Mutagenetix > Incidental Mutation

Incidental Mutation 'R4280:Pramel24'

322834

Institutional Source

Beutler Lab

Gene Symbol

Pramel24

Ensembl Gene

ENSMUSG00000046435

Gene Name

PRAME like 24

Synonyms

Gm13078

MMRRC Submission

041648-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.154) question?

Stock #

R4280 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

143446025-143455728 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 143452592 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 8 (T8A)

Ref Sequence

ENSEMBL: ENSMUSP00000077761 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000078695]

AlphaFold

A2AGW8

Predicted Effect

possibly damaging
Transcript: ENSMUST00000078695
AA Change: T8A

PolyPhen 2 Score 0.945 (Sensitivity: 0.80; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000077761
Gene: ENSMUSG00000046435
AA Change: T8A

Domain	Start	End	E-Value	Type
SCOP:d1a4ya_	204	412	4e-12	SMART

Meta Mutation Damage Score

0.1795

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.4%
20x: 95.4%

Validation Efficiency

100% (51/51)

Allele List at MGI

Other mutations in this stock

Total: 46 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Arhgap32	T	C	9: 32,171,185 (GRCm39)	C1322R	probably damaging	Het
Arl6ip1	AAAATAAATAAATAAATAAATAAATA	AAAATAAATAAATAAATAAATAAATAAATA	7: 117,721,122 (GRCm39)		probably benign	Het
Arvcf	G	A	16: 18,216,741 (GRCm39)	R292H	probably damaging	Het
Ccdc102a	C	A	8: 95,634,444 (GRCm39)	G382*	probably null	Het
Cd274	A	T	19: 29,357,871 (GRCm39)	M188L	probably benign	Het
Cep76	T	A	18: 67,773,229 (GRCm39)	D23V	probably benign	Het
Cimip3	T	C	17: 47,724,780 (GRCm39)	M17V	probably benign	Het
Clec12a	A	G	6: 129,340,892 (GRCm39)	Y224C	probably damaging	Het
Cplx2	A	G	13: 54,527,377 (GRCm39)	E87G	probably damaging	Het
Ctr9	A	G	7: 110,645,930 (GRCm39)		probably benign	Het
Dgat2	A	G	7: 98,808,204 (GRCm39)	I157T	probably damaging	Het
Epha1	G	T	6: 42,341,986 (GRCm39)	P355T	probably damaging	Het
Fabp3	C	T	4: 130,206,245 (GRCm39)		probably null	Het
Gmip	T	A	8: 70,266,251 (GRCm39)		probably benign	Het
Hephl1	A	G	9: 15,023,330 (GRCm39)	V24A	probably benign	Het
Itgb4	T	A	11: 115,881,761 (GRCm39)	M771K	probably damaging	Het
Mov10	A	C	3: 104,707,095 (GRCm39)	F635V	probably damaging	Het
Mtres1	A	T	10: 43,408,905 (GRCm39)	F79L	probably benign	Het
Or10ag60	A	G	2: 87,438,595 (GRCm39)	T288A	possibly damaging	Het
Or5an9	A	G	19: 12,187,302 (GRCm39)	Y124C	probably damaging	Het
Pbrm1	T	C	14: 30,829,269 (GRCm39)		probably null	Het
Plscr1l1	T	C	9: 92,225,701 (GRCm39)	Y8H	possibly damaging	Het
Plxnd1	A	T	6: 115,933,056 (GRCm39)		probably null	Het
Plxnd1	C	A	6: 115,933,055 (GRCm39)		probably benign	Het
Pnma5	T	C	X: 72,079,036 (GRCm39)	M549V	probably benign	Het
Polq	C	A	16: 36,902,419 (GRCm39)	Q2205K	probably damaging	Het
Ppp4r3c1	A	T	X: 88,976,105 (GRCm39)	W31R	probably damaging	Het
Psma8	T	A	18: 14,854,292 (GRCm39)	D57E	probably benign	Het
Rbm47	T	C	5: 66,183,520 (GRCm39)	Y361C	probably damaging	Het
Rec8	A	G	14: 55,856,091 (GRCm39)	H11R	probably damaging	Het
Ric1	A	G	19: 29,563,950 (GRCm39)	Y568C	probably damaging	Het
Rrp36	G	A	17: 46,983,302 (GRCm39)	T104I	probably damaging	Het
Rrs1	G	A	1: 9,616,364 (GRCm39)	G206S	probably damaging	Het
Scgb2b6	A	G	7: 31,318,367 (GRCm39)		noncoding transcript	Het
Skint5	T	A	4: 113,799,749 (GRCm39)	K126I	probably damaging	Het
Slc38a10	C	T	11: 120,028,704 (GRCm39)	G202D	probably damaging	Het
Supt5	G	A	7: 28,016,498 (GRCm39)	R761W	probably damaging	Het
Tmtc2	A	G	10: 105,184,294 (GRCm39)		probably null	Het
Tob1	T	C	11: 94,105,148 (GRCm39)	V228A	probably benign	Het
Traj44	T	C	14: 54,411,148 (GRCm39)		probably benign	Het
Trps1	G	A	15: 50,709,478 (GRCm39)	L291F	probably benign	Het
Ttn	T	A	2: 76,585,168 (GRCm39)	I22042F	probably damaging	Het
Ush2a	A	G	1: 188,310,658 (GRCm39)	Q2078R	probably benign	Het
Zbtb24	T	C	10: 41,340,916 (GRCm39)	S649P	probably benign	Het
Zfp28	A	T	7: 6,396,700 (GRCm39)	Q378H	probably benign	Het
Zfp429	A	C	13: 67,538,914 (GRCm39)	C177G	probably damaging	Het

Other mutations in Pramel24

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00976:Pramel24	APN	4	143,453,585 (GRCm39)	missense	probably damaging	1.00
IGL01122:Pramel24	APN	4	143,454,971 (GRCm39)	missense	probably benign	0.13
IGL02314:Pramel24	APN	4	143,455,012 (GRCm39)	missense	probably benign	0.00
IGL03089:Pramel24	APN	4	143,452,703 (GRCm39)	missense	probably benign	0.43
IGL03338:Pramel24	APN	4	143,453,312 (GRCm39)	missense	probably benign	0.01
R0233:Pramel24	UTSW	4	143,452,633 (GRCm39)	missense	possibly damaging	0.71
R0233:Pramel24	UTSW	4	143,452,633 (GRCm39)	missense	possibly damaging	0.71
R0349:Pramel24	UTSW	4	143,453,629 (GRCm39)	missense	probably benign	0.00
R0681:Pramel24	UTSW	4	143,454,622 (GRCm39)	missense	probably benign
R0963:Pramel24	UTSW	4	143,453,678 (GRCm39)	missense	possibly damaging	0.50
R1114:Pramel24	UTSW	4	143,453,425 (GRCm39)	missense	probably benign	0.01
R2070:Pramel24	UTSW	4	143,453,472 (GRCm39)	nonsense	probably null
R2475:Pramel24	UTSW	4	143,453,395 (GRCm39)	missense	probably benign	0.14
R3824:Pramel24	UTSW	4	143,453,255 (GRCm39)	missense	probably benign	0.00
R4050:Pramel24	UTSW	4	143,453,692 (GRCm39)	missense	probably benign	0.01
R4125:Pramel24	UTSW	4	143,452,850 (GRCm39)	nonsense	probably null
R4273:Pramel24	UTSW	4	143,453,416 (GRCm39)	nonsense	probably null
R4921:Pramel24	UTSW	4	143,454,896 (GRCm39)	missense	possibly damaging	0.95
R5223:Pramel24	UTSW	4	143,454,591 (GRCm39)	missense	probably benign	0.00
R7256:Pramel24	UTSW	4	143,452,849 (GRCm39)	missense	probably benign	0.23
R7640:Pramel24	UTSW	4	143,453,276 (GRCm39)	missense	probably benign	0.00
R7666:Pramel24	UTSW	4	143,455,085 (GRCm39)	missense	probably benign	0.00
R7683:Pramel24	UTSW	4	143,453,284 (GRCm39)	nonsense	probably null
R7981:Pramel24	UTSW	4	143,453,452 (GRCm39)	missense	probably benign	0.01
R8856:Pramel24	UTSW	4	143,453,303 (GRCm39)	missense	probably benign	0.33
R9050:Pramel24	UTSW	4	143,453,329 (GRCm39)	missense	probably benign	0.03
R9739:Pramel24	UTSW	4	143,454,997 (GRCm39)	missense	possibly damaging	0.94
R9757:Pramel24	UTSW	4	143,454,992 (GRCm39)	missense	probably benign	0.00
Z1088:Pramel24	UTSW	4	143,453,603 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TATTACCAGAAGGACCTTGAAGGATC -3'
(R):5'- GTTGGGAAAGGCCATGCTAC -3'

Sequencing Primer
(F):5'- ACCTTGAAGGATCTTTGGCAATGAG -3'
(R):5'- ACCACCATCTGCCTTAGTATGTTAGG -3'

Posted On

2015-06-20