Mutagenetix > Incidental Mutation

Incidental Mutation 'R2128:Zbtb26'

227692

Institutional Source

Beutler Lab

Gene Symbol

Zbtb26

Ensembl Gene

ENSMUSG00000050714

Gene Name

zinc finger and BTB domain containing 26

Synonyms

A630026F21Rik

MMRRC Submission

040131-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.365) question?

Stock #

R2128 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

37322180-37333147 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 37326563 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Lysine at position 158 (Q158K)

Ref Sequence

ENSEMBL: ENSMUSP00000099850 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000067043] [ENSMUST00000102789] [ENSMUST00000112932]

AlphaFold

Q8C8S0

Predicted Effect

probably benign
Transcript: ENSMUST00000067043
AA Change: Q147K

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)

SMART Domains

Protein: ENSMUSP00000070071
Gene: ENSMUSG00000050714
AA Change: Q147K

Domain	Start	End	E-Value	Type
BTB	33	127	4.38e-12	SMART
low complexity region	169	179	N/A	INTRINSIC
ZnF_C2H2	273	295	1.36e-2	SMART
ZnF_C2H2	298	320	1.4e-4	SMART
ZnF_C2H2	326	348	2.99e-4	SMART
ZnF_C2H2	354	377	2.09e-3	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000102789
AA Change: Q158K

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)

SMART Domains

Protein: ENSMUSP00000099850
Gene: ENSMUSG00000050714
AA Change: Q158K

Domain	Start	End	E-Value	Type
BTB	44	138	4.38e-12	SMART
low complexity region	180	190	N/A	INTRINSIC
ZnF_C2H2	284	306	1.36e-2	SMART
ZnF_C2H2	309	331	1.4e-4	SMART
ZnF_C2H2	337	359	2.99e-4	SMART
ZnF_C2H2	365	388	2.09e-3	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000112932

SMART Domains

Protein: ENSMUSP00000108554
Gene: ENSMUSG00000066798

Domain	Start	End	E-Value	Type
BTB	33	127	2.67e-16	SMART
Blast:BTB	161	196	1e-5	BLAST
ZnF_C2H2	300	322	7.15e-2	SMART
ZnF_C2H2	325	347	1.58e-3	SMART
ZnF_C2H2	353	375	3.63e-3	SMART
ZnF_C2H2	381	404	8.81e-2	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000203522

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.4%
20x: 95.4%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 94 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700113H08Rik	A	G	10: 87,066,066 (GRCm39)	E249G	possibly damaging	Het
2610028H24Rik	A	G	10: 76,293,349 (GRCm39)	M136V	possibly damaging	Het
4930523C07Rik	A	T	1: 159,902,945 (GRCm39)	K72*	probably null	Het
Abca6	A	G	11: 110,110,475 (GRCm39)	I558T	probably benign	Het
Acot10	T	C	15: 20,666,712 (GRCm39)	T10A	probably benign	Het
Adgrl4	T	A	3: 151,205,838 (GRCm39)	D233E	probably benign	Het
Adgrv1	A	T	13: 81,705,199 (GRCm39)	F1537Y	probably damaging	Het
Aqp3	T	A	4: 41,098,061 (GRCm39)	I17F	probably benign	Het
Arap1	T	A	7: 101,058,527 (GRCm39)	L1375H	probably damaging	Het
Aspm	T	C	1: 139,385,373 (GRCm39)	V339A	probably benign	Het
Atp13a3	G	A	16: 30,173,094 (GRCm39)	A261V	probably damaging	Het
Casp8ap2	T	C	4: 32,640,142 (GRCm39)	Y399H	probably benign	Het
Cept1	A	G	3: 106,420,195 (GRCm39)	V213A	probably damaging	Het
Cit	A	G	5: 116,123,566 (GRCm39)	D1469G	possibly damaging	Het
Cnga2	A	G	X: 71,051,394 (GRCm39)	Y182C	possibly damaging	Het
Cox20	A	G	1: 178,149,512 (GRCm39)	I54V	probably benign	Het
Dhx8	C	A	11: 101,629,235 (GRCm39)	D261E	probably benign	Het
Dnah2	A	T	11: 69,349,011 (GRCm39)	I2486N	probably benign	Het
Dnah5	A	G	15: 28,408,467 (GRCm39)	Q3484R	probably benign	Het
Drd1	T	C	13: 54,207,572 (GRCm39)	Y207C	probably damaging	Het
Dtl	C	T	1: 191,290,222 (GRCm39)	V222I	probably damaging	Het
Dync1h1	T	C	12: 110,607,316 (GRCm39)	Y2636H	probably damaging	Het
Endog	C	A	2: 30,062,048 (GRCm39)	D154E	probably benign	Het
Epc1	A	T	18: 6,462,954 (GRCm39)	V14E	probably damaging	Het
Ercc4	C	A	16: 12,965,798 (GRCm39)	T810K	probably damaging	Het
Fam43b	T	A	4: 138,123,299 (GRCm39)	N7I	possibly damaging	Het
Fgd1	T	C	X: 149,869,213 (GRCm39)		probably null	Het
Filip1	G	T	9: 79,726,612 (GRCm39)	T669N	probably damaging	Het
Fndc1	A	G	17: 7,997,497 (GRCm39)		probably benign	Het
Foxk1	C	A	5: 142,420,943 (GRCm39)	S189*	probably null	Het
Gatm	T	C	2: 122,431,017 (GRCm39)	N274S	probably damaging	Het
Gdf9	A	G	11: 53,328,334 (GRCm39)	Y430C	probably damaging	Het
Gga1	C	T	15: 78,772,648 (GRCm39)	P260S	probably damaging	Het
Gm11595	A	T	11: 99,663,327 (GRCm39)	C118S	unknown	Het
Gm382	G	T	X: 125,970,274 (GRCm39)	V820L	possibly damaging	Het
Gzmk	T	A	13: 113,308,548 (GRCm39)	I179F	probably damaging	Het
Hsp90b1	T	C	10: 86,531,570 (GRCm39)	D421G	probably damaging	Het
Hus1	A	G	11: 8,956,011 (GRCm39)	M174T	probably damaging	Het
Ifngr2	T	A	16: 91,359,761 (GRCm39)	Y289*	probably null	Het
Il6st	T	A	13: 112,640,709 (GRCm39)	H828Q	probably benign	Het
Impg2	T	A	16: 56,038,742 (GRCm39)	Y127N	probably damaging	Het
Irf3	T	A	7: 44,651,168 (GRCm39)	W345R	probably damaging	Het
Kif1b	G	A	4: 149,272,097 (GRCm39)	S1568L	possibly damaging	Het
Klhl42	A	G	6: 147,003,251 (GRCm39)	T342A	probably benign	Het
Kndc1	G	T	7: 139,510,025 (GRCm39)	R1289L	probably damaging	Het
Knl1	A	T	2: 118,902,300 (GRCm39)	T1334S	possibly damaging	Het
L3mbtl3	G	T	10: 26,189,766 (GRCm39)	D499E	unknown	Het
Ldhd	T	A	8: 112,353,680 (GRCm39)	M478L	probably benign	Het
Loxl4	C	G	19: 42,592,402 (GRCm39)	E385D	probably damaging	Het
Lrriq1	G	A	10: 103,050,718 (GRCm39)	T678I	probably benign	Het
Macf1	T	A	4: 123,386,567 (GRCm39)	I1017F	probably benign	Het
Madcam1	A	G	10: 79,501,406 (GRCm39)	E157G	possibly damaging	Het
Mamdc4	T	C	2: 25,459,270 (GRCm39)	D195G	probably damaging	Het
Mctp1	A	G	13: 76,972,941 (GRCm39)	D648G	probably damaging	Het
Mycbp2	T	C	14: 103,438,666 (GRCm39)	M2072V	probably benign	Het
Nck1	A	G	9: 100,379,600 (GRCm39)		probably null	Het
Ndufaf4	G	T	4: 24,898,608 (GRCm39)	D55Y	probably damaging	Het
Nek11	A	T	9: 105,177,560 (GRCm39)	D230E	probably benign	Het
Nit2	T	C	16: 56,981,559 (GRCm39)	K67E	possibly damaging	Het
Or12j2	C	T	7: 139,916,342 (GRCm39)	T189M	probably damaging	Het
Or5ae1	T	C	7: 84,565,701 (GRCm39)	F238S	probably damaging	Het
Or6a2	T	C	7: 106,600,455 (GRCm39)	D204G	probably damaging	Het
Or6c1	A	T	10: 129,518,401 (GRCm39)	V69E	possibly damaging	Het
Pakap	A	G	4: 57,854,890 (GRCm39)	Y134C	probably benign	Het
Pccb	G	C	9: 100,867,884 (GRCm39)	D347E	probably damaging	Het
Plcl1	T	A	1: 55,736,997 (GRCm39)	F779L	probably damaging	Het
Prune2	C	A	19: 17,099,786 (GRCm39)	D1763E	probably benign	Het
Pwwp2a	A	G	11: 43,596,145 (GRCm39)	S437G	probably benign	Het
Rabgap1l	A	T	1: 160,566,527 (GRCm39)	D90E	probably benign	Het
Rapgef4	T	A	2: 72,056,897 (GRCm39)	I552N	possibly damaging	Het
Scn7a	A	T	2: 66,528,330 (GRCm39)	I720K	probably damaging	Het
Scn9a	T	A	2: 66,356,998 (GRCm39)	N1101I	probably damaging	Het
Siglec1	A	T	2: 130,922,417 (GRCm39)	Y553N	probably damaging	Het
Slc22a23	A	G	13: 34,387,953 (GRCm39)	L381P	possibly damaging	Het
Slc7a11	T	A	3: 50,338,558 (GRCm39)	T284S	probably damaging	Het
Slc8a2	T	A	7: 15,874,417 (GRCm39)		probably null	Het
Snx29	T	A	16: 11,218,835 (GRCm39)	S224T	probably damaging	Het
Stimate	T	C	14: 30,588,581 (GRCm39)	Y103H	probably damaging	Het
Stox1	T	C	10: 62,500,314 (GRCm39)	T749A	probably benign	Het
Tg	A	G	15: 66,566,743 (GRCm39)	I1264V	probably benign	Het
Top2a	A	C	11: 98,900,633 (GRCm39)	V609G	probably damaging	Het
Trmt44	G	A	5: 35,732,176 (GRCm39)	P72S	probably benign	Het
Ttll3	G	C	6: 113,389,895 (GRCm39)	S760T	probably benign	Het
Ttn	T	C	2: 76,579,022 (GRCm39)	D23957G	probably damaging	Het
Ttn	G	A	2: 76,664,241 (GRCm39)		probably benign	Het
Ubxn1	T	G	19: 8,849,434 (GRCm39)	V59G	probably benign	Het
Ubxn4	T	C	1: 128,172,247 (GRCm39)	S14P	probably benign	Het
Uso1	T	A	5: 92,343,229 (GRCm39)	M771K	probably benign	Het
Utp20	A	G	10: 88,649,917 (GRCm39)	F431S	probably damaging	Het
Vmn1r206	T	C	13: 22,804,782 (GRCm39)	S142G	probably benign	Het
Vmn2r19	A	G	6: 123,285,289 (GRCm39)		probably null	Het
Vps36	G	T	8: 22,708,305 (GRCm39)		probably null	Het
Wnt3	A	G	11: 103,703,474 (GRCm39)	H319R	possibly damaging	Het
Zfp648	T	C	1: 154,080,353 (GRCm39)	S171P	probably benign	Het

Other mutations in Zbtb26

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00579:Zbtb26	APN	2	37,326,454 (GRCm39)	missense	possibly damaging	0.82
IGL00899:Zbtb26	APN	2	37,326,270 (GRCm39)	nonsense	probably null
IGL01598:Zbtb26	APN	2	37,326,283 (GRCm39)	missense	probably damaging	1.00
IGL01940:Zbtb26	APN	2	37,325,987 (GRCm39)	missense	possibly damaging	0.93
IGL02152:Zbtb26	APN	2	37,326,703 (GRCm39)	missense	possibly damaging	0.95
IGL02867:Zbtb26	APN	2	37,326,261 (GRCm39)	missense	probably benign	0.00
IGL02889:Zbtb26	APN	2	37,326,261 (GRCm39)	missense	probably benign	0.00
IGL03081:Zbtb26	APN	2	37,326,612 (GRCm39)	missense	possibly damaging	0.67
R0138:Zbtb26	UTSW	2	37,326,053 (GRCm39)	missense	probably benign	0.16
R0328:Zbtb26	UTSW	2	37,326,807 (GRCm39)	missense	possibly damaging	0.81
R0927:Zbtb26	UTSW	2	37,326,337 (GRCm39)	missense	possibly damaging	0.91
R1671:Zbtb26	UTSW	2	37,326,377 (GRCm39)	missense	probably benign	0.00
R1813:Zbtb26	UTSW	2	37,326,347 (GRCm39)	missense	possibly damaging	0.68
R1896:Zbtb26	UTSW	2	37,326,347 (GRCm39)	missense	possibly damaging	0.68
R2374:Zbtb26	UTSW	2	37,326,497 (GRCm39)	missense	probably benign
R4050:Zbtb26	UTSW	2	37,327,000 (GRCm39)	start codon destroyed	probably null	0.46
R4631:Zbtb26	UTSW	2	37,326,968 (GRCm39)	missense	probably benign	0.00
R4940:Zbtb26	UTSW	2	37,326,781 (GRCm39)	missense	probably damaging	0.98
R5071:Zbtb26	UTSW	2	37,325,941 (GRCm39)	missense	probably benign	0.26
R6348:Zbtb26	UTSW	2	37,325,687 (GRCm39)	missense	probably benign	0.43
R6962:Zbtb26	UTSW	2	37,326,106 (GRCm39)	missense	possibly damaging	0.71
R6990:Zbtb26	UTSW	2	37,326,557 (GRCm39)	missense	probably benign	0.00
R7261:Zbtb26	UTSW	2	37,326,667 (GRCm39)	missense	possibly damaging	0.71
R7981:Zbtb26	UTSW	2	37,326,887 (GRCm39)	missense	possibly damaging	0.51
R8013:Zbtb26	UTSW	2	37,327,013 (GRCm39)	critical splice acceptor site	probably null
R8014:Zbtb26	UTSW	2	37,327,013 (GRCm39)	critical splice acceptor site	probably null
R8872:Zbtb26	UTSW	2	37,326,913 (GRCm39)	missense	probably damaging	0.99
R8876:Zbtb26	UTSW	2	37,326,896 (GRCm39)	missense	probably benign
R8905:Zbtb26	UTSW	2	37,326,927 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- TGCAAAGCAGTGGGTTCAG -3'
(R):5'- AAGTGGGGAGACAATTGCTC -3'

Sequencing Primer
(F):5'- GGTTCAGAAGAAATGTACTGGTTCTC -3'
(R):5'- GACAATTGCTCTTGTCCTGTTATAG -3'

Posted On

2014-09-17