Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02132:4921513I03Rik'

281027

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

4921513I03Rik

Ensembl Gene

ENSMUSG00000044544

Gene Name

RIKEN cDNA 4921513I03 gene

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL02132

Quality Score

Status

Chromosome

Chromosomal Location

120601637-120614791 bp(+) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

G to A at 120614635 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000089781 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000092143]

AlphaFold

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000056994

SMART Domains

Protein: ENSMUSP00000059458
Gene: ENSMUSG00000044544

Domain	Start	End	E-Value	Type
low complexity region	62	74	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000092143

SMART Domains

Protein: ENSMUSP00000089781
Gene: ENSMUSG00000051236

Domain	Start	End	E-Value	Type
Pfam:SelR	41	161	1.9e-56	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000219219

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 37 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930432E11Rik	C	T	7: 29,262,704 (GRCm39)		noncoding transcript	Het
Adcy10	T	C	1: 165,400,112 (GRCm39)	V1507A	probably damaging	Het
Ap3b2	T	A	7: 81,110,746 (GRCm39)	M1010L	unknown	Het
Bmp10	T	C	6: 87,411,130 (GRCm39)	S308P	probably benign	Het
Cnih3	C	A	1: 181,282,274 (GRCm39)	Y169*	probably null	Het
Cpsf4l	A	G	11: 113,590,685 (GRCm39)	S222P	possibly damaging	Het
Cyp2d10	G	A	15: 82,288,808 (GRCm39)		probably benign	Het
Dcstamp	A	T	15: 39,617,928 (GRCm39)	E112D	probably damaging	Het
Fras1	C	T	5: 96,929,496 (GRCm39)	Q3967*	probably null	Het
Gcm1	C	A	9: 77,972,121 (GRCm39)	P354H	possibly damaging	Het
Gen1	A	G	12: 11,291,867 (GRCm39)	S706P	probably benign	Het
Glb1l3	G	T	9: 26,736,466 (GRCm39)	T532N	probably benign	Het
Gm5069	T	A	1: 180,154,872 (GRCm39)		probably benign	Het
Gzmc	A	C	14: 56,471,422 (GRCm39)	F40V	probably benign	Het
Itgb2	G	T	10: 77,385,895 (GRCm39)	C286F	probably damaging	Het
Jak3	A	G	8: 72,131,124 (GRCm39)	Y48C	probably damaging	Het
Lrp2	G	A	2: 69,367,960 (GRCm39)	S184L	probably benign	Het
Myo1f	T	A	17: 33,798,945 (GRCm39)	N203K	probably benign	Het
Nrxn2	G	A	19: 6,522,306 (GRCm39)	G182R	probably damaging	Het
Or4k15c	T	C	14: 50,321,943 (GRCm39)	N65S	probably damaging	Het
Or4p8	A	G	2: 88,727,503 (GRCm39)	V146A	probably benign	Het
Or5g23	A	C	2: 85,438,664 (GRCm39)	L197V	probably benign	Het
Otog	C	T	7: 45,954,903 (GRCm39)	S2692L	probably damaging	Het
Pde9a	C	T	17: 31,672,444 (GRCm39)	T34I	probably benign	Het
Phip	T	C	9: 82,763,394 (GRCm39)	T1295A	possibly damaging	Het
Pik3cb	A	G	9: 98,953,430 (GRCm39)	V451A	probably benign	Het
Psd2	T	G	18: 36,137,809 (GRCm39)		probably benign	Het
Pycr2	T	C	1: 180,733,762 (GRCm39)	I118T	probably damaging	Het
Rnf17	T	G	14: 56,658,623 (GRCm39)	M104R	probably benign	Het
Rp1l1	T	C	14: 64,266,259 (GRCm39)	V615A	probably benign	Het
Sel1l3	T	A	5: 53,327,747 (GRCm39)	R511W	possibly damaging	Het
Sis	T	C	3: 72,854,804 (GRCm39)	N478D	probably benign	Het
Trps1	T	A	15: 50,685,674 (GRCm39)	S584C	probably damaging	Het
Vmn2r124	T	C	17: 18,284,491 (GRCm39)		probably benign	Het
Vmn2r9	G	A	5: 108,991,502 (GRCm39)	L620F	probably damaging	Het
Zc3h13	T	C	14: 75,567,787 (GRCm39)	S1027P	probably benign	Het
Zfp644	A	T	5: 106,783,760 (GRCm39)	I929K	probably benign	Het

Other mutations in 4921513I03Rik

Allele	Source	Chr	Coord	Type	Predicted Effect
R0062:4921513I03Rik	UTSW	10	120,614,511 (GRCm39)	unclassified	probably benign
R0062:4921513I03Rik	UTSW	10	120,614,511 (GRCm39)	unclassified	probably benign
R1694:4921513I03Rik	UTSW	10	120,614,533 (GRCm39)	unclassified	probably benign
R5740:4921513I03Rik	UTSW	10	120,614,413 (GRCm39)	unclassified	probably benign
R5923:4921513I03Rik	UTSW	10	120,614,675 (GRCm39)	unclassified	probably benign
X0022:4921513I03Rik	UTSW	10	120,614,705 (GRCm39)	unclassified	probably benign

Posted On

2015-04-16