Mutagenetix > Incidental Mutation

Incidental Mutation 'R5423:Zfp874a'

426724

Institutional Source

Beutler Lab

Gene Symbol

Zfp874a

Ensembl Gene

ENSMUSG00000069206

Gene Name

zinc finger protein 874a

Synonyms

C330011K17Rik, Zfp874, Rslcan15

MMRRC Submission

042989-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.078) question?

Stock #

R5423 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

67588550-67599743 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 67590473 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Phenylalanine at position 404 (L404F)

Ref Sequence

ENSEMBL: ENSMUSP00000074735 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000057241] [ENSMUST00000075255] [ENSMUST00000180580] [ENSMUST00000223682] [ENSMUST00000225479]

AlphaFold

Q8BX23

Predicted Effect

probably benign
Transcript: ENSMUST00000057241

SMART Domains

Protein: ENSMUSP00000077307
Gene: ENSMUSG00000069206

Domain	Start	End	E-Value	Type
KRAB	5	65	1.73e-27	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000075255
AA Change: L404F

PolyPhen 2 Score 0.747 (Sensitivity: 0.85; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000074735
Gene: ENSMUSG00000069206
AA Change: L404F

Domain	Start	End	E-Value	Type
KRAB	5	65	1.73e-27	SMART
ZnF_C2H2	137	159	9.58e-3	SMART
ZnF_C2H2	165	187	5.99e-4	SMART
ZnF_C2H2	193	215	7.26e-3	SMART
ZnF_C2H2	221	243	2.4e-3	SMART
ZnF_C2H2	249	269	1.88e2	SMART
ZnF_C2H2	277	299	5.21e-4	SMART
ZnF_C2H2	305	327	2.12e-4	SMART
ZnF_C2H2	333	355	2.12e-4	SMART
ZnF_C2H2	361	383	8.47e-4	SMART
ZnF_C2H2	389	411	1.79e-2	SMART
ZnF_C2H2	417	438	2.86e-1	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000180580

SMART Domains

Protein: ENSMUSP00000137953
Gene: ENSMUSG00000069206

Domain	Start	End	E-Value	Type
KRAB	5	65	1.73e-27	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000223682

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000224239

Predicted Effect

probably benign
Transcript: ENSMUST00000225479

Predicted Effect

probably benign
Transcript: ENSMUST00000225778

Meta Mutation Damage Score

0.0984

Coding Region Coverage

1x: 99.3%
3x: 98.6%
10x: 97.3%
20x: 95.3%

Validation Efficiency

98% (60/61)

Allele List at MGI

Other mutations in this stock

Total: 54 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acyp2	C	T	11: 30,456,354 (GRCm39)	E98K	possibly damaging	Het
Adam22	C	A	5: 8,140,182 (GRCm39)	G202W	probably damaging	Het
Adamts9	A	G	6: 92,857,678 (GRCm39)	I289T	possibly damaging	Het
Ak4	T	G	4: 101,317,760 (GRCm39)	I110S	probably damaging	Het
Arhgap9	T	G	10: 127,165,418 (GRCm39)	I609S	probably damaging	Het
Arid4a	C	A	12: 71,116,634 (GRCm39)	S242*	probably null	Het
Ceacam1	T	G	7: 25,173,951 (GRCm39)	I235L	probably benign	Het
Chil3	T	C	3: 106,055,978 (GRCm39)	D365G	probably damaging	Het
Ckap2	A	C	8: 22,667,212 (GRCm39)	S216R	probably benign	Het
Cyp2e1	G	T	7: 140,350,031 (GRCm39)	V239L	probably benign	Het
Dnah7b	T	A	1: 46,397,431 (GRCm39)	M3954K	probably benign	Het
Ercc6l2	A	T	13: 64,020,072 (GRCm39)		probably benign	Het
Etv5	T	C	16: 22,202,404 (GRCm39)	D468G	probably damaging	Het
Fbxo44	T	A	4: 148,238,686 (GRCm39)	I213F	probably benign	Het
Gm5084	A	G	13: 60,360,356 (GRCm39)		noncoding transcript	Het
Gpr17	G	A	18: 32,080,694 (GRCm39)	T123I	probably damaging	Het
Grin3a	A	G	4: 49,770,376 (GRCm39)		probably benign	Het
H2-D1	T	G	17: 35,484,883 (GRCm39)	L248R	probably damaging	Het
Hmcn1	T	C	1: 150,577,723 (GRCm39)	I2013V	probably damaging	Het
Hp1bp3	A	T	4: 137,953,208 (GRCm39)	D84V	probably damaging	Het
Ift140	T	C	17: 25,252,059 (GRCm39)	F33S	probably damaging	Het
Inhbc	C	G	10: 127,193,296 (GRCm39)	C240S	probably damaging	Het
Iqgap1	T	A	7: 80,449,610 (GRCm39)	E62V	probably damaging	Het
Kcna4	G	A	2: 107,126,151 (GRCm39)	W295*	probably null	Het
Kdm4a	C	T	4: 117,996,105 (GRCm39)	A975T	probably damaging	Het
Lrrtm3	T	C	10: 63,923,931 (GRCm39)	D412G	possibly damaging	Het
Midn	A	C	10: 79,991,027 (GRCm39)	I346L	probably benign	Het
Ndufa10	C	T	1: 92,390,042 (GRCm39)	D259N	probably benign	Het
Nefh	C	A	11: 4,890,985 (GRCm39)	A545S	possibly damaging	Het
Prpf8	A	G	11: 75,399,784 (GRCm39)	Y2281C	probably damaging	Het
Psip1	G	A	4: 83,378,367 (GRCm39)		probably benign	Het
Ptpro	G	T	6: 137,419,705 (GRCm39)	A184S	probably damaging	Het
Rab37	T	A	11: 115,047,853 (GRCm39)	I65K	possibly damaging	Het
Rasgrp4	T	C	7: 28,844,561 (GRCm39)	L247P	probably damaging	Het
Rnf20	T	C	4: 49,644,620 (GRCm39)	V295A	probably damaging	Het
Serpina3g	A	G	12: 104,204,253 (GRCm39)		probably benign	Het
Shox2	A	G	3: 66,881,087 (GRCm39)		probably benign	Het
Skint6	T	G	4: 112,707,937 (GRCm39)	D977A	possibly damaging	Het
Slc25a23	C	T	17: 57,360,597 (GRCm39)	V248M	probably damaging	Het
Slco1a7	T	A	6: 141,690,188 (GRCm39)	K188N	probably damaging	Het
Smg1	A	T	7: 117,745,294 (GRCm39)	D3008E	possibly damaging	Het
St18	A	G	1: 6,872,840 (GRCm39)	S192G	possibly damaging	Het
Supt20	T	A	3: 54,616,746 (GRCm39)	V306E	probably damaging	Het
T	T	C	17: 8,660,597 (GRCm39)	Y403H	probably damaging	Het
Tars3	C	A	7: 65,333,567 (GRCm39)	N588K	probably benign	Het
Tmem132c	T	C	5: 127,640,907 (GRCm39)	V1026A	probably benign	Het
Trpv4	T	C	5: 114,774,506 (GRCm39)	T193A	probably benign	Het
Ubqln4	A	G	3: 88,470,506 (GRCm39)	N326S	probably damaging	Het
Uggt2	G	A	14: 119,256,898 (GRCm39)	T1112I	probably damaging	Het
Vasn	C	T	16: 4,466,284 (GRCm39)	P77L	probably benign	Het
Vps9d1	A	C	8: 123,974,704 (GRCm39)		probably null	Het
Washc4	C	A	10: 83,415,418 (GRCm39)	Q803K	possibly damaging	Het
Zcchc2	C	T	1: 105,958,430 (GRCm39)	T967I	probably damaging	Het
Zscan30	T	C	18: 24,104,773 (GRCm39)		noncoding transcript	Het

Other mutations in Zfp874a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02490:Zfp874a	APN	13	67,590,819 (GRCm39)	nonsense	probably null
R1052:Zfp874a	UTSW	13	67,590,539 (GRCm39)	missense	possibly damaging	0.89
R1991:Zfp874a	UTSW	13	67,590,623 (GRCm39)	missense	probably benign	0.03
R2085:Zfp874a	UTSW	13	67,590,967 (GRCm39)	missense	probably damaging	1.00
R2103:Zfp874a	UTSW	13	67,590,623 (GRCm39)	missense	probably benign	0.03
R5129:Zfp874a	UTSW	13	67,591,100 (GRCm39)	missense	probably damaging	1.00
R5336:Zfp874a	UTSW	13	67,590,799 (GRCm39)	missense	probably damaging	1.00
R5713:Zfp874a	UTSW	13	67,597,476 (GRCm39)	missense	probably benign	0.16
R5855:Zfp874a	UTSW	13	67,590,812 (GRCm39)	missense	probably benign	0.03
R6496:Zfp874a	UTSW	13	67,590,694 (GRCm39)	missense	possibly damaging	0.62
R7046:Zfp874a	UTSW	13	67,590,418 (GRCm39)	missense	probably damaging	1.00
R7065:Zfp874a	UTSW	13	67,590,401 (GRCm39)	missense	probably damaging	0.97
R7233:Zfp874a	UTSW	13	67,590,776 (GRCm39)	missense	possibly damaging	0.83
R7271:Zfp874a	UTSW	13	67,591,415 (GRCm39)	missense	probably benign	0.00
R7465:Zfp874a	UTSW	13	67,590,376 (GRCm39)	missense	probably damaging	0.99
R7468:Zfp874a	UTSW	13	67,573,723 (GRCm39)	splice site	probably null
R8108:Zfp874a	UTSW	13	67,591,353 (GRCm39)	nonsense	probably null
R8109:Zfp874a	UTSW	13	67,597,563 (GRCm39)	missense	possibly damaging	0.46
R8843:Zfp874a	UTSW	13	67,590,764 (GRCm39)	missense	probably damaging	1.00
R8859:Zfp874a	UTSW	13	67,590,647 (GRCm39)	missense	probably benign	0.17
R9137:Zfp874a	UTSW	13	67,590,841 (GRCm39)	missense	probably damaging	1.00
R9673:Zfp874a	UTSW	13	67,591,156 (GRCm39)	missense	probably benign	0.03
X0063:Zfp874a	UTSW	13	67,591,106 (GRCm39)	missense	probably damaging	1.00
Z1177:Zfp874a	UTSW	13	67,590,781 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TTCCTGTAGGTGGAAAGAACTAGAA -3'
(R):5'- TGCTATCGTTCATATCTTAGGGAA -3'

Sequencing Primer
(F):5'- GGAAAGAACTAGAAAATCTTTTGCC -3'
(R):5'- AGAATGCATTCTGGAGAGTATCCC -3'

Posted On

2016-09-01