Busch Lab

ZMP

LOC571439

Ensembl ID:
ENSDARG00000087780
Human Orthologue:
TIAM2
Human Description:
T-cell lymphoma invasion and metastasis 2 [Source:HGNC Symbol;Acc:11806]
Mouse Orthologue:
Tiam2
Mouse Description:
T-cell lymphoma invasion and metastasis 2 Gene [Source:MGI Symbol;Acc:MGI:1344338]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa23184 Essential Splice Site Available for shipment Available now
sa10201 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa23184
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
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000130685 Essential Splice Site 1107 1677 19 31
Genomic Location (Zv9):
Chromosome 17 (position 49345939)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 49107023
GRCz11 17 49189998
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACGCAAGGTCATCCAGGAATTAGTGGATACAGAGAAATCCTACGTAAAG[G/A]TGAGAACCGACTCCATAATCCCCTATTAACATCGTTCAACAGAGCGAAGT
Long Flanking Sequence:
TTGCAAATATAGTGTTATTAGATATTAAACAATGCAGATGGCATGGAAGGAATTTGTAAAGTGCTCTGGCTAGCCAAAATTGCAAGCCTCTCTAAATTTTGCGTTGTTTACTTGATTTTGCATTACATTCAGTGACTGCAGGATCACAAAACATGCCTATTTTTAAATTCATTTTGGTCATGAAATTCAGGTTTTTAGTCGACAAAAGTCAGTAAAAAGTCAGCAAAGTAGAAACCCTACTGCAGTTATTCTGTTTACCTCCTTATCAGTTGACATCATGCTTAATGTTCCTATCTTAATTGTGTCTGCAGAGTGTGGACACGGTGTGTTCGCTGTACCACTCCTACCAGGAAGGCTCTGGAGGTCTGATGGAGAGCCAGGAGGAGCAAACGGGGCCTGAACCCGCTATCCTCAGGCCCTGTCCGCGTCATATGTCTGCCACAGAGAGACTACGCAAGGTCATCCAGGAATTAGTGGATACAGAGAAATCCTACGTAAAG[G/A]TGAGAACCGACTCCATAATCCCCTATTAACATCGTTCAACAGAGCGAAGTGAGCAGTCATGGCGAGTAGAGCTCCGTGTTGTTGCCCAACCCCAGACTTCATTAAAACTGAACGACTTGACCTTTTCGTCTTGACCAAAAAAGTCACGTCAGCAGCGCTTTAAAGCTGGATTTAATGATAGAAACGTGAGGTGAAATGGTTTGACGGATAGCTGCTGGAAGATTCCTCATGGAGTCCCGAAGGATCAGCTATTAATTAACTCCTCTAGACGGTGAAAAGCAGACGCCTCCCCTCTCATCTGTTTCCTGAAGATTCCCCAGGCTTGCATATGATTGTTTATGCGGTGCTGGTTTTATTCTGACGGTGTTCATAGTGAGCCTTTAAAACCGTGCTGTCATAATGCGTTCCTGGTGGTTAATAGTTGTCAGGGATGCATCTGATTATTCTGTGATTTGTGGGAGGGAGAGAAGCAACATCCCAGAGTCCCGCACTGGAGCCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10201
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000130685 Essential Splice Site 1107 1677 19 31
Genomic Location (Zv9):
Chromosome 17 (position 49345940)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 49107024
GRCz11 17 49189999
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGCAAGGTCATCCAGGAATTAGTGGATACAGAGAAATCCTACGTAAAGG[T/C]GAGAACCGACTCCATAATCCCCTATTAACATCGTTCAACAGAGCRAAGTG
Long Flanking Sequence:
TGCAAATATAGTGTTATTAGATATTAAACAATGCAGATGGCATGGAAGGAATTTGTAAAGTGCTCTGGCTAGCCAAAATTGCAAGCCTCTCTAAATTTTGCGTTGTTTACTTGATTTTGCATTACATTCAGTGACTGCAGGATCACAAAACATGCCTATTTTTAAATTCATTTTGGTCATGAAATTCAGGTTTTTAGTCGACAAAAGTCAGTAAAAAGTCAGCAAAGTAGAAACCCTACTGCAGTTATTCTGTTTACCTCCTTATCAGTTGACATCATGCTTAATGTTCCTATCTTAATTGTGTCTGCAGAGTGTGGACACGGTGTGTTCGCTGTACCACTCCTACCAGGAAGGCTCTGGAGGTCTGATGGAGAGCCAGGAGGAGCAAACGGGGCCTGAACCCGCTATCCTCAGGCCCTGTCCGCGTCATATGTCTGCCACAGAGAGACTACGCAAGGTCATCCAGGAATTAGTGGATACAGAGAAATCCTACGTAAAGG[T/C]GAGAACCGACTCCATAATCCCCTATTAACATCGTTCAACAGAGCGAAGTGAGCAGTCATGGCGAGTAGAGCTCCGTGTTGTTGCCCAACCCCAGACTTCATTAAAACTGAACGACTTGACCTTTTCGTCTTGACCAAAAAAGTCACGTCAGCAGCGCTTTAAAGCTGGATTTAATGATAGAAACGTGAGGTGAAATGGTTTGACGGATAGCTGCTGGAAGATTCCTCATGGAGTCCCGAAGGATCAGCTATTAATTAACTCCTCTAGACGGTGAAAAGCAGACGCCTCCCCTCTCATCTGTTTCCTGAAGATTCCCCAGGCTTGCATATGATTGTTTATGCGGTGCTGGTTTTATTCTGACGGTGTTCATAGTGAGCCTTTAAAACCGTGCTGTCATAATGCGTTCCTGGTGGTTAATAGTTGTCAGGGATGCATCTGATTATTCTGTGATTTGTGGGAGGGAGAGAAGCAACATCCCAGAGTCCCGCACTGGAGCCATT
Associated Phenotype:
Not determined