Mutagenetix > Incidental Mutation

Incidental Mutation 'R1037:Dbnl'

93877

Institutional Source

Beutler Lab

Gene Symbol

Dbnl

Ensembl Gene

ENSMUSG00000020476

Gene Name

drebrin-like

Synonyms

ABP1, SH3P7, mAbp1

MMRRC Submission

039136-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.241) question?

Stock #

R1037 (G1)

Quality Score

185

Status

Validated

Chromosome

Chromosomal Location

5738488-5750962 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 5746807 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Serine at position 179 (F179S)

Ref Sequence

ENSEMBL: ENSMUSP00000105471 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000020768] [ENSMUST00000020769] [ENSMUST00000102928] [ENSMUST00000109845]

AlphaFold

Q62418

Predicted Effect

probably benign
Transcript: ENSMUST00000020768

SMART Domains

Protein: ENSMUSP00000020768
Gene: ENSMUSG00000020475

Domain	Start	End	E-Value	Type
PGAM	5	193	8.71e-20	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000020769
AA Change: F179S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000020769
Gene: ENSMUSG00000020476
AA Change: F179S

Domain	Start	End	E-Value	Type
ADF	7	133	2.39e-31	SMART
coiled coil region	180	233	N/A	INTRINSIC
low complexity region	334	345	N/A	INTRINSIC
SH3	380	436	1.62e-16	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000102928
AA Change: F179S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000099992
Gene: ENSMUSG00000020476
AA Change: F179S

Domain	Start	End	E-Value	Type
ADF	7	133	2.39e-31	SMART
coiled coil region	180	233	N/A	INTRINSIC
low complexity region	331	342	N/A	INTRINSIC
SH3	377	433	1.62e-16	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000109845
AA Change: F179S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000105471
Gene: ENSMUSG00000020476
AA Change: F179S

Domain	Start	End	E-Value	Type
ADF	7	133	2.39e-31	SMART
coiled coil region	180	233	N/A	INTRINSIC
low complexity region	330	341	N/A	INTRINSIC
SH3	376	432	1.62e-16	SMART

Meta Mutation Damage Score

0.6294

Coding Region Coverage

1x: 99.4%
3x: 98.1%
10x: 94.3%
20x: 85.9%

Validation Efficiency

100% (58/58)

MGI Phenotype

PHENOTYPE: Targeted mutation causes abnormal structure and function in organs including the spleen, heart and lungs. Vesicle transport is impaired in the brain and neurological impairment is observed. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 54 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4933405L10Rik	A	G	8: 106,436,144 (GRCm39)	S139G	probably benign	Het
Abca2	T	A	2: 25,328,240 (GRCm39)		probably benign	Het
Abcb1b	A	T	5: 8,875,657 (GRCm39)	N610I	probably benign	Het
Ahnak	T	C	19: 8,984,982 (GRCm39)	F2089L	probably benign	Het
Cacnb1	T	C	11: 97,895,843 (GRCm39)		probably benign	Het
Cep57	T	C	9: 13,730,275 (GRCm39)	I61V	possibly damaging	Het
Ckap5	T	C	2: 91,380,974 (GRCm39)	I110T	probably benign	Het
Clasp2	T	C	9: 113,725,702 (GRCm39)		probably benign	Het
Col11a1	A	C	3: 113,987,801 (GRCm39)	E265A	probably damaging	Het
Cst13	A	G	2: 148,672,251 (GRCm39)		probably benign	Het
Cyp24a1	G	A	2: 170,333,537 (GRCm39)	T272M	probably damaging	Het
Cyp4a14	A	C	4: 115,347,193 (GRCm39)	L415R	probably damaging	Het
Eepd1	T	C	9: 25,498,079 (GRCm39)	L388P	possibly damaging	Het
Exosc8	G	T	3: 54,640,159 (GRCm39)	A55E	probably damaging	Het
Fam72a	G	A	1: 131,461,557 (GRCm39)	V81I	probably damaging	Het
Fasn	C	T	11: 120,700,277 (GRCm39)	M2182I	probably benign	Het
Fras1	C	T	5: 96,862,322 (GRCm39)	P2234S	probably damaging	Het
Grn	C	A	11: 102,323,896 (GRCm39)	D33E	possibly damaging	Het
Gsap	A	G	5: 21,456,163 (GRCm39)		probably benign	Het
H2bc15	T	A	13: 21,938,417 (GRCm39)	V42E	probably damaging	Het
Hook3	T	C	8: 26,562,378 (GRCm39)	Q229R	possibly damaging	Het
Itgb6	T	C	2: 60,480,412 (GRCm39)	E308G	probably damaging	Het
Kmo	C	T	1: 175,479,184 (GRCm39)	P240L	possibly damaging	Het
Lrrc4c	A	G	2: 97,460,330 (GRCm39)	M319V	probably benign	Het
Mia3	T	C	1: 183,138,698 (GRCm39)	I672M	probably benign	Het
Mib2	C	T	4: 155,743,917 (GRCm39)	G42S	probably damaging	Het
Mlc1	A	G	15: 88,849,664 (GRCm39)	L223P	probably damaging	Het
Mmp21	T	C	7: 133,276,182 (GRCm39)	K554E	probably benign	Het
Nup160	C	T	2: 90,524,246 (GRCm39)	T383I	probably damaging	Het
Opcml	T	A	9: 28,814,595 (GRCm39)	D290E	probably damaging	Het
Or10a3b	T	A	7: 108,445,191 (GRCm39)	T9S	probably benign	Het
Or4a27	T	A	2: 88,559,376 (GRCm39)	D189V	probably damaging	Het
Or5ac19	C	T	16: 59,089,307 (GRCm39)	C241Y	probably damaging	Het
Or5d38	A	G	2: 87,954,573 (GRCm39)	I252T	probably damaging	Het
Or5k14	T	C	16: 58,693,333 (GRCm39)	Y60C	probably damaging	Het
Palm3	C	A	8: 84,755,901 (GRCm39)	T471K	probably benign	Het
Prl2c5	T	A	13: 13,360,492 (GRCm39)	L50*	probably null	Het
Pzp	T	C	6: 128,496,389 (GRCm39)	N281S	probably benign	Het
Qser1	T	C	2: 104,590,900 (GRCm39)	Y1722C	probably damaging	Het
Ryr3	A	G	2: 112,699,453 (GRCm39)	V879A	probably benign	Het
Sbno1	A	G	5: 124,531,975 (GRCm39)	S736P	possibly damaging	Het
Septin5	G	A	16: 18,441,844 (GRCm39)		probably benign	Het
Slc17a6	A	G	7: 51,298,996 (GRCm39)		probably benign	Het
Spag17	A	T	3: 100,010,433 (GRCm39)	T1976S	probably benign	Het
Swt1	A	T	1: 151,246,320 (GRCm39)		probably benign	Het
Tenm4	T	C	7: 96,446,688 (GRCm39)	W853R	probably damaging	Het
Thbs1	A	T	2: 117,953,532 (GRCm39)	Q983L	probably damaging	Het
Tmem191	A	G	16: 17,094,347 (GRCm39)		probably benign	Het
Tmprss11g	A	T	5: 86,638,606 (GRCm39)	V294D	probably damaging	Het
Tor1aip2	A	G	1: 155,941,082 (GRCm39)	S463G	probably benign	Het
Trim36	A	G	18: 46,329,385 (GRCm39)		probably benign	Het
Ttc1	A	G	11: 43,621,326 (GRCm39)	V285A	possibly damaging	Het
Uckl1	C	T	2: 181,214,278 (GRCm39)	R303H	possibly damaging	Het
Vwa8	C	A	14: 79,324,094 (GRCm39)	C1132*	probably null	Het

Other mutations in Dbnl

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00902:Dbnl	APN	11	5,748,105 (GRCm39)	missense	probably benign
IGL01101:Dbnl	APN	11	5,743,722 (GRCm39)	missense	possibly damaging	0.94
IGL01596:Dbnl	APN	11	5,748,279 (GRCm39)	missense	probably damaging	1.00
IGL01924:Dbnl	APN	11	5,747,142 (GRCm39)	missense	probably damaging	1.00
IGL02331:Dbnl	APN	11	5,749,997 (GRCm39)	makesense	probably null
R0433:Dbnl	UTSW	11	5,746,825 (GRCm39)	critical splice donor site	probably null
R0646:Dbnl	UTSW	11	5,745,441 (GRCm39)	splice site	probably benign
R0656:Dbnl	UTSW	11	5,747,321 (GRCm39)	missense	probably benign
R1691:Dbnl	UTSW	11	5,747,174 (GRCm39)	missense	probably null	0.12
R1883:Dbnl	UTSW	11	5,749,247 (GRCm39)	missense	probably benign	0.01
R1884:Dbnl	UTSW	11	5,749,247 (GRCm39)	missense	probably benign	0.01
R7033:Dbnl	UTSW	11	5,748,102 (GRCm39)	missense	probably benign	0.44
R7541:Dbnl	UTSW	11	5,745,486 (GRCm39)	missense	probably damaging	0.99
R7702:Dbnl	UTSW	11	5,748,048 (GRCm39)	missense	probably benign
R7761:Dbnl	UTSW	11	5,738,597 (GRCm39)	missense	probably benign	0.33
R7904:Dbnl	UTSW	11	5,741,779 (GRCm39)	splice site	probably null
R8725:Dbnl	UTSW	11	5,738,582 (GRCm39)	missense	probably benign	0.07
R8727:Dbnl	UTSW	11	5,738,582 (GRCm39)	missense	probably benign	0.07
R8837:Dbnl	UTSW	11	5,741,839 (GRCm39)	missense	possibly damaging	0.95
Z1088:Dbnl	UTSW	11	5,746,797 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- AAAACCTGCCTCAGCCTCTTGG -3'
(R):5'- TTCTGCAAAGGAGCTGCTCACTC -3'

Sequencing Primer
(F):5'- TTGAGCCTACCAGATGCAGTC -3'
(R):5'- TCACTCAGCCATGTGCAG -3'

Posted On

2014-01-05