Mutagenetix > Incidental Mutation

Incidental Mutation 'R5243:4930447C04Rik'

401005

Institutional Source

Beutler Lab

Gene Symbol

4930447C04Rik

Ensembl Gene

ENSMUSG00000021098

Gene Name

RIKEN cDNA 4930447C04 gene

Synonyms

Six6os1, Six6as

MMRRC Submission

042814-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.161) question?

Stock #

R5243 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

72926967-72964742 bp(-) (GRCm39)

Type of Mutation

critical splice donor site (2 bp from exon)

DNA Base Change (assembly)

A to T at 72956543 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000106115 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000044000] [ENSMUST00000044000] [ENSMUST00000110489] [ENSMUST00000110489] [ENSMUST00000130635] [ENSMUST00000131033] [ENSMUST00000132067] [ENSMUST00000136075]

AlphaFold

Q9CTN5

Predicted Effect

probably null
Transcript: ENSMUST00000044000

SMART Domains

Protein: ENSMUSP00000035376
Gene: ENSMUSG00000021098

Domain	Start	End	E-Value	Type
low complexity region	137	147	N/A	INTRINSIC
coiled coil region	197	233	N/A	INTRINSIC
low complexity region	247	261	N/A	INTRINSIC
low complexity region	264	275	N/A	INTRINSIC
low complexity region	478	489	N/A	INTRINSIC
low complexity region	522	534	N/A	INTRINSIC
low complexity region	552	565	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000044000

SMART Domains

Protein: ENSMUSP00000035376
Gene: ENSMUSG00000021098

Domain	Start	End	E-Value	Type
low complexity region	137	147	N/A	INTRINSIC
coiled coil region	197	233	N/A	INTRINSIC
low complexity region	247	261	N/A	INTRINSIC
low complexity region	264	275	N/A	INTRINSIC
low complexity region	478	489	N/A	INTRINSIC
low complexity region	522	534	N/A	INTRINSIC
low complexity region	552	565	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000110489

SMART Domains

Protein: ENSMUSP00000106115
Gene: ENSMUSG00000021098

Domain	Start	End	E-Value	Type
Pfam:S6OS1	31	575	1.1e-277	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000110489

SMART Domains

Protein: ENSMUSP00000106115
Gene: ENSMUSG00000021098

Domain	Start	End	E-Value	Type
Pfam:S6OS1	31	575	1.1e-277	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000130635

Predicted Effect

probably benign
Transcript: ENSMUST00000131033
AA Change: Y186N

PolyPhen 2 Score 0.074 (Sensitivity: 0.93; Specificity: 0.85)

SMART Domains

Protein: ENSMUSP00000119777
Gene: ENSMUSG00000021098
AA Change: Y186N

Domain	Start	End	E-Value	Type
low complexity region	137	147	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000132016

Predicted Effect

probably benign
Transcript: ENSMUST00000132067

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000132901

Predicted Effect

probably benign
Transcript: ENSMUST00000143960

SMART Domains

Protein: ENSMUSP00000116391
Gene: ENSMUSG00000021098

Domain	Start	End	E-Value	Type
Pfam:S6OS1	1	70	6.1e-21	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000136075

Meta Mutation Damage Score

0.9488

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.1%
20x: 95.0%

Validation Efficiency

95% (62/65)

MGI Phenotype

PHENOTYPE: Mice homozygous for a null mutation display male and female infertility with meiotic arrest and defective synaptic formation. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 60 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aatk	A	G	11: 119,907,594 (GRCm39)	L78P	probably damaging	Het
Acadsb	T	A	7: 131,045,972 (GRCm39)	I412K	probably damaging	Het
Acer3	T	C	7: 97,867,277 (GRCm39)	R246G	possibly damaging	Het
Atp1a3	T	A	7: 24,693,994 (GRCm39)	I387F	probably damaging	Het
Atp6v1b2	A	T	8: 69,556,391 (GRCm39)	M300L	probably benign	Het
Aurkb	T	A	11: 68,936,752 (GRCm39)		probably benign	Het
Card10	C	A	15: 78,664,872 (GRCm39)	G694V	possibly damaging	Het
Ccdc171	A	G	4: 83,522,344 (GRCm39)	N336S	probably damaging	Het
Copg2	T	C	6: 30,750,626 (GRCm39)	T720A	probably benign	Het
Coro2a	A	T	4: 46,545,620 (GRCm39)	W272R	probably damaging	Het
Cpne6	T	A	14: 55,750,204 (GRCm39)	C112S	probably damaging	Het
Ddx21	A	G	10: 62,437,992 (GRCm39)	M1T	probably null	Het
Dohh	A	G	10: 81,223,203 (GRCm39)	R161G	probably benign	Het
Dsc1	A	C	18: 20,232,216 (GRCm39)	V264G	probably damaging	Het
E4f1	A	T	17: 24,666,292 (GRCm39)	C198S	probably damaging	Het
Evpl	T	A	11: 116,113,795 (GRCm39)	E1298D	probably damaging	Het
Grid2ip	A	T	5: 143,363,260 (GRCm39)	I246F	probably damaging	Het
H2-M1	A	G	17: 36,982,193 (GRCm39)	F136S	possibly damaging	Het
Hck	T	C	2: 152,986,412 (GRCm39)	V387A	probably damaging	Het
Hdac1	G	A	4: 129,410,646 (GRCm39)		probably benign	Het
Hydin	A	C	8: 111,232,380 (GRCm39)	Q1633P	possibly damaging	Het
Igkv12-41	A	G	6: 69,835,686 (GRCm39)	I22T	probably damaging	Het
Ints3	CA	CAA	3: 90,308,451 (GRCm39)		probably null	Het
Itpr2	C	G	6: 146,089,044 (GRCm39)	W2188C	probably damaging	Het
Kcnt1	A	G	2: 25,798,086 (GRCm39)	E899G	probably damaging	Het
Lgals8	C	A	13: 12,469,645 (GRCm39)	V12L	probably benign	Het
Lgr6	T	C	1: 135,037,010 (GRCm39)		probably benign	Het
Lrrc8b	T	G	5: 105,628,812 (GRCm39)	I386S	probably damaging	Het
Mks1	T	C	11: 87,747,504 (GRCm39)		probably benign	Het
Mon1b	A	G	8: 114,364,553 (GRCm39)	D110G	possibly damaging	Het
Mpdz	G	T	4: 81,225,116 (GRCm39)	A1437E	probably damaging	Het
Nbeal1	T	A	1: 60,309,487 (GRCm39)	N1753K	probably damaging	Het
Nceh1	T	C	3: 27,295,837 (GRCm39)	V366A	probably damaging	Het
Ncor1	A	T	11: 62,229,788 (GRCm39)	D893E	probably damaging	Het
Npc1	T	A	18: 12,331,688 (GRCm39)		probably benign	Het
Or1j15	T	C	2: 36,458,655 (GRCm39)	L15P	probably damaging	Het
Or9i1b	A	G	19: 13,897,025 (GRCm39)	I214V	probably damaging	Het
Podxl2	T	C	6: 88,826,356 (GRCm39)	T317A	probably benign	Het
Prl8a9	T	G	13: 27,746,446 (GRCm39)	Q54P	probably damaging	Het
Prpf31	C	T	7: 3,641,753 (GRCm39)	R351*	probably null	Het
Pspc1	C	T	14: 57,001,648 (GRCm39)	G242D	probably damaging	Het
Rbmxl2	G	C	7: 106,809,044 (GRCm39)	G110R	probably damaging	Het
Rif1	T	A	2: 52,001,836 (GRCm39)	H1763Q	possibly damaging	Het
Rpusd3	T	C	6: 113,395,025 (GRCm39)	T85A	probably benign	Het
Rttn	A	G	18: 89,126,187 (GRCm39)	I1853M	possibly damaging	Het
Sacs	T	A	14: 61,443,406 (GRCm39)	C1817*	probably null	Het
Scrib	A	T	15: 75,937,101 (GRCm39)	V335E	probably benign	Het
Sdk2	A	G	11: 113,715,912 (GRCm39)	L1549P	possibly damaging	Het
Slc25a11	C	T	11: 70,536,924 (GRCm39)	G44S	probably damaging	Het
Slc6a3	A	G	13: 73,719,570 (GRCm39)	Y533C	possibly damaging	Het
Slc7a5	A	G	8: 122,623,274 (GRCm39)	V191A	probably damaging	Het
Son	A	G	16: 91,451,621 (GRCm39)	K123E	probably damaging	Het
Tcstv3	T	A	13: 120,779,125 (GRCm39)	M8K	probably benign	Het
Tie1	A	G	4: 118,339,548 (GRCm39)	V411A	probably damaging	Het
Upk3bl	C	A	5: 136,088,977 (GRCm39)	D1E	possibly damaging	Het
Vmn2r5	T	C	3: 64,411,497 (GRCm39)	D357G	probably damaging	Het
Vmn2r75	T	C	7: 85,813,447 (GRCm39)	N452D	probably damaging	Het
Wnk2	T	A	13: 49,226,054 (GRCm39)	N1043I	possibly damaging	Het
Zfp407	A	T	18: 84,579,216 (GRCm39)	H632Q	probably damaging	Het
Zfp423	T	C	8: 88,500,275 (GRCm39)	K1174R	probably benign	Het

Other mutations in 4930447C04Rik

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00801:4930447C04Rik	APN	12	72,928,160 (GRCm39)	missense	possibly damaging	0.71
IGL01611:4930447C04Rik	APN	12	72,954,644 (GRCm39)	missense	possibly damaging	0.93
IGL02352:4930447C04Rik	APN	12	72,941,829 (GRCm39)	splice site	probably null
IGL02359:4930447C04Rik	APN	12	72,941,829 (GRCm39)	splice site	probably null
FR4304:4930447C04Rik	UTSW	12	72,928,061 (GRCm39)	small deletion	probably benign
R0650:4930447C04Rik	UTSW	12	72,956,830 (GRCm39)	missense	probably damaging	0.99
R0651:4930447C04Rik	UTSW	12	72,956,830 (GRCm39)	missense	probably damaging	0.99
R1271:4930447C04Rik	UTSW	12	72,939,657 (GRCm39)	missense	possibly damaging	0.71
R1321:4930447C04Rik	UTSW	12	72,945,318 (GRCm39)	splice site	probably benign
R1387:4930447C04Rik	UTSW	12	72,962,208 (GRCm39)	missense	probably benign	0.04
R1424:4930447C04Rik	UTSW	12	72,939,669 (GRCm39)	nonsense	probably null
R1440:4930447C04Rik	UTSW	12	72,928,195 (GRCm39)	missense	possibly damaging	0.85
R1538:4930447C04Rik	UTSW	12	72,928,120 (GRCm39)	missense	possibly damaging	0.92
R1694:4930447C04Rik	UTSW	12	72,931,992 (GRCm39)	splice site	probably null
R1888:4930447C04Rik	UTSW	12	72,960,030 (GRCm39)	missense	unknown
R1888:4930447C04Rik	UTSW	12	72,960,030 (GRCm39)	missense	unknown
R2151:4930447C04Rik	UTSW	12	72,954,725 (GRCm39)	splice site	probably null
R4930:4930447C04Rik	UTSW	12	72,953,008 (GRCm39)	missense	possibly damaging	0.71
R4967:4930447C04Rik	UTSW	12	72,956,502 (GRCm39)	nonsense	probably null
R6312:4930447C04Rik	UTSW	12	72,936,541 (GRCm39)	missense	possibly damaging	0.86
R6825:4930447C04Rik	UTSW	12	72,954,654 (GRCm39)	missense	probably benign	0.32
R7275:4930447C04Rik	UTSW	12	72,956,795 (GRCm39)	missense	possibly damaging	0.71
R8427:4930447C04Rik	UTSW	12	72,950,060 (GRCm39)	missense	possibly damaging	0.86
R8669:4930447C04Rik	UTSW	12	72,949,234 (GRCm39)	missense	probably benign	0.32
R8674:4930447C04Rik	UTSW	12	72,956,696 (GRCm39)	missense	probably benign	0.00
R9065:4930447C04Rik	UTSW	12	72,939,604 (GRCm39)	missense	possibly damaging	0.86
R9801:4930447C04Rik	UTSW	12	72,945,540 (GRCm39)	missense	probably benign	0.12
RF041:4930447C04Rik	UTSW	12	72,928,050 (GRCm39)	small deletion	probably benign
Z1088:4930447C04Rik	UTSW	12	72,986,169 (GRCm39)	unclassified	probably benign
Z1176:4930447C04Rik	UTSW	12	72,963,500 (GRCm39)	missense	probably benign	0.18

Predicted Primers

PCR Primer
(F):5'- GCCACTTTAAAGCCAGATGACTATAC -3'
(R):5'- GGCATGTACTGAACAACTACAATTG -3'

Sequencing Primer
(F):5'- AACTGCTTGCTTCTGATCACATAGG -3'
(R):5'- ACTGAACAACTACAATTGAATGAAAC -3'

Posted On

2016-07-06