Busch Lab

ZMP

SHROOM3 (2 of 2)

Ensembl ID:
ENSDARG00000078705
Description:
shroom family member 3 [Source:HGNC Symbol;Acc:30422]
Human Orthologue:
SHROOM3
Human Description:
shroom family member 3 [Source:HGNC Symbol;Acc:30422]
Mouse Orthologue:
Shroom3
Mouse Description:
shroom family member 3 Gene [Source:MGI Symbol;Acc:MGI:1351655]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa36528 Nonsense Mutation detected in F1 DNA Not yet available
sa17759 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa36528
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109205 Nonsense 345 1577 5 9
Genomic Location (Zv9):
Chromosome 17 (position 49964078)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 5654011
GRCz11 21 5760928
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCAGCAGTAGTAGTGAAAGCAGTGGGAGTAGTGGAAGCACTTCCAGCT[C/A]ACAACGGCAGAGTTTTGGGCCAGTCTGGGATCCAATGCACAGCCGGCACT
Long Flanking Sequence:
TTTTCCCTGCAGTGCTTCCACCACAGACCTATCAGGATTTGAGACGGGATTTCTTAGGAAGAGCCCTGATCAGTATAGTTCCCGGGGCAGCATGGAAAGCCTTGACCACAGTCACCCAGCTTACAGCTCCTGCTATCATCTATCATCCTCGAAATCATCCAGCAGCATCGATCATCTACACAACAAGCGGGATTCTGCATACAGCTCGTTCTCCACCAGCTCCAGTATCCCAGAGTACCTTGCAGCCACACCATCATTTAACAAGGAAAGGTCCTATTCCATGGAGAATGTTCCACAGAGGGAAGGGATGCAGCAGGCGGATATACGCTACGTACGCACTGTGTATGACAACCAACAGGGGGTGTCTGAGGAGCACGAGATCACCTCTGCAGCTCTAATGAGAACCAATGACAGCAGAGCACGGTCTAAAAGTGGCATAATCTGTCATCGTGGCAGCAGTAGTAGTGAAAGCAGTGGGAGTAGTGGAAGCACTTCCAGCT[C/A]ACAACGGCAGAGTTTTGGGCCAGTCTGGGATCCAATGCACAGCCGGCACTCCTTTGAGAACCTAAAGGGGGCACCAGCTCCCCCATTACGCAGTGACAGCTATGCAGCATTTCGCAATCACGAACGTCCAAACTCTTGGTCGAGTCTTGAACATGCTCGGTCACAAAGGGCACTTTCAAAGGGTTTCTGGCAACACTCTAGTGGTTCTGTGGCAACAGGAAAGTCCTCATTTGGAGCTGAAGGTCAGTTGCATACAGTGATTGAAAAAAGTCCTGAAAGTAGCCCCACAACCAAACCCAAGCAAGGCATTCCTCAGCCCGCACAACCTGGCCGCTTCATGTTACCAACTGGCGTCTACCCTGTTCCTCCTCCAGAGCCTCATTTTGCACAAATCCCAACCAGCAACCCTAATTCTGGTAGTGTATACCCAGCACTGGCCAAGGAGAGCAAGCACAACAATCACTGTGACCGCTTGGGTGGACTTGTAAAAGAGGACAGGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17759
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
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109205 Nonsense 809 1577 5 9
Genomic Location (Zv9):
Chromosome 17 (position 49965469)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 5655402
GRCz11 21 5762319
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TMCAATATCACCAGCAACAAGACCCTACAGTCACTCAGAAGAAGTATCTT[C/T]AAAGGAGTAAGAGCACCTTTCAGCTTGGTGAGGGTAATGGTAAAGGAGAT
Long Flanking Sequence:
GAAATGACAACATAGTCAAACCTTCAATGCACTACAGTGACTCTAGTGCTCTCCGGCAGAGAGGTCAAGACTTGGATAACCCCCTGACCAGACTGGAGAATGCACTTGCAGAGGTTCAGCGATGTGTAAGTCCTGAAAGTACAACCAGCCATTGCAGTTTTCAGAGTGAGCGTAGCATGTCAGTCCTGGAGAAAGTCAGTCATTTTGAGAGACAGCAAGTCAAACCTCGCAGTCAGAGCAGCCTGTCCCATTATGGATCCACACCTCGGCTGAACCAACCAGCGAGACCCTCCAGTGCCAAGGGTTCCTTTTCTGGTAAGGACGGTGTGCGCACCATGTTGGAGAGAAGCAACAGCTCAGTTACTGAGAGTTACCAGAGAACTGAGAGCTATGATGGACATGCTGATATGCAGCAGGATTTCCATACAAGACGTGGGAGTAGTGATCAAATACAATATCACCAGCAACAAGACCCTACAGTCACTCAGAAGAAGTATCTT[C/T]AAAGGAGTAAGAGCACCTTTCAGCTTGGTGAGGGTAATGGTAAAGGAGATATTCATGACATGTTGGGTGCTATTCAAGACACATCTTTTAACAGAGCATACAGAGACAGCCTTAAAGATGCCCAGTCTAAGGTTTTGAGATCAACTTCCTTCAGAAGGCGTGACTTTGGTGTTAACCCTCCACCAGTACCAGCCAAGCACATGTCCCTAGAGCGAAAAGGAACCAATACAAGTCCCAAAGCAGTTACAACATCACCACACACTCCAAAAGAACGCCATGTTGTTCCTGTTGAAGCACAAAACAGAACCACTCCTCCTGAACTCCCCAGTGTCCCAGCTGTTGGACCCCCAGTTTTGCGGATTTGTGGACGCAAACGGTTCACAATGGAGCAAAAGAAACGATCATATTCTGAGCCTGAAAATATGCATGAAGTTGGAGTGACTCAGGAAATCAATCAAGTTGAGAGGAGGGTTCAACAGCAGTTTCTGTCAAGTGAGACA
Associated Phenotype:
Not determined