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
sa36526 Essential Splice Site Mutation detected in F1 DNA Not yet available

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

Mutation Details

Allele Name:
sa36526
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000130685 Essential Splice Site 1397 1677 28 31
Genomic Location (Zv9):
Chromosome 17 (position 49368183)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 49129267
GRCz11 17 49212242
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGCTCATTCCCCTGTCAGCGCTACAGGTCAGACTGGGCAACACTGCAG[G/A]TAAGAGACGCATCTGGCATGTTTGAGTTTATAGAGATGCTAGTAATCAAC
Long Flanking Sequence:
CTTATACTATATGTGAAGCACCACCATGTCGAAATGAATTGCCCCAAGGGGATTAATAAAGTTTTAAAATAAACTTATTACTCACATGCACGAGCACCAATTTGCCAGCGATTTCTCAAAAACTGTCGGCGAGTCAAAATCAGGGCTAAAATCATGCAGTCTGGACTCGGCATTACACTCATATATAAAACTCGACTATTCTGTGGTTAAATTGTGTACTAGGACGGACATAAAATTAAACGTTGCGATTTTCTAGGAGGTCGATATTACTTGGAACTATACTTACATTGTTGTGTAATAATCAAGGAACTTTTCTGCCGTACTATAACAACAGCATTGTAATAATTATTGAAATAAAATGTGTTTAAAGATCCATAAATGGTGTCAATATTTTGTTTGGAAGGTGACTTCAAGATCAGCCCACGGAGATCAGGATTCATTCAAGTTTCGCTGGCTCATTCCCCTGTCAGCGCTACAGGTCAGACTGGGCAACACTGCAG[G/A]TAAGAGACGCATCTGGCATGTTTGAGTTTATAGAGATGCTAGTAATCAACAGGTGTAAATAAATCTTTGCTTTTCGATGTTGCCTGAAGACACAGACTGCCTCTGGGAGCTGATTCACACCAAATCACAAAAGGAGGGCAGGCCTGAGACGGTGTTCCAGTTGTGCAGCAGGTAGGAGTTACCTACTTGGTCTTTTCAAAAATGAAGTGTCCCATTTTATTCCATATAGAGCTTACCATTTTTTATGTTGTGTCATTTGCAGCACACCAGAGTGCAAAGTGAATATCATCAAGGTGATGCGCTCCATCTTGCGGGAGAACCTGCGTCGAAACATGCAAAGGGTTGAACAGTCTGAGAGAACCTGTAAAAAGCGGCTTACTCCCCTTCGGAAAAGCCTGCCAGCTTCGGCTAGGATAGGTCAGTGTGGTCTTCCCTTTACTTGCACATCTGATACTCTTGAAGCTGTGGTCAAGAAAGCCATAACCTGACTTTAACAGCAA
Associated Phenotype:
Not determined