Mutagenetix > Incidental Mutation

Incidental Mutation 'R2156:Ninl'

234783

Institutional Source

Beutler Lab

Gene Symbol

Ninl

Ensembl Gene

ENSMUSG00000068115

Gene Name

ninein-like

Synonyms

LOC381388, 4930519N13Rik, LOC381387

MMRRC Submission

040159-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R2156 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

150776439-150851330 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 150786503 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Lysine at position 1146 (Q1146K)

Ref Sequence

ENSEMBL: ENSMUSP00000105522 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000109896] [ENSMUST00000124135]

AlphaFold

Q6ZQ12

Predicted Effect

probably damaging
Transcript: ENSMUST00000109896
AA Change: Q1146K

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

SMART Domains

Protein: ENSMUSP00000105522
Gene: ENSMUSG00000068115
AA Change: Q1146K

Domain	Start	End	E-Value	Type
EFh	12	40	6.56e0	SMART
low complexity region	76	93	N/A	INTRINSIC
EFh	201	229	4.45e1	SMART
EFh	238	266	8.98e-4	SMART
low complexity region	295	306	N/A	INTRINSIC
coiled coil region	381	423	N/A	INTRINSIC
coiled coil region	461	517	N/A	INTRINSIC
coiled coil region	541	584	N/A	INTRINSIC
coiled coil region	620	699	N/A	INTRINSIC
coiled coil region	728	751	N/A	INTRINSIC
coiled coil region	835	863	N/A	INTRINSIC
coiled coil region	1058	1334	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000117833

Predicted Effect

probably benign
Transcript: ENSMUST00000124135
AA Change: Q161K

PolyPhen 2 Score 0.271 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000122069
Gene: ENSMUSG00000068115
AA Change: Q161K

Domain	Start	End	E-Value	Type
coiled coil region	16	61	N/A	INTRINSIC
coiled coil region	92	266	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000150036

Coding Region Coverage

1x: 99.2%
3x: 98.7%
10x: 97.5%
20x: 95.6%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice homozygous for a knock-out allele exhibit bone-marrow myeloid hyperplasia. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 85 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1810065E05Rik	T	A	11: 58,313,134 (GRCm39)		probably null	Het
Acaa2	T	C	18: 74,926,476 (GRCm39)		probably null	Het
Adam7	T	C	14: 68,748,792 (GRCm39)	Q485R	probably benign	Het
Adcy4	T	G	14: 56,006,627 (GRCm39)	T1069P	probably benign	Het
Arsj	T	C	3: 126,232,337 (GRCm39)	L361P	probably damaging	Het
Birc2	A	C	9: 7,826,939 (GRCm39)	L349R	probably damaging	Het
C1qa	T	C	4: 136,623,727 (GRCm39)	Y159C	probably damaging	Het
Cdh13	A	G	8: 119,963,703 (GRCm39)	K428E	probably damaging	Het
Cenpe	T	C	3: 134,953,235 (GRCm39)	M1563T	probably benign	Het
Col10a1	T	C	10: 34,271,696 (GRCm39)	V556A	probably benign	Het
Creg2	G	A	1: 39,662,338 (GRCm39)	L265F	probably damaging	Het
Cyp1a2	T	A	9: 57,589,433 (GRCm39)	D127V	probably damaging	Het
Cyp3a44	A	T	5: 145,740,480 (GRCm39)	Y53*	probably null	Het
Cyth1	C	T	11: 118,073,634 (GRCm39)	R233Q	probably damaging	Het
Dnmbp	G	A	19: 43,890,346 (GRCm39)	H474Y	possibly damaging	Het
Dvl1	G	A	4: 155,932,273 (GRCm39)	V28I	possibly damaging	Het
Ercc2	G	A	7: 19,120,717 (GRCm39)	R206H	possibly damaging	Het
Evx2	T	A	2: 74,486,360 (GRCm39)	H343L	probably damaging	Het
Fcrl2	T	A	3: 87,164,648 (GRCm39)	I293F	probably benign	Het
Gcnt4	A	G	13: 97,082,974 (GRCm39)	E90G	probably damaging	Het
Gid8	T	G	2: 180,358,751 (GRCm39)	C139G	probably benign	Het
Gm11938	C	A	11: 99,493,933 (GRCm39)	C54F	probably damaging	Het
Gm3336	G	A	8: 71,174,509 (GRCm39)	V158I	probably benign	Het
Gucy1b1	T	C	3: 81,968,327 (GRCm39)	N60D	probably benign	Het
Hdac7	T	C	15: 97,691,944 (GRCm39)	K810E	probably benign	Het
Hsp90ab1	A	G	17: 45,880,629 (GRCm39)	F361L	possibly damaging	Het
Igf2bp3	A	T	6: 49,085,858 (GRCm39)		probably null	Het
Inpp4b	T	A	8: 82,775,118 (GRCm39)	I772N	probably damaging	Het
Iqca1	A	G	1: 90,017,238 (GRCm39)	L390P	possibly damaging	Het
Itgb2	C	T	10: 77,396,082 (GRCm39)	R586W	probably benign	Het
Itih1	A	G	14: 30,655,432 (GRCm39)	S588P	possibly damaging	Het
Iyd	T	A	10: 3,497,166 (GRCm39)		probably null	Het
Kl	A	G	5: 150,912,425 (GRCm39)	K725E	probably benign	Het
Layn	T	A	9: 50,968,697 (GRCm39)	M349L	probably benign	Het
Map3k5	T	C	10: 19,900,683 (GRCm39)	Y286H	probably damaging	Het
Med4	C	T	14: 73,755,472 (GRCm39)		probably benign	Het
Mfn1	T	A	3: 32,588,400 (GRCm39)	N42K	possibly damaging	Het
Mindy2	T	C	9: 70,563,874 (GRCm39)	D152G	probably benign	Het
Mrc2	A	G	11: 105,238,682 (GRCm39)		probably null	Het
Mrpl11	C	A	19: 5,012,497 (GRCm39)	A26E	probably damaging	Het
Msh6	G	A	17: 88,293,568 (GRCm39)	W774*	probably null	Het
Mtch1	A	T	17: 29,561,841 (GRCm39)	V121E	probably damaging	Het
Mtg2	G	T	2: 179,725,923 (GRCm39)	E178*	probably null	Het
Nbas	A	T	12: 13,491,510 (GRCm39)	N1461Y	probably damaging	Het
Ndfip2	A	G	14: 105,525,204 (GRCm39)	T65A	probably benign	Het
Notch1	T	C	2: 26,350,873 (GRCm39)	D2089G	possibly damaging	Het
Notch3	C	T	17: 32,366,818 (GRCm39)	V906M	probably damaging	Het
Or51l14	A	G	7: 103,101,371 (GRCm39)	I276V	probably benign	Het
Or6b6	A	G	7: 106,570,775 (GRCm39)	Y259H	probably damaging	Het
Osmr	A	T	15: 6,873,891 (GRCm39)	Y169N	probably benign	Het
Ovgp1	T	C	3: 105,885,033 (GRCm39)	V124A	possibly damaging	Het
P2rx1	T	C	11: 72,904,939 (GRCm39)	M369T	probably benign	Het
Pde4dip	T	C	3: 97,631,534 (GRCm39)	Q1125R	probably damaging	Het
Podn	A	T	4: 107,878,892 (GRCm39)	V180E	probably damaging	Het
Pold1	A	T	7: 44,188,542 (GRCm39)	V475E	probably damaging	Het
Polg	A	G	7: 79,111,468 (GRCm39)	I261T	possibly damaging	Het
Satb1	G	T	17: 52,047,438 (GRCm39)	Q595K	probably benign	Het
Scaf8	T	A	17: 3,214,407 (GRCm39)		probably null	Het
Semp2l1	T	A	1: 32,585,128 (GRCm39)	M261L	probably benign	Het
Serpinb3a	C	T	1: 106,975,202 (GRCm39)		probably null	Het
Slc22a26	T	C	19: 7,779,480 (GRCm39)	D112G	probably damaging	Het
Slc25a23	A	G	17: 57,352,562 (GRCm39)	F441L	probably benign	Het
Slc25a53	T	C	X: 135,884,216 (GRCm39)	T42A	probably damaging	Het
Slc6a15	T	C	10: 103,229,269 (GRCm39)	Y103H	probably damaging	Het
Slx4	A	G	16: 3,804,223 (GRCm39)	S864P	probably benign	Het
Snap91	T	C	9: 86,707,130 (GRCm39)	E220G	probably damaging	Het
Spam1	T	C	6: 24,796,267 (GRCm39)	F73L	probably damaging	Het
Sphkap	C	T	1: 83,255,710 (GRCm39)	V393M	probably benign	Het
Spred2	T	C	11: 19,971,241 (GRCm39)	Y370H	probably damaging	Het
Sqle	T	C	15: 59,195,578 (GRCm39)		probably null	Het
Srrm2	A	G	17: 24,037,237 (GRCm39)	T1390A	probably benign	Het
Tas1r2	A	G	4: 139,396,352 (GRCm39)	R564G	possibly damaging	Het
Tbl2	G	T	5: 135,185,374 (GRCm39)		probably null	Het
Tcof1	T	C	18: 60,964,901 (GRCm39)	D606G	possibly damaging	Het
Tdpoz3	T	A	3: 93,734,087 (GRCm39)	L254H	probably damaging	Het
Trpm1	A	T	7: 63,884,736 (GRCm39)	I806F	probably damaging	Het
Ttc22	A	G	4: 106,496,237 (GRCm39)	D429G	probably benign	Het
Ube2o	C	A	11: 116,471,972 (GRCm39)	G90C	probably damaging	Het
Usp34	T	A	11: 23,332,602 (GRCm39)	F1110I	probably damaging	Het
Vmn2r82	T	C	10: 79,214,722 (GRCm39)	L235P	probably damaging	Het
Vps35	A	G	8: 86,013,129 (GRCm39)	V116A	probably benign	Het
Wdfy3	A	G	5: 102,046,291 (GRCm39)		probably null	Het
Zeb2	T	C	2: 44,878,821 (GRCm39)	K1138E	probably benign	Het
Zfp513	G	A	5: 31,357,866 (GRCm39)	T169I	probably benign	Het
Zfp629	T	C	7: 127,211,551 (GRCm39)	D86G	probably benign	Het

Other mutations in Ninl

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00230:Ninl	APN	2	150,808,161 (GRCm39)	missense	probably damaging	0.98
IGL01697:Ninl	APN	2	150,781,867 (GRCm39)	missense	probably damaging	1.00
IGL01756:Ninl	APN	2	150,821,436 (GRCm39)	missense	probably damaging	1.00
IGL01925:Ninl	APN	2	150,812,979 (GRCm39)	missense	probably damaging	1.00
IGL02341:Ninl	APN	2	150,786,525 (GRCm39)	nonsense	probably null
IGL02838:Ninl	APN	2	150,797,631 (GRCm39)	splice site	probably null
IGL02868:Ninl	APN	2	150,778,974 (GRCm39)	missense	probably benign
IGL03116:Ninl	APN	2	150,806,139 (GRCm39)	missense	probably damaging	1.00
IGL03396:Ninl	APN	2	150,808,132 (GRCm39)	missense	possibly damaging	0.88
R0117:Ninl	UTSW	2	150,779,593 (GRCm39)	missense	probably damaging	0.98
R0685:Ninl	UTSW	2	150,781,775 (GRCm39)	missense	possibly damaging	0.73
R0928:Ninl	UTSW	2	150,805,395 (GRCm39)	missense	probably damaging	0.99
R1051:Ninl	UTSW	2	150,812,046 (GRCm39)	missense	probably damaging	1.00
R1441:Ninl	UTSW	2	150,813,044 (GRCm39)	missense	probably benign	0.10
R1493:Ninl	UTSW	2	150,822,015 (GRCm39)	missense	probably damaging	1.00
R1499:Ninl	UTSW	2	150,822,096 (GRCm39)	missense	possibly damaging	0.70
R1539:Ninl	UTSW	2	150,817,867 (GRCm39)	missense	probably damaging	1.00
R1658:Ninl	UTSW	2	150,806,079 (GRCm39)	missense	probably damaging	1.00
R2038:Ninl	UTSW	2	150,817,763 (GRCm39)	nonsense	probably null
R2232:Ninl	UTSW	2	150,791,970 (GRCm39)	missense	probably benign	0.00
R2373:Ninl	UTSW	2	150,822,037 (GRCm39)	missense	probably damaging	1.00
R3743:Ninl	UTSW	2	150,792,168 (GRCm39)	missense	probably benign	0.01
R3906:Ninl	UTSW	2	150,822,039 (GRCm39)	missense	probably damaging	1.00
R3950:Ninl	UTSW	2	150,794,408 (GRCm39)	missense	possibly damaging	0.90
R4283:Ninl	UTSW	2	150,795,336 (GRCm39)	unclassified	probably benign
R4798:Ninl	UTSW	2	150,801,801 (GRCm39)	nonsense	probably null
R4963:Ninl	UTSW	2	150,781,829 (GRCm39)	missense	probably benign	0.04
R4998:Ninl	UTSW	2	150,795,284 (GRCm39)	missense	probably damaging	1.00
R5343:Ninl	UTSW	2	150,813,110 (GRCm39)	missense	probably benign	0.01
R5810:Ninl	UTSW	2	150,792,088 (GRCm39)	missense	probably benign	0.31
R5825:Ninl	UTSW	2	150,782,644 (GRCm39)	missense	probably damaging	1.00
R6436:Ninl	UTSW	2	150,808,098 (GRCm39)	missense	probably damaging	1.00
R6728:Ninl	UTSW	2	150,817,777 (GRCm39)	nonsense	probably null
R6734:Ninl	UTSW	2	150,787,003 (GRCm39)	critical splice donor site	probably null
R6997:Ninl	UTSW	2	150,808,145 (GRCm39)	missense	probably benign	0.08
R7135:Ninl	UTSW	2	150,797,524 (GRCm39)	missense	probably benign	0.00
R7157:Ninl	UTSW	2	150,791,263 (GRCm39)	missense	possibly damaging	0.63
R7315:Ninl	UTSW	2	150,791,970 (GRCm39)	missense	probably benign	0.00
R7840:Ninl	UTSW	2	150,808,016 (GRCm39)	missense	probably benign	0.00
R8134:Ninl	UTSW	2	150,792,234 (GRCm39)	missense	probably benign	0.01
R8319:Ninl	UTSW	2	150,801,827 (GRCm39)	missense	probably damaging	1.00
R8802:Ninl	UTSW	2	150,777,172 (GRCm39)	missense	probably damaging	1.00
R8997:Ninl	UTSW	2	150,801,816 (GRCm39)	missense	probably damaging	0.98
R9231:Ninl	UTSW	2	150,792,129 (GRCm39)	missense	probably benign
R9465:Ninl	UTSW	2	150,782,726 (GRCm39)	missense	possibly damaging	0.83
R9474:Ninl	UTSW	2	150,782,726 (GRCm39)	missense	probably benign	0.27
R9571:Ninl	UTSW	2	150,791,803 (GRCm39)	missense	probably benign
R9789:Ninl	UTSW	2	150,791,701 (GRCm39)	missense	probably benign	0.05
X0062:Ninl	UTSW	2	150,811,966 (GRCm39)	missense	probably damaging	1.00
Z1177:Ninl	UTSW	2	150,795,318 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TTTTGGAAGGGAGGAGCCTAC -3'
(R):5'- ATTGGACACTCGTGCAGAC -3'

Sequencing Primer
(F):5'- GAGGAGCCTACAGTTCCTCAC -3'
(R):5'- CTCCATGCAGTGCTTGAGGTC -3'

Posted On

2014-10-01