Mutagenetix > Incidental Mutation

Incidental Mutation 'R1861:Asap1'

203962

Institutional Source

Beutler Lab

Gene Symbol

Asap1

Ensembl Gene

ENSMUSG00000022377

Gene Name

ArfGAP with SH3 domain, ankyrin repeat and PH domain1

Synonyms

Ddef1

MMRRC Submission

039884-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.120) question?

Stock #

R1861 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

63958706-64254768 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

G to A at 64007647 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000134825 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000023008] [ENSMUST00000110114] [ENSMUST00000110115] [ENSMUST00000175793] [ENSMUST00000175799] [ENSMUST00000176014] [ENSMUST00000176384] [ENSMUST00000177374] [ENSMUST00000177083] [ENSMUST00000177035] [ENSMUST00000177371]

AlphaFold

Q9QWY8

Predicted Effect

probably benign
Transcript: ENSMUST00000023008

SMART Domains

Protein: ENSMUSP00000023008
Gene: ENSMUSG00000022377

Domain	Start	End	E-Value	Type
low complexity region	2	16	N/A	INTRINSIC
low complexity region	122	136	N/A	INTRINSIC
low complexity region	147	164	N/A	INTRINSIC
PH	340	433	4.12e-15	SMART
ArfGap	454	577	2.18e-34	SMART
ANK	615	647	1.17e-1	SMART
ANK	651	680	3.46e-4	SMART
low complexity region	727	738	N/A	INTRINSIC
low complexity region	792	803	N/A	INTRINSIC
low complexity region	814	847	N/A	INTRINSIC
low complexity region	856	865	N/A	INTRINSIC
low complexity region	892	903	N/A	INTRINSIC
low complexity region	971	984	N/A	INTRINSIC
low complexity region	1065	1077	N/A	INTRINSIC
SH3	1088	1146	3.29e-17	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000110114

SMART Domains

Protein: ENSMUSP00000105741
Gene: ENSMUSG00000022377

Domain	Start	End	E-Value	Type
low complexity region	2	16	N/A	INTRINSIC
low complexity region	122	136	N/A	INTRINSIC
low complexity region	147	164	N/A	INTRINSIC
PH	340	433	4.12e-15	SMART
ArfGap	454	577	2.18e-34	SMART
ANK	615	647	1.17e-1	SMART
ANK	651	680	3.46e-4	SMART
low complexity region	727	738	N/A	INTRINSIC
low complexity region	792	803	N/A	INTRINSIC
low complexity region	835	846	N/A	INTRINSIC
low complexity region	914	927	N/A	INTRINSIC
low complexity region	1008	1020	N/A	INTRINSIC
SH3	1031	1089	3.29e-17	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000110115

SMART Domains

Protein: ENSMUSP00000105742
Gene: ENSMUSG00000022377

Domain	Start	End	E-Value	Type
low complexity region	2	16	N/A	INTRINSIC
low complexity region	122	136	N/A	INTRINSIC
low complexity region	147	164	N/A	INTRINSIC
PH	325	418	4.12e-15	SMART
ArfGap	439	562	2.18e-34	SMART
ANK	600	632	1.17e-1	SMART
ANK	636	665	3.46e-4	SMART
low complexity region	712	723	N/A	INTRINSIC
low complexity region	777	788	N/A	INTRINSIC
low complexity region	799	832	N/A	INTRINSIC
low complexity region	841	850	N/A	INTRINSIC
low complexity region	877	888	N/A	INTRINSIC
low complexity region	956	969	N/A	INTRINSIC
low complexity region	1050	1062	N/A	INTRINSIC
SH3	1073	1131	3.29e-17	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000175793

SMART Domains

Protein: ENSMUSP00000135718
Gene: ENSMUSG00000022377

Domain	Start	End	E-Value	Type
low complexity region	2	16	N/A	INTRINSIC
low complexity region	122	136	N/A	INTRINSIC
low complexity region	147	164	N/A	INTRINSIC
PH	328	421	4.12e-15	SMART
ArfGap	442	565	2.18e-34	SMART
ANK	603	635	1.17e-1	SMART
ANK	639	668	3.46e-4	SMART
low complexity region	715	726	N/A	INTRINSIC
low complexity region	780	791	N/A	INTRINSIC
low complexity region	802	835	N/A	INTRINSIC
low complexity region	844	853	N/A	INTRINSIC
low complexity region	880	891	N/A	INTRINSIC
low complexity region	959	972	N/A	INTRINSIC
low complexity region	1053	1065	N/A	INTRINSIC
SH3	1076	1134	3.29e-17	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000175799

SMART Domains

Protein: ENSMUSP00000135359
Gene: ENSMUSG00000022377

Domain	Start	End	E-Value	Type
low complexity region	2	16	N/A	INTRINSIC
low complexity region	122	136	N/A	INTRINSIC
low complexity region	147	164	N/A	INTRINSIC
PH	337	430	4.12e-15	SMART
ArfGap	451	574	2.18e-34	SMART
ANK	612	644	1.17e-1	SMART
ANK	648	677	3.46e-4	SMART
low complexity region	724	735	N/A	INTRINSIC
low complexity region	789	800	N/A	INTRINSIC
low complexity region	832	843	N/A	INTRINSIC
low complexity region	911	924	N/A	INTRINSIC
low complexity region	1005	1017	N/A	INTRINSIC
SH3	1028	1086	3.29e-17	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000176014

SMART Domains

Protein: ENSMUSP00000135172
Gene: ENSMUSG00000022377

Domain	Start	End	E-Value	Type
low complexity region	2	16	N/A	INTRINSIC
low complexity region	122	136	N/A	INTRINSIC
low complexity region	147	164	N/A	INTRINSIC
PH	337	430	4.12e-15	SMART
ArfGap	451	574	2.18e-34	SMART
ANK	612	644	1.17e-1	SMART
ANK	648	677	3.46e-4	SMART
low complexity region	724	735	N/A	INTRINSIC
low complexity region	789	800	N/A	INTRINSIC
low complexity region	811	844	N/A	INTRINSIC
low complexity region	853	862	N/A	INTRINSIC
low complexity region	889	900	N/A	INTRINSIC
low complexity region	968	981	N/A	INTRINSIC
low complexity region	1062	1074	N/A	INTRINSIC
SH3	1085	1143	3.29e-17	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000176384

SMART Domains

Protein: ENSMUSP00000135190
Gene: ENSMUSG00000022377

Domain	Start	End	E-Value	Type
low complexity region	2	16	N/A	INTRINSIC
low complexity region	122	136	N/A	INTRINSIC
low complexity region	147	164	N/A	INTRINSIC
low complexity region	310	328	N/A	INTRINSIC
PH	340	433	4.12e-15	SMART
ArfGap	454	577	2.18e-34	SMART
ANK	615	647	1.17e-1	SMART
ANK	651	680	3.46e-4	SMART
low complexity region	727	738	N/A	INTRINSIC
low complexity region	792	803	N/A	INTRINSIC
low complexity region	835	846	N/A	INTRINSIC
low complexity region	914	927	N/A	INTRINSIC
low complexity region	1008	1020	N/A	INTRINSIC
SH3	1031	1089	3.29e-17	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000177374

SMART Domains

Protein: ENSMUSP00000134825
Gene: ENSMUSG00000022377

Domain	Start	End	E-Value	Type
low complexity region	2	16	N/A	INTRINSIC
Pfam:BAR	18	267	1.8e-11	PFAM
Pfam:BAR_3	52	286	1.2e-29	PFAM
low complexity region	310	328	N/A	INTRINSIC
PH	340	433	4.12e-15	SMART
ArfGap	454	577	2.18e-34	SMART
ANK	615	647	1.17e-1	SMART
ANK	651	680	3.46e-4	SMART
low complexity region	727	738	N/A	INTRINSIC
low complexity region	792	803	N/A	INTRINSIC
low complexity region	814	847	N/A	INTRINSIC
low complexity region	856	865	N/A	INTRINSIC
low complexity region	892	903	N/A	INTRINSIC
low complexity region	971	984	N/A	INTRINSIC
low complexity region	1065	1077	N/A	INTRINSIC
SH3	1088	1146	3.29e-17	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000177083

SMART Domains

Protein: ENSMUSP00000134877
Gene: ENSMUSG00000022377

Domain	Start	End	E-Value	Type
low complexity region	102	116	N/A	INTRINSIC
low complexity region	127	144	N/A	INTRINSIC
PH	305	398	4.12e-15	SMART
ArfGap	419	542	2.18e-34	SMART
ANK	580	612	1.17e-1	SMART
ANK	616	645	3.46e-4	SMART
low complexity region	692	703	N/A	INTRINSIC
low complexity region	757	768	N/A	INTRINSIC
low complexity region	779	812	N/A	INTRINSIC
low complexity region	821	830	N/A	INTRINSIC
low complexity region	857	868	N/A	INTRINSIC
low complexity region	936	949	N/A	INTRINSIC
low complexity region	1030	1042	N/A	INTRINSIC
SH3	1053	1111	3.29e-17	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000177035

SMART Domains

Protein: ENSMUSP00000135346
Gene: ENSMUSG00000022377

Domain	Start	End	E-Value	Type
low complexity region	2	16	N/A	INTRINSIC
low complexity region	122	136	N/A	INTRINSIC
low complexity region	147	164	N/A	INTRINSIC
PH	325	418	4.12e-15	SMART
ArfGap	439	562	2.18e-34	SMART
ANK	600	632	1.17e-1	SMART
ANK	636	665	3.46e-4	SMART
low complexity region	712	723	N/A	INTRINSIC
low complexity region	777	788	N/A	INTRINSIC
low complexity region	820	831	N/A	INTRINSIC
low complexity region	899	912	N/A	INTRINSIC
low complexity region	993	1005	N/A	INTRINSIC
SH3	1016	1074	3.29e-17	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000177371

SMART Domains

Protein: ENSMUSP00000135643
Gene: ENSMUSG00000022377

Domain	Start	End	E-Value	Type
low complexity region	102	116	N/A	INTRINSIC
low complexity region	127	144	N/A	INTRINSIC
PH	317	410	4.12e-15	SMART
ArfGap	431	554	2.18e-34	SMART
ANK	592	624	1.17e-1	SMART
ANK	628	657	3.46e-4	SMART
low complexity region	704	715	N/A	INTRINSIC
low complexity region	769	780	N/A	INTRINSIC
low complexity region	791	824	N/A	INTRINSIC
low complexity region	833	842	N/A	INTRINSIC
low complexity region	869	880	N/A	INTRINSIC
low complexity region	948	961	N/A	INTRINSIC
low complexity region	1042	1054	N/A	INTRINSIC
SH3	1065	1123	3.29e-17	SMART

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 97.4%
3x: 96.9%
10x: 95.2%
20x: 92.0%

Validation Efficiency

97% (117/121)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes an ADP-ribosylation factor (ARF) GTPase-activating protein. The GTPase-activating activity is stimulated by phosphatidylinositol 4,5-biphosphate (PIP2), and is greater towards ARF1 and ARF5, and lesser for ARF6. This gene maybe involved in regulation of membrane trafficking and cytoskeleton remodeling. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]

Allele List at MGI

All alleles(13) : Gene trapped(13)

Other mutations in this stock

Total: 113 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930579C12Rik	C	A	9: 89,034,884 (GRCm39)		noncoding transcript	Het
Abra	C	A	15: 41,732,430 (GRCm39)	R212L	probably damaging	Het
Actr1a	T	C	19: 46,372,714 (GRCm39)	E87G	probably damaging	Het
Adam26a	A	G	8: 44,022,578 (GRCm39)	V304A	possibly damaging	Het
Alg2	T	A	4: 47,471,670 (GRCm39)	K379N	probably benign	Het
Alk	G	T	17: 72,181,933 (GRCm39)		probably benign	Het
Aopep	A	G	13: 63,163,597 (GRCm39)	Y206C	probably damaging	Het
Arhgef17	A	G	7: 100,531,475 (GRCm39)	Y331H	probably damaging	Het
Art3	A	G	5: 92,560,094 (GRCm39)		probably benign	Het
Atad2	A	T	15: 57,960,114 (GRCm39)		probably null	Het
Atp8b5	G	A	4: 43,372,906 (GRCm39)	R1150H	probably damaging	Het
Bltp2	C	T	11: 78,178,755 (GRCm39)		probably benign	Het
Brdt	T	C	5: 107,507,324 (GRCm39)	S575P	probably benign	Het
Capn3	T	A	2: 120,316,963 (GRCm39)		probably benign	Het
Casd1	T	A	6: 4,640,951 (GRCm39)	Y691N	probably damaging	Het
Ccdc127	T	G	13: 74,505,098 (GRCm39)	H215Q	possibly damaging	Het
Cenpe	T	C	3: 134,974,740 (GRCm39)	L2300P	probably damaging	Het
Clasp1	T	C	1: 118,498,661 (GRCm39)	F898L	possibly damaging	Het
Clcn1	C	A	6: 42,290,925 (GRCm39)	P933Q	possibly damaging	Het
Cntn3	T	A	6: 102,222,032 (GRCm39)	N489I	probably benign	Het
Col16a1	T	C	4: 129,955,517 (GRCm39)		probably benign	Het
Col24a1	G	A	3: 145,243,022 (GRCm39)		probably null	Het
Col8a2	C	T	4: 126,205,417 (GRCm39)		probably benign	Het
Cpd	T	C	11: 76,675,208 (GRCm39)		probably benign	Het
Csmd3	A	T	15: 47,522,588 (GRCm39)	C2694S	probably damaging	Het
Cyp2c40	T	C	19: 39,775,319 (GRCm39)	Y311C	probably benign	Het
Dennd5b	T	A	6: 148,969,760 (GRCm39)	N231I	probably damaging	Het
Dgkh	T	A	14: 78,816,232 (GRCm39)	H936L	probably benign	Het
Dmtf1	T	C	5: 9,170,347 (GRCm39)		probably null	Het
Dnai2	T	C	11: 114,643,777 (GRCm39)	V481A	possibly damaging	Het
Dnai3	T	C	3: 145,788,801 (GRCm39)	Y260C	probably damaging	Het
Dpyd	T	G	3: 118,710,780 (GRCm39)	V396G	probably damaging	Het
Elmo3	A	G	8: 106,035,213 (GRCm39)	D448G	probably damaging	Het
Emsy	A	T	7: 98,290,822 (GRCm39)	V100E	probably damaging	Het
Erbb2	T	C	11: 98,303,563 (GRCm39)		probably null	Het
Faah	T	C	4: 115,865,432 (GRCm39)	K85R	probably benign	Het
Fam149a	A	T	8: 45,792,399 (GRCm39)	Y686*	probably null	Het
Fat4	T	C	3: 39,064,633 (GRCm39)	V4863A	probably benign	Het
Fbxl8	A	G	8: 105,995,561 (GRCm39)	T358A	probably damaging	Het
Fcgbpl1	A	G	7: 27,854,157 (GRCm39)	Y1707C	probably damaging	Het
Fgfr3	A	G	5: 33,887,090 (GRCm39)	T165A	probably damaging	Het
Fnbp1l	A	T	3: 122,354,581 (GRCm39)	H180Q	probably damaging	Het
Gm8180	T	A	14: 44,021,196 (GRCm39)	H4L	probably benign	Het
Gon4l	T	C	3: 88,802,794 (GRCm39)	V1135A	probably damaging	Het
Gstcd	G	T	3: 132,688,868 (GRCm39)	N627K	probably damaging	Het
Gtf2a1l	G	A	17: 89,022,382 (GRCm39)	V458I	probably damaging	Het
Gtf3c3	T	C	1: 54,477,997 (GRCm39)	E26G	possibly damaging	Het
Hrct1	A	T	4: 43,727,404 (GRCm39)	T15S	probably benign	Het
Ift122	C	A	6: 115,868,889 (GRCm39)	R459S	probably damaging	Het
Irf1	T	A	11: 53,665,183 (GRCm39)	C187S	possibly damaging	Het
Kcnh7	A	G	2: 62,607,736 (GRCm39)	V615A	probably damaging	Het
Kif1c	T	C	11: 70,594,168 (GRCm39)	S61P	probably damaging	Het
Mamdc2	T	C	19: 23,336,517 (GRCm39)	T331A	probably damaging	Het
Mark2	T	C	19: 7,268,128 (GRCm39)	D25G	possibly damaging	Het
Me2	T	C	18: 73,918,785 (GRCm39)	D432G	probably benign	Het
Mfap3	T	C	11: 57,419,032 (GRCm39)	V64A	probably benign	Het
Nadk2	T	A	15: 9,108,399 (GRCm39)	M416K	probably benign	Het
Ndufs1	C	T	1: 63,186,576 (GRCm39)	G631D	probably benign	Het
Nomo1	G	A	7: 45,727,525 (GRCm39)	V1055I	probably benign	Het
Nuggc	T	A	14: 65,879,450 (GRCm39)		probably benign	Het
Nwd2	T	C	5: 63,962,197 (GRCm39)	S594P	probably damaging	Het
Or13c3	T	A	4: 52,856,373 (GRCm39)	I47L	probably benign	Het
Or4a27	T	G	2: 88,559,674 (GRCm39)	I90L	probably damaging	Het
Or4b1b	C	A	2: 90,112,502 (GRCm39)	C139F	probably damaging	Het
Or5b113	T	A	19: 13,342,705 (GRCm39)	S238T	possibly damaging	Het
Or6p1	T	C	1: 174,258,657 (GRCm39)	I221T	probably damaging	Het
Or8c10	C	T	9: 38,278,902 (GRCm39)	S10L	probably benign	Het
Pakap	A	G	4: 57,709,468 (GRCm39)	I138V	probably damaging	Het
Pcyt2	G	A	11: 120,501,968 (GRCm39)	P332S	probably benign	Het
Phaf1	A	G	8: 105,966,703 (GRCm39)	E150G	probably null	Het
Phf14	A	T	6: 11,987,610 (GRCm39)	M630L	probably benign	Het
Piezo1	T	C	8: 123,222,489 (GRCm39)	N919S	possibly damaging	Het
Pif1	A	T	9: 65,496,735 (GRCm39)	I283F	probably damaging	Het
Pknox2	G	A	9: 36,834,957 (GRCm39)	H171Y	probably damaging	Het
Pramel17	A	T	4: 101,694,135 (GRCm39)	D249E	probably benign	Het
Prkg2	T	A	5: 99,095,275 (GRCm39)	D632V	probably damaging	Het
Prr29	G	A	11: 106,266,264 (GRCm39)	A6T	probably damaging	Het
Rims1	T	A	1: 22,635,639 (GRCm39)	Y114F	probably damaging	Het
Ryr1	A	T	7: 28,708,977 (GRCm39)	D4796E	unknown	Het
Scnn1b	G	A	7: 121,513,484 (GRCm39)	C399Y	probably damaging	Het
Scp2	T	C	4: 107,948,518 (GRCm39)	Y153C	probably damaging	Het
Sema3d	A	G	5: 12,547,570 (GRCm39)	K164R	probably benign	Het
Siglecf	A	G	7: 43,001,648 (GRCm39)	T153A	probably benign	Het
Siglecf	A	G	7: 43,004,967 (GRCm39)	N399S	probably benign	Het
Skint2	T	C	4: 112,504,315 (GRCm39)		probably benign	Het
Slc22a8	G	A	19: 8,583,503 (GRCm39)	R236H	probably damaging	Het
Slc25a40	T	A	5: 8,492,431 (GRCm39)		probably null	Het
Slc26a5	T	C	5: 22,021,956 (GRCm39)	D490G	possibly damaging	Het
Slc26a7	G	T	4: 14,522,873 (GRCm39)	D482E	probably benign	Het
Smarca2	A	T	19: 26,601,284 (GRCm39)	M77L	probably benign	Het
Sos2	A	G	12: 69,664,137 (GRCm39)	L449P	probably damaging	Het
Spaca1	A	G	4: 34,044,206 (GRCm39)	V96A	probably damaging	Het
Spata31d1b	T	A	13: 59,865,150 (GRCm39)	I766N	possibly damaging	Het
Specc1l	T	C	10: 75,145,693 (GRCm39)	Y1113H	probably damaging	Het
Speg	A	G	1: 75,365,649 (GRCm39)	R677G	probably damaging	Het
Taf5l	A	T	8: 124,724,729 (GRCm39)	D363E	probably damaging	Het
Tex56	A	T	13: 35,116,490 (GRCm39)	I80F	possibly damaging	Het
Tmem208	A	G	8: 106,061,438 (GRCm39)	K155E	possibly damaging	Het
Tppp2	A	C	14: 52,158,062 (GRCm39)	N169T	probably benign	Het
Trrap	T	A	5: 144,752,727 (GRCm39)		probably null	Het
Ttll6	T	A	11: 96,029,700 (GRCm39)	Y204*	probably null	Het
Ttn	A	T	2: 76,602,992 (GRCm39)	I18410K	probably benign	Het
V1rd19	T	A	7: 23,703,149 (GRCm39)	V205D	probably damaging	Het
Vdac3	A	T	8: 23,070,515 (GRCm39)	I132K	possibly damaging	Het
Vmn2r95	T	G	17: 18,672,530 (GRCm39)	C756G	probably damaging	Het
Zc3h15	A	G	2: 83,494,334 (GRCm39)	T421A	unknown	Het
Zc3hc1	T	C	6: 30,374,837 (GRCm39)	T235A	probably benign	Het
Zcchc14	A	G	8: 122,335,990 (GRCm39)		probably benign	Het
Zfp318	T	A	17: 46,722,366 (GRCm39)	N1456K	possibly damaging	Het
Zfp606	A	G	7: 12,214,858 (GRCm39)		probably benign	Het
Zfp811	T	A	17: 33,016,399 (GRCm39)	H546L	probably damaging	Het
Zfp94	A	T	7: 24,008,541 (GRCm39)	Y33N	probably damaging	Het
Zfyve9	G	T	4: 108,539,492 (GRCm39)		probably benign	Het

Other mutations in Asap1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00428:Asap1	APN	15	63,991,803 (GRCm39)	splice site	probably benign
IGL00473:Asap1	APN	15	64,045,064 (GRCm39)	splice site	probably benign
IGL00519:Asap1	APN	15	63,982,791 (GRCm39)	missense	probably damaging	1.00
IGL01304:Asap1	APN	15	64,184,298 (GRCm39)	missense	probably damaging	1.00
IGL01510:Asap1	APN	15	64,030,777 (GRCm39)	missense	probably damaging	1.00
IGL02208:Asap1	APN	15	63,993,882 (GRCm39)	missense	probably damaging	1.00
IGL02338:Asap1	APN	15	63,995,519 (GRCm39)	critical splice donor site	probably null
IGL02429:Asap1	APN	15	64,039,589 (GRCm39)	missense	probably damaging	1.00
IGL02565:Asap1	APN	15	64,001,014 (GRCm39)	splice site	probably benign
IGL02644:Asap1	APN	15	63,982,911 (GRCm39)	missense	probably damaging	1.00
IGL02684:Asap1	APN	15	63,966,018 (GRCm39)	missense	probably benign
IGL02707:Asap1	APN	15	64,001,123 (GRCm39)	missense	probably damaging	1.00
IGL03052:Asap1	APN	15	64,025,683 (GRCm39)	splice site	probably benign
IGL03153:Asap1	APN	15	64,032,123 (GRCm39)	missense	probably damaging	1.00
A4554:Asap1	UTSW	15	63,996,560 (GRCm39)	splice site	probably benign
PIT4378001:Asap1	UTSW	15	64,007,697 (GRCm39)	missense	probably damaging	0.99
R0081:Asap1	UTSW	15	63,971,413 (GRCm39)	missense	probably damaging	1.00
R0555:Asap1	UTSW	15	63,966,213 (GRCm39)	missense	probably damaging	1.00
R1414:Asap1	UTSW	15	64,030,733 (GRCm39)	missense	possibly damaging	0.92
R1437:Asap1	UTSW	15	63,991,956 (GRCm39)	missense	probably damaging	0.96
R1474:Asap1	UTSW	15	63,991,869 (GRCm39)	missense	probably benign	0.01
R1489:Asap1	UTSW	15	64,044,579 (GRCm39)	missense	probably damaging	1.00
R1553:Asap1	UTSW	15	64,024,701 (GRCm39)	missense	probably benign	0.31
R1603:Asap1	UTSW	15	64,001,106 (GRCm39)	missense	probably damaging	1.00
R1636:Asap1	UTSW	15	63,995,761 (GRCm39)	missense	probably damaging	1.00
R1645:Asap1	UTSW	15	63,961,324 (GRCm39)	missense	probably damaging	0.99
R2136:Asap1	UTSW	15	63,982,808 (GRCm39)	missense	probably damaging	1.00
R2351:Asap1	UTSW	15	64,007,653 (GRCm39)	critical splice donor site	probably null
R4436:Asap1	UTSW	15	64,221,692 (GRCm39)	missense	probably benign	0.03
R4618:Asap1	UTSW	15	64,024,744 (GRCm39)	missense	probably damaging	1.00
R4868:Asap1	UTSW	15	63,966,030 (GRCm39)	missense	probably benign
R5077:Asap1	UTSW	15	63,999,272 (GRCm39)	missense	probably damaging	1.00
R5333:Asap1	UTSW	15	63,999,263 (GRCm39)	missense	possibly damaging	0.79
R5391:Asap1	UTSW	15	63,965,901 (GRCm39)	missense	possibly damaging	0.57
R5493:Asap1	UTSW	15	64,002,000 (GRCm39)	missense	possibly damaging	0.85
R5665:Asap1	UTSW	15	64,184,302 (GRCm39)	missense	probably damaging	1.00
R5756:Asap1	UTSW	15	64,039,556 (GRCm39)	missense	probably damaging	1.00
R5790:Asap1	UTSW	15	63,966,114 (GRCm39)	missense	probably damaging	1.00
R6139:Asap1	UTSW	15	64,038,388 (GRCm39)	missense	possibly damaging	0.87
R6194:Asap1	UTSW	15	64,001,058 (GRCm39)	missense	probably damaging	1.00
R6361:Asap1	UTSW	15	64,221,672 (GRCm39)	splice site	probably null
R6751:Asap1	UTSW	15	63,966,261 (GRCm39)	missense	possibly damaging	0.86
R7143:Asap1	UTSW	15	64,063,377 (GRCm39)	missense	probably damaging	1.00
R7218:Asap1	UTSW	15	64,002,099 (GRCm39)	missense	probably damaging	1.00
R7225:Asap1	UTSW	15	64,002,099 (GRCm39)	missense	probably damaging	1.00
R7305:Asap1	UTSW	15	64,002,099 (GRCm39)	missense	probably damaging	1.00
R7310:Asap1	UTSW	15	63,971,379 (GRCm39)	critical splice donor site	probably null
R7439:Asap1	UTSW	15	64,002,105 (GRCm39)	missense	probably damaging	1.00
R7441:Asap1	UTSW	15	64,002,105 (GRCm39)	missense	probably damaging	1.00
R7488:Asap1	UTSW	15	63,991,974 (GRCm39)	missense	probably benign	0.29
R7597:Asap1	UTSW	15	64,184,304 (GRCm39)	missense	probably benign	0.37
R7708:Asap1	UTSW	15	64,024,721 (GRCm39)	missense	probably damaging	1.00
R7871:Asap1	UTSW	15	63,963,925 (GRCm39)	missense	probably damaging	1.00
R7990:Asap1	UTSW	15	64,044,586 (GRCm39)	splice site	probably null
R8163:Asap1	UTSW	15	63,963,899 (GRCm39)	missense	probably damaging	1.00
R8171:Asap1	UTSW	15	63,982,815 (GRCm39)	missense	probably damaging	1.00
R8416:Asap1	UTSW	15	64,002,072 (GRCm39)	missense	possibly damaging	0.83
R8778:Asap1	UTSW	15	63,999,258 (GRCm39)	missense	probably benign	0.02
R9462:Asap1	UTSW	15	64,038,328 (GRCm39)	missense	probably damaging	0.98

Predicted Primers

PCR Primer
(F):5'- TGTTCTCAGAGAGCTTAGGGTC -3'
(R):5'- AAGTGAATTGTTGCACTGCTG -3'

Sequencing Primer
(F):5'- AGAGCTTAGGGTCTCTAAATGC -3'
(R):5'- CTCTCCTTTCTGAGATGTTG -3'

Posted On

2014-06-23