Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL00419:Atp1a4'

7326

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Atp1a4

Ensembl Gene

ENSMUSG00000007107

Gene Name

ATPase, Na+/K+ transporting, alpha 4 polypeptide

Synonyms

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL00419

Quality Score

Status

Chromosome

Chromosomal Location

172051080-172085981 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 172067373 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Lysine at position 586 (N586K)

Ref Sequence

ENSEMBL: ENSMUSP00000106874 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000111243]

AlphaFold

Q9WV27

Predicted Effect

probably damaging
Transcript: ENSMUST00000111243
AA Change: N586K

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

SMART Domains

Protein: ENSMUSP00000106874
Gene: ENSMUSG00000007107
AA Change: N586K

Domain	Start	End	E-Value	Type
low complexity region	33	50	N/A	INTRINSIC
Cation_ATPase_N	51	125	1.22e-14	SMART
Pfam:E1-E2_ATPase	144	375	2.6e-59	PFAM
Pfam:Hydrolase	380	738	8.1e-19	PFAM
Pfam:HAD	383	735	1.6e-17	PFAM
Pfam:Cation_ATPase	437	531	9.2e-25	PFAM
Pfam:Cation_ATPase_C	808	1017	1.2e-47	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000191616

Coding Region Coverage

Validation Efficiency

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 family of P-type cation transport ATPases, and to the subfamily of Na+/K+ -ATPases. Na+/K+ -ATPase is an integral membrane protein responsible for establishing and maintaining the electrochemical gradients of Na and K ions across the plasma membrane. These gradients are essential for osmoregulation, for sodium-coupled transport of a variety of organic and inorganic molecules, and for electrical excitability of nerve and muscle. This enzyme is composed of two subunits, a large catalytic subunit (alpha) and a smaller glycoprotein subunit (beta). The catalytic subunit of Na+/K+ -ATPase is encoded by multiple genes. This gene encodes an alpha 4 subunit. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
PHENOTYPE: Male mice homozygous for a knock-out allele exhibit infertility associated with asthenozoospermia and teratozoospermia. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 25 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
AU040320	T	C	4: 126,686,027 (GRCm39)	M201T	probably benign	Het
Bcap29	A	T	12: 31,680,871 (GRCm39)	F38L	probably benign	Het
Bdkrb2	A	G	12: 105,554,562 (GRCm39)		probably benign	Het
Ceacam5	G	T	7: 17,493,481 (GRCm39)	E835*	probably null	Het
Cenpp	T	C	13: 49,801,132 (GRCm39)		probably null	Het
Clca3a2	A	G	3: 144,804,574 (GRCm39)	V51A	probably damaging	Het
Dmxl2	T	C	9: 54,313,951 (GRCm39)	N1660D	probably damaging	Het
Exosc9	T	C	3: 36,607,288 (GRCm39)		probably benign	Het
Ezh1	T	C	11: 101,085,332 (GRCm39)		probably null	Het
Fbxo24	G	A	5: 137,622,563 (GRCm39)	R68C	probably damaging	Het
Gbp9	T	C	5: 105,241,943 (GRCm39)	I205V	probably benign	Het
Gpc5	A	G	14: 115,607,436 (GRCm39)	Y346C	probably damaging	Het
Hectd1	A	G	12: 51,810,818 (GRCm39)	Y1706H	probably damaging	Het
Igsf9b	A	G	9: 27,230,951 (GRCm39)	Y318C	probably damaging	Het
Map1a	A	T	2: 121,129,508 (GRCm39)	Q182L	probably damaging	Het
Rab11fip3	A	T	17: 26,210,783 (GRCm39)		probably benign	Het
Rbm20	G	A	19: 53,831,695 (GRCm39)	R643Q	probably damaging	Het
Ros1	A	T	10: 51,967,150 (GRCm39)	C1707S	probably damaging	Het
Rpgrip1l	G	T	8: 91,990,202 (GRCm39)	R747S	possibly damaging	Het
Rsph10b	T	C	5: 143,873,905 (GRCm39)	*166R	probably null	Het
Sft2d1	G	A	17: 8,539,437 (GRCm39)	C80Y	possibly damaging	Het
Zdhhc14	T	C	17: 5,802,959 (GRCm39)		probably benign	Het
Zfp300	T	A	X: 20,948,531 (GRCm39)	Y411F	probably damaging	Het
Zfp92	T	C	X: 72,463,764 (GRCm39)		probably benign	Het
Zhx1	A	G	15: 57,916,711 (GRCm39)	F512L	probably damaging	Het

Other mutations in Atp1a4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00924:Atp1a4	APN	1	172,074,339 (GRCm39)	missense	probably damaging	1.00
IGL01288:Atp1a4	APN	1	172,085,474 (GRCm39)	missense	possibly damaging	0.77
IGL01665:Atp1a4	APN	1	172,074,291 (GRCm39)	missense	probably benign
IGL02156:Atp1a4	APN	1	172,085,529 (GRCm39)	missense	probably benign
IGL02170:Atp1a4	APN	1	172,062,103 (GRCm39)	missense	possibly damaging	0.94
IGL02228:Atp1a4	APN	1	172,082,452 (GRCm39)	missense	possibly damaging	0.69
IGL02505:Atp1a4	APN	1	172,062,642 (GRCm39)	missense	probably damaging	1.00
IGL02653:Atp1a4	APN	1	172,078,973 (GRCm39)	missense	possibly damaging	0.81
IGL02792:Atp1a4	APN	1	172,054,866 (GRCm39)	critical splice donor site	probably null
IGL02794:Atp1a4	APN	1	172,071,653 (GRCm39)	missense	probably benign	0.13
IGL03102:Atp1a4	APN	1	172,058,718 (GRCm39)	missense	probably damaging	1.00
R0046:Atp1a4	UTSW	1	172,067,664 (GRCm39)	missense	probably benign	0.09
R0046:Atp1a4	UTSW	1	172,067,664 (GRCm39)	missense	probably benign	0.09
R0276:Atp1a4	UTSW	1	172,085,468 (GRCm39)	missense	probably damaging	1.00
R0309:Atp1a4	UTSW	1	172,062,554 (GRCm39)	missense	probably damaging	1.00
R0525:Atp1a4	UTSW	1	172,067,255 (GRCm39)	splice site	probably benign
R0615:Atp1a4	UTSW	1	172,059,627 (GRCm39)	splice site	probably benign
R0730:Atp1a4	UTSW	1	172,067,774 (GRCm39)	splice site	probably benign
R1412:Atp1a4	UTSW	1	172,059,576 (GRCm39)	missense	probably damaging	0.97
R1652:Atp1a4	UTSW	1	172,082,470 (GRCm39)	missense	probably damaging	1.00
R1898:Atp1a4	UTSW	1	172,062,615 (GRCm39)	missense	probably damaging	0.99
R1968:Atp1a4	UTSW	1	172,067,731 (GRCm39)	missense	probably benign
R2291:Atp1a4	UTSW	1	172,072,473 (GRCm39)	missense	probably damaging	1.00
R2897:Atp1a4	UTSW	1	172,074,257 (GRCm39)	missense	probably damaging	1.00
R2908:Atp1a4	UTSW	1	172,062,044 (GRCm39)	missense	probably benign
R3119:Atp1a4	UTSW	1	172,067,393 (GRCm39)	missense	probably damaging	0.99
R3731:Atp1a4	UTSW	1	172,061,528 (GRCm39)	missense	probably damaging	1.00
R4447:Atp1a4	UTSW	1	172,061,998 (GRCm39)	missense	probably damaging	0.99
R4602:Atp1a4	UTSW	1	172,067,332 (GRCm39)	missense	probably damaging	1.00
R4670:Atp1a4	UTSW	1	172,062,567 (GRCm39)	missense	probably benign	0.07
R4674:Atp1a4	UTSW	1	172,085,223 (GRCm39)	missense	possibly damaging	0.81
R4675:Atp1a4	UTSW	1	172,085,223 (GRCm39)	missense	possibly damaging	0.81
R4785:Atp1a4	UTSW	1	172,081,677 (GRCm39)	nonsense	probably null
R4958:Atp1a4	UTSW	1	172,058,718 (GRCm39)	missense	probably damaging	1.00
R5015:Atp1a4	UTSW	1	172,081,649 (GRCm39)	missense	probably damaging	1.00
R5149:Atp1a4	UTSW	1	172,059,572 (GRCm39)	missense	probably damaging	1.00
R5234:Atp1a4	UTSW	1	172,054,737 (GRCm39)	missense	possibly damaging	0.73
R5501:Atp1a4	UTSW	1	172,074,399 (GRCm39)	missense	probably damaging	1.00
R5682:Atp1a4	UTSW	1	172,081,730 (GRCm39)	missense	probably damaging	0.99
R5872:Atp1a4	UTSW	1	172,071,975 (GRCm39)	missense	probably damaging	1.00
R5933:Atp1a4	UTSW	1	172,059,841 (GRCm39)	missense	possibly damaging	0.91
R6722:Atp1a4	UTSW	1	172,085,617 (GRCm39)	unclassified	probably benign
R7087:Atp1a4	UTSW	1	172,074,269 (GRCm39)	missense	probably damaging	1.00
R7122:Atp1a4	UTSW	1	172,059,503 (GRCm39)	missense	possibly damaging	0.47
R7381:Atp1a4	UTSW	1	172,067,682 (GRCm39)	missense	possibly damaging	0.70
R7431:Atp1a4	UTSW	1	172,078,474 (GRCm39)	missense	probably benign	0.31
R8269:Atp1a4	UTSW	1	172,059,892 (GRCm39)	missense	probably damaging	1.00
R8400:Atp1a4	UTSW	1	172,062,061 (GRCm39)	missense	probably damaging	1.00
R8559:Atp1a4	UTSW	1	172,078,897 (GRCm39)	missense	probably damaging	1.00
R8680:Atp1a4	UTSW	1	172,078,566 (GRCm39)	missense	probably damaging	1.00
R8777:Atp1a4	UTSW	1	172,059,869 (GRCm39)	missense	probably damaging	1.00
R8777-TAIL:Atp1a4	UTSW	1	172,059,869 (GRCm39)	missense	probably damaging	1.00
R8867:Atp1a4	UTSW	1	172,072,491 (GRCm39)	missense	probably damaging	0.99
R8869:Atp1a4	UTSW	1	172,054,690 (GRCm39)	missense	probably benign
R9260:Atp1a4	UTSW	1	172,074,359 (GRCm39)	missense	probably damaging	1.00
R9300:Atp1a4	UTSW	1	172,067,398 (GRCm39)	missense	probably damaging	1.00
R9545:Atp1a4	UTSW	1	172,078,464 (GRCm39)	missense	probably benign	0.35
Z1176:Atp1a4	UTSW	1	172,059,521 (GRCm39)	missense	probably benign	0.44

Posted On

2012-04-20