Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01598:2410124H12Rik'

91739

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

2410124H12Rik

Ensembl Gene

ENSMUSG00000051297

Gene Name

RIKEN cDNA 2410124H12 gene

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL01598

Quality Score

Status

Chromosome

Chromosomal Location

92275630-92294258 bp(+) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

T to A at 92275817 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: ENSMUST00000160494

SMART Domains

Protein: ENSMUSP00000123968
Gene: ENSMUSG00000051297

Domain	Start	End	E-Value	Type
low complexity region	4	22	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 31 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Apc2	T	A	10: 80,148,882 (GRCm39)	L1283Q	probably damaging	Het
Apol6	G	A	15: 76,934,916 (GRCm39)	A62T	probably damaging	Het
AU018091	A	T	7: 3,212,110 (GRCm39)	I204N	possibly damaging	Het
B4galnt4	G	T	7: 140,650,428 (GRCm39)	R765L	probably benign	Het
Brca1	T	C	11: 101,415,156 (GRCm39)	T993A	probably benign	Het
Cadps	C	T	14: 12,522,202 (GRCm38)		probably null	Het
Ccdc177	A	G	12: 80,805,519 (GRCm39)	S252P	unknown	Het
Cdc73	A	G	1: 143,575,017 (GRCm39)	S59P	probably damaging	Het
Cep63	G	T	9: 102,467,657 (GRCm39)	Q570K	possibly damaging	Het
Ces1c	A	T	8: 93,845,041 (GRCm39)	I120K	probably benign	Het
Cpeb1	T	C	7: 81,011,549 (GRCm39)	M131V	probably benign	Het
Dync1h1	G	A	12: 110,624,562 (GRCm39)	V3701I	probably damaging	Het
Fxr1	T	C	3: 34,118,381 (GRCm39)	S535P	possibly damaging	Het
Gldc	A	T	19: 30,111,156 (GRCm39)	V540D	probably damaging	Het
Iqcf6	A	G	9: 106,504,707 (GRCm39)	T124A	probably benign	Het
Itih4	A	G	14: 30,609,774 (GRCm39)	I35V	possibly damaging	Het
Kmt2c	T	C	5: 25,478,664 (GRCm39)	*1525W	probably null	Het
Kmt2c	A	T	5: 25,559,769 (GRCm39)	V963E	probably damaging	Het
Lmnb2	T	C	10: 80,742,999 (GRCm39)	S202G	probably benign	Het
Med23	T	G	10: 24,779,696 (GRCm39)	S924R	probably benign	Het
Or5b102	T	C	19: 13,041,513 (GRCm39)	V246A	probably damaging	Het
Pcif1	T	C	2: 164,728,531 (GRCm39)	F263L	possibly damaging	Het
Pon2	A	T	6: 5,272,331 (GRCm39)	L163H	probably damaging	Het
Scn1a	C	T	2: 66,132,829 (GRCm39)	V165M	possibly damaging	Het
Sema6d	C	A	2: 124,507,018 (GRCm39)	P961Q	probably damaging	Het
Snx27	A	G	3: 94,469,150 (GRCm39)	Y64H	probably damaging	Het
Srsf11	C	T	3: 157,717,672 (GRCm39)		probably benign	Het
Taok1	A	G	11: 77,462,510 (GRCm39)	V193A	probably damaging	Het
Tut4	A	G	4: 108,408,017 (GRCm39)		probably benign	Het
Vps13d	T	C	4: 144,743,471 (GRCm39)	T4137A	probably benign	Het
Zbtb26	T	C	2: 37,326,283 (GRCm39)	Y251C	probably damaging	Het

Posted On

2013-12-09