Busch Lab

ZMP

LOC556398

Ensembl ID:
ENSDARG00000075249
Human Orthologue:
FAM171A2
Human Description:
family with sequence similarity 171, member A2 [Source:HGNC Symbol;Acc:30480]
Mouse Orthologue:
Fam171a2
Mouse Description:
family with sequence similarity 171, member A2 Gene [Source:MGI Symbol;Acc:MGI:2448496]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa33149 Nonsense Mutation detected in F1 DNA Not yet available
sa15965 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa33149
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000114906 Nonsense 559 828 8 8
Genomic Location (Zv9):
Chromosome 3 (position 21496350)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 21152741
GRCz11 3 21283289
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTGTCCTCTGACTTGACAGCTGTGGAGCAGGCAATGGAACGGCAACAA[C/T]AGCTGCAGCACGATATGGAGGGCATCCAGGTTAGTATGACTCTACCAAGG
Long Flanking Sequence:
TTAAACATGGTCCCACCCAAAGACAACACAACTCCAGGACGAATGCTGACTCAAAACGAGGAGAGAGCTTCCCATTGAAAGCTACACGCTCTTCAAACACAGGAACTCGAGATCTGCTTCTTCAGGATGACTACGGCAAAGGTTACAGCTCTGCTGAGGACTCAGATGATCGCAAATACAATCACCATAATGCTAAAGACAACCAGGGCTATTCATCAGACCCACCATCTCCACCTCCACTTTTGCCACCATTTGCCGGCCACTACCAGGATCTCAATCGGGACAGCAAGCCTCCAGAGTATTATGCATCAGCAGGGGATCACCTCAATCGGCCCTCTTCGGTCAATACCCAGCCTGGCCAACTGATCTTCTGTCACTCAATGGAGCAGATGAAAGAGAGCATGTACCACAGCATGGTACCCACATTGGTCATCCCTGCACATTACATGCATCTGTCCTCTGACTTGACAGCTGTGGAGCAGGCAATGGAACGGCAACAA[C/T]AGCTGCAGCACGATATGGAGGGCATCCAGGTTAGTATGACTCTACCAAGGCAGCAGAATCAAAAGCAACAACAGCAGCAGGCCAGGGCTGATAATGAAGAGGAAGAGTCAGGCAAACAAGCAGATGGATCTTCGGAGGAGAACTGGGGATCAGACCAATCCAGTGCCCCAGTACGTATTCCAGTGCTTTTCAATGATTCAACCATTGCTCAAATGAATGGAGAGCTGCAAGCGATGACAGAGAAGAAGTTGCTGGAGCTTGGGGTGAAGCCACACCCTCGTGCCTGGTTCGTTTCCCTTGATGGCCGTTCAAACTCTCTTGTTAGACACTCCTACATTGAGCTGAGCAATGAAGCCTTGCGTCCACCCATGGGCGCCTGCAATCAAACACTAGACCAGCGTACTGAAGCAATCCCCACGAATTCAGGGAAACCTTCCCACCGAAAATTAAAAGAGGATGGCAAGGTAAAGGAGGGAGGTGAAAGAAAAGCTCATGGTAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15965
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000114906 Nonsense 814 828 8 8
Genomic Location (Zv9):
Chromosome 3 (position 21495583)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 21151974
GRCz11 3 21282522
KASP Assay ID:
2259-3334.1 (used for ordering genotyping assays)
KASP Sequence:
GACRATAATGATGACAAAGATGATGACGGAGAGAATAAGAAGAGCCCCTG[G/A]CAAAAGCGTGAAGAAAGACCCCTCATGGTGTTTAATGTCAAGTAATGCTG
Long Flanking Sequence:
AAGCCACACCCTCGTGCCTGGTTCGTTTCCCTTGATGGCCGTTCAAACTCTCTTGTTAGACACTCCTACATTGAGCTGAGCAATGAAGCCTTGCGTCCACCCATGGGCGCCTGCAATCAAACACTAGACCAGCGTACTGAAGCAATCCCCACGAATTCAGGGAAACCTTCCCACCGAAAATTAAAAGAGGATGGCAAGGTAAAGGAGGGAGGTGAAAGAAAAGCTCATGGTAAAATTTATTCCAAGCTTCCCGTTATTGAAACTCCAGACTCAAGCAGCGAGAGCCATTCAGCCATGTACTCACCTGAGGAGAACTCAACAGCGCCGCTACTTGATGAAACTGCAGAGGTGTCCAAAGGTGGGACGTTCCCGCGTAAAGGCCGCAGCCGAGACAACAGCACCCGTAGTAGTGCCAGTGAGGTCCACCGAGACTCAGTCACCAGTCCTGATGACGATAATGATGACAAAGATGATGACGGAGAGAATAAGAAGAGCCCCTG[G/A]CAAAAGCGTGAAGAAAGACCCCTCATGGTGTTTAATGTCAAGTAATGCTGCCCAGGACTGGTTAGGGCATCGTCTTGGCTGTACCCTTCTTTTGCATAGATACTCACTAGTGATGAGGTGTGAGGATACAGAGCTGGAAGAAAGTCTGATGAAAAGCACAATATGAGATATGGCACTTACTTGAGTGATCTGTTTCAACCATCAAGACTAGGTACAAAGAATAAGCACTGAATGCCACCTGCAAAGAAGCATCTGAAGTCGTCACACCCTCTTAGATATCCTTCAGACAGTTTATACACCTGATGTTGTTCTGGCAGTTCATCAGGTCAAAGGGAGTTGAACTGAATCTCAAGATGTTGTCTTGCTTTCTTTGAGGGTTACCCAGTTTTTGTAAGAATGACCATGAGCCATTTTAAAACTAACTTTGGGAAGCAATCCATAAGCCTTAAAGAGCTTTTTCCTTTACTTAAGAAATATAAATGAATATAAATTTGATATGA
Associated Phenotype:
Not determined