Mutagenetix > Incidental Mutations

Incidental Mutation 'R7223:Mybl2'

561925

Institutional Source

Beutler Lab

Gene Symbol

Mybl2

Ensembl Gene

ENSMUSG00000017861

Gene Name

myeloblastosis oncogene-like 2

Synonyms

B-Myb, Bmyb

MMRRC Submission

Accession Numbers

Is this an essential gene?

Essential (E-score: 1.000) question?

Stock #

R7223 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

163054687-163084688 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 163072705 bp

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 248 (T248A)

Ref Sequence

ENSEMBL: ENSMUSP00000018005 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000018005] [ENSMUST00000142729]

PDB Structure

Solution Structure of RSGI RUH-050, a myb DNA-binding domain in mouse cDNA [SOLUTION NMR]

Predicted Effect

probably benign
Transcript: ENSMUST00000018005
AA Change: T248A

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)

SMART Domains

Protein: ENSMUSP00000018005
Gene: ENSMUSG00000017861
AA Change: T248A

Domain	Start	End	E-Value	Type
SANT	30	79	1.38e-16	SMART
SANT	82	131	5.77e-19	SMART
SANT	134	182	2.12e-17	SMART
low complexity region	232	252	N/A	INTRINSIC
low complexity region	339	366	N/A	INTRINSIC
Pfam:Cmyb_C	454	610	6.4e-62	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000142729

SMART Domains

Protein: ENSMUSP00000114710
Gene: ENSMUSG00000017861

Domain	Start	End	E-Value	Type
Pfam:Cmyb_C	16	71	1.9e-23	PFAM
Pfam:Cmyb_C	99	215	4e-36	PFAM

Coding Region Coverage

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

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene, a member of the MYB family of transcription factor genes, is a nuclear protein involved in cell cycle progression. The encoded protein is phosphorylated by cyclin A/cyclin-dependent kinase 2 during the S-phase of the cell cycle and possesses both activator and repressor activities. It has been shown to activate the cell division cycle 2, cyclin D1, and insulin-like growth factor-binding protein 5 genes. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2013]
PHENOTYPE: Mice homozygous for disruptions in this gene die as embryos shortly after implantation. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 82 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcb11	A	T	2: 69,274,143	V733E	probably benign	Het
Adam34	A	T	8: 43,652,004	N201K	probably benign	Het
Aldh3b2	A	C	19: 3,979,592	S322R	probably damaging	Het
Anpep	A	T	7: 79,825,310	L914Q	probably damaging	Het
Arhgap30	T	C	1: 171,407,571	F535S	probably damaging	Het
Baiap3	G	A	17: 25,243,840	R1075C	probably benign	Het
Baz2a	G	T	10: 128,112,606	G252V	probably damaging	Het
Brinp3	T	A	1: 146,901,074	S420T	possibly damaging	Het
Carmil3	T	C	14: 55,496,238	F359S	possibly damaging	Het
Ccdc124	A	T	8: 70,868,526	L190Q	probably damaging	Het
Ccr6	T	C	17: 8,256,140	V59A	probably damaging	Het
Ccr8	T	A	9: 120,094,617	I266N	probably damaging	Het
Cdh23	T	A	10: 60,331,817	E1798V	probably damaging	Het
Cdk5rap2	T	C	4: 70,235,447	N1713S	probably benign	Het
Cep19	T	A	16: 32,104,015	I33N	probably damaging	Het
Cers3	A	T	7: 66,783,415	Y196F	probably damaging	Het
Cidea	T	C	18: 67,366,421	I126T	probably damaging	Het
Copg2	A	T	6: 30,812,754	Y546*	probably null	Het
Cul3	A	T	1: 80,287,000	V261E	probably benign	Het
Cyp2g1	A	T	7: 26,814,632	D221V	probably damaging	Het
Cyp8b1	G	A	9: 121,915,097	H390Y	probably damaging	Het
Daam1	T	C	12: 71,988,943	F971L	probably damaging	Het
Dnajc24	G	A	2: 106,001,966	S24L	possibly damaging	Het
Dpysl3	T	C	18: 43,438,042	S56G	probably benign	Het
Esp1	A	G	17: 40,731,081	D88G	probably benign	Het
Fam171b	A	G	2: 83,878,230	T359A	probably damaging	Het
Fam186b	T	C	15: 99,279,837	E536G	possibly damaging	Het
Fbxo3	T	C	2: 104,043,012	V156A	possibly damaging	Het
Gls2	C	A	10: 128,199,194	H65Q	probably benign	Het
Gp2	A	G	7: 119,451,498		probably null	Het
Gpcpd1	T	A	2: 132,534,056	K435I	probably benign	Het
Gpx6	T	A	13: 21,317,670		probably null	Het
Hps3	A	T	3: 20,030,419	S202T	probably benign	Het
Htr1d	T	A	4: 136,443,501	L347H	probably damaging	Het
Igfals	T	C	17: 24,881,234	L433P	probably damaging	Het
Ilvbl	C	T	10: 78,583,696	H537Y	probably benign	Het
Iqgap2	A	T	13: 95,628,972	M1530K	probably damaging	Het
Jarid2	A	G	13: 44,896,322	T247A	possibly damaging	Het
L3hypdh	C	T	12: 72,074,009	V323I	possibly damaging	Het
Lama3	C	T	18: 12,582,608	T1707I	possibly damaging	Het
Map6	G	T	7: 99,268,025	A2S	probably damaging	Het
Mfap3	T	A	11: 57,530,240	I349K	probably benign	Het
N6amt1	A	G	16: 87,362,660	*151W	probably null	Het
Nhlrc1	A	G	13: 47,014,208	V191A	probably benign	Het
Nkx2-5	T	C	17: 26,839,620	E120G	possibly damaging	Het
Olfr1066	T	A	2: 86,455,867	I135F	possibly damaging	Het
Olfr1380	T	A	11: 49,564,098	M59K	probably damaging	Het
Olfr582	C	A	7: 103,041,632	T46N	possibly damaging	Het
Olfr890	T	C	9: 38,143,753	V201A	probably benign	Het
Pcdha8	T	G	18: 36,993,148	L228V	probably benign	Het
Pcsk2	A	G	2: 143,690,333	T134A	possibly damaging	Het
Phldb3	G	A	7: 24,624,653	R484Q	probably benign	Het
Pipox	A	G	11: 77,881,186	S371P	probably damaging	Het
Plekhg1	T	C	10: 3,873,343	S159P		Het
Psme4	C	T	11: 30,874,226	P1737S	probably benign	Het
Pygm	G	A	19: 6,388,863	D328N	probably benign	Het
Rabgef1	A	T	5: 130,190,960	E88V	probably benign	Het
Rims2	G	T	15: 39,437,032	R245L	probably benign	Het
Slc38a4	T	C	15: 97,010,345	I172V	probably damaging	Het
Slc4a10	T	A	2: 62,268,665	Y586N	probably damaging	Het
Snap91	C	T	9: 86,879,557		probably benign	Het
Sorcs1	C	T	19: 50,190,042	V881I	probably benign	Het
Spef2	A	T	15: 9,601,640	V1512E	unknown	Het
Sufu	T	C	19: 46,453,277	I292T	possibly damaging	Het
Tet1	T	C	10: 62,813,671	N87D	possibly damaging	Het
Tmem108	T	C	9: 103,499,534	T239A	not run	Het
Tmem121	A	T	12: 113,188,494	K111*	probably null	Het
Tpp2	T	A	1: 43,968,888	D417E	probably damaging	Het
Tpr	G	A	1: 150,439,256	E2025K	possibly damaging	Het
Trappc3	C	T	4: 126,275,152	A145V	possibly damaging	Het
Ttn	T	C	2: 76,890,981	D6754G	probably null	Het
Unc13c	T	A	9: 73,629,191	M1627L	probably benign	Het
Ush2a	A	G	1: 188,810,217	I3327V	probably benign	Het
Vmn1r74	C	T	7: 11,846,967	Q65*	probably null	Het
Wdr18	G	A	10: 79,960,368	R69H	probably damaging	Het
Zbed5	G	T	5: 129,900,438	D132Y	probably damaging	Het
Zfp644	A	T	5: 106,637,582	Y366*	probably null	Het
Zfyve26	T	C	12: 79,246,171	N2068S	probably damaging	Het
Zic2	T	C	14: 122,476,091	F139S	probably damaging	Het
Zmynd11	T	C	13: 9,710,162	Q141R	probably benign	Het
Zrsr1	A	G	11: 22,973,388	E54G	probably benign	Het
Zscan10	G	A	17: 23,609,482	D333N	probably benign	Het

Other mutations in Mybl2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02331:Mybl2	APN	2	163074685	missense	probably damaging	1.00
IGL03112:Mybl2	APN	2	163062536	missense	probably damaging	1.00
R0129:Mybl2	UTSW	2	163059491	splice site	probably benign
R0393:Mybl2	UTSW	2	163061608	splice site	probably benign
R0488:Mybl2	UTSW	2	163072614	unclassified	probably benign
R0839:Mybl2	UTSW	2	163075768	missense	probably benign	0.00
R1268:Mybl2	UTSW	2	163074716	missense	probably benign	0.06
R1462:Mybl2	UTSW	2	163072708	missense	probably benign
R1462:Mybl2	UTSW	2	163072708	missense	probably benign
R1667:Mybl2	UTSW	2	163075696	missense	probably damaging	1.00
R1829:Mybl2	UTSW	2	163059583	missense	probably benign	0.41
R4793:Mybl2	UTSW	2	163074763	missense	probably damaging	1.00
R4953:Mybl2	UTSW	2	163080796	missense	probably damaging	1.00
R5738:Mybl2	UTSW	2	163068283	nonsense	probably null
R6524:Mybl2	UTSW	2	163074530	missense	possibly damaging	0.65
R6957:Mybl2	UTSW	2	163072808	missense	possibly damaging	0.86
R7244:Mybl2	UTSW	2	163082685	missense	probably benign	0.10
R7376:Mybl2	UTSW	2	163082593	missense	possibly damaging	0.56
R7451:Mybl2	UTSW	2	163072706	missense	possibly damaging	0.86
R7623:Mybl2	UTSW	2	163072832	missense	probably damaging	1.00
R8463:Mybl2	UTSW	2	163074718	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- AGTGCTCAGTACAGTTGAAATGTC -3'
(R):5'- AGTCCAGAGCTTCAGAGAGG -3'

Sequencing Primer
(F):5'- GTCCCTGTGAGTTCCTTTGATGC -3'
(R):5'- AGCTTCAGAGAGGCTGGACC -3'

Posted On

2019-06-26