Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02221:1700013D24Rik'

285137

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

1700013D24Rik

Ensembl Gene

ENSMUSG00000079346

Gene Name

RIKEN cDNA 1700013D24 gene

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.107) question?

Stock #

IGL02221

Quality Score

Status

Chromosome

Chromosomal Location

124324546-124334003 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 124333907 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Methionine at position 24 (I24M)

Ref Sequence

ENSEMBL: ENSMUSP00000108156 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000112537]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000112537
AA Change: I24M

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)

SMART Domains

Protein: ENSMUSP00000108156
Gene: ENSMUSG00000079346
AA Change: I24M

Domain	Start	End	E-Value	Type
transmembrane domain	15	37	N/A	INTRINSIC
low complexity region	83	98	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000203817

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 35 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ano5	G	A	7: 51,220,071 (GRCm39)	D390N	probably damaging	Het
Atp2c2	A	G	8: 120,471,073 (GRCm39)	Y407C	probably damaging	Het
B430306N03Rik	T	C	17: 48,631,223 (GRCm39)		probably benign	Het
Cd44	A	T	2: 102,676,858 (GRCm39)	M269K	probably benign	Het
Cdin1	T	C	2: 115,469,547 (GRCm39)		probably null	Het
Cpped1	G	T	16: 11,646,392 (GRCm39)	P144Q	probably damaging	Het
Epas1	C	T	17: 87,135,275 (GRCm39)	T636M	possibly damaging	Het
Hsd17b3	G	T	13: 64,236,865 (GRCm39)	H26Q	probably benign	Het
Ighv8-9	A	G	12: 115,431,947 (GRCm39)		probably benign	Het
Itih1	A	T	14: 30,651,544 (GRCm39)	C883S	probably damaging	Het
Krt16	A	T	11: 100,137,162 (GRCm39)		probably benign	Het
Lcn3	A	T	2: 25,656,172 (GRCm39)	M76L	probably benign	Het
Lin9	A	T	1: 180,478,399 (GRCm39)	M53L	probably benign	Het
Mast1	A	G	8: 85,645,384 (GRCm39)	V687A	possibly damaging	Het
Mmd2	C	T	5: 142,555,212 (GRCm39)		probably benign	Het
Mroh2b	T	C	15: 4,953,123 (GRCm39)	L619S	probably damaging	Het
Ngef	T	C	1: 87,468,418 (GRCm39)	T114A	probably benign	Het
Nlrp12	T	C	7: 3,289,597 (GRCm39)	D305G	possibly damaging	Het
Nlrp1a	A	T	11: 71,013,944 (GRCm39)	F435L	possibly damaging	Het
Nup188	A	G	2: 30,220,653 (GRCm39)	I909V	possibly damaging	Het
Osbpl3	A	C	6: 50,304,347 (GRCm39)		probably benign	Het
P2ry2	G	T	7: 100,647,321 (GRCm39)	P328H	possibly damaging	Het
Prex2	A	T	1: 11,131,569 (GRCm39)	N46I	probably benign	Het
Prss42	T	C	9: 110,632,243 (GRCm39)	F325L	possibly damaging	Het
Reep5	A	G	18: 34,482,850 (GRCm39)	F120L	probably damaging	Het
Scg3	G	T	9: 75,590,939 (GRCm39)	F23L	probably damaging	Het
Scx	A	G	15: 76,343,295 (GRCm39)	D200G	probably benign	Het
Setd5	C	T	6: 113,098,131 (GRCm39)		probably benign	Het
Tcf4	T	A	18: 69,480,438 (GRCm39)	S23R	probably damaging	Het
Ttc4	A	G	4: 106,533,793 (GRCm39)		probably null	Het
Tyro3	T	A	2: 119,643,071 (GRCm39)	C627S	probably benign	Het
Yipf2	T	C	9: 21,502,764 (GRCm39)	N106S	possibly damaging	Het
Zfp619	T	C	7: 39,186,334 (GRCm39)	L788P	probably benign	Het
Zfp831	G	A	2: 174,485,519 (GRCm39)	V65I	probably benign	Het
Zgpat	T	C	2: 181,020,651 (GRCm39)	S275P	probably benign	Het

Other mutations in 1700013D24Rik

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL03369:1700013D24Rik	APN	6	124,333,380 (GRCm39)	missense	possibly damaging	0.66
R0760:1700013D24Rik	UTSW	6	124,324,661 (GRCm39)	missense	possibly damaging	0.46
R1984:1700013D24Rik	UTSW	6	124,324,778 (GRCm39)	missense	probably damaging	0.99
R2146:1700013D24Rik	UTSW	6	124,324,803 (GRCm39)	splice site	probably null
R4035:1700013D24Rik	UTSW	6	124,333,879 (GRCm39)	missense	probably benign	0.27
R4119:1700013D24Rik	UTSW	6	124,333,863 (GRCm39)	missense	probably damaging	0.97
R6502:1700013D24Rik	UTSW	6	124,333,908 (GRCm39)	missense	probably benign	0.12
R8425:1700013D24Rik	UTSW	6	124,324,745 (GRCm39)	missense	possibly damaging	0.82
R9179:1700013D24Rik	UTSW	6	124,333,882 (GRCm39)	missense	probably benign	0.01

Posted On

2015-04-16