Mutagenetix > Incidental Mutation

Incidental Mutation 'R7029:Zfp874b'

546193

Institutional Source

Beutler Lab

Gene Symbol

Zfp874b

Ensembl Gene

ENSMUSG00000059839

Gene Name

zinc finger protein 874b

Synonyms

9630025I21Rik

MMRRC Submission

045130-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.103) question?

Stock #

R7029 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

67619632-67632377 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 67622392 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Cysteine at position 302 (Y302C)

Ref Sequence

ENSEMBL: ENSMUSP00000019572 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000019572] [ENSMUST00000223868]

AlphaFold

Q7M6X2

Predicted Effect

probably damaging
Transcript: ENSMUST00000019572
AA Change: Y302C

PolyPhen 2 Score 0.976 (Sensitivity: 0.76; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000019572
Gene: ENSMUSG00000059839
AA Change: Y302C

Domain	Start	End	E-Value	Type
KRAB	5	65	4.48e-26	SMART
ZnF_C2H2	136	158	5.9e-3	SMART
ZnF_C2H2	164	186	3.16e-3	SMART
ZnF_C2H2	192	214	6.78e-3	SMART
ZnF_C2H2	220	242	2.4e-3	SMART
ZnF_C2H2	248	268	1.88e2	SMART
ZnF_C2H2	276	298	6.42e-4	SMART
ZnF_C2H2	304	326	2.12e-4	SMART
ZnF_C2H2	332	354	1.28e-3	SMART
ZnF_C2H2	360	382	8.47e-4	SMART
ZnF_C2H2	388	410	1.79e-2	SMART
ZnF_C2H2	416	438	1.47e-3	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000223868

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.0%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 41 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700034J05Rik	T	C	6: 146,853,841 (GRCm39)	Q271R	probably benign	Het
Abhd4	T	A	14: 54,500,164 (GRCm39)	W63R	probably damaging	Het
Adcy5	A	G	16: 35,120,018 (GRCm39)	M1176V	probably null	Het
Bach1	G	A	16: 87,516,179 (GRCm39)	R240Q	probably benign	Het
Brox	G	A	1: 183,065,750 (GRCm39)	P206L	possibly damaging	Het
Ccn3	A	G	15: 54,611,171 (GRCm39)	D102G	possibly damaging	Het
Def6	A	G	17: 28,444,943 (GRCm39)	K447R	probably benign	Het
Dna2	T	C	10: 62,799,773 (GRCm39)	S726P	probably damaging	Het
Ell	G	A	8: 71,031,879 (GRCm39)	V15I	probably damaging	Het
Entrep2	T	A	7: 64,409,075 (GRCm39)	T440S	probably benign	Het
Epha3	T	A	16: 63,593,698 (GRCm39)	D130V	probably benign	Het
Gys1	A	G	7: 45,089,008 (GRCm39)	T200A	possibly damaging	Het
Habp4	A	T	13: 64,309,939 (GRCm39)	H47L	probably benign	Het
Iqcn	G	T	8: 71,161,511 (GRCm39)	V235L	possibly damaging	Het
Kcnj10	C	A	1: 172,196,563 (GRCm39)	R26S	probably benign	Het
Klhl1	T	A	14: 96,755,632 (GRCm39)	D41V	probably benign	Het
Lyn	A	G	4: 3,782,996 (GRCm39)	T410A	probably damaging	Het
Mga	A	G	2: 119,754,031 (GRCm39)	T847A	probably damaging	Het
Mrgpra3	G	T	7: 47,239,290 (GRCm39)	T212N	probably benign	Het
Myh4	T	C	11: 67,137,251 (GRCm39)	F491L	probably benign	Het
Neurl4	T	A	11: 69,801,562 (GRCm39)	I1206N	probably damaging	Het
Pcdhb15	T	A	18: 37,608,621 (GRCm39)	W618R	possibly damaging	Het
Pomc	A	G	12: 4,010,146 (GRCm39)	H129R	probably damaging	Het
Ppm1l	C	A	3: 69,460,399 (GRCm39)	H325Q	probably benign	Het
Psme4	A	G	11: 30,722,474 (GRCm39)		probably benign	Het
Reep2	A	G	18: 34,978,342 (GRCm39)	I74V	probably null	Het
Robo2	T	G	16: 73,745,225 (GRCm39)	E850A	probably damaging	Het
Scrn2	T	A	11: 96,921,262 (GRCm39)		probably benign	Het
Sfpq	G	A	4: 126,923,675 (GRCm39)	R673K	probably benign	Het
Sh2d3c	T	C	2: 32,644,581 (GRCm39)	*703R	probably null	Het
Spp1	A	G	5: 104,587,167 (GRCm39)	M85V	probably benign	Het
Srebf1	T	C	11: 60,097,810 (GRCm39)	E98G	probably damaging	Het
Srrm4	T	A	5: 116,582,851 (GRCm39)		probably benign	Het
Ticam1	A	T	17: 56,578,154 (GRCm39)	S314T	possibly damaging	Het
Tie1	T	C	4: 118,341,823 (GRCm39)	I209V	possibly damaging	Het
Vapa	G	A	17: 65,889,586 (GRCm39)	R194*	probably null	Het
Vcan	C	T	13: 89,838,360 (GRCm39)	D2395N	probably damaging	Het
Whamm	A	G	7: 81,241,574 (GRCm39)	H295R	probably benign	Het
Zdhhc14	A	G	17: 5,698,186 (GRCm39)	Y85C	probably damaging	Het
Zfp35	T	A	18: 24,136,583 (GRCm39)	F309Y	probably damaging	Het
Zfp423	C	A	8: 88,414,694 (GRCm39)	C1187F	probably damaging	Het

Other mutations in Zfp874b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02172:Zfp874b	APN	13	67,622,135 (GRCm39)	missense	probably damaging	1.00
R0432:Zfp874b	UTSW	13	67,629,955 (GRCm39)	missense	probably damaging	1.00
R0653:Zfp874b	UTSW	13	67,623,052 (GRCm39)	missense	possibly damaging	0.69
R0727:Zfp874b	UTSW	13	67,622,831 (GRCm39)	missense	probably damaging	1.00
R1475:Zfp874b	UTSW	13	67,622,211 (GRCm39)	splice site	probably null
R1726:Zfp874b	UTSW	13	67,622,839 (GRCm39)	missense	probably damaging	1.00
R5484:Zfp874b	UTSW	13	67,629,373 (GRCm39)	missense	possibly damaging	0.76
R6386:Zfp874b	UTSW	13	67,622,962 (GRCm39)	missense	possibly damaging	0.70
R7150:Zfp874b	UTSW	13	67,622,622 (GRCm39)	nonsense	probably null
R7726:Zfp874b	UTSW	13	67,621,975 (GRCm39)	missense	probably benign	0.01
R7778:Zfp874b	UTSW	13	67,622,093 (GRCm39)	missense	probably benign	0.03
R7824:Zfp874b	UTSW	13	67,622,093 (GRCm39)	missense	probably benign	0.03
R7918:Zfp874b	UTSW	13	67,622,279 (GRCm39)	missense	possibly damaging	0.74
R7939:Zfp874b	UTSW	13	67,622,622 (GRCm39)	nonsense	probably null
R8053:Zfp874b	UTSW	13	67,622,217 (GRCm39)	missense	probably damaging	0.96
R8881:Zfp874b	UTSW	13	67,622,141 (GRCm39)	missense	probably damaging	0.99
X0028:Zfp874b	UTSW	13	67,622,179 (GRCm39)	missense	probably damaging	0.96

Predicted Primers

PCR Primer
(F):5'- CTCATGGGGAGTGTCTACAGA -3'
(R):5'- TGGAGAGAAACTTGACAAGTGTG -3'

Sequencing Primer
(F):5'- ACACTCTTCACACGTGTAGGG -3'
(R):5'- CTTGACAAGTGTGAAGAATGTGG -3'

Posted On

2019-05-13