Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01665:C230029F24Rik'

103277

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

C230029F24Rik

Ensembl Gene

ENSMUSG00000051616

Gene Name

RIKEN cDNA C230029F24 gene

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.146) question?

Stock #

IGL01665

Quality Score

Status

Chromosome

Chromosomal Location

49283775-49379590 bp(+) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

T to A at 49377253 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s):

AlphaFold

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000056879

SMART Domains

Protein: ENSMUSP00000051252
Gene: ENSMUSG00000051616

Domain	Start	End	E-Value	Type
low complexity region	33	77	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000188673

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 27 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acsbg1	T	A	9: 54,530,004 (GRCm39)	I231L	probably benign	Het
Adcyap1	T	A	17: 93,507,506 (GRCm39)	V22D	probably damaging	Het
Adgra3	T	C	5: 50,164,272 (GRCm39)	T236A	possibly damaging	Het
Adipor2	A	T	6: 119,338,887 (GRCm39)	L122H	probably benign	Het
Atp1a4	T	C	1: 172,074,291 (GRCm39)	I321V	probably benign	Het
Bhmt2	A	T	13: 93,799,661 (GRCm39)	Y258*	probably null	Het
Ccpg1	T	A	9: 72,913,159 (GRCm39)	F232I	probably damaging	Het
Cd83	A	T	13: 43,955,153 (GRCm39)	T195S	probably benign	Het
Cdcp3	G	T	7: 130,848,386 (GRCm39)	G847*	probably null	Het
Cfap70	G	A	14: 20,453,186 (GRCm39)	T897M	probably damaging	Het
Cyp3a11	T	A	5: 145,805,475 (GRCm39)	M181L	probably benign	Het
Frem2	C	T	3: 53,457,083 (GRCm39)	V2090I	probably benign	Het
Gm45234	A	G	6: 124,723,571 (GRCm39)		probably benign	Het
Gm7964	T	A	7: 83,406,341 (GRCm39)		noncoding transcript	Het
Igsf9	T	A	1: 172,319,738 (GRCm39)	C39*	probably null	Het
Il1rap	A	T	16: 26,541,463 (GRCm39)	D568V	probably damaging	Het
Ints7	C	T	1: 191,345,331 (GRCm39)		probably benign	Het
Lsamp	C	T	16: 41,964,375 (GRCm39)	R250*	probably null	Het
Oit3	T	A	10: 59,274,731 (GRCm39)	D23V	probably damaging	Het
Pcdh17	T	A	14: 84,684,442 (GRCm39)	L303Q	probably damaging	Het
Pcdhb1	T	A	18: 37,400,450 (GRCm39)	N800K	probably benign	Het
Plce1	A	G	19: 38,513,331 (GRCm39)	D210G	probably benign	Het
Plekhb2	T	A	1: 34,908,411 (GRCm39)	Y152N	probably damaging	Het
Rbp3	T	C	14: 33,678,088 (GRCm39)	S679P	probably benign	Het
Rps6kc1	T	C	1: 190,643,854 (GRCm39)	T2A	possibly damaging	Het
Tmem167	T	A	13: 90,246,504 (GRCm39)	S9R	probably damaging	Het
Xpnpep1	A	T	19: 52,985,463 (GRCm39)	S522T	probably benign	Het

Other mutations in C230029F24Rik

Allele	Source	Chr	Coord	Type	Predicted Effect
R0501:C230029F24Rik	UTSW	1	49,374,629 (GRCm39)	critical splice donor site	noncoding transcript
R3925:C230029F24Rik	UTSW	1	49,350,088 (GRCm39)	exon	noncoding transcript
R4190:C230029F24Rik	UTSW	1	49,350,088 (GRCm39)	exon	noncoding transcript
R4995:C230029F24Rik	UTSW	1	49,377,295 (GRCm39)	exon	noncoding transcript
R5799:C230029F24Rik	UTSW	1	49,377,307 (GRCm39)	exon	noncoding transcript

Posted On

2014-01-21