Mutagenetix > Incidental Mutation

Incidental Mutation 'R1759:Zfp507'

195184

Institutional Source

Beutler Lab

Gene Symbol

Zfp507

Ensembl Gene

ENSMUSG00000044452

Gene Name

zinc finger protein 507

Synonyms

A230056M16Rik, 1810022O10Rik

MMRRC Submission

039791-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.228) question?

Stock #

R1759 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

35471768-35502428 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 35475403 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Alanine to Serine at position 145 (A145S)

Ref Sequence

ENSEMBL: ENSMUSP00000140940 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000061586] [ENSMUST00000187282] [ENSMUST00000206615]

AlphaFold

Q6ZPY5

Predicted Effect

probably benign
Transcript: ENSMUST00000061586
AA Change: A937S

PolyPhen 2 Score 0.199 (Sensitivity: 0.92; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000058609
Gene: ENSMUSG00000044452
AA Change: A937S

Domain	Start	End	E-Value	Type
ZnF_C2H2	122	144	1.56e-2	SMART
ZnF_C2H2	152	175	2.49e-1	SMART
low complexity region	178	192	N/A	INTRINSIC
ZnF_C2H2	237	259	8.52e0	SMART
ZnF_C2H2	630	652	2.75e-3	SMART
ZnF_C2H2	658	680	1.26e-2	SMART
ZnF_C2H2	686	709	5.42e-2	SMART
ZnF_C2H2	746	768	4.79e-3	SMART
ZnF_C2H2	774	796	1.45e-2	SMART
ZnF_C2H2	899	921	3.83e-2	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000181078

Predicted Effect

probably damaging
Transcript: ENSMUST00000187282
AA Change: A145S

PolyPhen 2 Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000140940
Gene: ENSMUSG00000044452
AA Change: A145S

Domain	Start	End	E-Value	Type
ZnF_C2H2	107	129	1.6e-4	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000206615

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000206761

Coding Region Coverage

1x: 97.5%
3x: 96.9%
10x: 95.4%
20x: 92.5%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 87 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
9330159F19Rik	A	T	10: 29,094,272 (GRCm39)	M53L	possibly damaging	Het
Abca5	T	C	11: 110,184,674 (GRCm39)	D944G	probably benign	Het
Ankdd1b	T	C	13: 96,556,211 (GRCm39)	Y433C	probably damaging	Het
Aox3	A	G	1: 58,209,805 (GRCm39)		probably null	Het
Ap1g1	G	A	8: 110,559,853 (GRCm39)	G260E	probably damaging	Het
Arsi	G	A	18: 61,049,723 (GRCm39)	G202E	probably benign	Het
Atp13a4	T	A	16: 29,275,429 (GRCm39)	T352S	probably damaging	Het
Ccdc33	T	A	9: 58,024,729 (GRCm39)	N166Y	possibly damaging	Het
Ces2h	T	A	8: 105,743,243 (GRCm39)	D159E	probably damaging	Het
Chd1	T	A	17: 17,607,533 (GRCm39)	D360E	probably benign	Het
Col16a1	G	T	4: 129,978,062 (GRCm39)	G781V	probably damaging	Het
Col6a5	T	A	9: 105,808,045 (GRCm39)	E1001V	unknown	Het
Cracdl	A	T	1: 37,664,791 (GRCm39)	I369N	probably benign	Het
Cyp3a59	T	G	5: 146,035,060 (GRCm39)	M246R	probably benign	Het
Dcn	T	C	10: 97,349,517 (GRCm39)	V263A	probably benign	Het
Dnttip2	A	G	3: 122,069,798 (GRCm39)	N338D	probably benign	Het
Entpd1	G	T	19: 40,600,968 (GRCm39)		probably null	Het
Epb41l1	A	G	2: 156,363,894 (GRCm39)	D801G	probably benign	Het
Fam186a	T	A	15: 99,864,762 (GRCm39)	K23*	probably null	Het
Gbe1	T	C	16: 70,284,929 (GRCm39)	M417T	probably benign	Het
Gmnc	T	A	16: 26,784,497 (GRCm39)	S3C	possibly damaging	Het
Gpr156	T	C	16: 37,768,583 (GRCm39)	S35P	probably damaging	Het
Grid1	T	C	14: 35,167,988 (GRCm39)	M504T	possibly damaging	Het
Gsdma3	T	C	11: 98,526,071 (GRCm39)	V265A	possibly damaging	Het
Hsd3b3	A	T	3: 98,649,399 (GRCm39)	I308N	probably damaging	Het
Inpp4b	A	G	8: 82,494,732 (GRCm39)	D49G	probably benign	Het
Ipmk	C	A	10: 71,217,133 (GRCm39)	Q227K	probably damaging	Het
Kalrn	T	A	16: 34,181,320 (GRCm39)	D88V	probably damaging	Het
Kansl1l	C	T	1: 66,841,047 (GRCm39)	M84I	probably damaging	Het
Kcnab2	T	G	4: 152,477,509 (GRCm39)	K363Q	probably damaging	Het
Kdm7a	C	A	6: 39,124,633 (GRCm39)		probably null	Het
Kiss1r	T	C	10: 79,757,612 (GRCm39)	L322P	probably damaging	Het
Lce1e	A	T	3: 92,615,178 (GRCm39)	C56*	probably null	Het
Lrpprc	T	C	17: 85,047,509 (GRCm39)	K908E	probably damaging	Het
Mak	C	A	13: 41,210,110 (GRCm39)	W42L	probably damaging	Het
Map3k21	A	G	8: 126,671,519 (GRCm39)	T936A	probably benign	Het
Marchf7	C	T	2: 60,064,888 (GRCm39)	S388F	probably damaging	Het
Matcap1	A	T	8: 106,012,182 (GRCm39)	S88R	probably damaging	Het
Mgat2	A	T	12: 69,232,301 (GRCm39)	I292F	probably benign	Het
Myh3	C	A	11: 66,987,717 (GRCm39)	R1397S	probably damaging	Het
Myo5a	A	G	9: 75,089,275 (GRCm39)	D1135G	possibly damaging	Het
N4bp2	A	G	5: 65,983,956 (GRCm39)	E1667G	probably damaging	Het
Nbr1	A	G	11: 101,450,369 (GRCm39)	T43A	probably damaging	Het
Nip7	A	G	8: 107,784,767 (GRCm39)	N124S	probably benign	Het
Or3a1	G	A	11: 74,225,808 (GRCm39)	S83F	possibly damaging	Het
Or51l14	T	C	7: 103,101,356 (GRCm39)	S271P	probably benign	Het
Or6c75	T	A	10: 129,336,775 (GRCm39)	S7R	probably benign	Het
Or7g25	C	T	9: 19,160,384 (GRCm39)	V104I	probably benign	Het
Or8b55	T	C	9: 38,727,194 (GRCm39)	Y132H	probably damaging	Het
Otoa	T	C	7: 120,733,326 (GRCm39)	L731P	probably damaging	Het
Pcnx2	G	A	8: 126,500,717 (GRCm39)	P1458S	probably damaging	Het
Pfpl	A	G	19: 12,407,224 (GRCm39)	T492A	probably damaging	Het
Pgm1	A	G	4: 99,824,305 (GRCm39)	D326G	probably damaging	Het
Plekhh1	T	A	12: 79,119,535 (GRCm39)	Y953N	probably damaging	Het
Pnkd	G	A	1: 74,387,922 (GRCm39)	A195T	probably damaging	Het
Ppib	C	T	9: 65,968,764 (GRCm39)	Q51*	probably null	Het
Ppip5k1	G	T	2: 121,181,067 (GRCm39)	T13K	probably benign	Het
Psmg2	A	T	18: 67,781,246 (GRCm39)	S113C	probably benign	Het
Rapgef2	A	G	3: 78,974,038 (GRCm39)	M1584T	possibly damaging	Het
Rbm12b1	A	C	4: 12,145,424 (GRCm39)	R465S	probably damaging	Het
Reln	A	G	5: 22,215,287 (GRCm39)	Y1055H	probably damaging	Het
Ros1	A	T	10: 51,996,922 (GRCm39)	I1250K	probably damaging	Het
Samd9l	C	A	6: 3,373,401 (GRCm39)	V1287F	probably damaging	Het
Sgce	A	T	6: 4,689,765 (GRCm39)	I356N	probably damaging	Het
Sh3tc1	C	T	5: 35,863,248 (GRCm39)	E980K	possibly damaging	Het
Sil1	T	C	18: 35,551,151 (GRCm39)	E68G	possibly damaging	Het
Slc18a1	A	G	8: 69,518,237 (GRCm39)	I259T	possibly damaging	Het
Slc6a20b	A	C	9: 123,438,062 (GRCm39)		probably null	Het
Smg7	G	T	1: 152,724,597 (GRCm39)	T536K	probably benign	Het
Smyd4	A	G	11: 75,273,192 (GRCm39)	Y84C	probably damaging	Het
Snrnp40	C	G	4: 130,271,836 (GRCm39)		probably null	Het
Sorbs2	A	T	8: 46,216,056 (GRCm39)	*50C	probably null	Het
Speg	A	T	1: 75,377,806 (GRCm39)	M855L	possibly damaging	Het
Srrt	G	T	5: 137,301,212 (GRCm39)	H71Q	probably damaging	Het
St6galnac5	A	G	3: 152,552,130 (GRCm39)	S146P	probably damaging	Het
Syne1	T	A	10: 5,299,369 (GRCm39)	Q962L	probably damaging	Het
Tiam2	A	G	17: 3,566,278 (GRCm39)	H1441R	probably damaging	Het
Tmem45a	C	T	16: 56,642,765 (GRCm39)	M135I	probably benign	Het
Tpr	A	T	1: 150,305,275 (GRCm39)	E1521D	probably benign	Het
Uba3	C	T	6: 97,173,865 (GRCm39)	G107R	probably damaging	Het
Unc45b	G	T	11: 82,820,325 (GRCm39)	V590F	probably benign	Het
Vmn1r14	A	T	6: 57,211,297 (GRCm39)	T292S	probably benign	Het
Vmn2r102	T	A	17: 19,914,755 (GRCm39)	N773K	probably damaging	Het
Vps13d	A	T	4: 144,882,427 (GRCm39)	D1055E	probably benign	Het
Wfs1	G	C	5: 37,124,359 (GRCm39)	A844G	probably damaging	Het
Zfp398	A	G	6: 47,836,412 (GRCm39)	T71A	possibly damaging	Het
Zfp971	A	T	2: 177,675,722 (GRCm39)	E440D	probably damaging	Het

Other mutations in Zfp507

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00715:Zfp507	APN	7	35,494,137 (GRCm39)	missense	possibly damaging	0.93
IGL00835:Zfp507	APN	7	35,475,463 (GRCm39)	missense	probably damaging	1.00
IGL01083:Zfp507	APN	7	35,493,463 (GRCm39)	missense	probably benign	0.00
IGL01359:Zfp507	APN	7	35,493,927 (GRCm39)	missense	probably damaging	1.00
IGL01418:Zfp507	APN	7	35,493,237 (GRCm39)	splice site	probably null
IGL02122:Zfp507	APN	7	35,475,520 (GRCm39)	missense	probably damaging	1.00
IGL02506:Zfp507	APN	7	35,475,891 (GRCm39)	missense	probably damaging	1.00
IGL02601:Zfp507	APN	7	35,491,136 (GRCm39)	missense	probably damaging	1.00
IGL02643:Zfp507	APN	7	35,494,656 (GRCm39)	missense	probably damaging	0.99
IGL03129:Zfp507	APN	7	35,493,631 (GRCm39)	missense	probably damaging	1.00
R0400:Zfp507	UTSW	7	35,491,171 (GRCm39)	missense	probably damaging	1.00
R0812:Zfp507	UTSW	7	35,502,048 (GRCm39)	intron	probably benign
R1183:Zfp507	UTSW	7	35,494,315 (GRCm39)	missense	probably damaging	0.99
R1381:Zfp507	UTSW	7	35,475,435 (GRCm39)	missense	possibly damaging	0.91
R1542:Zfp507	UTSW	7	35,494,226 (GRCm39)	missense	possibly damaging	0.71
R1626:Zfp507	UTSW	7	35,494,858 (GRCm39)	missense	probably damaging	1.00
R1843:Zfp507	UTSW	7	35,493,150 (GRCm39)	missense	probably damaging	0.97
R1852:Zfp507	UTSW	7	35,487,176 (GRCm39)	missense	probably damaging	1.00
R1893:Zfp507	UTSW	7	35,502,052 (GRCm39)	intron	probably benign
R1923:Zfp507	UTSW	7	35,493,150 (GRCm39)	missense	probably damaging	0.97
R1925:Zfp507	UTSW	7	35,493,150 (GRCm39)	missense	probably damaging	0.97
R1927:Zfp507	UTSW	7	35,493,150 (GRCm39)	missense	probably damaging	0.97
R2139:Zfp507	UTSW	7	35,493,148 (GRCm39)	missense	probably damaging	1.00
R2191:Zfp507	UTSW	7	35,494,268 (GRCm39)	missense	probably damaging	1.00
R2431:Zfp507	UTSW	7	35,494,827 (GRCm39)	missense	probably benign	0.08
R2921:Zfp507	UTSW	7	35,494,224 (GRCm39)	missense	probably damaging	1.00
R2922:Zfp507	UTSW	7	35,494,224 (GRCm39)	missense	probably damaging	1.00
R3436:Zfp507	UTSW	7	35,487,195 (GRCm39)	missense	probably damaging	1.00
R4483:Zfp507	UTSW	7	35,487,141 (GRCm39)	critical splice donor site	probably null
R4751:Zfp507	UTSW	7	35,493,807 (GRCm39)	missense	probably damaging	0.99
R4852:Zfp507	UTSW	7	35,493,480 (GRCm39)	missense	probably benign	0.01
R5298:Zfp507	UTSW	7	35,475,421 (GRCm39)	missense	probably damaging	0.99
R5602:Zfp507	UTSW	7	35,475,663 (GRCm39)	nonsense	probably null
R5707:Zfp507	UTSW	7	35,493,588 (GRCm39)	missense	probably damaging	1.00
R5785:Zfp507	UTSW	7	35,487,167 (GRCm39)	missense	probably benign	0.20
R6140:Zfp507	UTSW	7	35,493,613 (GRCm39)	missense	probably damaging	1.00
R6674:Zfp507	UTSW	7	35,494,159 (GRCm39)	missense	probably damaging	0.98
R6714:Zfp507	UTSW	7	35,487,152 (GRCm39)	missense	probably damaging	0.99
R7045:Zfp507	UTSW	7	35,494,978 (GRCm39)	missense	possibly damaging	0.56
R7334:Zfp507	UTSW	7	35,475,505 (GRCm39)	missense	probably damaging	1.00
R7365:Zfp507	UTSW	7	35,475,843 (GRCm39)	missense	unknown
R7569:Zfp507	UTSW	7	35,493,969 (GRCm39)	missense	probably damaging	0.99
R7662:Zfp507	UTSW	7	35,487,229 (GRCm39)	nonsense	probably null
R7846:Zfp507	UTSW	7	35,493,963 (GRCm39)	missense	probably damaging	1.00
R9100:Zfp507	UTSW	7	35,494,446 (GRCm39)	missense	probably benign	0.39
R9136:Zfp507	UTSW	7	35,475,883 (GRCm39)	missense	probably damaging	0.96
R9513:Zfp507	UTSW	7	35,475,573 (GRCm39)	missense	probably benign	0.00
Z1088:Zfp507	UTSW	7	35,493,702 (GRCm39)	missense	possibly damaging	0.88

Predicted Primers

PCR Primer
(F):5'- TGGAGACAGTGGAAGTCACTGACC -3'
(R):5'- TGAAGTTATGGACGCCAGCGAG -3'

Sequencing Primer
(F):5'- ATCACACCAGTGTGGCTCTG -3'
(R):5'- GAGCTTGAGAAACTGAACCCC -3'

Posted On

2014-05-23