Mutagenetix > Incidental Mutation

Incidental Mutation 'R8794:1700010I14Rik'

671151

Institutional Source

Beutler Lab

Gene Symbol

1700010I14Rik

Ensembl Gene

ENSMUSG00000023873

Gene Name

RIKEN cDNA 1700010I14 gene

Synonyms

MMRRC Submission

068723-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R8794 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

9207152-9227151 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 9226939 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Aspartic acid at position 498 (V498D)

Ref Sequence

ENSEMBL: ENSMUSP00000024650 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000024650] [ENSMUST00000151609]

AlphaFold

Q7TPG0

Predicted Effect

unknown
Transcript: ENSMUST00000024650
AA Change: V498D

SMART Domains

Protein: ENSMUSP00000024650
Gene: ENSMUSG00000023873
AA Change: V498D

Domain	Start	End	E-Value	Type
coiled coil region	135	165	N/A	INTRINSIC
Pfam:TSNAXIP1_N	239	349	6.1e-36	PFAM
low complexity region	351	364	N/A	INTRINSIC
low complexity region	372	385	N/A	INTRINSIC
coiled coil region	421	466	N/A	INTRINSIC
low complexity region	501	519	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000151609

SMART Domains

Protein: ENSMUSP00000118841
Gene: ENSMUSG00000023873

Domain	Start	End	E-Value	Type
coiled coil region	135	165	N/A	INTRINSIC
coiled coil region	321	370	N/A	INTRINSIC
low complexity region	372	385	N/A	INTRINSIC
coiled coil region	421	466	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.9%
20x: 99.6%

Validation Efficiency

100% (86/86)

Allele List at MGI

Other mutations in this stock

Total: 86 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Actn1	C	T	12: 80,245,754 (GRCm39)		probably benign	Het
Actrt2	T	C	4: 154,751,176 (GRCm39)	E320G	probably damaging	Het
Adamts7	C	T	9: 90,076,239 (GRCm39)	Q1265*	probably null	Het
Adra1a	A	G	14: 66,875,064 (GRCm39)	N13S	probably benign	Het
Alpk3	G	T	7: 80,707,403 (GRCm39)	R9L	unknown	Het
Ankrd42	A	G	7: 92,263,674 (GRCm39)	F225L	probably benign	Het
C3	T	C	17: 57,528,011 (GRCm39)	E736G	probably benign	Het
Ccng1	A	G	11: 40,644,826 (GRCm39)	S24P	probably benign	Het
Cdc42bpa	A	T	1: 179,894,816 (GRCm39)	N332I	probably damaging	Het
Cep131	G	A	11: 119,972,074 (GRCm39)	P90S	probably benign	Het
Chd8	A	G	14: 52,441,904 (GRCm39)	S2154P	probably damaging	Het
Cilp	A	G	9: 65,186,535 (GRCm39)	S877G	probably benign	Het
Clic6	T	A	16: 92,324,987 (GRCm39)	S382T	possibly damaging	Het
Coq8a	G	T	1: 180,006,773 (GRCm39)	P85Q	probably benign	Het
Creb3l4	A	G	3: 90,145,225 (GRCm39)	I309T	probably benign	Het
Cux2	T	C	5: 122,007,306 (GRCm39)	E785G	probably benign	Het
Cyfip2	A	G	11: 46,144,800 (GRCm39)	F685L	possibly damaging	Het
Epha6	T	C	16: 60,026,035 (GRCm39)	D469G	probably benign	Het
Erc1	A	T	6: 119,607,616 (GRCm39)	V962E	probably damaging	Het
Esrrb	A	T	12: 86,517,038 (GRCm39)	S57C	probably damaging	Het
Fam169a	A	G	13: 97,250,628 (GRCm39)	T320A	possibly damaging	Het
Farsb	C	T	1: 78,401,678 (GRCm39)		probably benign	Het
Frem3	T	C	8: 81,338,907 (GRCm39)	V400A	probably damaging	Het
Frem3	A	T	8: 81,342,851 (GRCm39)	M1715L	probably benign	Het
Frmpd1	A	G	4: 45,279,632 (GRCm39)	T786A	probably benign	Het
Gapvd1	A	T	2: 34,594,330 (GRCm39)	S886T	possibly damaging	Het
Gba2	A	G	4: 43,568,077 (GRCm39)	S737P	probably damaging	Het
Gm525	A	G	11: 88,979,479 (GRCm39)	N85S	probably damaging	Het
Gnpda1	T	A	18: 38,465,091 (GRCm39)	D175V	probably benign	Het
Heatr5b	T	C	17: 79,123,015 (GRCm39)	I655V	probably benign	Het
Hmcn1	G	A	1: 150,591,469 (GRCm39)	T1910I	probably benign	Het
Idh1	CA	CAA	1: 65,204,347 (GRCm39)		probably null	Het
Ier2	A	T	8: 85,389,096 (GRCm39)	D95E	probably damaging	Het
Ifi208	A	G	1: 173,523,370 (GRCm39)	R547G	possibly damaging	Het
Itih3	T	A	14: 30,634,854 (GRCm39)	S639C	possibly damaging	Het
Kif19b	A	G	5: 140,461,785 (GRCm39)	E529G	probably damaging	Het
Marchf7	G	A	2: 60,074,015 (GRCm39)		probably null	Het
Mep1b	A	C	18: 21,224,325 (GRCm39)	T373P	probably damaging	Het
Mlh3	G	A	12: 85,282,497 (GRCm39)	P1379S	probably damaging	Het
Nav3	T	A	10: 109,605,032 (GRCm39)	K1014*	probably null	Het
Nme1	A	T	11: 93,851,658 (GRCm39)	F78I	probably benign	Het
Nos3	T	A	5: 24,576,745 (GRCm39)	V458D	probably damaging	Het
Noxa1	A	G	2: 24,984,852 (GRCm39)	F29L	probably benign	Het
Nrcam	G	A	12: 44,624,958 (GRCm39)	G1055D	probably benign	Het
Nutf2	A	T	8: 106,602,171 (GRCm39)		probably benign	Het
Oog3	A	G	4: 143,884,556 (GRCm39)	I460T	probably benign	Het
Or4b1b	A	T	2: 90,112,150 (GRCm39)	Y256*	probably null	Het
Or4c113	T	C	2: 88,885,477 (GRCm39)	M98V	probably benign	Het
Or5p78	A	T	7: 108,211,580 (GRCm39)	D22V	probably benign	Het
Or7e175	A	T	9: 20,048,630 (GRCm39)	M73L	possibly damaging	Het
Pde2a	A	T	7: 101,155,136 (GRCm39)	Y559F	possibly damaging	Het
Pde6d	G	A	1: 86,475,209 (GRCm39)	Q61*	probably null	Het
Pdpr	A	G	8: 111,852,240 (GRCm39)	T536A	possibly damaging	Het
Pias4	T	A	10: 80,999,846 (GRCm39)	K69M	probably damaging	Het
Pigo	A	T	4: 43,023,787 (GRCm39)	D188E	possibly damaging	Het
Pik3r2	A	G	8: 71,224,007 (GRCm39)	V270A	probably benign	Het
Plod2	T	A	9: 92,482,801 (GRCm39)	W456R	probably damaging	Het
Pmpcb	T	C	5: 21,961,832 (GRCm39)	V450A	probably benign	Het
Poln	G	A	5: 34,286,871 (GRCm39)	T99I	possibly damaging	Het
Prg2	A	G	2: 84,812,404 (GRCm39)	D38G	possibly damaging	Het
Psmd7	A	C	8: 108,310,831 (GRCm39)	Y138D	probably damaging	Het
Ptprk	T	A	10: 28,139,504 (GRCm39)	Y76*	probably null	Het
Ranbp2	T	A	10: 58,328,414 (GRCm39)	V2810E	probably damaging	Het
Rgma	A	T	7: 73,067,648 (GRCm39)	H411L	probably damaging	Het
Sapcd1	T	C	17: 35,246,814 (GRCm39)	T25A	probably damaging	Het
Serpinb6e	T	C	13: 34,024,977 (GRCm39)	I105V	possibly damaging	Het
Serpinb9f	A	T	13: 33,513,396 (GRCm39)	T158S	probably benign	Het
Sirpb1b	T	A	3: 15,613,843 (GRCm39)	T80S	probably benign	Het
Skint6	A	T	4: 113,049,869 (GRCm39)	S265R	possibly damaging	Het
Slc23a2	A	T	2: 131,902,629 (GRCm39)	F524L	probably benign	Het
Slc2a13	C	A	15: 91,234,302 (GRCm39)	G345C	probably damaging	Het
Sp110	A	G	1: 85,511,231 (GRCm39)		probably null	Het
Srcin1	A	G	11: 97,439,803 (GRCm39)	V109A	probably benign	Het
Tfcp2l1	A	G	1: 118,560,118 (GRCm39)	N70S	probably damaging	Het
Tmem30c	T	A	16: 57,090,553 (GRCm39)	H218L	probably benign	Het
Tmprss11d	G	A	5: 86,486,680 (GRCm39)	T70I	probably damaging	Het
Tnpo2	A	T	8: 85,765,114 (GRCm39)	Q32L	probably benign	Het
Trav16n	A	C	14: 53,588,867 (GRCm39)	T48P	probably damaging	Het
Ufc1	A	G	1: 171,117,095 (GRCm39)	Y110H	probably damaging	Het
Wars2	A	G	3: 99,123,888 (GRCm39)	K250E	probably damaging	Het
Wdfy4	G	T	14: 32,869,049 (GRCm39)	N326K	probably benign	Het
Xirp2	A	T	2: 67,341,557 (GRCm39)	E1266V	probably damaging	Het
Zfp423	A	C	8: 88,507,857 (GRCm39)	L829R	probably damaging	Het
Zfp735	A	G	11: 73,603,029 (GRCm39)	K658E	possibly damaging	Het
Zscan12	T	A	13: 21,547,847 (GRCm39)	C10S	possibly damaging	Het
Zswim3	T	A	2: 164,662,687 (GRCm39)	M389K	probably damaging	Het

Other mutations in 1700010I14Rik

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00988:1700010I14Rik	APN	17	9,215,937 (GRCm39)	critical splice donor site	probably null
IGL01569:1700010I14Rik	APN	17	9,215,827 (GRCm39)	missense	probably benign	0.33
IGL03024:1700010I14Rik	APN	17	9,212,464 (GRCm39)	missense	probably benign	0.33
IGL03410:1700010I14Rik	APN	17	9,220,728 (GRCm39)	missense	probably damaging	1.00
R0017:1700010I14Rik	UTSW	17	9,226,938 (GRCm39)	utr 3 prime	probably benign
R0017:1700010I14Rik	UTSW	17	9,226,938 (GRCm39)	utr 3 prime	probably benign
R0324:1700010I14Rik	UTSW	17	9,219,989 (GRCm39)	missense	probably benign	0.33
R0361:1700010I14Rik	UTSW	17	9,211,378 (GRCm39)	missense	probably benign	0.39
R0482:1700010I14Rik	UTSW	17	9,207,255 (GRCm39)	critical splice donor site	probably null
R0529:1700010I14Rik	UTSW	17	9,211,228 (GRCm39)	missense	probably benign	0.32
R1102:1700010I14Rik	UTSW	17	9,211,460 (GRCm39)	missense	probably damaging	1.00
R1964:1700010I14Rik	UTSW	17	9,211,324 (GRCm39)	missense	probably damaging	0.99
R3620:1700010I14Rik	UTSW	17	9,226,864 (GRCm39)	missense	probably benign	0.15
R4259:1700010I14Rik	UTSW	17	9,214,066 (GRCm39)	missense	probably damaging	1.00
R4261:1700010I14Rik	UTSW	17	9,214,066 (GRCm39)	missense	probably damaging	1.00
R4687:1700010I14Rik	UTSW	17	9,210,985 (GRCm39)	missense	probably damaging	1.00
R4707:1700010I14Rik	UTSW	17	9,224,544 (GRCm39)	missense	probably damaging	1.00
R4839:1700010I14Rik	UTSW	17	9,226,845 (GRCm39)	missense	probably benign	0.41
R4979:1700010I14Rik	UTSW	17	9,220,643 (GRCm39)	missense	probably damaging	1.00
R5225:1700010I14Rik	UTSW	17	9,226,839 (GRCm39)	nonsense	probably null
R5383:1700010I14Rik	UTSW	17	9,211,532 (GRCm39)	missense	possibly damaging	0.86
R6031:1700010I14Rik	UTSW	17	9,214,084 (GRCm39)	missense	possibly damaging	0.85
R6031:1700010I14Rik	UTSW	17	9,214,084 (GRCm39)	missense	possibly damaging	0.85
R6505:1700010I14Rik	UTSW	17	9,220,772 (GRCm39)	missense	probably benign	0.08
R6736:1700010I14Rik	UTSW	17	9,211,100 (GRCm39)	missense	probably benign	0.01
R7089:1700010I14Rik	UTSW	17	9,226,927 (GRCm39)	missense	probably benign	0.00
R7097:1700010I14Rik	UTSW	17	9,224,052 (GRCm39)	missense	probably damaging	1.00
R7292:1700010I14Rik	UTSW	17	9,215,861 (GRCm39)	nonsense	probably null
R7405:1700010I14Rik	UTSW	17	9,220,649 (GRCm39)	missense	probably damaging	0.99
R7567:1700010I14Rik	UTSW	17	9,226,838 (GRCm39)	missense	probably damaging	1.00
R7877:1700010I14Rik	UTSW	17	9,220,665 (GRCm39)	missense	probably damaging	1.00
R8805:1700010I14Rik	UTSW	17	9,226,737 (GRCm39)	nonsense	probably null
R9007:1700010I14Rik	UTSW	17	9,226,935 (GRCm39)	missense	probably benign	0.01
R9308:1700010I14Rik	UTSW	17	9,220,667 (GRCm39)	nonsense	probably null
R9400:1700010I14Rik	UTSW	17	9,211,118 (GRCm39)	missense	probably benign	0.01

Predicted Primers

PCR Primer
(F):5'- GCGCTGTGGGATCTCATTAG -3'
(R):5'- TTAAATGCACGTGTGGAAACATGTC -3'

Sequencing Primer
(F):5'- TGGGATCTCATTAGGGAATATTCAG -3'
(R):5'- AACCTGTTTTGTCCAGTTC -3'

Posted On

2021-04-30