Mutagenetix > Incidental Mutation

Incidental Mutation 'R0335:Wapl'

26222

Institutional Source

Beutler Lab

Gene Symbol

Wapl

Ensembl Gene

ENSMUSG00000041408

Gene Name

WAPL cohesin release factor

Synonyms

A530089A20Rik, Wapal

MMRRC Submission

038544-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R0335 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

34395885-34469940 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 34414281 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Asparagine at position 381 (I381N)

Ref Sequence

ENSEMBL: ENSMUSP00000130547 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000048263] [ENSMUST00000090027] [ENSMUST00000169910]

AlphaFold

Q65Z40

Predicted Effect

probably damaging
Transcript: ENSMUST00000048263
AA Change: I381N

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000040232
Gene: ENSMUSG00000041408
AA Change: I381N

Domain	Start	End	E-Value	Type
low complexity region	436	455	N/A	INTRINSIC
low complexity region	465	477	N/A	INTRINSIC
low complexity region	493	513	N/A	INTRINSIC
Pfam:WAPL	645	1009	6.5e-153	PFAM
low complexity region	1018	1033	N/A	INTRINSIC
low complexity region	1101	1112	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000090027
AA Change: I381N

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000087481
Gene: ENSMUSG00000041408
AA Change: I381N

Domain	Start	End	E-Value	Type
low complexity region	436	455	N/A	INTRINSIC
low complexity region	465	477	N/A	INTRINSIC
low complexity region	493	513	N/A	INTRINSIC
Pfam:WAPL	639	1003	2.6e-153	PFAM
low complexity region	1012	1027	N/A	INTRINSIC
low complexity region	1095	1106	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000111895

Predicted Effect

probably damaging
Transcript: ENSMUST00000169910
AA Change: I381N

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000130547
Gene: ENSMUSG00000041408
AA Change: I381N

Domain	Start	End	E-Value	Type
low complexity region	436	455	N/A	INTRINSIC
low complexity region	465	477	N/A	INTRINSIC
low complexity region	493	513	N/A	INTRINSIC
Pfam:WAPL	647	1008	3.5e-120	PFAM
low complexity region	1018	1033	N/A	INTRINSIC
low complexity region	1101	1112	N/A	INTRINSIC

Meta Mutation Damage Score

0.6467

Coding Region Coverage

1x: 98.8%
3x: 97.6%
10x: 94.6%
20x: 87.5%

Validation Efficiency

100% (89/89)

MGI Phenotype

FUNCTION: Studies suggest that the protein encoded by this gene is important for the release of cohesin from chromatin. This gene product is thought to be essential for development, and reduced expression of this gene in cells causes defects in chromatin structure. High levels of expression of the human ortholog of this gene are observed in cervical cancers, and expression of the human ortholog of this gene in mice results in tumor formation. Alternative splicing results in multiple transcript variants encoding different protein isoforms. [provided by RefSeq, Aug 2014]
PHENOTYPE: Mice homozygous for a targeted allele exhibit prenatal lethality. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 88 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts12	G	T	15: 11,311,144 (GRCm39)	D1134Y	possibly damaging	Het
Add3	A	G	19: 53,225,259 (GRCm39)	T460A	probably benign	Het
Amer3	A	C	1: 34,618,381 (GRCm39)		probably benign	Het
Arhgap22	C	T	14: 33,081,065 (GRCm39)		probably benign	Het
Arhgap32	T	G	9: 32,171,056 (GRCm39)	S1279A	probably benign	Het
Bcas1	G	A	2: 170,260,601 (GRCm39)	T26M	probably damaging	Het
Begain	A	T	12: 109,004,860 (GRCm39)	F256I	probably damaging	Het
Bltp1	T	C	3: 37,023,301 (GRCm39)	V2210A	probably damaging	Het
Cabin1	A	T	10: 75,492,883 (GRCm39)	I1804N	probably damaging	Het
Cad	G	A	5: 31,231,329 (GRCm39)		probably benign	Het
Carmil1	G	A	13: 24,257,966 (GRCm39)	S762L	probably damaging	Het
Ccdc93	T	A	1: 121,420,706 (GRCm39)	L529Q	probably damaging	Het
Cdh12	T	A	15: 21,578,635 (GRCm39)		probably null	Het
Cep15	A	G	14: 12,301,266 (GRCm38)	E124G	possibly damaging	Het
Clip2	T	A	5: 134,564,069 (GRCm39)		probably benign	Het
Cmip	T	C	8: 118,172,105 (GRCm39)	I480T	probably damaging	Het
Cnot1	A	T	8: 96,498,628 (GRCm39)	I203K	probably benign	Het
Col18a1	G	A	10: 76,895,197 (GRCm39)	P1155S	probably damaging	Het
Col1a2	T	A	6: 4,531,956 (GRCm39)		probably benign	Het
Crybg3	A	T	16: 59,364,503 (GRCm39)	L2373Q	probably damaging	Het
D130043K22Rik	A	T	13: 25,071,860 (GRCm39)	I935F	probably damaging	Het
Dapl1	T	A	2: 59,326,938 (GRCm39)	D61E	possibly damaging	Het
Def6	A	G	17: 28,447,043 (GRCm39)	D558G	possibly damaging	Het
Dnah6	T	C	6: 73,046,382 (GRCm39)		probably benign	Het
Dvl2	G	A	11: 69,891,861 (GRCm39)		probably benign	Het
Ecd	A	C	14: 20,370,802 (GRCm39)	V639G	probably benign	Het
Epg5	C	T	18: 78,029,687 (GRCm39)	T1350M	probably benign	Het
Erbb4	C	A	1: 68,298,418 (GRCm39)	M657I	probably benign	Het
Evi5	T	C	5: 107,960,277 (GRCm39)	R431G	probably benign	Het
Fbxo11	G	A	17: 88,323,041 (GRCm39)	A115V	possibly damaging	Het
Fgfr2	T	C	7: 129,797,979 (GRCm39)	T192A	probably benign	Het
Gas7	C	T	11: 67,552,878 (GRCm39)	A146V	possibly damaging	Het
Gatad2b	T	A	3: 90,263,489 (GRCm39)	S529T	probably benign	Het
Gm10722	G	T	9: 3,001,048 (GRCm39)	Q41H	probably null	Het
Gm10801	G	C	2: 98,494,352 (GRCm39)	R143T	possibly damaging	Het
Gm7535	A	G	17: 18,131,374 (GRCm39)		probably benign	Het
Gstm1	T	A	3: 107,920,012 (GRCm39)	N193I	possibly damaging	Het
Heatr5b	G	A	17: 79,135,375 (GRCm39)	P252L	probably benign	Het
Hmgb1	A	G	5: 148,987,441 (GRCm39)	V36A	probably benign	Het
Hrh1	G	T	6: 114,457,193 (GRCm39)	W158L	probably damaging	Het
Ighv6-4	T	C	12: 114,370,294 (GRCm39)	M53V	probably benign	Het
Iqgap2	T	A	13: 95,772,141 (GRCm39)	D1346V	probably damaging	Het
Kcng3	A	T	17: 83,895,166 (GRCm39)	N433K	possibly damaging	Het
Kif1a	T	A	1: 92,980,288 (GRCm39)		probably benign	Het
Lctl	C	A	9: 64,026,169 (GRCm39)	Q75K	probably benign	Het
Ldb3	T	A	14: 34,300,608 (GRCm39)	I89F	possibly damaging	Het
Lrrc49	A	T	9: 60,584,378 (GRCm39)	L156Q	probably damaging	Het
Mark2	G	T	19: 7,259,193 (GRCm39)	T83K	probably benign	Het
Ms4a15	A	T	19: 10,957,574 (GRCm39)	D170E	probably damaging	Het
Msantd2	A	G	9: 37,434,056 (GRCm39)	S99G	possibly damaging	Het
Nemf	G	T	12: 69,400,577 (GRCm39)	T124N	probably benign	Het
Nlrp9c	A	T	7: 26,093,561 (GRCm39)	F35I	possibly damaging	Het
Nwd2	A	G	5: 63,962,116 (GRCm39)	I567V	probably benign	Het
Optn	C	T	2: 5,028,926 (GRCm39)	G526R	probably damaging	Het
Or11l3	T	C	11: 58,516,566 (GRCm39)	Y102C	probably damaging	Het
Or13p8	A	G	4: 118,584,367 (GRCm39)	I308V	probably null	Het
Or5v1b	A	C	17: 37,841,533 (GRCm39)	I222L	probably benign	Het
Or7g16	T	A	9: 18,727,290 (GRCm39)	Q100L	probably damaging	Het
Pdk4	T	C	6: 5,491,138 (GRCm39)	E209G	probably benign	Het
Plch1	T	C	3: 63,618,399 (GRCm39)	Q712R	probably damaging	Het
Pnpla1	T	A	17: 29,105,852 (GRCm39)	V569E	possibly damaging	Het
Prkar2a	A	T	9: 108,596,457 (GRCm39)	D134V	probably damaging	Het
Ptov1	T	A	7: 44,514,046 (GRCm39)	Q40L	possibly damaging	Het
Ptprq	T	C	10: 107,544,589 (GRCm39)	I314V	probably benign	Het
Rabl2	T	C	15: 89,468,169 (GRCm39)	K66E	probably damaging	Het
Rnf38	A	G	4: 44,152,507 (GRCm39)	V19A	possibly damaging	Het
Scn2a	T	A	2: 65,512,435 (GRCm39)	W191R	probably damaging	Het
Sec22b	T	A	3: 97,828,572 (GRCm39)	F212I	possibly damaging	Het
Sec24c	T	A	14: 20,738,783 (GRCm39)		probably null	Het
Septin2	T	C	1: 93,423,321 (GRCm39)	S51P	probably damaging	Het
Serpinb1a	T	C	13: 33,032,639 (GRCm39)	N90S	probably damaging	Het
Slc1a2	C	T	2: 102,574,208 (GRCm39)	T206I	probably benign	Het
Slc25a19	C	A	11: 115,515,032 (GRCm39)	R42L	probably damaging	Het
St14	G	A	9: 31,002,620 (GRCm39)		probably benign	Het
Stxbp1	C	T	2: 32,692,917 (GRCm39)		probably benign	Het
Tas2r131	C	T	6: 132,934,792 (GRCm39)	V6I	probably benign	Het
Tdo2	T	A	3: 81,871,307 (GRCm39)	M235L	probably benign	Het
Tenm3	T	G	8: 48,685,140 (GRCm39)	H2432P	probably damaging	Het
Tmprss15	C	T	16: 78,821,630 (GRCm39)		probably benign	Het
Tmx1	A	G	12: 70,500,030 (GRCm39)	N30D	probably benign	Het
Tom1	A	G	8: 75,791,020 (GRCm39)		probably null	Het
Top2a	T	C	11: 98,913,781 (GRCm39)	N20S	probably benign	Het
Ttc23l	T	A	15: 10,540,049 (GRCm39)	T145S	probably benign	Het
Unc13b	T	A	4: 43,236,983 (GRCm39)	M3351K	possibly damaging	Het
Vmn1r47	T	C	6: 89,999,641 (GRCm39)	S258P	probably damaging	Het
Vmn2r8	T	G	5: 108,945,317 (GRCm39)		probably null	Het
Vps11	T	C	9: 44,265,135 (GRCm39)	Q641R	probably null	Het
Zmym6	G	A	4: 127,016,601 (GRCm39)	G794E	probably damaging	Het

Other mutations in Wapl

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00335:Wapl	APN	14	34,414,593 (GRCm39)	missense	probably benign	0.00
IGL00539:Wapl	APN	14	34,416,965 (GRCm39)	missense	probably damaging	1.00
IGL00846:Wapl	APN	14	34,414,701 (GRCm39)	splice site	probably benign
IGL01070:Wapl	APN	14	34,467,579 (GRCm39)	unclassified	probably benign
IGL01516:Wapl	APN	14	34,414,038 (GRCm39)	missense	probably damaging	1.00
IGL02021:Wapl	APN	14	34,444,293 (GRCm39)	missense	probably benign
IGL02209:Wapl	APN	14	34,399,218 (GRCm39)	missense	possibly damaging	0.46
IGL02309:Wapl	APN	14	34,466,820 (GRCm39)	missense	probably damaging	0.98
IGL02471:Wapl	APN	14	34,413,877 (GRCm39)	missense	possibly damaging	0.68
IGL02965:Wapl	APN	14	34,461,181 (GRCm39)	intron	probably benign
IGL03076:Wapl	APN	14	34,414,046 (GRCm39)	missense	probably benign	0.26
IGL03197:Wapl	APN	14	34,467,588 (GRCm39)	missense	possibly damaging	0.77
Mcclintock	UTSW	14	34,452,619 (GRCm39)	critical splice donor site	probably null
Tatum	UTSW	14	34,451,152 (GRCm39)	missense	probably damaging	1.00
R0045:Wapl	UTSW	14	34,455,751 (GRCm39)	missense	probably benign	0.18
R0278:Wapl	UTSW	14	34,414,569 (GRCm39)	missense	possibly damaging	0.68
R1018:Wapl	UTSW	14	34,413,863 (GRCm39)	missense	possibly damaging	0.91
R1295:Wapl	UTSW	14	34,446,726 (GRCm39)	missense	probably damaging	1.00
R1553:Wapl	UTSW	14	34,451,147 (GRCm39)	missense	probably damaging	1.00
R1868:Wapl	UTSW	14	34,414,415 (GRCm39)	missense	probably benign	0.00
R1909:Wapl	UTSW	14	34,413,869 (GRCm39)	missense	probably damaging	1.00
R2698:Wapl	UTSW	14	34,413,734 (GRCm39)	missense	probably benign
R2990:Wapl	UTSW	14	34,458,665 (GRCm39)	missense	probably damaging	0.98
R3121:Wapl	UTSW	14	34,451,172 (GRCm39)	missense	possibly damaging	0.93
R3122:Wapl	UTSW	14	34,451,172 (GRCm39)	missense	possibly damaging	0.93
R3147:Wapl	UTSW	14	34,447,106 (GRCm39)	missense	probably damaging	1.00
R3732:Wapl	UTSW	14	34,458,721 (GRCm39)	missense	probably damaging	0.99
R3732:Wapl	UTSW	14	34,458,721 (GRCm39)	missense	probably damaging	0.99
R3733:Wapl	UTSW	14	34,458,721 (GRCm39)	missense	probably damaging	0.99
R3878:Wapl	UTSW	14	34,414,104 (GRCm39)	missense	probably damaging	1.00
R4034:Wapl	UTSW	14	34,459,871 (GRCm39)	missense	possibly damaging	0.92
R4934:Wapl	UTSW	14	34,414,052 (GRCm39)	missense	probably benign	0.11
R5079:Wapl	UTSW	14	34,446,714 (GRCm39)	missense	probably damaging	1.00
R5104:Wapl	UTSW	14	34,414,016 (GRCm39)	nonsense	probably null
R5113:Wapl	UTSW	14	34,446,711 (GRCm39)	missense	probably damaging	1.00
R5121:Wapl	UTSW	14	34,399,119 (GRCm39)	missense	probably benign	0.01
R5222:Wapl	UTSW	14	34,458,642 (GRCm39)	nonsense	probably null
R5299:Wapl	UTSW	14	34,455,765 (GRCm39)	critical splice donor site	probably null
R5387:Wapl	UTSW	14	34,399,252 (GRCm39)	missense	probably benign	0.00
R5541:Wapl	UTSW	14	34,452,619 (GRCm39)	critical splice donor site	probably null
R5618:Wapl	UTSW	14	34,413,863 (GRCm39)	missense	possibly damaging	0.91
R5802:Wapl	UTSW	14	34,414,277 (GRCm39)	missense	probably damaging	1.00
R6029:Wapl	UTSW	14	34,461,204 (GRCm39)	missense	possibly damaging	0.94
R6292:Wapl	UTSW	14	34,451,152 (GRCm39)	missense	probably damaging	1.00
R6482:Wapl	UTSW	14	34,414,649 (GRCm39)	missense	probably benign	0.01
R6487:Wapl	UTSW	14	34,414,249 (GRCm39)	missense	probably damaging	1.00
R6925:Wapl	UTSW	14	34,399,320 (GRCm39)	missense	probably benign	0.31
R6937:Wapl	UTSW	14	34,444,311 (GRCm39)	missense	probably benign	0.01
R7080:Wapl	UTSW	14	34,414,313 (GRCm39)	missense	probably benign	0.03
R7203:Wapl	UTSW	14	34,458,648 (GRCm39)	missense	probably benign
R7944:Wapl	UTSW	14	34,399,105 (GRCm39)	missense	probably benign	0.00
R7945:Wapl	UTSW	14	34,399,105 (GRCm39)	missense	probably benign	0.00
R7969:Wapl	UTSW	14	34,452,604 (GRCm39)	missense	probably damaging	1.00
R8038:Wapl	UTSW	14	34,413,639 (GRCm39)	missense	probably benign
R8053:Wapl	UTSW	14	34,414,278 (GRCm39)	missense	probably damaging	1.00
R8688:Wapl	UTSW	14	34,414,549 (GRCm39)	missense	possibly damaging	0.94
R8864:Wapl	UTSW	14	34,414,159 (GRCm39)	missense	probably benign	0.03
R8988:Wapl	UTSW	14	34,451,139 (GRCm39)	missense	probably damaging	1.00
R9072:Wapl	UTSW	14	34,399,417 (GRCm39)	missense	possibly damaging	0.81
R9197:Wapl	UTSW	14	34,444,244 (GRCm39)	missense	probably damaging	1.00
R9259:Wapl	UTSW	14	34,463,052 (GRCm39)	missense	probably benign	0.00
R9545:Wapl	UTSW	14	34,399,050 (GRCm39)	missense	probably damaging	1.00
R9613:Wapl	UTSW	14	34,453,520 (GRCm39)	missense	probably benign	0.29
R9624:Wapl	UTSW	14	34,414,063 (GRCm39)	missense	possibly damaging	0.89
Z1177:Wapl	UTSW	14	34,467,647 (GRCm39)	makesense	probably null

Predicted Primers

PCR Primer
(F):5'- AGCAACTGTAGGACGTACTGTAGGG -3'
(R):5'- ACTTTCGCTGAGATCGTCAAAGCC -3'

Sequencing Primer
(F):5'- TTGATAAGCTAATGGATGGCACC -3'
(R):5'- TTGTAATTAGAACTTCCAGAACCCC -3'

Posted On

2013-04-16