Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01955:4930432E11Rik'

181421

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

4930432E11Rik

Ensembl Gene

ENSMUSG00000046958

Gene Name

RIKEN cDNA 4930432E11 gene

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.082) question?

Stock #

IGL01955

Quality Score

Status

Chromosome

Chromosomal Location

29255998-29276204 bp(+) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

G to T at 29273420 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s):

AlphaFold

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000053635

SMART Domains

Protein: ENSMUSP00000049518
Gene: ENSMUSG00000046958

Domain	Start	End	E-Value	Type
Blast:WD40	43	79	3e-11	BLAST
WD40	131	172	1.97e2	SMART
WD40	175	214	2.24e-2	SMART
Blast:WD40	257	296	4e-15	BLAST
WD40	393	437	1.32e2	SMART
WD40	494	533	2.15e-4	SMART
low complexity region	598	617	N/A	INTRINSIC
low complexity region	1082	1094	N/A	INTRINSIC
low complexity region	1107	1148	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000063585

SMART Domains

Protein: ENSMUSP00000063695
Gene: ENSMUSG00000051976

Domain	Start	End	E-Value	Type
low complexity region	15	28	N/A	INTRINSIC
internal_repeat_1	35	67	3.29e-5	PROSPERO
internal_repeat_1	73	102	3.29e-5	PROSPERO
low complexity region	122	135	N/A	INTRINSIC
coiled coil region	161	182	N/A	INTRINSIC
low complexity region	216	233	N/A	INTRINSIC
low complexity region	239	249	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000187265

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 39 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc1	T	A	16: 14,228,659 (GRCm39)	I302N	probably damaging	Het
Abhd16a	A	G	17: 35,320,316 (GRCm39)	S394G	probably damaging	Het
Adgrv1	T	C	13: 81,330,902 (GRCm39)	Y71C	probably damaging	Het
Apol8	A	G	15: 77,633,899 (GRCm39)	C226R	probably benign	Het
Bbs7	A	G	3: 36,664,471 (GRCm39)	S45P	probably benign	Het
Cacna1b	T	C	2: 24,529,149 (GRCm39)	Y1575C	probably damaging	Het
Cckbr	T	A	7: 105,084,169 (GRCm39)	V301E	probably damaging	Het
Cwc27	A	G	13: 104,944,245 (GRCm39)	Y79H	probably damaging	Het
Dchs1	T	C	7: 105,406,798 (GRCm39)	T2236A	probably benign	Het
Ddx50	T	C	10: 62,482,962 (GRCm39)	R36G	probably benign	Het
Extl3	T	A	14: 65,313,415 (GRCm39)	Y589F	probably benign	Het
Gab2	T	C	7: 96,953,430 (GRCm39)	V601A	probably damaging	Het
Hsd3b1	T	A	3: 98,760,463 (GRCm39)	N176I	probably benign	Het
L3mbtl3	A	T	10: 26,194,336 (GRCm39)	S420R	unknown	Het
Odad2	C	T	18: 7,127,291 (GRCm39)	R974Q	possibly damaging	Het
Or2ak6	T	C	11: 58,592,955 (GRCm39)	S143P	probably damaging	Het
Or52e2	T	A	7: 102,804,061 (GRCm39)	K298*	probably null	Het
Or5g23	A	G	2: 85,439,051 (GRCm39)	F68L	probably benign	Het
Polr2a	T	C	11: 69,632,674 (GRCm39)	D974G	probably damaging	Het
Ptges3l	T	C	11: 101,314,644 (GRCm39)	K13E	possibly damaging	Het
Ptprk	A	G	10: 28,471,861 (GRCm39)		probably benign	Het
Rassf3	T	C	10: 121,253,027 (GRCm39)	Y60C	probably damaging	Het
Rnf157	T	C	11: 116,250,722 (GRCm39)	T160A	probably damaging	Het
Secisbp2l	A	G	2: 125,585,732 (GRCm39)		probably null	Het
Setd2	A	G	9: 110,378,386 (GRCm39)	T734A	probably benign	Het
Skint5	A	G	4: 113,480,933 (GRCm39)		probably null	Het
Slc38a9	A	G	13: 112,831,952 (GRCm39)		probably benign	Het
Snx17	T	G	5: 31,354,426 (GRCm39)		probably benign	Het
Tas2r113	A	T	6: 132,870,817 (GRCm39)	M282L	probably benign	Het
Tbc1d31	A	G	15: 57,805,766 (GRCm39)	N404D	probably benign	Het
Tmem63c	A	T	12: 87,123,982 (GRCm39)	I487F	probably benign	Het
Tpm3	A	G	3: 89,995,742 (GRCm39)	M164V	probably benign	Het
Trafd1	G	T	5: 121,513,217 (GRCm39)	N340K	probably benign	Het
Trpv4	T	A	5: 114,760,743 (GRCm39)	K863*	probably null	Het
Ttn	A	T	2: 76,627,696 (GRCm39)	M13003K	possibly damaging	Het
Tulp1	G	A	17: 28,575,398 (GRCm39)	T103M	probably damaging	Het
Unc5b	T	C	10: 60,614,034 (GRCm39)	T272A	probably benign	Het
Vmn1r82	A	C	7: 12,039,650 (GRCm39)		probably null	Het
Zc3h7b	A	G	15: 81,676,205 (GRCm39)	N704D	probably benign	Het

Other mutations in 4930432E11Rik

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01121:4930432E11Rik	APN	7	29,273,426 (GRCm39)	unclassified	noncoding transcript
IGL01971:4930432E11Rik	APN	7	29,273,987 (GRCm39)	unclassified	noncoding transcript
IGL02132:4930432E11Rik	APN	7	29,262,704 (GRCm39)	unclassified	noncoding transcript
IGL02484:4930432E11Rik	APN	7	29,262,777 (GRCm39)	unclassified	noncoding transcript
P0016:4930432E11Rik	UTSW	7	29,262,537 (GRCm39)	unclassified	noncoding transcript
R0051:4930432E11Rik	UTSW	7	29,278,526 (GRCm39)	exon	noncoding transcript
R0060:4930432E11Rik	UTSW	7	29,273,595 (GRCm39)	unclassified	noncoding transcript
R0094:4930432E11Rik	UTSW	7	29,260,236 (GRCm39)	exon	noncoding transcript
R0268:4930432E11Rik	UTSW	7	29,274,027 (GRCm39)	unclassified	noncoding transcript
R0423:4930432E11Rik	UTSW	7	29,261,825 (GRCm39)	exon	noncoding transcript
R0478:4930432E11Rik	UTSW	7	29,262,014 (GRCm39)	exon	noncoding transcript
R0646:4930432E11Rik	UTSW	7	29,260,710 (GRCm39)	exon	noncoding transcript
R1208:4930432E11Rik	UTSW	7	29,260,708 (GRCm39)	exon	noncoding transcript
R1778:4930432E11Rik	UTSW	7	29,260,131 (GRCm39)	exon	noncoding transcript
R1779:4930432E11Rik	UTSW	7	29,278,591 (GRCm39)	exon	noncoding transcript
R1918:4930432E11Rik	UTSW	7	29,273,514 (GRCm39)	unclassified	noncoding transcript
R2360:4930432E11Rik	UTSW	7	29,274,214 (GRCm39)	unclassified	noncoding transcript
R3736:4930432E11Rik	UTSW	7	29,273,996 (GRCm39)	unclassified	noncoding transcript
R3780:4930432E11Rik	UTSW	7	29,260,263 (GRCm39)	exon	noncoding transcript
R4427:4930432E11Rik	UTSW	7	29,278,678 (GRCm39)	exon	noncoding transcript
R4835:4930432E11Rik	UTSW	7	29,274,326 (GRCm39)	unclassified	noncoding transcript
R4929:4930432E11Rik	UTSW	7	29,273,467 (GRCm39)	unclassified	noncoding transcript
R5042:4930432E11Rik	UTSW	7	29,273,927 (GRCm39)	unclassified	noncoding transcript
R5129:4930432E11Rik	UTSW	7	29,260,786 (GRCm39)	exon	noncoding transcript
R5371:4930432E11Rik	UTSW	7	29,261,918 (GRCm39)	exon	noncoding transcript
R5381:4930432E11Rik	UTSW	7	29,262,393 (GRCm39)	unclassified	noncoding transcript
R5586:4930432E11Rik	UTSW	7	29,277,153 (GRCm39)	unclassified	noncoding transcript
R5874:4930432E11Rik	UTSW	7	29,280,610 (GRCm39)	exon	noncoding transcript

Posted On

2014-05-07