Incidental Mutation 'R2149:Anp32a'
ID234119
Institutional Source Beutler Lab
Gene Symbol Anp32a
Ensembl Gene ENSMUSG00000032249
Gene Nameacidic (leucine-rich) nuclear phosphoprotein 32 family, member A
Synonymspp32, Anp32
MMRRC Submission 040152-MU
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #R2149 (G1)
Quality Score225
Status Not validated
Chromosome9
Chromosomal Location62341293-62378812 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to A at 62371802 bp
ZygosityHeterozygous
Amino Acid Change Phenylalanine to Tyrosine at position 46 (F46Y)
Ref Sequence ENSEMBL: ENSMUSP00000082652 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000085519] [ENSMUST00000128636] [ENSMUST00000135395]
PDB Structure
Structure of the Leucine-Rich Repeat domain of LANP [SOLUTION NMR]
Predicted Effect probably benign
Transcript: ENSMUST00000085519
AA Change: F46Y

PolyPhen 2 Score 0.185 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000082652
Gene: ENSMUSG00000032249
AA Change: F46Y

DomainStartEndE-ValueType
Pfam:LRR_4 64 107 5.2e-9 PFAM
Pfam:LRR_8 64 125 1.9e-9 PFAM
LRRcap 128 146 3.19e-2 SMART
coiled coil region 167 199 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000126451
Predicted Effect probably benign
Transcript: ENSMUST00000128636
AA Change: F49Y

PolyPhen 2 Score 0.010 (Sensitivity: 0.96; Specificity: 0.77)
SMART Domains Protein: ENSMUSP00000123574
Gene: ENSMUSG00000032249
AA Change: F49Y

DomainStartEndE-ValueType
Pfam:LRR_8 67 128 3.1e-10 PFAM
Pfam:LRR_4 77 111 3e-8 PFAM
Pfam:LRR_6 90 110 7.2e-6 PFAM
Pfam:LRR_7 91 107 9.5e-4 PFAM
Pfam:LRR_1 92 115 1.7e-4 PFAM
LRRcap 131 149 3.19e-2 SMART
coiled coil region 170 198 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000129026
Predicted Effect probably benign
Transcript: ENSMUST00000135395
AA Change: F32Y

PolyPhen 2 Score 0.034 (Sensitivity: 0.95; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000122165
Gene: ENSMUSG00000032249
AA Change: F32Y

DomainStartEndE-ValueType
Pfam:LRR_8 50 111 4.9e-10 PFAM
Pfam:LRR_6 73 93 9e-6 PFAM
Pfam:LRR_7 74 90 1.2e-3 PFAM
Pfam:LRR_1 75 98 2.2e-4 PFAM
LRRcap 114 132 3.19e-2 SMART
coiled coil region 153 185 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000136603
Predicted Effect noncoding transcript
Transcript: ENSMUST00000138226
Predicted Effect noncoding transcript
Transcript: ENSMUST00000141277
Predicted Effect noncoding transcript
Transcript: ENSMUST00000145679
Predicted Effect unknown
Transcript: ENSMUST00000156461
AA Change: F41Y
SMART Domains Protein: ENSMUSP00000115293
Gene: ENSMUSG00000032249
AA Change: F41Y

DomainStartEndE-ValueType
Pfam:LRR_9 5 138 8e-13 PFAM
Pfam:LRR_4 60 104 9.7e-10 PFAM
Pfam:LRR_8 60 121 8.6e-10 PFAM
Pfam:LRR_4 84 129 2.8e-9 PFAM
Pfam:LRR_1 85 106 1.4e-3 PFAM
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.1%
Validation Efficiency
MGI Phenotype PHENOTYPE: Homozygous mutant mice are viable, fertile, behaviorally normal, and show no defects of the central nervous system. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 85 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1500015O10Rik A G 1: 43,742,336 D126G probably damaging Het
1700006A11Rik T C 3: 124,409,686 E414G probably benign Het
3632451O06Rik T C 14: 49,751,571 D647G probably benign Het
Abca12 C A 1: 71,263,488 V2191L probably benign Het
Abca13 A G 11: 9,267,508 T317A possibly damaging Het
Acap3 T G 4: 155,905,625 L750R probably damaging Het
Anapc7 T A 5: 122,443,826 S511T probably benign Het
Anxa2 TCCC TCC 9: 69,489,754 probably null Het
Arfgef1 C T 1: 10,199,878 A349T probably benign Het
Arid2 T C 15: 96,370,835 I943T probably damaging Het
Auh G A 13: 52,835,496 P308L probably benign Het
BC003331 A T 1: 150,388,559 N66K probably benign Het
Btnl6 T C 17: 34,514,347 N218S possibly damaging Het
Capn11 T C 17: 45,633,107 probably null Het
Clcnkb C T 4: 141,408,017 G470D probably damaging Het
Clic6 T A 16: 92,499,207 S252T probably benign Het
Col28a1 T C 6: 8,155,383 K318E possibly damaging Het
Col5a3 A T 9: 20,771,270 V1626D unknown Het
Col6a4 C A 9: 106,076,929 A404S probably benign Het
Cyp2j5 G T 4: 96,641,340 H265N possibly damaging Het
Dennd3 A T 15: 73,555,060 H762L probably benign Het
Dock2 A G 11: 34,229,472 probably null Het
Emilin2 T C 17: 71,273,992 S580G probably benign Het
Fbn2 C A 18: 58,102,325 probably null Het
Gfm1 T C 3: 67,474,560 L693P probably damaging Het
Glb1 T C 9: 114,450,648 Y375H probably damaging Het
Gpha2 A G 19: 6,226,982 T38A probably damaging Het
Gtf2h3 T C 5: 124,599,785 probably benign Het
Hmgxb3 T C 18: 61,157,674 T376A probably benign Het
Hspa12b A G 2: 131,143,057 D416G probably damaging Het
Immt C T 6: 71,844,675 R28* probably null Het
Iqgap1 T C 7: 80,762,560 Y180C probably damaging Het
Kcnq3 T A 15: 66,023,729 D322V probably damaging Het
Kifc2 C A 15: 76,662,221 L268I probably benign Het
Lama1 T C 17: 67,773,865 M1296T possibly damaging Het
Lipk A G 19: 34,021,617 N104S possibly damaging Het
Lrrc14b T A 13: 74,363,757 N68I possibly damaging Het
Lrrc28 A T 7: 67,531,682 D268E probably damaging Het
Ly6c2 T C 15: 75,108,543 *132W probably null Het
Msh6 A G 17: 87,986,088 E757G probably damaging Het
Mtss1l T C 8: 110,726,383 V47A possibly damaging Het
Muc2 CGTG CGTGTG 7: 141,699,185 probably null Het
Nalcn A T 14: 123,370,017 I680N probably benign Het
Nup214 C T 2: 32,034,466 S1669F probably damaging Het
Olfr1501 A C 19: 13,838,582 V197G probably damaging Het
Olfr61 C T 7: 140,638,052 T117M probably damaging Het
Olfr713 A T 7: 107,036,338 Y61F possibly damaging Het
Olfr912 T C 9: 38,581,508 V77A probably benign Het
Oosp2 A T 19: 11,649,614 L17* probably null Het
Parvb A G 15: 84,232,168 K33E possibly damaging Het
Pde4dip T A 3: 97,792,836 Q300L possibly damaging Het
Phf2 T C 13: 48,804,689 K950E unknown Het
Pira2 G A 7: 3,844,171 P124L probably damaging Het
Plpp4 C T 7: 129,379,371 T157I probably benign Het
Polrmt G A 10: 79,740,275 Q545* probably null Het
Ptprs A G 17: 56,417,706 F1511L probably damaging Het
Sbno1 T C 5: 124,402,119 probably null Het
Setd1a T A 7: 127,786,518 V256D possibly damaging Het
Slamf1 T C 1: 171,767,272 S16P probably damaging Het
Slc16a14 T C 1: 84,907,399 D473G probably damaging Het
Slc8a2 A T 7: 16,159,164 H917L probably damaging Het
Sorbs2 A C 8: 45,795,443 D442A probably damaging Het
Srp68 G T 11: 116,260,867 T301K possibly damaging Het
Stab2 A T 10: 86,865,040 C457* probably null Het
Stk31 T G 6: 49,439,218 S652R possibly damaging Het
Stra6 T G 9: 58,152,539 S594R probably benign Het
Tbc1d9 G A 8: 83,271,449 E1212K probably damaging Het
Thada C T 17: 84,441,764 R593Q probably damaging Het
Tmem131 C A 1: 36,812,609 V938L probably benign Het
Tmem132c T A 5: 127,462,962 W351R probably damaging Het
Tmem206 T G 1: 191,345,109 F210V probably benign Het
Trim10 C T 17: 36,877,014 A374V probably benign Het
Try10 T C 6: 41,356,561 V80A probably benign Het
Ttn T C 2: 76,729,363 T29565A possibly damaging Het
Uggt2 G T 14: 119,075,345 Q351K probably benign Het
Vmn1r120 A T 7: 21,052,964 V274D probably damaging Het
Vmn1r62 A T 7: 5,675,359 H13L probably benign Het
Vmn2r101 C T 17: 19,588,963 T118I probably benign Het
Vmn2r114 ATTT ATT 17: 23,290,932 probably null Het
Vps51 A G 19: 6,068,134 V777A probably benign Het
Wnt5a A G 14: 28,513,317 Y86C probably damaging Het
Xpa T C 4: 46,183,189 E200G probably damaging Het
Zc3h12a C T 4: 125,126,642 R136K possibly damaging Het
Zc3hav1 T C 6: 38,336,537 H191R probably damaging Het
Zfp804a A G 2: 82,258,664 T946A probably benign Het
Other mutations in Anp32a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00655:Anp32a APN 9 62371712 splice site probably benign
IGL01799:Anp32a APN 9 62371810 missense probably benign 0.06
IGL02066:Anp32a APN 9 62377333 unclassified probably benign
IGL02536:Anp32a APN 9 62371828 missense probably damaging 0.98
R1608:Anp32a UTSW 9 62372093 missense probably damaging 0.99
R5287:Anp32a UTSW 9 62341993 missense possibly damaging 0.50
R5381:Anp32a UTSW 9 62372177 missense probably damaging 0.97
R5403:Anp32a UTSW 9 62341993 missense possibly damaging 0.50
R5427:Anp32a UTSW 9 62377316 unclassified probably benign
R6856:Anp32a UTSW 9 62372115 missense possibly damaging 0.95
R6906:Anp32a UTSW 9 62377569 unclassified probably benign
Predicted Primers PCR Primer
(F):5'- AGTGCTGATCTGGATAAGGC -3'
(R):5'- GTACACTTAACACCCAGCTCGG -3'

Sequencing Primer
(F):5'- CTGATCTGGATAAGGCAATTGATG -3'
(R):5'- TACTCTCCCCAGGCAGC -3'
Posted On2014-10-01