Mutagenetix > Incidental Mutation

Incidental Mutation 'R8117:2010315B03Rik'

631282

Institutional Source

Beutler Lab

Gene Symbol

2010315B03Rik

Ensembl Gene

ENSMUSG00000074829

Gene Name

RIKEN cDNA 2010315B03 gene

Synonyms

MMRRC Submission

067546-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.065) question?

Stock #

R8117 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

124054434-124075326 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 124058078 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 14 (T14A)

Ref Sequence

ENSEMBL: ENSMUSP00000137258 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000071300] [ENSMUST00000177714] [ENSMUST00000185949] [ENSMUST00000189915]

AlphaFold

J3QK55

Predicted Effect

probably damaging
Transcript: ENSMUST00000071300
AA Change: T35A

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

SMART Domains

Protein: ENSMUSP00000071269
Gene: ENSMUSG00000074829
AA Change: T35A

Domain	Start	End	E-Value	Type
KRAB	24	86	5.28e-14	SMART
ZnF_C2H2	95	117	5.9e-3	SMART
ZnF_C2H2	123	145	1.26e-2	SMART
ZnF_C2H2	151	173	2.95e-3	SMART
ZnF_C2H2	179	201	4.24e-4	SMART
ZnF_C2H2	207	229	1.38e-3	SMART
ZnF_C2H2	235	257	3.21e-4	SMART
ZnF_C2H2	263	285	1.26e-2	SMART
ZnF_C2H2	291	312	6.08e0	SMART
ZnF_C2H2	318	340	8.6e-5	SMART
ZnF_C2H2	346	368	1.36e-2	SMART
ZnF_C2H2	374	396	8.02e-5	SMART
ZnF_C2H2	402	424	9.58e-3	SMART

Predicted Effect

SMART Domains

Protein: ENSMUSP00000137258
Gene: ENSMUSG00000074829
AA Change: T14A

Domain	Start	End	E-Value	Type
KRAB	28	90	5.28e-14	SMART
ZnF_C2H2	99	121	5.9e-3	SMART
ZnF_C2H2	127	149	1.26e-2	SMART
ZnF_C2H2	155	177	2.95e-3	SMART
ZnF_C2H2	183	205	4.24e-4	SMART
ZnF_C2H2	211	233	1.38e-3	SMART
ZnF_C2H2	239	261	3.21e-4	SMART
ZnF_C2H2	267	289	1.26e-2	SMART
ZnF_C2H2	295	316	6.08e0	SMART
ZnF_C2H2	322	344	8.6e-5	SMART
ZnF_C2H2	350	372	1.36e-2	SMART
ZnF_C2H2	378	400	8.02e-5	SMART
ZnF_C2H2	406	428	9.58e-3	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000185949
AA Change: T39A

PolyPhen 2 Score 0.992 (Sensitivity: 0.70; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000140144
Gene: ENSMUSG00000074829
AA Change: T39A

Domain	Start	End	E-Value	Type
KRAB	29	91	2.3e-16	SMART
ZnF_C2H2	100	122	2.5e-5	SMART
ZnF_C2H2	128	150	5.3e-5	SMART
ZnF_C2H2	156	175	5.1e-1	SMART

Predicted Effect

SMART Domains

Protein: ENSMUSP00000140738
Gene: ENSMUSG00000074829
AA Change: T11A

Domain	Start	End	E-Value	Type
KRAB	1	63	2.3e-16	SMART
ZnF_C2H2	72	94	2.5e-5	SMART
ZnF_C2H2	100	122	5.3e-5	SMART
ZnF_C2H2	128	150	1.2e-5	SMART

Coding Region Coverage

1x: 99.8%
3x: 99.5%
10x: 98.5%
20x: 94.4%

Validation Efficiency

99% (73/74)

Allele List at MGI

Other mutations in this stock

Total: 71 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2610008E11Rik	T	C	10: 78,930,289 (GRCm39)	N42D	probably benign	Het
Ajm1	A	G	2: 25,469,246 (GRCm39)	F222L	probably benign	Het
Ankrd54	T	A	15: 78,939,641 (GRCm39)	M183L		Het
Apob	G	A	12: 8,056,435 (GRCm39)	G1639D	probably damaging	Het
B3gat2	A	G	1: 23,884,061 (GRCm39)	T283A	probably benign	Het
Bmpr2	T	G	1: 59,886,252 (GRCm39)	S296R	probably damaging	Het
Cand1	G	A	10: 119,042,721 (GRCm39)	T1123I	probably damaging	Het
Cc2d2a	T	C	5: 43,869,781 (GRCm39)	F943S	probably damaging	Het
Ccdc40	T	C	11: 119,144,211 (GRCm39)	I912T	probably benign	Het
Cdkn2d	G	A	9: 21,200,447 (GRCm39)	S108L	probably benign	Het
Cep295	G	A	9: 15,245,660 (GRCm39)	T932I	probably damaging	Het
Cntn5	A	G	9: 9,673,955 (GRCm39)	S716P	probably benign	Het
Col18a1	T	C	10: 76,895,808 (GRCm39)	E903G	probably benign	Het
Ctrc	T	A	4: 141,565,972 (GRCm39)	I229F	probably damaging	Het
Cyb561d2	C	T	9: 107,418,771 (GRCm39)	A18T	probably benign	Het
Dnajb4	T	A	3: 151,899,089 (GRCm39)	K46*	probably null	Het
Dsc2	C	T	18: 20,165,331 (GRCm39)	G881R	possibly damaging	Het
Dsg1c	C	T	18: 20,410,016 (GRCm39)	H495Y	probably benign	Het
Eif2b3	A	G	4: 116,879,414 (GRCm39)	D18G	probably damaging	Het
Enam	A	T	5: 88,651,385 (GRCm39)	I965L	probably benign	Het
Fhod3	T	A	18: 25,248,910 (GRCm39)	I1363K	probably damaging	Het
Fras1	A	G	5: 96,855,245 (GRCm39)	Y1918C	probably damaging	Het
Fsip2	T	A	2: 82,823,296 (GRCm39)	I6343N	possibly damaging	Het
Gpr45	G	C	1: 43,072,475 (GRCm39)	V373L	probably damaging	Het
Hdac2	G	T	10: 36,873,966 (GRCm39)	Q365H	probably damaging	Het
Hspa12b	A	G	2: 130,980,389 (GRCm39)	T103A	possibly damaging	Het
Ifrd1	A	T	12: 40,262,350 (GRCm39)	S287T	probably benign	Het
Igkv6-15	G	A	6: 70,383,622 (GRCm39)	P60S	possibly damaging	Het
Ippk	C	T	13: 49,599,818 (GRCm39)	P226S		Het
Kctd19	T	A	8: 106,122,069 (GRCm39)	D109V	unknown	Het
Matn4	G	A	2: 164,234,851 (GRCm39)	S540L	probably damaging	Het
Matn4	T	C	2: 164,241,682 (GRCm39)	K248E	probably benign	Het
Muc16	G	A	9: 18,420,206 (GRCm39)	Q97*	probably null	Het
Mup18	A	G	4: 61,592,238 (GRCm39)	C9R	unknown	Het
Myh1	A	G	11: 67,113,031 (GRCm39)	K1845R	probably damaging	Het
Mysm1	G	A	4: 94,848,627 (GRCm39)	R469*	probably null	Het
Naip1	T	C	13: 100,563,509 (GRCm39)	D552G	possibly damaging	Het
Nrcam	A	G	12: 44,618,371 (GRCm39)	D787G	probably benign	Het
Nrcam	G	A	12: 44,645,365 (GRCm39)	V1256I	probably damaging	Het
Obscn	G	T	11: 58,932,980 (GRCm39)	H4799N	possibly damaging	Het
Or1f12	T	C	13: 21,722,122 (GRCm39)	K3E	probably benign	Het
Or4p4	A	G	2: 88,482,729 (GRCm39)	K78E	probably damaging	Het
Or52e18	T	C	7: 104,609,356 (GRCm39)	I194M	probably damaging	Het
Or7g22	A	G	9: 19,048,353 (GRCm39)	I21M	probably benign	Het
Pcdhgb5	T	C	18: 37,866,302 (GRCm39)	F699S	probably damaging	Het
Phtf2	T	C	5: 21,007,038 (GRCm39)	E175G	probably benign	Het
Pira1	G	A	7: 3,740,075 (GRCm39)	T340I	probably damaging	Het
Ppp2r5c	A	G	12: 110,517,519 (GRCm39)	H218R	possibly damaging	Het
Ptgs2	A	G	1: 149,979,785 (GRCm39)	R297G	probably damaging	Het
Rapgef3	A	T	15: 97,648,747 (GRCm39)	D619E	probably benign	Het
Ric1	G	A	19: 29,552,191 (GRCm39)	V321I	probably benign	Het
Ripor1	T	C	8: 106,344,105 (GRCm39)	V413A	probably damaging	Het
Rsf1	G	T	7: 97,288,464 (GRCm39)		probably null	Het
Sccpdh	A	G	1: 179,504,017 (GRCm39)	D122G	probably damaging	Het
Sec16a	A	T	2: 26,331,441 (GRCm39)	H191Q	probably benign	Het
Slco1a5	G	T	6: 142,208,418 (GRCm39)	N124K	probably damaging	Het
Snrnp200	A	G	2: 127,071,051 (GRCm39)	T1111A	probably benign	Het
Stard9	G	A	2: 120,534,911 (GRCm39)	G3723S	probably benign	Het
Tanc2	T	A	11: 105,725,988 (GRCm39)	V384E	probably damaging	Het
Tbrg1	A	G	9: 37,568,296 (GRCm39)	F49L	possibly damaging	Het
Tecta	A	G	9: 42,288,927 (GRCm39)	F546S	probably damaging	Het
Tmem132c	A	G	5: 127,437,176 (GRCm39)	R222G	probably benign	Het
Trub2	C	T	2: 29,668,739 (GRCm39)		probably null	Het
Tti1	G	T	2: 157,849,418 (GRCm39)	P607Q	probably damaging	Het
Vmn1r62	T	A	7: 5,678,726 (GRCm39)	F136I	possibly damaging	Het
Vmn2r111	T	A	17: 22,790,469 (GRCm39)	H179L	probably benign	Het
Wdfy4	A	T	14: 32,699,063 (GRCm39)	C2703*	probably null	Het
Wdfy4	G	A	14: 32,826,072 (GRCm39)	P1193L		Het
Wipf3	A	G	6: 54,460,816 (GRCm39)	K88R	probably benign	Het
Zfp641	C	T	15: 98,186,856 (GRCm39)	G256R	probably damaging	Het
Zfp993	T	A	4: 146,741,972 (GRCm39)	C99S	probably benign	Het

Other mutations in 2010315B03Rik

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01872:2010315B03Rik	APN	9	124,058,120 (GRCm39)	splice site	probably benign
P4748:2010315B03Rik	UTSW	9	124,057,789 (GRCm39)	critical splice acceptor site	probably benign
R0090:2010315B03Rik	UTSW	9	124,057,789 (GRCm39)	critical splice acceptor site	probably benign
R0122:2010315B03Rik	UTSW	9	124,057,789 (GRCm39)	critical splice acceptor site	probably benign
R0140:2010315B03Rik	UTSW	9	124,057,789 (GRCm39)	critical splice acceptor site	probably benign
R0164:2010315B03Rik	UTSW	9	124,057,789 (GRCm39)	critical splice acceptor site	probably benign
R0164:2010315B03Rik	UTSW	9	124,057,789 (GRCm39)	critical splice acceptor site	probably benign
R0388:2010315B03Rik	UTSW	9	124,057,789 (GRCm39)	critical splice acceptor site	probably benign
R0775:2010315B03Rik	UTSW	9	124,057,789 (GRCm39)	critical splice acceptor site	probably benign
R0798:2010315B03Rik	UTSW	9	124,057,789 (GRCm39)	critical splice acceptor site	probably benign
R1467:2010315B03Rik	UTSW	9	124,058,093 (GRCm39)	missense	possibly damaging	0.91
R1569:2010315B03Rik	UTSW	9	124,056,427 (GRCm39)	nonsense	probably null
R2566:2010315B03Rik	UTSW	9	124,055,783 (GRCm39)	missense	probably damaging	0.99
R2566:2010315B03Rik	UTSW	9	124,055,701 (GRCm39)	missense	probably damaging	0.97
R3853:2010315B03Rik	UTSW	9	124,055,976 (GRCm39)	missense	probably damaging	1.00
R4092:2010315B03Rik	UTSW	9	124,055,903 (GRCm39)	missense	probably benign	0.03
R4109:2010315B03Rik	UTSW	9	124,057,733 (GRCm39)	missense	probably benign	0.01
R4646:2010315B03Rik	UTSW	9	124,056,228 (GRCm39)	missense	probably benign	0.00
R4648:2010315B03Rik	UTSW	9	124,056,228 (GRCm39)	missense	probably benign	0.00
R4705:2010315B03Rik	UTSW	9	124,056,631 (GRCm39)	missense	possibly damaging	0.86
R4764:2010315B03Rik	UTSW	9	124,056,396 (GRCm39)	missense	probably benign	0.01
R5110:2010315B03Rik	UTSW	9	124,057,987 (GRCm39)	critical splice donor site	probably null
R5117:2010315B03Rik	UTSW	9	124,055,715 (GRCm39)	missense	probably benign	0.00
R5162:2010315B03Rik	UTSW	9	124,056,301 (GRCm39)	missense	probably benign	0.08
R5226:2010315B03Rik	UTSW	9	124,056,706 (GRCm39)	missense	possibly damaging	0.91
R5426:2010315B03Rik	UTSW	9	124,056,633 (GRCm39)	missense	probably damaging	1.00
R6793:2010315B03Rik	UTSW	9	124,058,052 (GRCm39)	missense	possibly damaging	0.85
R6975:2010315B03Rik	UTSW	9	124,056,687 (GRCm39)	missense	probably benign	0.02
R7213:2010315B03Rik	UTSW	9	124,056,530 (GRCm39)	nonsense	probably null
R8011:2010315B03Rik	UTSW	9	124,056,529 (GRCm39)	missense
R8086:2010315B03Rik	UTSW	9	124,055,808 (GRCm39)	missense
R8363:2010315B03Rik	UTSW	9	124,055,800 (GRCm39)	missense
R8941:2010315B03Rik	UTSW	9	124,056,679 (GRCm39)	missense	probably benign	0.05
R9523:2010315B03Rik	UTSW	9	124,056,652 (GRCm39)	missense

Predicted Primers

PCR Primer
(F):5'- ACAATGCTTGATTTATTCACCTCAT -3'
(R):5'- ATGAGACAGTACACCCAGACTGC -3'

Sequencing Primer
(F):5'- TGCTTGATTTATTCACCTCATTTTTC -3'
(R):5'- GCAAGGCTATATCCTATTCAAAGGGC -3'

Posted On

2020-06-30