Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01869:1700026F02Rik'

178664

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

1700026F02Rik

Ensembl Gene

ENSMUSG00000101854

Gene Name

RIKEN cDNA 1700026F02 gene

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL01869

Quality Score

Status

Chromosome

Chromosomal Location

71459372-71479399 bp(-) (GRCm39)

Type of Mutation

intron

DNA Base Change (assembly)

A to G at 71495689 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: ENSMUST00000170101

SMART Domains

Protein: ENSMUSP00000125974
Gene: ENSMUSG00000091388

Domain	Start	End	E-Value	Type
KRAB	3	55	2.15e-14	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000212266

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000212780

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 33 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam29	T	C	8: 56,324,732 (GRCm39)	H574R	probably damaging	Het
Arap1	C	A	7: 101,049,490 (GRCm39)	T984K	probably damaging	Het
Ccdc146	A	T	5: 21,521,837 (GRCm39)	S396T	probably benign	Het
Col6a3	T	C	1: 90,700,770 (GRCm39)	K2587E	unknown	Het
Cyp3a44	A	G	5: 145,727,496 (GRCm39)	S278P	probably damaging	Het
Daw1	T	G	1: 83,159,965 (GRCm39)		probably benign	Het
Dnah17	T	C	11: 117,943,502 (GRCm39)	K3200R	probably benign	Het
Efhd2	A	G	4: 141,601,913 (GRCm39)	F89S	probably damaging	Het
Fras1	A	G	5: 96,856,642 (GRCm39)		probably benign	Het
Ggps1	T	C	13: 14,228,979 (GRCm39)	D68G	probably damaging	Het
Gm10718	A	T	9: 3,025,118 (GRCm39)	Y194F	probably benign	Het
Gm21738	G	A	14: 19,416,979 (GRCm38)	S144L	probably benign	Het
Gm3604	A	T	13: 62,517,954 (GRCm39)	C134S	probably damaging	Het
Gpaa1	A	G	15: 76,217,198 (GRCm39)	T178A	probably benign	Het
Lama3	A	G	18: 12,657,820 (GRCm39)	N312S	possibly damaging	Het
Npepps	T	C	11: 97,126,948 (GRCm39)	I437M	probably damaging	Het
Or10q12	A	G	19: 13,746,534 (GRCm39)	D276G	probably benign	Het
Or11i1	C	T	3: 106,729,342 (GRCm39)	D178N	probably benign	Het
Rcor1	C	A	12: 111,070,193 (GRCm39)	T330K	possibly damaging	Het
Sbno2	A	G	10: 79,896,226 (GRCm39)		probably null	Het
Sema3g	A	G	14: 30,945,624 (GRCm39)	E478G	probably damaging	Het
Smg9	A	G	7: 24,115,949 (GRCm39)	D280G	probably damaging	Het
Smtnl1	A	T	2: 84,641,741 (GRCm39)	*460R	probably null	Het
Syde1	A	G	10: 78,424,753 (GRCm39)	C360R	possibly damaging	Het
Szt2	A	G	4: 118,256,268 (GRCm39)	V197A	possibly damaging	Het
Tnrc6c	T	C	11: 117,646,274 (GRCm39)	V1405A	possibly damaging	Het
Ttbk1	A	G	17: 46,757,989 (GRCm39)	S882P	probably damaging	Het
Tubgcp4	T	A	2: 121,006,269 (GRCm39)	H116Q	possibly damaging	Het
Vmn1r192	T	A	13: 22,371,750 (GRCm39)	N157Y	probably damaging	Het
Vmn1r60	C	T	7: 5,547,228 (GRCm39)	V291M	probably benign	Het
Vmn2r129	C	T	4: 156,690,549 (GRCm39)		noncoding transcript	Het
Xpo5	C	T	17: 46,553,133 (GRCm39)	P1184L	possibly damaging	Het
Zfp946	T	G	17: 22,673,684 (GRCm39)	I146S	probably benign	Het

Posted On

2014-05-07