Mutagenetix > Incidental Mutations

Incidental Mutation 'IGL03007:Tex101'

407609

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Tex101

Ensembl Gene

ENSMUSG00000062773

Gene Name

testis expressed gene 101

Synonyms

TES101RP, 1700008H15Rik

Accession Numbers

Is this an essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL03007

Quality Score

Status

Chromosome

Chromosomal Location

24668007-24676675 bp(-) (GRCm38)

Type of Mutation

splice site

DNA Base Change (assembly)

G to A at 24670481 bp

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000146082 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000078001] [ENSMUST00000205488] [ENSMUST00000206390]

Predicted Effect

probably benign
Transcript: ENSMUST00000078001

SMART Domains

Protein: ENSMUSP00000077150
Gene: ENSMUSG00000062773

Domain	Start	End	E-Value	Type
signal peptide	1	25	N/A	INTRINSIC
Pfam:UPAR_LY6	141	217	3.9e-15	PFAM
low complexity region	232	246	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000205488

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000206367

Predicted Effect

probably benign
Transcript: ENSMUST00000206390

Coding Region Coverage

Validation Efficiency

MGI Phenotype

PHENOTYPE: Male mice homozygous for a knockout allele of this marker are infertile due to the failure of sperm to migrate into the oviduct. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 35 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
9330159F19Rik	A	G	10: 29,222,038	N144D	possibly damaging	Het
A830010M20Rik	T	A	5: 107,503,676	V145E	probably benign	Het
A830031A19Rik	T	C	11: 24,049,248		probably benign	Het
Ankfy1	T	C	11: 72,750,521	F640S	probably damaging	Het
Asb8	A	G	15: 98,142,734	Y16H	probably damaging	Het
Astn1	T	C	1: 158,668,623		probably benign	Het
Celf3	A	G	3: 94,487,137	T183A	probably benign	Het
Dctn1	T	C	6: 83,182,708	V56A	probably damaging	Het
Erbb2	A	C	11: 98,428,993		probably benign	Het
Ighv6-4	A	T	12: 114,406,593	Y80N	possibly damaging	Het
Igsf9b	T	C	9: 27,333,082	S782P	probably damaging	Het
Itsn1	A	T	16: 91,784,162		probably benign	Het
Kcnt2	T	A	1: 140,354,507	Y77N	possibly damaging	Het
Lig3	T	C	11: 82,789,575	F359S	probably damaging	Het
Mtmr6	G	T	14: 60,289,535		probably benign	Het
Muc4	C	T	16: 32,752,048	S642F	possibly damaging	Het
Ncoa1	T	A	12: 4,339,114	I54F	possibly damaging	Het
Nfx1	C	A	4: 40,984,962	T362K	probably benign	Het
Ntrk1	T	C	3: 87,782,743	S449G	possibly damaging	Het
Odc1	T	A	12: 17,548,810	H230Q	probably benign	Het
Olfr26	C	T	9: 38,855,296	T78I	probably damaging	Het
Olfr348	T	C	2: 36,786,800	S92P	probably damaging	Het
Olfr63	A	G	17: 33,268,883	E53G	probably damaging	Het
Olfr963	T	C	9: 39,669,471	V138A	possibly damaging	Het
Plekhh2	A	C	17: 84,574,960	S665R	possibly damaging	Het
Qpct	T	A	17: 79,070,865	F155I	probably damaging	Het
Rcor2	C	A	19: 7,274,353	T379K	probably benign	Het
Rint1	A	G	5: 23,815,701	N574S	probably benign	Het
Rsbn1	C	T	3: 103,928,879	A411V	probably damaging	Het
Sbno2	A	T	10: 80,058,550		probably benign	Het
Sptb	A	G	12: 76,621,341	S661P	probably damaging	Het
Syn3	A	T	10: 86,064,914	M370K	possibly damaging	Het
Tmem255b	C	T	8: 13,457,066	T265I	possibly damaging	Het
Trio	G	T	15: 27,902,742	A211D	probably damaging	Het
Zfp638	C	A	6: 83,984,884	Q1902K	probably damaging	Het

Other mutations in Tex101

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02313:Tex101	APN	7	24668325	missense	probably damaging	1.00
IGL03357:Tex101	APN	7	24668333	missense	probably damaging	0.96
R1935:Tex101	UTSW	7	24668225	missense	probably benign	0.33
R1936:Tex101	UTSW	7	24668225	missense	probably benign	0.33
R4632:Tex101	UTSW	7	24668368	nonsense	probably null
R6109:Tex101	UTSW	7	24668313	missense	possibly damaging	0.79
R7049:Tex101	UTSW	7	24668258	missense	probably benign	0.03
R7276:Tex101	UTSW	7	24670404	missense	probably damaging	1.00
R7860:Tex101	UTSW	7	24669765	missense	probably damaging	1.00
R8092:Tex101	UTSW	7	24670353	missense	probably damaging	1.00
R8435:Tex101	UTSW	7	24668366	missense	probably damaging	1.00
R8514:Tex101	UTSW	7	24668532	missense	possibly damaging	0.87

Posted On

2016-08-02