Incidental Mutation 'R9335:Afm'
ID 707062
Institutional Source Beutler Lab
Gene Symbol Afm
Ensembl Gene ENSMUSG00000029369
Gene Name afamin
Synonyms alpha albumin, Alf
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.054) question?
Stock # R9335 (G1)
Quality Score 225.009
Status Not validated
Chromosome 5
Chromosomal Location 90666808-90701403 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 90698086 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Valine at position 496 (D496V)
Ref Sequence ENSEMBL: ENSMUSP00000108804 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000113179] [ENSMUST00000128740]
AlphaFold O89020
Predicted Effect probably damaging
Transcript: ENSMUST00000113179
AA Change: D496V

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000108804
Gene: ENSMUSG00000029369
AA Change: D496V

DomainStartEndE-ValueType
ALBUMIN 20 205 3.69e-55 SMART
ALBUMIN 212 397 6.42e-64 SMART
ALBUMIN 404 593 3.07e-61 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000128740
SMART Domains Protein: ENSMUSP00000117180
Gene: ENSMUSG00000029369

DomainStartEndE-ValueType
ALBUMIN 20 205 3.69e-55 SMART
ALBUMIN 212 397 6.42e-64 SMART
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.4%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of the albumin gene family, which is comprised of four genes that localize to chromosome 4 in a tandem arrangement. These four genes encode structurally-related serum transport proteins that are known to be evolutionarily related. The protein encoded by this gene is regulated developmentally, expressed in the liver and secreted into the bloodstream. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 77 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4932438H23Rik G T 16: 90,852,830 (GRCm39) T102K probably damaging Het
Aldh1l2 C T 10: 83,342,510 (GRCm39) M546I probably damaging Het
Apol7c G T 15: 77,409,889 (GRCm39) N352K probably benign Het
Arfgef1 A T 1: 10,228,236 (GRCm39) D1319E probably damaging Het
Atl2 A G 17: 80,160,207 (GRCm39) I460T probably benign Het
Brms1l C A 12: 55,888,431 (GRCm39) T73K possibly damaging Het
C1rl A T 6: 124,482,341 (GRCm39) H154L probably benign Het
Cacna2d4 T A 6: 119,279,014 (GRCm39) L709Q probably damaging Het
Cd101 A T 3: 100,915,431 (GRCm39) V716D probably benign Het
Cd177 A G 7: 24,443,711 (GRCm39) S796P probably benign Het
D430041D05Rik A T 2: 104,078,674 (GRCm39) M530K probably damaging Het
Dcbld2 A T 16: 58,272,141 (GRCm39) Q399L probably benign Het
Dennd4b T C 3: 90,175,611 (GRCm39) Y138H probably damaging Het
Dmxl1 A G 18: 49,992,187 (GRCm39) N311S probably damaging Het
Dnai2 A G 11: 114,625,489 (GRCm39) I107V probably benign Het
Dync2h1 A C 9: 7,112,149 (GRCm39) V2480G possibly damaging Het
Ect2l T A 10: 18,077,032 (GRCm39) T24S probably null Het
Egfr C A 11: 16,820,991 (GRCm39) T302K probably damaging Het
Eid1 T G 2: 125,515,578 (GRCm39) I156S possibly damaging Het
Elmod1 A T 9: 53,843,116 (GRCm39) W21R probably benign Het
Enah G A 1: 181,749,450 (GRCm39) P463L probably damaging Het
Epha7 A G 4: 28,966,529 (GRCm39) Y602C probably benign Het
Ermap T A 4: 119,035,545 (GRCm39) Y481F probably damaging Het
Fam114a2 G T 11: 57,397,748 (GRCm39) T231N possibly damaging Het
Gdap1 A G 1: 17,231,389 (GRCm39) T245A probably benign Het
Glmp T A 3: 88,235,563 (GRCm39) V368D probably damaging Het
Gm10203 C T 6: 149,031,815 (GRCm39) A40V unknown Het
Gm4553 ACCCTTGCAGCCACCACAGGAGCCACAGCCCCCACAGGAGCTACAGCCTCCCTTGCAGCCACCACAGGAGCCACAGCCCCCACAGGAGCTACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCC ACCCTTGCAGCCACCACAGGAGCCACAGCCCCCACAGGAGCTACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCC 7: 141,719,157 (GRCm39) probably benign Het
Grid1 G A 14: 35,043,664 (GRCm39) D340N probably damaging Het
Hao2 C A 3: 98,791,010 (GRCm39) V55L possibly damaging Het
Hemgn A T 4: 46,394,647 (GRCm39) S488T probably benign Het
Ighv12-3 C T 12: 114,330,312 (GRCm39) G61E probably damaging Het
Itga2b T C 11: 102,346,478 (GRCm39) E986G probably damaging Het
Laptm5 T G 4: 130,656,839 (GRCm39) S167A Het
Lmtk3 A T 7: 45,442,165 (GRCm39) Y377F probably damaging Het
Lrp2 A G 2: 69,258,983 (GRCm39) I4569T probably benign Het
Magi2 A G 5: 20,866,263 (GRCm39) N176D Het
Mcf2l C A 8: 13,050,812 (GRCm39) H356N possibly damaging Het
Mettl4 T A 17: 95,042,936 (GRCm39) Y300F probably damaging Het
Naaladl2 T G 3: 24,467,532 (GRCm39) K307N possibly damaging Het
Or1a1b T A 11: 74,097,832 (GRCm39) D70V probably damaging Het
Or2aj4 G A 16: 19,385,513 (GRCm39) T40I probably benign Het
Or51ag1 C T 7: 103,155,727 (GRCm39) R142H probably benign Het
Or6c8b C T 10: 128,882,614 (GRCm39) G106E probably damaging Het
Phip T A 9: 82,814,979 (GRCm39) M248L probably benign Het
Picalm A G 7: 89,825,491 (GRCm39) T300A probably benign Het
Ppa1 T G 10: 61,484,562 (GRCm39) V19G possibly damaging Het
Ppp4r3a T C 12: 101,007,013 (GRCm39) Y793C probably damaging Het
Prlr A T 15: 10,325,357 (GRCm39) I177F probably benign Het
Prodh C A 16: 17,894,160 (GRCm39) G457V probably damaging Het
Prrt3 T C 6: 113,475,058 (GRCm39) K55E probably benign Het
Prx G T 7: 27,217,496 (GRCm39) V805L probably damaging Het
Ptk6 T G 2: 180,844,146 (GRCm39) D51A probably damaging Het
Rec114 T A 9: 58,565,041 (GRCm39) Q205L probably null Het
Rfwd3 T G 8: 112,006,567 (GRCm39) K510Q possibly damaging Het
Sdhb C T 4: 140,700,250 (GRCm39) R117C probably benign Het
Serinc2 T G 4: 130,158,220 (GRCm39) T21P probably benign Het
Serpinb3a A C 1: 106,974,886 (GRCm39) F216V probably damaging Het
Sertm1 T C 3: 54,806,929 (GRCm39) D32G probably damaging Het
Setx A G 2: 29,035,963 (GRCm39) D816G probably benign Het
Sfxn4 T A 19: 60,839,494 (GRCm39) N188I probably damaging Het
Slc26a4 T C 12: 31,575,553 (GRCm39) D711G probably damaging Het
Sp9 T C 2: 73,104,621 (GRCm39) F392L probably damaging Het
Ssbp1 T C 6: 40,454,955 (GRCm39) L138P probably damaging Het
Sv2a G A 3: 96,092,588 (GRCm39) G96E probably damaging Het
Tbc1d9 G T 8: 83,937,160 (GRCm39) G81C possibly damaging Het
Tmem67 G A 4: 12,040,640 (GRCm39) Q968* probably null Het
Tnni2 T C 7: 141,998,003 (GRCm39) S169P probably damaging Het
Tpk1 T C 6: 43,446,084 (GRCm39) probably null Het
Unc13b T A 4: 43,216,123 (GRCm39) Y141N possibly damaging Het
Unc13b A T 4: 43,255,551 (GRCm39) E1057D probably damaging Het
Usf3 G T 16: 44,041,936 (GRCm39) G2139C probably damaging Het
Vmn1r36 A T 6: 66,693,430 (GRCm39) Y148* probably null Het
Vmn2r42 A C 7: 8,197,758 (GRCm39) M287R probably damaging Het
Vmn2r60 A T 7: 41,844,332 (GRCm39) H565L probably damaging Het
Zfp518a G A 19: 40,901,225 (GRCm39) V385I probably benign Het
Zfp974 A T 7: 27,611,476 (GRCm39) M83K probably benign Het
Other mutations in Afm
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00911:Afm APN 5 90,673,450 (GRCm39) missense probably benign 0.01
IGL01140:Afm APN 5 90,672,726 (GRCm39) missense probably damaging 1.00
IGL01789:Afm APN 5 90,673,443 (GRCm39) missense probably benign 0.32
IGL01819:Afm APN 5 90,672,765 (GRCm39) missense probably benign 0.01
IGL01826:Afm APN 5 90,672,787 (GRCm39) splice site probably benign
IGL01875:Afm APN 5 90,696,742 (GRCm39) utr 3 prime probably benign
IGL02337:Afm APN 5 90,695,770 (GRCm39) missense probably benign
IGL02902:Afm APN 5 90,674,222 (GRCm39) missense possibly damaging 0.58
IGL02950:Afm APN 5 90,679,466 (GRCm39) missense probably damaging 1.00
R0009:Afm UTSW 5 90,693,243 (GRCm39) splice site probably benign
R0009:Afm UTSW 5 90,693,243 (GRCm39) splice site probably benign
R0135:Afm UTSW 5 90,698,181 (GRCm39) missense probably benign 0.00
R0582:Afm UTSW 5 90,672,639 (GRCm39) splice site probably benign
R1416:Afm UTSW 5 90,674,238 (GRCm39) missense possibly damaging 0.74
R1465:Afm UTSW 5 90,698,200 (GRCm39) missense probably damaging 1.00
R1465:Afm UTSW 5 90,698,200 (GRCm39) missense probably damaging 1.00
R1834:Afm UTSW 5 90,674,283 (GRCm39) missense probably benign 0.01
R1919:Afm UTSW 5 90,672,779 (GRCm39) nonsense probably null
R2071:Afm UTSW 5 90,671,594 (GRCm39) missense probably benign 0.17
R2843:Afm UTSW 5 90,674,324 (GRCm39) nonsense probably null
R2979:Afm UTSW 5 90,670,022 (GRCm39) missense probably benign 0.19
R4853:Afm UTSW 5 90,699,326 (GRCm39) missense probably damaging 1.00
R5400:Afm UTSW 5 90,699,257 (GRCm39) missense possibly damaging 0.86
R5551:Afm UTSW 5 90,679,511 (GRCm39) missense probably null 0.97
R5583:Afm UTSW 5 90,695,740 (GRCm39) missense probably damaging 1.00
R5780:Afm UTSW 5 90,699,290 (GRCm39) missense possibly damaging 0.87
R7378:Afm UTSW 5 90,699,259 (GRCm39) missense probably benign 0.00
R7470:Afm UTSW 5 90,679,486 (GRCm39) missense probably damaging 0.99
R7785:Afm UTSW 5 90,698,032 (GRCm39) missense possibly damaging 0.93
R7799:Afm UTSW 5 90,671,713 (GRCm39) missense probably benign 0.00
R7809:Afm UTSW 5 90,672,675 (GRCm39) missense probably damaging 1.00
R7897:Afm UTSW 5 90,695,727 (GRCm39) missense probably benign 0.00
R8236:Afm UTSW 5 90,671,747 (GRCm39) missense probably damaging 1.00
R8497:Afm UTSW 5 90,699,202 (GRCm39) critical splice acceptor site probably null
R8752:Afm UTSW 5 90,700,424 (GRCm39) missense probably benign 0.00
R8949:Afm UTSW 5 90,679,374 (GRCm39) nonsense probably null
R8971:Afm UTSW 5 90,696,675 (GRCm39) missense probably damaging 0.99
R9013:Afm UTSW 5 90,671,594 (GRCm39) missense probably damaging 0.99
R9067:Afm UTSW 5 90,671,674 (GRCm39) missense probably benign 0.01
R9082:Afm UTSW 5 90,698,095 (GRCm39) missense probably damaging 1.00
X0022:Afm UTSW 5 90,693,273 (GRCm39) missense probably damaging 1.00
Z1177:Afm UTSW 5 90,679,475 (GRCm39) missense probably damaging 1.00
Z1177:Afm UTSW 5 90,679,365 (GRCm39) missense probably benign 0.07
Z1177:Afm UTSW 5 90,669,805 (GRCm39) missense probably benign 0.05
Z1177:Afm UTSW 5 90,699,242 (GRCm39) missense possibly damaging 0.87
Predicted Primers PCR Primer
(F):5'- AAGTAAGGTTGTTGGTGATCTCAC -3'
(R):5'- ACCATGGTGTGTTTTCTGAGAC -3'

Sequencing Primer
(F):5'- GTGATCTCACAACTAGCTATTCATC -3'
(R):5'- ACAGATGTGTCTCTGGGCTTCATAC -3'
Posted On 2022-04-18