Mutagenetix > Incidental Mutation

Incidental Mutation 'R7633:Atr'

589763

Institutional Source

Beutler Lab

Gene Symbol

Atr

Ensembl Gene

ENSMUSG00000032409

Gene Name

ataxia telangiectasia and Rad3 related

Synonyms

MMRRC Submission

045721-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R7633 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

95857597-95951781 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 95947118 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Glutamic Acid at position 2508 (V2508E)

Ref Sequence

ENSEMBL: ENSMUSP00000149953 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000034980] [ENSMUST00000215311]

AlphaFold

no structure available at present

Predicted Effect

SMART Domains

Protein: ENSMUSP00000034980
Gene: ENSMUSG00000032409
AA Change: V2502E

Domain	Start	End	E-Value	Type
low complexity region	431	449	N/A	INTRINSIC
low complexity region	889	897	N/A	INTRINSIC
low complexity region	998	1013	N/A	INTRINSIC
UME	1119	1225	2.3e-43	SMART
low complexity region	1352	1362	N/A	INTRINSIC
Pfam:FAT	1771	2092	9.2e-51	PFAM
PI3Kc	2320	2630	7.51e-124	SMART
FATC	2609	2641	6.22e-13	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000215311
AA Change: V2508E

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

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.0%

Validation Efficiency

100% (52/52)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs the PI3/PI4-kinase family, and is most closely related to ATM, a protein kinase encoded by the gene mutated in ataxia telangiectasia. This protein and ATM share similarity with Schizosaccharomyces pombe rad3, a cell cycle checkpoint gene required for cell cycle arrest and DNA damage repair in response to DNA damage. This kinase has been shown to phosphorylate checkpoint kinase CHK1, checkpoint proteins RAD17, and RAD9, as well as tumor suppressor protein BRCA1. Mutations of this gene are associated with Seckel syndrome. An alternatively spliced transcript variant of this gene has been reported, however, its full length nature is not known. Transcript variants utilizing alternative polyA sites exist. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit early embryonic lethality. Mice heterozygous for a knock-out allele exhibit premature death and increased tumor incidence. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 54 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A530084C06Rik	G	T	13: 31,558,995 (GRCm38)	R92S	unknown	Het
Acaca	A	G	11: 84,372,639 (GRCm38)	I2029V	probably benign	Het
Anks1b	A	C	10: 90,948,584 (GRCm38)	D1138A	probably damaging	Het
C4b	C	T	17: 34,729,399 (GRCm38)		probably null	Het
Calhm4	G	A	10: 34,043,908 (GRCm38)	T121M	possibly damaging	Het
Cd46	A	T	1: 195,083,619 (GRCm38)	M146K	probably null	Het
Chp1	A	G	2: 119,560,745 (GRCm38)	I28V	probably benign	Het
Chrnb1	T	A	11: 69,792,873 (GRCm38)	R216W	probably damaging	Het
Clmn	G	A	12: 104,782,112 (GRCm38)	T392M	probably benign	Het
Cracd	A	G	5: 76,857,520 (GRCm38)	E576G	unknown	Het
Dcxr	A	C	11: 120,726,453 (GRCm38)	L88R	probably benign	Het
Dedd	C	T	1: 171,338,910 (GRCm38)	P138L	probably benign	Het
Degs1	A	G	1: 182,279,698 (GRCm38)	S35P	probably damaging	Het
Ehmt1	T	C	2: 24,815,780 (GRCm38)	D851G	possibly damaging	Het
Fam117b	A	G	1: 59,981,534 (GRCm38)	D521G	probably damaging	Het
Gm6882	A	G	7: 21,427,652 (GRCm38)	V97A	probably damaging	Het
Hgs	A	T	11: 120,474,302 (GRCm38)	Q172L	probably damaging	Het
Hormad2	T	C	11: 4,346,662 (GRCm38)	Q274R	probably benign	Het
Igkv8-19	C	T	6: 70,341,399 (GRCm38)		probably benign	Het
Ikbkb	T	C	8: 22,671,741 (GRCm38)	N377S	probably benign	Het
Intu	G	A	3: 40,654,253 (GRCm38)	G232S	probably damaging	Het
Lypd9	C	A	11: 58,447,478 (GRCm38)	M29I	probably benign	Het
Mov10	A	G	3: 104,797,065 (GRCm38)	S806P	possibly damaging	Het
Mrgprb1	A	G	7: 48,447,583 (GRCm38)	F194L	probably benign	Het
Notch3	A	T	17: 32,158,622 (GRCm38)	I160K	probably benign	Het
Nup155	C	G	15: 8,109,453 (GRCm38)	S3W	probably damaging	Het
Or4k41	A	G	2: 111,449,622 (GRCm38)	I161V	probably benign	Het
Or8s5	A	G	15: 98,340,086 (GRCm38)	I301T	probably damaging	Het
Plxdc1	A	T	11: 97,956,151 (GRCm38)	F147L	possibly damaging	Het
Ppfia1	T	C	7: 144,552,436 (GRCm38)	D33G	possibly damaging	Het
Prdm11	G	A	2: 92,980,654 (GRCm38)	A200V	probably damaging	Het
Qrich2	A	T	11: 116,456,629 (GRCm38)	I1123K	unknown	Het
Rgs1	A	G	1: 144,248,477 (GRCm38)		probably null	Het
Skint7	T	A	4: 111,984,140 (GRCm38)	V259E	probably benign	Het
Slc25a3	A	T	10: 91,118,042 (GRCm38)		probably null	Het
Slc28a2b	A	T	2: 122,486,680 (GRCm38)	R7S	probably null	Het
Slco1a6	A	T	6: 142,145,755 (GRCm38)	I73N	probably damaging	Het
Sltm	C	G	9: 70,586,673 (GRCm38)	P802R	possibly damaging	Het
Smc4	CTA	CTATA	3: 69,018,067 (GRCm38)		probably benign	Het
Spock2	G	A	10: 60,126,180 (GRCm38)	D206N	probably damaging	Het
Stard3nl	T	G	13: 19,367,838 (GRCm38)	R185S	probably damaging	Het
Supt16	A	G	14: 52,197,099 (GRCm38)	Y18H	probably benign	Het
Synpo	G	A	18: 60,603,428 (GRCm38)	T482I	probably damaging	Het
Tcstv7b	G	A	13: 120,240,840 (GRCm38)	W57*	probably null	Het
Tmc6	G	T	11: 117,769,220 (GRCm38)	T694K	probably benign	Het
Trim59	T	A	3: 69,037,926 (GRCm38)	H27L	probably damaging	Het
Trpv2	G	A	11: 62,591,006 (GRCm38)		probably null	Het
Tyw5	A	T	1: 57,393,485 (GRCm38)	D117E	probably benign	Het
Usp17la	T	C	7: 104,861,147 (GRCm38)	Y320H	probably damaging	Het
Usp31	T	C	7: 121,658,962 (GRCm38)	D694G	probably damaging	Het
Vmn1r159	T	A	7: 22,843,023 (GRCm38)	T195S	probably damaging	Het
Vmn2r57	C	T	7: 41,425,089 (GRCm38)	V517M	possibly damaging	Het
Yipf1	A	G	4: 107,318,996 (GRCm38)	N29S	probably benign	Het
Zfp954	A	T	7: 7,115,824 (GRCm38)	F240L	possibly damaging	Het

Other mutations in Atr

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00640:Atr	APN	9	95,865,052 (GRCm38)	missense	probably damaging	1.00
IGL00922:Atr	APN	9	95,907,345 (GRCm38)	missense	probably damaging	0.97
IGL01020:Atr	APN	9	95,862,783 (GRCm38)	missense	probably damaging	1.00
IGL01345:Atr	APN	9	95,940,949 (GRCm38)	missense	probably damaging	1.00
IGL01364:Atr	APN	9	95,865,624 (GRCm38)	missense	probably benign	0.29
IGL01456:Atr	APN	9	95,950,565 (GRCm38)	missense	possibly damaging	0.62
IGL01534:Atr	APN	9	95,865,546 (GRCm38)	missense	probably damaging	0.99
IGL01761:Atr	APN	9	95,951,448 (GRCm38)	splice site	probably benign
IGL01791:Atr	APN	9	95,921,781 (GRCm38)	missense	probably benign	0.05
IGL01831:Atr	APN	9	95,870,754 (GRCm38)	missense	probably benign	0.18
IGL01973:Atr	APN	9	95,871,674 (GRCm38)	missense	probably damaging	1.00
IGL02008:Atr	APN	9	95,881,420 (GRCm38)	splice site	probably benign
IGL02016:Atr	APN	9	95,927,175 (GRCm38)	missense	probably benign	0.09
IGL02035:Atr	APN	9	95,866,682 (GRCm38)	missense	probably benign	0.01
IGL02058:Atr	APN	9	95,871,487 (GRCm38)	missense	probably damaging	0.99
IGL02081:Atr	APN	9	95,883,205 (GRCm38)	missense	probably damaging	1.00
IGL02224:Atr	APN	9	95,878,629 (GRCm38)	missense	probably damaging	0.98
IGL02234:Atr	APN	9	95,947,250 (GRCm38)	splice site	probably benign
IGL02367:Atr	APN	9	95,899,141 (GRCm38)	nonsense	probably null
IGL02621:Atr	APN	9	95,908,400 (GRCm38)	missense	probably benign	0.00
IGL02728:Atr	APN	9	95,936,475 (GRCm38)	missense	probably damaging	1.00
IGL02833:Atr	APN	9	95,862,852 (GRCm38)	missense	probably damaging	1.00
IGL02939:Atr	APN	9	95,865,261 (GRCm38)	missense	probably benign
IGL03107:Atr	APN	9	95,897,730 (GRCm38)	missense	probably benign	0.28
IGL03382:Atr	APN	9	95,920,822 (GRCm38)	nonsense	probably null
PIT4812001:Atr	UTSW	9	95,910,649 (GRCm38)	missense	probably benign	0.41
R0042:Atr	UTSW	9	95,927,356 (GRCm38)	splice site	probably benign
R0042:Atr	UTSW	9	95,927,356 (GRCm38)	splice site	probably benign
R0281:Atr	UTSW	9	95,937,566 (GRCm38)	missense	probably benign	0.26
R0282:Atr	UTSW	9	95,862,798 (GRCm38)	missense	probably benign	0.12
R0512:Atr	UTSW	9	95,935,526 (GRCm38)	missense	probably damaging	0.99
R0547:Atr	UTSW	9	95,899,165 (GRCm38)	splice site	probably benign
R0567:Atr	UTSW	9	95,865,829 (GRCm38)	missense	probably benign	0.00
R0631:Atr	UTSW	9	95,874,777 (GRCm38)	missense	possibly damaging	0.92
R1116:Atr	UTSW	9	95,867,636 (GRCm38)	nonsense	probably null
R1171:Atr	UTSW	9	95,907,323 (GRCm38)	missense	probably damaging	1.00
R1241:Atr	UTSW	9	95,950,636 (GRCm38)	missense	probably benign	0.08
R1345:Atr	UTSW	9	95,920,355 (GRCm38)	missense	probably benign	0.25
R1400:Atr	UTSW	9	95,862,848 (GRCm38)	missense	probably benign	0.32
R1413:Atr	UTSW	9	95,932,442 (GRCm38)	missense	probably damaging	1.00
R1527:Atr	UTSW	9	95,870,043 (GRCm38)	missense	possibly damaging	0.82
R1557:Atr	UTSW	9	95,871,449 (GRCm38)	missense	probably damaging	1.00
R1591:Atr	UTSW	9	95,945,385 (GRCm38)	missense	probably damaging	1.00
R1602:Atr	UTSW	9	95,951,557 (GRCm38)	missense	probably damaging	1.00
R1605:Atr	UTSW	9	95,936,463 (GRCm38)	missense	probably damaging	1.00
R1670:Atr	UTSW	9	95,861,456 (GRCm38)	missense	probably benign	0.38
R1709:Atr	UTSW	9	95,871,076 (GRCm38)	missense	probably benign	0.00
R1728:Atr	UTSW	9	95,897,581 (GRCm38)	missense	probably benign	0.01
R1729:Atr	UTSW	9	95,897,581 (GRCm38)	missense	probably benign	0.01
R1739:Atr	UTSW	9	95,897,581 (GRCm38)	missense	probably benign	0.01
R1816:Atr	UTSW	9	95,866,694 (GRCm38)	missense	probably benign	0.00
R1824:Atr	UTSW	9	95,936,421 (GRCm38)	missense	probably damaging	1.00
R1844:Atr	UTSW	9	95,905,817 (GRCm38)	missense	probably benign	0.01
R1857:Atr	UTSW	9	95,865,097 (GRCm38)	missense	probably damaging	1.00
R1858:Atr	UTSW	9	95,865,097 (GRCm38)	missense	probably damaging	1.00
R1866:Atr	UTSW	9	95,870,605 (GRCm38)	splice site	probably null
R1913:Atr	UTSW	9	95,866,733 (GRCm38)	missense	probably benign	0.01
R2042:Atr	UTSW	9	95,870,022 (GRCm38)	missense	probably benign	0.00
R2210:Atr	UTSW	9	95,907,300 (GRCm38)	missense	probably damaging	1.00
R2230:Atr	UTSW	9	95,920,765 (GRCm38)	missense	probably damaging	1.00
R2361:Atr	UTSW	9	95,871,157 (GRCm38)	missense	probably benign	0.41
R2399:Atr	UTSW	9	95,871,599 (GRCm38)	missense	probably benign	0.00
R2431:Atr	UTSW	9	95,862,892 (GRCm38)	missense	probably benign	0.24
R2860:Atr	UTSW	9	95,874,243 (GRCm38)	missense	probably benign	0.07
R2861:Atr	UTSW	9	95,874,243 (GRCm38)	missense	probably benign	0.07
R3019:Atr	UTSW	9	95,905,818 (GRCm38)	missense	possibly damaging	0.52
R3684:Atr	UTSW	9	95,920,400 (GRCm38)	missense	probably damaging	0.96
R4155:Atr	UTSW	9	95,888,124 (GRCm38)	nonsense	probably null
R4295:Atr	UTSW	9	95,874,426 (GRCm38)	missense	probably benign	0.04
R4359:Atr	UTSW	9	95,951,536 (GRCm38)	missense	probably damaging	1.00
R4506:Atr	UTSW	9	95,865,237 (GRCm38)	missense	probably benign	0.21
R4523:Atr	UTSW	9	95,862,863 (GRCm38)	missense	probably damaging	1.00
R4536:Atr	UTSW	9	95,874,418 (GRCm38)	missense	probably benign	0.26
R4588:Atr	UTSW	9	95,865,667 (GRCm38)	missense	probably benign
R4646:Atr	UTSW	9	95,871,197 (GRCm38)	critical splice donor site	probably null
R4702:Atr	UTSW	9	95,920,355 (GRCm38)	missense	possibly damaging	0.92
R4743:Atr	UTSW	9	95,862,792 (GRCm38)	missense	probably benign	0.14
R4782:Atr	UTSW	9	95,862,797 (GRCm38)	missense	probably benign	0.00
R4928:Atr	UTSW	9	95,907,299 (GRCm38)	missense	probably damaging	1.00
R5031:Atr	UTSW	9	95,865,702 (GRCm38)	missense	probably damaging	0.98
R5138:Atr	UTSW	9	95,937,596 (GRCm38)	missense	probably benign	0.15
R5188:Atr	UTSW	9	95,921,725 (GRCm38)	missense	probably benign	0.00
R5219:Atr	UTSW	9	95,881,238 (GRCm38)	missense	probably damaging	0.99
R5307:Atr	UTSW	9	95,878,544 (GRCm38)	missense	probably benign	0.01
R5414:Atr	UTSW	9	95,870,704 (GRCm38)	missense	probably benign	0.00
R5628:Atr	UTSW	9	95,874,226 (GRCm38)	nonsense	probably null
R5664:Atr	UTSW	9	95,905,813 (GRCm38)	missense	probably benign	0.00
R5678:Atr	UTSW	9	95,951,487 (GRCm38)	nonsense	probably null
R5724:Atr	UTSW	9	95,866,588 (GRCm38)	missense	probably damaging	1.00
R5759:Atr	UTSW	9	95,874,402 (GRCm38)	missense	probably benign	0.01
R5763:Atr	UTSW	9	95,945,123 (GRCm38)	missense	probably benign	0.04
R5922:Atr	UTSW	9	95,903,682 (GRCm38)	missense	probably benign	0.00
R6051:Atr	UTSW	9	95,908,369 (GRCm38)	missense	possibly damaging	0.85
R6161:Atr	UTSW	9	95,865,319 (GRCm38)	missense	probably benign
R6171:Atr	UTSW	9	95,881,271 (GRCm38)	nonsense	probably null
R6532:Atr	UTSW	9	95,908,408 (GRCm38)	missense	probably benign
R6774:Atr	UTSW	9	95,927,213 (GRCm38)	missense	probably benign	0.00
R6894:Atr	UTSW	9	95,927,197 (GRCm38)	missense	probably damaging	1.00
R6930:Atr	UTSW	9	95,866,635 (GRCm38)	missense	probably benign	0.21
R7018:Atr	UTSW	9	95,866,694 (GRCm38)	missense	probably benign	0.17
R7056:Atr	UTSW	9	95,862,863 (GRCm38)	missense	probably damaging	1.00
R7103:Atr	UTSW	9	95,865,372 (GRCm38)	missense	probably damaging	0.98
R7154:Atr	UTSW	9	95,865,045 (GRCm38)	missense	probably benign
R7157:Atr	UTSW	9	95,869,900 (GRCm38)	missense	probably benign	0.00
R7188:Atr	UTSW	9	95,862,791 (GRCm38)	nonsense	probably null
R7189:Atr	UTSW	9	95,862,791 (GRCm38)	nonsense	probably null
R7300:Atr	UTSW	9	95,865,370 (GRCm38)	missense	probably benign	0.00
R7337:Atr	UTSW	9	95,871,448 (GRCm38)	missense	probably damaging	1.00
R7584:Atr	UTSW	9	95,942,713 (GRCm38)	missense	probably damaging	1.00
R7602:Atr	UTSW	9	95,907,383 (GRCm38)	missense	possibly damaging	0.64
R7640:Atr	UTSW	9	95,907,293 (GRCm38)	splice site	probably null
R7677:Atr	UTSW	9	95,885,462 (GRCm38)	missense	probably damaging	1.00
R7699:Atr	UTSW	9	95,875,690 (GRCm38)	nonsense	probably null
R7700:Atr	UTSW	9	95,875,690 (GRCm38)	nonsense	probably null
R7790:Atr	UTSW	9	95,874,180 (GRCm38)	missense	probably damaging	1.00
R8027:Atr	UTSW	9	95,865,756 (GRCm38)	missense	probably damaging	0.99
R8147:Atr	UTSW	9	95,899,060 (GRCm38)	missense	probably damaging	1.00
R8204:Atr	UTSW	9	95,935,513 (GRCm38)	missense
R8306:Atr	UTSW	9	95,920,370 (GRCm38)	missense
R8462:Atr	UTSW	9	95,867,526 (GRCm38)	missense	probably benign
R8716:Atr	UTSW	9	95,907,415 (GRCm38)	missense	probably benign	0.09
R8748:Atr	UTSW	9	95,932,423 (GRCm38)	missense	probably benign	0.00
R8795:Atr	UTSW	9	95,867,531 (GRCm38)	missense	probably damaging	1.00
R8891:Atr	UTSW	9	95,905,760 (GRCm38)	missense	probably benign	0.03
R8976:Atr	UTSW	9	95,890,766 (GRCm38)	missense	probably benign	0.00
R9024:Atr	UTSW	9	95,907,363 (GRCm38)	missense	possibly damaging	0.93
R9116:Atr	UTSW	9	95,865,798 (GRCm38)	missense	probably benign	0.00
R9523:Atr	UTSW	9	95,910,557 (GRCm38)	missense	possibly damaging	0.89
R9524:Atr	UTSW	9	95,910,557 (GRCm38)	missense	possibly damaging	0.89
R9525:Atr	UTSW	9	95,910,557 (GRCm38)	missense	possibly damaging	0.89
R9527:Atr	UTSW	9	95,885,376 (GRCm38)	missense	probably damaging	1.00
R9563:Atr	UTSW	9	95,920,780 (GRCm38)	missense	probably damaging	0.98
R9629:Atr	UTSW	9	95,865,045 (GRCm38)	missense	probably benign
R9642:Atr	UTSW	9	95,939,241 (GRCm38)	missense	probably damaging	1.00
R9652:Atr	UTSW	9	95,874,834 (GRCm38)	missense	probably damaging	1.00
R9660:Atr	UTSW	9	95,914,997 (GRCm38)	missense	probably benign	0.40
R9678:Atr	UTSW	9	95,910,557 (GRCm38)	missense	possibly damaging	0.89
R9728:Atr	UTSW	9	95,914,997 (GRCm38)	missense	probably benign	0.40
R9731:Atr	UTSW	9	95,865,039 (GRCm38)	missense	possibly damaging	0.52
R9732:Atr	UTSW	9	95,861,385 (GRCm38)	missense	probably damaging	1.00
R9749:Atr	UTSW	9	95,937,650 (GRCm38)	critical splice donor site	probably null
X0019:Atr	UTSW	9	95,940,871 (GRCm38)	missense	probably damaging	1.00
Z1088:Atr	UTSW	9	95,885,320 (GRCm38)	splice site	probably null
Z1177:Atr	UTSW	9	95,888,100 (GRCm38)	missense	probably benign	0.01

Predicted Primers

PCR Primer
(F):5'- CCAAACTCTTTGAGCAAAGGTTTTG -3'
(R):5'- TATTTACATTCGAGGCCACTAGTAG -3'

Sequencing Primer
(F):5'- CTCACAGTCAGCTATTGGATGGATC -3'
(R):5'- TCGAGGCCACTAGTAGATTATTTAC -3'

Posted On

2019-10-24