Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02411:Gm5414'

292299

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm5414

Ensembl Gene

ENSMUSG00000064232

Gene Name

predicted gene 5414

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.134) question?

Stock #

IGL02411

Quality Score

Status

Chromosome

Chromosomal Location

101532463-101536623 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 101536269 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Asparagine at position 119 (Y119N)

Ref Sequence

ENSEMBL: ENSMUSP00000059101 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000062879]

AlphaFold

Q6IFZ8

Predicted Effect

probably benign
Transcript: ENSMUST00000062879
AA Change: Y119N

PolyPhen 2 Score 0.049 (Sensitivity: 0.94; Specificity: 0.83)

SMART Domains

Protein: ENSMUSP00000059101
Gene: ENSMUSG00000064232
AA Change: Y119N

Domain	Start	End	E-Value	Type
Pfam:Keratin_2_head	15	148	3.3e-29	PFAM
Filament	151	464	1.4e-143	SMART
low complexity region	489	507	N/A	INTRINSIC
low complexity region	511	549	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 42 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
0610040J01Rik	A	G	5: 64,055,459 (GRCm39)	E65G	probably benign	Het
Abcc8	G	A	7: 45,756,431 (GRCm39)	R1425C	probably damaging	Het
Adcy3	A	T	12: 4,259,407 (GRCm39)		probably null	Het
AI661453	T	G	17: 47,778,263 (GRCm39)		probably benign	Het
Arhgef10	A	T	8: 15,004,819 (GRCm39)	Y445F	probably benign	Het
Atrx	G	T	X: 104,874,587 (GRCm39)	S1924R	possibly damaging	Het
Clca3a1	T	C	3: 144,733,763 (GRCm39)	T58A	possibly damaging	Het
Clec1b	A	G	6: 129,378,804 (GRCm39)	Y97C	probably damaging	Het
Cobll1	A	G	2: 64,928,084 (GRCm39)	S1080P	probably damaging	Het
Crb1	C	A	1: 139,176,213 (GRCm39)	C529F	probably damaging	Het
Crim1	C	T	17: 78,642,763 (GRCm39)	R494*	probably null	Het
Cyp3a25	A	T	5: 145,938,257 (GRCm39)		probably benign	Het
Dntt	T	A	19: 41,041,424 (GRCm39)		probably null	Het
Gjb1	T	C	X: 100,428,611 (GRCm39)	C280R	probably damaging	Het
Glp1r	T	A	17: 31,143,485 (GRCm39)	C174S	probably damaging	Het
Gm9631	G	A	11: 121,834,478 (GRCm39)			Het
Gm9796	G	T	11: 95,588,756 (GRCm39)		noncoding transcript	Het
Gm9956	T	C	10: 56,621,388 (GRCm39)	F17L	unknown	Het
Il1rap	A	T	16: 26,529,366 (GRCm39)	D396V	probably damaging	Het
Impa1	T	C	3: 10,388,018 (GRCm39)	K135E	possibly damaging	Het
Iqub	G	A	6: 24,449,810 (GRCm39)	A685V	probably damaging	Het
Jade3	T	C	X: 20,379,063 (GRCm39)	V512A	probably benign	Het
Kif3a	C	A	11: 53,461,525 (GRCm39)	P57T	probably damaging	Het
Kndc1	G	T	7: 139,501,829 (GRCm39)		probably null	Het
Lyst	G	A	13: 13,835,541 (GRCm39)	C1741Y	probably benign	Het
Maged2	G	T	X: 149,592,755 (GRCm39)	D343E	probably benign	Het
Magi2	T	C	5: 19,883,707 (GRCm39)	S120P	probably damaging	Het
Nxph3	A	T	11: 95,401,656 (GRCm39)	*253R	probably null	Het
Oog2	A	T	4: 143,921,618 (GRCm39)	H194L	probably damaging	Het
Pcbd2	T	G	13: 55,880,764 (GRCm39)	W7G	probably benign	Het
Pcdhb14	T	G	18: 37,582,823 (GRCm39)	L643R	possibly damaging	Het
Plch1	G	T	3: 63,605,177 (GRCm39)		probably null	Het
Poln	G	T	5: 34,270,666 (GRCm39)	S455*	probably null	Het
Ppp2r1a	T	C	17: 21,171,596 (GRCm39)		probably benign	Het
Rsu1	T	G	2: 13,082,308 (GRCm39)		probably benign	Het
Serpina10	A	T	12: 103,583,202 (GRCm39)	M360K	possibly damaging	Het
Sox30	A	T	11: 45,871,951 (GRCm39)	K269*	probably null	Het
Thbs1	T	C	2: 117,945,451 (GRCm39)	V310A	probably benign	Het
Tie1	C	A	4: 118,343,760 (GRCm39)	E61*	probably null	Het
Tm2d1	G	T	4: 98,268,911 (GRCm39)	P62Q	probably damaging	Het
Tpp1	G	T	7: 105,398,826 (GRCm39)	P201Q	probably damaging	Het
Trim13	A	G	14: 61,842,598 (GRCm39)	E205G	probably damaging	Het

Other mutations in Gm5414

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01011:Gm5414	APN	15	101,536,569 (GRCm39)	missense	probably benign	0.00
IGL01774:Gm5414	APN	15	101,535,410 (GRCm39)	missense	probably benign	0.13
IGL01939:Gm5414	APN	15	101,534,105 (GRCm39)	splice site	probably benign
IGL02205:Gm5414	APN	15	101,534,304 (GRCm39)	missense	probably benign	0.44
IGL02720:Gm5414	APN	15	101,533,990 (GRCm39)	missense	probably damaging	1.00
IGL02900:Gm5414	APN	15	101,536,242 (GRCm39)	missense	probably damaging	0.99
IGL03283:Gm5414	APN	15	101,535,522 (GRCm39)	missense	probably damaging	1.00
PIT4480001:Gm5414	UTSW	15	101,536,181 (GRCm39)	missense	probably damaging	1.00
PIT4504001:Gm5414	UTSW	15	101,534,258 (GRCm39)	missense	probably damaging	0.98
R1905:Gm5414	UTSW	15	101,533,075 (GRCm39)	missense	probably damaging	1.00
R2070:Gm5414	UTSW	15	101,536,495 (GRCm39)	missense	possibly damaging	0.52
R3011:Gm5414	UTSW	15	101,534,047 (GRCm39)	missense	probably damaging	1.00
R3033:Gm5414	UTSW	15	101,533,044 (GRCm39)	missense	probably damaging	1.00
R4074:Gm5414	UTSW	15	101,533,988 (GRCm39)	missense	probably benign
R4257:Gm5414	UTSW	15	101,533,107 (GRCm39)	missense	probably damaging	1.00
R4396:Gm5414	UTSW	15	101,534,101 (GRCm39)	missense	probably damaging	1.00
R4648:Gm5414	UTSW	15	101,536,543 (GRCm39)	missense	possibly damaging	0.72
R4912:Gm5414	UTSW	15	101,533,445 (GRCm39)	missense	possibly damaging	0.46
R5095:Gm5414	UTSW	15	101,532,473 (GRCm39)	missense	probably benign	0.01
R5135:Gm5414	UTSW	15	101,536,203 (GRCm39)	missense	probably damaging	0.97
R5177:Gm5414	UTSW	15	101,534,252 (GRCm39)	missense	possibly damaging	0.91
R5330:Gm5414	UTSW	15	101,533,099 (GRCm39)	missense	probably damaging	1.00
R5331:Gm5414	UTSW	15	101,533,099 (GRCm39)	missense	probably damaging	1.00
R5432:Gm5414	UTSW	15	101,533,069 (GRCm39)	missense	probably damaging	1.00
R5521:Gm5414	UTSW	15	101,536,422 (GRCm39)	missense	probably benign	0.33
R5623:Gm5414	UTSW	15	101,534,246 (GRCm39)	missense	probably damaging	1.00
R6781:Gm5414	UTSW	15	101,534,096 (GRCm39)	missense	possibly damaging	0.91
R8298:Gm5414	UTSW	15	101,532,605 (GRCm39)	missense	unknown
R8912:Gm5414	UTSW	15	101,536,620 (GRCm39)	missense	possibly damaging	0.94
R9092:Gm5414	UTSW	15	101,536,345 (GRCm39)	missense	probably benign	0.01
R9721:Gm5414	UTSW	15	101,536,582 (GRCm39)	nonsense	probably null
RF001:Gm5414	UTSW	15	101,536,388 (GRCm39)	missense	probably benign

Posted On

2015-04-16