Mutagenetix > Incidental Mutation

Incidental Mutation 'R0505:Zscan5b'

47468

Institutional Source

Beutler Lab

Gene Symbol

Zscan5b

Ensembl Gene

ENSMUSG00000058028

Gene Name

zinc finger and SCAN domain containing 5B

Synonyms

Zfg1, Zfp371

MMRRC Submission

038700-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0505 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

6222278-6239423 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 6239075 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Asparagine at position 431 (I431N)

Ref Sequence

ENSEMBL: ENSMUSP00000126044 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000072662] [ENSMUST00000165445]

AlphaFold

B2RTN3

Predicted Effect

probably damaging
Transcript: ENSMUST00000072662
AA Change: I431N

PolyPhen 2 Score 0.987 (Sensitivity: 0.73; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000072449
Gene: ENSMUSG00000058028
AA Change: I431N

Domain	Start	End	E-Value	Type
Pfam:SCAN	31	121	1.6e-25	PFAM
low complexity region	157	166	N/A	INTRINSIC
low complexity region	178	189	N/A	INTRINSIC
low complexity region	302	314	N/A	INTRINSIC
ZnF_C2H2	326	348	3.11e-2	SMART
ZnF_C2H2	354	376	1.28e-3	SMART
ZnF_C2H2	382	404	1.36e-2	SMART
ZnF_C2H2	410	432	3.16e-3	SMART
ZnF_C2H2	438	460	1.06e-4	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000165445
AA Change: I431N

PolyPhen 2 Score 0.987 (Sensitivity: 0.73; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000126044
Gene: ENSMUSG00000058028
AA Change: I431N

Domain	Start	End	E-Value	Type
Pfam:SCAN	33	120	1e-25	PFAM
low complexity region	157	166	N/A	INTRINSIC
low complexity region	178	189	N/A	INTRINSIC
low complexity region	302	314	N/A	INTRINSIC
ZnF_C2H2	326	348	3.11e-2	SMART
ZnF_C2H2	354	376	1.28e-3	SMART
ZnF_C2H2	382	404	1.36e-2	SMART
ZnF_C2H2	410	432	3.16e-3	SMART
ZnF_C2H2	438	460	1.06e-4	SMART

Meta Mutation Damage Score

0.6467

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.8%
20x: 94.1%

Validation Efficiency

98% (119/121)

Allele List at MGI

Other mutations in this stock

Total: 117 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca13	T	C	11: 9,291,058 (GRCm38)	Y974H	probably benign	Het
Abca2	G	T	2: 25,434,894 (GRCm38)	G300V	probably benign	Het
Abi1	A	G	2: 22,962,504 (GRCm38)		probably benign	Het
Actr10	T	A	12: 70,959,964 (GRCm38)	Y332N	probably damaging	Het
Adam25	G	T	8: 40,755,224 (GRCm38)	C509F	probably damaging	Het
Adck1	A	T	12: 88,371,691 (GRCm38)		probably benign	Het
Adgra3	A	G	5: 50,009,334 (GRCm38)		probably null	Het
Adgrl1	G	T	8: 83,934,650 (GRCm38)		probably benign	Het
Akr1c21	A	G	13: 4,576,307 (GRCm38)	Y110C	probably damaging	Het
Arhgef25	T	C	10: 127,183,697 (GRCm38)	I463V	probably null	Het
Atp6v1e2	C	T	17: 86,944,578 (GRCm38)	V131M	probably benign	Het
Bdnf	A	G	2: 109,675,343 (GRCm38)		probably null	Het
C7	A	T	15: 4,994,142 (GRCm38)		probably benign	Het
Cdc27	T	C	11: 104,528,288 (GRCm38)	T273A	probably benign	Het
Cdo1	T	A	18: 46,715,611 (GRCm38)	I187F	probably benign	Het
Cep104	A	T	4: 153,996,304 (GRCm38)	T742S	probably benign	Het
Ckm	A	T	7: 19,419,452 (GRCm38)	K223*	probably null	Het
Cmtr1	C	T	17: 29,676,285 (GRCm38)	P586L	probably benign	Het
Csmd1	C	T	8: 15,992,758 (GRCm38)	R2325Q	probably damaging	Het
Dcpp1	A	T	17: 23,882,594 (GRCm38)	I106L	possibly damaging	Het
Diaph3	A	C	14: 87,090,964 (GRCm38)		probably benign	Het
Dnah11	A	G	12: 118,106,510 (GRCm38)	V1520A	probably damaging	Het
Dnajc25	T	A	4: 59,020,438 (GRCm38)	M168K		Het
Dpp3	T	C	19: 4,914,654 (GRCm38)	N542D	probably damaging	Het
Ebf2	A	T	14: 67,371,736 (GRCm38)	K199*	probably null	Het
Efcab11	T	A	12: 99,719,035 (GRCm38)	Q160L	probably benign	Het
Eif2ak4	T	A	2: 118,431,036 (GRCm38)	S686T	probably benign	Het
Epha6	C	T	16: 60,205,732 (GRCm38)	S449N	possibly damaging	Het
Ercc4	T	C	16: 13,126,467 (GRCm38)	V329A	probably benign	Het
Faf1	T	C	4: 109,840,403 (GRCm38)	F309L	possibly damaging	Het
Fam102b	T	C	3: 108,980,204 (GRCm38)	E248G	probably benign	Het
G6pd2	C	A	5: 61,809,567 (GRCm38)	D228E	probably benign	Het
Ggt1	T	G	10: 75,585,957 (GRCm38)	V546G	probably damaging	Het
Gm14139	T	A	2: 150,193,080 (GRCm38)	C471*	probably null	Het
Gpatch4	G	T	3: 88,051,217 (GRCm38)	V3F	probably damaging	Het
Gprin3	A	G	6: 59,353,387 (GRCm38)	L645P	probably damaging	Het
Hyal2	A	G	9: 107,572,071 (GRCm38)	Y342C	probably benign	Het
Igf2bp2	A	G	16: 22,089,099 (GRCm38)	I16T	possibly damaging	Het
Inca1	T	C	11: 70,690,199 (GRCm38)	Y61C	probably damaging	Het
Ipo5	T	C	14: 120,942,733 (GRCm38)	W860R	possibly damaging	Het
Kcnj9	C	T	1: 172,323,024 (GRCm38)	A341T	probably benign	Het
Kdm5b	T	C	1: 134,602,571 (GRCm38)	V440A	probably damaging	Het
L3mbtl1	C	T	2: 162,947,335 (GRCm38)		probably benign	Het
Lin54	G	A	5: 100,452,293 (GRCm38)	T307I	probably damaging	Het
Lrrc18	C	A	14: 33,009,139 (GRCm38)	Q212K	probably benign	Het
Lrrc37a	A	G	11: 103,503,025 (GRCm38)	S525P	probably benign	Het
Lrrc71	T	A	3: 87,745,699 (GRCm38)	S137C	probably damaging	Het
Lrrk1	A	T	7: 66,290,908 (GRCm38)		probably null	Het
Man2b2	G	A	5: 36,816,198 (GRCm38)	S58L	probably benign	Het
Masp1	T	A	16: 23,458,138 (GRCm38)	H539L	probably benign	Het
Med1	G	A	11: 98,156,904 (GRCm38)	P1022L	probably damaging	Het
Meis1	T	A	11: 19,011,360 (GRCm38)	H171L	probably damaging	Het
Mier1	T	A	4: 103,155,623 (GRCm38)		probably benign	Het
Mkl2	C	T	16: 13,412,526 (GRCm38)	T1025I	possibly damaging	Het
Mmp13	A	T	9: 7,272,929 (GRCm38)	R96S	probably damaging	Het
Mms19	G	A	19: 41,953,734 (GRCm38)	T38I	probably damaging	Het
Mrc1	G	A	2: 14,310,032 (GRCm38)	C976Y	probably damaging	Het
Naalad2	A	G	9: 18,385,895 (GRCm38)	Y32H	probably benign	Het
Ndufs1	A	G	1: 63,143,926 (GRCm38)		probably benign	Het
Nefm	C	T	14: 68,124,159 (GRCm38)	D219N	probably damaging	Het
Nwd1	C	T	8: 72,662,337 (GRCm38)	P172L	probably damaging	Het
Nwd2	T	A	5: 63,805,111 (GRCm38)	D679E	probably damaging	Het
Ogdh	T	A	11: 6,339,936 (GRCm38)		probably benign	Het
Olfm3	T	A	3: 115,122,681 (GRCm38)	S421T	possibly damaging	Het
Olfr1281	A	T	2: 111,329,328 (GRCm38)	N303I	probably benign	Het
Olfr1445	A	G	19: 12,884,546 (GRCm38)	T222A	probably damaging	Het
Olfr1445	T	C	19: 12,884,079 (GRCm38)	L66P	probably damaging	Het
Olfr559	T	A	7: 102,724,029 (GRCm38)	I154F	probably damaging	Het
Olfr628	T	C	7: 103,732,376 (GRCm38)	V150A	probably benign	Het
Olfr988	A	G	2: 85,353,749 (GRCm38)	M59T	possibly damaging	Het
Opn5	T	G	17: 42,592,953 (GRCm38)	T164P	possibly damaging	Het
Pde7b	C	T	10: 20,438,746 (GRCm38)	V166M	probably damaging	Het
Pik3ap1	T	C	19: 41,324,564 (GRCm38)	N370S	probably damaging	Het
Pkhd1l1	A	T	15: 44,589,418 (GRCm38)	D3913V	probably damaging	Het
Pld1	A	G	3: 28,120,822 (GRCm38)	I90V	possibly damaging	Het
Plxna2	A	G	1: 194,644,348 (GRCm38)	T197A	possibly damaging	Het
Plxna4	A	T	6: 32,202,119 (GRCm38)	M987K	probably benign	Het
Pmch	A	G	10: 88,091,359 (GRCm38)	N75D	probably benign	Het
Prom2	T	A	2: 127,532,867 (GRCm38)	Q583L	possibly damaging	Het
Pyroxd1	T	A	6: 142,353,562 (GRCm38)	M148K	possibly damaging	Het
R3hdm2	C	T	10: 127,457,700 (GRCm38)	L158F	probably damaging	Het
Rapgef6	A	T	11: 54,625,963 (GRCm38)	T349S	probably benign	Het
Rfx5	C	T	3: 94,956,355 (GRCm38)	T105I	probably damaging	Het
Rif1	C	A	2: 52,110,737 (GRCm38)	P1401Q	probably damaging	Het
Robo3	G	A	9: 37,416,759 (GRCm38)		probably benign	Het
Rpn1	T	A	6: 88,090,242 (GRCm38)	S195T	probably benign	Het
Rslcan18	C	A	13: 67,102,119 (GRCm38)	K17N	probably benign	Het
Rsph3b	A	T	17: 6,941,727 (GRCm38)	I48N	probably damaging	Het
Sbf2	A	T	7: 110,399,343 (GRCm38)	Y628N	probably damaging	Het
Sis	T	C	3: 72,960,296 (GRCm38)	T139A	probably benign	Het
Slc22a14	A	G	9: 119,172,034 (GRCm38)		probably benign	Het
Slitrk6	A	T	14: 110,749,932 (GRCm38)	L781H	probably damaging	Het
Smarcb1	T	C	10: 75,897,066 (GRCm38)	T372A	probably damaging	Het
Spidr	T	A	16: 16,037,667 (GRCm38)	H328L	probably damaging	Het
Sun5	T	A	2: 153,870,952 (GRCm38)	D16V	probably damaging	Het
Syde2	G	A	3: 146,014,380 (GRCm38)	E1053K	possibly damaging	Het
Syne2	T	C	12: 76,099,464 (GRCm38)	S6419P	probably damaging	Het
Tenm3	G	A	8: 48,341,160 (GRCm38)		probably benign	Het
Timm44	C	A	8: 4,260,532 (GRCm38)	E407*	probably null	Het
Tmem189	A	T	2: 167,644,987 (GRCm38)		probably benign	Het
Tnpo2	A	G	8: 85,047,362 (GRCm38)	T342A	probably benign	Het
Trio	A	G	15: 27,767,907 (GRCm38)	C1964R	probably benign	Het
Trip11	A	C	12: 101,885,672 (GRCm38)	L711R	probably damaging	Het
Trp53bp1	A	T	2: 121,269,969 (GRCm38)	H101Q	probably damaging	Het
Trpm6	A	G	19: 18,873,902 (GRCm38)		probably benign	Het
Ttn	A	T	2: 76,849,991 (GRCm38)		probably benign	Het
Ucp1	T	A	8: 83,295,307 (GRCm38)	M256K	possibly damaging	Het
Uhrf1bp1l	T	C	10: 89,791,443 (GRCm38)	S145P	probably damaging	Het
Unc5a	T	A	13: 55,004,954 (GRCm38)	S838T	probably damaging	Het
Uxs1	T	C	1: 43,764,886 (GRCm38)		probably null	Het
Vmn2r108	A	T	17: 20,462,834 (GRCm38)	C703S	possibly damaging	Het
Zc3hav1	C	T	6: 38,332,664 (GRCm38)	G408R	probably damaging	Het
Zfp609	G	A	9: 65,703,462 (GRCm38)	L740F	possibly damaging	Het
Zfp69	T	C	4: 120,931,095 (GRCm38)	E341G	probably damaging	Het
Zfp707	A	T	15: 75,975,256 (GRCm38)	H312L	probably damaging	Het
Zfp773	T	C	7: 7,133,024 (GRCm38)	D191G	probably benign	Het
Zgrf1	C	A	3: 127,573,238 (GRCm38)	D755E	probably benign	Het

Other mutations in Zscan5b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01511:Zscan5b	APN	7	6,231,422 (GRCm38)	missense	probably benign	0.00
R0535:Zscan5b	UTSW	7	6,233,912 (GRCm38)	missense	possibly damaging	0.72
R1401:Zscan5b	UTSW	7	6,230,426 (GRCm38)	missense	probably damaging	1.00
R1537:Zscan5b	UTSW	7	6,233,851 (GRCm38)	missense	probably benign	0.00
R1613:Zscan5b	UTSW	7	6,230,375 (GRCm38)	missense	probably damaging	1.00
R1820:Zscan5b	UTSW	7	6,239,163 (GRCm38)	missense	probably damaging	1.00
R1833:Zscan5b	UTSW	7	6,238,966 (GRCm38)	missense	possibly damaging	0.67
R2191:Zscan5b	UTSW	7	6,231,443 (GRCm38)	missense	possibly damaging	0.53
R3177:Zscan5b	UTSW	7	6,231,346 (GRCm38)	missense	possibly damaging	0.86
R3277:Zscan5b	UTSW	7	6,231,346 (GRCm38)	missense	possibly damaging	0.86
R4911:Zscan5b	UTSW	7	6,239,190 (GRCm38)	makesense	probably null
R5624:Zscan5b	UTSW	7	6,230,519 (GRCm38)	missense	probably benign	0.00
R8213:Zscan5b	UTSW	7	6,233,947 (GRCm38)	missense	possibly damaging	0.93
R8214:Zscan5b	UTSW	7	6,233,947 (GRCm38)	missense	possibly damaging	0.93
R8326:Zscan5b	UTSW	7	6,233,947 (GRCm38)	missense	possibly damaging	0.93
R8327:Zscan5b	UTSW	7	6,233,947 (GRCm38)	missense	possibly damaging	0.93
R8328:Zscan5b	UTSW	7	6,233,947 (GRCm38)	missense	possibly damaging	0.93
R8985:Zscan5b	UTSW	7	6,238,835 (GRCm38)	missense	probably damaging	0.99
R9474:Zscan5b	UTSW	7	6,231,473 (GRCm38)	missense	probably benign	0.00
R9717:Zscan5b	UTSW	7	6,231,526 (GRCm38)	missense	possibly damaging	0.73
X0018:Zscan5b	UTSW	7	6,230,276 (GRCm38)	missense	probably damaging	0.97
X0024:Zscan5b	UTSW	7	6,238,949 (GRCm38)	missense	probably benign	0.00
X0025:Zscan5b	UTSW	7	6,238,615 (GRCm38)	missense	probably benign	0.18
Z1177:Zscan5b	UTSW	7	6,230,217 (GRCm38)	frame shift	probably null

Predicted Primers

PCR Primer
(F):5'- AAGACACTGTTGTGGATGCTGTACC -3'
(R):5'- GCAACCCAACCTCCATTTCTCTGAG -3'

Sequencing Primer
(F):5'- caccagaggtcacacacag -3'
(R):5'- CTCCATTTCTCTGAGAAAAGACTTC -3'

Posted On

2013-06-12