Mutagenetix > Incidental Mutation

Incidental Mutation 'R0457:Bub1b'

41194

Institutional Source

Beutler Lab

Gene Symbol

Bub1b

Ensembl Gene

ENSMUSG00000040084

Gene Name

BUB1B, mitotic checkpoint serine/threonine kinase

Synonyms

BUBR1

MMRRC Submission

038657-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R0457 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

118428692-118472072 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 118440340 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Serine at position 148 (F148S)

Ref Sequence

ENSEMBL: ENSMUSP00000037126 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000038341]

AlphaFold

Q9Z1S0

Predicted Effect

probably damaging
Transcript: ENSMUST00000038341
AA Change: F148S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000037126
Gene: ENSMUSG00000040084
AA Change: F148S

Domain	Start	End	E-Value	Type
PDB:4GGD\|D	14	35	6e-6	PDB
Mad3_BUB1_I	49	173	1.83e-68	SMART
low complexity region	198	214	N/A	INTRINSIC
low complexity region	382	395	N/A	INTRINSIC
coiled coil region	418	457	N/A	INTRINSIC
low complexity region	671	686	N/A	INTRINSIC
low complexity region	717	726	N/A	INTRINSIC
Pfam:Pkinase	806	942	4.5e-7	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000127356

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.4%
20x: 92.9%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a kinase involved in spindle checkpoint function. The protein has been localized to the kinetochore and plays a role in the inhibition of the anaphase-promoting complex/cyclosome (APC/C), delaying the onset of anaphase and ensuring proper chromosome segregation. Impaired spindle checkpoint function has been found in many forms of cancer. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous mutant embryos undergo extensive apoptosis and die during early gestation. Heterozygous mice are viable and exhibit splenomegaly, abnormal megakaryopoiesis, and an increased susceptibility to intestinal tumorigenesis. Hypomorphic homozygotes display infertility and premature aging. [provided by MGI curators]

Allele List at MGI

All alleles(22) : Targeted, knock-out(1) Targeted, other(3) Gene trapped(18)

Other mutations in this stock

Total: 70 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aadacl2fm1	A	G	3: 59,844,054 (GRCm39)	I249M	possibly damaging	Het
Adcy5	T	C	16: 35,094,915 (GRCm39)	S691P	probably benign	Het
Ajm1	G	T	2: 25,468,358 (GRCm39)	R518S	possibly damaging	Het
Aspscr1	A	G	11: 120,568,444 (GRCm39)	E12G	probably benign	Het
Atp2a2	T	C	5: 122,607,777 (GRCm39)	Q244R	probably benign	Het
Birc6	A	G	17: 74,959,023 (GRCm39)	M3818V	probably benign	Het
Birc6	C	T	17: 74,969,620 (GRCm39)	A4230V	probably damaging	Het
C1ra	T	C	6: 124,499,712 (GRCm39)	S633P	probably benign	Het
Cacna2d1	A	G	5: 16,472,414 (GRCm39)	T274A	probably damaging	Het
Cmya5	A	G	13: 93,232,095 (GRCm39)	W998R	possibly damaging	Het
Crbn	T	C	6: 106,758,018 (GRCm39)	K404R	probably benign	Het
Cryga	T	C	1: 65,142,204 (GRCm39)	Y63C	probably damaging	Het
Csmd1	C	A	8: 16,551,407 (GRCm39)		probably null	Het
Defa-ps1	A	T	8: 22,185,758 (GRCm39)		noncoding transcript	Het
Dnajc10	T	A	2: 80,175,290 (GRCm39)	V559D	possibly damaging	Het
Dock1	A	T	7: 134,739,874 (GRCm39)	E1423D	possibly damaging	Het
Dpf3	A	T	12: 83,319,179 (GRCm39)	S44T	probably damaging	Het
Dyrk3	A	T	1: 131,064,094 (GRCm39)	V31D	possibly damaging	Het
F5	T	C	1: 164,021,769 (GRCm39)	S1415P	probably benign	Het
Fam186b	A	C	15: 99,169,166 (GRCm39)	I927S	probably benign	Het
Fcho1	C	T	8: 72,165,204 (GRCm39)	A418T	probably benign	Het
Fer1l6	G	A	15: 58,509,943 (GRCm39)		probably null	Het
Fndc7	G	T	3: 108,783,861 (GRCm39)	S249R	probably benign	Het
Ganab	A	G	19: 8,884,614 (GRCm39)	E139G	possibly damaging	Het
Gbp5	A	G	3: 142,213,518 (GRCm39)	D478G	probably damaging	Het
Gm17324	T	A	9: 78,355,580 (GRCm39)	M1K	probably null	Het
Gtpbp6	T	A	5: 110,254,608 (GRCm39)	R126S	probably damaging	Het
Hapln4	G	A	8: 70,541,122 (GRCm39)	W385*	probably null	Het
Hmcn2	T	A	2: 31,305,296 (GRCm39)		probably null	Het
Hsp90ab1	A	G	17: 45,879,914 (GRCm39)	V534A	probably damaging	Het
Kat6b	C	A	14: 21,720,598 (GRCm39)	T1650K	probably damaging	Het
Kpna1	T	A	16: 35,823,275 (GRCm39)	D42E	probably benign	Het
Lrrc14b	A	G	13: 74,509,279 (GRCm39)	M376T	probably benign	Het
Lrrc40	A	G	3: 157,760,201 (GRCm39)		probably null	Het
Ltv1	T	C	10: 13,067,887 (GRCm39)	T34A	probably benign	Het
Mga	T	A	2: 119,746,969 (GRCm39)	N373K	probably damaging	Het
Msh3	A	T	13: 92,357,505 (GRCm39)	M101K	probably damaging	Het
Mthfd2l	T	C	5: 91,168,065 (GRCm39)	M320T	possibly damaging	Het
Mug1	G	A	6: 121,838,514 (GRCm39)	E506K	probably benign	Het
Ngb	T	C	12: 87,147,503 (GRCm39)	D54G	probably damaging	Het
Ntrk1	A	G	3: 87,699,014 (GRCm39)	F84L	probably benign	Het
Or1j18	A	T	2: 36,624,545 (GRCm39)	I71F	probably benign	Het
Or52n2b	T	A	7: 104,566,180 (GRCm39)	T108S	probably benign	Het
Phf12	T	A	11: 77,908,994 (GRCm39)	I358N	possibly damaging	Het
Plec	A	G	15: 76,061,801 (GRCm39)	F2577S	probably damaging	Het
Polr1c	T	A	17: 46,558,689 (GRCm39)	Y36F	probably benign	Het
Prkd1	A	T	12: 50,413,155 (GRCm39)	M672K	probably damaging	Het
Prob1	T	C	18: 35,785,539 (GRCm39)	Y905C	probably damaging	Het
Ptpn23	T	A	9: 110,215,361 (GRCm39)	H1433L	possibly damaging	Het
Rnf11	A	T	4: 109,314,149 (GRCm39)	L80Q	probably damaging	Het
Sbp	G	A	17: 24,164,286 (GRCm39)	G183D	probably benign	Het
Scgb2b7	A	T	7: 31,403,437 (GRCm39)	C90S	possibly damaging	Het
Slc4a9	T	C	18: 36,668,471 (GRCm39)	L710P	probably damaging	Het
Spire1	T	A	18: 67,685,670 (GRCm39)	I35F	probably damaging	Het
Sptbn2	T	C	19: 4,795,966 (GRCm39)	V1715A	possibly damaging	Het
St7	T	C	6: 17,819,281 (GRCm39)	F62L	probably damaging	Het
Svep1	C	T	4: 58,118,136 (GRCm39)	G862D	probably damaging	Het
Syne1	A	T	10: 4,972,041 (GRCm39)	M8789K	probably damaging	Het
Synpo2	A	G	3: 122,906,421 (GRCm39)	L965P	probably damaging	Het
Trhde	A	T	10: 114,284,167 (GRCm39)	M772K	probably benign	Het
Ttn	T	A	2: 76,608,851 (GRCm39)	K15976*	probably null	Het
Unc13a	A	C	8: 72,110,645 (GRCm39)		probably null	Het
Vcan	T	C	13: 89,851,318 (GRCm39)	E1214G	possibly damaging	Het
Vmn1r29	T	C	6: 58,285,072 (GRCm39)	V264A	probably benign	Het
Vmn1r60	T	A	7: 5,548,118 (GRCm39)		probably benign	Het
Wdr90	C	T	17: 26,079,459 (GRCm39)	R225H	probably benign	Het
Wnk1	G	A	6: 119,946,293 (GRCm39)	T620I	probably damaging	Het
Zan	C	T	5: 137,405,968 (GRCm39)		probably benign	Het
Zfp37	A	T	4: 62,109,902 (GRCm39)	C387*	probably null	Het
Zfp521	T	C	18: 13,977,897 (GRCm39)	T839A	probably benign	Het

Other mutations in Bub1b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00676:Bub1b	APN	2	118,460,619 (GRCm39)	missense	probably benign
IGL01319:Bub1b	APN	2	118,445,475 (GRCm39)	missense	possibly damaging	0.49
IGL01744:Bub1b	APN	2	118,467,230 (GRCm39)	missense	probably damaging	0.99
IGL03184:Bub1b	APN	2	118,440,258 (GRCm39)	splice site	probably benign
P0035:Bub1b	UTSW	2	118,452,666 (GRCm39)	missense	probably damaging	1.00
R0315:Bub1b	UTSW	2	118,457,457 (GRCm39)	splice site	probably benign
R0322:Bub1b	UTSW	2	118,470,099 (GRCm39)	splice site	probably benign
R0378:Bub1b	UTSW	2	118,471,604 (GRCm39)	missense	probably benign	0.01
R0845:Bub1b	UTSW	2	118,440,457 (GRCm39)	missense	probably damaging	1.00
R0960:Bub1b	UTSW	2	118,437,161 (GRCm39)	missense	probably benign	0.03
R1071:Bub1b	UTSW	2	118,462,928 (GRCm39)	frame shift	probably null
R1129:Bub1b	UTSW	2	118,445,487 (GRCm39)	missense	probably damaging	1.00
R1138:Bub1b	UTSW	2	118,453,570 (GRCm39)	missense	probably benign	0.01
R1171:Bub1b	UTSW	2	118,437,167 (GRCm39)	missense	probably benign	0.31
R1613:Bub1b	UTSW	2	118,470,222 (GRCm39)	critical splice donor site	probably null
R1667:Bub1b	UTSW	2	118,471,670 (GRCm39)	missense	probably benign	0.00
R1812:Bub1b	UTSW	2	118,462,902 (GRCm39)	missense	probably benign	0.00
R1828:Bub1b	UTSW	2	118,468,920 (GRCm39)	missense	probably benign	0.00
R2085:Bub1b	UTSW	2	118,452,676 (GRCm39)	missense	possibly damaging	0.88
R2137:Bub1b	UTSW	2	118,467,199 (GRCm39)	nonsense	probably null
R3749:Bub1b	UTSW	2	118,445,936 (GRCm39)	missense	possibly damaging	0.63
R3750:Bub1b	UTSW	2	118,445,936 (GRCm39)	missense	possibly damaging	0.63
R4211:Bub1b	UTSW	2	118,461,459 (GRCm39)	missense	possibly damaging	0.78
R4579:Bub1b	UTSW	2	118,453,657 (GRCm39)	nonsense	probably null
R4993:Bub1b	UTSW	2	118,467,251 (GRCm39)	missense	possibly damaging	0.63
R5144:Bub1b	UTSW	2	118,445,980 (GRCm39)	missense	possibly damaging	0.92
R5229:Bub1b	UTSW	2	118,460,470 (GRCm39)	missense	probably damaging	1.00
R5596:Bub1b	UTSW	2	118,461,463 (GRCm39)	missense	probably damaging	1.00
R5656:Bub1b	UTSW	2	118,435,912 (GRCm39)	missense	probably damaging	1.00
R5785:Bub1b	UTSW	2	118,440,325 (GRCm39)	missense	probably damaging	0.98
R5883:Bub1b	UTSW	2	118,440,363 (GRCm39)	missense	probably damaging	1.00
R6128:Bub1b	UTSW	2	118,448,293 (GRCm39)	missense	probably benign
R6187:Bub1b	UTSW	2	118,461,481 (GRCm39)	missense	probably damaging	1.00
R6333:Bub1b	UTSW	2	118,428,944 (GRCm39)	critical splice donor site	probably null
R6985:Bub1b	UTSW	2	118,437,095 (GRCm39)	missense	probably damaging	1.00
R6988:Bub1b	UTSW	2	118,467,311 (GRCm39)	missense	probably damaging	0.96
R7161:Bub1b	UTSW	2	118,456,534 (GRCm39)	missense	probably damaging	1.00
R7341:Bub1b	UTSW	2	118,467,267 (GRCm39)	missense	possibly damaging	0.95
R7575:Bub1b	UTSW	2	118,471,639 (GRCm39)	missense	possibly damaging	0.51
R7824:Bub1b	UTSW	2	118,457,448 (GRCm39)	splice site	probably null
R8129:Bub1b	UTSW	2	118,468,975 (GRCm39)	missense	probably benign	0.06
R8702:Bub1b	UTSW	2	118,468,975 (GRCm39)	missense	probably benign	0.06
R8787:Bub1b	UTSW	2	118,462,305 (GRCm39)	missense	probably damaging	1.00
R9569:Bub1b	UTSW	2	118,468,884 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGTTTGGCACATAACCGGCATTTG -3'
(R):5'- AGGGAATGGAGTCAGTCCATCCTC -3'

Sequencing Primer
(F):5'- GCACATAACCGGCATTTGATAAG -3'
(R):5'- CAACGGAGAACTCTTTGGATAC -3'

Posted On

2013-05-23