Mutagenetix > Incidental Mutation

Incidental Mutation 'R7685:Nme8'

593026

Institutional Source

Beutler Lab

Gene Symbol

Nme8

Ensembl Gene

ENSMUSG00000041138

Gene Name

NME/NM23 family member 8

Synonyms

Sptrx-2, 1700056P15Rik, Txndc3

MMRRC Submission

045750-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.137) question?

Stock #

R7685 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

19829248-19881964 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 19835145 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Leucine at position 514 (M514L)

Ref Sequence

ENSEMBL: ENSMUSP00000089358 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000039340] [ENSMUST00000091763] [ENSMUST00000223466]

AlphaFold

Q715T0

Predicted Effect

probably benign
Transcript: ENSMUST00000039340

SMART Domains

Protein: ENSMUSP00000047052
Gene: ENSMUSG00000041138

Domain	Start	End	E-Value	Type
Pfam:Thioredoxin	11	112	3.7e-12	PFAM
Pfam:NDK	155	283	2.3e-14	PFAM
NDK	312	452	3.8e-28	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000091763
AA Change: M514L

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

SMART Domains

Protein: ENSMUSP00000089358
Gene: ENSMUSG00000041138
AA Change: M514L

Domain	Start	End	E-Value	Type
Pfam:Thioredoxin	11	112	6.9e-12	PFAM
Pfam:NDK	155	284	1.1e-13	PFAM
NDK	312	449	2.75e-25	SMART
NDK	450	586	1.45e-33	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000223466

Coding Region Coverage

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

Validation Efficiency

99% (79/80)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein with an N-terminal thioredoxin domain and three C-terminal nucleoside diphosphate kinase (NDK) domains, but the NDK domains are thought to be catalytically inactive. The sea urchin ortholog of this gene encodes a component of sperm outer dynein arms, and the protein is implicated in ciliary function. Mutations in this gene are implicated in primary ciliary dyskinesia type 6.[provided by RefSeq, Nov 2009]
PHENOTYPE: Homozygous mutant displays normal reproductive system phenotype [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcg3	A	G	5: 105,116,081 (GRCm39)	L251S	probably damaging	Het
Acsbg1	C	T	9: 54,535,843 (GRCm39)	S53N	unknown	Het
Adamts18	A	G	8: 114,439,855 (GRCm39)	C913R	probably damaging	Het
Adck5	C	A	15: 76,479,588 (GRCm39)	Y524*	probably null	Het
Adgrv1	G	T	13: 81,251,443 (GRCm39)	Q6225K	possibly damaging	Het
Ahr	T	C	12: 35,554,016 (GRCm39)	N701S	probably damaging	Het
Apc	T	C	18: 34,447,261 (GRCm39)	C1386R	probably damaging	Het
Bbs1	A	G	19: 4,956,182 (GRCm39)	S38P	probably benign	Het
Celsr1	G	T	15: 85,862,933 (GRCm39)	C1366*	probably null	Het
Cep290	A	C	10: 100,375,919 (GRCm39)	H1424P	probably benign	Het
Clcn3	C	T	8: 61,386,119 (GRCm39)	R311K	possibly damaging	Het
Crat	C	T	2: 30,294,577 (GRCm39)	R497Q	probably benign	Het
Dhx9	A	G	1: 153,334,152 (GRCm39)	Y1002H	probably damaging	Het
Dnah8	C	T	17: 30,876,947 (GRCm39)	T533I	probably damaging	Het
Ermard	T	C	17: 15,279,724 (GRCm39)	S505P	probably benign	Het
Fbxw17	G	A	13: 50,579,680 (GRCm39)	D166N	probably damaging	Het
Fmo3	T	C	1: 162,785,901 (GRCm39)	K363R	possibly damaging	Het
Frey1	C	A	2: 92,213,817 (GRCm39)	P68Q	probably damaging	Het
Gadd45gip1	A	T	8: 85,558,980 (GRCm39)	R21W	probably damaging	Het
Galnt4	A	G	10: 98,945,826 (GRCm39)	N517S	probably benign	Het
Ganc	T	A	2: 120,264,273 (GRCm39)	W409R	probably damaging	Het
Glrx3	T	C	7: 137,060,920 (GRCm39)	S185P	probably damaging	Het
Gm49368	T	C	7: 127,712,414 (GRCm39)	S853P	probably damaging	Het
Gtf3c2	A	C	5: 31,325,611 (GRCm39)	L443V	probably damaging	Het
Gxylt2	A	T	6: 100,781,489 (GRCm39)	Q388L	probably benign	Het
Hcar2	C	T	5: 124,003,396 (GRCm39)	V36M	possibly damaging	Het
Ifit3b	A	T	19: 34,589,955 (GRCm39)	D377V	possibly damaging	Het
Ints5	A	G	19: 8,874,168 (GRCm39)	D709G	probably benign	Het
Lyst	A	G	13: 13,844,450 (GRCm39)	E1880G	probably benign	Het
Mep1a	C	T	17: 43,790,065 (GRCm39)	S428N	probably benign	Het
Mllt6	T	C	11: 97,567,790 (GRCm39)	L739P	probably damaging	Het
Mlst8	T	C	17: 24,695,031 (GRCm39)	Y284C	probably damaging	Het
Mmel1	T	C	4: 154,956,111 (GRCm39)	M1T	probably null	Het
Muc5ac	C	T	7: 141,363,120 (GRCm39)	P2144S	unknown	Het
Myh4	T	C	11: 67,131,756 (GRCm39)	V72A	probably benign	Het
Naa15	T	A	3: 51,377,395 (GRCm39)		probably null	Het
Nlrc5	A	G	8: 95,248,028 (GRCm39)		probably null	Het
Nudt9	C	A	5: 104,194,946 (GRCm39)	S14*	probably null	Het
Optn	G	A	2: 5,059,461 (GRCm39)	T19I	probably benign	Het
Or11h23	A	T	14: 50,948,215 (GRCm39)	I143F	possibly damaging	Het
Or13a24	T	C	7: 140,154,159 (GRCm39)	F31S	probably damaging	Het
Osbpl8	T	A	10: 111,112,370 (GRCm39)	L495*	probably null	Het
Panx2	T	C	15: 88,951,973 (GRCm39)	S147P	possibly damaging	Het
Pclo	T	A	5: 14,730,630 (GRCm39)	V3044D	unknown	Het
Pcnt	T	C	10: 76,258,642 (GRCm39)	K608E	probably benign	Het
Pde7a	T	A	3: 19,281,909 (GRCm39)	N447I	probably damaging	Het
Peli2	G	T	14: 48,517,491 (GRCm39)	C186F	not run	Het
Pgm5	A	G	19: 24,705,215 (GRCm39)	F433L	probably benign	Het
Plce1	G	A	19: 38,736,877 (GRCm39)	V1588I	probably benign	Het
Plin4	T	A	17: 56,409,413 (GRCm39)	H1295L	probably benign	Het
Poli	T	C	18: 70,658,590 (GRCm39)	E134G	probably benign	Het
Pramel11	T	A	4: 143,624,371 (GRCm39)	D42V	probably benign	Het
Ptprq	T	A	10: 107,479,839 (GRCm39)	I1144F	probably damaging	Het
Ptprz1	A	T	6: 23,024,977 (GRCm39)	T1738S	probably damaging	Het
Pxdc1	A	G	13: 34,836,267 (GRCm39)	L51P	probably damaging	Het
Rabepk	C	T	2: 34,669,308 (GRCm39)	G362S	probably damaging	Het
Rftn1	G	T	17: 50,354,408 (GRCm39)	A318D	probably damaging	Het
Rhd	T	A	4: 134,611,820 (GRCm39)		probably null	Het
Rpp14	T	C	14: 8,090,453 (GRCm38)	S126P	probably damaging	Het
Scn7a	C	T	2: 66,506,536 (GRCm39)	C1451Y	probably damaging	Het
Sdr39u1	G	A	14: 56,135,191 (GRCm39)	R251*	probably null	Het
Sephs2	G	T	7: 126,872,506 (GRCm39)	P196T	possibly damaging	Het
Slc22a16	T	C	10: 40,450,085 (GRCm39)	Y195H	possibly damaging	Het
Spg11	C	A	2: 121,899,361 (GRCm39)	V1575F	probably damaging	Het
Sqle	C	T	15: 59,187,890 (GRCm39)	S66L	probably benign	Het
Tas2r124	T	G	6: 132,732,056 (GRCm39)	W122G	probably damaging	Het
Tex52	A	T	6: 128,361,921 (GRCm39)		probably null	Het
Thoc1	T	A	18: 9,993,454 (GRCm39)	C604*	probably null	Het
Tmc3	T	C	7: 83,246,666 (GRCm39)	S136P	probably damaging	Het
Tmem212	T	A	3: 27,950,462 (GRCm39)	T11S	probably benign	Het
Ubn2	A	G	6: 38,468,727 (GRCm39)	N1147S	probably benign	Het
Uggt2	A	G	14: 119,312,759 (GRCm39)	I350T	probably damaging	Het
Ust	A	T	10: 8,083,339 (GRCm39)	Y346N	probably damaging	Het
Vwa8	A	G	14: 79,335,740 (GRCm39)	T1399A	probably benign	Het
Zc3h18	G	A	8: 123,140,615 (GRCm39)	R850Q	unknown	Het
Zfp800	C	A	6: 28,244,193 (GRCm39)	K257N	probably damaging	Het
Zfp985	T	A	4: 147,667,331 (GRCm39)	D66E	probably benign	Het

Other mutations in Nme8

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01984:Nme8	APN	13	19,873,150 (GRCm39)	missense	probably damaging	1.00
IGL02272:Nme8	APN	13	19,842,996 (GRCm39)	missense	probably damaging	0.99
IGL02344:Nme8	APN	13	19,858,574 (GRCm39)	missense	possibly damaging	0.94
IGL02395:Nme8	APN	13	19,862,078 (GRCm39)	missense	possibly damaging	0.64
IGL02621:Nme8	APN	13	19,859,818 (GRCm39)	missense	probably damaging	1.00
IGL02645:Nme8	APN	13	19,844,755 (GRCm39)	missense	probably damaging	1.00
IGL02807:Nme8	APN	13	19,860,001 (GRCm39)	unclassified	probably benign
IGL03059:Nme8	APN	13	19,836,414 (GRCm39)	missense	possibly damaging	0.92
IGL03288:Nme8	APN	13	19,880,776 (GRCm39)	missense	possibly damaging	0.94
IGL03323:Nme8	APN	13	19,873,120 (GRCm39)	missense	probably benign	0.06
R0139:Nme8	UTSW	13	19,862,018 (GRCm39)	missense	probably benign	0.19
R0616:Nme8	UTSW	13	19,875,029 (GRCm39)	missense	probably benign	0.00
R0632:Nme8	UTSW	13	19,842,206 (GRCm39)	missense	probably damaging	0.96
R1233:Nme8	UTSW	13	19,844,682 (GRCm39)	missense	possibly damaging	0.71
R1288:Nme8	UTSW	13	19,858,619 (GRCm39)	missense	possibly damaging	0.87
R1305:Nme8	UTSW	13	19,881,077 (GRCm39)	missense	possibly damaging	0.90
R1773:Nme8	UTSW	13	19,881,206 (GRCm39)	start codon destroyed	probably damaging	1.00
R1942:Nme8	UTSW	13	19,859,978 (GRCm39)	missense	probably damaging	1.00
R1970:Nme8	UTSW	13	19,836,492 (GRCm39)	missense	probably damaging	1.00
R2012:Nme8	UTSW	13	19,881,053 (GRCm39)	missense	probably damaging	1.00
R2093:Nme8	UTSW	13	19,835,042 (GRCm39)	missense	probably damaging	1.00
R2392:Nme8	UTSW	13	19,873,113 (GRCm39)	critical splice donor site	probably null
R2436:Nme8	UTSW	13	19,862,029 (GRCm39)	missense	probably damaging	1.00
R2901:Nme8	UTSW	13	19,859,834 (GRCm39)	missense	probably benign	0.02
R2902:Nme8	UTSW	13	19,859,834 (GRCm39)	missense	probably benign	0.02
R4665:Nme8	UTSW	13	19,858,605 (GRCm39)	missense	probably damaging	1.00
R4751:Nme8	UTSW	13	19,859,808 (GRCm39)	critical splice donor site	probably null
R4785:Nme8	UTSW	13	19,842,100 (GRCm39)	missense	probably damaging	0.96
R5101:Nme8	UTSW	13	19,875,017 (GRCm39)	critical splice donor site	probably null
R5217:Nme8	UTSW	13	19,880,861 (GRCm39)	missense	probably damaging	1.00
R5251:Nme8	UTSW	13	19,844,795 (GRCm39)	missense	probably benign	0.33
R5356:Nme8	UTSW	13	19,836,469 (GRCm39)	missense	probably damaging	1.00
R5397:Nme8	UTSW	13	19,878,549 (GRCm39)	missense	probably damaging	1.00
R5624:Nme8	UTSW	13	19,862,038 (GRCm39)	missense	possibly damaging	0.94
R6679:Nme8	UTSW	13	19,875,140 (GRCm39)	splice site	probably null
R7040:Nme8	UTSW	13	19,878,498 (GRCm39)	missense	probably damaging	1.00
R7111:Nme8	UTSW	13	19,859,817 (GRCm39)	missense	probably benign	0.06
R7185:Nme8	UTSW	13	19,862,053 (GRCm39)	missense	probably damaging	1.00
R7670:Nme8	UTSW	13	19,842,999 (GRCm39)	missense	probably benign	0.01
R8108:Nme8	UTSW	13	19,835,130 (GRCm39)	missense	probably benign	0.00
R8331:Nme8	UTSW	13	19,843,036 (GRCm39)	missense	probably damaging	1.00
R8413:Nme8	UTSW	13	19,858,689 (GRCm39)	missense	probably benign	0.01
R8808:Nme8	UTSW	13	19,859,978 (GRCm39)	missense	probably damaging	1.00
R9227:Nme8	UTSW	13	19,874,384 (GRCm39)	missense	probably benign
R9230:Nme8	UTSW	13	19,874,384 (GRCm39)	missense	probably benign
R9422:Nme8	UTSW	13	19,859,918 (GRCm39)	missense	probably benign	0.01
Z1088:Nme8	UTSW	13	19,873,127 (GRCm39)	missense	possibly damaging	0.82

Predicted Primers

PCR Primer
(F):5'- TGCTTCAGAAAAGTTAGACGCC -3'
(R):5'- CCCAGGGGAGTAAAAGTATGAATCC -3'

Sequencing Primer
(F):5'- AGTTAGACGCCCCATGGACAG -3'
(R):5'- CCATTTGCATAATTCTCAAGGGTC -3'

Posted On

2019-11-12