Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02598:4933414I15Rik'

299968

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

4933414I15Rik

Ensembl Gene

ENSMUSG00000072983

Gene Name

RIKEN cDNA 4933414I15 gene

Synonyms

ENSMUSG00000051192

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.087) question?

Stock #

IGL02598

Quality Score

Status

Chromosome

Chromosomal Location

50940711-50943765 bp(-) (GRCm38)

Type of Mutation

start codon destroyed

DNA Base Change (assembly)

A to T at 50943621 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Lysine at position 1 (M1K)

Ref Sequence

ENSEMBL: ENSMUSP00000104751 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000109123]

AlphaFold

Q9D4D5

Predicted Effect

probably null
Transcript: ENSMUST00000109123
AA Change: M1K

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000156329

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca13	C	T	11: 9,431,898	T3850I	probably damaging	Het
Abcc4	A	T	14: 118,668,369	L95*	probably null	Het
Acacb	A	G	5: 114,246,037	Y2209C	probably damaging	Het
Acadm	A	G	3: 153,938,544		probably benign	Het
Arid2	G	A	15: 96,371,536	V1177M	probably damaging	Het
Atp8a1	A	T	5: 67,682,756		probably null	Het
BC048403	G	A	10: 121,739,971		probably benign	Het
Catsperd	A	G	17: 56,647,815		probably null	Het
Cd28	A	G	1: 60,763,339		probably benign	Het
Cep164	A	G	9: 45,770,704	Y1934H	probably damaging	Het
Cep350	T	C	1: 155,862,967	I2377V	probably benign	Het
Csmd3	T	C	15: 47,669,690	K1581E	probably damaging	Het
Dab2	A	T	15: 6,429,366	N232I	probably damaging	Het
Dyrk4	G	A	6: 126,884,019		probably benign	Het
Efcab14	T	A	4: 115,740,434	C75*	probably null	Het
Elovl1	T	C	4: 118,431,419		probably null	Het
Eps8l2	T	G	7: 141,354,936		probably benign	Het
Gm4907	A	T	X: 23,907,471	T404S	probably benign	Het
Grik1	A	T	16: 87,947,984	V460E	probably damaging	Het
Gtf2f2	A	G	14: 76,007,742	S35P	probably benign	Het
Ifi203	A	G	1: 173,935,002		probably benign	Het
Ifi209	T	C	1: 173,644,715	V374A	probably damaging	Het
Lars	A	G	18: 42,227,277	S705P	possibly damaging	Het
Lcmt1	A	G	7: 123,421,648		probably benign	Het
Limd1	T	A	9: 123,480,171	Y312N	probably benign	Het
Limd1	T	C	9: 123,516,868	S571P	probably benign	Het
Lin28b	A	T	10: 45,420,526	D125E	possibly damaging	Het
Lmtk3	T	C	7: 45,793,140	S416P	probably damaging	Het
Map7d3	T	C	X: 56,809,786	T446A	probably benign	Het
Masp1	T	A	16: 23,459,631	M523L	probably benign	Het
Mroh4	C	A	15: 74,611,243		probably null	Het
Mtmr6	G	A	14: 60,300,504	A651T	probably damaging	Het
Myocd	A	G	11: 65,183,470	S738P	probably benign	Het
Olfr1176	A	T	2: 88,340,251	I229F	possibly damaging	Het
Olfr685	A	G	7: 105,180,956	V134A	probably damaging	Het
Olfr714	A	T	7: 107,074,716	N296I	possibly damaging	Het
Olfr803	A	T	10: 129,691,273	I256N	possibly damaging	Het
Olfr984	A	T	9: 40,100,565	F308L	probably benign	Het
Parg	G	T	14: 32,214,324	V479L	probably damaging	Het
Pcdhb10	C	A	18: 37,413,781	H637N	possibly damaging	Het
Plekhg2	G	A	7: 28,360,475	T1118I	possibly damaging	Het
Podxl	T	C	6: 31,524,420	E400G	probably damaging	Het
Prss54	C	A	8: 95,565,709	V81F	probably damaging	Het
Pzp	A	G	6: 128,487,457	L1369P	probably benign	Het
Rfx8	A	T	1: 39,695,968		probably benign	Het
Rgs6	C	T	12: 83,091,797	P302S	probably benign	Het
Rnf148	A	C	6: 23,654,457	I180S	probably damaging	Het
Sacm1l	A	G	9: 123,578,996	D350G	probably benign	Het
Slc33a1	C	T	3: 63,943,332	G524S	probably benign	Het
Slc5a7	A	G	17: 54,284,193	V237A	probably benign	Het
Spink7	T	C	18: 62,594,285	D56G	probably damaging	Het
Syn3	A	G	10: 86,467,199	S31P	probably damaging	Het
Thrb	C	A	14: 18,008,606	P110Q	possibly damaging	Het
Vmn2r76	G	T	7: 86,228,671	T506K	probably benign	Het
Vps45	A	G	3: 96,031,042	L486P	probably benign	Het
Zan	G	A	5: 137,446,211	T1823M	unknown	Het
Zdhhc6	T	A	19: 55,314,527	Q14L	probably benign	Het
Zfp990	A	T	4: 145,536,963	N177I	possibly damaging	Het

Other mutations in 4933414I15Rik

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL02269:4933414I15Rik	APN	11	50942598	missense	unknown
BB010:4933414I15Rik	UTSW	11	50942400	missense	unknown
BB020:4933414I15Rik	UTSW	11	50942400	missense	unknown
R2384:4933414I15Rik	UTSW	11	50942506	missense	unknown
R5226:4933414I15Rik	UTSW	11	50942589	missense	unknown
R6514:4933414I15Rik	UTSW	11	50942742	missense	unknown
R7933:4933414I15Rik	UTSW	11	50942400	missense	unknown
R8219:4933414I15Rik	UTSW	11	50942536	missense	unknown
R8700:4933414I15Rik	UTSW	11	50942517	missense	unknown

Posted On

2015-04-16