Mutagenetix > Incidental Mutation

Incidental Mutation 'R6232:Dysf'

504666

Institutional Source

Beutler Lab

Gene Symbol

Dysf

Ensembl Gene

ENSMUSG00000033788

Gene Name

dysferlin

Synonyms

2310004N10Rik

MMRRC Submission

044360-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R6232 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

83985572-84188042 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 84075235 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Threonine at position 583 (I583T)

Ref Sequence

ENSEMBL: ENSMUSP00000144748 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000081904] [ENSMUST00000089595] [ENSMUST00000113818] [ENSMUST00000113821] [ENSMUST00000113823] [ENSMUST00000153860] [ENSMUST00000168387] [ENSMUST00000203803] [ENSMUST00000204354] [ENSMUST00000204591] [ENSMUST00000204987] [ENSMUST00000203695]

AlphaFold

Q9ESD7

Predicted Effect

probably benign
Transcript: ENSMUST00000081904
AA Change: I600T

PolyPhen 2 Score 0.113 (Sensitivity: 0.93; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000080579
Gene: ENSMUSG00000033788
AA Change: I600T

Domain	Start	End	E-Value	Type
C2	1	101	2.11e-14	SMART
low complexity region	126	147	N/A	INTRINSIC
low complexity region	213	232	N/A	INTRINSIC
C2	255	351	4.84e-14	SMART
FerI	337	408	5.3e-39	SMART
C2	414	528	2.96e-9	SMART
FerA	714	779	6.3e-23	SMART
FerB	806	880	2.49e-44	SMART
DysFN	894	953	1.42e-22	SMART
DysFN	966	1022	2.65e-22	SMART
DysFC	1031	1069	1.33e-13	SMART
DysFC	1088	1121	1.1e-10	SMART
C2	1173	1281	2.63e-15	SMART
C2	1350	1457	7.13e0	SMART
C2	1599	1698	2.52e-12	SMART
C2	1832	1961	1.55e-3	SMART
Pfam:Ferlin_C	1991	2095	6.7e-25	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000089595
AA Change: I583T

PolyPhen 2 Score 0.259 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000087022
Gene: ENSMUSG00000033788
AA Change: I583T

Domain	Start	End	E-Value	Type
C2	1	101	2.11e-14	SMART
low complexity region	126	147	N/A	INTRINSIC
low complexity region	182	201	N/A	INTRINSIC
C2	224	320	4.84e-14	SMART
FerI	306	377	5.3e-39	SMART
C2	383	497	1.12e-9	SMART
FerA	697	762	6.3e-23	SMART
FerB	789	863	2.49e-44	SMART
DysFN	877	936	1.42e-22	SMART
DysFN	949	1005	2.65e-22	SMART
DysFC	1014	1052	1.33e-13	SMART
DysFC	1071	1104	1.1e-10	SMART
C2	1156	1264	2.63e-15	SMART
C2	1333	1440	7.13e0	SMART
C2	1582	1681	2.52e-12	SMART
C2	1815	1944	1.55e-3	SMART
Pfam:Ferlin_C	1974	2078	3.7e-25	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000113818
AA Change: I569T

PolyPhen 2 Score 0.113 (Sensitivity: 0.93; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000109449
Gene: ENSMUSG00000033788
AA Change: I569T

Domain	Start	End	E-Value	Type
C2	1	101	2.11e-14	SMART
low complexity region	126	147	N/A	INTRINSIC
low complexity region	182	201	N/A	INTRINSIC
C2	224	320	4.84e-14	SMART
FerI	306	377	5.3e-39	SMART
C2	383	497	2.96e-9	SMART
FerA	683	748	6.3e-23	SMART
FerB	775	849	2.49e-44	SMART
DysFN	863	922	1.42e-22	SMART
DysFN	935	991	2.65e-22	SMART
DysFC	1000	1038	1.33e-13	SMART
DysFC	1057	1090	1.1e-10	SMART
C2	1142	1250	2.63e-15	SMART
C2	1319	1426	7.13e0	SMART
C2	1568	1667	2.52e-12	SMART
C2	1801	1930	1.55e-3	SMART
transmembrane domain	2034	2056	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000113821
AA Change: I582T

PolyPhen 2 Score 0.135 (Sensitivity: 0.92; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000109452
Gene: ENSMUSG00000033788
AA Change: I582T

Domain	Start	End	E-Value	Type
C2	1	100	1.62e-15	SMART
low complexity region	125	146	N/A	INTRINSIC
low complexity region	181	200	N/A	INTRINSIC
C2	223	319	4.84e-14	SMART
FerI	305	376	5.3e-39	SMART
C2	382	496	1.12e-9	SMART
FerA	696	761	6.3e-23	SMART
FerB	788	862	2.49e-44	SMART
DysFN	876	935	1.42e-22	SMART
DysFN	948	1004	2.65e-22	SMART
DysFC	1013	1051	1.33e-13	SMART
DysFC	1070	1103	1.1e-10	SMART
C2	1155	1263	2.63e-15	SMART
C2	1332	1439	7.13e0	SMART
C2	1581	1680	2.52e-12	SMART
C2	1814	1943	1.55e-3	SMART
transmembrane domain	2047	2069	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000113823
AA Change: I599T

PolyPhen 2 Score 0.069 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000109454
Gene: ENSMUSG00000033788
AA Change: I599T

Domain	Start	End	E-Value	Type
C2	1	100	1.62e-15	SMART
low complexity region	125	146	N/A	INTRINSIC
low complexity region	212	231	N/A	INTRINSIC
C2	254	350	4.84e-14	SMART
FerI	336	407	5.3e-39	SMART
C2	413	527	2.96e-9	SMART
FerA	713	778	6.3e-23	SMART
FerB	805	879	2.49e-44	SMART
DysFN	893	952	1.42e-22	SMART
DysFN	965	1021	2.65e-22	SMART
DysFC	1030	1068	1.33e-13	SMART
DysFC	1087	1120	1.1e-10	SMART
C2	1172	1280	2.63e-15	SMART
C2	1349	1456	7.13e0	SMART
C2	1598	1697	2.52e-12	SMART
C2	1831	1960	1.55e-3	SMART
transmembrane domain	2064	2086	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000137673

Predicted Effect

probably benign
Transcript: ENSMUST00000153860
AA Change: I582T

PolyPhen 2 Score 0.069 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000145518
Gene: ENSMUSG00000033788
AA Change: I582T

Domain	Start	End	E-Value	Type
C2	1	100	1.1e-17	SMART
low complexity region	125	146	N/A	INTRINSIC
low complexity region	181	200	N/A	INTRINSIC
C2	223	319	3.2e-16	SMART
FerI	305	376	2.6e-43	SMART
C2	382	496	7.4e-12	SMART
FerA	696	761	3.1e-27	SMART
FerB	788	862	1.2e-48	SMART
DysFN	876	935	5.3e-25	SMART
DysFN	948	1004	9.6e-25	SMART
DysFC	1013	1051	4.7e-16	SMART
DysFC	1070	1103	4.1e-13	SMART
C2	1155	1263	1.7e-17	SMART
C2	1332	1439	4.7e-2	SMART
C2	1602	1701	1.7e-14	SMART
C2	1835	1964	1.1e-5	SMART
Pfam:Ferlin_C	1994	2098	4.4e-22	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000168387
AA Change: I582T

PolyPhen 2 Score 0.069 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000132297
Gene: ENSMUSG00000033788
AA Change: I582T

Domain	Start	End	E-Value	Type
C2	1	100	1.62e-15	SMART
low complexity region	125	146	N/A	INTRINSIC
low complexity region	181	200	N/A	INTRINSIC
C2	223	319	4.84e-14	SMART
FerI	305	376	5.3e-39	SMART
C2	382	496	1.12e-9	SMART
FerA	704	769	6.3e-23	SMART
FerB	796	870	2.49e-44	SMART
DysFN	884	943	1.42e-22	SMART
DysFN	956	1012	2.65e-22	SMART
DysFC	1021	1059	1.33e-13	SMART
DysFC	1078	1111	1.1e-10	SMART
C2	1163	1271	2.63e-15	SMART
C2	1340	1447	7.13e0	SMART
C2	1589	1688	2.52e-12	SMART
C2	1822	1951	1.55e-3	SMART
transmembrane domain	2055	2077	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000203803
AA Change: I613T

PolyPhen 2 Score 0.259 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000145511
Gene: ENSMUSG00000033788
AA Change: I613T

Domain	Start	End	E-Value	Type
C2	1	100	1.1e-17	SMART
low complexity region	125	146	N/A	INTRINSIC
low complexity region	212	231	N/A	INTRINSIC
C2	254	350	3.2e-16	SMART
FerI	336	407	2.6e-43	SMART
C2	413	527	7.4e-12	SMART
FerA	727	792	3.1e-27	SMART
FerB	819	893	1.2e-48	SMART
DysFN	907	966	5.3e-25	SMART
DysFN	979	1035	9.6e-25	SMART
DysFC	1044	1082	4.7e-16	SMART
DysFC	1101	1134	4.1e-13	SMART
C2	1186	1294	1.7e-17	SMART
C2	1353	1460	4.7e-2	SMART
C2	1602	1701	1.7e-14	SMART
C2	1835	1964	1.1e-5	SMART
Pfam:Ferlin_C	1994	2098	4.4e-22	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000204354
AA Change: I569T

PolyPhen 2 Score 0.069 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000144705
Gene: ENSMUSG00000033788
AA Change: I569T

Domain	Start	End	E-Value	Type
C2	1	101	1.4e-16	SMART
low complexity region	126	147	N/A	INTRINSIC
low complexity region	182	201	N/A	INTRINSIC
C2	224	320	3.2e-16	SMART
FerI	306	377	2.6e-43	SMART
C2	383	497	2e-11	SMART
FerA	683	748	3.1e-27	SMART
FerB	775	849	1.2e-48	SMART
DysFN	863	922	5.3e-25	SMART
DysFN	935	991	9.6e-25	SMART
DysFC	1000	1038	4.7e-16	SMART
DysFC	1057	1090	4.1e-13	SMART
C2	1142	1250	1.7e-17	SMART
C2	1319	1426	4.7e-2	SMART
C2	1589	1688	1.7e-14	SMART
C2	1822	1951	1.1e-5	SMART
Pfam:Ferlin_C	1981	2085	4.4e-22	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000204591
AA Change: I599T

PolyPhen 2 Score 0.038 (Sensitivity: 0.94; Specificity: 0.82)

SMART Domains

Protein: ENSMUSP00000144970
Gene: ENSMUSG00000033788
AA Change: I599T

Domain	Start	End	E-Value	Type
C2	1	100	1.1e-17	SMART
low complexity region	125	146	N/A	INTRINSIC
low complexity region	212	231	N/A	INTRINSIC
C2	254	350	3.2e-16	SMART
FerI	336	407	2.6e-43	SMART
C2	413	527	2e-11	SMART
FerA	713	778	3.1e-27	SMART
FerB	805	879	1.2e-48	SMART
DysFN	893	952	5.3e-25	SMART
DysFN	965	1021	9.6e-25	SMART
DysFC	1030	1068	4.7e-16	SMART
DysFC	1087	1120	4.1e-13	SMART
C2	1172	1280	1.7e-17	SMART
C2	1349	1456	4.7e-2	SMART
C2	1619	1718	1.7e-14	SMART
C2	1852	1981	1.1e-5	SMART
Pfam:Ferlin_C	2011	2115	4.4e-22	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000204987
AA Change: I583T

PolyPhen 2 Score 0.259 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000144748
Gene: ENSMUSG00000033788
AA Change: I583T

Domain	Start	End	E-Value	Type
C2	1	101	1.4e-16	SMART
low complexity region	126	147	N/A	INTRINSIC
low complexity region	182	201	N/A	INTRINSIC
C2	224	320	3.2e-16	SMART
FerI	306	377	2.6e-43	SMART
C2	383	497	7.4e-12	SMART
FerA	697	762	3.1e-27	SMART
FerB	789	863	1.2e-48	SMART
DysFN	877	936	5.3e-25	SMART
DysFN	949	1005	9.6e-25	SMART
DysFC	1014	1052	4.7e-16	SMART
DysFC	1071	1104	4.1e-13	SMART
C2	1156	1264	1.7e-17	SMART
C2	1333	1440	4.7e-2	SMART
C2	1603	1702	1.7e-14	SMART
C2	1836	1965	1.1e-5	SMART
Pfam:Ferlin_C	1995	2099	4.4e-22	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000203695
AA Change: I614T

PolyPhen 2 Score 0.038 (Sensitivity: 0.94; Specificity: 0.82)

SMART Domains

Protein: ENSMUSP00000145292
Gene: ENSMUSG00000033788
AA Change: I614T

Domain	Start	End	E-Value	Type
C2	1	101	1.4e-16	SMART
low complexity region	126	147	N/A	INTRINSIC
low complexity region	213	232	N/A	INTRINSIC
C2	255	351	3.2e-16	SMART
FerI	337	408	2.6e-43	SMART
C2	414	528	7.4e-12	SMART
FerA	728	793	3.1e-27	SMART
FerB	820	894	1.2e-48	SMART
DysFN	908	967	5.3e-25	SMART
DysFN	980	1036	9.6e-25	SMART
DysFC	1045	1083	4.7e-16	SMART
DysFC	1102	1135	4.1e-13	SMART
C2	1187	1295	1.7e-17	SMART
C2	1364	1471	4.7e-2	SMART
C2	1613	1712	1.7e-14	SMART
C2	1846	1975	1.1e-5	SMART
Pfam:Ferlin_C	2005	2109	4.4e-22	PFAM

Meta Mutation Damage Score

0.1178

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 98.5%
20x: 95.7%

Validation Efficiency

94% (64/68)

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 to the ferlin family and is a skeletal muscle protein found associated with the sarcolemma. It is involved in muscle contraction and contains C2 domains that play a role in calcium-mediated membrane fusion events, suggesting that it may be involved in membrane regeneration and repair. In addition, the protein encoded by this gene binds caveolin-3, a skeletal muscle membrane protein which is important in the formation of caveolae. Specific mutations in this gene have been shown to cause autosomal recessive limb girdle muscular dystrophy type 2B (LGMD2B) as well as Miyoshi myopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2008]
PHENOTYPE: Homozygotes display dystrophic muscle changes and progressive muscle weakness developing over time. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 72 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acsl5	T	C	19: 55,268,933 (GRCm39)	V198A	possibly damaging	Het
Adam34l	T	G	8: 44,078,949 (GRCm39)	N425T	probably benign	Het
Adgra2	A	T	8: 27,609,193 (GRCm39)	M805L	probably benign	Het
Arhgap39	T	C	15: 76,620,712 (GRCm39)	S630G	probably damaging	Het
Bcl3	T	A	7: 19,546,409 (GRCm39)	N142I	probably damaging	Het
Cfap210	C	T	2: 69,602,398 (GRCm39)	E338K	possibly damaging	Het
Chuk	A	T	19: 44,085,431 (GRCm39)	D238E	probably benign	Het
Cnga4	T	G	7: 105,056,906 (GRCm39)	Y336*	probably null	Het
Cyp2j8	A	T	4: 96,395,427 (GRCm39)	L66Q	possibly damaging	Het
Dnase1l1	C	T	X: 73,320,644 (GRCm39)		probably null	Homo
Dst	T	A	1: 34,227,253 (GRCm39)	D1290E	probably damaging	Het
Eif1ad13	A	T	12: 87,762,351 (GRCm39)	R24*	probably null	Het
Fbxl2	T	A	9: 113,815,516 (GRCm39)	D249V	probably damaging	Het
Fbxo30	A	T	10: 11,165,602 (GRCm39)	Y108F	possibly damaging	Het
Fibin	G	T	2: 110,193,041 (GRCm39)	H34N	probably damaging	Het
Gabrr1	A	G	4: 33,161,632 (GRCm39)	I319V	probably benign	Het
Gfm1	G	T	3: 67,375,215 (GRCm39)	L559F	possibly damaging	Het
Gm5134	T	A	10: 75,821,859 (GRCm39)	L231Q	possibly damaging	Het
Grm5	A	G	7: 87,251,638 (GRCm39)		probably benign	Het
Hbs1l	T	A	10: 21,183,657 (GRCm39)		probably null	Het
Hsf5	C	G	11: 87,508,120 (GRCm39)	T8S	probably benign	Het
Hspa4	C	T	11: 53,153,766 (GRCm39)	E702K	probably benign	Het
Inpp4b	A	G	8: 82,678,813 (GRCm39)	Q281R	probably damaging	Het
Krt40	G	A	11: 99,433,920 (GRCm39)	A22V	possibly damaging	Het
Ldlrap1	C	T	4: 134,486,345 (GRCm39)	R38Q	possibly damaging	Het
Lepr	A	G	4: 101,671,588 (GRCm39)		probably null	Het
Map3k12	A	G	15: 102,412,081 (GRCm39)	S328P	probably damaging	Het
Mrpl2	T	C	17: 46,958,356 (GRCm39)	V46A	probably benign	Het
Muc16	A	T	9: 18,568,294 (GRCm39)	N1408K	unknown	Het
Myh7	T	A	14: 55,226,753 (GRCm39)	Q366L	probably benign	Het
Nbeal2	A	G	9: 110,467,802 (GRCm39)	V462A	probably damaging	Het
Nradd	G	T	9: 110,450,655 (GRCm39)	T174N	probably damaging	Het
Nup155	T	C	15: 8,138,963 (GRCm39)	S12P	probably benign	Het
Obscn	C	A	11: 58,943,337 (GRCm39)	E4832*	probably null	Het
Opn3	G	A	1: 175,490,669 (GRCm39)	R331W	probably damaging	Het
Or2ag15	A	T	7: 106,340,761 (GRCm39)	C127S	probably damaging	Het
Or2w3	T	A	11: 58,556,757 (GRCm39)	V124E	possibly damaging	Het
Or4a66	G	T	2: 88,531,161 (GRCm39)	H171N	probably benign	Het
Or52ae9	T	A	7: 103,389,661 (GRCm39)	H262L	probably damaging	Het
Or5b120	G	A	19: 13,480,427 (GRCm39)	C240Y	probably damaging	Het
Or6b2	T	C	1: 92,408,305 (GRCm39)	I13V	probably benign	Het
Phip	A	G	9: 82,785,234 (GRCm39)	V827A	probably benign	Het
Phldb1	G	A	9: 44,607,414 (GRCm39)	R1264W	probably damaging	Het
Pibf1	T	G	14: 99,424,014 (GRCm39)	I529S	probably benign	Het
Pkp1	T	A	1: 135,814,599 (GRCm39)	I241F	probably benign	Het
Pla2g4f	G	T	2: 120,132,702 (GRCm39)	D711E	possibly damaging	Het
Pold1	A	G	7: 44,190,266 (GRCm39)		probably null	Het
Pold2	T	C	11: 5,823,691 (GRCm39)	S287G	probably benign	Het
Prg4	T	C	1: 150,331,567 (GRCm39)		probably benign	Het
Prl8a1	T	C	13: 27,759,557 (GRCm39)	E160G	possibly damaging	Het
Rfc4	C	T	16: 22,932,840 (GRCm39)		probably benign	Het
Robo3	T	G	9: 37,332,225 (GRCm39)	Y891S	probably damaging	Het
Rsf1	ATGGCG	ATGGCGACGGTGGCG	7: 97,229,111 (GRCm39)		probably benign	Homo
Rsph14	G	A	10: 74,797,520 (GRCm39)	R156W	probably benign	Het
Sec61a1	T	C	6: 88,482,150 (GRCm39)	Y457C	probably benign	Het
Sec63	T	A	10: 42,704,861 (GRCm39)		probably null	Het
Spen	T	C	4: 141,244,333 (GRCm39)	E234G	unknown	Het
Sphkap	T	A	1: 83,258,200 (GRCm39)	E181V	probably damaging	Het
Stau2	C	T	1: 16,445,035 (GRCm39)	A298T	probably benign	Het
Tbc1d2	C	T	4: 46,629,912 (GRCm39)	G252R	probably benign	Het
Tbc1d23	T	C	16: 56,990,796 (GRCm39)	I661V	probably benign	Het
Thoc6	A	C	17: 23,889,295 (GRCm39)		probably null	Het
Trpv1	T	A	11: 73,141,636 (GRCm39)	M553K	possibly damaging	Het
Ttn	T	C	2: 76,641,579 (GRCm39)	I11760V	probably benign	Het
Vmn1r61	G	A	7: 5,613,850 (GRCm39)	H155Y	probably damaging	Het
Vmn2r41	A	G	7: 8,153,214 (GRCm39)		probably null	Het
Vmn2r74	A	G	7: 85,607,498 (GRCm39)	I75T	possibly damaging	Het
Wwp2	C	A	8: 108,232,977 (GRCm39)	T205K	probably benign	Het
Zfp1003	A	T	2: 177,546,195 (GRCm39)	T40S	probably benign	Het
Zfp747	C	T	7: 126,973,306 (GRCm39)	G288D	probably damaging	Het
Zfp871	CCACAC	CC	17: 32,994,494 (GRCm39)		probably null	Het
Zfp953	G	A	13: 67,491,161 (GRCm39)	L264F	possibly damaging	Het

Other mutations in Dysf

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00309:Dysf	APN	6	84,085,081 (GRCm39)	missense	probably damaging	1.00
IGL00340:Dysf	APN	6	84,118,933 (GRCm39)	missense	probably benign	0.02
IGL00429:Dysf	APN	6	84,166,826 (GRCm39)	missense	probably damaging	1.00
IGL00465:Dysf	APN	6	84,176,830 (GRCm39)	critical splice donor site	probably null
IGL00800:Dysf	APN	6	84,126,980 (GRCm39)	missense	probably damaging	1.00
IGL01069:Dysf	APN	6	84,176,767 (GRCm39)	missense	possibly damaging	0.94
IGL01094:Dysf	APN	6	84,171,368 (GRCm39)	missense	probably damaging	1.00
IGL01420:Dysf	APN	6	84,126,741 (GRCm39)	nonsense	probably null
IGL01649:Dysf	APN	6	84,176,821 (GRCm39)	missense	probably damaging	1.00
IGL01923:Dysf	APN	6	84,187,811 (GRCm39)	makesense	probably null
IGL01991:Dysf	APN	6	84,090,600 (GRCm39)	missense	probably damaging	1.00
IGL01999:Dysf	APN	6	84,090,600 (GRCm39)	missense	probably damaging	1.00
IGL02002:Dysf	APN	6	84,187,769 (GRCm39)	splice site	probably benign
IGL02136:Dysf	APN	6	84,085,149 (GRCm39)	missense	probably benign	0.43
IGL02318:Dysf	APN	6	84,163,446 (GRCm39)	missense	possibly damaging	0.50
IGL02378:Dysf	APN	6	84,088,887 (GRCm39)	missense	probably damaging	1.00
IGL02404:Dysf	APN	6	84,093,043 (GRCm39)	missense	probably damaging	1.00
IGL02416:Dysf	APN	6	84,169,896 (GRCm39)	missense	possibly damaging	0.92
IGL02535:Dysf	APN	6	84,126,679 (GRCm39)	missense	possibly damaging	0.45
IGL02553:Dysf	APN	6	84,107,109 (GRCm39)	missense	possibly damaging	0.95
IGL02559:Dysf	APN	6	84,044,428 (GRCm39)	splice site	probably benign
IGL02563:Dysf	APN	6	84,163,498 (GRCm39)	splice site	probably benign
IGL02647:Dysf	APN	6	84,114,355 (GRCm39)	missense	probably damaging	1.00
IGL02820:Dysf	APN	6	84,077,187 (GRCm39)	missense	probably damaging	0.99
IGL02858:Dysf	APN	6	84,076,471 (GRCm39)	missense	probably benign	0.01
IGL02860:Dysf	APN	6	84,167,880 (GRCm39)	critical splice donor site	probably null
IGL02861:Dysf	APN	6	84,016,519 (GRCm39)	missense	probably damaging	0.99
IGL03008:Dysf	APN	6	84,050,876 (GRCm39)	missense	probably benign	0.01
IGL03023:Dysf	APN	6	84,169,989 (GRCm39)	missense	probably damaging	1.00
IGL03074:Dysf	APN	6	84,165,208 (GRCm39)	missense	probably benign	0.25
IGL03342:Dysf	APN	6	84,167,854 (GRCm39)	missense	probably benign
PIT4305001:Dysf	UTSW	6	84,077,216 (GRCm39)	nonsense	probably null
R0067:Dysf	UTSW	6	84,040,313 (GRCm39)	missense	possibly damaging	0.58
R0106:Dysf	UTSW	6	84,090,318 (GRCm39)	missense	probably benign	0.07
R0106:Dysf	UTSW	6	84,090,318 (GRCm39)	missense	probably benign	0.07
R0124:Dysf	UTSW	6	84,042,084 (GRCm39)	splice site	probably benign
R0219:Dysf	UTSW	6	84,106,443 (GRCm39)	splice site	probably benign
R0238:Dysf	UTSW	6	84,041,461 (GRCm39)	nonsense	probably null
R0238:Dysf	UTSW	6	84,041,461 (GRCm39)	nonsense	probably null
R0239:Dysf	UTSW	6	84,041,461 (GRCm39)	nonsense	probably null
R0239:Dysf	UTSW	6	84,041,461 (GRCm39)	nonsense	probably null
R0426:Dysf	UTSW	6	84,126,739 (GRCm39)	missense	probably damaging	1.00
R0455:Dysf	UTSW	6	84,117,649 (GRCm39)	missense	probably benign	0.29
R0482:Dysf	UTSW	6	84,129,387 (GRCm39)	missense	probably benign	0.03
R0545:Dysf	UTSW	6	84,076,443 (GRCm39)	missense	probably damaging	0.99
R0625:Dysf	UTSW	6	84,088,969 (GRCm39)	splice site	probably null
R0676:Dysf	UTSW	6	84,090,318 (GRCm39)	missense	probably benign	0.07
R0699:Dysf	UTSW	6	84,167,828 (GRCm39)	missense	probably benign	0.00
R1165:Dysf	UTSW	6	84,044,051 (GRCm39)	missense	probably damaging	0.98
R1455:Dysf	UTSW	6	84,090,368 (GRCm39)	missense	probably benign	0.01
R1582:Dysf	UTSW	6	84,074,749 (GRCm39)	missense	probably damaging	1.00
R1584:Dysf	UTSW	6	84,044,029 (GRCm39)	missense	probably benign	0.04
R1605:Dysf	UTSW	6	84,083,923 (GRCm39)	missense	probably damaging	0.96
R1674:Dysf	UTSW	6	84,156,697 (GRCm39)	missense	probably benign	0.01
R1739:Dysf	UTSW	6	84,089,217 (GRCm39)	critical splice donor site	probably null
R1765:Dysf	UTSW	6	84,167,884 (GRCm39)	splice site	probably null
R1813:Dysf	UTSW	6	84,128,906 (GRCm39)	missense	possibly damaging	0.83
R1900:Dysf	UTSW	6	84,016,549 (GRCm39)	missense	probably damaging	0.97
R1960:Dysf	UTSW	6	84,050,885 (GRCm39)	missense	probably benign	0.12
R2216:Dysf	UTSW	6	84,184,227 (GRCm39)	splice site	probably null
R2242:Dysf	UTSW	6	84,163,491 (GRCm39)	critical splice donor site	probably null
R2243:Dysf	UTSW	6	84,163,491 (GRCm39)	critical splice donor site	probably null
R2245:Dysf	UTSW	6	84,163,491 (GRCm39)	critical splice donor site	probably null
R2246:Dysf	UTSW	6	84,163,491 (GRCm39)	critical splice donor site	probably null
R2280:Dysf	UTSW	6	84,041,476 (GRCm39)	missense	probably damaging	0.99
R2374:Dysf	UTSW	6	84,074,711 (GRCm39)	missense	probably damaging	1.00
R2403:Dysf	UTSW	6	84,016,549 (GRCm39)	missense	possibly damaging	0.84
R2763:Dysf	UTSW	6	84,083,914 (GRCm39)	missense	probably benign	0.00
R2895:Dysf	UTSW	6	84,163,491 (GRCm39)	critical splice donor site	probably null
R2916:Dysf	UTSW	6	84,163,491 (GRCm39)	critical splice donor site	probably null
R2918:Dysf	UTSW	6	84,163,491 (GRCm39)	critical splice donor site	probably null
R3402:Dysf	UTSW	6	84,163,491 (GRCm39)	critical splice donor site	probably null
R3403:Dysf	UTSW	6	84,163,491 (GRCm39)	critical splice donor site	probably null
R3434:Dysf	UTSW	6	84,047,870 (GRCm39)	missense	probably benign	0.00
R3772:Dysf	UTSW	6	84,129,333 (GRCm39)	missense	possibly damaging	0.63
R3781:Dysf	UTSW	6	84,163,491 (GRCm39)	critical splice donor site	probably null
R3789:Dysf	UTSW	6	84,163,491 (GRCm39)	critical splice donor site	probably null
R3822:Dysf	UTSW	6	84,184,070 (GRCm39)	splice site	probably benign
R3918:Dysf	UTSW	6	84,163,491 (GRCm39)	critical splice donor site	probably null
R3919:Dysf	UTSW	6	84,163,491 (GRCm39)	critical splice donor site	probably null
R3939:Dysf	UTSW	6	84,163,491 (GRCm39)	critical splice donor site	probably null
R3942:Dysf	UTSW	6	84,163,491 (GRCm39)	critical splice donor site	probably null
R4177:Dysf	UTSW	6	84,044,013 (GRCm39)	nonsense	probably null
R4179:Dysf	UTSW	6	84,163,491 (GRCm39)	critical splice donor site	probably null
R4180:Dysf	UTSW	6	84,163,491 (GRCm39)	critical splice donor site	probably null
R4299:Dysf	UTSW	6	84,045,059 (GRCm39)	missense	possibly damaging	0.78
R4419:Dysf	UTSW	6	84,184,224 (GRCm39)	critical splice donor site	probably null
R4446:Dysf	UTSW	6	84,182,854 (GRCm39)	missense	probably damaging	1.00
R4577:Dysf	UTSW	6	84,114,308 (GRCm39)	missense	probably damaging	1.00
R4680:Dysf	UTSW	6	84,074,697 (GRCm39)	missense	probably damaging	0.99
R4708:Dysf	UTSW	6	84,074,697 (GRCm39)	missense	probably damaging	0.99
R4709:Dysf	UTSW	6	84,074,697 (GRCm39)	missense	probably damaging	0.99
R4710:Dysf	UTSW	6	84,074,697 (GRCm39)	missense	probably damaging	0.99
R4725:Dysf	UTSW	6	84,074,738 (GRCm39)	missense	probably damaging	1.00
R4742:Dysf	UTSW	6	84,074,697 (GRCm39)	missense	probably damaging	0.99
R4743:Dysf	UTSW	6	84,074,697 (GRCm39)	missense	probably damaging	0.99
R4749:Dysf	UTSW	6	84,043,990 (GRCm39)	missense	probably damaging	1.00
R4787:Dysf	UTSW	6	84,180,310 (GRCm39)	nonsense	probably null
R4850:Dysf	UTSW	6	84,074,697 (GRCm39)	missense	probably damaging	0.99
R4868:Dysf	UTSW	6	84,156,675 (GRCm39)	missense	probably damaging	1.00
R4871:Dysf	UTSW	6	84,044,005 (GRCm39)	missense	possibly damaging	0.93
R4951:Dysf	UTSW	6	84,091,102 (GRCm39)	critical splice donor site	probably null
R4952:Dysf	UTSW	6	84,126,968 (GRCm39)	missense	possibly damaging	0.79
R5009:Dysf	UTSW	6	84,128,968 (GRCm39)	missense	probably damaging	1.00
R5072:Dysf	UTSW	6	84,114,254 (GRCm39)	missense	probably damaging	1.00
R5073:Dysf	UTSW	6	84,114,254 (GRCm39)	missense	probably damaging	1.00
R5074:Dysf	UTSW	6	84,114,254 (GRCm39)	missense	probably damaging	1.00
R5252:Dysf	UTSW	6	84,163,450 (GRCm39)	missense	probably damaging	0.98
R5260:Dysf	UTSW	6	84,127,016 (GRCm39)	missense	probably damaging	1.00
R5447:Dysf	UTSW	6	84,172,245 (GRCm39)	missense	probably damaging	0.98
R5501:Dysf	UTSW	6	84,064,800 (GRCm39)	missense	probably damaging	0.99
R5533:Dysf	UTSW	6	84,163,453 (GRCm39)	missense	probably damaging	0.99
R5611:Dysf	UTSW	6	84,041,860 (GRCm39)	missense	probably damaging	0.98
R5618:Dysf	UTSW	6	84,083,806 (GRCm39)	missense	probably benign	0.03
R5884:Dysf	UTSW	6	84,163,063 (GRCm39)	missense	probably damaging	1.00
R5927:Dysf	UTSW	6	84,184,194 (GRCm39)	missense	probably damaging	1.00
R6045:Dysf	UTSW	6	84,091,054 (GRCm39)	missense	probably damaging	0.99
R6056:Dysf	UTSW	6	84,083,844 (GRCm39)	missense	probably benign
R6084:Dysf	UTSW	6	84,089,101 (GRCm39)	missense	probably damaging	1.00
R6084:Dysf	UTSW	6	83,996,586 (GRCm39)	missense	probably damaging	0.98
R6146:Dysf	UTSW	6	84,180,181 (GRCm39)	missense	probably damaging	0.96
R6220:Dysf	UTSW	6	84,126,727 (GRCm39)	missense	probably damaging	0.97
R6247:Dysf	UTSW	6	84,043,981 (GRCm39)	missense	probably damaging	1.00
R6298:Dysf	UTSW	6	84,084,118 (GRCm39)	splice site	probably null
R6306:Dysf	UTSW	6	84,114,248 (GRCm39)	missense	possibly damaging	0.91
R6377:Dysf	UTSW	6	83,985,945 (GRCm39)	missense	probably benign
R6415:Dysf	UTSW	6	84,117,024 (GRCm39)	missense	probably damaging	1.00
R6444:Dysf	UTSW	6	84,167,822 (GRCm39)	missense	probably benign	0.36
R6470:Dysf	UTSW	6	84,043,926 (GRCm39)	missense	possibly damaging	0.93
R6504:Dysf	UTSW	6	83,985,907 (GRCm39)	missense	probably benign	0.03
R6557:Dysf	UTSW	6	84,163,366 (GRCm39)	missense	probably damaging	0.99
R6665:Dysf	UTSW	6	84,107,098 (GRCm39)	missense	probably benign
R6701:Dysf	UTSW	6	84,089,172 (GRCm39)	missense	probably damaging	1.00
R6776:Dysf	UTSW	6	84,041,876 (GRCm39)	missense	possibly damaging	0.88
R6909:Dysf	UTSW	6	84,169,920 (GRCm39)	missense	probably damaging	1.00
R7007:Dysf	UTSW	6	84,090,962 (GRCm39)	missense	probably damaging	1.00
R7013:Dysf	UTSW	6	84,114,340 (GRCm39)	missense	probably damaging	1.00
R7035:Dysf	UTSW	6	84,163,374 (GRCm39)	missense	probably benign	0.02
R7094:Dysf	UTSW	6	84,077,184 (GRCm39)	missense	probably benign	0.43
R7124:Dysf	UTSW	6	84,167,883 (GRCm39)	splice site	probably null
R7156:Dysf	UTSW	6	84,064,858 (GRCm39)	critical splice donor site	probably null
R7261:Dysf	UTSW	6	84,169,992 (GRCm39)	missense	probably damaging	0.98
R7296:Dysf	UTSW	6	84,083,880 (GRCm39)	missense	probably benign	0.33
R7356:Dysf	UTSW	6	84,044,443 (GRCm39)	missense	probably damaging	1.00
R7359:Dysf	UTSW	6	84,172,306 (GRCm39)	splice site	probably null
R7384:Dysf	UTSW	6	84,091,087 (GRCm39)	missense	probably benign	0.17
R7409:Dysf	UTSW	6	84,126,664 (GRCm39)	missense	probably benign	0.00
R7449:Dysf	UTSW	6	84,114,362 (GRCm39)	missense	possibly damaging	0.90
R7476:Dysf	UTSW	6	84,041,878 (GRCm39)	missense	probably benign	0.08
R7496:Dysf	UTSW	6	84,044,460 (GRCm39)	missense	probably benign	0.43
R7573:Dysf	UTSW	6	84,107,104 (GRCm39)	missense	possibly damaging	0.59
R7616:Dysf	UTSW	6	84,078,945 (GRCm39)	missense	probably benign	0.01
R7684:Dysf	UTSW	6	84,077,117 (GRCm39)	missense	probably benign	0.00
R7808:Dysf	UTSW	6	84,047,911 (GRCm39)	missense	possibly damaging	0.86
R7836:Dysf	UTSW	6	84,114,380 (GRCm39)	missense	probably damaging	1.00
R7868:Dysf	UTSW	6	84,091,081 (GRCm39)	missense	probably benign	0.00
R7873:Dysf	UTSW	6	84,060,747 (GRCm39)	missense	probably benign
R7956:Dysf	UTSW	6	83,985,978 (GRCm39)	missense	probably benign	0.01
R8130:Dysf	UTSW	6	84,114,358 (GRCm39)	missense	probably damaging	0.97
R8357:Dysf	UTSW	6	84,165,227 (GRCm39)	missense	probably benign	0.01
R8383:Dysf	UTSW	6	83,996,565 (GRCm39)	missense	probably damaging	1.00
R8457:Dysf	UTSW	6	84,165,227 (GRCm39)	missense	probably benign	0.01
R8693:Dysf	UTSW	6	84,088,952 (GRCm39)	missense	probably damaging	1.00
R8738:Dysf	UTSW	6	84,171,353 (GRCm39)	missense	probably damaging	1.00
R8808:Dysf	UTSW	6	83,996,466 (GRCm39)	start gained	probably benign
R8836:Dysf	UTSW	6	84,093,105 (GRCm39)	missense	probably damaging	1.00
R8915:Dysf	UTSW	6	84,156,736 (GRCm39)	missense	probably benign
R8959:Dysf	UTSW	6	84,078,945 (GRCm39)	missense	probably benign	0.01
R9091:Dysf	UTSW	6	84,077,216 (GRCm39)	nonsense	probably null
R9095:Dysf	UTSW	6	84,156,666 (GRCm39)	missense	probably benign	0.01
R9162:Dysf	UTSW	6	84,089,215 (GRCm39)	missense	probably damaging	1.00
R9164:Dysf	UTSW	6	84,180,308 (GRCm39)	missense	probably damaging	1.00
R9166:Dysf	UTSW	6	84,126,959 (GRCm39)	missense	probably damaging	1.00
R9173:Dysf	UTSW	6	84,171,379 (GRCm39)	missense	probably benign	0.10
R9191:Dysf	UTSW	6	84,045,048 (GRCm39)	missense	probably benign	0.43
R9270:Dysf	UTSW	6	84,077,216 (GRCm39)	nonsense	probably null
R9328:Dysf	UTSW	6	84,050,895 (GRCm39)	missense	probably damaging	1.00
R9470:Dysf	UTSW	6	84,090,352 (GRCm39)	missense	possibly damaging	0.59
R9509:Dysf	UTSW	6	84,187,779 (GRCm39)	missense	probably damaging	0.98
R9511:Dysf	UTSW	6	84,090,650 (GRCm39)	missense	probably damaging	1.00
R9526:Dysf	UTSW	6	84,128,885 (GRCm39)	missense	probably damaging	0.99
R9751:Dysf	UTSW	6	84,163,450 (GRCm39)	missense	probably damaging	0.98
X0063:Dysf	UTSW	6	84,040,336 (GRCm39)	missense	probably damaging	0.97
X0066:Dysf	UTSW	6	84,091,084 (GRCm39)	missense	possibly damaging	0.77
Z1176:Dysf	UTSW	6	84,049,667 (GRCm39)	missense	probably damaging	1.00
Z1177:Dysf	UTSW	6	84,064,799 (GRCm39)	missense	probably benign	0.39
Z1177:Dysf	UTSW	6	84,041,505 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- TCCCCATCTATAGGGGTGAACTATAG -3'
(R):5'- TAAGCCTCAAAGCATCCCTGG -3'

Sequencing Primer
(F):5'- GAACTATAGTATGCTGTCATGCG -3'
(R):5'- GGATGGGGACGGAATATCACAC -3'

Posted On

2018-02-28