Mutagenetix > Incidental Mutation

Incidental Mutation 'R4795:Atp13a4'

368984

Institutional Source

Beutler Lab

Gene Symbol

Atp13a4

Ensembl Gene

ENSMUSG00000038094

Gene Name

ATPase type 13A4

Synonyms

9330174J19Rik, 4631413J11Rik

MMRRC Submission

041996-MU

Accession Numbers

Genbank: NM_001164612, NM_172613, NM_001164613

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R4795 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

29395853-29544864 bp(-) (GRCm38)

Type of Mutation

critical splice donor site (2 bp from exon)

DNA Base Change (assembly)

A to G at 29490008 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000138479 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000039090] [ENSMUST00000039090] [ENSMUST00000039090] [ENSMUST00000039090] [ENSMUST00000057018] [ENSMUST00000057018] [ENSMUST00000182013] [ENSMUST00000182013] [ENSMUST00000182627] [ENSMUST00000182627] [ENSMUST00000182627] [ENSMUST00000182627]

AlphaFold

no structure available at present

Predicted Effect

probably null
Transcript: ENSMUST00000039090

SMART Domains

Protein: ENSMUSP00000048753
Gene: ENSMUSG00000038094

Domain	Start	End	E-Value	Type
Pfam:P5-ATPase	17	143	8.4e-31	PFAM
Cation_ATPase_N	147	223	1.09e-1	SMART
Pfam:E1-E2_ATPase	229	476	1.7e-36	PFAM
Pfam:Hydrolase	481	769	3.9e-11	PFAM
Pfam:HAD	484	787	4.1e-14	PFAM
Pfam:Hydrolase_like2	574	637	1.2e-9	PFAM
transmembrane domain	824	846	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000039090

SMART Domains

Protein: ENSMUSP00000048753
Gene: ENSMUSG00000038094

Domain	Start	End	E-Value	Type
Pfam:P5-ATPase	17	143	8.4e-31	PFAM
Cation_ATPase_N	147	223	1.09e-1	SMART
Pfam:E1-E2_ATPase	229	476	1.7e-36	PFAM
Pfam:Hydrolase	481	769	3.9e-11	PFAM
Pfam:HAD	484	787	4.1e-14	PFAM
Pfam:Hydrolase_like2	574	637	1.2e-9	PFAM
transmembrane domain	824	846	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000039090

SMART Domains

Protein: ENSMUSP00000048753
Gene: ENSMUSG00000038094

Domain	Start	End	E-Value	Type
Pfam:P5-ATPase	17	143	8.4e-31	PFAM
Cation_ATPase_N	147	223	1.09e-1	SMART
Pfam:E1-E2_ATPase	229	476	1.7e-36	PFAM
Pfam:Hydrolase	481	769	3.9e-11	PFAM
Pfam:HAD	484	787	4.1e-14	PFAM
Pfam:Hydrolase_like2	574	637	1.2e-9	PFAM
transmembrane domain	824	846	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000039090

SMART Domains

Protein: ENSMUSP00000048753
Gene: ENSMUSG00000038094

Domain	Start	End	E-Value	Type
Pfam:P5-ATPase	17	143	8.4e-31	PFAM
Cation_ATPase_N	147	223	1.09e-1	SMART
Pfam:E1-E2_ATPase	229	476	1.7e-36	PFAM
Pfam:Hydrolase	481	769	3.9e-11	PFAM
Pfam:HAD	484	787	4.1e-14	PFAM
Pfam:Hydrolase_like2	574	637	1.2e-9	PFAM
transmembrane domain	824	846	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000057018

SMART Domains

Protein: ENSMUSP00000060987
Gene: ENSMUSG00000038094

Domain	Start	End	E-Value	Type
Pfam:P5-ATPase	17	142	9.6e-34	PFAM
Cation_ATPase_N	147	223	1.09e-1	SMART
Pfam:E1-E2_ATPase	228	476	1.6e-34	PFAM
Pfam:Hydrolase	481	767	1.1e-10	PFAM
Pfam:HAD	484	858	3.3e-23	PFAM
Pfam:Cation_ATPase	573	637	4.9e-8	PFAM
transmembrane domain	902	924	N/A	INTRINSIC
transmembrane domain	934	951	N/A	INTRINSIC
transmembrane domain	972	994	N/A	INTRINSIC
low complexity region	1014	1023	N/A	INTRINSIC
transmembrane domain	1040	1057	N/A	INTRINSIC
transmembrane domain	1070	1092	N/A	INTRINSIC
transmembrane domain	1107	1126	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000057018

SMART Domains

Protein: ENSMUSP00000060987
Gene: ENSMUSG00000038094

Domain	Start	End	E-Value	Type
Pfam:P5-ATPase	17	142	9.6e-34	PFAM
Cation_ATPase_N	147	223	1.09e-1	SMART
Pfam:E1-E2_ATPase	228	476	1.6e-34	PFAM
Pfam:Hydrolase	481	767	1.1e-10	PFAM
Pfam:HAD	484	858	3.3e-23	PFAM
Pfam:Cation_ATPase	573	637	4.9e-8	PFAM
transmembrane domain	902	924	N/A	INTRINSIC
transmembrane domain	934	951	N/A	INTRINSIC
transmembrane domain	972	994	N/A	INTRINSIC
low complexity region	1014	1023	N/A	INTRINSIC
transmembrane domain	1040	1057	N/A	INTRINSIC
transmembrane domain	1070	1092	N/A	INTRINSIC
transmembrane domain	1107	1126	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000182013

SMART Domains

Protein: ENSMUSP00000138583
Gene: ENSMUSG00000038094

Domain	Start	End	E-Value	Type
Pfam:P5-ATPase	17	84	4.2e-26	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000182013

SMART Domains

Protein: ENSMUSP00000138583
Gene: ENSMUSG00000038094

Domain	Start	End	E-Value	Type
Pfam:P5-ATPase	17	84	4.2e-26	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000182627

SMART Domains

Protein: ENSMUSP00000138479
Gene: ENSMUSG00000038094

Domain	Start	End	E-Value	Type
Pfam:P5-ATPase	17	143	2.1e-29	PFAM
Cation_ATPase_N	147	223	1.09e-1	SMART
Pfam:E1-E2_ATPase	229	476	3.9e-35	PFAM
Pfam:Hydrolase	481	861	4.2e-16	PFAM
Pfam:HAD	484	858	1.9e-23	PFAM
Pfam:Hydrolase_like2	574	637	2.2e-8	PFAM
transmembrane domain	902	924	N/A	INTRINSIC
transmembrane domain	934	951	N/A	INTRINSIC
transmembrane domain	972	994	N/A	INTRINSIC
low complexity region	1014	1023	N/A	INTRINSIC
transmembrane domain	1040	1057	N/A	INTRINSIC
transmembrane domain	1070	1092	N/A	INTRINSIC
transmembrane domain	1107	1126	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000182627

SMART Domains

Protein: ENSMUSP00000138479
Gene: ENSMUSG00000038094

Domain	Start	End	E-Value	Type
Pfam:P5-ATPase	17	143	2.1e-29	PFAM
Cation_ATPase_N	147	223	1.09e-1	SMART
Pfam:E1-E2_ATPase	229	476	3.9e-35	PFAM
Pfam:Hydrolase	481	861	4.2e-16	PFAM
Pfam:HAD	484	858	1.9e-23	PFAM
Pfam:Hydrolase_like2	574	637	2.2e-8	PFAM
transmembrane domain	902	924	N/A	INTRINSIC
transmembrane domain	934	951	N/A	INTRINSIC
transmembrane domain	972	994	N/A	INTRINSIC
low complexity region	1014	1023	N/A	INTRINSIC
transmembrane domain	1040	1057	N/A	INTRINSIC
transmembrane domain	1070	1092	N/A	INTRINSIC
transmembrane domain	1107	1126	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000182627

SMART Domains

Protein: ENSMUSP00000138479
Gene: ENSMUSG00000038094

Domain	Start	End	E-Value	Type
Pfam:P5-ATPase	17	143	2.1e-29	PFAM
Cation_ATPase_N	147	223	1.09e-1	SMART
Pfam:E1-E2_ATPase	229	476	3.9e-35	PFAM
Pfam:Hydrolase	481	861	4.2e-16	PFAM
Pfam:HAD	484	858	1.9e-23	PFAM
Pfam:Hydrolase_like2	574	637	2.2e-8	PFAM
transmembrane domain	902	924	N/A	INTRINSIC
transmembrane domain	934	951	N/A	INTRINSIC
transmembrane domain	972	994	N/A	INTRINSIC
low complexity region	1014	1023	N/A	INTRINSIC
transmembrane domain	1040	1057	N/A	INTRINSIC
transmembrane domain	1070	1092	N/A	INTRINSIC
transmembrane domain	1107	1126	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000182627

SMART Domains

Protein: ENSMUSP00000138479
Gene: ENSMUSG00000038094

Domain	Start	End	E-Value	Type
Pfam:P5-ATPase	17	143	2.1e-29	PFAM
Cation_ATPase_N	147	223	1.09e-1	SMART
Pfam:E1-E2_ATPase	229	476	3.9e-35	PFAM
Pfam:Hydrolase	481	861	4.2e-16	PFAM
Pfam:HAD	484	858	1.9e-23	PFAM
Pfam:Hydrolase_like2	574	637	2.2e-8	PFAM
transmembrane domain	902	924	N/A	INTRINSIC
transmembrane domain	934	951	N/A	INTRINSIC
transmembrane domain	972	994	N/A	INTRINSIC
low complexity region	1014	1023	N/A	INTRINSIC
transmembrane domain	1040	1057	N/A	INTRINSIC
transmembrane domain	1070	1092	N/A	INTRINSIC
transmembrane domain	1107	1126	N/A	INTRINSIC

Meta Mutation Damage Score

0.9492

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.7%
20x: 93.7%

Validation Efficiency

98% (123/125)

Allele List at MGI

Other mutations in this stock

Total: 105 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca4	T	G	3: 122,176,123 (GRCm38)	L2259R	probably damaging	Het
Acd	A	G	8: 105,701,015 (GRCm38)	S2P	possibly damaging	Het
Acsf3	A	G	8: 122,780,157 (GRCm38)	Y63C	possibly damaging	Het
Adam21	T	C	12: 81,560,974 (GRCm38)	I5V	probably benign	Het
Adamts6	C	A	13: 104,444,128 (GRCm38)	S783*	probably null	Het
Adamtsl1	T	C	4: 86,243,769 (GRCm38)		probably null	Het
Adck2	T	A	6: 39,576,393 (GRCm38)	S313T	probably benign	Het
Adgb	A	G	10: 10,357,872 (GRCm38)	I1285T	probably benign	Het
Angptl1	T	A	1: 156,860,583 (GRCm38)	M485K	possibly damaging	Het
Ank3	G	A	10: 69,858,265 (GRCm38)	V289I	probably benign	Het
Atp1a1	A	G	3: 101,583,775 (GRCm38)	L648P	probably benign	Het
Atp2a3	A	G	11: 72,973,029 (GRCm38)	I194V	probably benign	Het
Bglap	A	C	3: 88,384,405 (GRCm38)	I4S	unknown	Het
Cacna1b	T	A	2: 24,637,487 (GRCm38)	T1621S	possibly damaging	Het
Ccdc112	T	A	18: 46,287,672 (GRCm38)	Q337L	probably benign	Het
Cd34	T	G	1: 194,951,011 (GRCm38)	S194A	probably damaging	Het
Cdh20	A	G	1: 104,941,264 (GRCm38)	D160G	probably damaging	Het
Clock	T	C	5: 76,265,916 (GRCm38)	K44R	probably damaging	Het
Commd9	A	G	2: 101,898,896 (GRCm38)	N116D	probably benign	Het
Dab2	C	A	15: 6,429,611 (GRCm38)	P335T	probably benign	Het
Epb41l3	T	A	17: 69,248,719 (GRCm38)		probably null	Het
Epha2	A	G	4: 141,322,416 (GRCm38)		probably null	Het
Fam78b	T	C	1: 167,078,647 (GRCm38)	V125A	probably benign	Het
Fars2	A	T	13: 36,537,426 (GRCm38)	E448V	probably damaging	Het
Fkbpl	G	A	17: 34,645,329 (GRCm38)	A24T	probably benign	Het
Glyr1	A	C	16: 5,047,758 (GRCm38)	V44G	probably benign	Het
Gm1527	A	G	3: 28,920,663 (GRCm38)	I542V	possibly damaging	Het
Gm18856	C	A	13: 13,965,208 (GRCm38)		probably benign	Het
Gm44501	A	G	17: 40,578,714 (GRCm38)	K40E	probably benign	Het
Gm6583	A	G	5: 112,355,299 (GRCm38)	S180P	possibly damaging	Het
Hdhd5	T	C	6: 120,523,446 (GRCm38)	H97R	probably benign	Het
Hmcn1	A	G	1: 150,753,611 (GRCm38)	V965A	probably benign	Het
Hsf5	A	G	11: 87,635,620 (GRCm38)	M373V	probably benign	Het
Igbp1b	C	T	6: 138,657,805 (GRCm38)	E214K	probably benign	Het
Iigp1	T	A	18: 60,389,892 (GRCm38)	F27L	probably benign	Het
Isl1	T	C	13: 116,305,430 (GRCm38)	N89S	probably benign	Het
Itga1	C	A	13: 115,035,385 (GRCm38)	W61C	probably damaging	Het
Itga5	T	C	15: 103,347,760 (GRCm38)	R922G	probably benign	Het
Kbtbd3	G	A	9: 4,331,073 (GRCm38)	W482*	probably null	Het
Kcnq1	A	G	7: 143,182,757 (GRCm38)	T168A	probably benign	Het
Lrch3	A	G	16: 33,005,704 (GRCm38)	N631S	probably damaging	Het
Lrrk1	T	A	7: 66,262,665 (GRCm38)	I1716F	possibly damaging	Het
Ly75	T	C	2: 60,349,940 (GRCm38)	E631G	probably benign	Het
Map4	T	C	9: 110,035,263 (GRCm38)	S519P	probably benign	Het
Mkl1	C	T	15: 81,017,033 (GRCm38)	S419N	probably damaging	Het
Mroh2a	A	G	1: 88,258,664 (GRCm38)	S64G	probably benign	Het
Muc5b	A	G	7: 141,849,567 (GRCm38)	E755G	unknown	Het
Ncaph2	T	G	15: 89,370,807 (GRCm38)	V478G	probably damaging	Het
Ncbp1	A	G	4: 46,152,967 (GRCm38)	R247G	possibly damaging	Het
Necab1	G	T	4: 15,111,208 (GRCm38)	D73E	possibly damaging	Het
Nedd9	T	C	13: 41,317,900 (GRCm38)	K208E	probably benign	Het
Nfyb	A	T	10: 82,752,368 (GRCm38)		probably benign	Het
Nol4	T	C	18: 22,921,887 (GRCm38)	Q162R	probably damaging	Het
Nwd2	G	A	5: 63,805,433 (GRCm38)	D787N	probably benign	Het
Olfr2	C	T	7: 107,001,335 (GRCm38)	G175D	probably damaging	Het
Olfr205	C	T	16: 59,328,850 (GRCm38)	V220I	probably benign	Het
Olfr49	A	G	14: 54,282,547 (GRCm38)	M116T	probably damaging	Het
Olfr535	A	G	7: 140,493,007 (GRCm38)	D123G	probably damaging	Het
Olfr713	A	T	7: 107,036,914 (GRCm38)	Y253F	probably benign	Het
Olfr740	A	C	14: 50,453,417 (GRCm38)	M122L	probably damaging	Het
Olfr908	T	A	9: 38,516,503 (GRCm38)	M157K	probably damaging	Het
Orai3	T	C	7: 127,773,888 (GRCm38)	V187A	probably benign	Het
Parn	T	C	16: 13,606,202 (GRCm38)	T444A	probably benign	Het
Pcdh11x	A	C	X: 120,400,240 (GRCm38)	N460T	probably damaging	Het
Pcnt	C	T	10: 76,370,024 (GRCm38)	R2516H	probably benign	Het
Pde4d	T	A	13: 109,938,171 (GRCm38)		probably benign	Het
Pdgfra	A	G	5: 75,189,311 (GRCm38)	N952S	probably benign	Het
Pgm1	A	G	5: 64,103,874 (GRCm38)	Y237C	probably damaging	Het
Plcb2	A	G	2: 118,711,124 (GRCm38)	V975A	probably benign	Het
Polk	T	C	13: 96,489,256 (GRCm38)	T347A	probably benign	Het
Ppp6r1	C	T	7: 4,641,054 (GRCm38)	V430M	possibly damaging	Het
Ptges2	C	A	2: 32,396,322 (GRCm38)	C16*	probably null	Het
Relb	A	T	7: 19,619,839 (GRCm38)	I38N	probably damaging	Het
Runx1t1	T	A	4: 13,837,767 (GRCm38)	N51K	probably damaging	Het
Samsn1	A	G	16: 75,883,845 (GRCm38)		probably benign	Het
Scrn1	A	G	6: 54,520,769 (GRCm38)	V279A	possibly damaging	Het
Sec31b	A	G	19: 44,531,746 (GRCm38)	S200P	probably benign	Het
Selp	A	G	1: 164,144,906 (GRCm38)	T705A	probably benign	Het
Slc2a1	G	A	4: 119,132,445 (GRCm38)	R61Q	probably damaging	Het
Slit3	G	A	11: 35,651,820 (GRCm38)		probably null	Het
Smo	T	A	6: 29,755,574 (GRCm38)	V415E	probably damaging	Het
Spag8	C	A	4: 43,652,035 (GRCm38)	V350L	possibly damaging	Het
Tbck	T	G	3: 132,707,798 (GRCm38)	L132R	possibly damaging	Het
Thnsl1	T	A	2: 21,212,045 (GRCm38)	C203*	probably null	Het
Tm9sf2	T	A	14: 122,149,840 (GRCm38)		probably null	Het
Tmem131	A	G	1: 36,841,676 (GRCm38)	V171A	probably damaging	Het
Tmem209	T	C	6: 30,501,955 (GRCm38)	T83A	probably benign	Het
Tmem63a	T	C	1: 180,954,851 (GRCm38)	Y138H	probably damaging	Het
Trim80	A	G	11: 115,447,943 (GRCm38)	Y533C	probably damaging	Het
Trpv2	A	G	11: 62,581,180 (GRCm38)	D66G	possibly damaging	Het
Trrap	T	A	5: 144,832,488 (GRCm38)	I2620N	probably benign	Het
Ttyh3	A	T	5: 140,634,786 (GRCm38)	I232N	probably damaging	Het
Ube2dnl1	G	A	X: 114,905,785 (GRCm38)	C119Y	possibly damaging	Het
Unc13c	T	A	9: 73,932,187 (GRCm38)	S461C	probably damaging	Het
Unc80	T	G	1: 66,527,941 (GRCm38)	I902S	probably damaging	Het
Usp42	C	A	5: 143,723,937 (GRCm38)	G170W	probably damaging	Het
Vldlr	T	C	19: 27,238,852 (GRCm38)		probably null	Het
Ywhab	A	G	2: 164,015,345 (GRCm38)	Y180C	probably damaging	Het
Zan	A	T	5: 137,380,850 (GRCm38)	C5329*	probably null	Het
Zbtb40	C	T	4: 136,998,642 (GRCm38)	M535I	probably benign	Het
Zdhhc1	CGGGGG	CGGGGGG	8: 105,483,744 (GRCm38)		probably null	Het
Zfp318	A	G	17: 46,412,062 (GRCm38)	T1664A	probably benign	Het
Zfp7	T	A	15: 76,891,346 (GRCm38)	C529*	probably null	Het
Zfp768	T	C	7: 127,343,375 (GRCm38)	Q527R	possibly damaging	Het
Zfp975	T	A	7: 42,665,146 (GRCm38)		probably null	Het

Other mutations in Atp13a4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00563:Atp13a4	APN	16	29,403,778 (GRCm38)	splice site	probably benign
IGL01577:Atp13a4	APN	16	29,441,284 (GRCm38)	missense	possibly damaging	0.77
IGL01834:Atp13a4	APN	16	29,415,777 (GRCm38)	splice site	probably benign
IGL02165:Atp13a4	APN	16	29,434,010 (GRCm38)	missense	probably damaging	1.00
IGL02194:Atp13a4	APN	16	29,456,629 (GRCm38)	missense	probably damaging	1.00
IGL02322:Atp13a4	APN	16	29,440,102 (GRCm38)	missense	probably benign	0.00
IGL02553:Atp13a4	APN	16	29,422,703 (GRCm38)	missense	probably benign	0.03
IGL02821:Atp13a4	APN	16	29,441,307 (GRCm38)	missense	probably benign	0.01
IGL03349:Atp13a4	APN	16	29,456,671 (GRCm38)	missense	probably benign	0.01
G5030:Atp13a4	UTSW	16	29,455,488 (GRCm38)	missense	probably damaging	1.00
R0091:Atp13a4	UTSW	16	29,455,395 (GRCm38)	missense	probably damaging	1.00
R0100:Atp13a4	UTSW	16	29,421,724 (GRCm38)	missense	probably damaging	1.00
R0278:Atp13a4	UTSW	16	29,454,834 (GRCm38)	missense	probably damaging	1.00
R1263:Atp13a4	UTSW	16	29,471,953 (GRCm38)	missense	possibly damaging	0.60
R1378:Atp13a4	UTSW	16	29,420,428 (GRCm38)	missense	probably damaging	1.00
R1575:Atp13a4	UTSW	16	29,409,710 (GRCm38)	missense	probably benign	0.01
R1720:Atp13a4	UTSW	16	29,408,928 (GRCm38)	missense	probably damaging	0.99
R1759:Atp13a4	UTSW	16	29,456,611 (GRCm38)	missense	probably damaging	0.99
R1967:Atp13a4	UTSW	16	29,479,854 (GRCm38)	missense	probably damaging	0.99
R2030:Atp13a4	UTSW	16	29,422,684 (GRCm38)	missense	probably damaging	1.00
R2113:Atp13a4	UTSW	16	29,441,284 (GRCm38)	missense	possibly damaging	0.77
R3409:Atp13a4	UTSW	16	29,413,749 (GRCm38)	missense	probably damaging	1.00
R3410:Atp13a4	UTSW	16	29,413,749 (GRCm38)	missense	probably damaging	1.00
R4032:Atp13a4	UTSW	16	29,418,571 (GRCm38)	missense	probably damaging	1.00
R4163:Atp13a4	UTSW	16	29,541,250 (GRCm38)	missense	possibly damaging	0.87
R4652:Atp13a4	UTSW	16	29,452,603 (GRCm38)	missense	probably damaging	1.00
R4772:Atp13a4	UTSW	16	29,420,835 (GRCm38)	intron	probably benign
R4898:Atp13a4	UTSW	16	29,408,961 (GRCm38)	nonsense	probably null
R4996:Atp13a4	UTSW	16	29,472,004 (GRCm38)	missense	probably damaging	1.00
R5112:Atp13a4	UTSW	16	29,409,868 (GRCm38)	missense	possibly damaging	0.87
R5259:Atp13a4	UTSW	16	29,456,610 (GRCm38)	missense	probably damaging	1.00
R5395:Atp13a4	UTSW	16	29,456,604 (GRCm38)	missense	possibly damaging	0.94
R5395:Atp13a4	UTSW	16	29,420,888 (GRCm38)	nonsense	probably null
R5640:Atp13a4	UTSW	16	29,415,831 (GRCm38)	missense	probably damaging	0.98
R5809:Atp13a4	UTSW	16	29,433,987 (GRCm38)	missense	possibly damaging	0.56
R5856:Atp13a4	UTSW	16	29,433,987 (GRCm38)	missense	possibly damaging	0.94
R5912:Atp13a4	UTSW	16	29,456,571 (GRCm38)	missense	probably benign	0.33
R6282:Atp13a4	UTSW	16	29,434,004 (GRCm38)	missense	probably benign	0.00
R6404:Atp13a4	UTSW	16	29,471,901 (GRCm38)	nonsense	probably null
R6497:Atp13a4	UTSW	16	29,479,901 (GRCm38)	missense	probably damaging	1.00
R6577:Atp13a4	UTSW	16	29,479,841 (GRCm38)	missense	probably benign	0.03
R6806:Atp13a4	UTSW	16	29,469,280 (GRCm38)	missense	probably damaging	1.00
R7229:Atp13a4	UTSW	16	29,420,905 (GRCm38)	missense	probably benign	0.05
R7438:Atp13a4	UTSW	16	29,441,196 (GRCm38)	missense
R7493:Atp13a4	UTSW	16	29,471,956 (GRCm38)	missense
R7712:Atp13a4	UTSW	16	29,459,487 (GRCm38)	missense
R7739:Atp13a4	UTSW	16	29,456,601 (GRCm38)	missense
R7897:Atp13a4	UTSW	16	29,396,466 (GRCm38)	missense
R7950:Atp13a4	UTSW	16	29,449,917 (GRCm38)	missense
R8217:Atp13a4	UTSW	16	29,403,801 (GRCm38)	missense
R8227:Atp13a4	UTSW	16	29,403,845 (GRCm38)	missense
R8273:Atp13a4	UTSW	16	29,471,902 (GRCm38)	missense
R8488:Atp13a4	UTSW	16	29,417,836 (GRCm38)	missense	possibly damaging	0.63
R8508:Atp13a4	UTSW	16	29,454,769 (GRCm38)	nonsense	probably null
R8773:Atp13a4	UTSW	16	29,441,580 (GRCm38)	missense
R8921:Atp13a4	UTSW	16	29,454,774 (GRCm38)	missense
R8940:Atp13a4	UTSW	16	29,454,690 (GRCm38)	critical splice donor site	probably null
R9056:Atp13a4	UTSW	16	29,471,888 (GRCm38)	critical splice donor site	probably null
R9272:Atp13a4	UTSW	16	29,449,979 (GRCm38)	missense
R9292:Atp13a4	UTSW	16	29,422,682 (GRCm38)	missense
R9415:Atp13a4	UTSW	16	29,409,003 (GRCm38)	missense
R9453:Atp13a4	UTSW	16	29,420,841 (GRCm38)	missense	unknown
R9497:Atp13a4	UTSW	16	29,469,312 (GRCm38)	critical splice acceptor site	probably null
R9541:Atp13a4	UTSW	16	29,422,726 (GRCm38)	missense
R9614:Atp13a4	UTSW	16	29,441,580 (GRCm38)	missense
R9622:Atp13a4	UTSW	16	29,420,459 (GRCm38)	missense
R9727:Atp13a4	UTSW	16	29,409,771 (GRCm38)	missense
Z1176:Atp13a4	UTSW	16	29,422,587 (GRCm38)	missense	probably null

Predicted Primers

PCR Primer
(F):5'- ACACGTTCACATTCGCTCTAAC -3'
(R):5'- TTGCAGGAAATATTTGGCTATCGG -3'

Sequencing Primer
(F):5'- TTCGCTCTAACACTTGCAAAAGTAGC -3'
(R):5'- ATATTTGGCTATCGGACTCAAGGC -3'

Posted On

2016-02-04