Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03007:A830031A19Rik'

407611

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

A830031A19Rik

Ensembl Gene

ENSMUSG00000055010

Gene Name

RIKEN cDNA A830031A19 gene

Synonyms

LOC268391

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.249) question?

Stock #

IGL03007

Quality Score

Status

Chromosome

Chromosomal Location

23998955-24025054 bp(-) (GRCm39)

Type of Mutation

utr 3 prime

DNA Base Change (assembly)

T to C at 23999248 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000063283 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000068360]

AlphaFold

Q8BNT5

Predicted Effect

probably benign
Transcript: ENSMUST00000068360

SMART Domains

Protein: ENSMUSP00000063283
Gene: ENSMUSG00000055010

Domain	Start	End	E-Value	Type
low complexity region	42	57	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 35 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
9330159F19Rik	A	G	10: 29,098,034 (GRCm39)	N144D	possibly damaging	Het
Ankfy1	T	C	11: 72,641,347 (GRCm39)	F640S	probably damaging	Het
Asb8	A	G	15: 98,040,615 (GRCm39)	Y16H	probably damaging	Het
Astn1	T	C	1: 158,496,193 (GRCm39)		probably benign	Het
Btbd8	T	A	5: 107,651,542 (GRCm39)	V145E	probably benign	Het
Celf3	A	G	3: 94,394,444 (GRCm39)	T183A	probably benign	Het
Dctn1	T	C	6: 83,159,690 (GRCm39)	V56A	probably damaging	Het
Erbb2	A	C	11: 98,319,819 (GRCm39)		probably benign	Het
Ighv6-4	A	T	12: 114,370,213 (GRCm39)	Y80N	possibly damaging	Het
Igsf9b	T	C	9: 27,244,378 (GRCm39)	S782P	probably damaging	Het
Itsn1	A	T	16: 91,581,050 (GRCm39)		probably benign	Het
Kcnt2	T	A	1: 140,282,245 (GRCm39)	Y77N	possibly damaging	Het
Lig3	T	C	11: 82,680,401 (GRCm39)	F359S	probably damaging	Het
Mtmr6	G	T	14: 60,526,984 (GRCm39)		probably benign	Het
Muc4	C	T	16: 32,570,866 (GRCm39)	S642F	possibly damaging	Het
Ncoa1	T	A	12: 4,389,114 (GRCm39)	I54F	possibly damaging	Het
Nfx1	C	A	4: 40,984,962 (GRCm39)	T362K	probably benign	Het
Ntrk1	T	C	3: 87,690,050 (GRCm39)	S449G	possibly damaging	Het
Odc1	T	A	12: 17,598,811 (GRCm39)	H230Q	probably benign	Het
Or10d4	T	C	9: 39,580,767 (GRCm39)	V138A	possibly damaging	Het
Or10h28	A	G	17: 33,487,857 (GRCm39)	E53G	probably damaging	Het
Or1j19	T	C	2: 36,676,812 (GRCm39)	S92P	probably damaging	Het
Or8d1	C	T	9: 38,766,592 (GRCm39)	T78I	probably damaging	Het
Plekhh2	A	C	17: 84,882,388 (GRCm39)	S665R	possibly damaging	Het
Qpct	T	A	17: 79,378,294 (GRCm39)	F155I	probably damaging	Het
Rcor2	C	A	19: 7,251,718 (GRCm39)	T379K	probably benign	Het
Rint1	A	G	5: 24,020,699 (GRCm39)	N574S	probably benign	Het
Rsbn1	C	T	3: 103,836,195 (GRCm39)	A411V	probably damaging	Het
Sbno2	A	T	10: 79,894,384 (GRCm39)		probably benign	Het
Sptb	A	G	12: 76,668,115 (GRCm39)	S661P	probably damaging	Het
Syn3	A	T	10: 85,900,778 (GRCm39)	M370K	possibly damaging	Het
Tex101	G	A	7: 24,369,906 (GRCm39)		probably benign	Het
Tmem255b	C	T	8: 13,507,066 (GRCm39)	T265I	possibly damaging	Het
Trio	G	T	15: 27,902,828 (GRCm39)	A211D	probably damaging	Het
Zfp638	C	A	6: 83,961,866 (GRCm39)	Q1902K	probably damaging	Het

Other mutations in A830031A19Rik

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R1019:A830031A19Rik	UTSW	11	23,999,438 (GRCm39)	missense	unknown
R5524:A830031A19Rik	UTSW	11	24,008,776 (GRCm39)	missense	unknown

Posted On

2016-08-02