Mutagenetix > Incidental Mutation

Incidental Mutation 'R7354:Recql5'

570823

Institutional Source

Beutler Lab

Gene Symbol

Recql5

Ensembl Gene

ENSMUSG00000020752

Gene Name

RecQ protein-like 5

Synonyms

Recql5b, Recq5b

MMRRC Submission

045440-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.383) question?

Stock #

R7354 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

115783421-115824303 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 115819027 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Cysteine at position 180 (R180C)

Ref Sequence

ENSEMBL: ENSMUSP00000021097 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000021097] [ENSMUST00000131578] [ENSMUST00000134208] [ENSMUST00000140174]

AlphaFold

Q8VID5

Predicted Effect

probably damaging
Transcript: ENSMUST00000021097
AA Change: R180C

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

SMART Domains

Protein: ENSMUSP00000021097
Gene: ENSMUSG00000020752
AA Change: R180C

Domain	Start	End	E-Value	Type
DEXDc	25	230	1.13e-29	SMART
HELICc	274	355	8.68e-22	SMART
Pfam:RecQ_Zn_bind	366	436	1.8e-12	PFAM
low complexity region	472	499	N/A	INTRINSIC
PDB:4BK0\|B	516	621	2e-51	PDB
Pfam:RecQ5	626	818	3.1e-97	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000131578

SMART Domains

Protein: ENSMUSP00000136178
Gene: ENSMUSG00000020752

Domain	Start	End	E-Value	Type
HELICc	1	82	8.68e-22	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000134208

SMART Domains

Protein: ENSMUSP00000137157
Gene: ENSMUSG00000020752

Domain	Start	End	E-Value	Type
Blast:DEXDc	25	96	4e-34	BLAST
HELICc	160	241	8.68e-22	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000140174
AA Change: R180C

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

SMART Domains

Protein: ENSMUSP00000136506
Gene: ENSMUSG00000020752
AA Change: R180C

Domain	Start	End	E-Value	Type
DEXDc	25	230	1.13e-29	SMART

Coding Region Coverage

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

Validation Efficiency

100% (82/82)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a helicase that is important for genome stability. The encoded protein also prevents aberrant homologous recombination by displacing RAD51 from ssDNA. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2011]
PHENOTYPE: Mice homozygous for disruptions in this gene express elevated levels of sister chromatid exchange due to a failure to suppress crossovers. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 79 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ago3	T	A	4: 126,311,099 (GRCm39)	Q38L	possibly damaging	Het
Apon	T	A	10: 128,090,607 (GRCm39)	I95N	probably benign	Het
Arid1a	G	T	4: 133,421,258 (GRCm39)	P464Q	unknown	Het
Arid4b	A	G	13: 14,339,455 (GRCm39)	D503G	probably benign	Het
Asxl2	T	C	12: 3,505,637 (GRCm39)		probably benign	Het
Atp2a1	A	T	7: 126,048,028 (GRCm39)	V594D	probably damaging	Het
Begain	A	G	12: 108,999,215 (GRCm39)	F519L	possibly damaging	Het
Bora	A	G	14: 99,284,794 (GRCm39)	T15A	probably damaging	Het
Btbd7	A	T	12: 102,804,464 (GRCm39)	M192K	probably benign	Het
Ccdc125	T	G	13: 100,814,382 (GRCm39)		probably null	Het
Cdcp3	G	A	7: 130,858,458 (GRCm39)	C1042Y	possibly damaging	Het
Cdcp3	G	T	7: 130,873,762 (GRCm39)	C1696F	unknown	Het
Cfap74	G	T	4: 155,549,804 (GRCm39)	V146L	unknown	Het
Crisp1	G	A	17: 40,630,071 (GRCm39)		probably benign	Het
Ctbp1	A	T	5: 33,407,732 (GRCm39)	H292Q	possibly damaging	Het
Defb5	T	A	8: 19,300,750 (GRCm39)	M34K	probably benign	Het
Dnajc27	A	G	12: 4,146,249 (GRCm39)	I93V	probably benign	Het
Dqx1	T	A	6: 83,037,957 (GRCm39)	Y448*	probably null	Het
Dynap	A	T	18: 70,374,371 (GRCm39)	C52S	possibly damaging	Het
Ehd4	C	A	2: 119,932,613 (GRCm39)	R271L	probably damaging	Het
Ercc2	T	G	7: 19,127,579 (GRCm39)	I619S	possibly damaging	Het
Etf1	A	G	18: 35,039,040 (GRCm39)	I409T	probably damaging	Het
Fam117a	A	G	11: 95,271,529 (GRCm39)	D367G	probably damaging	Het
Fancd2	A	G	6: 113,572,907 (GRCm39)	D1447G	unknown	Het
Fbxw9	T	C	8: 85,788,825 (GRCm39)	S192P	probably damaging	Het
Frzb	A	T	2: 80,277,153 (GRCm39)	L11Q	probably damaging	Het
Gm14496	T	C	2: 181,642,479 (GRCm39)	S717P	probably damaging	Het
Gm3250	A	G	10: 77,618,367 (GRCm39)		probably benign	Het
Gm4353	C	T	7: 115,683,146 (GRCm39)	R145Q	probably benign	Het
Gpr12	A	T	5: 146,520,772 (GRCm39)	V50D	probably damaging	Het
Hes1	T	C	16: 29,884,746 (GRCm39)		probably null	Het
Hmcn1	A	T	1: 150,682,196 (GRCm39)	C451*	probably null	Het
Iars1	T	C	13: 49,857,796 (GRCm39)	V347A	probably benign	Het
Igfn1	A	G	1: 135,903,770 (GRCm39)	S323P	possibly damaging	Het
Itga6	G	A	2: 71,650,574 (GRCm39)	A207T	probably damaging	Het
Lgi4	T	A	7: 30,760,047 (GRCm39)	L81H	probably damaging	Het
Lrp1	T	C	10: 127,407,277 (GRCm39)	E1888G	probably damaging	Het
Man2a1	C	T	17: 65,059,539 (GRCm39)	T1142M	probably damaging	Het
Mdfic2	T	A	6: 98,215,242 (GRCm39)	D127V	probably damaging	Het
Mgam	A	T	6: 40,721,732 (GRCm39)	Y350F	probably damaging	Het
Miga1	T	C	3: 151,996,137 (GRCm39)	D351G	probably damaging	Het
Mro	A	G	18: 74,006,385 (GRCm39)	T111A	probably benign	Het
Mtrr	A	T	13: 68,714,326 (GRCm39)	V471E	probably damaging	Het
Myh3	C	A	11: 66,987,708 (GRCm39)	L1394I	probably damaging	Het
Myocd	A	G	11: 65,078,319 (GRCm39)	V492A	probably benign	Het
Nbeal2	A	G	9: 110,458,247 (GRCm39)	F2115S	probably damaging	Het
Nlrp1b	A	T	11: 71,072,376 (GRCm39)	M489K	possibly damaging	Het
Or12j5	A	C	7: 140,084,099 (GRCm39)	I91R	probably damaging	Het
Or14j7	A	G	17: 38,235,284 (GRCm39)	I276V	probably benign	Het
Or1e1c	A	T	11: 73,266,201 (GRCm39)	I212F	probably benign	Het
Or4c122	T	C	2: 89,079,031 (GRCm39)		probably null	Het
Or4k44	C	T	2: 111,367,909 (GRCm39)	A242T	possibly damaging	Het
Orc2	A	G	1: 58,508,906 (GRCm39)	S462P	possibly damaging	Het
Pcdh9	T	C	14: 94,125,706 (GRCm39)	T155A	probably benign	Het
Pcdhb16	G	A	18: 37,611,177 (GRCm39)	V46I	possibly damaging	Het
Pcdhb22	A	G	18: 37,653,311 (GRCm39)	D336G	probably damaging	Het
Pde4dip	T	A	3: 97,626,646 (GRCm39)	R1297S	probably damaging	Het
Plin4	A	G	17: 56,411,427 (GRCm39)	M868T	probably benign	Het
Plxnb2	A	G	15: 89,049,928 (GRCm39)	M531T	possibly damaging	Het
Poc5	T	C	13: 96,531,033 (GRCm39)	V77A	probably benign	Het
Rho	C	A	6: 115,912,464 (GRCm39)	Y268*	probably null	Het
Riok1	A	T	13: 38,231,288 (GRCm39)	H182L	probably benign	Het
Rnf207	T	C	4: 152,398,548 (GRCm39)	D273G	probably damaging	Het
Serpinb11	A	G	1: 107,305,263 (GRCm39)	Y213C	probably benign	Het
Slc16a10	T	C	10: 39,952,951 (GRCm39)	Y181C	probably damaging	Het
Slc22a15	G	A	3: 101,771,897 (GRCm39)	H401Y	probably benign	Het
Slc5a5	C	A	8: 71,342,247 (GRCm39)	R268L	probably damaging	Het
Slc9a8	T	C	2: 167,316,051 (GRCm39)	F576S	possibly damaging	Het
Slx4	T	C	16: 3,804,963 (GRCm39)	E617G	probably benign	Het
Spata31d1e	A	T	13: 59,889,648 (GRCm39)	L724*	probably null	Het
Top1	T	C	2: 160,546,878 (GRCm39)	I386T	probably damaging	Het
Tor1aip1	G	T	1: 155,911,859 (GRCm39)	D41E	probably damaging	Het
Tsc22d4	G	A	5: 137,766,371 (GRCm39)	R479Q	probably benign	Het
Unc79	C	T	12: 103,108,961 (GRCm39)	T2191I	possibly damaging	Het
Vmn2r109	A	T	17: 20,761,043 (GRCm39)	D771E	probably damaging	Het
Vmn2r82	A	C	10: 79,192,464 (GRCm39)	M14L	probably benign	Het
Zc3h7a	C	T	16: 10,966,378 (GRCm39)	S583N	probably damaging	Het
Zfp518b	G	A	5: 38,840,122 (GRCm39)		probably benign	Het
Zswim4	A	G	8: 84,955,478 (GRCm39)	W314R	probably damaging	Het

Other mutations in Recql5

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01108:Recql5	APN	11	115,788,007 (GRCm39)	missense	probably benign	0.04
IGL01589:Recql5	APN	11	115,785,495 (GRCm39)	missense	probably damaging	1.00
IGL02040:Recql5	APN	11	115,823,623 (GRCm39)	missense	possibly damaging	0.89
IGL02131:Recql5	APN	11	115,814,068 (GRCm39)	missense	probably benign	0.01
IGL02198:Recql5	APN	11	115,785,499 (GRCm39)	missense	probably benign	0.00
IGL02236:Recql5	APN	11	115,784,856 (GRCm39)	missense	probably benign	0.01
IGL02501:Recql5	APN	11	115,785,917 (GRCm39)	missense	probably benign	0.26
IGL02980:Recql5	APN	11	115,784,770 (GRCm39)	splice site	probably null
IGL03028:Recql5	APN	11	115,785,257 (GRCm39)	missense	possibly damaging	0.94
PIT4581001:Recql5	UTSW	11	115,823,682 (GRCm39)	missense	possibly damaging	0.53
R0152:Recql5	UTSW	11	115,785,499 (GRCm39)	missense	probably benign
R0269:Recql5	UTSW	11	115,819,050 (GRCm39)	missense	possibly damaging	0.91
R0317:Recql5	UTSW	11	115,785,499 (GRCm39)	missense	probably benign
R0511:Recql5	UTSW	11	115,819,209 (GRCm39)	missense	probably benign	0.00
R0786:Recql5	UTSW	11	115,786,628 (GRCm39)	missense	probably benign
R0975:Recql5	UTSW	11	115,814,082 (GRCm39)	missense	probably damaging	1.00
R1170:Recql5	UTSW	11	115,788,060 (GRCm39)	missense	probably damaging	0.98
R1208:Recql5	UTSW	11	115,783,982 (GRCm39)	missense	probably damaging	0.98
R1208:Recql5	UTSW	11	115,783,982 (GRCm39)	missense	probably damaging	0.98
R1807:Recql5	UTSW	11	115,785,941 (GRCm39)	missense	possibly damaging	0.63
R1872:Recql5	UTSW	11	115,814,135 (GRCm39)	missense	probably benign	0.15
R1878:Recql5	UTSW	11	115,785,927 (GRCm39)	missense	probably benign	0.00
R1935:Recql5	UTSW	11	115,788,017 (GRCm39)	missense	probably benign	0.00
R1936:Recql5	UTSW	11	115,788,017 (GRCm39)	missense	probably benign	0.00
R1945:Recql5	UTSW	11	115,819,123 (GRCm39)	nonsense	probably null
R2011:Recql5	UTSW	11	115,787,923 (GRCm39)	missense	probably benign	0.20
R2012:Recql5	UTSW	11	115,787,923 (GRCm39)	missense	probably benign	0.20
R2023:Recql5	UTSW	11	115,784,466 (GRCm39)	missense	probably benign
R2183:Recql5	UTSW	11	115,787,613 (GRCm39)	missense	probably benign	0.00
R3881:Recql5	UTSW	11	115,784,780 (GRCm39)	missense	probably benign
R3881:Recql5	UTSW	11	115,784,781 (GRCm39)	missense	probably benign	0.00
R4093:Recql5	UTSW	11	115,795,714 (GRCm39)	missense	probably benign	0.05
R4857:Recql5	UTSW	11	115,819,038 (GRCm39)	missense	probably damaging	1.00
R5245:Recql5	UTSW	11	115,784,385 (GRCm39)	missense	probably damaging	1.00
R5323:Recql5	UTSW	11	115,818,215 (GRCm39)	missense	probably damaging	1.00
R5796:Recql5	UTSW	11	115,818,691 (GRCm39)	intron	probably benign
R6160:Recql5	UTSW	11	115,823,613 (GRCm39)	critical splice donor site	probably null
R6229:Recql5	UTSW	11	115,821,540 (GRCm39)	missense	probably damaging	0.96
R6824:Recql5	UTSW	11	115,814,038 (GRCm39)	missense	possibly damaging	0.83
R7013:Recql5	UTSW	11	115,785,402 (GRCm39)	missense	probably benign	0.02
R7043:Recql5	UTSW	11	115,821,502 (GRCm39)	critical splice donor site	probably null
R7135:Recql5	UTSW	11	115,821,498 (GRCm39)	splice site	probably null
R7373:Recql5	UTSW	11	115,819,198 (GRCm39)	missense	possibly damaging	0.92
R7503:Recql5	UTSW	11	115,785,881 (GRCm39)	missense	probably benign	0.00
R7574:Recql5	UTSW	11	115,819,248 (GRCm39)	missense	probably benign
R7597:Recql5	UTSW	11	115,819,207 (GRCm39)	missense	probably benign	0.03
R7658:Recql5	UTSW	11	115,814,102 (GRCm39)	missense	probably damaging	1.00
R8025:Recql5	UTSW	11	115,818,938 (GRCm39)	missense	probably damaging	1.00
R8038:Recql5	UTSW	11	115,818,178 (GRCm39)	missense	possibly damaging	0.90
R8316:Recql5	UTSW	11	115,784,861 (GRCm39)	missense	possibly damaging	0.46
R8463:Recql5	UTSW	11	115,787,619 (GRCm39)	nonsense	probably null
R8770:Recql5	UTSW	11	115,787,943 (GRCm39)	missense	probably benign	0.00
R8788:Recql5	UTSW	11	115,786,628 (GRCm39)	missense	probably benign
R9083:Recql5	UTSW	11	115,785,475 (GRCm39)	missense	possibly damaging	0.46
R9653:Recql5	UTSW	11	115,788,032 (GRCm39)	missense	probably benign	0.01
R9711:Recql5	UTSW	11	115,784,367 (GRCm39)	missense	probably damaging	1.00
X0026:Recql5	UTSW	11	115,814,087 (GRCm39)	missense	probably damaging	1.00
X0028:Recql5	UTSW	11	115,785,432 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- CCTTAAGGCAGAAGTCCCTCAG -3'
(R):5'- TGACCTGGAGCGAGACAAAC -3'

Sequencing Primer
(F):5'- TCAGATTGCCATAGACGTCG -3'
(R):5'- ACCTCGGACCAAACTTTTGTAC -3'

Posted On

2019-09-13