Mutagenetix > Incidental Mutation

Incidental Mutation 'R2321:Rad51ap2'

245650

Institutional Source

Beutler Lab

Gene Symbol

Rad51ap2

Ensembl Gene

ENSMUSG00000086022

Gene Name

RAD51 associated protein 2

Synonyms

MMRRC Submission

040313-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R2321 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

11506080-11512929 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 11507058 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glycine to Arginine at position 327 (G327R)

Ref Sequence

ENSEMBL: ENSMUSP00000128854 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000124065]

AlphaFold

G3UW63

Predicted Effect

probably damaging
Transcript: ENSMUST00000124065
AA Change: G327R

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000128854
Gene: ENSMUSG00000086022
AA Change: G327R

Domain	Start	End	E-Value	Type
low complexity region	17	32	N/A	INTRINSIC
low complexity region	428	438	N/A	INTRINSIC
low complexity region	702	713	N/A	INTRINSIC
Pfam:RAD51_interact	937	975	1.3e-20	PFAM

Meta Mutation Damage Score

0.6467

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.2%
20x: 94.7%

Validation Efficiency

100% (39/39)

Allele List at MGI

Other mutations in this stock

Total: 36 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A2ml1	C	T	6: 128,557,349 (GRCm39)	A115T	probably benign	Het
Abcf2	A	T	5: 24,772,251 (GRCm39)	Y492*	probably null	Het
Adcy9	A	G	16: 4,106,132 (GRCm39)	V994A	probably damaging	Het
Arhgef40	T	C	14: 52,231,733 (GRCm39)		probably benign	Het
Bhlha15	T	C	5: 144,128,014 (GRCm39)	L42P	probably damaging	Het
Clca4b	C	A	3: 144,638,134 (GRCm39)	A43S	probably benign	Het
Cpq	A	G	15: 33,594,291 (GRCm39)	H434R	probably benign	Het
Crybg2	A	G	4: 133,801,822 (GRCm39)	E994G	probably benign	Het
Dcaf1	T	C	9: 106,715,672 (GRCm39)	L263S	probably benign	Het
Dnajc12	G	T	10: 63,242,990 (GRCm39)		probably benign	Het
Fbxo32	T	C	15: 58,054,689 (GRCm39)	I215V	possibly damaging	Het
Krtap17-1	T	C	11: 99,884,746 (GRCm39)	D7G	unknown	Het
Men1	A	G	19: 6,389,868 (GRCm39)	D466G	possibly damaging	Het
Myh15	T	A	16: 48,933,436 (GRCm39)	F624I	possibly damaging	Het
Ncam1	A	C	9: 49,456,132 (GRCm39)		probably benign	Het
Or2y1d	A	G	11: 49,322,107 (GRCm39)	N268S	probably benign	Het
Otol1	T	A	3: 69,925,858 (GRCm39)	L11*	probably null	Het
Plekhg4	T	C	8: 106,104,172 (GRCm39)	S447P	probably benign	Het
Pnma8b	G	T	7: 16,679,490 (GRCm39)	R158L	unknown	Het
Ppp1r2	A	T	16: 31,084,121 (GRCm39)		probably null	Het
Rbm26	T	C	14: 105,390,863 (GRCm39)	T208A	unknown	Het
Reln	T	C	5: 22,120,018 (GRCm39)	Y2878C	probably damaging	Het
Rnps1	T	A	17: 24,641,142 (GRCm39)	F181I	probably damaging	Het
Senp6	A	C	9: 80,031,022 (GRCm39)	I575L	possibly damaging	Het
Serpinh1	T	C	7: 98,995,592 (GRCm39)	D330G	probably damaging	Het
Slamf9	G	T	1: 172,304,980 (GRCm39)	C198F	probably damaging	Het
Slc22a13	A	T	9: 119,024,694 (GRCm39)	V261D	possibly damaging	Het
Slc26a4	A	G	12: 31,590,543 (GRCm39)	V370A	probably damaging	Het
Tasp1	A	G	2: 139,899,332 (GRCm39)	M7T	probably benign	Het
Tet2	T	C	3: 133,192,100 (GRCm39)	N778S	possibly damaging	Het
Tm9sf4	T	A	2: 153,046,506 (GRCm39)	Y582N	probably damaging	Het
Tmem131l	T	A	3: 83,843,330 (GRCm39)	H508L	probably damaging	Het
Tmem71	T	G	15: 66,423,849 (GRCm39)	D139A	possibly damaging	Het
Uroc1	A	G	6: 90,324,229 (GRCm39)	R418G	possibly damaging	Het
Wdr64	A	C	1: 175,622,653 (GRCm39)	K810T	possibly damaging	Het
Zgrf1	C	A	3: 127,356,056 (GRCm39)	Y427*	probably null	Het

Other mutations in Rad51ap2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01879:Rad51ap2	APN	12	11,508,139 (GRCm39)	missense	probably benign	0.10
IGL01908:Rad51ap2	APN	12	11,508,592 (GRCm39)	missense	probably damaging	1.00
IGL02415:Rad51ap2	APN	12	11,506,930 (GRCm39)	missense	possibly damaging	0.91
IGL02731:Rad51ap2	APN	12	11,506,897 (GRCm39)	missense	probably damaging	0.99
IGL03407:Rad51ap2	APN	12	11,507,198 (GRCm39)	missense	possibly damaging	0.96
R0190:Rad51ap2	UTSW	12	11,508,540 (GRCm39)	missense	probably benign	0.01
R0281:Rad51ap2	UTSW	12	11,507,043 (GRCm39)	missense	possibly damaging	0.93
R0564:Rad51ap2	UTSW	12	11,507,897 (GRCm39)	missense	probably benign	0.20
R0674:Rad51ap2	UTSW	12	11,508,818 (GRCm39)	critical splice donor site	probably null
R0699:Rad51ap2	UTSW	12	11,507,601 (GRCm39)	missense	probably benign	0.03
R1033:Rad51ap2	UTSW	12	11,506,252 (GRCm39)	missense	probably damaging	0.98
R1255:Rad51ap2	UTSW	12	11,508,095 (GRCm39)	missense	possibly damaging	0.54
R1572:Rad51ap2	UTSW	12	11,507,113 (GRCm39)	missense	probably damaging	0.99
R1746:Rad51ap2	UTSW	12	11,507,776 (GRCm39)	missense	probably benign
R1882:Rad51ap2	UTSW	12	11,506,251 (GRCm39)	missense	possibly damaging	0.85
R2038:Rad51ap2	UTSW	12	11,507,025 (GRCm39)	missense	possibly damaging	0.73
R2151:Rad51ap2	UTSW	12	11,507,986 (GRCm39)	missense	probably benign	0.02
R2152:Rad51ap2	UTSW	12	11,507,986 (GRCm39)	missense	probably benign	0.02
R2154:Rad51ap2	UTSW	12	11,507,986 (GRCm39)	missense	probably benign	0.02
R2159:Rad51ap2	UTSW	12	11,507,752 (GRCm39)	missense	possibly damaging	0.87
R2355:Rad51ap2	UTSW	12	11,507,109 (GRCm39)	missense	probably benign
R2393:Rad51ap2	UTSW	12	11,507,798 (GRCm39)	missense	probably damaging	0.98
R2407:Rad51ap2	UTSW	12	11,508,502 (GRCm39)	missense	probably damaging	0.99
R2518:Rad51ap2	UTSW	12	11,507,068 (GRCm39)	missense	probably damaging	0.99
R2929:Rad51ap2	UTSW	12	11,507,185 (GRCm39)	missense	probably benign	0.07
R3085:Rad51ap2	UTSW	12	11,506,758 (GRCm39)	missense	possibly damaging	0.53
R4009:Rad51ap2	UTSW	12	11,507,052 (GRCm39)	missense	probably benign	0.33
R4108:Rad51ap2	UTSW	12	11,508,396 (GRCm39)	missense	probably damaging	1.00
R4282:Rad51ap2	UTSW	12	11,506,465 (GRCm39)	missense	probably benign	0.01
R4536:Rad51ap2	UTSW	12	11,507,850 (GRCm39)	missense	possibly damaging	0.90
R4594:Rad51ap2	UTSW	12	11,507,881 (GRCm39)	missense	probably benign	0.01
R4678:Rad51ap2	UTSW	12	11,506,552 (GRCm39)	missense	probably damaging	0.96
R4679:Rad51ap2	UTSW	12	11,506,552 (GRCm39)	missense	probably damaging	0.96
R4810:Rad51ap2	UTSW	12	11,507,406 (GRCm39)	missense	probably damaging	1.00
R5151:Rad51ap2	UTSW	12	11,507,516 (GRCm39)	missense	probably benign	0.09
R5421:Rad51ap2	UTSW	12	11,509,368 (GRCm39)	nonsense	probably null
R5517:Rad51ap2	UTSW	12	11,508,313 (GRCm39)	missense	probably benign	0.19
R5786:Rad51ap2	UTSW	12	11,506,921 (GRCm39)	missense	probably damaging	1.00
R5884:Rad51ap2	UTSW	12	11,507,534 (GRCm39)	small deletion	probably benign
R5932:Rad51ap2	UTSW	12	11,508,387 (GRCm39)	missense	probably damaging	1.00
R6022:Rad51ap2	UTSW	12	11,508,523 (GRCm39)	missense	probably damaging	1.00
R6064:Rad51ap2	UTSW	12	11,507,418 (GRCm39)	missense	possibly damaging	0.80
R6112:Rad51ap2	UTSW	12	11,507,290 (GRCm39)	missense	probably benign	0.01
R6235:Rad51ap2	UTSW	12	11,507,517 (GRCm39)	missense	possibly damaging	0.70
R6282:Rad51ap2	UTSW	12	11,507,560 (GRCm39)	missense	probably benign	0.12
R6488:Rad51ap2	UTSW	12	11,508,161 (GRCm39)	missense	possibly damaging	0.56
R6668:Rad51ap2	UTSW	12	11,507,647 (GRCm39)	missense	probably benign	0.17
R6759:Rad51ap2	UTSW	12	11,507,145 (GRCm39)	missense	possibly damaging	0.91
R7030:Rad51ap2	UTSW	12	11,507,432 (GRCm39)	missense	possibly damaging	0.93
R7080:Rad51ap2	UTSW	12	11,506,366 (GRCm39)	missense	probably benign
R7105:Rad51ap2	UTSW	12	11,508,278 (GRCm39)	missense	possibly damaging	0.84
R7269:Rad51ap2	UTSW	12	11,506,807 (GRCm39)	missense	possibly damaging	0.67
R7286:Rad51ap2	UTSW	12	11,507,692 (GRCm39)	missense	probably benign	0.19
R7305:Rad51ap2	UTSW	12	11,507,344 (GRCm39)	missense	possibly damaging	0.68
R7451:Rad51ap2	UTSW	12	11,507,982 (GRCm39)	missense	probably benign	0.05
R7632:Rad51ap2	UTSW	12	11,507,116 (GRCm39)	missense	possibly damaging	0.85
R7833:Rad51ap2	UTSW	12	11,506,656 (GRCm39)	missense	probably benign
R7839:Rad51ap2	UTSW	12	11,507,238 (GRCm39)	missense	possibly damaging	0.83
R7953:Rad51ap2	UTSW	12	11,512,593 (GRCm39)	nonsense	probably null
R8040:Rad51ap2	UTSW	12	11,508,792 (GRCm39)	missense	probably benign	0.03
R8879:Rad51ap2	UTSW	12	11,507,401 (GRCm39)	missense	possibly damaging	0.55
R8963:Rad51ap2	UTSW	12	11,506,255 (GRCm39)	missense	possibly damaging	0.91
R9010:Rad51ap2	UTSW	12	11,508,675 (GRCm39)	missense	probably benign	0.01
R9328:Rad51ap2	UTSW	12	11,507,772 (GRCm39)	missense	probably benign	0.03
R9691:Rad51ap2	UTSW	12	11,509,413 (GRCm39)	missense	possibly damaging	0.70
R9712:Rad51ap2	UTSW	12	11,507,593 (GRCm39)	missense	possibly damaging	0.95
RF023:Rad51ap2	UTSW	12	11,508,076 (GRCm39)	missense	possibly damaging	0.94
X0026:Rad51ap2	UTSW	12	11,508,097 (GRCm39)	missense	possibly damaging	0.93

Predicted Primers

PCR Primer
(F):5'- GCCAAACCTAGCTATTTTAGAGATAGC -3'
(R):5'- GATCTGTCACAGTCCAAGTTTTG -3'

Sequencing Primer
(F):5'- CAAGGGATTTAAATAGCAACATGTCC -3'
(R):5'- CTGTCACAGTCCAAGTTTTGAAATTC -3'

Posted On

2014-10-30