Mutagenetix > Incidental Mutation

Incidental Mutation 'R5270:Zfp607a'

400195

Institutional Source

Beutler Lab

Gene Symbol

Zfp607a

Ensembl Gene

ENSMUSG00000020420

Gene Name

zinc finger protein 607A

Synonyms

Zfp607, 4732475C15Rik

MMRRC Submission

042835-MU

Accession Numbers

Essential gene?

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

Stock #

R5270 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

27556952-27580250 bp(+) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

A to T at 27577730 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Stop codon at position 267 (K267*)

Ref Sequence

ENSEMBL: ENSMUSP00000146006 (fasta)

Gene Model

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

AlphaFold

Q3TQG9

Predicted Effect

probably null
Transcript: ENSMUST00000053722
AA Change: K267*

SMART Domains

Protein: ENSMUSP00000051496
Gene: ENSMUSG00000020420
AA Change: K267*

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 null
Transcript: ENSMUST00000205534
AA Change: K267*

Predicted Effect

probably null
Transcript: ENSMUST00000205715
AA Change: K267*

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000206136

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.3%
20x: 95.6%

Validation Efficiency

98% (59/60)

Allele List at MGI

Other mutations in this stock

Total: 50 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acsl5	T	C	19: 55,282,650 (GRCm39)	V585A	possibly damaging	Het
Adam6a	A	T	12: 113,507,747 (GRCm39)	H40L	possibly damaging	Het
Adamts20	G	A	15: 94,180,400 (GRCm39)	P1752S	probably benign	Het
Atp5if1	A	G	4: 132,260,611 (GRCm39)	F27L	probably damaging	Het
B230104I21Rik	A	G	4: 154,434,050 (GRCm39)		probably benign	Het
Ciz1	C	A	2: 32,264,511 (GRCm39)		probably null	Het
Crb1	T	A	1: 139,164,602 (GRCm39)	Y1174F	probably damaging	Het
Csf2rb2	A	T	15: 78,176,182 (GRCm39)		probably null	Het
Cyp3a25	A	T	5: 145,918,312 (GRCm39)	M433K	probably benign	Het
Dock4	A	G	12: 40,783,270 (GRCm39)	I735V	probably benign	Het
Dpp6	C	T	5: 27,839,532 (GRCm39)	S349L	probably damaging	Het
Epg5	T	A	18: 78,026,778 (GRCm39)	N1256K	possibly damaging	Het
Epha4	A	G	1: 77,483,244 (GRCm39)	V255A	probably damaging	Het
Gabrb1	A	T	5: 72,265,669 (GRCm39)	D155V	probably damaging	Het
Gpr35	A	T	1: 92,910,299 (GRCm39)	T4S	probably benign	Het
Hcrt	T	C	11: 100,652,823 (GRCm39)	T64A	probably damaging	Het
Henmt1	G	A	3: 108,867,530 (GRCm39)	R355H	probably benign	Het
Hrh1	C	A	6: 114,458,179 (GRCm39)	R487S	possibly damaging	Het
Ints2	T	C	11: 86,106,621 (GRCm39)	S930G	probably damaging	Het
Irs2	G	A	8: 11,056,678 (GRCm39)	Q585*	probably null	Het
Kcns1	C	A	2: 164,010,249 (GRCm39)	R170L	probably benign	Het
Kdm3b	T	C	18: 34,960,467 (GRCm39)	S1351P	probably damaging	Het
Ly9	T	C	1: 171,428,730 (GRCm39)	T297A	probably damaging	Het
M6pr	G	A	6: 122,292,048 (GRCm39)	D127N	possibly damaging	Het
Macir	T	C	1: 97,573,720 (GRCm39)	Q115R	probably damaging	Het
Nhsl3	T	C	4: 129,118,005 (GRCm39)	T208A	possibly damaging	Het
Nit2	G	A	16: 56,977,494 (GRCm39)	P179S	probably damaging	Het
Per1	T	C	11: 68,994,424 (GRCm39)	M516T	probably benign	Het
Pkdrej	A	T	15: 85,702,528 (GRCm39)	I1136N	probably damaging	Het
Pramel27	A	G	4: 143,578,468 (GRCm39)	M243V	probably damaging	Het
Prdm9	G	T	17: 15,773,625 (GRCm39)	T257K	probably benign	Het
Prkdc	T	C	16: 15,552,819 (GRCm39)	L2085P	probably damaging	Het
Rasgrf1	A	C	9: 89,908,747 (GRCm39)	E1240D	probably benign	Het
Rrh	T	C	3: 129,606,998 (GRCm39)	I142V	probably benign	Het
Saal1	G	T	7: 46,351,157 (GRCm39)		probably benign	Het
Sdcbp2	A	G	2: 151,426,812 (GRCm39)	I70V	probably benign	Het
Skida1	C	A	2: 18,052,460 (GRCm39)	A231S	probably benign	Het
Smtnl2	T	A	11: 72,290,743 (GRCm39)	T401S	probably benign	Het
Sntb1	C	G	15: 55,506,191 (GRCm39)	G461R	probably damaging	Het
Spag4	G	T	2: 155,907,853 (GRCm39)		probably benign	Het
Tbc1d9	A	G	8: 83,960,283 (GRCm39)	M179V	probably benign	Het
Tm9sf1	G	T	14: 55,873,938 (GRCm39)	T520N	probably damaging	Het
Tmem163	G	A	1: 127,419,289 (GRCm39)		probably benign	Het
Vmn1r47	A	T	6: 89,999,525 (GRCm39)	Q219L	probably damaging	Het
Vmn2r104	A	T	17: 20,258,528 (GRCm39)	C539S	probably damaging	Het
Wdr17	G	T	8: 55,096,221 (GRCm39)	S1024R	probably benign	Het
Zc3h4	A	G	7: 16,168,440 (GRCm39)	T850A	unknown	Het
Zfa-ps	A	G	10: 52,419,552 (GRCm39)		noncoding transcript	Het
Zfp146	G	T	7: 29,861,900 (GRCm39)	N47K	probably benign	Het
Zfp353-ps	G	T	8: 42,534,572 (GRCm39)		noncoding transcript	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
R0071:Zfp607a	UTSW	7	27,577,694 (GRCm39)	missense	probably damaging	0.96
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
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'- TCACACCTGCCAGACTCTTG -3'
(R):5'- ATGAAGCTCTTCCCACAGTCC -3'

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

Posted On

2016-07-06