect

probably null
Transcript: ENSMUST00000023179
AA Change: C365*

SMART Domains

Protein: ENSMUSP00000023179
Gene: ENSMUSG00000033669
AA Change: C365*

Domain	Start	End	E-Value	Type
KRAB	4	65	3.07e-33	SMART
ZnF_C2H2	192	214	6.88e-4	SMART
ZnF_C2H2	220	242	4.24e-4	SMART
ZnF_C2H2	248	270	2.09e-3	SMART
ZnF_C2H2	276	298	1.45e-2	SMART
ZnF_C2H2	304	326	1.13e-4	SMART
ZnF_C2H2	332	354	9.08e-4	SMART
ZnF_C2H2	360	383	2.24e-3	SMART
ZnF_C2H2	412	434	9.08e-4	SMART
ZnF_C2H2	440	462	1.67e-2	SMART
ZnF_C2H2	468	490	3.44e-4	SMART
ZnF_C2H2	496	518	8.47e-4	SMART
ZnF_C2H2	524	546	4.54e-4	SMART
ZnF_C2H2	552	574	7.9e-4	SMART
ZnF_C2H2	580	602	1.72e-4	SMART
ZnF_C2H2	633	655	1.98e-4	SMART
ZnF_C2H2	661	683	4.79e-3	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000229729

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000229782

Predicted Effect

probably benign
Transcript: ENSMUST00000229831

Predicted Effect

probably benign
Transcript: ENSMUST00000229990

Predicted Effect

probably null
Transcript: ENSMUST00000230106
AA Change: C365*

Predicted Effect

probably benign
Transcript: ENSMUST00000230214

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000230954

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: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcg5	A	T	17: 84,978,557 (GRCm39)	D300E	probably damaging	Het
Apbb1ip	T	C	2: 22,725,960 (GRCm39)	V244A	possibly damaging	Het
Arhgap32	T	C	9: 32,159,678 (GRCm39)	S232P	probably benign	Het
Atf7ip	G	A	6: 136,564,255 (GRCm39)	V833M	probably damaging	Het
Casp7	A	G	19: 56,421,770 (GRCm39)		probably null	Het
Ccdc9b	T	C	2: 118,590,067 (GRCm39)	D259G	probably damaging	Het
Celsr2	T	A	3: 108,299,974 (GRCm39)	E2911D	probably benign	Het
Cep350	T	C	1: 155,770,469 (GRCm39)	D1807G	probably benign	Het
Cfap251	C	T	5: 123,425,240 (GRCm39)	T294M	probably damaging	Het
Chrd	A	G	16: 20,557,660 (GRCm39)	T753A	possibly damaging	Het
Clasp2	A	G	9: 113,733,014 (GRCm39)	D971G	probably damaging	Het
Cnnm2	A	G	19: 46,865,727 (GRCm39)	T772A	possibly damaging	Het
Cntn1	A	T	15: 92,192,958 (GRCm39)	N687Y	probably damaging	Het
Col6a3	G	A	1: 90,709,761 (GRCm39)	R1812*	probably null	Het
Dsc2	T	C	18: 20,168,360 (GRCm39)	I700V	possibly damaging	Het
Flt3	G	A	5: 147,291,905 (GRCm39)	Q540*	probably null	Het
Fmo4	T	A	1: 162,632,842 (GRCm39)	I170F	probably benign	Het
Fra10ac1	T	A	19: 38,207,910 (GRCm39)	D72V	possibly damaging	Het
Garin2	G	A	12: 78,761,890 (GRCm39)	E185K	probably damaging	Het
Gemin6	T	G	17: 80,535,178 (GRCm39)	V46G	probably damaging	Het
Gm2381	T	G	7: 42,469,425 (GRCm39)	H233P	probably damaging	Het
Gm5148	T	A	3: 37,768,995 (GRCm39)	Q75L	probably damaging	Het
Gm8369	T	C	19: 11,482,170 (GRCm39)	V27A	possibly damaging	Het
Gpr157	T	C	4: 150,186,825 (GRCm39)	S318P	probably benign	Het
Hectd4	G	A	5: 121,404,337 (GRCm39)	V405M	probably benign	Het
Hemgn	T	C	4: 46,400,738 (GRCm39)	R41G	probably benign	Het
Hhipl1	T	A	12: 108,294,467 (GRCm39)	L791Q	probably damaging	Het
Hjurp	T	G	1: 88,194,038 (GRCm39)	K290T	probably benign	Het
Ifi207	T	C	1: 173,555,363 (GRCm39)	E773G	probably damaging	Het
Kcnh6	T	C	11: 105,914,685 (GRCm39)	Y697H	probably damaging	Het
Lonrf2	T	C	1: 38,846,234 (GRCm39)	T313A	probably benign	Het
Lrba	G	T	3: 86,275,902 (GRCm39)	V1757L	probably benign	Het
Lrrc24	T	C	15: 76,600,306 (GRCm39)	T278A	probably benign	Het
Ltbp2	T	C	12: 84,856,428 (GRCm39)	I679V	probably null	Het
Mapk4	G	T	18: 74,064,073 (GRCm39)	T383K	probably benign	Het
Mdn1	C	T	4: 32,723,690 (GRCm39)	P2542L	probably damaging	Het
Mia3	A	G	1: 183,117,471 (GRCm39)	V208A	probably benign	Het
Myo15a	C	A	11: 60,411,603 (GRCm39)	C3234*	probably null	Het
Nlrp1b	G	T	11: 71,108,701 (GRCm39)	Q267K	probably benign	Het
Nphp3	A	G	9: 103,881,922 (GRCm39)	K37E	probably damaging	Het
Nwd2	T	C	5: 63,962,681 (GRCm39)	M755T	probably damaging	Het
Or10u4	T	A	10: 129,802,158 (GRCm39)	H137L	probably benign	Het
Or52ac1	A	G	7: 104,246,028 (GRCm39)	F120S	probably damaging	Het
Or5p58	A	G	7: 107,693,949 (GRCm39)	V276A	possibly damaging	Het
Pdlim5	C	T	3: 142,058,495 (GRCm39)	R83K	probably null	Het
Plekha5	A	T	6: 140,498,459 (GRCm39)	R173*	probably null	Het
Pramel25	T	A	4: 143,521,707 (GRCm39)	V441E	possibly damaging	Het
Rbms3	T	A	9: 117,080,853 (GRCm39)	D6V	possibly damaging	Het
Rhoq	A	T	17: 87,271,755 (GRCm39)	Y57F	probably benign	Het
Rrm1	A	T	7: 102,100,230 (GRCm39)	T204S	possibly damaging	Het
Slf1	A	T	13: 77,239,323 (GRCm39)	I447N	probably benign	Het
Smarcc2	T	A	10: 128,323,943 (GRCm39)		probably benign	Het
Spdye4c	C	T	2: 128,438,484 (GRCm39)	Q281*	probably null	Het
Tert	T	A	13: 73,792,403 (GRCm39)	M890K	probably benign	Het
Tln1	C	A	4: 43,543,905 (GRCm39)	R1198L	probably benign	Het
Tmco4	A	G	4: 138,748,178 (GRCm39)	M253V	probably damaging	Het
Usp19	G	T	9: 108,375,119 (GRCm39)	V782F	possibly damaging	Het
Usp33	T	A	3: 152,080,260 (GRCm39)	S464T	probably damaging	Het
Usp47	A	T	7: 111,673,928 (GRCm39)	Y397F	probably damaging	Het
Vmn1r12	A	G	6: 57,136,466 (GRCm39)	T144A	probably benign	Het
Vmn2r90	A	T	17: 17,954,386 (GRCm39)	H850L	probably benign	Het
Zfhx3	A	T	8: 109,682,842 (GRCm39)	Q3427L	unknown	Het
Zfp236	G	T	18: 82,700,281 (GRCm39)	Q63K	probably benign	Het
Zfp786	T	C	6: 47,796,619 (GRCm39)	E773G	probably damaging	Het

Other mutations in Zfp7

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00576:Zfp7	APN	15	76,775,101 (GRCm39)	intron	probably benign
IGL01509:Zfp7	APN	15	76,765,333 (GRCm39)	missense	probably damaging	1.00
IGL01694:Zfp7	APN	15	76,774,995 (GRCm39)	nonsense	probably null
IGL01731:Zfp7	APN	15	76,772,505 (GRCm39)	nonsense	probably null
IGL02025:Zfp7	APN	15	76,772,464 (GRCm39)	missense	probably damaging	1.00
R0841:Zfp7	UTSW	15	76,775,704 (GRCm39)	missense	probably damaging	1.00
R1345:Zfp7	UTSW	15	76,774,908 (GRCm39)	missense	probably damaging	1.00
R1625:Zfp7	UTSW	15	76,765,374 (GRCm39)	missense	probably damaging	1.00
R1872:Zfp7	UTSW	15	76,775,977 (GRCm39)	missense	probably benign	0.00
R2330:Zfp7	UTSW	15	76,775,509 (GRCm39)	missense	probably damaging	1.00
R4170:Zfp7	UTSW	15	76,775,818 (GRCm39)	missense	probably benign	0.00
R4795:Zfp7	UTSW	15	76,775,546 (GRCm39)	nonsense	probably null
R4796:Zfp7	UTSW	15	76,775,546 (GRCm39)	nonsense	probably null
R5038:Zfp7	UTSW	15	76,776,010 (GRCm39)	missense	probably benign	0.01
R5277:Zfp7	UTSW	15	76,765,403 (GRCm39)	missense	probably damaging	1.00
R5285:Zfp7	UTSW	15	76,775,422 (GRCm39)	missense	probably damaging	1.00
R5287:Zfp7	UTSW	15	76,775,422 (GRCm39)	missense	probably damaging	1.00
R5655:Zfp7	UTSW	15	76,775,629 (GRCm39)	missense	probably damaging	1.00
R6320:Zfp7	UTSW	15	76,774,810 (GRCm39)	missense	possibly damaging	0.79
R7063:Zfp7	UTSW	15	76,775,919 (GRCm39)	missense	possibly damaging	0.82
R8110:Zfp7	UTSW	15	76,775,131 (GRCm39)	missense	possibly damaging	0.94
R9058:Zfp7	UTSW	15	76,764,981 (GRCm39)	start codon destroyed	probably null	0.77
R9205:Zfp7	UTSW	15	76,774,800 (GRCm39)	intron	probably benign
R9206:Zfp7	UTSW	15	76,774,800 (GRCm39)	intron	probably benign
R9352:Zfp7	UTSW	15	76,775,674 (GRCm39)	missense	probably damaging	1.00
R9364:Zfp7	UTSW	15	76,774,800 (GRCm39)	intron	probably benign
R9368:Zfp7	UTSW	15	76,774,800 (GRCm39)	intron	probably benign
R9369:Zfp7	UTSW	15	76,774,800 (GRCm39)	intron	probably benign
R9372:Zfp7	UTSW	15	76,774,800 (GRCm39)	intron	probably benign
R9373:Zfp7	UTSW	15	76,774,800 (GRCm39)	intron	probably benign
R9373:Zfp7	UTSW	15	76,774,798 (GRCm39)	intron	probably benign
R9513:Zfp7	UTSW	15	76,775,484 (GRCm39)	missense	probably damaging	1.00
R9515:Zfp7	UTSW	15	76,775,484 (GRCm39)	missense	probably damaging	1.00
R9516:Zfp7	UTSW	15	76,775,484 (GRCm39)	missense	probably damaging	1.00
R9623:Zfp7	UTSW	15	76,774,531 (GRCm39)	missense	probably benign	0.16

Predicted Primers

PCR Primer
(F):5'- GCCTGAATCAGCACAAACTG -3'
(R):5'- CTGAAAGCTTTGCCACACTG -3'

Sequencing Primer
(F):5'- TTCATACTGGAGAGAAGCCTTACCG -3'
(R):5'- ACACTGCTCACACTTAAATGGCTTC -3'

Posted On

2016-09-01