C10orf71 (1 of 2)

Ensembl ID:
ENSDARG00000086970
Description:
chromosome 10 open reading frame 71 [Source:HGNC Symbol;Acc:26973]
Human Orthologue:
C10orf71
Human Description:
chromosome 10 open reading frame 71 [Source:HGNC Symbol;Acc:26973]
Mouse Orthologue:
3425401B19Rik
Mouse Description:
RIKEN cDNA 3425401B19 gene Gene [Source:MGI Symbol;Acc:MGI:3588196]

Alleles

There are 17 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa42226 Nonsense Mutation detected in F1 DNA During 2016
sa35522 Nonsense Mutation detected in F1 DNA During 2016
sa16604 Nonsense Available for shipment Available now
sa12297 Nonsense Available for shipment Available now
sa42225 Nonsense Mutation detected in F1 DNA During 2016
sa38950 Nonsense Mutation detected in F1 DNA During 2016
sa42224 Nonsense Mutation detected in F1 DNA During 2016
sa35521 Nonsense Mutation detected in F1 DNA During 2016
sa17126 Nonsense Available for shipment Available now
sa28133 Nonsense Mutation detected in F1 DNA During 2016
sa42223 Nonsense Mutation detected in F1 DNA During 2016
sa35520 Nonsense Mutation detected in F1 DNA During 2016
sa18600 Nonsense Available for shipment Available now
sa18475 Nonsense Available for shipment Available now
sa4510 Nonsense F2 line generated During 2016
sa35519 Nonsense Mutation detected in F1 DNA During 2016
sa13671 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa42226
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
G > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 853 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31157115)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30803063
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
ATAAAGCCCAAAAGAATGAAGAACTGTACTCTTATCAGCCATATAAGTAT[G/T]AGCATAACAAACAGTGGCACATGTCAACAAGTGAAGACAGGCACACCAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35522
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
A > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 961 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31156791)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30802739
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GAGATAACGAGCAGGCAAGAAGACTAAAGGATAATTCAGTTAGTATGTCT[A/T]AATCAGAAAATTCACAAAGTCAAGTGAAATTGGATGCAGCTGAAAAACTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16604
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 1622 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31154808)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30800756
KASP Assay ID:
2260-6577.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GARATGAAGACATKACAAAGTCTTTGCTCTATTTCAATAAWGAAGATGTA[C/T]AAGCATTARCTAWCAAAAACATTAAAWCAAAGGAAAATGTTTTGGATAAY
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12297
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 1673 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31154655)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30800603
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
AAAAGATGGACAGTCAGTCAAAACTAGAAACARGTAAAGAATCCCTARCA[C/T]AAATGGCATCAGTTAAAGCAAAARAAAAANTCTATGCAAAAWGAACTCCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42225
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 1707 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31154553)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30800501
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
AAGATGATGAAAATGATAAGGTGCTACTATGTTTTAACAATGAAGATGGA[C/T]AAGCAATAATGATCAAAAACATTAAAACAAAGGAAAATGTTTTGGATAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38950
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
G > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 1959 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31153797)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30799745
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
ATCAAGTTGATGAAAGTACAAAGTCTTTGCTAAGCTTTAATAAGGAAGAT[G/T]GACAAGCATTATTAATCAAAGATAGTAAAGCAAAGCAAAATATTATGGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42224
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 1978 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31153740)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30799688
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CATTATTAATCAAAGATAGTAAAGCAAAGCAAAATATTATGGATAATCAA[C/T]AAAGCAATGCATCACAAGAAAAGTCTACTCCTGCAAACCAAATGGTGGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35521
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
A > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 1998 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31153680)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30799628
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CATCACAAGAAAAGTCTACTCCTGCAAACCAAATGGTGGACAGTCGGTCC[A/T]AACCAGGATCAAATAAAGAATCACTAAAACACAAGACTTCAGCTAAAGCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17126
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 2171 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31153159)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30799107
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
ACACCTAGCAAAGTGGAGTCTGCAGAGGAGCCGAWGATTTACAATATYTG[T/A]GTGTCAAGCAAAACGGAAGCAGCCTCAGAYGATGAGCCCATGATCTACAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa28133
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 2201 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31153071)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30799019
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CCATGATCTACACTATATGTGTGTCAAGTAAGTGTCATATTGATGAGCAA[C/T]AAAATTCAGTCAAACAAGAAGAGGAGAGTTCTGTTGAAACTGAAATAAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42223
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 2347 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31152633)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30798581
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CCAAAGAAAAAAGCTCAGGTGACAAACAAACACATTCAGATGACTCAAGA[C/T]AAGCCTCCAGTCAAAAGACGTCTATTACAAGTCAACCTTTAAAGGAAGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35520
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
A > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 2410 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31152444)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30798392
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GCCTTGGCCATTCTACAAGTGATACCACCCTAATACCAAAAGATATAAAT[A/T]GACATGTTGAACAAGACAGAGTTACACAAAATATTGAACCATCAAGTCAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18600
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 2829 3591 1 1
ENSDART00000128847 Nonsense 2829 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31151187)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30797135
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GCAGTCTCGAAGGAAAGCAAGTAAAACATATTGAAGCTACTGAGACAAAA[C/T]AAGCTCATCAACCTAATACAAACCAGAATCAGCCTGGGAGAGGTTTGGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18475
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 2829 3591 1 1
ENSDART00000128847 Nonsense 2829 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31151187)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30797135
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GCAGTCTCGAAGGAAAGCAAGTAAAACATATTGAAGCTACTGAGACAAAA[C/T]AAGCTCATCAACCTAATACAAACCAGAATCAGCCTGGGAGAGGTTTGGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa4510
Current Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 2854 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31151110)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30797058
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
AATCAGCCTGGGAGAGGTTTGGAGCCTGAAAAAGAAAGAAGTGCAAGCTA[T/A]GAACTAGAACATGCACAGATATATCAAAAGGACGCCAAGAAAGAAGGTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35519
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2016.
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 3029 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31150587)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30796535
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
AGCAAACAAAAACAGGAGAAAGTTACAAAACATACCAGTCCAGGAATCCC[C/T]AAGGAGACAATATTGCAGCATTGCAAGCTGAGAGTACAATAAACCGATCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13671
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128847 Nonsense 3490 3591 1 1
Genomic Location (Zv9):
Chromosome 13 (position 31149202)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 30795150
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
CAGGGTGCTYTAACACAGCCAGCACMAGTTGAAATGTTAAATGCTCCTTA[C/A]ATGCTGTATCGTGGCTTTCTGCCAATGGCTGCATCCTCATTATCACCCTT
Associated Phenotype:
Not determined

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