Mutagenetix > Incidental Mutation

Incidental Mutation 'R9651:Spaca6'

727137

Institutional Source

Beutler Lab

Gene Symbol

Spaca6

Ensembl Gene

ENSMUSG00000080316

Gene Name

sperm acrosome associated 6

Synonyms

B230206P06Rik, 4930546H06Rik, Ncrna00085

MMRRC Submission

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.056) question?

Stock #

R9651 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

18047420-18063271 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 18057829 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glutamic Acid at position 164 (D164E)

Ref Sequence

ENSEMBL: ENSMUSP00000128732 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000139969] [ENSMUST00000150302] [ENSMUST00000172097] [ENSMUST00000226899] [ENSMUST00000228490]

AlphaFold

E9Q8Q8

Predicted Effect

probably benign
Transcript: ENSMUST00000139969
AA Change: D144E

PolyPhen 2 Score 0.136 (Sensitivity: 0.92; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000119658
Gene: ENSMUSG00000080316
AA Change: D144E

Domain	Start	End	E-Value	Type
signal peptide	1	21	N/A	INTRINSIC
Blast:IG	151	186	1e-17	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000150302
AA Change: D64E

PolyPhen 2 Score 0.136 (Sensitivity: 0.92; Specificity: 0.86)

Predicted Effect

probably benign
Transcript: ENSMUST00000154301

SMART Domains

Protein: ENSMUSP00000117377
Gene: ENSMUSG00000080316

Domain	Start	End	E-Value	Type
Blast:IG	27	78	2e-32	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000172097
AA Change: D164E

PolyPhen 2 Score 0.136 (Sensitivity: 0.92; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000128732
Gene: ENSMUSG00000080316
AA Change: D164E

Domain	Start	End	E-Value	Type
transmembrane domain	15	37	N/A	INTRINSIC
IG	171	260	2.08e-1	SMART
transmembrane domain	310	332	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000226899
AA Change: D73E

PolyPhen 2 Score 0.060 (Sensitivity: 0.94; Specificity: 0.84)

Predicted Effect

probably benign
Transcript: ENSMUST00000228490

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.0%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice homozygous for a transgene insertion that inactivates this gene exhibit impaired fertilization and male infertility. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 82 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4933405L10Rik	T	C	8: 106,436,604 (GRCm39)	S267P		Het
Abca13	C	T	11: 9,243,741 (GRCm39)	P1868L	probably benign	Het
Abca13	A	G	11: 9,535,484 (GRCm39)	S4703G	probably benign	Het
Abca9	A	T	11: 110,006,319 (GRCm39)	M1262K	probably benign	Het
Acta1	A	T	8: 124,619,431 (GRCm39)	Y220*	probably null	Het
Actr6	A	G	10: 89,564,877 (GRCm39)	V24A	probably damaging	Het
Adam30	T	C	3: 98,069,936 (GRCm39)	Y590H	possibly damaging	Het
Akap8l	T	C	17: 32,557,783 (GRCm39)	N35D	probably damaging	Het
Ankle2	A	G	5: 110,385,661 (GRCm39)	I337V	probably benign	Het
Arid2	T	C	15: 96,256,822 (GRCm39)	V220A	probably benign	Het
Atp8b2	T	C	3: 89,865,603 (GRCm39)	D99G	probably damaging	Het
Baz1b	A	T	5: 135,252,022 (GRCm39)	H940L	probably benign	Het
Cacna1d	C	T	14: 29,764,881 (GRCm39)	V2017I	probably benign	Het
Ccn1	G	T	3: 145,354,583 (GRCm39)	N109K	probably damaging	Het
Cd226	T	A	18: 89,265,395 (GRCm39)	C224*	probably null	Het
Cdrt4	T	A	11: 62,883,466 (GRCm39)	I56N	possibly damaging	Het
Ces3b	G	T	8: 105,812,257 (GRCm39)	A169S	probably damaging	Het
Cramp1	C	A	17: 25,201,783 (GRCm39)	K566N	probably damaging	Het
Cryz	A	G	3: 154,327,765 (GRCm39)	Q289R	probably benign	Het
Csn1s2b	T	A	5: 87,968,820 (GRCm39)	M94K	probably benign	Het
Ctnnd1	T	C	2: 84,439,899 (GRCm39)	K804E	possibly damaging	Het
Cwh43	T	C	5: 73,572,340 (GRCm39)	S193P	probably benign	Het
Dcstamp	A	T	15: 39,623,792 (GRCm39)	D469V	probably benign	Het
Dffa	A	G	4: 149,190,674 (GRCm39)	T68A	probably damaging	Het
Dnah2	C	T	11: 69,341,824 (GRCm39)		probably null	Het
Dst	T	A	1: 34,219,458 (GRCm39)	I1966N	probably benign	Het
Efcab5	G	A	11: 77,022,934 (GRCm39)	T593I	probably damaging	Het
Epn3	C	T	11: 94,383,687 (GRCm39)		probably null	Het
Fem1c	A	T	18: 46,657,674 (GRCm39)	D13E		Het
Foxo3	C	T	10: 42,073,021 (GRCm39)	V499M	probably damaging	Het
Fpr2	T	A	17: 18,113,484 (GRCm39)	I160N	probably benign	Het
Gabra1	A	G	11: 42,045,853 (GRCm39)	Y86H	probably damaging	Het
Gabrb3	T	C	7: 57,415,202 (GRCm39)	Y91H	probably damaging	Het
Gcn1	T	C	5: 115,747,665 (GRCm39)		probably null	Het
Gp5	A	C	16: 30,128,393 (GRCm39)	F94V	probably damaging	Het
Gpr152	T	G	19: 4,192,614 (GRCm39)	W52G	probably damaging	Het
Hsd17b12	A	G	2: 93,988,081 (GRCm39)	V45A	probably benign	Het
Htr5a	A	G	5: 28,047,838 (GRCm39)	N131S	possibly damaging	Het
Il16	T	A	7: 83,332,064 (GRCm39)	N172I	probably damaging	Het
Itga2	G	A	13: 115,020,991 (GRCm39)	P120L	probably benign	Het
Itpkb	G	T	1: 180,160,056 (GRCm39)	E61*	probably null	Het
Lama1	T	C	17: 68,101,215 (GRCm39)	S1903P		Het
Llgl2	A	T	11: 115,742,941 (GRCm39)		probably null	Het
Mical1	A	T	10: 41,362,022 (GRCm39)		probably null	Het
Muc2	C	T	7: 141,288,014 (GRCm39)	P262S	probably damaging	Het
Myo9a	A	G	9: 59,778,764 (GRCm39)	R1507G	probably damaging	Het
Ndst1	G	A	18: 60,833,539 (GRCm39)	H491Y	probably damaging	Het
Nfasc	T	C	1: 132,527,791 (GRCm39)	T872A	probably benign	Het
Nipal3	A	T	4: 135,174,634 (GRCm39)	C372*	probably null	Het
Nmrk1	A	G	19: 18,616,929 (GRCm39)	H26R	probably benign	Het
Nubp2	G	A	17: 25,103,382 (GRCm39)	T165I	probably damaging	Het
Or2m12	C	T	16: 19,105,489 (GRCm39)	M1I	probably null	Het
Or51d1	T	A	7: 102,347,832 (GRCm39)	M129K	probably damaging	Het
Or5au1	T	C	14: 52,273,205 (GRCm39)	D121G	probably damaging	Het
Or5b102	T	G	19: 13,041,256 (GRCm39)	D160E	probably benign	Het
P2ry12	T	C	3: 59,134,931 (GRCm39)		probably benign	Het
Pax8	T	A	2: 24,331,173 (GRCm39)	D174V	probably damaging	Het
Pbxip1	A	G	3: 89,352,795 (GRCm39)	D147G	probably damaging	Het
Pnpla7	T	C	2: 24,892,931 (GRCm39)	S451P	probably benign	Het
Polm	A	G	11: 5,781,732 (GRCm39)	Y255H	probably damaging	Het
Polr1has	C	T	17: 37,276,353 (GRCm39)	Q242*	probably null	Het
Rdh14	T	A	12: 10,441,118 (GRCm39)	C93*	probably null	Het
Rnf213	C	A	11: 119,331,238 (GRCm39)	S2150Y		Het
Rpap1	G	A	2: 119,598,484 (GRCm39)	P1111L	probably damaging	Het
Rpl3l	T	A	17: 24,947,328 (GRCm39)	L14Q	probably damaging	Het
Sbp	A	G	17: 24,164,419 (GRCm39)	*200W	probably null	Het
Scn10a	A	G	9: 119,439,063 (GRCm39)	M1601T	probably benign	Het
Sertad4	C	T	1: 192,528,836 (GRCm39)	D327N	probably damaging	Het
Slc4a1	A	T	11: 102,242,256 (GRCm39)	I821N	probably damaging	Het
Synj1	T	C	16: 90,735,412 (GRCm39)	T1514A	probably benign	Het
Synj1	C	T	16: 90,757,343 (GRCm39)	V902I	possibly damaging	Het
Tctn1	A	G	5: 122,384,576 (GRCm39)	Y443H	probably benign	Het
Thoc5	C	T	11: 4,849,883 (GRCm39)	R25W	possibly damaging	Het
Tmem200c	A	G	17: 69,149,181 (GRCm39)	H588R	probably benign	Het
Trim45	C	T	3: 100,832,705 (GRCm39)	Q313*	probably null	Het
Ubqlnl	T	C	7: 103,799,122 (GRCm39)	D125G	possibly damaging	Het
Ubr4	A	T	4: 139,206,859 (GRCm39)	E4926V	unknown	Het
Usp5	T	C	6: 124,799,501 (GRCm39)	D349G	possibly damaging	Het
Vmn1r25	T	A	6: 57,956,306 (GRCm39)		probably benign	Het
Xirp2	A	G	2: 67,344,167 (GRCm39)	Q2136R	possibly damaging	Het
Zfp28	G	A	7: 6,395,623 (GRCm39)	R134H		Het
Zfp712	A	G	13: 67,188,824 (GRCm39)	S568P	probably benign	Het

Other mutations in Spaca6

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01433:Spaca6	APN	17	18,051,429 (GRCm39)	missense	probably benign	0.41
IGL02630:Spaca6	APN	17	18,051,351 (GRCm39)	missense	probably damaging	1.00
IGL03010:Spaca6	APN	17	18,058,667 (GRCm39)	missense	probably benign	0.01
IGL03352:Spaca6	APN	17	18,058,401 (GRCm39)	missense	probably damaging	1.00
R0021:Spaca6	UTSW	17	18,058,498 (GRCm39)	nonsense	probably null
R0964:Spaca6	UTSW	17	18,058,653 (GRCm39)	missense	possibly damaging	0.46
R1941:Spaca6	UTSW	17	18,058,692 (GRCm39)	missense	probably damaging	0.99
R1941:Spaca6	UTSW	17	18,058,664 (GRCm39)	missense	probably benign	0.05
R2197:Spaca6	UTSW	17	18,056,416 (GRCm39)	critical splice donor site	probably null
R2235:Spaca6	UTSW	17	18,058,507 (GRCm39)	critical splice donor site	probably null
R4602:Spaca6	UTSW	17	18,051,387 (GRCm39)	missense	probably damaging	0.99
R4645:Spaca6	UTSW	17	18,056,307 (GRCm39)	intron	probably benign
R4672:Spaca6	UTSW	17	18,057,005 (GRCm39)	nonsense	probably null
R5044:Spaca6	UTSW	17	18,051,458 (GRCm39)	missense	probably benign	0.00
R5212:Spaca6	UTSW	17	18,058,656 (GRCm39)	missense	probably benign	0.01
R5222:Spaca6	UTSW	17	18,058,367 (GRCm39)	missense	probably benign	0.02
R5528:Spaca6	UTSW	17	18,051,344 (GRCm39)	missense	probably benign
R5854:Spaca6	UTSW	17	18,051,509 (GRCm39)	nonsense	probably null
R6029:Spaca6	UTSW	17	18,051,458 (GRCm39)	missense	probably benign	0.00
R7041:Spaca6	UTSW	17	18,056,358 (GRCm39)	missense	probably benign	0.14
R7268:Spaca6	UTSW	17	18,052,369 (GRCm39)	missense	probably benign	0.09
R8281:Spaca6	UTSW	17	18,052,321 (GRCm39)	missense	possibly damaging	0.78
R8840:Spaca6	UTSW	17	18,051,365 (GRCm39)	missense	possibly damaging	0.59
R8926:Spaca6	UTSW	17	18,058,790 (GRCm39)	critical splice donor site	probably null
R8965:Spaca6	UTSW	17	18,058,718 (GRCm39)	missense	probably damaging	0.98
R9404:Spaca6	UTSW	17	18,057,800 (GRCm39)	missense	probably damaging	1.00
R9713:Spaca6	UTSW	17	18,058,498 (GRCm39)	nonsense	probably null
Z1177:Spaca6	UTSW	17	18,051,314 (GRCm39)	missense	probably benign	0.18

Predicted Primers

PCR Primer
(F):5'- AGAAGGTTAGCCAGGGCCTTAC -3'
(R):5'- GACTCTGGCAACTCGAAAGC -3'

Sequencing Primer
(F):5'- CAGAAAAGACTGGGTCTGTCTTCC -3'
(R):5'- GCAACTCGAAAGCCACGATACAAG -3'

Posted On

2022-10-06