Mutagenetix > Incidental Mutation

Incidental Mutation 'R4490:Zfp9'

330680

Institutional Source

Beutler Lab

Gene Symbol

Zfp9

Ensembl Gene

ENSMUSG00000072623

Gene Name

zinc finger protein 9

Synonyms

Zfp-9, Krox-4, 1810048F22Rik

MMRRC Submission

041746-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.428) question?

Stock #

R4490 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

118438911-118456281 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 118442273 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 130 (S130P)

Ref Sequence

ENSEMBL: ENSMUSP00000123810 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000161170]

AlphaFold

Q8BIS1

Predicted Effect

probably benign
Transcript: ENSMUST00000161170
AA Change: S130P

PolyPhen 2 Score 0.061 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000123810
Gene: ENSMUSG00000072623
AA Change: S130P

Domain	Start	End	E-Value	Type
KRAB	8	68	2.26e-31	SMART
ZnF_C2H2	117	139	1.82e-3	SMART
ZnF_C2H2	144	166	4.17e-3	SMART
ZnF_C2H2	172	194	5.99e-4	SMART
ZnF_C2H2	200	222	2.79e-4	SMART
ZnF_C2H2	228	250	1.56e-2	SMART
ZnF_C2H2	256	278	6.88e-4	SMART
ZnF_C2H2	284	306	7.9e-4	SMART
ZnF_C2H2	312	334	2.75e-3	SMART
ZnF_C2H2	340	362	5.14e-3	SMART
ZnF_C2H2	368	390	1.26e-2	SMART
ZnF_C2H2	396	418	1.6e-4	SMART
ZnF_C2H2	424	446	9.08e-4	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000204066

Meta Mutation Damage Score

0.2457

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.2%
20x: 95.1%

Validation Efficiency

100% (45/45)

Allele List at MGI

Other mutations in this stock

Total: 40 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abl2	T	C	1: 156,461,349 (GRCm39)	V417A	probably damaging	Het
Adgrb2	T	C	4: 129,906,121 (GRCm39)	V881A	possibly damaging	Het
Arl5c	G	A	11: 97,886,662 (GRCm39)	R10*	probably null	Het
Atad1	A	G	19: 32,673,197 (GRCm39)	C229R	probably benign	Het
Atp6v0a2	T	C	5: 124,784,674 (GRCm39)	V319A	probably damaging	Het
Cage1	A	G	13: 38,207,393 (GRCm39)	S257P	possibly damaging	Het
Ccndbp1	A	G	2: 120,842,876 (GRCm39)	D179G	probably damaging	Het
Cngb3	T	C	4: 19,415,684 (GRCm39)	I398T	probably benign	Het
Crmp1	A	G	5: 37,433,675 (GRCm39)	D178G	probably damaging	Het
Csmd3	C	T	15: 48,177,429 (GRCm39)	V370I	possibly damaging	Het
Dapk1	A	G	13: 60,865,942 (GRCm39)	T180A	probably benign	Het
Dmtf1	A	G	5: 9,190,379 (GRCm39)		probably benign	Het
Dnah12	T	C	14: 26,455,758 (GRCm39)	L827S	possibly damaging	Het
F5	T	C	1: 164,044,964 (GRCm39)	V2084A	probably benign	Het
Fan1	A	T	7: 64,018,928 (GRCm39)	S476T	possibly damaging	Het
Far2	T	C	6: 148,074,907 (GRCm39)	L380P	possibly damaging	Het
Gbp2	A	G	3: 142,329,525 (GRCm39)	N24S	probably benign	Het
Gm14325	T	C	2: 177,474,776 (GRCm39)	H101R	possibly damaging	Het
Gpr55	C	T	1: 85,869,540 (GRCm39)	V14M	probably damaging	Het
Herc6	A	T	6: 57,631,480 (GRCm39)	Y724F	probably damaging	Het
Impg1	T	A	9: 80,301,341 (GRCm39)	Q195L	probably damaging	Het
Inf2	T	C	12: 112,566,638 (GRCm39)	F68L	probably damaging	Het
Kcnh8	T	C	17: 53,268,905 (GRCm39)		probably null	Het
Klb	A	G	5: 65,533,137 (GRCm39)	N482S	probably benign	Het
Kpnb1	A	G	11: 97,062,424 (GRCm39)	V447A	probably benign	Het
Nckap5l	G	A	15: 99,324,011 (GRCm39)	P831S	probably benign	Het
Ncor2	A	G	5: 125,113,879 (GRCm39)		probably null	Het
Or4b1d	A	T	2: 89,969,261 (GRCm39)	V74D	probably damaging	Het
Pgm3	T	C	9: 86,443,893 (GRCm39)	Y337C	probably damaging	Het
Prdm1	G	T	10: 44,322,903 (GRCm39)	Y197*	probably null	Het
Prdm4	A	T	10: 85,736,763 (GRCm39)	C626S	probably damaging	Het
Prex2	T	A	1: 11,232,487 (GRCm39)	S851R	probably benign	Het
Ranbp6	A	G	19: 29,787,733 (GRCm39)	L873P	probably damaging	Het
Rin2	A	G	2: 145,664,194 (GRCm39)	T23A	possibly damaging	Het
Rxra	G	T	2: 27,631,207 (GRCm39)	R118L	probably damaging	Het
Spice1	T	C	16: 44,202,476 (GRCm39)	L750P	probably damaging	Het
Trpm1	C	T	7: 63,858,660 (GRCm39)	Q228*	probably null	Het
Tsc1	A	G	2: 28,560,937 (GRCm39)	D265G	probably damaging	Het
Usp29	T	C	7: 6,964,949 (GRCm39)	I264T	possibly damaging	Het
Vmn2r26	T	C	6: 124,027,697 (GRCm39)	L479P	possibly damaging	Het

Other mutations in Zfp9

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00336:Zfp9	APN	6	118,441,436 (GRCm39)	missense	probably damaging	1.00
IGL01093:Zfp9	APN	6	118,442,800 (GRCm39)	missense	probably benign	0.14
IGL01512:Zfp9	APN	6	118,444,292 (GRCm39)	missense	probably damaging	1.00
R0491:Zfp9	UTSW	6	118,442,163 (GRCm39)	missense	probably damaging	0.96
R1716:Zfp9	UTSW	6	118,441,712 (GRCm39)	missense	probably damaging	1.00
R1858:Zfp9	UTSW	6	118,442,021 (GRCm39)	missense	probably benign	0.15
R4088:Zfp9	UTSW	6	118,441,730 (GRCm39)	missense	probably damaging	1.00
R4627:Zfp9	UTSW	6	118,441,937 (GRCm39)	missense	probably damaging	1.00
R4951:Zfp9	UTSW	6	118,441,408 (GRCm39)	missense	probably damaging	1.00
R5344:Zfp9	UTSW	6	118,442,140 (GRCm39)	missense	probably damaging	1.00
R5594:Zfp9	UTSW	6	118,442,000 (GRCm39)	missense	probably damaging	0.98
R6198:Zfp9	UTSW	6	118,454,282 (GRCm39)	start codon destroyed	probably null
R6682:Zfp9	UTSW	6	118,444,202 (GRCm39)	missense	possibly damaging	0.82
R6986:Zfp9	UTSW	6	118,441,426 (GRCm39)	missense	possibly damaging	0.77
R7147:Zfp9	UTSW	6	118,441,963 (GRCm39)	missense	probably damaging	1.00
R7799:Zfp9	UTSW	6	118,441,843 (GRCm39)	missense	probably damaging	1.00
R7921:Zfp9	UTSW	6	118,442,032 (GRCm39)	missense	possibly damaging	0.70
R7934:Zfp9	UTSW	6	118,441,847 (GRCm39)	missense	probably damaging	0.99
R8111:Zfp9	UTSW	6	118,441,561 (GRCm39)	missense	probably damaging	1.00
R8369:Zfp9	UTSW	6	118,441,353 (GRCm39)	missense	probably damaging	0.99
R8916:Zfp9	UTSW	6	118,442,223 (GRCm39)	nonsense	probably null
R9660:Zfp9	UTSW	6	118,443,851 (GRCm39)	missense	probably benign
R9728:Zfp9	UTSW	6	118,443,851 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- AATGGCTTCTCCCCTGTGTG -3'
(R):5'- GCCCTATGAATGTGACAAACAGG -3'

Sequencing Primer
(F):5'- ACACTGGCTACATTCGTAGG -3'
(R):5'- GGATTATGGAAATTATCATCAAGGGG -3'

Posted On

2015-07-21