Mutagenetix > Incidental Mutation

Incidental Mutation 'R1457:Zfp949'

158585

Institutional Source

Beutler Lab

Gene Symbol

Zfp949

Ensembl Gene

ENSMUSG00000032425

Gene Name

zinc finger protein 949

Synonyms

4930422I07Rik

MMRRC Submission

039512-MU

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.067) question?

Stock #

R1457 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

88548020-88571061 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 88569838 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Isoleucine at position 487 (T487I)

Ref Sequence

ENSEMBL: ENSMUSP00000125325 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000160652] [ENSMUST00000161458] [ENSMUST00000162827]

AlphaFold

E9Q732

Predicted Effect

probably benign
Transcript: ENSMUST00000160652

Predicted Effect

probably damaging
Transcript: ENSMUST00000161458
AA Change: T487I

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000125017
Gene: ENSMUSG00000032425
AA Change: T487I

Domain	Start	End	E-Value	Type
KRAB	8	68	2.63e-32	SMART
ZnF_C2H2	268	290	5.99e1	SMART
ZnF_C2H2	296	318	5.5e-3	SMART
ZnF_C2H2	324	346	6.42e-4	SMART
ZnF_C2H2	352	374	2.91e-2	SMART
ZnF_C2H2	380	402	4.11e-2	SMART
ZnF_C2H2	408	430	3.63e-3	SMART
ZnF_C2H2	436	458	5.67e-5	SMART
ZnF_C2H2	464	486	7.9e-4	SMART
ZnF_C2H2	492	514	2.43e-4	SMART
ZnF_C2H2	520	542	2.95e-3	SMART
ZnF_C2H2	548	570	1.03e-2	SMART
ZnF_C2H2	576	598	1.4e-4	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000162827
AA Change: T487I

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000125325
Gene: ENSMUSG00000032425
AA Change: T487I

Domain	Start	End	E-Value	Type
KRAB	8	68	2.63e-32	SMART
ZnF_C2H2	268	290	5.99e1	SMART
ZnF_C2H2	296	318	5.5e-3	SMART
ZnF_C2H2	324	346	6.42e-4	SMART
ZnF_C2H2	352	374	2.91e-2	SMART
ZnF_C2H2	380	402	4.11e-2	SMART
ZnF_C2H2	408	430	3.63e-3	SMART
ZnF_C2H2	436	458	5.67e-5	SMART
ZnF_C2H2	464	486	7.9e-4	SMART
ZnF_C2H2	492	514	2.43e-4	SMART
ZnF_C2H2	520	542	2.95e-3	SMART
ZnF_C2H2	548	570	1.03e-2	SMART
ZnF_C2H2	576	598	1.4e-4	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000162985

SMART Domains

Protein: ENSMUSP00000124007
Gene: ENSMUSG00000032425

Domain	Start	End	E-Value	Type
KRAB	8	68	2.63e-32	SMART

Coding Region Coverage

1x: 98.9%
3x: 97.8%
10x: 94.7%
20x: 87.3%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice homozygous for a knock-out allele exhibit embryonic lethality during organogenesis with defects in growth, development, cell proliferation, apoptosis and turning. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2010300C02Rik	A	T	1: 37,626,012	Y268*	probably null	Het
Abca14	A	T	7: 120,289,460	I1210F	probably benign	Het
Ankrd17	T	C	5: 90,285,846	H688R	possibly damaging	Het
Arhgap24	T	A	5: 102,664,106	N66K	probably damaging	Het
Atp1a1	C	T	3: 101,590,466	G335D	probably damaging	Het
Cacna1g	C	T	11: 94,459,555	R488H	possibly damaging	Het
Cacna1h	A	T	17: 25,397,620	V149E	probably damaging	Het
Cd22	G	T	7: 30,873,170	P338Q	probably benign	Het
Cntln	G	T	4: 85,096,839	M1122I	probably benign	Het
Cntrl	A	G	2: 35,122,756	N302S	probably benign	Het
Cog8	T	C	8: 107,052,896	R250G	probably damaging	Het
Creld2	T	C	15: 88,823,753	C232R	probably damaging	Het
Cyp2b23	G	A	7: 26,673,149	P347L	probably damaging	Het
Dnah5	T	C	15: 28,403,542		probably null	Het
Eml6	C	T	11: 30,024,459	V40I	probably damaging	Het
Epb42	C	T	2: 121,029,967		probably null	Het
Fcrla	A	G	1: 170,921,004	L190P	probably damaging	Het
Galnt18	A	T	7: 111,779,428	Y40*	probably null	Het
Gdf7	A	T	12: 8,298,073	M416K	probably damaging	Het
Gm11232	T	A	4: 71,756,919		probably null	Het
Gpam	T	A	19: 55,088,176	N198Y	probably damaging	Het
Grip1	C	T	10: 119,986,350	S327F	possibly damaging	Het
Hey2	C	T	10: 30,834,356	A134T	probably benign	Het
Kat6a	T	C	8: 22,938,652	I1341T	probably benign	Het
Kcnd3	T	C	3: 105,668,186	L542P	probably benign	Het
Lars	G	A	18: 42,210,050	R1101C	probably damaging	Het
Lman2	T	C	13: 55,351,251	D234G	probably benign	Het
Map3k19	A	C	1: 127,817,898	I1273R	probably damaging	Het
Matn1	T	A	4: 130,950,019	F180I	possibly damaging	Het
Meikin	T	A	11: 54,370,941	L61*	probably null	Het
Mroh2b	G	T	15: 4,925,684	D720Y	probably damaging	Het
Myh13	T	C	11: 67,331,046	I199T	probably damaging	Het
Myh4	T	A	11: 67,248,461	S535T	probably damaging	Het
Myo5a	T	C	9: 75,213,065	M1715T	probably damaging	Het
Nat8	A	T	6: 85,830,989	V54D	probably damaging	Het
Nbea	A	G	3: 56,085,327	V286A	probably damaging	Het
Ndnf	A	G	6: 65,704,014	K426E	possibly damaging	Het
Nup210l	T	A	3: 90,190,972	N1410K	possibly damaging	Het
Oca2	A	T	7: 56,321,521	T399S	probably damaging	Het
Olfr1045	A	G	2: 86,198,252	S167P	probably damaging	Het
Olfr118	A	T	17: 37,672,925	K301*	probably null	Het
Olfr250	G	A	9: 38,368,196	V217I	probably benign	Het
Olfr366	A	C	2: 37,219,659	T57P	possibly damaging	Het
Olfr644	A	T	7: 104,068,459	C191S	probably damaging	Het
Olfr652	T	A	7: 104,565,071	N283K	probably damaging	Het
Otogl	A	C	10: 107,878,152		probably null	Het
Pde4b	C	T	4: 102,605,176	T511I	probably damaging	Het
Proser3	A	G	7: 30,539,747		probably null	Het
Psmd12	G	A	11: 107,479,646	V24M	probably damaging	Het
Rbm17	A	T	2: 11,593,461	M170K	probably benign	Het
Rims2	C	T	15: 39,511,314	T1064I	possibly damaging	Het
Ripor3	C	T	2: 167,992,653	V281M	probably damaging	Het
Rreb1	C	A	13: 37,946,928	Q1353K	possibly damaging	Het
Sgo2a	A	G	1: 58,015,806	D383G	probably benign	Het
Sik3	C	T	9: 46,221,148	T1346M	probably damaging	Het
Slx1b	A	T	7: 126,692,796	V63E	probably damaging	Het
Son	A	G	16: 91,657,086	D907G	probably damaging	Het
Src	G	A	2: 157,469,212	V401M	probably damaging	Het
St3gal4	T	C	9: 35,054,757	K24E	possibly damaging	Het
Stat6	A	G	10: 127,658,245	K647R	probably damaging	Het
Tbl1xr1	G	A	3: 22,193,169		probably null	Het
Tlk2	G	A	11: 105,256,952		probably null	Het
Tmbim6	T	A	15: 99,401,615	I3K	probably benign	Het
Tmeff2	A	T	1: 51,181,867	I334F	probably damaging	Het
Ttn	T	C	2: 76,840,315		probably null	Het
Ubl7	T	A	9: 57,914,611	I81N	probably damaging	Het
Ugt1a10	A	G	1: 88,055,711	Y77C	probably damaging	Het
Uqcrfs1	A	G	13: 30,540,907	C217R	probably damaging	Het
Usp50	T	C	2: 126,761,634	T331A	probably benign	Het
Vmn1r65	A	G	7: 6,009,157	V26A	probably benign	Het
Wdfy3	A	C	5: 101,917,579	V1241G	possibly damaging	Het
Wtap	A	C	17: 12,981,744		probably null	Het
Zbtb40	C	A	4: 136,984,837	A1187S	possibly damaging	Het
Zfp57	T	C	17: 37,006,098	S20P	probably damaging	Het
Zfp592	A	G	7: 81,024,479	D397G	probably damaging	Het
Zfp747	A	T	7: 127,374,504	S165T	probably benign	Het
Zscan4d	A	G	7: 11,164,994	C119R	probably damaging	Het

Other mutations in Zfp949

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL03201:Zfp949	APN	9	88568664	missense	probably benign	0.23
R0034:Zfp949	UTSW	9	88567640	intron	probably benign
R0462:Zfp949	UTSW	9	88568734	missense	possibly damaging	0.63
R1574:Zfp949	UTSW	9	88569777	nonsense	probably null
R1574:Zfp949	UTSW	9	88569777	nonsense	probably null
R1878:Zfp949	UTSW	9	88569303	missense	probably damaging	0.99
R1917:Zfp949	UTSW	9	88570062	missense	probably damaging	0.98
R4488:Zfp949	UTSW	9	88570089	missense	probably damaging	0.98
R4839:Zfp949	UTSW	9	88569994	missense	probably damaging	0.97
R5309:Zfp949	UTSW	9	88567183	missense	possibly damaging	0.92
R5312:Zfp949	UTSW	9	88567183	missense	possibly damaging	0.92
R5461:Zfp949	UTSW	9	88569484	missense	probably benign	0.00
R6530:Zfp949	UTSW	9	88567287	critical splice donor site	probably null
R6844:Zfp949	UTSW	9	88569411	missense	possibly damaging	0.91
R7749:Zfp949	UTSW	9	88569870	missense	probably damaging	1.00
R7937:Zfp949	UTSW	9	88569270	missense	probably damaging	1.00
R8150:Zfp949	UTSW	9	88570000	missense	probably benign
R8290:Zfp949	UTSW	9	88569240	missense	probably damaging	0.98
R8349:Zfp949	UTSW	9	88567249	missense	possibly damaging	0.84
R8449:Zfp949	UTSW	9	88567249	missense	possibly damaging	0.84
R8808:Zfp949	UTSW	9	88569364	missense	probably damaging	1.00
R8949:Zfp949	UTSW	9	88568718	missense	possibly damaging	0.78
R9219:Zfp949	UTSW	9	88569670	missense	probably damaging	1.00
R9396:Zfp949	UTSW	9	88567207	missense	probably damaging	0.99
R9486:Zfp949	UTSW	9	88570129	missense	probably benign	0.01
R9488:Zfp949	UTSW	9	88570129	missense	probably benign	0.01
R9643:Zfp949	UTSW	9	88554447	start gained	probably benign
R9727:Zfp949	UTSW	9	88569860	nonsense	probably null
R9778:Zfp949	UTSW	9	88567287	critical splice donor site	probably null

Predicted Primers

PCR Primer
(F):5'- TGCCTTGAAAGTAAGAAAACCTTTCCCA -3'
(R):5'- TTGCTGAGGACTAACTTCCACTGAAAC -3'

Sequencing Primer
(F):5'- ctcaaaacgcaccagagaac -3'
(R):5'- cgttttcccacatttattgcactc -3'

Posted On

2014-03-14