Mutagenetix > Incidental Mutation

Incidental Mutation 'R8774:Zfp867'

664614

Institutional Source

Beutler Lab

Gene Symbol

Zfp867

Ensembl Gene

ENSMUSG00000054519

Gene Name

zinc finger protein 867

Synonyms

MMRRC Submission

068628-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.438) question?

Stock #

R8774 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

59352023-59363300 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 59354837 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Serine at position 164 (F164S)

Ref Sequence

ENSEMBL: ENSMUSP00000050746 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000057799]

AlphaFold

E9Q2M4

Predicted Effect

probably damaging
Transcript: ENSMUST00000057799
AA Change: F164S

PolyPhen 2 Score 0.961 (Sensitivity: 0.78; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000050746
Gene: ENSMUSG00000054519
AA Change: F164S

Domain	Start	End	E-Value	Type
KRAB	12	70	1.36e-16	SMART
low complexity region	84	90	N/A	INTRINSIC
ZnF_C2H2	121	143	4.47e-3	SMART
ZnF_C2H2	149	171	5.59e-4	SMART
ZnF_C2H2	177	199	5.5e-3	SMART
ZnF_C2H2	205	227	5.14e-3	SMART
ZnF_C2H2	233	255	1.2e-3	SMART
ZnF_C2H2	261	283	5.5e-3	SMART
ZnF_C2H2	289	311	1.38e-3	SMART
ZnF_C2H2	317	339	5.42e-2	SMART
ZnF_C2H2	346	368	1.47e-3	SMART
ZnF_C2H2	374	396	7.11e0	SMART
ZnF_C2H2	402	424	1.69e-3	SMART

Meta Mutation Damage Score

0.4466

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.2%

Validation Efficiency

100% (67/67)

Allele List at MGI

Other mutations in this stock

Total: 66 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca1	A	G	4: 53,090,358 (GRCm39)	S364P	possibly damaging	Het
Abcc2	T	A	19: 43,787,577 (GRCm39)	Y208N	probably damaging	Het
Acy1	A	T	9: 106,313,913 (GRCm39)	D82E	probably damaging	Het
Ankub1	A	G	3: 57,597,802 (GRCm39)	L56P	probably damaging	Het
Aoc1	T	A	6: 48,885,529 (GRCm39)	F678Y	probably damaging	Het
Asxl3	C	A	18: 22,657,101 (GRCm39)	Q1704K	probably damaging	Het
Atg9b	T	C	5: 24,595,571 (GRCm39)	D236G	probably damaging	Het
Auh	A	T	13: 52,993,631 (GRCm39)	M261K	probably benign	Het
C2cd6	A	T	1: 59,099,825 (GRCm39)	M372K	possibly damaging	Het
Ccdc88b	A	T	19: 6,825,090 (GRCm39)	N1287K	probably damaging	Het
Cebpz	A	G	17: 79,229,073 (GRCm39)	S958P	probably benign	Het
Cgn	T	A	3: 94,680,810 (GRCm39)	Q576L	probably damaging	Het
Chd7	T	A	4: 8,854,692 (GRCm39)	M2011K	probably damaging	Het
Cntnap4	A	G	8: 113,529,820 (GRCm39)	E676G	probably benign	Het
Cspp1	A	T	1: 10,183,139 (GRCm39)	E781D	possibly damaging	Het
Cyb5d2	A	C	11: 72,679,901 (GRCm39)		probably null	Het
Epn3	G	T	11: 94,383,220 (GRCm39)	P335T	possibly damaging	Het
Far2	T	A	6: 148,047,629 (GRCm39)	S103T	probably benign	Het
Fhip1a	G	C	3: 85,580,097 (GRCm39)	Q703E	probably benign	Het
Fhl2	A	G	1: 43,162,751 (GRCm39)	S255P	probably damaging	Het
Fmnl2	T	A	2: 52,932,321 (GRCm39)	V100D		Het
Gabbr1	T	C	17: 37,382,749 (GRCm39)	L814P	probably damaging	Het
Gzmg	C	T	14: 56,394,193 (GRCm39)	V234I	probably benign	Het
Ift172	A	G	5: 31,415,207 (GRCm39)	V1334A	probably benign	Het
Itga8	C	G	2: 12,187,495 (GRCm39)	G728A	probably damaging	Het
Klrg1	T	C	6: 122,255,193 (GRCm39)	T80A	probably benign	Het
Lrp4	A	G	2: 91,308,043 (GRCm39)	N496S	probably benign	Het
Lsmem1	G	T	12: 40,227,145 (GRCm39)	N113K	probably damaging	Het
Map3k2	G	A	18: 32,345,117 (GRCm39)	S314N	probably damaging	Het
Mtpap	C	T	18: 4,387,032 (GRCm39)	R361*	probably null	Het
Muc5b	T	A	7: 141,418,831 (GRCm39)	S3926T	probably benign	Het
Nat10	C	A	2: 103,561,752 (GRCm39)	R643L	probably damaging	Het
Ncbp3	T	C	11: 72,938,808 (GRCm39)	V28A	probably benign	Het
Nlrp9a	T	C	7: 26,257,984 (GRCm39)	L534P	possibly damaging	Het
Nmi	T	C	2: 51,848,974 (GRCm39)	K39E	probably benign	Het
Nxpe4	A	G	9: 48,304,692 (GRCm39)	N260D	probably benign	Het
Or4k38	T	C	2: 111,166,318 (GRCm39)	Y35C	probably damaging	Het
Or51aa2	C	A	7: 103,187,965 (GRCm39)	V159L	probably benign	Het
Or6c213	T	A	10: 129,573,926 (GRCm39)	I287F	probably damaging	Het
Or8c19-ps1	G	A	9: 38,220,600 (GRCm39)	A170T	unknown	Het
Phf2	G	T	13: 48,971,878 (GRCm39)		probably benign	Het
Pirb	G	T	7: 3,720,728 (GRCm39)	L257M	probably damaging	Het
Plcg2	A	T	8: 118,306,585 (GRCm39)	D313V	possibly damaging	Het
Ppard	G	A	17: 28,517,864 (GRCm39)	V311I	possibly damaging	Het
Ptcd1	A	T	5: 145,092,175 (GRCm39)	M308K	probably damaging	Het
Pygo1	A	G	9: 72,852,436 (GRCm39)	N208D	possibly damaging	Het
Robo1	T	G	16: 72,832,719 (GRCm39)	D1497E	probably benign	Het
Sdk2	T	C	11: 113,730,169 (GRCm39)	D1022G	probably damaging	Het
Shc3	G	A	13: 51,615,475 (GRCm39)	H161Y	probably damaging	Het
Slc15a1	G	T	14: 121,724,423 (GRCm39)	Q150K	probably damaging	Het
Slc6a11	C	A	6: 114,206,995 (GRCm39)		probably benign	Het
Sod1	T	G	16: 90,023,039 (GRCm39)	V120G	probably damaging	Het
Spata31g1	T	C	4: 42,971,087 (GRCm39)	L140P	probably damaging	Het
Sprr2f	T	A	3: 92,273,323 (GRCm39)	C41S	unknown	Het
Svil	A	T	18: 5,049,068 (GRCm39)	Y115F	probably damaging	Het
Tdp1	T	C	12: 99,877,917 (GRCm39)	S400P	probably damaging	Het
Thbs4	A	T	13: 92,898,030 (GRCm39)	D596E	probably damaging	Het
Tshz1	T	A	18: 84,033,101 (GRCm39)	M436L	possibly damaging	Het
Ube3c	C	T	5: 29,812,029 (GRCm39)	T423I	probably benign	Het
Unc93a	A	T	17: 13,341,837 (GRCm39)	I98N	probably damaging	Het
Usp33	T	A	3: 152,085,213 (GRCm39)	Y624*	probably null	Het
Utp20	A	G	10: 88,588,763 (GRCm39)		probably benign	Het
Vmn1r217	T	A	13: 23,298,108 (GRCm39)	M265L	probably benign	Het
Vmn1r222	A	T	13: 23,416,418 (GRCm39)	M265K	probably benign	Het
Vmn2r16	C	T	5: 109,488,231 (GRCm39)	T368M	probably benign	Het
Zswim1	C	T	2: 164,668,062 (GRCm39)	T438I	probably benign	Het

Other mutations in Zfp867

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL03156:Zfp867	APN	11	59,355,834 (GRCm39)	splice site	probably benign
IGL03338:Zfp867	APN	11	59,355,003 (GRCm39)	nonsense	probably null
R0040:Zfp867	UTSW	11	59,354,691 (GRCm39)	missense	possibly damaging	0.88
R1997:Zfp867	UTSW	11	59,354,417 (GRCm39)	missense	probably damaging	0.98
R2251:Zfp867	UTSW	11	59,356,319 (GRCm39)	nonsense	probably null
R4015:Zfp867	UTSW	11	59,354,520 (GRCm39)	missense	probably damaging	1.00
R4429:Zfp867	UTSW	11	59,355,863 (GRCm39)	missense	possibly damaging	0.55
R4697:Zfp867	UTSW	11	59,354,487 (GRCm39)	missense	probably damaging	1.00
R7428:Zfp867	UTSW	11	59,354,760 (GRCm39)	missense	probably benign	0.03
R7736:Zfp867	UTSW	11	59,354,016 (GRCm39)	missense	probably damaging	1.00
R8075:Zfp867	UTSW	11	59,355,066 (GRCm39)	missense	probably benign
R8774-TAIL:Zfp867	UTSW	11	59,354,837 (GRCm39)	missense	probably damaging	0.96
R9674:Zfp867	UTSW	11	59,355,850 (GRCm39)	missense	probably benign	0.06

Predicted Primers

PCR Primer
(F):5'- TCATAGGGCTTCTCTCCAGTG -3'
(R):5'- CACAGTATAGGAGCTCTTTCATTTCTC -3'

Sequencing Primer
(F):5'- TTCATGAATTTGGAGATAACTGGGAC -3'
(R):5'- AGGAGCTCTTTCATTTCTCTTATGAG -3'

Posted On

2021-03-08