Incidental Mutation 'R4821:Prr13'
ID 370253
Institutional Source Beutler Lab
Gene Symbol Prr13
Ensembl Gene ENSMUSG00000023048
Gene Name proline rich 13
Synonyms 2010324E22Rik, 1110020C13Rik
MMRRC Submission 042437-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.425) question?
Stock # R4821 (G1)
Quality Score 225
Status Validated
Chromosome 15
Chromosomal Location 102367605-102371241 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to T at 102369120 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000129218 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000023810] [ENSMUST00000164688] [ENSMUST00000164938] [ENSMUST00000164957] [ENSMUST00000171245]
AlphaFold Q9CQJ5
Predicted Effect unknown
Transcript: ENSMUST00000023810
AA Change: H112L
SMART Domains Protein: ENSMUSP00000023810
Gene: ENSMUSG00000023048
AA Change: H112L

DomainStartEndE-ValueType
low complexity region 22 48 N/A INTRINSIC
low complexity region 50 85 N/A INTRINSIC
low complexity region 102 136 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000158543
Predicted Effect unknown
Transcript: ENSMUST00000164688
AA Change: H112L
SMART Domains Protein: ENSMUSP00000130498
Gene: ENSMUSG00000023048
AA Change: H112L

DomainStartEndE-ValueType
low complexity region 22 48 N/A INTRINSIC
low complexity region 50 85 N/A INTRINSIC
low complexity region 102 136 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000164938
SMART Domains Protein: ENSMUSP00000129218
Gene: ENSMUSG00000023048

DomainStartEndE-ValueType
low complexity region 22 48 N/A INTRINSIC
low complexity region 50 79 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000164957
AA Change: H112L
SMART Domains Protein: ENSMUSP00000125784
Gene: ENSMUSG00000023048
AA Change: H112L

DomainStartEndE-ValueType
low complexity region 22 48 N/A INTRINSIC
low complexity region 50 85 N/A INTRINSIC
low complexity region 102 136 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000171245
AA Change: H112L
SMART Domains Protein: ENSMUSP00000132636
Gene: ENSMUSG00000023048
AA Change: H112L

DomainStartEndE-ValueType
low complexity region 22 48 N/A INTRINSIC
low complexity region 50 85 N/A INTRINSIC
low complexity region 102 136 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000181328
Meta Mutation Damage Score 0.1545 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.3%
  • 10x: 96.3%
  • 20x: 92.5%
Validation Efficiency 100% (79/79)
Allele List at MGI
Other mutations in this stock
Total: 70 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4921539E11Rik T C 4: 103,092,871 (GRCm39) K150R probably damaging Het
Aak1 T C 6: 86,827,171 (GRCm39) V46A probably damaging Het
Abcb9 T C 5: 124,228,212 (GRCm39) T10A probably benign Het
Acaca A G 11: 84,185,813 (GRCm39) D116G possibly damaging Het
Adam33 G A 2: 130,903,115 (GRCm39) P43L probably benign Het
Adamtsl2 T A 2: 26,988,604 (GRCm39) probably null Het
Akap13 A G 7: 75,327,255 (GRCm39) probably benign Het
Art1 T A 7: 101,756,385 (GRCm39) L192Q probably damaging Het
Baalc A G 15: 38,796,575 (GRCm39) probably benign Het
Baz2a A G 10: 127,946,978 (GRCm39) E164G probably damaging Het
Bcs1l A G 1: 74,631,144 (GRCm39) I391V probably benign Het
Cacna1c T C 6: 118,673,386 (GRCm39) T497A probably damaging Het
Cap2 C A 13: 46,763,586 (GRCm39) T164N probably damaging Het
Ccdc57 A G 11: 120,751,225 (GRCm39) probably null Het
Ccdc88c T C 12: 100,904,338 (GRCm39) N1120S probably benign Het
Cfap210 T C 2: 69,612,452 (GRCm39) E96G possibly damaging Het
Chd7 T A 4: 8,844,706 (GRCm39) V1605D probably damaging Het
Col12a1 A T 9: 79,622,622 (GRCm39) probably benign Het
Commd3 T C 2: 18,677,339 (GRCm39) S22P probably benign Het
Cpd T C 11: 76,737,063 (GRCm39) I244V probably benign Het
Cpeb2 C A 5: 43,390,817 (GRCm39) probably benign Het
Cyp2c65 A G 19: 39,060,635 (GRCm39) D165G probably damaging Het
Ddx1 T C 12: 13,289,148 (GRCm39) Y152C probably damaging Het
Dennd4a G A 9: 64,804,531 (GRCm39) C1290Y possibly damaging Het
Ebf4 G A 2: 130,148,965 (GRCm39) M232I probably benign Het
Farp2 A G 1: 93,502,192 (GRCm39) probably null Het
Frk T C 10: 34,360,233 (GRCm39) V78A probably benign Het
Gm5799 A G 14: 43,782,098 (GRCm39) D90G probably damaging Het
Gpr45 C G 1: 43,069,613 (GRCm39) probably benign Het
Hfm1 C T 5: 107,002,606 (GRCm39) probably null Het
Igkv4-57-1 T A 6: 69,521,387 (GRCm39) D105V probably damaging Het
Impdh2-ps A G 8: 100,757,995 (GRCm39) noncoding transcript Het
Kctd4 G A 14: 76,200,217 (GRCm39) V63I probably benign Het
Lcn6 T A 2: 25,570,822 (GRCm39) L137M probably damaging Het
Lonrf1 T C 8: 36,687,126 (GRCm39) N737D probably benign Het
Mcu C T 10: 59,303,511 (GRCm39) V109M probably damaging Het
Mecom C A 3: 30,039,500 (GRCm39) K186N probably damaging Het
Muc4 T C 16: 32,753,802 (GRCm38) I1226T probably benign Het
Mybpc1 T C 10: 88,384,727 (GRCm39) D533G probably damaging Het
Nae1 A C 8: 105,246,416 (GRCm39) C294G probably damaging Het
Ncapg2 T G 12: 116,379,077 (GRCm39) H190Q probably damaging Het
Nkx2-2 A T 2: 147,027,763 (GRCm39) L59Q possibly damaging Het
Nrxn3 C T 12: 90,171,483 (GRCm39) T295I probably damaging Het
Obscn C T 11: 58,897,652 (GRCm39) probably benign Het
Obscn A T 11: 58,931,293 (GRCm39) M5781K probably damaging Het
Or11g24 A G 14: 50,662,206 (GRCm39) T77A possibly damaging Het
Or4k39 T C 2: 111,239,570 (GRCm39) noncoding transcript Het
Or4z4 T A 19: 12,076,110 (GRCm39) M298L probably benign Het
Pcdhb6 C A 18: 37,467,381 (GRCm39) P101T probably damaging Het
Pot1b A G 17: 55,979,885 (GRCm39) S324P possibly damaging Het
Potefam1 T C 2: 111,034,490 (GRCm39) probably null Het
Ppcdc C T 9: 57,342,194 (GRCm39) V43I probably benign Het
Rab10os T A 12: 3,287,322 (GRCm39) noncoding transcript Het
Rabgap1 T C 2: 37,422,531 (GRCm39) S595P probably damaging Het
Rap1gap T C 4: 137,439,440 (GRCm39) S126P probably damaging Het
Rgs6 A T 12: 83,114,185 (GRCm39) probably null Het
Slc5a6 T A 5: 31,194,228 (GRCm39) K610* probably null Het
Sun5 C T 2: 153,711,386 (GRCm39) V27I probably benign Het
Tmco5b T C 2: 113,120,102 (GRCm39) I126T probably benign Het
Tmed7 G A 18: 46,726,480 (GRCm39) Q92* probably null Het
Trav7d-2 A G 14: 52,921,885 (GRCm39) D98G probably benign Het
Trbv16 T A 6: 41,128,936 (GRCm39) L40Q probably damaging Het
Ush2a T C 1: 188,485,848 (GRCm39) V2986A probably benign Het
Usp33 T C 3: 152,064,310 (GRCm39) V58A probably benign Het
Vmn2r94 T A 17: 18,477,293 (GRCm39) M373L probably benign Het
Ywhaq T C 12: 21,467,512 (GRCm39) probably benign Het
Zbbx G A 3: 74,989,054 (GRCm39) H345Y possibly damaging Het
Zfp346 G T 13: 55,261,626 (GRCm39) probably benign Het
Zfp616 C T 11: 73,975,033 (GRCm39) A434V probably benign Het
Zfp992 C T 4: 146,551,976 (GRCm39) H566Y probably damaging Het
Other mutations in Prr13
AlleleSourceChrCoordTypePredicted EffectPPH Score
FR4304:Prr13 UTSW 15 102,370,612 (GRCm39) small insertion probably benign
FR4548:Prr13 UTSW 15 102,370,609 (GRCm39) small insertion probably benign
FR4737:Prr13 UTSW 15 102,370,608 (GRCm39) small insertion probably benign
FR4976:Prr13 UTSW 15 102,370,611 (GRCm39) small insertion probably benign
FR4976:Prr13 UTSW 15 102,370,606 (GRCm39) small insertion probably benign
R0650:Prr13 UTSW 15 102,370,650 (GRCm39) makesense probably null
R1901:Prr13 UTSW 15 102,369,133 (GRCm39) unclassified probably benign
R1902:Prr13 UTSW 15 102,369,133 (GRCm39) unclassified probably benign
Predicted Primers PCR Primer
(F):5'- TTATCCTGTACCACAACCAGG -3'
(R):5'- TGGGAGTGATCTGATGCCTC -3'

Sequencing Primer
(F):5'- TGTACCACAACCAGGGTGTC -3'
(R):5'- CTACATCTGCTAAAGCGACAAGGTTG -3'
Posted On 2016-02-04