Incidental Mutation 'R4232:Atg14'
ID 320927
Institutional Source Beutler Lab
Gene Symbol Atg14
Ensembl Gene ENSMUSG00000037526
Gene Name autophagy related 14
Synonyms Barkor, D14Ertd436e, D14Ertd114e
MMRRC Submission 041051-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.864) question?
Stock # R4232 (G1)
Quality Score 225
Status Validated
Chromosome 14
Chromosomal Location 47778350-47805891 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 47788802 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Glutamic Acid at position 184 (K184E)
Ref Sequence ENSEMBL: ENSMUSP00000153718 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000042988] [ENSMUST00000226299]
AlphaFold Q8CDJ3
Predicted Effect probably benign
Transcript: ENSMUST00000042988
AA Change: K184E

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000039047
Gene: ENSMUSG00000037526
AA Change: K184E

DomainStartEndE-ValueType
Pfam:Atg14 43 393 1.1e-79 PFAM
low complexity region 447 464 N/A INTRINSIC
low complexity region 465 480 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000226299
AA Change: K184E

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.1%
  • 20x: 94.9%
Validation Efficiency 92% (58/63)
MGI Phenotype PHENOTYPE: Mice homozygous for a conditional allele following delivery of a Tat-cre exhibit increased mucin accumulation in colonic epithelial spheroids. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930567H17Rik C T X: 69,438,135 (GRCm39) A53T probably benign Het
Ajuba T C 14: 54,806,983 (GRCm39) R490G probably damaging Het
Akap6 T A 12: 53,186,454 (GRCm39) N1289K probably damaging Het
Arhgap21 A G 2: 20,891,948 (GRCm39) V161A probably damaging Het
Aven A G 2: 112,458,113 (GRCm39) D167G probably damaging Het
Celsr2 A G 3: 108,321,088 (GRCm39) F575L probably benign Het
Cflar A T 1: 58,780,152 (GRCm39) Q249L possibly damaging Het
Col7a1 G A 9: 108,801,881 (GRCm39) probably null Het
Dmxl2 T C 9: 54,327,193 (GRCm39) D944G possibly damaging Het
Dnah1 T C 14: 31,026,873 (GRCm39) N717S probably benign Het
Dnaja3 T A 16: 4,517,735 (GRCm39) N322K possibly damaging Het
Dnajb3 A G 1: 88,132,974 (GRCm39) S143P possibly damaging Het
Dtx3 A G 10: 127,029,058 (GRCm39) I60T possibly damaging Het
Dvl3 A G 16: 20,342,983 (GRCm39) probably benign Het
Fkbp7 A T 2: 76,493,661 (GRCm39) D177E possibly damaging Het
Galnt7 T C 8: 58,106,000 (GRCm39) I5V probably benign Het
Garin3 C A 11: 46,298,232 (GRCm39) T512K possibly damaging Het
Helz2 A T 2: 180,871,695 (GRCm39) L2639Q probably damaging Het
Hnrnpr T C 4: 136,066,500 (GRCm39) M394T probably benign Het
Ip6k2 G A 9: 108,682,847 (GRCm39) R319Q probably benign Het
Kif14 T A 1: 136,444,101 (GRCm39) C1364* probably null Het
Macf1 T C 4: 123,326,185 (GRCm39) E5104G probably damaging Het
Mrps30 T C 13: 118,523,376 (GRCm39) D132G probably damaging Het
Mrtfa T A 15: 80,907,796 (GRCm39) K29M probably damaging Het
Mtbp CATGA CATGAATGA 15: 55,484,073 (GRCm39) probably null Het
Nfkb1 A G 3: 135,309,531 (GRCm39) V521A probably damaging Het
Or2b7 T C 13: 21,739,631 (GRCm39) D187G probably damaging Het
Or7g32 G T 9: 19,389,022 (GRCm39) L175M probably damaging Het
P2rx6 T C 16: 17,388,631 (GRCm39) L335P probably damaging Het
Pcdhga5 A G 18: 37,829,001 (GRCm39) D483G possibly damaging Het
Pgpep1l T C 7: 67,886,827 (GRCm39) T161A probably benign Het
Prss40 A G 1: 34,599,873 (GRCm39) V38A probably benign Het
Ptk2 C A 15: 73,181,698 (GRCm39) R104L possibly damaging Het
Ralgapa1 C T 12: 55,687,429 (GRCm39) R2019Q probably damaging Het
Rin2 C T 2: 145,702,366 (GRCm39) T354I probably benign Het
Rtp4 A G 16: 23,431,833 (GRCm39) N122D possibly damaging Het
Samd8 A G 14: 21,830,213 (GRCm39) Y213C probably benign Het
Shcbp1 T A 8: 4,786,372 (GRCm39) T577S probably benign Het
Tiprl A G 1: 165,050,156 (GRCm39) V153A probably damaging Het
Tmprss7 A T 16: 45,476,936 (GRCm39) D775E probably damaging Het
Tnr T C 1: 159,713,785 (GRCm39) S738P possibly damaging Het
Tsc22d4 T C 5: 137,749,632 (GRCm39) probably null Het
Ttc21a A T 9: 119,771,684 (GRCm39) H161L probably benign Het
Ubqln3 T A 7: 103,791,010 (GRCm39) E360V probably benign Het
Ugt1a10 C A 1: 87,983,932 (GRCm39) D243E probably benign Het
Vmn2r19 G A 6: 123,306,871 (GRCm39) V460I probably benign Het
Vmn2r58 T A 7: 41,487,011 (GRCm39) Y628F possibly damaging Het
Wnk1 A T 6: 119,926,222 (GRCm39) S1588T possibly damaging Het
Wscd2 A G 5: 113,699,045 (GRCm39) D200G probably benign Het
Zfp831 G C 2: 174,547,447 (GRCm39) W1543C possibly damaging Het
Other mutations in Atg14
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02088:Atg14 APN 14 47,780,316 (GRCm39) missense probably benign 0.00
IGL02513:Atg14 APN 14 47,783,081 (GRCm39) splice site probably benign
IGL02513:Atg14 APN 14 47,786,451 (GRCm39) missense probably benign 0.03
PIT4243001:Atg14 UTSW 14 47,792,031 (GRCm39) missense possibly damaging 0.77
R1463:Atg14 UTSW 14 47,786,451 (GRCm39) missense probably benign 0.03
R1479:Atg14 UTSW 14 47,784,696 (GRCm39) critical splice donor site probably null
R1499:Atg14 UTSW 14 47,798,102 (GRCm39) missense probably benign
R1781:Atg14 UTSW 14 47,786,607 (GRCm39) critical splice acceptor site probably null
R1974:Atg14 UTSW 14 47,783,298 (GRCm39) missense probably damaging 1.00
R2089:Atg14 UTSW 14 47,780,352 (GRCm39) missense probably damaging 1.00
R2091:Atg14 UTSW 14 47,780,352 (GRCm39) missense probably damaging 1.00
R2091:Atg14 UTSW 14 47,780,352 (GRCm39) missense probably damaging 1.00
R2113:Atg14 UTSW 14 47,788,781 (GRCm39) missense probably damaging 1.00
R4231:Atg14 UTSW 14 47,788,802 (GRCm39) missense probably benign 0.00
R4233:Atg14 UTSW 14 47,788,802 (GRCm39) missense probably benign 0.00
R4234:Atg14 UTSW 14 47,788,802 (GRCm39) missense probably benign 0.00
R4236:Atg14 UTSW 14 47,788,802 (GRCm39) missense probably benign 0.00
R4360:Atg14 UTSW 14 47,805,827 (GRCm39) missense probably benign 0.00
R4711:Atg14 UTSW 14 47,783,298 (GRCm39) missense probably damaging 1.00
R4883:Atg14 UTSW 14 47,788,771 (GRCm39) missense probably damaging 1.00
R5025:Atg14 UTSW 14 47,783,273 (GRCm39) missense probably damaging 1.00
R5235:Atg14 UTSW 14 47,805,656 (GRCm39) missense probably damaging 0.98
R5250:Atg14 UTSW 14 47,805,656 (GRCm39) missense probably damaging 0.98
R5297:Atg14 UTSW 14 47,805,656 (GRCm39) missense probably damaging 0.98
R5301:Atg14 UTSW 14 47,805,656 (GRCm39) missense probably damaging 0.98
R5338:Atg14 UTSW 14 47,805,656 (GRCm39) missense probably damaging 0.98
R5450:Atg14 UTSW 14 47,788,921 (GRCm39) missense probably benign
R5475:Atg14 UTSW 14 47,805,793 (GRCm39) missense possibly damaging 0.83
R5799:Atg14 UTSW 14 47,784,752 (GRCm39) missense possibly damaging 0.63
R6489:Atg14 UTSW 14 47,786,480 (GRCm39) missense probably damaging 0.97
R7589:Atg14 UTSW 14 47,780,547 (GRCm39) missense probably benign 0.00
R7908:Atg14 UTSW 14 47,806,050 (GRCm39) unclassified probably benign
R9478:Atg14 UTSW 14 47,783,138 (GRCm39) missense probably damaging 1.00
R9643:Atg14 UTSW 14 47,788,780 (GRCm39) missense probably damaging 0.99
Z1088:Atg14 UTSW 14 47,805,749 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- ATGAGGCCCAGTAAAAGTGC -3'
(R):5'- AGTGAAGTTCCTCTGCGTG -3'

Sequencing Primer
(F):5'- GCCCAGTAAAAGTGCTGAAC -3'
(R):5'- GAAGTTCCTCTGCGTGCACAC -3'
Posted On 2015-06-12