Mutagenetix > Incidental Mutation

Incidental Mutation 'R7981:Zbtb26'

651194

Institutional Source

Beutler Lab

Gene Symbol

Zbtb26

Ensembl Gene

ENSMUSG00000050714

Gene Name

zinc finger and BTB domain containing 26

Synonyms

A630026F21Rik

MMRRC Submission

046022-MU

Accession Numbers

Essential gene?

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

Stock #

R7981 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

37322180-37333147 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 37326887 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Leucine at position 50 (I50L)

Ref Sequence

ENSEMBL: ENSMUSP00000099850 (fasta)

Gene Model

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

AlphaFold

Q8C8S0

Predicted Effect

possibly damaging
Transcript: ENSMUST00000067043
AA Change: I39L

PolyPhen 2 Score 0.511 (Sensitivity: 0.88; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000070071
Gene: ENSMUSG00000050714
AA Change: I39L

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

possibly damaging
Transcript: ENSMUST00000102789
AA Change: I50L

PolyPhen 2 Score 0.511 (Sensitivity: 0.88; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000099850
Gene: ENSMUSG00000050714
AA Change: I50L

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

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.8%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 50 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aadacl2fm3	T	A	3: 59,784,360 (GRCm39)	F278I	probably damaging	Het
Abca8a	T	C	11: 109,980,739 (GRCm39)	T100A	probably benign	Het
Adam34l	A	G	8: 44,078,850 (GRCm39)	F458S	probably damaging	Het
Agbl1	A	G	7: 76,094,588 (GRCm39)	T740A	unknown	Het
Aldh1a2	A	T	9: 71,171,102 (GRCm39)	I197F	probably damaging	Het
Ankrd28	T	C	14: 31,424,114 (GRCm39)	T1009A	probably benign	Het
Antxrl	T	C	14: 33,787,838 (GRCm39)	V287A	probably damaging	Het
Baiap2l1	G	A	5: 144,294,700 (GRCm39)		probably benign	Het
Catsperd	T	C	17: 56,938,562 (GRCm39)	V30A	possibly damaging	Het
Ccdc150	A	T	1: 54,407,551 (GRCm39)	K1109M	probably damaging	Het
Ccdc28a	A	G	10: 18,094,127 (GRCm39)	L164P	probably benign	Het
Cnot1	C	T	8: 96,489,797 (GRCm39)	V469M	probably damaging	Het
Col16a1	T	G	4: 129,980,347 (GRCm39)		probably null	Het
Coq9	A	G	8: 95,569,285 (GRCm39)	H39R	probably benign	Het
Crh	T	A	3: 19,748,216 (GRCm39)	E142V	probably benign	Het
Depdc1a	A	G	3: 159,226,488 (GRCm39)	N265S	probably benign	Het
Dlg5	T	C	14: 24,208,213 (GRCm39)	T998A	probably benign	Het
Epg5	T	C	18: 78,052,929 (GRCm39)		probably null	Het
Gcc1	G	A	6: 28,419,140 (GRCm39)	L398F	probably benign	Het
Gde1	T	C	7: 118,288,264 (GRCm39)	T320A	probably damaging	Het
Gemin5	T	C	11: 58,036,231 (GRCm39)	D704G	probably damaging	Het
Gfi1	G	A	5: 107,873,543 (GRCm39)		probably benign	Het
Insc	A	G	7: 114,428,302 (GRCm39)	T92A	probably damaging	Het
Krtap6-2	T	C	16: 89,216,562 (GRCm39)	Y135C	unknown	Het
Lpcat2	T	C	8: 93,582,182 (GRCm39)	S34P	probably damaging	Het
Mansc1	T	C	6: 134,587,274 (GRCm39)	D301G	possibly damaging	Het
Mbl2	C	A	19: 30,216,737 (GRCm39)	T183K	probably damaging	Het
Mri1	A	C	8: 84,983,792 (GRCm39)	V33G	possibly damaging	Het
Mrps7	T	C	11: 115,497,687 (GRCm39)	M184T	possibly damaging	Het
Mug1	A	T	6: 121,858,723 (GRCm39)	Y1147F	probably damaging	Het
N4bp2	C	T	5: 65,969,485 (GRCm39)	H1416Y	probably benign	Het
Naa15	T	C	3: 51,366,092 (GRCm39)	F487S	probably damaging	Het
Nin	C	T	12: 70,089,591 (GRCm39)	V1275I		Het
Or4c116	A	G	2: 88,942,400 (GRCm39)	F152S	probably damaging	Het
Or55b3	A	T	7: 102,127,036 (GRCm39)	Y14N	probably damaging	Het
Pik3c2b	A	T	1: 133,003,547 (GRCm39)		probably null	Het
Pkn1	G	T	8: 84,407,637 (GRCm39)	N463K	probably damaging	Het
Pramel24	T	G	4: 143,453,452 (GRCm39)	F187V	probably benign	Het
Rab11fip3	C	T	17: 26,216,963 (GRCm39)	S816N	probably damaging	Het
Rassf4	G	T	6: 116,617,218 (GRCm39)	D262E	probably damaging	Het
Sec16a	A	G	2: 26,311,384 (GRCm39)		probably null	Het
Sspo	A	G	6: 48,445,428 (GRCm39)	T2290A	probably benign	Het
Sumf1	A	G	6: 108,129,186 (GRCm39)		probably null	Het
Syne1	T	C	10: 5,179,248 (GRCm39)	K4409E	probably benign	Het
Tasor	T	C	14: 27,168,373 (GRCm39)	V305A	possibly damaging	Het
Tmco4	T	G	4: 138,785,772 (GRCm39)	L614R	probably damaging	Het
Tmem67	G	T	4: 12,070,592 (GRCm39)	N245K	probably damaging	Het
Trim58	T	C	11: 58,542,138 (GRCm39)	V366A	probably benign	Het
Vmn1r123	T	C	7: 20,896,914 (GRCm39)	S269P	probably damaging	Het
Vmn2r91	T	A	17: 18,327,887 (GRCm39)	S494T	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
R2128:Zbtb26	UTSW	2	37,326,563 (GRCm39)	missense	probably benign	0.00
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
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'- GTTCCATCTCAGGGAATTCCAG -3'
(R):5'- ACAAGCATGACAACACATTTGG -3'

Sequencing Primer
(F):5'- TCTCAGGGAATTCCAGCACAC -3'
(R):5'- GCATGACAACACATTTGGTTTTG -3'

Posted On

2020-09-15