Mutagenetix > Incidental Mutation

Incidental Mutation 'R3825:6030468B19Rik'

275359

Institutional Source

Beutler Lab

Gene Symbol

6030468B19Rik

Ensembl Gene

ENSMUSG00000025573

Gene Name

RIKEN cDNA 6030468B19 gene

Synonyms

MMRRC Submission

040774-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.049) question?

Stock #

R3825 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

117688486-117698127 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 117693739 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Glutamic Acid at position 69 (K69E)

Ref Sequence

ENSEMBL: ENSMUSP00000101938 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000106331]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000106331
AA Change: K69E

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000101938
Gene: ENSMUSG00000025573
AA Change: K69E

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
Pfam:Ig_3	31	100	6.1e-5	PFAM
Pfam:Ig_3	120	195	1.2e-6	PFAM

Meta Mutation Damage Score

0.2944

Coding Region Coverage

1x: 99.2%
3x: 98.7%
10x: 97.6%
20x: 96.0%

Validation Efficiency

98% (63/64)

MGI Phenotype

PHENOTYPE: No notable phenotype was detected in a high-throughput screen of homozygous null mice. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 62 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcb5	C	T	12: 118,865,087 (GRCm39)		probably null	Het
Acot1	G	T	12: 84,061,194 (GRCm39)	G167*	probably null	Het
Agbl1	C	T	7: 76,069,715 (GRCm39)	H164Y	probably damaging	Het
Atp4b	T	C	8: 13,443,549 (GRCm39)	Y43C	probably damaging	Het
Bsn	T	C	9: 107,984,055 (GRCm39)	D3333G	unknown	Het
Ccdc27	A	C	4: 154,120,742 (GRCm39)	D351E	unknown	Het
Cd200r4	T	C	16: 44,641,313 (GRCm39)	F19L	probably benign	Het
Dbndd1	T	A	8: 124,236,731 (GRCm39)	I75F	probably damaging	Het
Dennd5b	T	C	6: 148,946,334 (GRCm39)	K426E	probably benign	Het
Drg2	A	G	11: 60,350,334 (GRCm39)	T98A	possibly damaging	Het
Fabp3	C	T	4: 130,206,245 (GRCm39)		probably null	Het
Fmo1	T	C	1: 162,678,916 (GRCm39)		probably benign	Het
Foxn2	A	T	17: 88,791,837 (GRCm39)	I236F	probably damaging	Het
Glmp	G	A	3: 88,233,718 (GRCm39)	V107I	probably damaging	Het
Gpr15	A	G	16: 58,538,723 (GRCm39)	F122S	probably damaging	Het
Gvin-ps3	T	C	7: 105,682,780 (GRCm39)	I158M	possibly damaging	Het
Hmcn1	A	T	1: 150,462,716 (GRCm39)	D5140E	probably benign	Het
Hspa1a	C	T	17: 35,190,703 (GRCm39)	V67M	probably damaging	Het
Igfbp4	A	G	11: 98,939,061 (GRCm39)	E27G	probably damaging	Het
Il7	A	G	3: 7,642,226 (GRCm39)		probably benign	Het
Kat6a	G	T	8: 23,352,380 (GRCm39)	V55F	probably damaging	Het
Kynu	A	G	2: 43,571,451 (GRCm39)	T456A	probably benign	Het
Lcorl	A	G	5: 45,932,729 (GRCm39)		probably benign	Het
Lrp5	G	A	19: 3,655,290 (GRCm39)	R1077*	probably null	Het
Mab21l2	T	C	3: 86,454,211 (GRCm39)	E263G	possibly damaging	Het
Macf1	T	A	4: 123,338,744 (GRCm39)	D1436V	probably benign	Het
Map4k2	C	A	19: 6,394,081 (GRCm39)	T252N	probably benign	Het
Mterf2	A	T	10: 84,956,147 (GRCm39)	L159Q	probably damaging	Het
Muc5ac	C	A	7: 141,368,460 (GRCm39)	T3063K	possibly damaging	Het
Myo18a	T	A	11: 77,668,292 (GRCm39)	S51T	possibly damaging	Het
Ncoa3	G	T	2: 165,896,718 (GRCm39)	G503V	possibly damaging	Het
Ncor1	A	T	11: 62,264,183 (GRCm39)	H406Q	probably benign	Het
Nectin2	T	C	7: 19,458,510 (GRCm39)	K434E	possibly damaging	Het
Nipal2	A	T	15: 34,578,852 (GRCm39)		probably null	Het
Nub1	G	C	5: 24,912,851 (GRCm39)	S517T	probably benign	Het
Or10a4	T	C	7: 106,696,816 (GRCm39)	L48P	possibly damaging	Het
Or4d10c	A	G	19: 12,065,391 (GRCm39)	V255A	probably damaging	Het
Or8b101	A	T	9: 38,020,134 (GRCm39)	I51F	possibly damaging	Het
Or8c17	T	G	9: 38,179,814 (GRCm39)	S2A	probably benign	Het
Plscr3	G	A	11: 69,740,964 (GRCm39)	V267M	probably benign	Het
Plxnb2	G	T	15: 89,050,602 (GRCm39)	N451K	probably benign	Het
Ppp2r2a	A	G	14: 67,259,892 (GRCm39)	L268P	probably damaging	Het
Ptprb	A	T	10: 116,186,694 (GRCm39)	I1743F	probably benign	Het
Rack1	A	G	11: 48,693,131 (GRCm39)	T105A	probably benign	Het
Rhot1	G	A	11: 80,116,907 (GRCm39)	V94I	probably damaging	Het
Rin2	C	T	2: 145,702,366 (GRCm39)	T354I	probably benign	Het
Smc6	T	A	12: 11,351,517 (GRCm39)		probably benign	Het
Spink8	T	A	9: 109,645,861 (GRCm39)	V11D	probably damaging	Het
Ss18l1	A	T	2: 179,705,103 (GRCm39)	Q365L	unknown	Het
Tbc1d31	T	A	15: 57,779,474 (GRCm39)	H62Q	probably benign	Het
Tbc1d9b	T	C	11: 50,061,954 (GRCm39)	V1171A	possibly damaging	Het
Tln1	G	A	4: 43,536,413 (GRCm39)		probably benign	Het
Tmem220	G	A	11: 66,916,077 (GRCm39)	A25T	possibly damaging	Het
Tmem259	T	C	10: 79,814,282 (GRCm39)	N334S	possibly damaging	Het
Tmod3	A	T	9: 75,414,809 (GRCm39)		probably benign	Het
Tmprss2	A	T	16: 97,398,021 (GRCm39)	Y52N	probably damaging	Het
Tsga10	A	T	1: 37,873,278 (GRCm39)	N200K	possibly damaging	Het
Ube2frt	T	C	12: 36,141,036 (GRCm39)		probably benign	Het
Vmn1r189	T	A	13: 22,286,382 (GRCm39)	T152S	probably benign	Het
Vmn2r76	C	T	7: 85,880,415 (GRCm39)	M90I	probably benign	Het
Zfr	C	T	15: 12,166,277 (GRCm39)	A849V	probably damaging	Het
Znhit6	T	C	3: 145,284,099 (GRCm39)	M95T	probably benign	Het

Other mutations in 6030468B19Rik

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02168:6030468B19Rik	APN	11	117,689,244 (GRCm39)	splice site	probably benign
IGL03388:6030468B19Rik	APN	11	117,693,596 (GRCm39)	splice site	probably benign
PIT4434001:6030468B19Rik	UTSW	11	117,696,869 (GRCm39)	missense	probably benign	0.01
R0477:6030468B19Rik	UTSW	11	117,693,787 (GRCm39)	missense	probably benign	0.00
R3824:6030468B19Rik	UTSW	11	117,693,739 (GRCm39)	missense	probably damaging	0.99
R4114:6030468B19Rik	UTSW	11	117,693,793 (GRCm39)	missense	probably damaging	1.00
R4283:6030468B19Rik	UTSW	11	117,697,087 (GRCm39)	missense	probably benign	0.01
R4779:6030468B19Rik	UTSW	11	117,696,834 (GRCm39)	missense	probably benign	0.14
R4916:6030468B19Rik	UTSW	11	117,697,092 (GRCm39)	nonsense	probably null
R5068:6030468B19Rik	UTSW	11	117,693,701 (GRCm39)	missense	possibly damaging	0.85
R5725:6030468B19Rik	UTSW	11	117,696,883 (GRCm39)	missense	probably damaging	0.98
R6139:6030468B19Rik	UTSW	11	117,697,150 (GRCm39)	missense	probably damaging	0.98
R6992:6030468B19Rik	UTSW	11	117,688,594 (GRCm39)	start codon destroyed	probably null
R7157:6030468B19Rik	UTSW	11	117,693,780 (GRCm39)	missense	probably damaging	0.98
R8757:6030468B19Rik	UTSW	11	117,697,112 (GRCm39)	missense	probably benign	0.01
R8759:6030468B19Rik	UTSW	11	117,697,112 (GRCm39)	missense	probably benign	0.01

Predicted Primers

PCR Primer
(F):5'- AACCTGGAGTTTCTTTTAGGCG -3'
(R):5'- GCAAACAGTCTGCCCTTGTC -3'

Sequencing Primer
(F):5'- CTTTTAGGCGTCTGATTGGC -3'
(R):5'- AAACAGTCTGCCCTTGTCCACTC -3'

Posted On

2015-04-02