Mutagenetix > Incidental Mutation

Incidental Mutation 'R8461:Aurkb'

655285

Institutional Source

Beutler Lab

Gene Symbol

Aurkb

Ensembl Gene

ENSMUSG00000020897

Gene Name

aurora kinase B

Synonyms

Stk5, IPL1, STK-1, AIRK2, aurora B, Aik2, Stk12

MMRRC Submission

067837-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R8461 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

68936473-68942490 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 68941727 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 293 (V293A)

Ref Sequence

ENSEMBL: ENSMUSP00000021277 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000021277] [ENSMUST00000108666]

AlphaFold

O70126

Predicted Effect

probably damaging
Transcript: ENSMUST00000021277
AA Change: V293A

PolyPhen 2 Score 0.975 (Sensitivity: 0.76; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000021277
Gene: ENSMUSG00000020897
AA Change: V293A

Domain	Start	End	E-Value	Type
S_TKc	82	332	2.75e-94	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000108666
AA Change: V293A

PolyPhen 2 Score 0.975 (Sensitivity: 0.76; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000104306
Gene: ENSMUSG00000020897
AA Change: V293A

Domain	Start	End	E-Value	Type
S_TKc	82	332	2.75e-94	SMART

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.6%

Validation Efficiency

MGI Phenotype

FUNCTION: This gene encodes a member of the aurora kinase subfamily of serine/threonine kinases. The genes encoding the other two members of this subfamily are located on chromosomes 2 and 7. These kinases participate in the regulation of alignment and segregation of chromosomes during mitosis and meiosis through association with microtubules. [provided by RefSeq, Sep 2015]
PHENOTYPE: Heterozygous null mice may develop oligospermia and show premature death and increased tumor incidence. Homozygous null embryos are small and die post-implantation showing reduced inner cell mass outgrowth, mitotic defects, aberrant trophoblast giant cells, edema, hemorrhage and increased apoptosis. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 56 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700067P10Rik	G	T	17: 48,400,849 (GRCm39)	E45*	probably null	Het
4921539E11Rik	T	C	4: 103,112,712 (GRCm39)	D132G	probably benign	Het
Abca16	T	C	7: 120,035,918 (GRCm39)	F334L	possibly damaging	Het
Ache	T	C	5: 137,288,582 (GRCm39)	F96S	probably damaging	Het
Actg1	T	C	11: 120,239,010 (GRCm39)	T27A	unknown	Het
Ankrd27	T	C	7: 35,326,911 (GRCm39)	L752P	probably damaging	Het
Atp1a1	T	A	3: 101,496,405 (GRCm39)	T417S	probably benign	Het
Atp6v0a1	T	G	11: 100,935,400 (GRCm39)	L653R	possibly damaging	Het
C2cd5	A	T	6: 142,980,802 (GRCm39)	D654E	probably damaging	Het
Cacna1s	T	C	1: 136,001,440 (GRCm39)	V297A	possibly damaging	Het
Catsperg2	T	C	7: 29,404,744 (GRCm39)	D773G	possibly damaging	Het
Ccdc187	A	G	2: 26,183,814 (GRCm39)	L62P	probably damaging	Het
Cdh2	A	G	18: 16,783,522 (GRCm39)	V69A	probably benign	Het
D430041D05Rik	A	G	2: 103,998,280 (GRCm39)	V1156A	possibly damaging	Het
Defb37	G	A	8: 19,036,386 (GRCm39)	H45Y	unknown	Het
Dgke	T	C	11: 88,939,819 (GRCm39)	M367V	possibly damaging	Het
Dnah1	T	C	14: 31,027,915 (GRCm39)	K640R	probably benign	Het
Gm5478	A	T	15: 101,554,652 (GRCm39)	L148Q	probably damaging	Het
Hhla1	A	T	15: 65,795,723 (GRCm39)	S494R	probably benign	Het
Kcne4	G	A	1: 78,795,433 (GRCm39)	S27N	probably benign	Het
Klhdc7b	A	T	15: 89,271,824 (GRCm39)	H244L	probably damaging	Het
Lrrc40	T	C	3: 157,764,371 (GRCm39)	S429P	possibly damaging	Het
Map3k21	A	T	8: 126,671,361 (GRCm39)	D883V	probably benign	Het
Med4	T	C	14: 73,755,468 (GRCm39)	S259P	unknown	Het
Mrm3	T	C	11: 76,135,158 (GRCm39)	I123T	probably damaging	Het
Mrpl1	T	A	5: 96,361,646 (GRCm39)	V11D	probably damaging	Het
Myl1	G	A	1: 66,983,994 (GRCm39)	P24L	unknown	Het
Necap2	T	C	4: 140,797,531 (GRCm39)	K168R	probably damaging	Het
Nnt	A	G	13: 119,505,038 (GRCm39)	S559P	unknown	Het
Nox4	T	C	7: 86,966,479 (GRCm39)	F197L	probably damaging	Het
Nup93	T	C	8: 95,007,963 (GRCm39)		probably null	Het
Nxph2	T	C	2: 23,211,529 (GRCm39)	V10A	unknown	Het
Or1e16	T	A	11: 73,285,982 (GRCm39)	I289F	probably damaging	Het
Or8c11	T	A	9: 38,289,777 (GRCm39)	V194D	probably damaging	Het
Or8k38	G	A	2: 86,487,890 (GRCm39)	T304I	probably benign	Het
P2ry2	G	T	7: 100,647,895 (GRCm39)	R137S	possibly damaging	Het
Plxnb3	T	C	X: 72,803,103 (GRCm39)	Y324H	probably damaging	Het
Pmpca	G	C	2: 26,285,046 (GRCm39)	E424Q	possibly damaging	Het
Ppme1	T	C	7: 100,021,012 (GRCm39)	S7G	probably benign	Het
Rabep1	T	A	11: 70,775,681 (GRCm39)	M85K	possibly damaging	Het
Ranbp2	T	C	10: 58,312,216 (GRCm39)	Y979H	probably damaging	Het
Rapgef5	T	C	12: 117,677,844 (GRCm39)	S360P	probably benign	Het
Rbm33	T	A	5: 28,592,970 (GRCm39)	H623Q	probably damaging	Het
Rev1	G	T	1: 38,122,868 (GRCm39)	T450K	possibly damaging	Het
Sec23ip	T	A	7: 128,373,926 (GRCm39)	L716Q	probably benign	Het
Sp2	T	C	11: 96,846,739 (GRCm39)	T535A	possibly damaging	Het
Syne1	A	G	10: 5,011,463 (GRCm39)	S61P	probably benign	Het
Tcf4	T	C	18: 69,598,501 (GRCm39)	V72A	probably benign	Het
Tmem131	G	A	1: 36,833,902 (GRCm39)	S1726F	probably damaging	Het
Trim13	T	C	14: 61,842,921 (GRCm39)	Y313H	probably benign	Het
Ttn	A	G	2: 76,611,437 (GRCm39)	V17365A	possibly damaging	Het
Uap1l1	G	A	2: 25,255,422 (GRCm39)	A69V	probably benign	Het
Upp2	A	G	2: 58,670,068 (GRCm39)	D258G	probably benign	Het
Vmn1r44	A	T	6: 89,870,701 (GRCm39)	H149L	possibly damaging	Het
Zbtb49	T	C	5: 38,358,453 (GRCm39)	D600G	probably benign	Het
Zfp869	G	T	8: 70,160,305 (GRCm39)	H89Q	probably benign	Het

Other mutations in Aurkb

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01582:Aurkb	APN	11	68,939,605 (GRCm39)	missense	probably damaging	1.00
R0193:Aurkb	UTSW	11	68,939,370 (GRCm39)	missense	probably damaging	1.00
R0924:Aurkb	UTSW	11	68,936,822 (GRCm39)	nonsense	probably null
R4622:Aurkb	UTSW	11	68,939,188 (GRCm39)	missense	probably damaging	1.00
R4664:Aurkb	UTSW	11	68,939,435 (GRCm39)	missense	probably damaging	0.98
R4933:Aurkb	UTSW	11	68,938,970 (GRCm39)	intron	probably benign
R5243:Aurkb	UTSW	11	68,936,752 (GRCm39)	splice site	probably benign
R5705:Aurkb	UTSW	11	68,939,641 (GRCm39)	missense	possibly damaging	0.87
R6457:Aurkb	UTSW	11	68,939,172 (GRCm39)	missense	possibly damaging	0.77
R6604:Aurkb	UTSW	11	68,939,388 (GRCm39)	nonsense	probably null
R7739:Aurkb	UTSW	11	68,939,058 (GRCm39)	nonsense	probably null
R9289:Aurkb	UTSW	11	68,941,175 (GRCm39)	missense	probably damaging	1.00
Z1186:Aurkb	UTSW	11	68,938,696 (GRCm39)	missense	probably benign
Z1186:Aurkb	UTSW	11	68,938,692 (GRCm39)	missense	probably damaging	1.00
Z1187:Aurkb	UTSW	11	68,938,696 (GRCm39)	missense	probably benign
Z1187:Aurkb	UTSW	11	68,938,692 (GRCm39)	missense	probably damaging	1.00
Z1188:Aurkb	UTSW	11	68,938,696 (GRCm39)	missense	probably benign
Z1188:Aurkb	UTSW	11	68,938,692 (GRCm39)	missense	probably damaging	1.00
Z1189:Aurkb	UTSW	11	68,938,696 (GRCm39)	missense	probably benign
Z1189:Aurkb	UTSW	11	68,938,692 (GRCm39)	missense	probably damaging	1.00
Z1190:Aurkb	UTSW	11	68,938,696 (GRCm39)	missense	probably benign
Z1190:Aurkb	UTSW	11	68,938,692 (GRCm39)	missense	probably damaging	1.00
Z1191:Aurkb	UTSW	11	68,938,696 (GRCm39)	missense	probably benign
Z1191:Aurkb	UTSW	11	68,938,692 (GRCm39)	missense	probably damaging	1.00
Z1192:Aurkb	UTSW	11	68,938,696 (GRCm39)	missense	probably benign
Z1192:Aurkb	UTSW	11	68,938,692 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GTTCCATGCTCTCAAAAGAAACAA -3'
(R):5'- GTTCCCACCCCTTCTCAGAACA -3'

Sequencing Primer
(F):5'- TGACGGGATGAGTAGTCAG -3'
(R):5'- AACACTGAAAAATGACAGGGAC -3'

Posted On

2020-10-20