Mutagenetix > Incidental Mutation

Incidental Mutation 'R4941:Fam227a'

383130

Institutional Source

Beutler Lab

Gene Symbol

Fam227a

Ensembl Gene

ENSMUSG00000042564

Gene Name

family with sequence similarity 227, member A

Synonyms

4933432B09Rik

MMRRC Submission

042539-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.055) question?

Stock #

R4941 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

79493777-79543157 bp(-) (GRCm39)

Type of Mutation

critical splice donor site (1 bp from exon)

DNA Base Change (assembly)

C to A at 79524204 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000155261 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000109646] [ENSMUST00000109646] [ENSMUST00000109648] [ENSMUST00000109648] [ENSMUST00000187519] [ENSMUST00000191401] [ENSMUST00000229064] [ENSMUST00000230366]

AlphaFold

Q9D3V8

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000046816

SMART Domains

Protein: ENSMUSP00000048277
Gene: ENSMUSG00000042564

Domain	Start	End	E-Value	Type
Pfam:FWWh	128	242	6.3e-32	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000109646

SMART Domains

Protein: ENSMUSP00000105273
Gene: ENSMUSG00000042564

Domain	Start	End	E-Value	Type
low complexity region	156	175	N/A	INTRINSIC
low complexity region	204	211	N/A	INTRINSIC
low complexity region	243	253	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000109646

SMART Domains

Protein: ENSMUSP00000105273
Gene: ENSMUSG00000042564

Domain	Start	End	E-Value	Type
low complexity region	156	175	N/A	INTRINSIC
low complexity region	204	211	N/A	INTRINSIC
low complexity region	243	253	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000109648

SMART Domains

Protein: ENSMUSP00000105275
Gene: ENSMUSG00000042564

Domain	Start	End	E-Value	Type
Pfam:FWWh	134	295	1.4e-51	PFAM
low complexity region	512	531	N/A	INTRINSIC
low complexity region	560	567	N/A	INTRINSIC
low complexity region	599	609	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000109648

SMART Domains

Protein: ENSMUSP00000105275
Gene: ENSMUSG00000042564

Domain	Start	End	E-Value	Type
Pfam:FWWh	134	295	1.4e-51	PFAM
low complexity region	512	531	N/A	INTRINSIC
low complexity region	560	567	N/A	INTRINSIC
low complexity region	599	609	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000187519

SMART Domains

Protein: ENSMUSP00000139524
Gene: ENSMUSG00000042564

Domain	Start	End	E-Value	Type
Pfam:FWWh	132	295	1e-47	PFAM
low complexity region	512	531	N/A	INTRINSIC
low complexity region	560	567	N/A	INTRINSIC
low complexity region	599	609	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000191401

Predicted Effect

probably null
Transcript: ENSMUST00000229064

Predicted Effect

probably benign
Transcript: ENSMUST00000230366

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000230475

Meta Mutation Damage Score

0.9471

Coding Region Coverage

1x: 98.9%
3x: 98.0%
10x: 95.4%
20x: 89.0%

Validation Efficiency

97% (112/116)

Allele List at MGI

Other mutations in this stock

Total: 98 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A4galt	T	A	15: 83,112,529 (GRCm39)	I85F	probably damaging	Het
Abcc6	T	A	7: 45,661,947 (GRCm39)	I435F	probably benign	Het
Adam3	T	C	8: 25,167,332 (GRCm39)		probably benign	Het
Adrb3	T	C	8: 27,717,450 (GRCm39)	Y333C	probably damaging	Het
Ago4	A	T	4: 126,419,847 (GRCm39)	D43E	probably benign	Het
Agt	T	A	8: 125,283,727 (GRCm39)	Q464L	probably benign	Het
Amdhd1	A	T	10: 93,367,463 (GRCm39)	D230E	probably damaging	Het
Aplf	A	G	6: 87,645,405 (GRCm39)	I33T	probably damaging	Het
Aplf	A	T	6: 87,623,331 (GRCm39)	N249K	probably benign	Het
Arap2	A	G	5: 62,906,821 (GRCm39)	M66T	probably benign	Het
Atf4	T	C	15: 80,140,434 (GRCm39)		probably benign	Het
Bahcc1	A	C	11: 120,177,491 (GRCm39)	H2068P	probably benign	Het
Bcor	C	T	X: 11,906,725 (GRCm39)	R1551Q	probably damaging	Het
Bltp1	A	C	3: 36,971,851 (GRCm39)	H528P	probably damaging	Het
Bltp1	G	A	3: 36,974,050 (GRCm39)	S600N	probably benign	Het
Catsper1	C	A	19: 5,391,466 (GRCm39)	A616D	possibly damaging	Het
Cdkn3	A	G	14: 47,007,320 (GRCm39)	D159G	possibly damaging	Het
Cep162	T	C	9: 87,108,022 (GRCm39)		probably benign	Het
Clca3a1	T	A	3: 144,721,414 (GRCm39)	I386L	probably damaging	Het
Cldn10	G	A	14: 119,025,725 (GRCm39)	G53S	possibly damaging	Het
Cmtm3	T	C	8: 105,070,460 (GRCm39)	L73P	probably damaging	Het
Cnksr3	A	C	10: 7,102,925 (GRCm39)	L149R	probably benign	Het
Cope	T	C	8: 70,755,584 (GRCm39)		probably null	Het
Cpa6	T	A	1: 10,479,562 (GRCm39)	M224L	probably benign	Het
Cyp2d41-ps	T	C	15: 82,666,154 (GRCm39)		noncoding transcript	Het
Ddx55	T	A	5: 124,706,779 (GRCm39)	L592*	probably null	Het
Deup1	T	C	9: 15,499,323 (GRCm39)	M333V	probably benign	Het
Eif4a1	T	C	11: 69,558,640 (GRCm39)		probably benign	Het
Eif4g3	A	C	4: 137,897,876 (GRCm39)	D1026A	probably damaging	Het
Eif5b	T	C	1: 38,090,280 (GRCm39)	V1153A	probably damaging	Het
Ercc8	G	T	13: 108,297,301 (GRCm39)		probably benign	Het
Fat1	A	G	8: 45,489,312 (GRCm39)	I3505V	probably benign	Het
Fat3	T	G	9: 16,286,448 (GRCm39)	E1025A	probably damaging	Het
Fat4	C	T	3: 39,011,601 (GRCm39)	R2234W	probably damaging	Het
Fer1l4	G	T	2: 155,887,009 (GRCm39)	F634L	probably damaging	Het
Fetub	G	A	16: 22,756,624 (GRCm39)	V162I	probably benign	Het
Fgd4	T	C	16: 16,302,402 (GRCm39)	Q51R	probably benign	Het
Fgfr2	T	C	7: 129,800,175 (GRCm39)	H140R	probably benign	Het
Flt3	T	A	5: 147,293,185 (GRCm39)		probably null	Het
Gabrb1	A	G	5: 72,294,121 (GRCm39)	N465S	probably damaging	Het
Gapdhs	T	C	7: 30,432,691 (GRCm39)	I206V	probably benign	Het
Gkn3	C	T	6: 87,360,507 (GRCm39)	A163T	probably damaging	Het
Glp2r	T	C	11: 67,637,529 (GRCm39)		probably null	Het
Gm4956	T	A	1: 21,368,306 (GRCm39)		noncoding transcript	Het
Gtf2a1l	A	T	17: 89,022,350 (GRCm39)	D447V	probably damaging	Het
Hsd3b5	A	G	3: 98,526,379 (GRCm39)	W356R	probably damaging	Het
Idh2	A	T	7: 79,745,847 (GRCm39)	V335D	probably damaging	Het
Isyna1	T	C	8: 71,048,146 (GRCm39)	I184T	probably damaging	Het
Kcnh2	A	G	5: 24,536,085 (GRCm39)	S320P	probably damaging	Het
Klk14	G	A	7: 43,341,501 (GRCm39)	C51Y	probably damaging	Het
Kpna6	A	G	4: 129,541,825 (GRCm39)	F524S	probably damaging	Het
Lap3	A	T	5: 45,663,539 (GRCm39)	M338L	probably benign	Het
Lins1	T	C	7: 66,359,198 (GRCm39)		probably benign	Het
Llgl1	C	T	11: 60,600,394 (GRCm39)	P581L	probably benign	Het
Lrrc43	A	G	5: 123,639,126 (GRCm39)	D385G	probably benign	Het
Maf	T	C	8: 116,433,532 (GRCm39)	D24G	unknown	Het
Nell1	T	C	7: 49,712,386 (GRCm39)	S69P	probably benign	Het
Nkapd1	G	T	9: 50,518,809 (GRCm39)	Q268K	probably benign	Het
Or13p4	C	T	4: 118,547,089 (GRCm39)	V187I	possibly damaging	Het
Or2h1	C	T	17: 37,404,484 (GRCm39)	G94E	probably damaging	Het
Or2j6	T	A	7: 139,980,792 (GRCm39)	M56L	probably benign	Het
Or51af1	T	C	7: 103,141,458 (GRCm39)	D209G	probably damaging	Het
Or5an10	A	G	19: 12,276,260 (GRCm39)	S79P	possibly damaging	Het
Or8g54	T	C	9: 39,707,160 (GRCm39)	M163T	possibly damaging	Het
Oxld1	T	C	11: 120,347,862 (GRCm39)	T112A	probably benign	Het
Parp14	T	C	16: 35,666,403 (GRCm39)	N1210S	probably benign	Het
Pcdhb10	C	A	18: 37,545,887 (GRCm39)	T321K	probably benign	Het
Pcdhb8	C	T	18: 37,489,059 (GRCm39)	L246F	probably benign	Het
Pcdhga1	T	A	18: 37,795,659 (GRCm39)	I221K	probably benign	Het
Pcdhga9	T	A	18: 37,871,185 (GRCm39)	V338E	probably damaging	Het
Pdcd11	T	C	19: 47,108,325 (GRCm39)	S1231P	probably damaging	Het
Pde6c	A	T	19: 38,140,013 (GRCm39)	L325F	probably damaging	Het
Pnpla7	T	A	2: 24,887,276 (GRCm39)		probably null	Het
Pparg	T	A	6: 115,467,071 (GRCm39)	V478E	probably damaging	Het
Ppib	T	C	9: 65,967,672 (GRCm39)	V42A	probably benign	Het
Ppox	T	C	1: 171,105,166 (GRCm39)	M341V	probably damaging	Het
Proc	T	C	18: 32,258,166 (GRCm39)	K260E	possibly damaging	Het
Ptpro	C	T	6: 137,369,763 (GRCm39)	P525L	probably damaging	Het
Rnf14	C	A	18: 38,441,435 (GRCm39)	A275E	probably damaging	Het
Scnn1b	C	T	7: 121,511,231 (GRCm39)	P306L	probably damaging	Het
Sec14l5	A	G	16: 4,994,364 (GRCm39)	E386G	probably damaging	Het
Sftpa1	T	A	14: 40,854,509 (GRCm39)	I32N	probably damaging	Het
Slc26a5	A	G	5: 22,025,384 (GRCm39)	I408T	probably damaging	Het
Slc7a13	A	G	4: 19,841,467 (GRCm39)	Y438C	probably damaging	Het
Spire1	T	C	18: 67,652,384 (GRCm39)	E231G	possibly damaging	Het
Stab1	T	A	14: 30,873,528 (GRCm39)	I1014F	probably benign	Het
Steap2	T	C	5: 5,727,651 (GRCm39)	Y228C	probably damaging	Het
Tmem131l	T	C	3: 83,806,546 (GRCm39)	T1487A	probably benign	Het
Tmem171	A	G	13: 98,828,803 (GRCm39)	F116L	possibly damaging	Het
Tmem215	T	C	4: 40,474,520 (GRCm39)	V199A	probably damaging	Het
Tmem45a	T	C	16: 56,642,652 (GRCm39)	N173S	possibly damaging	Het
Uqcrc2	C	T	7: 120,242,301 (GRCm39)	R148C	probably benign	Het
Vmn2r116	A	G	17: 23,620,116 (GRCm39)	K617E	probably damaging	Het
Xrcc6	T	C	15: 81,924,013 (GRCm39)	L229P	probably damaging	Het
Yju2	A	G	17: 56,271,149 (GRCm39)	D97G	possibly damaging	Het
Zfp184	A	G	13: 22,133,891 (GRCm39)	D46G	probably damaging	Het
Zfp790	T	A	7: 29,528,916 (GRCm39)	C534S	possibly damaging	Het
Zfp990	A	T	4: 145,263,407 (GRCm39)	N135I	probably damaging	Het

Other mutations in Fam227a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01650:Fam227a	APN	15	79,518,274 (GRCm39)	missense	possibly damaging	0.66
IGL01807:Fam227a	APN	15	79,533,856 (GRCm39)	missense	probably benign	0.03
IGL01936:Fam227a	APN	15	79,496,747 (GRCm39)	missense	possibly damaging	0.90
IGL02355:Fam227a	APN	15	79,528,139 (GRCm39)	intron	probably benign
IGL02362:Fam227a	APN	15	79,528,139 (GRCm39)	intron	probably benign
IGL02569:Fam227a	APN	15	79,518,323 (GRCm39)	missense	probably benign
IGL02713:Fam227a	APN	15	79,520,997 (GRCm39)	splice site	probably benign
IGL02734:Fam227a	APN	15	79,502,042 (GRCm39)	splice site	probably benign
IGL02816:Fam227a	APN	15	79,510,497 (GRCm39)	missense	possibly damaging	0.66
IGL03354:Fam227a	APN	15	79,520,951 (GRCm39)	missense	possibly damaging	0.91
R0105:Fam227a	UTSW	15	79,505,033 (GRCm39)	missense	possibly damaging	0.90
R0194:Fam227a	UTSW	15	79,524,870 (GRCm39)	nonsense	probably null
R0437:Fam227a	UTSW	15	79,528,189 (GRCm39)	missense	possibly damaging	0.90
R0786:Fam227a	UTSW	15	79,510,469 (GRCm39)	missense	probably benign	0.01
R0925:Fam227a	UTSW	15	79,505,006 (GRCm39)	missense	probably benign	0.04
R1200:Fam227a	UTSW	15	79,496,738 (GRCm39)	missense	possibly damaging	0.66
R1424:Fam227a	UTSW	15	79,518,309 (GRCm39)	missense	probably benign	0.34
R1474:Fam227a	UTSW	15	79,499,582 (GRCm39)	missense	probably damaging	0.97
R1495:Fam227a	UTSW	15	79,510,446 (GRCm39)	missense	probably benign	0.00
R1561:Fam227a	UTSW	15	79,520,963 (GRCm39)	missense	possibly damaging	0.95
R1661:Fam227a	UTSW	15	79,504,878 (GRCm39)	splice site	probably null
R1669:Fam227a	UTSW	15	79,504,878 (GRCm39)	splice site	probably null
R1967:Fam227a	UTSW	15	79,521,335 (GRCm39)	missense	possibly damaging	0.93
R1976:Fam227a	UTSW	15	79,510,477 (GRCm39)	missense	possibly damaging	0.83
R2197:Fam227a	UTSW	15	79,507,668 (GRCm39)	missense	probably damaging	0.97
R2230:Fam227a	UTSW	15	79,499,582 (GRCm39)	missense	possibly damaging	0.66
R2231:Fam227a	UTSW	15	79,499,582 (GRCm39)	missense	possibly damaging	0.66
R2232:Fam227a	UTSW	15	79,499,582 (GRCm39)	missense	possibly damaging	0.66
R2910:Fam227a	UTSW	15	79,520,935 (GRCm39)	missense	possibly damaging	0.81
R3027:Fam227a	UTSW	15	79,532,934 (GRCm39)	splice site	probably null
R3943:Fam227a	UTSW	15	79,505,060 (GRCm39)	splice site	probably benign
R4811:Fam227a	UTSW	15	79,499,628 (GRCm39)	missense	possibly damaging	0.66
R4845:Fam227a	UTSW	15	79,533,912 (GRCm39)	missense	probably damaging	0.99
R4896:Fam227a	UTSW	15	79,521,255 (GRCm39)	missense	probably benign	0.32
R4934:Fam227a	UTSW	15	79,521,262 (GRCm39)	missense	possibly damaging	0.71
R5225:Fam227a	UTSW	15	79,520,936 (GRCm39)	missense	possibly damaging	0.90
R5369:Fam227a	UTSW	15	79,499,637 (GRCm39)	missense	probably benign	0.27
R5593:Fam227a	UTSW	15	79,524,259 (GRCm39)	utr 3 prime	probably benign
R6311:Fam227a	UTSW	15	79,524,895 (GRCm39)	missense	probably benign	0.23
R6362:Fam227a	UTSW	15	79,527,551 (GRCm39)	missense	possibly damaging	0.53
R6532:Fam227a	UTSW	15	79,520,921 (GRCm39)	missense	probably benign	0.00
R7239:Fam227a	UTSW	15	79,518,263 (GRCm39)	critical splice donor site	probably null
R7619:Fam227a	UTSW	15	79,501,967 (GRCm39)	missense	probably benign
R7719:Fam227a	UTSW	15	79,504,913 (GRCm39)	missense	possibly damaging	0.53
R8006:Fam227a	UTSW	15	79,518,299 (GRCm39)	missense	possibly damaging	0.61
R8048:Fam227a	UTSW	15	79,533,959 (GRCm39)	start codon destroyed	probably null
R8175:Fam227a	UTSW	15	79,524,861 (GRCm39)	missense	probably damaging	0.97
R8439:Fam227a	UTSW	15	79,514,271 (GRCm39)	missense	possibly damaging	0.53
R9014:Fam227a	UTSW	15	79,504,958 (GRCm39)	missense	possibly damaging	0.96
R9034:Fam227a	UTSW	15	79,532,952 (GRCm39)	missense	probably benign	0.00
R9582:Fam227a	UTSW	15	79,501,978 (GRCm39)	missense	probably benign	0.33
R9613:Fam227a	UTSW	15	79,518,284 (GRCm39)	missense	probably benign	0.09
R9668:Fam227a	UTSW	15	79,526,444 (GRCm39)	missense	probably benign	0.41

Predicted Primers

PCR Primer
(F):5'- ACCAGCCAAGATGTACTGTC -3'
(R):5'- AGATTTCGGGTGTGAGAACG -3'

Sequencing Primer
(F):5'- GTCACATCTTCCCAGTGAGTATAGG -3'
(R):5'- TGAGAACGGTGCTTCGC -3'

Posted On

2016-04-27