Mutagenetix > Incidental Mutation

Incidental Mutation 'R0071:Zfp607a'

43847

Institutional Source

Beutler Lab

Gene Symbol

Zfp607a

Ensembl Gene

ENSMUSG00000020420

Gene Name

zinc finger protein 607A

Synonyms

Zfp607, 4732475C15Rik

MMRRC Submission

038362-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.058) question?

Stock #

R0071 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

27556952-27580250 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 27577694 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Glutamic Acid at position 255 (K255E)

Ref Sequence

ENSEMBL: ENSMUSP00000146006 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000053722] [ENSMUST00000205534] [ENSMUST00000205715]

AlphaFold

Q3TQG9

Predicted Effect

probably damaging
Transcript: ENSMUST00000053722
AA Change: K255E

PolyPhen 2 Score 0.962 (Sensitivity: 0.78; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000051496
Gene: ENSMUSG00000020420
AA Change: K255E

Domain	Start	End	E-Value	Type
KRAB	14	75	8.48e-36	SMART
ZnF_C2H2	173	195	2.91e-2	SMART
ZnF_C2H2	201	223	3.44e-4	SMART
ZnF_C2H2	229	251	3.83e-2	SMART
ZnF_C2H2	257	279	4.87e-4	SMART
ZnF_C2H2	285	307	1.38e-3	SMART
ZnF_C2H2	313	335	4.17e-3	SMART
ZnF_C2H2	341	363	2.86e-1	SMART
ZnF_C2H2	369	391	5.14e-3	SMART
ZnF_C2H2	397	419	1.2e-3	SMART
ZnF_C2H2	425	447	4.47e-3	SMART
ZnF_C2H2	453	475	1.1e-2	SMART
ZnF_C2H2	481	503	1.45e-2	SMART
ZnF_C2H2	509	531	1.12e-3	SMART
ZnF_C2H2	537	559	1.5e-4	SMART
ZnF_C2H2	565	587	8.34e-3	SMART
ZnF_C2H2	593	615	1.12e-3	SMART
ZnF_C2H2	621	643	6.42e-4	SMART
ZnF_C2H2	649	671	6.23e-2	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000205534
AA Change: K255E

PolyPhen 2 Score 0.962 (Sensitivity: 0.78; Specificity: 0.95)

Predicted Effect

probably damaging
Transcript: ENSMUST00000205715
AA Change: K255E

PolyPhen 2 Score 0.962 (Sensitivity: 0.78; Specificity: 0.95)

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000206136

Coding Region Coverage

1x: 99.1%
3x: 98.2%
10x: 96.0%
20x: 92.2%

Validation Efficiency

99% (78/79)

Allele List at MGI

Other mutations in this stock

Total: 78 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930474N05Rik	A	G	14: 35,812,746 (GRCm39)		probably benign	Het
Acot12	T	C	13: 91,929,293 (GRCm39)		probably benign	Het
Acrbp	T	C	6: 125,027,915 (GRCm39)		probably benign	Het
Amotl1	G	A	9: 14,460,069 (GRCm39)	A890V	probably benign	Het
Aox3	T	A	1: 58,211,050 (GRCm39)	C931*	probably null	Het
Apob	T	A	12: 8,052,111 (GRCm39)	V1184E	probably damaging	Het
Arhgap44	A	T	11: 64,902,721 (GRCm39)	L582Q	possibly damaging	Het
Bbx	C	T	16: 50,100,755 (GRCm39)	E47K	probably benign	Het
Bccip	A	G	7: 133,315,960 (GRCm39)	D72G	probably damaging	Het
Bckdha	A	T	7: 25,329,868 (GRCm39)		probably null	Het
Bmerb1	A	G	16: 13,906,818 (GRCm39)	D11G	probably damaging	Het
Cald1	C	T	6: 34,735,069 (GRCm39)		probably benign	Het
Cby2	A	G	14: 75,821,621 (GRCm39)	S44P	probably benign	Het
Cdk11b	T	C	4: 155,733,880 (GRCm39)		probably benign	Het
Cebpe	G	T	14: 54,948,061 (GRCm39)	R261S	probably damaging	Het
Cep95	C	T	11: 106,681,554 (GRCm39)		probably benign	Het
Chi3l1	T	C	1: 134,113,017 (GRCm39)	Y150H	probably benign	Het
Chrnd	T	C	1: 87,120,559 (GRCm39)		probably benign	Het
Clec4g	T	A	8: 3,767,489 (GRCm39)		probably benign	Het
Cog2	T	C	8: 125,275,407 (GRCm39)		probably benign	Het
Coro7	A	T	16: 4,488,391 (GRCm39)	L93Q	probably damaging	Het
Csmd3	T	C	15: 47,460,217 (GRCm39)	T3525A	probably benign	Het
Ctsc	G	A	7: 87,957,357 (GRCm39)		probably benign	Het
Dnajc16	T	C	4: 141,495,318 (GRCm39)	T467A	probably benign	Het
Dnmt1	G	A	9: 20,819,916 (GRCm39)	T1409I	probably damaging	Het
Fam227b	T	A	2: 125,965,994 (GRCm39)	N144Y	probably benign	Het
Fam83h	A	G	15: 75,874,377 (GRCm39)	S987P	probably benign	Het
Fhod1	A	T	8: 106,063,857 (GRCm39)		probably null	Het
Folr1	A	G	7: 101,513,130 (GRCm39)		probably null	Het
Glis3	C	T	19: 28,241,255 (GRCm39)		probably benign	Het
Gm10069	T	C	6: 128,449,688 (GRCm39)		noncoding transcript	Het
Golgb1	G	A	16: 36,735,865 (GRCm39)	R1704Q	probably benign	Het
Gpr158	C	A	2: 21,815,479 (GRCm39)	T624K	probably benign	Het
Helz2	T	C	2: 180,878,200 (GRCm39)	Y866C	probably damaging	Het
Itpkb	T	A	1: 180,160,330 (GRCm39)	V152E	probably damaging	Het
Kcnma1	C	T	14: 23,576,835 (GRCm39)	R236H	probably damaging	Het
Klhl32	A	G	4: 24,743,907 (GRCm39)	V88A	probably damaging	Het
Lct	C	T	1: 128,219,755 (GRCm39)	W1631*	probably null	Het
Lipa	T	A	19: 34,472,482 (GRCm39)	K313M	probably damaging	Het
Ly75	T	C	2: 60,152,163 (GRCm39)	K1130R	probably benign	Het
Mamdc2	C	A	19: 23,280,994 (GRCm39)	E685*	probably null	Het
Mdm1	A	G	10: 117,982,701 (GRCm39)	E112G	probably damaging	Het
Metrnl	A	T	11: 121,606,826 (GRCm39)	M212L	probably benign	Het
Mettl2	A	G	11: 105,022,468 (GRCm39)		probably benign	Het
Mxd3	A	T	13: 55,477,449 (GRCm39)	L11Q	probably damaging	Het
Myo7a	A	T	7: 97,706,037 (GRCm39)	Y1836N	probably damaging	Het
Nsun7	A	G	5: 66,421,388 (GRCm39)	Y118C	probably benign	Het
Obscn	G	A	11: 58,955,027 (GRCm39)	T3962M	possibly damaging	Het
Or13a20	A	T	7: 140,232,170 (GRCm39)	I93F	probably benign	Het
Or2d36	A	G	7: 106,746,919 (GRCm39)	Y132C	probably damaging	Het
Or5k3	C	A	16: 58,969,578 (GRCm39)	R122S	probably benign	Het
Osbpl11	T	C	16: 33,034,708 (GRCm39)		probably benign	Het
Pcdhb22	A	T	18: 37,653,131 (GRCm39)	D276V	probably damaging	Het
Pik3cb	A	T	9: 98,926,918 (GRCm39)	D886E	probably benign	Het
Pkhd1	T	A	1: 20,271,568 (GRCm39)	Y2995F	probably benign	Het
Raver2	C	T	4: 100,977,642 (GRCm39)		probably benign	Het
Rhbdf1	A	G	11: 32,160,498 (GRCm39)	L684P	probably damaging	Het
Rufy2	C	A	10: 62,824,946 (GRCm39)	L75M	possibly damaging	Het
Sec22c	A	G	9: 121,521,979 (GRCm39)	F44L	probably damaging	Het
Sephs1	A	G	2: 4,904,371 (GRCm39)	T250A	probably benign	Het
Serpina1a	T	C	12: 103,822,002 (GRCm39)	K310R	probably benign	Het
Shoc1	A	G	4: 59,059,643 (GRCm39)	Y1006H	possibly damaging	Het
Sobp	A	G	10: 43,033,993 (GRCm39)	L111P	probably damaging	Het
Sparcl1	G	T	5: 104,233,707 (GRCm39)	Y547*	probably null	Het
Spata31d1b	G	A	13: 59,863,163 (GRCm39)	A104T	probably benign	Het
Spsb3	A	G	17: 25,106,878 (GRCm39)	D184G	probably damaging	Het
Sptan1	A	T	2: 29,893,354 (GRCm39)	K1148*	probably null	Het
Tdrd12	A	G	7: 35,228,671 (GRCm39)	V17A	possibly damaging	Het
Tlr9	A	G	9: 106,100,777 (GRCm39)	T23A	probably benign	Het
Tra2b	A	T	16: 22,073,151 (GRCm39)		probably benign	Het
Tspan15	A	G	10: 62,038,849 (GRCm39)		probably benign	Het
Ttc41	A	G	10: 86,572,710 (GRCm39)	N694S	probably benign	Het
Ttn	T	G	2: 76,597,813 (GRCm39)	D19700A	probably damaging	Het
Ube3b	G	A	5: 114,557,558 (GRCm39)	G1014D	probably damaging	Het
Unc5d	A	G	8: 29,209,854 (GRCm39)	V422A	possibly damaging	Het
Vmn2r80	C	T	10: 79,007,566 (GRCm39)	T514I	possibly damaging	Het
Zfp595	T	C	13: 67,464,917 (GRCm39)	K452E	possibly damaging	Het
Zxdc	T	G	6: 90,347,398 (GRCm39)	V253G	probably damaging	Het

Other mutations in Zfp607a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00164:Zfp607a	APN	7	27,577,214 (GRCm39)	missense	possibly damaging	0.55
IGL01019:Zfp607a	APN	7	27,578,042 (GRCm39)	missense	probably damaging	1.00
IGL01412:Zfp607a	APN	7	27,578,109 (GRCm39)	missense	probably damaging	0.99
IGL03206:Zfp607a	APN	7	27,577,248 (GRCm39)	missense	possibly damaging	0.52
R0304:Zfp607a	UTSW	7	27,578,637 (GRCm39)	missense	possibly damaging	0.92
R0685:Zfp607a	UTSW	7	27,577,901 (GRCm39)	missense	probably damaging	0.97
R0726:Zfp607a	UTSW	7	27,578,574 (GRCm39)	missense	probably benign	0.00
R1201:Zfp607a	UTSW	7	27,578,736 (GRCm39)	missense	probably damaging	1.00
R1304:Zfp607a	UTSW	7	27,565,000 (GRCm39)	missense	probably benign	0.00
R1648:Zfp607a	UTSW	7	27,578,493 (GRCm39)	missense	probably benign	0.02
R1732:Zfp607a	UTSW	7	27,577,884 (GRCm39)	missense	probably damaging	1.00
R2194:Zfp607a	UTSW	7	27,578,805 (GRCm39)	missense	possibly damaging	0.73
R3793:Zfp607a	UTSW	7	27,578,331 (GRCm39)	missense	probably benign	0.01
R3808:Zfp607a	UTSW	7	27,578,826 (GRCm39)	missense	probably benign	0.01
R4296:Zfp607a	UTSW	7	27,565,073 (GRCm39)	missense	probably damaging	1.00
R4786:Zfp607a	UTSW	7	27,578,838 (GRCm39)	missense	probably damaging	1.00
R4792:Zfp607a	UTSW	7	27,578,078 (GRCm39)	missense	probably benign	0.23
R4915:Zfp607a	UTSW	7	27,577,985 (GRCm39)	missense	probably benign	0.00
R4950:Zfp607a	UTSW	7	27,578,176 (GRCm39)	missense	probably damaging	1.00
R5123:Zfp607a	UTSW	7	27,578,523 (GRCm39)	missense	probably damaging	1.00
R5217:Zfp607a	UTSW	7	27,577,269 (GRCm39)	missense	probably damaging	0.97
R5270:Zfp607a	UTSW	7	27,577,730 (GRCm39)	nonsense	probably null
R5403:Zfp607a	UTSW	7	27,578,744 (GRCm39)	missense	possibly damaging	0.54
R6010:Zfp607a	UTSW	7	27,577,254 (GRCm39)	nonsense	probably null
R6224:Zfp607a	UTSW	7	27,578,007 (GRCm39)	missense	probably damaging	1.00
R6939:Zfp607a	UTSW	7	27,578,473 (GRCm39)	nonsense	probably null
R6953:Zfp607a	UTSW	7	27,577,790 (GRCm39)	missense	possibly damaging	0.59
R7082:Zfp607a	UTSW	7	27,578,183 (GRCm39)	missense	probably damaging	1.00
R7781:Zfp607a	UTSW	7	27,565,000 (GRCm39)	missense	possibly damaging	0.90
R7909:Zfp607a	UTSW	7	27,578,519 (GRCm39)	missense	probably damaging	1.00
R8191:Zfp607a	UTSW	7	27,578,868 (GRCm39)	missense	possibly damaging	0.93
R8224:Zfp607a	UTSW	7	27,577,536 (GRCm39)	missense	probably damaging	1.00
R8949:Zfp607a	UTSW	7	27,577,944 (GRCm39)	missense	possibly damaging	0.56
R8962:Zfp607a	UTSW	7	27,578,786 (GRCm39)	missense	possibly damaging	0.79
R9178:Zfp607a	UTSW	7	27,577,382 (GRCm39)	missense	probably benign	0.00
R9802:Zfp607a	UTSW	7	27,578,704 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CCTGCCAGACTCTTGCTCACAATAC -3'
(R):5'- GAAGCTCTTCCCACAGTCCTTACAC -3'

Sequencing Primer
(F):5'- tgttcatgctggagagaaacc -3'
(R):5'- AGTCCTTACACTGAAAGGGTCTC -3'

Posted On

2013-05-29