Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02824:9530002B09Rik'

361147

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

9530002B09Rik

Ensembl Gene

ENSMUSG00000023263

Gene Name

RIKEN cDNA 9530002B09 gene

Synonyms

Aump, Vpp1

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.083) question?

Stock #

IGL02824

Quality Score

Status

Chromosome

Chromosomal Location

122583068-122598922 bp(+) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

T to C at 122596112 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000024032 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000024032]

AlphaFold

Q9EPV7

Predicted Effect

probably benign
Transcript: ENSMUST00000024032

SMART Domains

Protein: ENSMUSP00000024032
Gene: ENSMUSG00000023263

Domain	Start	End	E-Value	Type
signal peptide	1	21	N/A	INTRINSIC
Pfam:Palm_thioest	37	129	1.9e-8	PFAM

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
Aadat	A	T	8: 60,969,056 (GRCm39)	K93N	probably benign	Het
Abcb5	A	G	12: 118,854,420 (GRCm39)	F832L	probably benign	Het
Abl1	A	T	2: 31,690,831 (GRCm39)	K783N	probably damaging	Het
Agxt2	A	G	15: 10,393,891 (GRCm39)	E423G	probably null	Het
Alkbh8	T	C	9: 3,368,021 (GRCm39)		probably null	Het
Ankrd36	T	C	11: 5,524,246 (GRCm39)	I171T	possibly damaging	Het
Ap1b1	G	T	11: 4,983,738 (GRCm39)	A664S	possibly damaging	Het
Cd19	T	C	7: 126,009,826 (GRCm39)	D446G	probably damaging	Het
Ces1d	C	A	8: 93,896,346 (GRCm39)		probably null	Het
Cyp4f39	T	C	17: 32,687,659 (GRCm39)		probably null	Het
Ehbp1l1	T	C	19: 5,769,326 (GRCm39)	D659G	probably benign	Het
Eif3l	A	G	15: 78,960,023 (GRCm39)		probably null	Het
F5	T	C	1: 164,021,916 (GRCm39)	S1464P	probably benign	Het
Fut9	T	C	4: 25,620,037 (GRCm39)	N259S	probably damaging	Het
Glb1l3	A	T	9: 26,761,405 (GRCm39)	I209N	probably damaging	Het
Gpd2	A	G	2: 57,254,339 (GRCm39)	E671G	probably null	Het
Heatr5b	T	C	17: 79,081,109 (GRCm39)	D1381G	probably damaging	Het
Ifi206	A	T	1: 173,309,438 (GRCm39)	I186K	possibly damaging	Het
Izumo1	A	G	7: 45,275,072 (GRCm39)	D236G	probably benign	Het
Klhl32	T	A	4: 24,682,237 (GRCm39)	R149*	probably null	Het
Lrrn1	T	C	6: 107,545,495 (GRCm39)	F431S	possibly damaging	Het
Man2b2	C	T	5: 36,979,195 (GRCm39)	V282I	probably benign	Het
Mboat2	A	G	12: 24,996,585 (GRCm39)	K164R	probably benign	Het
Mgarp	T	C	3: 51,296,508 (GRCm39)	T165A	probably damaging	Het
Midn	T	G	10: 79,989,486 (GRCm39)	I43S	possibly damaging	Het
Ndn	A	G	7: 61,998,582 (GRCm39)	I143V	possibly damaging	Het
Or6c69	T	C	10: 129,747,565 (GRCm39)	E194G	probably damaging	Het
Or8h9	T	C	2: 86,789,337 (GRCm39)	D155G	probably benign	Het
Pcnx4	T	C	12: 72,602,345 (GRCm39)	V278A	probably benign	Het
Prr30	A	G	14: 101,435,954 (GRCm39)	F203L	probably benign	Het
Scd4	T	C	19: 44,329,698 (GRCm39)	L223P	probably damaging	Het
Setdb1	T	C	3: 95,247,215 (GRCm39)		probably benign	Het
Smtn	A	G	11: 3,482,658 (GRCm39)	Y105H	probably damaging	Het
Spata19	A	G	9: 27,309,025 (GRCm39)	I54M	possibly damaging	Het
Syk	A	T	13: 52,777,319 (GRCm39)		probably benign	Het
Trim44	A	G	2: 102,230,540 (GRCm39)	F164L	possibly damaging	Het
Zfp503	C	T	14: 22,035,162 (GRCm39)	G585S	possibly damaging	Het

Other mutations in 9530002B09Rik

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
F5770:9530002B09Rik	UTSW	4	122,595,050 (GRCm39)	missense	possibly damaging	0.71
R0391:9530002B09Rik	UTSW	4	122,594,970 (GRCm39)	splice site	probably benign
R0553:9530002B09Rik	UTSW	4	122,596,128 (GRCm39)	missense	unknown
R2063:9530002B09Rik	UTSW	4	122,583,115 (GRCm39)	start gained	probably benign
R2064:9530002B09Rik	UTSW	4	122,583,115 (GRCm39)	start gained	probably benign
R2065:9530002B09Rik	UTSW	4	122,583,115 (GRCm39)	start gained	probably benign
R2066:9530002B09Rik	UTSW	4	122,583,115 (GRCm39)	start gained	probably benign
R2067:9530002B09Rik	UTSW	4	122,583,115 (GRCm39)	start gained	probably benign
R2095:9530002B09Rik	UTSW	4	122,596,151 (GRCm39)	nonsense	probably null
R2146:9530002B09Rik	UTSW	4	122,583,198 (GRCm39)	nonsense	probably null
R4584:9530002B09Rik	UTSW	4	122,594,979 (GRCm39)	missense	possibly damaging	0.84
R4965:9530002B09Rik	UTSW	4	122,594,285 (GRCm39)	missense	probably benign	0.05
R8844:9530002B09Rik	UTSW	4	122,595,011 (GRCm39)	missense	possibly damaging	0.71
R9532:9530002B09Rik	UTSW	4	122,596,133 (GRCm39)	missense	unknown
V7581:9530002B09Rik	UTSW	4	122,595,050 (GRCm39)	missense	possibly damaging	0.71
V7582:9530002B09Rik	UTSW	4	122,595,050 (GRCm39)	missense	possibly damaging	0.71
V7583:9530002B09Rik	UTSW	4	122,595,050 (GRCm39)	missense	possibly damaging	0.71

Posted On

2015-12-18