Mutagenetix > Incidental Mutations

Incidental Mutation 'R0648:Trp53bp1'

57320

Institutional Source

Beutler Lab

Gene Symbol

Trp53bp1

Ensembl Gene

ENSMUSG00000043909

Gene Name

transformation related protein 53 binding protein 1

Synonyms

53BP1, p53BP1

MMRRC Submission

038833-MU

Accession Numbers

Is this an essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0648 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

121193281-121271407 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 121235707 bp

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 846 (V846A)

Ref Sequence

ENSEMBL: ENSMUSP00000114457 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000110647] [ENSMUST00000110648] [ENSMUST00000129752] [ENSMUST00000131245]

Predicted Effect

probably benign
Transcript: ENSMUST00000110647
AA Change: V846A

PolyPhen 2 Score 0.062 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000106277
Gene: ENSMUSG00000043909
AA Change: V846A

Domain	Start	End	E-Value	Type
low complexity region	136	149	N/A	INTRINSIC
low complexity region	158	169	N/A	INTRINSIC
low complexity region	647	661	N/A	INTRINSIC
low complexity region	1031	1042	N/A	INTRINSIC
low complexity region	1099	1112	N/A	INTRINSIC
low complexity region	1260	1272	N/A	INTRINSIC
low complexity region	1290	1332	N/A	INTRINSIC
Pfam:53-BP1_Tudor	1430	1551	2.5e-80	PFAM
low complexity region	1581	1601	N/A	INTRINSIC
BRCT	1673	1785	7.13e-1	SMART
BRCT	1813	1901	1.03e-6	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000110648
AA Change: V846A

PolyPhen 2 Score 0.012 (Sensitivity: 0.96; Specificity: 0.78)

SMART Domains

Protein: ENSMUSP00000106278
Gene: ENSMUSG00000043909
AA Change: V846A

Domain	Start	End	E-Value	Type
low complexity region	136	149	N/A	INTRINSIC
low complexity region	158	169	N/A	INTRINSIC
low complexity region	647	661	N/A	INTRINSIC
low complexity region	1031	1042	N/A	INTRINSIC
low complexity region	1099	1112	N/A	INTRINSIC
low complexity region	1260	1272	N/A	INTRINSIC
low complexity region	1290	1332	N/A	INTRINSIC
low complexity region	1389	1409	N/A	INTRINSIC
Pfam:53-BP1_Tudor	1480	1601	1.5e-80	PFAM
low complexity region	1631	1651	N/A	INTRINSIC
BRCT	1723	1835	7.13e-1	SMART
BRCT	1863	1951	1.03e-6	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000124031

Predicted Effect

probably benign
Transcript: ENSMUST00000129752

Predicted Effect

probably benign
Transcript: ENSMUST00000131245
AA Change: V846A

PolyPhen 2 Score 0.204 (Sensitivity: 0.92; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000114457
Gene: ENSMUSG00000043909
AA Change: V846A

Domain	Start	End	E-Value	Type
low complexity region	136	149	N/A	INTRINSIC
low complexity region	158	169	N/A	INTRINSIC
low complexity region	647	661	N/A	INTRINSIC
low complexity region	991	1002	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000142400

Predicted Effect

unknown
Transcript: ENSMUST00000147540
AA Change: V100A

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.6%
20x: 96.0%

Validation Efficiency

100% (80/80)

MGI Phenotype

PHENOTYPE: Homozygous mutations in this gene result in growth retardation, immunodeficiency, thymic hypoplasia, and increased incidence of thymic lymphomas. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 80 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4922502D21Rik	A	G	6: 129,330,969	F46L	probably benign	Het
Abcc5	A	G	16: 20,365,882	V1009A	possibly damaging	Het
Acta2	T	C	19: 34,248,534	I87V	probably benign	Het
Arid1a	A	G	4: 133,685,204	Y1560H	unknown	Het
Bcor	C	T	X: 12,059,051	R102Q	probably damaging	Het
Camsap2	A	T	1: 136,304,319	D179E	probably damaging	Het
Ccdc18	T	A	5: 108,135,560	S46T	probably damaging	Het
Ccdc18	A	C	5: 108,174,987	Q651P	probably damaging	Het
Cdc73	T	C	1: 143,695,462	T80A	probably benign	Het
Cdh7	T	A	1: 110,065,607		probably benign	Het
Cenpe	G	A	3: 135,230,082	G426D	probably damaging	Het
Cenpt	A	G	8: 105,844,960	V487A	probably damaging	Het
Col4a1	G	A	8: 11,246,892	P84S	unknown	Het
Dennd2d	A	G	3: 106,500,555	I450M	probably damaging	Het
Dhps	C	A	8: 85,073,282		probably null	Het
Ebf1	A	T	11: 44,991,510	H431L	probably damaging	Het
Efcab6	A	G	15: 83,933,064		probably benign	Het
Egflam	T	C	15: 7,207,709	H990R	probably damaging	Het
Ercc6l2	A	G	13: 63,844,645	T303A	probably benign	Het
Fam160a1	A	C	3: 85,730,614	V126G	probably damaging	Het
Fam167b	T	C	4: 129,578,357	K7E	probably benign	Het
Fgd3	T	C	13: 49,296,573	I67V	probably benign	Het
Fn1	A	T	1: 71,597,585	V2045D	possibly damaging	Het
Gm10451	A	G	12: 76,451,296		noncoding transcript	Het
Gm8251	A	G	1: 44,056,563	S1792P	possibly damaging	Het
Gnl1	A	G	17: 35,982,598	N225S	probably damaging	Het
Gpx6	A	T	13: 21,318,877	N154Y	probably benign	Het
Haus8	C	A	8: 71,256,530	G79V	probably damaging	Het
Hdgfl1	A	T	13: 26,769,853	L79Q	probably damaging	Het
Hist2h2be	A	G	3: 96,221,535	S124G	probably benign	Het
Impdh2	T	C	9: 108,563,466	Y83H	probably benign	Het
Lama2	T	C	10: 26,989,376	T2929A	probably benign	Het
Lpin2	T	C	17: 71,229,312	S199P	probably benign	Het
Mkl1	A	G	15: 81,016,920	S457P	probably damaging	Het
Moap1	T	C	12: 102,742,517	T258A	probably benign	Het
Mrps35	C	A	6: 147,055,945	S156*	probably null	Het
Mtbp	C	T	15: 55,603,201	P537S	probably benign	Het
Ncstn	C	A	1: 172,067,887	V565F	probably benign	Het
Nhsl1	A	G	10: 18,531,726	N1536S	possibly damaging	Het
Nkain4	T	C	2: 180,943,112	Q103R	possibly damaging	Het
Nsun2	T	A	13: 69,627,587	N383K	probably damaging	Het
Olfr1342	C	T	4: 118,690,072	V127I	probably benign	Het
Olfr820	A	G	10: 130,017,481	N40S	probably damaging	Het
Parp1	C	T	1: 180,600,440		probably benign	Het
Pkd1	G	A	17: 24,594,937	R4125H	probably damaging	Het
Plxnd1	T	C	6: 115,994,001	I269V	possibly damaging	Het
Qrich1	T	A	9: 108,544,877	N563K	probably damaging	Het
Rab3il1	TGAAG	TGAAGAAG	19: 10,027,388		probably benign	Het
Rell1	G	A	5: 63,924,745	T271M	probably benign	Het
Rgl1	A	G	1: 152,536,265		probably null	Het
Rph3a	C	T	5: 120,959,270	R261H	possibly damaging	Het
Ryr2	A	T	13: 11,724,333	M2161K	possibly damaging	Het
Scaf11	T	C	15: 96,418,458	N1075S	possibly damaging	Het
Serpina3j	A	G	12: 104,314,679	D37G	probably benign	Het
Siah2	A	G	3: 58,676,214	V217A	probably damaging	Het
Sik2	T	C	9: 50,898,745	D506G	probably benign	Het
Skap2	A	C	6: 51,879,785	V279G	probably benign	Het
Slc8a3	G	T	12: 81,314,446	T533N	probably damaging	Het
Slc9a7	A	T	X: 20,162,420		probably benign	Het
Snai3	G	T	8: 122,454,994	F241L	probably damaging	Het
Speg	T	C	1: 75,427,978	S2805P	probably benign	Het
Spink5	A	T	18: 43,999,797		probably benign	Het
Tctn1	C	T	5: 122,251,698	E254K	probably benign	Het
Tdrd3	C	T	14: 87,472,182	T100M	probably damaging	Het
Tex47	T	C	5: 7,305,215	V132A	probably benign	Het
Thbs3	A	G	3: 89,216,665		probably null	Het
Tigit	T	A	16: 43,662,038	Y111F	probably damaging	Het
Tmem245	A	G	4: 56,906,270	I148T	probably benign	Het
Tmem97	A	G	11: 78,550,539	Y39H	probably benign	Het
Tnks2	T	A	19: 36,862,074		probably null	Het
Tulp2	T	G	7: 45,519,786	I259S	probably damaging	Het
Twistnb	C	T	12: 33,438,000	Q305*	probably null	Het
Ubxn1	G	A	19: 8,874,248	R215H	probably damaging	Het
Vmn1r17	A	G	6: 57,360,475	F253L	probably damaging	Het
Vmn2r10	T	C	5: 108,995,916	M723V	probably benign	Het
Xndc1	T	C	7: 102,078,824	V14A	possibly damaging	Het
Xpnpep1	A	G	19: 52,997,863		probably benign	Het
Yes1	T	A	5: 32,655,518	M322K	possibly damaging	Het
Zdhhc14	C	A	17: 5,493,602	N52K	probably benign	Het
Zfp42	A	G	8: 43,295,978	V162A	probably benign	Het

Other mutations in Trp53bp1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00336:Trp53bp1	APN	2	121256579	missense	possibly damaging	0.69
IGL00690:Trp53bp1	APN	2	121235995	missense	probably damaging	1.00
IGL00922:Trp53bp1	APN	2	121208482	missense	probably damaging	0.96
IGL01475:Trp53bp1	APN	2	121270319	splice site	probably null
IGL01639:Trp53bp1	APN	2	121202692	missense	possibly damaging	0.51
IGL01662:Trp53bp1	APN	2	121236025	missense	probably damaging	1.00
IGL01757:Trp53bp1	APN	2	121211304	missense	probably damaging	0.99
IGL01829:Trp53bp1	APN	2	121215896	missense	probably benign	0.39
IGL02247:Trp53bp1	APN	2	121236589	missense	probably damaging	1.00
IGL02349:Trp53bp1	APN	2	121199074	missense	probably damaging	1.00
IGL02391:Trp53bp1	APN	2	121202710	missense	possibly damaging	0.67
chives	UTSW	2	121251868	missense	probably null	0.13
concur	UTSW	2	121270319	splice site	probably null
confirmation	UTSW	2	121205113	critical splice acceptor site	probably null
Infra	UTSW	2	121247499	critical splice donor site	probably null
lentil	UTSW	2	121251868	missense	probably null	0.13
lentil2	UTSW	2	121207887	missense	probably damaging	1.00
Profundus	UTSW	2	121207803	missense	probably damaging	1.00
split_pea	UTSW	2	121228606	nonsense	probably null
verily	UTSW	2	121211313	missense	probably damaging	1.00
PIT1430001:Trp53bp1	UTSW	2	121271275	missense	probably damaging	1.00
R0045:Trp53bp1	UTSW	2	121204497	missense	probably benign
R0060:Trp53bp1	UTSW	2	121204525	missense	probably damaging	1.00
R0060:Trp53bp1	UTSW	2	121204525	missense	probably damaging	1.00
R0103:Trp53bp1	UTSW	2	121236759	missense	possibly damaging	0.92
R0103:Trp53bp1	UTSW	2	121236759	missense	possibly damaging	0.92
R0281:Trp53bp1	UTSW	2	121270237	missense	probably damaging	1.00
R0386:Trp53bp1	UTSW	2	121204943	missense	probably damaging	1.00
R0427:Trp53bp1	UTSW	2	121236017	missense	probably damaging	1.00
R0505:Trp53bp1	UTSW	2	121269969	missense	probably damaging	0.99
R0522:Trp53bp1	UTSW	2	121251868	missense	probably null	0.13
R0523:Trp53bp1	UTSW	2	121251868	missense	probably null	0.13
R0525:Trp53bp1	UTSW	2	121251868	missense	probably null	0.13
R0543:Trp53bp1	UTSW	2	121251868	missense	probably null	0.13
R0559:Trp53bp1	UTSW	2	121227801	missense	probably damaging	1.00
R0573:Trp53bp1	UTSW	2	121228172	splice site	probably benign
R0593:Trp53bp1	UTSW	2	121270528	missense	possibly damaging	0.95
R0680:Trp53bp1	UTSW	2	121251868	missense	probably null	0.13
R0732:Trp53bp1	UTSW	2	121248264	missense	probably null	0.96
R0905:Trp53bp1	UTSW	2	121204318	splice site	probably benign
R1377:Trp53bp1	UTSW	2	121270642	missense	probably damaging	1.00
R1415:Trp53bp1	UTSW	2	121236184	missense	probably damaging	1.00
R1725:Trp53bp1	UTSW	2	121252000	missense	possibly damaging	0.46
R1971:Trp53bp1	UTSW	2	121205036	missense	probably damaging	1.00
R2045:Trp53bp1	UTSW	2	121204483	missense	probably benign
R2143:Trp53bp1	UTSW	2	121216064	missense	probably benign	0.00
R2282:Trp53bp1	UTSW	2	121270273	nonsense	probably null
R2296:Trp53bp1	UTSW	2	121209247	missense	possibly damaging	0.96
R3106:Trp53bp1	UTSW	2	121236652	missense	probably damaging	1.00
R3792:Trp53bp1	UTSW	2	121200329	missense	probably damaging	1.00
R3793:Trp53bp1	UTSW	2	121200329	missense	probably damaging	1.00
R3946:Trp53bp1	UTSW	2	121228626	missense	probably damaging	0.99
R4001:Trp53bp1	UTSW	2	121205085	missense	probably damaging	1.00
R4327:Trp53bp1	UTSW	2	121256650	missense	probably damaging	1.00
R4585:Trp53bp1	UTSW	2	121207951	missense	probably damaging	1.00
R4630:Trp53bp1	UTSW	2	121207887	missense	probably damaging	1.00
R4744:Trp53bp1	UTSW	2	121211313	missense	probably damaging	1.00
R4751:Trp53bp1	UTSW	2	121227809	missense	probably damaging	1.00
R4754:Trp53bp1	UTSW	2	121207879	missense	probably damaging	1.00
R4755:Trp53bp1	UTSW	2	121228606	nonsense	probably null
R4850:Trp53bp1	UTSW	2	121205113	critical splice acceptor site	probably null
R4870:Trp53bp1	UTSW	2	121256641	missense	probably damaging	1.00
R4879:Trp53bp1	UTSW	2	121202603	missense	probably damaging	0.99
R4924:Trp53bp1	UTSW	2	121221220	nonsense	probably null
R4962:Trp53bp1	UTSW	2	121270546	missense	probably benign	0.12
R5019:Trp53bp1	UTSW	2	121270319	splice site	probably null
R5111:Trp53bp1	UTSW	2	121211387	missense	probably damaging	0.99
R5149:Trp53bp1	UTSW	2	121216117	missense	probably benign	0.00
R5252:Trp53bp1	UTSW	2	121243983	missense	probably benign	0.40
R5533:Trp53bp1	UTSW	2	121207746	missense	probably damaging	1.00
R5642:Trp53bp1	UTSW	2	121236662	missense	probably benign	0.00
R5773:Trp53bp1	UTSW	2	121243914	missense	probably damaging	1.00
R5819:Trp53bp1	UTSW	2	121208392	nonsense	probably null
R5886:Trp53bp1	UTSW	2	121205021	missense	probably damaging	1.00
R5908:Trp53bp1	UTSW	2	121236823	missense	probably benign	0.06
R6012:Trp53bp1	UTSW	2	121256602	missense	probably benign	0.07
R6351:Trp53bp1	UTSW	2	121269945	missense	probably damaging	1.00
R6406:Trp53bp1	UTSW	2	121270612	missense	probably damaging	0.99
R6575:Trp53bp1	UTSW	2	121228603	missense	probably damaging	1.00
R6619:Trp53bp1	UTSW	2	121247499	critical splice donor site	probably null
R6626:Trp53bp1	UTSW	2	121207803	missense	probably damaging	1.00
R6754:Trp53bp1	UTSW	2	121270576	missense	possibly damaging	0.83
R6765:Trp53bp1	UTSW	2	121209309	missense	probably damaging	1.00
R6806:Trp53bp1	UTSW	2	121228666	missense	probably damaging	0.99
R6860:Trp53bp1	UTSW	2	121199113	missense	probably damaging	1.00
R6991:Trp53bp1	UTSW	2	121208040	missense	probably damaging	1.00
R7278:Trp53bp1	UTSW	2	121199035	missense	probably damaging	1.00
R7339:Trp53bp1	UTSW	2	121236469	missense	probably benign	0.00
R7357:Trp53bp1	UTSW	2	121211300	missense	probably damaging	1.00
R7477:Trp53bp1	UTSW	2	121236346	missense	probably benign	0.34
R7577:Trp53bp1	UTSW	2	121236638	missense	possibly damaging	0.65
R7728:Trp53bp1	UTSW	2	121207899	missense	probably damaging	1.00
R7806:Trp53bp1	UTSW	2	121205061	missense	probably damaging	0.99
RF046:Trp53bp1	UTSW	2	121216001	frame shift	probably null
Z1088:Trp53bp1	UTSW	2	121253645	missense	probably benign	0.04

Predicted Primers

PCR Primer
(F):5'- ACCCTGAGTCCTGACAGTATGTGG -3'
(R):5'- TCGAGCTGATGTTTCCTGTGAACC -3'

Sequencing Primer
(F):5'- CCTGACAGTATGTGGGCTCTC -3'
(R):5'- TGGAGAAATGCTCTGACTCCC -3'

Posted On

2013-07-11