Mutagenetix > Incidental Mutation

Incidental Mutation 'R3002:Dnai2'

477315

Institutional Source

Beutler Lab

Gene Symbol

Dnai2

Ensembl Gene

ENSMUSG00000034706

Gene Name

dynein axonemal intermediate chain 2

Synonyms

C030015H18Rik, b2b3405Clo, Dnaic2

MMRRC Submission

040531-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.220) question?

Stock #

R3002 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

114618234-114648715 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 114641297 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Proline to Leucine at position 374 (P374L)

Ref Sequence

ENSEMBL: ENSMUSP00000114700 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000069325] [ENSMUST00000092469] [ENSMUST00000141762]

AlphaFold

A2AC93

Predicted Effect

probably damaging
Transcript: ENSMUST00000069325
AA Change: P374L

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000065787
Gene: ENSMUSG00000034706
AA Change: P374L

Domain	Start	End	E-Value	Type
low complexity region	127	146	N/A	INTRINSIC
WD40	206	245	2.86e0	SMART
WD40	248	293	3.33e-1	SMART
WD40	353	392	7.92e-3	SMART
WD40	396	436	2.05e1	SMART
WD40	441	480	4.93e1	SMART
low complexity region	519	545	N/A	INTRINSIC
low complexity region	559	608	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000092469
AA Change: P374L

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000090126
Gene: ENSMUSG00000034706
AA Change: P374L

Domain	Start	End	E-Value	Type
low complexity region	127	146	N/A	INTRINSIC
WD40	206	245	2.86e0	SMART
WD40	248	293	3.33e-1	SMART
WD40	353	392	7.92e-3	SMART
WD40	396	436	2.05e1	SMART
WD40	441	480	4.93e1	SMART
low complexity region	519	545	N/A	INTRINSIC
low complexity region	559	608	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000130692

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000136403

Predicted Effect

probably damaging
Transcript: ENSMUST00000141762
AA Change: P374L

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000114700
Gene: ENSMUSG00000034706
AA Change: P374L

Domain	Start	End	E-Value	Type
low complexity region	127	146	N/A	INTRINSIC
WD40	206	245	2.86e0	SMART
WD40	248	293	3.33e-1	SMART
WD40	353	392	7.92e-3	SMART
WD40	396	436	2.05e1	SMART
low complexity region	458	476	N/A	INTRINSIC
low complexity region	507	533	N/A	INTRINSIC
low complexity region	548	562	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000144872

Meta Mutation Damage Score

0.7861

Coding Region Coverage

1x: 99.1%
3x: 98.6%
10x: 97.3%
20x: 95.1%

Validation Efficiency

100% (41/41)

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 dynein intermediate chain family, and is part of the dynein complex of respiratory cilia and sperm flagella. Mutations in this gene are associated with primary ciliary dyskinesia type 9. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Mar 2010]
PHENOTYPE: Mice homozygous for an ENU-induced mutation exhibit situs inversus totalis and immotile respiratory cilia. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 70 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2810459M11Rik	T	C	1: 85,973,802 (GRCm39)	W40R	possibly damaging	Het
A2m	A	G	6: 121,638,406 (GRCm39)	S873G	possibly damaging	Het
Acd	C	T	8: 106,426,913 (GRCm39)		probably null	Het
Acly	T	C	11: 100,395,053 (GRCm39)	K469E	possibly damaging	Het
Adcy6	T	C	15: 98,494,541 (GRCm39)	T767A	probably benign	Het
Bnip3	T	C	7: 138,496,430 (GRCm39)	I93V	probably benign	Het
Casq2	A	G	3: 102,052,517 (GRCm39)	D269G	probably damaging	Het
Ccdc180	A	G	4: 45,899,988 (GRCm39)	D182G	probably benign	Het
Cep112	A	G	11: 108,331,329 (GRCm39)	E178G	probably damaging	Het
Chrd	T	G	16: 20,556,195 (GRCm39)	Y585*	probably null	Het
Cnksr3	T	C	10: 7,102,856 (GRCm39)		probably benign	Het
Csmd1	A	G	8: 16,246,184 (GRCm39)	F1072L	probably damaging	Het
Eif4g1	T	A	16: 20,511,134 (GRCm39)	F1289I	probably damaging	Het
Eprs1	T	C	1: 185,156,588 (GRCm39)		probably null	Het
Fasn	T	C	11: 120,700,671 (GRCm39)	D2114G	probably benign	Het
Fbxl17	T	A	17: 63,532,072 (GRCm39)	E590D	probably damaging	Het
Flnb	G	T	14: 7,907,162 (GRCm38)	R1245L	probably benign	Het
Folh1	A	C	7: 86,372,519 (GRCm39)	I678M	probably damaging	Het
Frrs1l	G	T	4: 56,990,139 (GRCm39)		probably benign	Het
Hal	G	A	10: 93,343,381 (GRCm39)	A542T	probably damaging	Het
Hs3st2	T	A	7: 121,099,910 (GRCm39)	M252K	probably damaging	Het
Il27ra	G	T	8: 84,758,660 (GRCm39)	S499*	probably null	Het
Klhdc1	T	A	12: 69,302,983 (GRCm39)	V173D	possibly damaging	Het
Knop1	CTCTTCTTCTTCTTCTTCTTCTTC	CTCTTCTTCTTCTTCTTC	7: 118,451,672 (GRCm39)		probably benign	Het
Lct	T	C	1: 128,231,963 (GRCm39)	M629V	probably damaging	Het
Lnx2	A	G	5: 146,955,825 (GRCm39)	V657A	probably benign	Het
Lrig1	G	A	6: 94,585,758 (GRCm39)	S810L	probably damaging	Het
Lyst	A	T	13: 13,871,290 (GRCm39)	M2676L	probably benign	Het
Mindy4	T	A	6: 55,195,349 (GRCm39)	S188T	probably benign	Het
Mrgprb3	C	T	7: 48,293,232 (GRCm39)	M106I	probably benign	Het
Ncam1	A	G	9: 49,468,526 (GRCm39)	I311T	probably damaging	Het
Ndufa8	T	A	2: 35,926,571 (GRCm39)	E155V	possibly damaging	Het
Nr4a1	A	G	15: 101,168,853 (GRCm39)		probably null	Het
Or2a12	A	G	6: 42,904,888 (GRCm39)	H241R	probably damaging	Het
Orc3	T	C	4: 34,571,790 (GRCm39)	T660A	probably benign	Het
Otub2	T	C	12: 103,370,536 (GRCm39)	S273P	probably damaging	Het
Otulinl	T	C	15: 27,664,792 (GRCm39)	T55A	probably benign	Het
Phf11c	A	G	14: 59,622,289 (GRCm39)	L241P	probably damaging	Het
Pik3ca	T	A	3: 32,516,946 (GRCm39)	I1058N	probably damaging	Het
Pkd2l1	A	G	19: 44,143,996 (GRCm39)	F359S	possibly damaging	Het
Plxnc1	A	T	10: 94,629,080 (GRCm39)	F1565I	probably damaging	Het
Polr1a	A	G	6: 71,890,000 (GRCm39)	N73S	probably benign	Het
Polr1a	T	A	6: 71,942,628 (GRCm39)	V1156E	probably benign	Het
Pon2	A	G	6: 5,268,976 (GRCm39)		probably null	Het
Ptcd1	G	A	5: 145,096,386 (GRCm39)	L236F	probably damaging	Het
Rgl2	A	G	17: 34,151,579 (GRCm39)	I208V	probably benign	Het
Rhox2e	C	A	X: 36,712,516 (GRCm39)	P69Q	probably damaging	Het
Rptor	G	A	11: 119,763,197 (GRCm39)	R927Q	possibly damaging	Het
Sec14l5	A	G	16: 4,989,746 (GRCm39)	Y230C	probably damaging	Het
Sele	G	T	1: 163,881,140 (GRCm39)	G447C	probably damaging	Het
Slc17a1	G	A	13: 24,062,564 (GRCm39)		probably null	Het
Slc2a4	A	T	11: 69,836,751 (GRCm39)	Y159*	probably null	Het
Slitrk5	A	G	14: 111,917,014 (GRCm39)	K213E	probably damaging	Het
Tdrd1	C	A	19: 56,850,182 (GRCm39)	Y981*	probably null	Het
Tex15	T	C	8: 34,064,556 (GRCm39)	Y1329H	probably benign	Het
Tgif2	C	G	2: 156,686,114 (GRCm39)	S2W	probably damaging	Het
Thoc5	A	G	11: 4,878,688 (GRCm39)	M620V	probably benign	Het
Tmeff2	C	T	1: 51,220,994 (GRCm39)	A323V	probably damaging	Het
Tmem181a	T	A	17: 6,346,061 (GRCm39)	L185H	probably damaging	Het
Tmem68	A	C	4: 3,569,588 (GRCm39)	L34W	probably damaging	Het
Tmtc4	A	T	14: 123,170,230 (GRCm39)		probably null	Het
Trpm2	A	T	10: 77,766,368 (GRCm39)		probably null	Het
Tut4	G	A	4: 108,370,125 (GRCm39)	E714K	probably damaging	Het
Tyk2	C	A	9: 21,020,617 (GRCm39)	R938L	probably benign	Het
Usp33	A	T	3: 152,063,579 (GRCm39)	T18S	probably damaging	Het
V1rd19	A	T	7: 23,703,310 (GRCm39)	I259F	probably benign	Het
Vmn2r24	A	C	6: 123,781,231 (GRCm39)	Q479P	probably benign	Het
Vmn2r98	A	G	17: 19,286,125 (GRCm39)	M208V	probably benign	Het
Wfdc6a	C	T	2: 164,422,225 (GRCm39)	V125I	probably benign	Het
Zkscan17	A	G	11: 59,378,077 (GRCm39)	C369R	probably damaging	Het

Other mutations in Dnai2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01359:Dnai2	APN	11	114,642,614 (GRCm39)	missense	probably benign	0.37
IGL01548:Dnai2	APN	11	114,643,768 (GRCm39)	missense	probably damaging	1.00
IGL02719:Dnai2	APN	11	114,642,737 (GRCm39)	missense	probably damaging	1.00
IGL03236:Dnai2	APN	11	114,648,075 (GRCm39)	unclassified	probably benign
R0096:Dnai2	UTSW	11	114,645,158 (GRCm39)	missense	probably benign	0.04
R0096:Dnai2	UTSW	11	114,645,158 (GRCm39)	missense	probably benign	0.04
R0305:Dnai2	UTSW	11	114,643,720 (GRCm39)	missense	probably benign	0.09
R0472:Dnai2	UTSW	11	114,636,015 (GRCm39)	splice site	probably benign
R0711:Dnai2	UTSW	11	114,645,158 (GRCm39)	missense	probably benign	0.04
R1756:Dnai2	UTSW	11	114,641,206 (GRCm39)	missense	probably benign	0.02
R1861:Dnai2	UTSW	11	114,643,777 (GRCm39)	missense	possibly damaging	0.56
R1916:Dnai2	UTSW	11	114,623,749 (GRCm39)	missense	possibly damaging	0.88
R1981:Dnai2	UTSW	11	114,623,755 (GRCm39)	missense	probably damaging	1.00
R1983:Dnai2	UTSW	11	114,626,682 (GRCm39)	splice site	probably null
R2430:Dnai2	UTSW	11	114,648,012 (GRCm39)	unclassified	probably benign
R2510:Dnai2	UTSW	11	114,647,993 (GRCm39)	unclassified	probably benign
R3001:Dnai2	UTSW	11	114,641,297 (GRCm39)	missense	probably damaging	1.00
R3113:Dnai2	UTSW	11	114,642,756 (GRCm39)	splice site	probably null
R3803:Dnai2	UTSW	11	114,629,551 (GRCm39)	missense	probably benign
R3874:Dnai2	UTSW	11	114,623,781 (GRCm39)	missense	probably damaging	1.00
R4853:Dnai2	UTSW	11	114,635,917 (GRCm39)	missense	probably benign	0.03
R5267:Dnai2	UTSW	11	114,631,293 (GRCm39)	missense	probably benign	0.02
R6008:Dnai2	UTSW	11	114,643,816 (GRCm39)	missense	probably benign	0.01
R6024:Dnai2	UTSW	11	114,643,734 (GRCm39)	missense	possibly damaging	0.85
R6819:Dnai2	UTSW	11	114,635,917 (GRCm39)	missense	probably benign	0.00
R7053:Dnai2	UTSW	11	114,629,521 (GRCm39)	missense	probably damaging	1.00
R7143:Dnai2	UTSW	11	114,645,076 (GRCm39)	missense	possibly damaging	0.86
R7208:Dnai2	UTSW	11	114,647,988 (GRCm39)	missense	unknown
R7275:Dnai2	UTSW	11	114,648,054 (GRCm39)	missense	unknown
R7463:Dnai2	UTSW	11	114,645,232 (GRCm39)	missense	probably benign	0.07
R7779:Dnai2	UTSW	11	114,645,235 (GRCm39)	missense	possibly damaging	0.50
R7899:Dnai2	UTSW	11	114,629,456 (GRCm39)	missense	probably benign	0.21
R8443:Dnai2	UTSW	11	114,645,275 (GRCm39)	missense	unknown
R8944:Dnai2	UTSW	11	114,641,302 (GRCm39)	missense	possibly damaging	0.58
R9081:Dnai2	UTSW	11	114,629,493 (GRCm39)	missense	probably damaging	0.97
R9182:Dnai2	UTSW	11	114,623,839 (GRCm39)	missense	probably benign	0.17
R9335:Dnai2	UTSW	11	114,625,489 (GRCm39)	missense	probably benign	0.01
R9380:Dnai2	UTSW	11	114,635,989 (GRCm39)	missense	probably benign	0.12
RF012:Dnai2	UTSW	11	114,641,242 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

Posted On

2017-05-15