Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02214:9430097D07Rik'

284799

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

9430097D07Rik

Ensembl Gene

ENSMUSG00000075405

Gene Name

RIKEN cDNA 9430097D07 gene

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.108) question?

Stock #

IGL02214

Quality Score

Status

Chromosome

Chromosomal Location

32464196-32465696 bp(-) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

T to C at 32464736 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000124665 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000028151] [ENSMUST00000048375] [ENSMUST00000055304] [ENSMUST00000100188] [ENSMUST00000100190] [ENSMUST00000140592]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000028151

SMART Domains

Protein: ENSMUSP00000028151
Gene: ENSMUSG00000026810

Domain	Start	End	E-Value	Type
Pfam:DPM2	5	80	4.2e-35	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000048375

SMART Domains

Protein: ENSMUSP00000044731
Gene: ENSMUSG00000039157

Domain	Start	End	E-Value	Type
Pfam:NT-C2	6	152	4.8e-32	PFAM
low complexity region	177	194	N/A	INTRINSIC
low complexity region	262	273	N/A	INTRINSIC
low complexity region	283	309	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000055304

SMART Domains

Protein: ENSMUSP00000051282
Gene: ENSMUSG00000046854

Domain	Start	End	E-Value	Type
Pfam:PIP5K	127	393	4.2e-62	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000100188

SMART Domains

Protein: ENSMUSP00000097763
Gene: ENSMUSG00000046854

Domain	Start	End	E-Value	Type
Pfam:PIP5K	165	358	4.3e-49	PFAM

Predicted Effect

unknown
Transcript: ENSMUST00000100190
AA Change: Y21C

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000128039

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000134204

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000150419

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000136816

Predicted Effect

probably benign
Transcript: ENSMUST00000140592

SMART Domains

Protein: ENSMUSP00000124665
Gene: ENSMUSG00000026810

Domain	Start	End	E-Value	Type
Pfam:DPM2	5	68	3e-30	PFAM

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
A330008L17Rik	T	A	8: 100,148,390 (GRCm39)		noncoding transcript	Het
A930004D18Rik	A	G	2: 18,032,067 (GRCm39)	L17P	unknown	Het
Abca14	A	T	7: 119,893,398 (GRCm39)	M1283L	probably benign	Het
Adarb1	A	T	10: 77,158,135 (GRCm39)	V104E	probably damaging	Het
Ano1	T	A	7: 144,209,445 (GRCm39)	N252Y	possibly damaging	Het
Atp6v0a1	A	G	11: 100,930,666 (GRCm39)	S498G	probably benign	Het
Bdp1	A	G	13: 100,178,043 (GRCm39)	V1942A	probably benign	Het
Carf	T	A	1: 60,187,240 (GRCm39)	D579E	probably damaging	Het
Cltc	A	T	11: 86,623,412 (GRCm39)	S200R	probably benign	Het
Cpeb1	T	C	7: 81,021,805 (GRCm39)	S113G	possibly damaging	Het
Csgalnact1	C	A	8: 68,854,144 (GRCm39)	G219V	probably damaging	Het
Ehd3	T	A	17: 74,127,541 (GRCm39)	L158H	probably damaging	Het
Etfa	C	A	9: 55,372,095 (GRCm39)	G289W	probably damaging	Het
Fndc3c1	G	A	X: 105,469,435 (GRCm39)	T1029I	probably benign	Het
Gipr	C	A	7: 18,891,471 (GRCm39)	G402V	possibly damaging	Het
Hacd1	C	T	2: 14,031,758 (GRCm39)	V242M	probably damaging	Het
Hecw1	A	G	13: 14,474,978 (GRCm39)	L520P	probably damaging	Het
Ibtk	A	T	9: 85,596,232 (GRCm39)		probably benign	Het
Igkv16-104	A	C	6: 68,402,778 (GRCm39)	I24L	probably benign	Het
Kcnh8	A	T	17: 53,184,939 (GRCm39)	Y407F	possibly damaging	Het
Mansc1	C	T	6: 134,587,323 (GRCm39)	V285M	probably benign	Het
Mindy4	A	G	6: 55,193,636 (GRCm39)	R110G	possibly damaging	Het
Morn1	C	T	4: 155,176,776 (GRCm39)	H100Y	probably damaging	Het
Naip6	A	T	13: 100,452,567 (GRCm39)	S165T	probably damaging	Het
Or13a24	A	T	7: 140,154,470 (GRCm39)	R135*	probably null	Het
Or5aq1	T	G	2: 86,965,849 (GRCm39)	K272T	probably damaging	Het
Prx	G	T	7: 27,218,337 (GRCm39)	R946M	probably damaging	Het
Ptchd1	A	G	X: 154,356,706 (GRCm39)	V833A	possibly damaging	Het
Rgl2	A	G	17: 34,154,163 (GRCm39)	D481G	probably benign	Het
Serpinb3a	A	G	1: 106,976,218 (GRCm39)		probably null	Het
Shtn1	T	C	19: 58,988,318 (GRCm39)		probably benign	Het
Slco1a7	T	A	6: 141,668,911 (GRCm39)	D507V	possibly damaging	Het
Sult1b1	C	T	5: 87,682,949 (GRCm39)		probably benign	Het
Tbl3	T	C	17: 24,923,106 (GRCm39)		probably benign	Het
Trappc9	C	T	15: 72,884,731 (GRCm39)	W416*	probably null	Het
Ubr4	T	C	4: 139,155,894 (GRCm39)	Y2240H	possibly damaging	Het
Ubr4	G	A	4: 139,189,138 (GRCm39)		probably null	Het
Vmn2r76	A	C	7: 85,879,138 (GRCm39)	F387L	probably benign	Het
Vps8	G	A	16: 21,336,035 (GRCm39)	C729Y	probably damaging	Het

Other mutations in 9430097D07Rik

Allele	Source	Chr	Coord	Type	Predicted Effect
R0356:9430097D07Rik	UTSW	2	32,464,418 (GRCm39)	unclassified	probably benign
R1776:9430097D07Rik	UTSW	2	32,464,767 (GRCm39)	unclassified	probably benign
R4525:9430097D07Rik	UTSW	2	32,464,388 (GRCm39)	unclassified	probably benign
R4886:9430097D07Rik	UTSW	2	32,464,630 (GRCm39)	unclassified	probably benign
R5010:9430097D07Rik	UTSW	2	32,464,440 (GRCm39)	unclassified	probably benign
R5613:9430097D07Rik	UTSW	2	32,465,346 (GRCm39)	unclassified	probably benign
R7059:9430097D07Rik	UTSW	2	32,464,509 (GRCm39)	unclassified	probably benign
R7919:9430097D07Rik	UTSW	2	32,464,461 (GRCm39)	missense	unknown
R7977:9430097D07Rik	UTSW	2	32,464,317 (GRCm39)	missense	unknown
R7987:9430097D07Rik	UTSW	2	32,464,317 (GRCm39)	missense	unknown
R9287:9430097D07Rik	UTSW	2	32,465,178 (GRCm39)	unclassified	probably benign
R9718:9430097D07Rik	UTSW	2	32,465,247 (GRCm39)	unclassified	probably benign

Posted On

2015-04-16