Mutagenetix > Incidental Mutation

Incidental Mutation 'RF035:A030005L19Rik'

604510

Institutional Source

Beutler Lab

Gene Symbol

A030005L19Rik

Ensembl Gene

ENSMUSG00000113880

Gene Name

RIKEN cDNA A030005L19 gene

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

RF035 (G1)

Quality Score

217.468

Status

Not validated

Chromosome

Chromosomal Location

82891046-82891851 bp(+) (GRCm39)

Type of Mutation

small insertion (3 aa in frame mutation)

DNA Base Change (assembly)

T to TTTGGCTGCC at 82891310 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000152156 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000220768]

AlphaFold

A0A1Y7VIU2

Predicted Effect

probably benign
Transcript: ENSMUST00000220768

Coding Region Coverage

1x: 99.8%
3x: 99.7%
10x: 99.4%
20x: 98.7%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 52 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acap3	TGCATCCTGGGCTGC	TGCATCCTGGGCTGCCGCATCCTGGGCTGC	4: 155,989,548 (GRCm39)		probably benign	Het
AI837181	G	GGCT	19: 5,475,266 (GRCm39)		probably benign	Het
Amfr	GCC	GCCGGCGCGAGCTCC	8: 94,738,920 (GRCm39)		probably benign	Het
Amot	GGAGCAGCAA	G	X: 144,233,984 (GRCm39)		probably benign	Het
Bltp1	TAT	TATTATTATTATTATGAT	3: 37,104,907 (GRCm39)		probably benign	Het
Cacna1f	GAG	GAGTAG	X: 7,486,293 (GRCm39)		probably null	Het
Calhm1	CTGTGGCTGTGGCTGTGGCTGTGG	CTGTGGCTGTGGTTGTGGCTGTGGCTGTGGCTGTGG	19: 47,129,692 (GRCm39)		probably benign	Het
Chga	G	GCAT	12: 102,527,686 (GRCm39)		probably benign	Het
E4f1	CGC	CGCTGC	17: 24,674,164 (GRCm39)		probably benign	Het
E4f1	CCG	CCGGCG	17: 24,674,169 (GRCm39)		probably benign	Het
Eps8	C	CTCAG	6: 137,494,068 (GRCm39)		probably null	Het
Exd2	GCAGCCACAGCAGCCGCAGCAGCCGCAGCCACAGCCACAGCCACAGCCACAGCCACAGC	GCAGCCACAGC	12: 80,522,674 (GRCm39)		probably benign	Het
Exd2	CAGCCAGAGC	CAGC	12: 80,522,729 (GRCm39)		probably benign	Het
Gm10447	AAAAAAAAAGAAAAA	AAAAAA	11: 53,347,165 (GRCm39)		probably benign	Het
Gm10521	CTCTCTCTCT	CTCTCTCTCTCTCT	1: 171,723,860 (GRCm39)		probably null	Het
Gm8369	TGTG	TGTGCGAGTG	19: 11,489,137 (GRCm39)		probably benign	Het
Gucy1b2	CACACACACACACACACTTAC	CAC	14: 62,646,090 (GRCm39)		probably benign	Het
Ier5l	TTGCTGCTGCTGCTGCTG	TTGCTGCTGCTGCTG	2: 30,363,832 (GRCm39)		probably benign	Het
Kmt2b	TTCTCCT	TTCTCCTTCTCCT	7: 30,285,782 (GRCm39)		probably benign	Het
Krtap28-10	CAG	CAGCCAAAG	1: 83,019,867 (GRCm39)		probably benign	Het
Krtap28-10	CCACCACAGC	CCACCACAGCCACAGTCACCACAGC	1: 83,020,002 (GRCm39)		probably benign	Het
Lmx1b	TCCATCTTGATGCCGTCCAACATCTTGATGCCGTCCA	TACATCTTGATGCCGTCCA	2: 33,530,501 (GRCm39)		probably null	Het
Mamld1	GCAACA	GCAACAACA	X: 70,162,418 (GRCm39)		probably benign	Het
Mamld1	AGC	AGCGGC	X: 70,162,456 (GRCm39)		probably benign	Het
Mamld1	AGC	AGCCGC	X: 70,162,444 (GRCm39)		probably benign	Het
Manbal	CGATAGAAT	C	2: 157,237,932 (GRCm39)		probably null	Het
Map1a	GCTCCAGCTCCAGCTCCA	GCTCCAGCTCCAGCTCCAGCTCCAGCTCCATCTCCAGCTCCAGCTCCA	2: 121,136,782 (GRCm39)		probably benign	Het
Mcph1	CTCT	CTCTTCT	8: 18,702,541 (GRCm39)		probably benign	Het
Nefh	CCTCACCTGGGGACTTGG	CCTCACCTGGGGACTTGGGCTCACCTGGGGACTTGG	11: 4,891,039 (GRCm39)		probably benign	Het
Nusap1	GATACACGTTAGCAGTGAGGAGCAAGCTGA	GATACACGTTAGCAGTGAGGAGCAAGCTGATATACACGTTAGCAGTGAGGAGCAAGCTGA	2: 119,458,060 (GRCm39)		probably benign	Het
Or2t49	TGGAGGTGGATTGG	TG	11: 58,393,208 (GRCm39)		probably benign	Het
P4ha2	CCAGGTG	C	11: 54,001,061 (GRCm39)		probably benign	Het
Pdik1l	CCACCA	CCACCAACACCA	4: 134,006,821 (GRCm39)		probably benign	Het
Polr1has	CACCAC	CACCACCCCCACCACCACCACAACCAC	17: 37,275,958 (GRCm39)		probably benign	Het
Rassf6	GCCTCACTCATGGTCCTGTAGAGCAATGGGGATTC	GCCTCACTCATGGTCCTGTAGAGCAATGGGGATTCTTCCTCACTCATGGTCCTGTAGAGCAATGGGGATTC	5: 90,756,767 (GRCm39)		probably benign	Het
Rfx4	TCTCTCTCTCTCTCT	TCTCTCTCTCTCTCTCGCTCTCTCTCTCTCT	10: 84,694,344 (GRCm39)		probably benign	Het
Rgs22	GCTAAAAAAAAAAAAAAAAA	G	15: 36,010,981 (GRCm39)		probably benign	Het
Rpgrip1	AGG	AGGGGG	14: 52,386,850 (GRCm39)		probably benign	Het
Slc39a4	TGTGGTC	TGTGGTCATCATGATCACCATGGTCACCATGAGCACGGTGGTC	15: 76,499,066 (GRCm39)		probably benign	Het
Srpk2	ATCCT	AT	5: 23,730,573 (GRCm39)		probably benign	Het
Strn	AGTC	AGTCCGTGCTCCCTTACCCCAGTCCGTGCTCCCTTACCCCTGTC	17: 78,984,714 (GRCm39)		probably null	Het
Tcof1	AAGAT	AAGATTGGCCCTTTCCCAGAGATGCCCTTGGCTGCTGAGAT	18: 60,966,625 (GRCm39)		probably benign	Het
Tfeb	AGC	AGCCGC	17: 48,097,036 (GRCm39)		probably benign	Het
Tmem59	T	TGTTTGTTG	4: 107,047,729 (GRCm39)		probably benign	Het
Trav6d-5	ATTTTT	ATTTTTTTTTT	14: 53,032,791 (GRCm39)		probably benign	Het
Triobp	CAGGACTCCCTGTGCCCAACGG	CAGGACTCCCTGTGCCCAACGGAACAACCCAAGGACTCCCTGTGCCCAACGG	15: 78,851,239 (GRCm39)		probably benign	Het
Tsen2	GGA	GGATGA	6: 115,537,028 (GRCm39)		probably benign	Het
Ttf2	TTCT	TTCTTCT	3: 100,870,473 (GRCm39)		probably benign	Het
Vat1l	C	T	8: 115,016,069 (GRCm39)	L320F	probably damaging	Het
Xirp2	TT	TTTAT	2: 67,355,888 (GRCm39)		probably benign	Het
Yipf3	AGAGGA	AGA	17: 46,559,898 (GRCm39)		probably benign	Het
Zfp933	TT	TTTGCGT	4: 147,910,188 (GRCm39)		probably null	Het

Other mutations in A030005L19Rik

Allele	Source	Chr	Coord	Type	Predicted Effect
RF001:A030005L19Rik	UTSW	1	82,891,311 (GRCm39)	small insertion	probably benign
RF005:A030005L19Rik	UTSW	1	82,891,306 (GRCm39)	small insertion	probably benign
RF011:A030005L19Rik	UTSW	1	82,891,307 (GRCm39)	small insertion	probably benign
RF011:A030005L19Rik	UTSW	1	82,891,294 (GRCm39)	small insertion	probably benign
RF011:A030005L19Rik	UTSW	1	82,891,290 (GRCm39)	small insertion	probably benign
RF016:A030005L19Rik	UTSW	1	82,891,298 (GRCm39)	small insertion	probably benign
RF018:A030005L19Rik	UTSW	1	82,891,293 (GRCm39)	small insertion	probably benign
RF021:A030005L19Rik	UTSW	1	82,891,290 (GRCm39)	small insertion	probably benign
RF023:A030005L19Rik	UTSW	1	82,891,117 (GRCm39)	small deletion	probably benign
RF028:A030005L19Rik	UTSW	1	82,891,301 (GRCm39)	small insertion	probably benign
RF028:A030005L19Rik	UTSW	1	82,891,299 (GRCm39)	small insertion	probably benign
RF034:A030005L19Rik	UTSW	1	82,891,301 (GRCm39)	small insertion	probably benign
RF038:A030005L19Rik	UTSW	1	82,891,301 (GRCm39)	small insertion	probably benign
RF040:A030005L19Rik	UTSW	1	82,891,311 (GRCm39)	small insertion	probably benign
RF040:A030005L19Rik	UTSW	1	82,891,298 (GRCm39)	small insertion	probably benign
RF042:A030005L19Rik	UTSW	1	82,891,305 (GRCm39)	small insertion	probably benign
RF044:A030005L19Rik	UTSW	1	82,891,310 (GRCm39)	small insertion	probably benign
RF053:A030005L19Rik	UTSW	1	82,891,294 (GRCm39)	small insertion	probably benign
RF059:A030005L19Rik	UTSW	1	82,891,300 (GRCm39)	small insertion	probably benign
RF060:A030005L19Rik	UTSW	1	82,891,308 (GRCm39)	small insertion	probably benign
RF060:A030005L19Rik	UTSW	1	82,891,300 (GRCm39)	nonsense	probably null
RF060:A030005L19Rik	UTSW	1	82,891,117 (GRCm39)	small deletion	probably benign

Predicted Primers

PCR Primer
(F):5'- GTCCTCTCTACTGACAACATGG -3'
(R):5'- CAGTGTGGCCTCCATATCTC -3'

Sequencing Primer
(F):5'- CAACATGGGTTGCTGTGGC -3'
(R):5'- GGCCTCCATATCTCCTAGGTAGG -3'

Posted On

2019-12-04