Incidental Mutation 'R9145:Nxt2'
ID 694609
Institutional Source Beutler Lab
Gene Symbol Nxt2
Ensembl Gene ENSMUSG00000042271
Gene Name nuclear transport factor 2-like export factor 2
Synonyms P15-2, 6330587F24Rik
MMRRC Submission
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.310) question?
Stock # R9145 (G1)
Quality Score 221.999
Status Validated
Chromosome X
Chromosomal Location 141009766-141022688 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 141020747 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Alanine to Valine at position 118 (A118V)
Ref Sequence ENSEMBL: ENSMUSP00000108536 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000042329] [ENSMUST00000112913] [ENSMUST00000112914] [ENSMUST00000112916]
AlphaFold Q3UNA4
Predicted Effect possibly damaging
Transcript: ENSMUST00000042329
AA Change: A118V

PolyPhen 2 Score 0.779 (Sensitivity: 0.85; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000048221
Gene: ENSMUSG00000042271
AA Change: A118V

DomainStartEndE-ValueType
Pfam:NTF2 17 136 3.5e-31 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000112913
AA Change: A90V

PolyPhen 2 Score 0.779 (Sensitivity: 0.85; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000108535
Gene: ENSMUSG00000042271
AA Change: A90V

DomainStartEndE-ValueType
Pfam:NTF2 1 108 1.4e-25 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000112914
AA Change: A118V

PolyPhen 2 Score 0.779 (Sensitivity: 0.85; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000108536
Gene: ENSMUSG00000042271
AA Change: A118V

DomainStartEndE-ValueType
Pfam:NTF2 17 136 3.5e-31 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000112916
AA Change: A174V

PolyPhen 2 Score 0.754 (Sensitivity: 0.85; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000108538
Gene: ENSMUSG00000042271
AA Change: A174V

DomainStartEndE-ValueType
Pfam:NTF2 73 192 1.5e-31 PFAM
Meta Mutation Damage Score 0.4261 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 100% (79/79)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene contains a nuclear transport factor 2 (NTF2) domain, which plays an important role in the trafficking of macromolecules, ions, and small molecules between the cytoplasm and nucleus. This protein may also have a role in mRNA nuclear export. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jun 2011]
Allele List at MGI
Other mutations in this stock
Total: 78 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A2ml1 T A 6: 128,536,032 (GRCm39) H720L probably benign Het
Abca15 T C 7: 119,987,388 (GRCm39) Y1225H probably benign Het
Adck1 C A 12: 88,335,193 (GRCm39) N26K probably benign Het
Adcy3 A G 12: 4,245,208 (GRCm39) D382G probably damaging Het
Ahi1 T A 10: 20,876,488 (GRCm39) C800S probably benign Het
Ahnak G T 19: 8,992,287 (GRCm39) V4524L probably benign Het
Aoc1l1 C A 6: 48,952,890 (GRCm39) R272S probably benign Het
Apol11a C T 15: 77,397,778 (GRCm39) A43V probably benign Het
Arid1a T C 4: 133,421,214 (GRCm39) M479V unknown Het
Atp13a2 T A 4: 140,724,056 (GRCm39) C324S probably damaging Het
C2cd2 T G 16: 97,677,486 (GRCm39) T413P probably damaging Het
Cct5 A C 15: 31,591,107 (GRCm39) D531E Het
Chst1 A T 2: 92,444,523 (GRCm39) I332F probably damaging Het
Col12a1 A T 9: 79,527,344 (GRCm39) V2662D probably benign Het
Cts3 A G 13: 61,712,800 (GRCm39) Y307H probably benign Het
D630023F18Rik G A 1: 65,160,371 (GRCm39) probably benign Het
Dhx9 A G 1: 153,336,826 (GRCm39) I807T probably damaging Het
Exoc3l4 T C 12: 111,388,586 (GRCm39) L25P probably benign Het
Ggcx T A 6: 72,402,905 (GRCm39) C288S probably benign Het
Gjb3 A G 4: 127,220,140 (GRCm39) Y131H probably damaging Het
Hdhd3 A G 4: 62,417,574 (GRCm39) S201P probably benign Het
Helz2 A T 2: 180,881,848 (GRCm39) V315E probably damaging Het
Hsp90aa1 A G 12: 110,662,684 (GRCm39) probably null Het
Ift70a1 A T 2: 75,810,423 (GRCm39) Y553* probably null Het
Il12a C T 3: 68,598,875 (GRCm39) R19W unknown Het
Isoc1 C T 18: 58,806,347 (GRCm39) A219V possibly damaging Het
Jup T A 11: 100,269,124 (GRCm39) T430S probably benign Het
Klra5 C T 6: 129,886,911 (GRCm39) C39Y probably benign Het
Map4 A T 9: 109,855,268 (GRCm39) Q131L probably damaging Het
Mau2 T A 8: 70,480,165 (GRCm39) K314M probably damaging Het
Mga A G 2: 119,794,493 (GRCm39) M2726V probably benign Het
Mgme1 G A 2: 144,114,405 (GRCm39) probably null Het
Msrb2 A G 2: 19,399,066 (GRCm39) E143G probably benign Het
Muc5b G T 7: 141,411,350 (GRCm39) C1432F unknown Het
Naglu T C 11: 100,961,940 (GRCm39) Y138H probably damaging Het
Nicn1 C T 9: 108,171,708 (GRCm39) R163C possibly damaging Het
Nlrp1b A G 11: 71,109,193 (GRCm39) Y103H probably benign Het
Nodal A G 10: 61,259,459 (GRCm39) N299D probably damaging Het
Notch1 T C 2: 26,349,587 (GRCm39) T2518A probably benign Het
Nr2e1 A C 10: 42,448,948 (GRCm39) S97A probably benign Het
Nuak1 A T 10: 84,210,587 (GRCm39) S500R probably benign Het
Nyap1 T C 5: 137,736,175 (GRCm39) E104G probably benign Het
Or3a1b C T 11: 74,012,526 (GRCm39) T137I probably benign Het
Or52e18 T A 7: 104,609,204 (GRCm39) H245L probably damaging Het
Palld T C 8: 62,330,107 (GRCm39) T257A probably benign Het
Pcnx4 C T 12: 72,603,043 (GRCm39) P435L probably damaging Het
Piezo1 T C 8: 123,208,753 (GRCm39) T2538A unknown Het
Plagl1 T C 10: 13,003,872 (GRCm39) L380P unknown Het
Polrmt G T 10: 79,576,415 (GRCm39) Q514K probably benign Het
Psg17 T G 7: 18,553,851 (GRCm39) D133A probably benign Het
Rab3b G A 4: 108,797,903 (GRCm39) D185N probably benign Het
Ranbp2 T A 10: 58,291,736 (GRCm39) S248T probably benign Het
Rdh10 C A 1: 16,199,430 (GRCm39) A212D probably damaging Het
Rinl A G 7: 28,495,089 (GRCm39) H154R Het
Selenbp1 T C 3: 94,851,414 (GRCm39) M389T probably benign Het
Serpina1c T A 12: 103,862,400 (GRCm39) H305L possibly damaging Het
Sh3rf2 T A 18: 42,282,746 (GRCm39) S467T Het
Sipa1l1 A G 12: 82,443,335 (GRCm39) D875G probably benign Het
Slc10a6 A T 5: 103,776,800 (GRCm39) V100D probably damaging Het
Slc13a4 T C 6: 35,247,290 (GRCm39) I577V possibly damaging Het
Slc20a2 T C 8: 23,030,447 (GRCm39) F168L probably benign Het
Slc25a1 A T 16: 17,745,108 (GRCm39) probably null Het
Slc5a12 A G 2: 110,471,242 (GRCm39) S495G probably benign Het
Smpdl3a A G 10: 57,677,028 (GRCm39) D42G possibly damaging Het
Spag16 G C 1: 70,420,459 (GRCm39) L482F probably damaging Het
Susd5 G A 9: 113,925,289 (GRCm39) G391R probably damaging Het
Sync G T 4: 129,187,618 (GRCm39) A217S Het
Tha1 T A 11: 117,759,512 (GRCm39) N326Y probably damaging Het
Tjp1 A T 7: 64,952,564 (GRCm39) F1590Y probably benign Het
Tle4 T C 19: 14,445,583 (GRCm39) N221S probably benign Het
Tln1 T C 4: 43,536,024 (GRCm39) T2054A probably damaging Het
Ttll4 A G 1: 74,718,949 (GRCm39) K267E probably benign Het
Usp32 C T 11: 84,913,118 (GRCm39) G930D probably damaging Het
Vmn2r75 T C 7: 85,813,447 (GRCm39) N452D probably damaging Het
Vmn2r81 T C 10: 79,104,028 (GRCm39) L217P possibly damaging Het
Wnt2 T A 6: 18,030,397 (GRCm39) probably benign Het
Zfp459 C T 13: 67,556,735 (GRCm39) S116N probably benign Het
Zfp981 C A 4: 146,622,410 (GRCm39) T445N possibly damaging Het
Other mutations in Nxt2
AlleleSourceChrCoordTypePredicted EffectPPH Score
R9016:Nxt2 UTSW X 141,020,747 (GRCm39) missense possibly damaging 0.78
R9018:Nxt2 UTSW X 141,020,747 (GRCm39) missense possibly damaging 0.78
R9064:Nxt2 UTSW X 141,020,747 (GRCm39) missense possibly damaging 0.78
R9065:Nxt2 UTSW X 141,020,747 (GRCm39) missense possibly damaging 0.78
R9066:Nxt2 UTSW X 141,020,747 (GRCm39) missense possibly damaging 0.78
R9114:Nxt2 UTSW X 141,020,747 (GRCm39) missense possibly damaging 0.78
R9115:Nxt2 UTSW X 141,020,747 (GRCm39) missense possibly damaging 0.78
R9144:Nxt2 UTSW X 141,020,747 (GRCm39) missense possibly damaging 0.78
R9146:Nxt2 UTSW X 141,020,747 (GRCm39) missense possibly damaging 0.78
R9147:Nxt2 UTSW X 141,020,747 (GRCm39) missense possibly damaging 0.78
R9148:Nxt2 UTSW X 141,020,747 (GRCm39) missense possibly damaging 0.78
R9149:Nxt2 UTSW X 141,020,747 (GRCm39) missense possibly damaging 0.78
R9326:Nxt2 UTSW X 141,020,747 (GRCm39) missense possibly damaging 0.78
R9327:Nxt2 UTSW X 141,020,747 (GRCm39) missense possibly damaging 0.78
R9480:Nxt2 UTSW X 141,020,747 (GRCm39) missense possibly damaging 0.78
R9521:Nxt2 UTSW X 141,020,747 (GRCm39) missense possibly damaging 0.78
X0064:Nxt2 UTSW X 141,012,590 (GRCm39) start codon destroyed probably null 1.00
Predicted Primers PCR Primer
(F):5'- TGGGATGCCTGCTTAAAGTACAG -3'
(R):5'- TCCAAACTGGCAGCTGATC -3'

Sequencing Primer
(F):5'- GCCTGCTTAAAGTACAGAATAGTC -3'
(R):5'- TGGACCAATAGAGTGGGT -3'
Posted On 2022-01-20