Mutagenetix > Incidental Mutation

Incidental Mutation 'R1159:Anp32b'

101943

Institutional Source

Beutler Lab

Gene Symbol

Anp32b

Ensembl Gene

ENSMUSG00000028333

Gene Name

acidic nuclear phosphoprotein 32 family member B

Synonyms

PAL31, PHAPI2a, 2410015B15Rik

MMRRC Submission

039232-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.786) question?

Stock #

R1159 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

46450926-46472657 bp(+) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

T to C at 46471478 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000099990 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000102926]

AlphaFold

Q9EST5

Predicted Effect

probably benign
Transcript: ENSMUST00000102926

SMART Domains

Protein: ENSMUSP00000099990
Gene: ENSMUSG00000028333

Domain	Start	End	E-Value	Type
Pfam:LRR_8	64	125	3.8e-9	PFAM
LRRcap	128	146	1.51e-3	SMART
low complexity region	170	259	N/A	INTRINSIC

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.1%
3x: 98.2%
10x: 96.1%
20x: 91.8%

Validation Efficiency

100% (42/42)

MGI Phenotype

PHENOTYPE: Mice homozygous for a knock-out allele exhibit background-sensitive partial perinatal lethality with failure to initiate breathing, craniofacial defects, enlarged brain ventricle, expanded inner ear cavities, plate closure defects, decreased body weight, premature aging, and premature death. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 39 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aass	G	A	6: 23,115,137 (GRCm39)	H164Y	probably damaging	Het
Acss2	T	C	2: 155,393,138 (GRCm39)	I288T	probably benign	Het
Akap9	C	T	5: 4,010,865 (GRCm39)	R541C	probably damaging	Het
Ano5	T	C	7: 51,229,222 (GRCm39)		probably benign	Het
Avil	T	C	10: 126,847,659 (GRCm39)	V528A	possibly damaging	Het
Cacna1c	C	T	6: 118,589,586 (GRCm39)	R1446H	probably damaging	Het
Cdk10	T	C	8: 123,955,062 (GRCm39)		probably benign	Het
Cfap65	A	T	1: 74,968,499 (GRCm39)	F111Y	probably damaging	Het
Cryge	A	G	1: 65,089,967 (GRCm39)	F72L	probably benign	Het
Ercc3	C	T	18: 32,397,611 (GRCm39)	T614I	possibly damaging	Het
Fgd5	T	C	6: 91,965,483 (GRCm39)	I572T	probably benign	Het
Fubp1	A	G	3: 151,921,229 (GRCm39)	D88G	possibly damaging	Het
Gcnt1	C	A	19: 17,307,168 (GRCm39)	V186F	possibly damaging	Het
Gldc	A	T	19: 30,138,162 (GRCm39)		probably benign	Het
Gxylt2	A	G	6: 100,781,602 (GRCm39)	M426V	possibly damaging	Het
Hps5	A	T	7: 46,421,978 (GRCm39)		probably null	Het
Igf2bp2	G	A	16: 21,880,603 (GRCm39)		probably benign	Het
Lamb2	T	C	9: 108,358,607 (GRCm39)	S215P	probably damaging	Het
Mfsd13b	T	C	7: 120,613,766 (GRCm39)	M421T	probably damaging	Het
Mtif2	C	A	11: 29,490,729 (GRCm39)	R478S	possibly damaging	Het
Nadk2	G	A	15: 9,106,925 (GRCm39)	R351H	possibly damaging	Het
Nt5dc1	T	C	10: 34,274,169 (GRCm39)	D167G	possibly damaging	Het
Nup98	T	A	7: 101,809,923 (GRCm39)	T536S	probably damaging	Het
Parp14	G	A	16: 35,677,130 (GRCm39)	A946V	probably benign	Het
Ppig	T	A	2: 69,580,568 (GRCm39)	S701T	unknown	Het
Pramel17	T	C	4: 101,695,224 (GRCm39)	E29G	possibly damaging	Het
Ptprc	A	G	1: 138,000,057 (GRCm39)	S830P	probably damaging	Het
Rev3l	T	A	10: 39,727,921 (GRCm39)	L2690*	probably null	Het
Rgs22	A	T	15: 36,040,839 (GRCm39)	S883T	probably damaging	Het
Rxfp4	A	G	3: 88,559,894 (GRCm39)	W186R	probably damaging	Het
Sacm1l	T	C	9: 123,395,476 (GRCm39)	S200P	probably benign	Het
Serpinb6d	T	A	13: 33,855,212 (GRCm39)	D295E	probably damaging	Het
Slc38a10	A	G	11: 119,996,301 (GRCm39)	V932A	probably benign	Het
Top2b	T	C	14: 16,430,329 (GRCm38)	S1568P	possibly damaging	Het
Tox	T	G	4: 6,697,600 (GRCm39)	N401T	probably benign	Het
Trim24	T	C	6: 37,933,412 (GRCm39)		probably null	Het
Unc79	T	G	12: 103,013,311 (GRCm39)		probably benign	Het
Vmn2r66	A	T	7: 84,644,613 (GRCm39)	I599N	probably benign	Het
Zfa-ps	T	A	10: 52,419,654 (GRCm39)		noncoding transcript	Het

Other mutations in Anp32b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R1753:Anp32b	UTSW	4	46,460,241 (GRCm39)	critical splice donor site	probably null
R5387:Anp32b	UTSW	4	46,468,573 (GRCm39)	missense	probably damaging	1.00
R5622:Anp32b	UTSW	4	46,469,930 (GRCm39)	missense	unknown
R5688:Anp32b	UTSW	4	46,469,868 (GRCm39)	splice site	probably null
R7875:Anp32b	UTSW	4	46,451,301 (GRCm39)	missense	probably benign	0.00
R9051:Anp32b	UTSW	4	46,468,592 (GRCm39)	missense	possibly damaging	0.95
R9233:Anp32b	UTSW	4	46,463,909 (GRCm39)	missense	probably damaging	0.99
X0026:Anp32b	UTSW	4	46,468,747 (GRCm39)	missense	unknown
X0062:Anp32b	UTSW	4	46,460,091 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

Posted On

2014-01-15