Mutagenetix > Incidental Mutation

Incidental Mutation 'R5543:Spmip10'

436131

Institutional Source

Beutler Lab

Gene Symbol

Spmip10

Ensembl Gene

ENSMUSG00000032900

Gene Name

sperm microtubule inner protein 10

Synonyms

Tex43, 1700065I17Rik

MMRRC Submission

043101-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.109) question?

Stock #

R5543 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

56721422-56727854 bp(+) (GRCm39)

Type of Mutation

utr 3 prime

DNA Base Change (assembly)

G to A at 56727760 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s): [ENSMUST00000035640] [ENSMUST00000127591]

AlphaFold

Q9D9I1

Predicted Effect

probably benign
Transcript: ENSMUST00000035640

SMART Domains

Protein: ENSMUSP00000038152
Gene: ENSMUSG00000032900

Domain	Start	End	E-Value	Type
Pfam:DUF4513	3	140	9.3e-75	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000127591

SMART Domains

Protein: ENSMUSP00000117284
Gene: ENSMUSG00000032900

Domain	Start	End	E-Value	Type
Pfam:DUF4513	1	72	2.7e-29	PFAM

Predicted Effect

unknown
Transcript: ENSMUST00000147775
AA Change: G78D

SMART Domains

Protein: ENSMUSP00000115084
Gene: ENSMUSG00000032900
AA Change: G78D

Domain	Start	End	E-Value	Type
Pfam:DUF4513	1	82	8.6e-26	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000153248

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.2%
20x: 94.7%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 54 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
9130023H24Rik	C	A	7: 127,836,353 (GRCm39)	S80I	probably benign	Het
Aak1	T	C	6: 86,959,627 (GRCm39)		probably null	Het
Abcc6	A	G	7: 45,638,960 (GRCm39)		probably null	Het
Acvr1	A	G	2: 58,353,157 (GRCm39)	S268P	probably damaging	Het
Apod	T	C	16: 31,122,351 (GRCm39)		probably null	Het
Atp5po	T	C	16: 91,723,418 (GRCm39)	I58V	probably benign	Het
AU040320	C	T	4: 126,735,017 (GRCm39)	T777M	probably damaging	Het
Ccne2	A	T	4: 11,194,026 (GRCm39)	N89I	probably benign	Het
Cspg4b	C	A	13: 113,457,407 (GRCm39)	T1151K	probably damaging	Het
Dnah7a	A	G	1: 53,543,228 (GRCm39)	V2314A	probably damaging	Het
Dop1b	T	C	16: 93,595,808 (GRCm39)	S1881P	probably damaging	Het
E4f1	A	G	17: 24,666,336 (GRCm39)	V24A	possibly damaging	Het
Esrrg	A	T	1: 187,882,451 (GRCm39)	D236V	probably damaging	Het
Fam240b	T	A	13: 64,633,736 (GRCm39)	I27F	possibly damaging	Het
Fat1	T	A	8: 45,476,516 (GRCm39)	I1854N	probably damaging	Het
Fchsd2	T	C	7: 100,920,906 (GRCm39)	Y480H	probably damaging	Het
Fras1	A	G	5: 96,676,394 (GRCm39)	N47S	probably benign	Het
Gabrr3	T	C	16: 59,253,870 (GRCm39)	S196P	probably damaging	Het
Gbp8	T	A	5: 105,165,696 (GRCm39)	D319V	possibly damaging	Het
Hrh3	G	T	2: 179,745,763 (GRCm39)	A61E	probably damaging	Het
Idua	T	C	5: 108,818,095 (GRCm39)	I89T	probably benign	Het
Ifitm3	T	A	7: 140,589,730 (GRCm39)	I108F	unknown	Het
Izumo4	T	C	10: 80,538,668 (GRCm39)	F40S	probably damaging	Het
Kifc2	A	G	15: 76,551,242 (GRCm39)	R679G	probably damaging	Het
Klk14	G	A	7: 43,341,501 (GRCm39)	C51Y	probably damaging	Het
Ldha	A	T	7: 46,500,314 (GRCm39)	I171F	possibly damaging	Het
Lrfn4	T	C	19: 4,662,191 (GRCm39)	S609G	probably benign	Het
Mmp15	T	C	8: 96,094,729 (GRCm39)	F201S	possibly damaging	Het
Myof	C	T	19: 37,969,778 (GRCm39)	V295I	probably benign	Het
Or1n2	C	T	2: 36,797,369 (GRCm39)	T137I	possibly damaging	Het
Or2z2	T	A	11: 58,345,993 (GRCm39)	M261L	probably damaging	Het
Or5m12	G	T	2: 85,734,672 (GRCm39)	A242D	probably damaging	Het
Parp14	T	C	16: 35,655,137 (GRCm39)	D1778G	probably benign	Het
Pcnt	A	T	10: 76,247,886 (GRCm39)	D969E	probably benign	Het
Pibf1	A	T	14: 99,350,428 (GRCm39)	N192I	probably benign	Het
Pitpnm3	A	G	11: 71,947,023 (GRCm39)	F792S	probably damaging	Het
Pkd2	T	A	5: 104,637,199 (GRCm39)	I604N	probably damaging	Het
Pla2g15	T	C	8: 106,887,775 (GRCm39)	Y188H	probably damaging	Het
Plxnc1	G	T	10: 94,700,636 (GRCm39)	D643E	probably benign	Het
Prrc2c	G	A	1: 162,501,080 (GRCm39)	P1241L	probably damaging	Het
Ptprd	T	C	4: 75,977,990 (GRCm39)	E173G	probably damaging	Het
Shank3	T	C	15: 89,416,557 (GRCm39)	V232A	probably damaging	Het
Shbg	A	G	11: 69,507,564 (GRCm39)	I171T	probably damaging	Het
Slc22a14	A	T	9: 119,002,674 (GRCm39)	F404L	probably benign	Het
Slc37a3	C	A	6: 39,331,960 (GRCm39)	G158C	probably damaging	Het
Slfn9	C	A	11: 82,873,207 (GRCm39)	L565F	probably damaging	Het
Trank1	T	A	9: 111,195,180 (GRCm39)	M1068K	probably damaging	Het
Trbv15	A	T	6: 41,118,187 (GRCm39)	I15L	probably benign	Het
Ttn	C	T	2: 76,569,918 (GRCm39)	V26992M	probably damaging	Het
Ttn	A	T	2: 76,641,587 (GRCm39)	L5176Q	possibly damaging	Het
Ugt2b34	T	A	5: 87,054,560 (GRCm39)	I74F	probably damaging	Het
Vamp3	A	G	4: 151,135,477 (GRCm39)	L47P	probably damaging	Het
Zfp143	T	A	7: 109,682,522 (GRCm39)	C363*	probably null	Het
Zfp438	T	C	18: 5,213,761 (GRCm39)	E399G	probably damaging	Het

Other mutations in Spmip10

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02487:Spmip10	APN	18	56,727,571 (GRCm39)	missense	possibly damaging	0.74
R1570:Spmip10	UTSW	18	56,727,606 (GRCm39)	missense	probably benign	0.06
R2062:Spmip10	UTSW	18	56,721,535 (GRCm39)	nonsense	probably null
R4411:Spmip10	UTSW	18	56,727,720 (GRCm39)	missense	probably benign	0.03
R4970:Spmip10	UTSW	18	56,725,494 (GRCm39)	missense	possibly damaging	0.71
R8056:Spmip10	UTSW	18	56,727,763 (GRCm39)	missense
R8137:Spmip10	UTSW	18	56,727,653 (GRCm39)	missense	probably damaging	1.00
R8165:Spmip10	UTSW	18	56,722,547 (GRCm39)	intron	probably benign
R8786:Spmip10	UTSW	18	56,727,568 (GRCm39)	missense	probably damaging	0.99
R8919:Spmip10	UTSW	18	56,725,537 (GRCm39)	missense	probably damaging	1.00
R9600:Spmip10	UTSW	18	56,725,450 (GRCm39)	missense	probably benign	0.14

Predicted Primers

PCR Primer
(F):5'- TTTGCCATGGGGAAGATCGG -3'
(R):5'- CAGGTAGCCTCAGAACTGAC -3'

Sequencing Primer
(F):5'- GAAAGCCGTCCTGAAGAAAGGC -3'
(R):5'- GCCCCTAAGATCTGTACATTACG -3'

Posted On

2016-10-24