Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02380:Txnl1'

291363

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Txnl1

Ensembl Gene

ENSMUSG00000024583

Gene Name

thioredoxin-like 1

Synonyms

TRP32, 32kDa

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.458) question?

Stock #

IGL02380

Quality Score

Status

Chromosome

Chromosomal Location

63795872-63825535 bp(-) (GRCm39)

Type of Mutation

splice site (6 bp from exon)

DNA Base Change (assembly)

A to G at 63807114 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000025476 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000025476] [ENSMUST00000025476]

AlphaFold

Q8CDN6

Predicted Effect

probably null
Transcript: ENSMUST00000025476

SMART Domains

Protein: ENSMUSP00000025476
Gene: ENSMUSG00000024583

Domain	Start	End	E-Value	Type
Pfam:Thioredoxin	6	106	5.8e-19	PFAM
Pfam:PITH	126	268	1.8e-44	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000025476

SMART Domains

Protein: ENSMUSP00000025476
Gene: ENSMUSG00000024583

Domain	Start	End	E-Value	Type
Pfam:Thioredoxin	6	106	5.8e-19	PFAM
Pfam:PITH	126	268	1.8e-44	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 46 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930433I11Rik	C	A	7: 40,643,968 (GRCm39)	P546T	possibly damaging	Het
Abca13	T	C	11: 9,241,599 (GRCm39)	I1154T	possibly damaging	Het
Abca8a	A	G	11: 109,969,641 (GRCm39)		probably benign	Het
Acsm5	A	T	7: 119,136,509 (GRCm39)	Q360L	probably benign	Het
Adamtsl5	T	C	10: 80,177,612 (GRCm39)	E350G	probably benign	Het
Adgrl2	A	T	3: 148,534,125 (GRCm39)	L1017*	probably null	Het
Aqr	T	C	2: 113,940,417 (GRCm39)	D1243G	probably damaging	Het
Arhgef17	G	T	7: 100,578,650 (GRCm39)	P766Q	possibly damaging	Het
Bclaf1	T	C	10: 20,201,113 (GRCm39)	V413A	possibly damaging	Het
Bcr	A	G	10: 75,011,131 (GRCm39)	D14G	probably benign	Het
Cadps2	C	T	6: 23,287,731 (GRCm39)	V1190I	probably benign	Het
Cdh9	A	G	15: 16,856,086 (GRCm39)	I709V	possibly damaging	Het
Cnbd1	C	A	4: 18,887,748 (GRCm39)		probably null	Het
Cnbd1	T	A	4: 18,887,749 (GRCm39)		probably null	Het
Col4a3	T	C	1: 82,650,509 (GRCm39)		probably benign	Het
Coro1a	T	A	7: 126,302,288 (GRCm39)	K20*	probably null	Het
Crb2	T	A	2: 37,673,447 (GRCm39)	D114E	probably damaging	Het
Dnah6	C	A	6: 73,053,623 (GRCm39)	K2870N	probably benign	Het
Fpr3	A	G	17: 18,191,254 (GRCm39)	H175R	probably benign	Het
Gk5	T	G	9: 96,032,533 (GRCm39)	S248A	possibly damaging	Het
Grm4	T	A	17: 27,653,635 (GRCm39)	I772F	probably damaging	Het
Gstt4	A	G	10: 75,653,073 (GRCm39)	I163T	possibly damaging	Het
Hr	A	G	14: 70,795,201 (GRCm39)	R278G	probably damaging	Het
Igfbp5	T	A	1: 72,903,108 (GRCm39)	R156*	probably null	Het
Ighv1-4	G	A	12: 114,450,753 (GRCm39)		probably benign	Het
Insyn2a	A	T	7: 134,500,873 (GRCm39)		probably null	Het
Kcna2	A	C	3: 107,012,274 (GRCm39)	Q285P	probably benign	Het
Klf5	A	T	14: 99,538,894 (GRCm39)	R102S	possibly damaging	Het
Ldb1	A	T	19: 46,022,929 (GRCm39)	M252K	possibly damaging	Het
Lrrc66	T	C	5: 73,787,009 (GRCm39)	I114V	possibly damaging	Het
Map1b	A	T	13: 99,567,651 (GRCm39)	I1690N	unknown	Het
Myo1a	A	G	10: 127,550,354 (GRCm39)	T565A	probably benign	Het
Nt5c	T	C	11: 115,382,127 (GRCm39)	D84G	possibly damaging	Het
Pde1b	A	G	15: 103,428,417 (GRCm39)	N51S	possibly damaging	Het
Pikfyve	T	A	1: 65,295,180 (GRCm39)	L1437Q	probably damaging	Het
Pld5	C	T	1: 175,967,610 (GRCm39)	V82I	probably damaging	Het
Psmb6	T	A	11: 70,416,737 (GRCm39)	N42K	probably benign	Het
Slco3a1	G	A	7: 74,204,238 (GRCm39)	S34F	probably damaging	Het
Slfn9	A	G	11: 82,872,046 (GRCm39)	Y897H	probably benign	Het
Spag6l	T	C	16: 16,581,033 (GRCm39)		probably null	Het
Srrm1	G	A	4: 135,052,415 (GRCm39)	P658L	unknown	Het
Tmem215	A	T	4: 40,474,534 (GRCm39)	I204F	probably benign	Het
Ube2q2	T	A	9: 55,070,296 (GRCm39)	D79E	probably benign	Het
Ugt2a3	T	C	5: 87,484,658 (GRCm39)	D122G	probably benign	Het
Vmn2r73	A	T	7: 85,507,383 (GRCm39)	I643K	probably benign	Het
Xkrx	T	A	X: 133,051,388 (GRCm39)	H421L	probably benign	Het

Other mutations in Txnl1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01637:Txnl1	APN	18	63,807,262 (GRCm39)	missense	probably damaging	0.98
R0631:Txnl1	UTSW	18	63,804,644 (GRCm39)	splice site	probably benign
R0638:Txnl1	UTSW	18	63,825,135 (GRCm39)	splice site	probably benign
R0948:Txnl1	UTSW	18	63,825,191 (GRCm39)	missense	possibly damaging	0.74
R1233:Txnl1	UTSW	18	63,808,539 (GRCm39)	missense	probably benign
R1990:Txnl1	UTSW	18	63,812,585 (GRCm39)	missense	probably benign
R1991:Txnl1	UTSW	18	63,812,585 (GRCm39)	missense	probably benign
R1992:Txnl1	UTSW	18	63,812,585 (GRCm39)	missense	probably benign
R2308:Txnl1	UTSW	18	63,804,691 (GRCm39)	missense	probably benign	0.38
R2979:Txnl1	UTSW	18	63,804,691 (GRCm39)	missense	probably benign	0.38
R4321:Txnl1	UTSW	18	63,812,561 (GRCm39)	missense	possibly damaging	0.63
R4352:Txnl1	UTSW	18	63,804,750 (GRCm39)	missense	possibly damaging	0.66
R4691:Txnl1	UTSW	18	63,804,750 (GRCm39)	missense	possibly damaging	0.66
R5218:Txnl1	UTSW	18	63,812,538 (GRCm39)	missense	probably benign	0.45
R5471:Txnl1	UTSW	18	63,809,997 (GRCm39)	missense	probably damaging	1.00
R5586:Txnl1	UTSW	18	63,797,396 (GRCm39)	missense	probably damaging	1.00
R7174:Txnl1	UTSW	18	63,804,667 (GRCm39)	missense	probably benign	0.06
R9273:Txnl1	UTSW	18	63,825,325 (GRCm39)	start gained	probably benign
R9308:Txnl1	UTSW	18	63,812,446 (GRCm39)	missense	probably benign	0.02
R9461:Txnl1	UTSW	18	63,810,050 (GRCm39)	missense	probably benign	0.00
X0026:Txnl1	UTSW	18	63,807,140 (GRCm39)	missense	probably damaging	1.00

Posted On

2015-04-16