Mutagenetix > Incidental Mutation

Incidental Mutation 'R8038:Tmem126b'

618334

Institutional Source

Beutler Lab

Gene Symbol

Tmem126b

Ensembl Gene

ENSMUSG00000030614

Gene Name

transmembrane protein 126B

Synonyms

1110001A23Rik

MMRRC Submission

067475-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.127) question?

Stock #

R8038 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

90118041-90125203 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 90118830 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Isoleucine at position 153 (V153I)

Ref Sequence

ENSEMBL: ENSMUSP00000032843 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000032843]

AlphaFold

Q9D1R1

Predicted Effect

probably benign
Transcript: ENSMUST00000032843
AA Change: V153I

PolyPhen 2 Score 0.406 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000032843
Gene: ENSMUSG00000030614
AA Change: V153I

Domain	Start	End	E-Value	Type
Pfam:DUF1370	51	228	2.9e-72	PFAM

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.3%

Validation Efficiency

100% (50/50)

Allele List at MGI

Other mutations in this stock

Total: 50 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acaca	T	A	11: 84,106,730 (GRCm39)	M143K	probably damaging	Het
Accs	A	T	2: 93,673,262 (GRCm39)		probably null	Het
Alkbh5	T	C	11: 60,429,811 (GRCm39)	V188A	probably damaging	Het
Cacna1h	C	T	17: 25,594,865 (GRCm39)	V2098I	probably damaging	Het
Chuk	A	G	19: 44,067,416 (GRCm39)	Y580H	probably damaging	Het
Col7a1	A	G	9: 108,786,360 (GRCm39)	N530S	unknown	Het
Cops2	A	T	2: 125,674,206 (GRCm39)	H420Q	probably benign	Het
Ctcfl	A	T	2: 172,943,698 (GRCm39)	C551S	probably damaging	Het
Depdc5	T	C	5: 33,116,692 (GRCm39)		probably null	Het
Dnmt1	A	C	9: 20,852,860 (GRCm39)	V82G	probably damaging	Het
Fam90a1a	A	T	8: 22,453,455 (GRCm39)	N270I	possibly damaging	Het
Foxn4	T	C	5: 114,394,658 (GRCm39)	D423G	probably damaging	Het
Hoxa5	A	G	6: 52,181,309 (GRCm39)	S8P	probably damaging	Het
Ighe	A	T	12: 113,233,053 (GRCm39)	V456D		Het
Ighv1-52	A	G	12: 115,109,210 (GRCm39)	F83S	probably damaging	Het
Itga2	A	T	13: 114,990,291 (GRCm39)	N921K	probably damaging	Het
Kdm2b	T	C	5: 123,098,958 (GRCm39)		probably benign	Het
Llgl2	T	G	11: 115,741,929 (GRCm39)	M657R	probably benign	Het
Lrrcc1	T	A	3: 14,630,890 (GRCm39)	I1019K	possibly damaging	Het
Lrriq3	A	T	3: 154,869,638 (GRCm39)	D321V	probably benign	Het
Lsm10	T	C	4: 125,991,890 (GRCm39)	V82A	probably damaging	Het
Mettl3	A	G	14: 52,537,421 (GRCm39)	S154P	possibly damaging	Het
Naip2	T	C	13: 100,298,570 (GRCm39)	I489V	probably benign	Het
Nat8f5	T	A	6: 85,794,667 (GRCm39)	T98S	possibly damaging	Het
Or10w1	G	A	19: 13,632,719 (GRCm39)	V309M	possibly damaging	Het
Or4c113	A	T	2: 88,885,212 (GRCm39)	L186Q	probably damaging	Het
Or7e166	G	T	9: 19,624,976 (GRCm39)	M284I	possibly damaging	Het
Or8d6	T	A	9: 39,854,177 (GRCm39)	V207D	probably damaging	Het
Pira1	C	G	7: 3,740,319 (GRCm39)	A301P	probably damaging	Het
Pld5	T	C	1: 175,872,463 (GRCm39)	I225V	probably benign	Het
Ppfia1	C	A	7: 144,068,653 (GRCm39)	A414S	possibly damaging	Het
Ppib	T	C	9: 65,967,615 (GRCm39)	V23A	probably benign	Het
Rabggta	A	T	14: 55,956,387 (GRCm39)	S361T	probably benign	Het
Rap1gap2	T	C	11: 74,283,109 (GRCm39)	S664G	probably benign	Het
Recql5	A	G	11: 115,818,178 (GRCm39)	V285A	possibly damaging	Het
Rtn4rl1	G	C	11: 75,156,707 (GRCm39)	E380Q	possibly damaging	Het
Scarb2	A	T	5: 92,599,307 (GRCm39)	S338T	probably damaging	Het
Skint4	T	G	4: 111,977,003 (GRCm39)		probably benign	Het
Slc13a5	T	C	11: 72,144,196 (GRCm39)	K294R	probably benign	Het
Spib	A	G	7: 44,179,310 (GRCm39)	F32S	probably benign	Het
Spint2	A	G	7: 28,959,554 (GRCm39)		probably benign	Het
Sycp2	A	T	2: 178,045,571 (GRCm39)	D16E	probably damaging	Het
Tab1	A	G	15: 80,044,471 (GRCm39)	T500A	probably benign	Het
Tecpr2	T	C	12: 110,902,854 (GRCm39)	F860L	probably benign	Het
Tg	A	G	15: 66,560,724 (GRCm39)	M1029V	probably benign	Het
Uba2	A	T	7: 33,847,022 (GRCm39)	Y440N	probably damaging	Het
Vwa2	A	G	19: 56,886,320 (GRCm39)	E129G	probably benign	Het
Wapl	A	G	14: 34,413,639 (GRCm39)	D167G	probably benign	Het
Zfp64	A	G	2: 168,741,932 (GRCm39)	F332S	probably damaging	Het
Zfp786	C	T	6: 47,798,188 (GRCm39)	R250H	probably benign	Het

Other mutations in Tmem126b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02111:Tmem126b	APN	7	90,118,269 (GRCm39)	missense	probably damaging	0.96
R1661:Tmem126b	UTSW	7	90,125,179 (GRCm39)	missense	probably damaging	1.00
R1665:Tmem126b	UTSW	7	90,125,179 (GRCm39)	missense	probably damaging	1.00
R1911:Tmem126b	UTSW	7	90,118,367 (GRCm39)	missense	possibly damaging	0.89
R2894:Tmem126b	UTSW	7	90,120,121 (GRCm39)	missense	probably damaging	0.99
R4519:Tmem126b	UTSW	7	90,118,316 (GRCm39)	missense	probably damaging	1.00
R5098:Tmem126b	UTSW	7	90,118,850 (GRCm39)	missense	probably damaging	1.00
R5425:Tmem126b	UTSW	7	90,120,155 (GRCm39)	missense	probably benign	0.06
R5750:Tmem126b	UTSW	7	90,118,865 (GRCm39)	missense	probably damaging	0.99
R7493:Tmem126b	UTSW	7	90,121,854 (GRCm39)	missense	probably benign	0.03
R8250:Tmem126b	UTSW	7	90,118,317 (GRCm39)	missense	probably damaging	0.99
R9580:Tmem126b	UTSW	7	90,118,231 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- GAAGAGTTTATCAGTACCACCCCTTC -3'
(R):5'- TGTTTACCTGTGGCTGCAAAC -3'

Sequencing Primer
(F):5'- GTGAGGACCAAAGTTTGATTCCC -3'
(R):5'- CCGTCTAGGTGACATAAGC -3'

Posted On

2020-01-23