Mutagenetix > Incidental Mutation

Incidental Mutation 'R1471:Nsun7'

164873

Institutional Source

Beutler Lab

Gene Symbol

Nsun7

Ensembl Gene

ENSMUSG00000029206

Gene Name

NOL1/NOP2/Sun domain family, member 7

Synonyms

4921525L17Rik

MMRRC Submission

039524-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1471 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

66417240-66455369 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 66441572 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Glutamic Acid at position 414 (K414E)

Ref Sequence

ENSEMBL: ENSMUSP00000144520 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000031109] [ENSMUST00000201100] [ENSMUST00000202994]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000031109
AA Change: K414E

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000031109
Gene: ENSMUSG00000029206
AA Change: K414E

Domain	Start	End	E-Value	Type
Pfam:Nol1_Nop2_Fmu	394	477	4.2e-7	PFAM
low complexity region	543	555	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000113720
AA Change: K414E

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000109349
Gene: ENSMUSG00000029206
AA Change: K414E

Domain	Start	End	E-Value	Type
Pfam:Nol1_Nop2_Fmu	312	479	4.4e-9	PFAM
low complexity region	543	555	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000201100
AA Change: K414E

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000144520
Gene: ENSMUSG00000029206
AA Change: K414E

Domain	Start	End	E-Value	Type
Pfam:Nol1_Nop2_Fmu	312	479	4.3e-9	PFAM
low complexity region	543	555	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000202994

SMART Domains

Protein: ENSMUSP00000144498
Gene: ENSMUSG00000029206

Domain	Start	End	E-Value	Type
PDB:2B9E\|A	205	479	5e-17	PDB
low complexity region	509	521	N/A	INTRINSIC

Coding Region Coverage

1x: 99.3%
3x: 98.6%
10x: 96.8%
20x: 94.4%

Validation Efficiency

MGI Phenotype

FUNCTION: This gene encodes a member of the NOL1/NOP2/sun domain RNA methyltransferase family. Mice with a mutation in this gene exhibit male sterility due to impaired sperm motility. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Nov 2014]
PHENOTYPE: Males homozygous for an ENU-induced mutation are either infertile or subfertile. Mutant sperm exhibit poor progressive motility linked to rigidity of the flagellar midpiece and abnormal electron density patterns in the mitochondrial sheath. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 96 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930486L24Rik	C	A	13: 61,001,336 (GRCm39)	K130N	probably damaging	Het
Adam6a	T	A	12: 113,508,013 (GRCm39)	S129T	probably damaging	Het
Adamts10	T	A	17: 33,772,112 (GRCm39)	F1087I	probably damaging	Het
Afp	T	A	5: 90,651,541 (GRCm39)	N385K	possibly damaging	Het
Ahnak	T	G	19: 8,990,296 (GRCm39)		probably benign	Het
Akap6	A	G	12: 53,188,279 (GRCm39)	T1898A	probably benign	Het
Antxr2	C	A	5: 98,123,199 (GRCm39)	V283F	possibly damaging	Het
Asgr1	T	C	11: 69,946,919 (GRCm39)	V55A	possibly damaging	Het
Asxl3	A	G	18: 22,649,411 (GRCm39)	K467E	probably damaging	Het
Atp5f1a	C	A	18: 77,868,969 (GRCm39)	Q398K	probably damaging	Het
Atxn2	T	A	5: 121,924,437 (GRCm39)	D455E	probably damaging	Het
B4galt6	C	T	18: 20,878,410 (GRCm39)	A39T	possibly damaging	Het
C130073F10Rik	C	T	4: 101,747,535 (GRCm39)	E165K	probably benign	Het
Cabin1	A	G	10: 75,530,626 (GRCm39)	C1519R	probably damaging	Het
Casp8ap2	C	T	4: 32,639,386 (GRCm39)	R147*	probably null	Het
Ccdc88b	A	G	19: 6,831,391 (GRCm39)	L517P	probably benign	Het
Cd109	G	A	9: 78,561,869 (GRCm39)	V220I	probably damaging	Het
Cd2ap	T	C	17: 43,131,488 (GRCm39)	K369R	probably benign	Het
Cd300c	A	G	11: 114,850,614 (GRCm39)	V63A	probably benign	Het
Cnot10	A	G	9: 114,420,619 (GRCm39)	V741A	probably benign	Het
Col18a1	G	T	10: 76,932,040 (GRCm39)	Q350K	unknown	Het
Crnkl1	T	C	2: 145,774,236 (GRCm39)	K76E	possibly damaging	Het
Cryzl2	A	G	1: 157,298,291 (GRCm39)	K227E	probably benign	Het
Cts6	G	A	13: 61,344,194 (GRCm39)	T286I	probably benign	Het
Cul1	T	C	6: 47,491,820 (GRCm39)	V392A	probably damaging	Het
Dcaf7	T	A	11: 105,937,573 (GRCm39)	F65L	probably benign	Het
Dgke	A	C	11: 88,946,320 (GRCm39)	V160G	possibly damaging	Het
Dock8	C	A	19: 25,178,400 (GRCm39)	Q2098K	possibly damaging	Het
Efhb	T	A	17: 53,706,140 (GRCm39)	D799V	possibly damaging	Het
Ephb2	T	C	4: 136,386,262 (GRCm39)	D829G	probably benign	Het
Exosc1	A	T	19: 41,913,157 (GRCm39)	S117R	probably damaging	Het
Fga	T	C	3: 82,935,925 (GRCm39)	S51P	probably benign	Het
Fmn1	T	C	2: 113,523,439 (GRCm39)	F1141L	possibly damaging	Het
Foxm1	C	T	6: 128,350,837 (GRCm39)	L713F	probably damaging	Het
Galnt4	A	G	10: 98,944,536 (GRCm39)	E87G	probably benign	Het
Gamt	T	C	10: 80,096,692 (GRCm39)	D15G	probably benign	Het
Gm15557	C	A	2: 155,784,174 (GRCm39)	D154E	possibly damaging	Het
Gnptab	A	G	10: 88,281,625 (GRCm39)	I1211V	probably benign	Het
Greb1	A	T	12: 16,761,775 (GRCm39)	M535K	probably damaging	Het
Grm8	C	A	6: 27,363,308 (GRCm39)	A736S	possibly damaging	Het
Hspa14	T	C	2: 3,492,645 (GRCm39)	I373M	probably benign	Het
Ifi207	T	A	1: 173,557,629 (GRCm39)	T370S	unknown	Het
Igf1r	A	G	7: 67,653,585 (GRCm39)	N41S	probably damaging	Het
Ikzf5	A	T	7: 130,993,496 (GRCm39)	V224D	probably damaging	Het
Il10	C	A	1: 130,949,110 (GRCm39)	Y90*	probably null	Het
Itga4	A	G	2: 79,117,376 (GRCm39)	D394G	probably benign	Het
Kif21a	A	T	15: 90,840,622 (GRCm39)	S1165T	probably benign	Het
Krtap14	A	G	16: 88,622,515 (GRCm39)	S155P	probably damaging	Het
Loxl2	A	G	14: 69,930,546 (GRCm39)	N770S	probably benign	Het
Man2b1	A	G	8: 85,813,474 (GRCm39)	D222G	probably damaging	Het
Mcub	T	A	3: 129,709,464 (GRCm39)	Y283F	probably damaging	Het
Meis3	T	A	7: 15,911,496 (GRCm39)	Y64*	probably null	Het
Mfsd6	T	A	1: 52,748,716 (GRCm39)	I50F	probably benign	Het
Micu2	T	C	14: 58,182,854 (GRCm39)	T165A	probably damaging	Het
Mtcl1	T	C	17: 66,686,143 (GRCm39)	E921G	probably damaging	Het
Muc5b	A	T	7: 141,396,971 (GRCm39)	N215Y	unknown	Het
Muc6	A	G	7: 141,234,176 (GRCm39)	F772L	possibly damaging	Het
Myt1	A	G	2: 181,438,904 (GRCm39)	D142G	probably benign	Het
Nol6	C	T	4: 41,120,281 (GRCm39)	V479I	probably benign	Het
Nup210l	A	C	3: 90,077,869 (GRCm39)	I914L	probably benign	Het
Obox3	G	A	7: 15,360,875 (GRCm39)	P88L	probably benign	Het
Or10ag57	A	G	2: 87,218,862 (GRCm39)	Y271C	probably damaging	Het
Or4f4b	T	C	2: 111,314,351 (GRCm39)	L192P	probably damaging	Het
Or8h8	C	T	2: 86,752,922 (GRCm39)		probably null	Het
Or8w1	T	C	2: 87,466,014 (GRCm39)	T26A	probably benign	Het
Pclo	T	C	5: 14,730,441 (GRCm39)		probably benign	Het
Pcsk5	T	C	19: 17,545,688 (GRCm39)	N745D	probably damaging	Het
Pdzrn3	T	A	6: 101,128,473 (GRCm39)	N731I	possibly damaging	Het
Pkdrej	T	A	15: 85,701,334 (GRCm39)	Q1534L	probably benign	Het
Pramel28	T	C	4: 143,691,523 (GRCm39)	N400S	probably benign	Het
Rell1	T	A	5: 64,093,428 (GRCm39)	D109V	probably damaging	Het
Rplp0	C	T	5: 115,701,403 (GRCm39)	T285I	probably damaging	Het
Sanbr	A	T	11: 23,565,222 (GRCm39)	M255K	probably damaging	Het
Sema3g	C	T	14: 30,950,002 (GRCm39)	R728C	probably damaging	Het
Slc15a2	A	G	16: 36,574,153 (GRCm39)	Y536H	probably damaging	Het
Slc26a5	T	A	5: 22,021,962 (GRCm39)	Y488F	probably benign	Het
Slc5a4a	A	T	10: 76,022,362 (GRCm39)	S566C	probably damaging	Het
Spink7	C	T	18: 62,729,275 (GRCm39)	E21K	possibly damaging	Het
Src	C	T	2: 157,299,107 (GRCm39)	Q35*	probably null	Het
Srrm2	T	A	17: 24,039,770 (GRCm39)	V2234E	probably damaging	Het
Stk36	A	T	1: 74,650,314 (GRCm39)	Q282L	probably benign	Het
Tas2r118	T	G	6: 23,969,170 (GRCm39)	E297A	probably damaging	Het
Terf1	A	G	1: 15,913,194 (GRCm39)	Y385C	probably damaging	Het
Tmc3	T	C	7: 83,247,498 (GRCm39)	S198P	probably damaging	Het
Tmprss11b	C	T	5: 86,808,355 (GRCm39)	R407H	possibly damaging	Het
Tspyl4	G	A	10: 34,174,107 (GRCm39)	E200K	probably damaging	Het
Ttc21a	T	C	9: 119,771,707 (GRCm39)	Y169H	probably damaging	Het
Ugt2b36	C	T	5: 87,239,930 (GRCm39)	D152N	probably damaging	Het
Unk	T	C	11: 115,940,235 (GRCm39)	I196T	probably benign	Het
Uroc1	T	G	6: 90,321,153 (GRCm39)	V243G	probably damaging	Het
Usp34	C	A	11: 23,438,862 (GRCm39)	Q3475K	probably benign	Het
Vmn2r117	T	A	17: 23,697,447 (GRCm39)	I82L	probably benign	Het
Vmn2r44	A	T	7: 8,380,882 (GRCm39)	V337E	probably damaging	Het
Zbtb14	C	A	17: 69,695,497 (GRCm39)	F398L	probably damaging	Het
Zfp362	T	C	4: 128,680,993 (GRCm39)	T111A	probably benign	Het
Zfp598	T	C	17: 24,899,046 (GRCm39)	V615A	probably benign	Het

Other mutations in Nsun7

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00960:Nsun7	APN	5	66,446,846 (GRCm39)	missense	probably benign	0.00
IGL01013:Nsun7	APN	5	66,440,944 (GRCm39)	missense	possibly damaging	0.87
IGL01355:Nsun7	APN	5	66,452,211 (GRCm39)	missense	probably damaging	1.00
IGL01768:Nsun7	APN	5	66,436,043 (GRCm39)	missense	probably benign	0.11
IGL01914:Nsun7	APN	5	66,433,977 (GRCm39)	missense	probably damaging	1.00
IGL01990:Nsun7	APN	5	66,418,416 (GRCm39)	missense	probably damaging	1.00
IGL02477:Nsun7	APN	5	66,433,992 (GRCm39)	missense	probably damaging	0.99
R0071:Nsun7	UTSW	5	66,421,388 (GRCm39)	missense	probably benign	0.00
R0071:Nsun7	UTSW	5	66,421,388 (GRCm39)	missense	probably benign	0.00
R0079:Nsun7	UTSW	5	66,452,856 (GRCm39)	missense	probably benign	0.00
R0255:Nsun7	UTSW	5	66,446,751 (GRCm39)	splice site	probably benign
R0503:Nsun7	UTSW	5	66,440,924 (GRCm39)	splice site	probably benign
R0540:Nsun7	UTSW	5	66,440,977 (GRCm39)	missense	probably damaging	0.98
R1416:Nsun7	UTSW	5	66,418,423 (GRCm39)	missense	probably damaging	0.98
R1942:Nsun7	UTSW	5	66,441,588 (GRCm39)	missense	probably benign	0.00
R1981:Nsun7	UTSW	5	66,418,557 (GRCm39)	missense	probably damaging	0.99
R2037:Nsun7	UTSW	5	66,418,429 (GRCm39)	missense	probably benign	0.06
R2098:Nsun7	UTSW	5	66,441,055 (GRCm39)	missense	probably damaging	0.98
R2226:Nsun7	UTSW	5	66,418,562 (GRCm39)	nonsense	probably null
R2996:Nsun7	UTSW	5	66,452,897 (GRCm39)	missense	probably benign	0.01
R3882:Nsun7	UTSW	5	66,435,983 (GRCm39)	missense	probably damaging	0.99
R4678:Nsun7	UTSW	5	66,418,407 (GRCm39)	missense	probably benign	0.00
R4681:Nsun7	UTSW	5	66,418,542 (GRCm39)	missense	probably benign	0.00
R4997:Nsun7	UTSW	5	66,453,182 (GRCm39)	missense	probably benign	0.02
R6108:Nsun7	UTSW	5	66,453,142 (GRCm39)	missense	probably damaging	0.99
R6465:Nsun7	UTSW	5	66,452,929 (GRCm39)	missense	probably benign	0.35
R6500:Nsun7	UTSW	5	66,452,827 (GRCm39)	missense	probably benign	0.11
R6746:Nsun7	UTSW	5	66,441,080 (GRCm39)	critical splice donor site	probably null
R6925:Nsun7	UTSW	5	66,434,415 (GRCm39)	missense	probably damaging	1.00
R7032:Nsun7	UTSW	5	66,421,378 (GRCm39)	missense	probably benign	0.02
R7084:Nsun7	UTSW	5	66,452,764 (GRCm39)	missense	probably damaging	1.00
R7098:Nsun7	UTSW	5	66,418,326 (GRCm39)	missense	probably damaging	0.98
R7216:Nsun7	UTSW	5	66,436,000 (GRCm39)	missense	probably damaging	1.00
R7276:Nsun7	UTSW	5	66,434,484 (GRCm39)	missense	probably benign	0.03
R7803:Nsun7	UTSW	5	66,433,884 (GRCm39)	nonsense	probably null
R8877:Nsun7	UTSW	5	66,453,294 (GRCm39)	nonsense	probably null
R9167:Nsun7	UTSW	5	66,435,994 (GRCm39)	missense	possibly damaging	0.95
R9222:Nsun7	UTSW	5	66,418,366 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- ATGTGAAGGTCATTCTGTTGCTACCTC -3'
(R):5'- GAACATTTTGTTTGAAGGCACTAGGGC -3'

Sequencing Primer
(F):5'- CTGCTTGTATTCATTGGATAAGGGAC -3'
(R):5'- GAAATTTTGCTTGTGGTTCCCGT -3'

Posted On

2014-03-28