Busch Lab

ZMP

tagap

Ensembl ID:
ENSDARG00000043475
ZFIN ID:
ZDB-GENE-040724-50
Description:
T-cell activation GTPase activating protein [Source:RefSeq peptide;Acc:NP_001004548]
Human Orthologue:
TAGAP
Human Description:
T-cell activation RhoGTPase activating protein [Source:HGNC Symbol;Acc:15669]
Mouse Orthologues:
CT485609.2, Tagap, Tagap1
Mouse Descriptions:
T-cell activation GTPase activating protein 1 Gene [Source:MGI Symbol;Acc:MGI:1919786]
T-cell activation Rho GTPase-activating protein Gene [Source:MGI Symbol;Acc:MGI:3615484]
T-cell activation Rho GTPase-activating protein [Source:UniProtKB/Swiss-Prot;Acc:B2RWW0]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa23651 Nonsense Mutation detected in F1 DNA Not yet available
sa17749 Nonsense Available for shipment Available now
sa43398 Nonsense Mutation detected in F1 DNA Not yet available
sa1810 Missense F2 line generated Not yet available

Mutation Details

Allele Name:
sa23651
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000063826 None None 687 1 10
ENSDART00000127654 Nonsense 164 876 5 14
Genomic Location (Zv9):
Chromosome 20 (position 13575276)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 13764522
GRCz11 20 13660502
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCCATGCTTTTTTCTGCATTGCAGCTTGCCTGAGCTGAGGGATCACTG[G/A]TTACAGACTTTACACAGGTGAGCACTCGTTTACAACTCTAACGTTTACTA
Long Flanking Sequence:
AATGTGTTAAAAAAACTTCTCTCTGTTAAATAGCACAACGATATTTAATAAATTGTTTAATATTCAGAGGAGGGCTAAAAGTTTTGTCTTCAACTTGTACCTCACCTCCGTGAGGAAGACACTTAGTCATCACTTCTGCAGAAAAAAGCTCTATCTTTATGTACTCCAAAAATAAAACTGTCAACACACATCTCAGCTACATGTTCTACTAGGTCCAATCTGACTGGAGGCCGTAGAGCTGCAAGTCTTTCAGATAAACTTTCCACTTGTCACCGAGACACGGTCTGAAAGAAGGAAGTGGTATCTCTAGCTGTGATGTTGCTTCCTGTCCTCGTGTCTCACTGAGACTTTCCTGCCCTTTTTGTTGTAAAGAGGTCGAGGGTGTGTGGCCTCTACACTCACAACATCATCATCATCACGCGAAATACGACTACTGTGGATTACTAACTCAAGCCATGCTTTTTTCTGCATTGCAGCTTGCCTGAGCTGAGGGATCACTG[G/A]TTACAGACTTTACACAGGTGAGCACTCGTTTACAACTCTAACGTTTACTACATGTACTTTTACAACAGTTGGAAAACATGCAAATCAAGAAATTATGAAATTCAGTTTTGCCACATATCTACAGTTAAAGGGGTAGTTCACAAAAAAGAAAATTTGCTCAATATTACTCAATATTTAAGTGATTCTAAACCTTTATGAGTTTCTTTCATCTGTTGAACACAAATAAAAAAAATGTTAAACTGTTAGAAACCTGTAACCACTGACTTCAATTGACAAATACTATTAAAGTCAATGATTAGCAGTTTTCAGCTTTTTTCAAAAAAAAAAAAAAAAAAACTTATTTTGTGTTCAACTGAAGAAAGTACTTCATCAAGGTTTCAAACAAGTAAAGAGTGATAAAATGGTGACAGACTTTTAGTTTTTGGTTAAAGCTATCTAACTTTAATGCTGCAAAAGCAAATTAACATGTTTTCTAGCTGCTCAGGCTAGTTGAGATATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17749
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000063826 None None 687 2 10
ENSDART00000127654 Nonsense 171 876 6 14
Genomic Location (Zv9):
Chromosome 20 (position 13574707)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 13763953
GRCz11 20 13659933
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTNACAGTAGTTGCAGAACTGAAATTTTGCAATTTGAAATGTGGWGACAGG[A/T]AAACTGTGGAGGCAAGGTTGTTAGCGGGCAGCACTTCCCCACCCCCCAGC
Long Flanking Sequence:
TTGGAAAACATGCAAATCAAGAAATTATGAAATTCAGTTTTGCCACATATCTACAGTTAAAGGGGTAGTTCACAAAAAAGAAAATTTGCTCAATATTACTCAATATTTAAGTGATTCTAAACCTTTATGAGTTTCTTTCATCTGTTGAACACAAATAAAAAAAATGTTAAACTGTTAGAAACCTGTAACCACTGACTTCAATTGACAAATACTATTAAAGTCAATGATTAGCAGTTTTCAGCTTTTTTCAAAAAAAAAAAAAAAAAAACTTATTTTGTGTTCAACTGAAGAAAGTACTTCATCAAGGTTTCAAACAAGTAAAGAGTGATAAAATGGTGACAGACTTTTAGTTTTTGGTTAAAGCTATCTAACTTTAATGCTGCAAAAGCAAATTAACATGTTTTCTAGCTGCTCAGGCTAGTTGAGATATTTGGTTTTGTTTACTTATTTTTACAGTAGTTGCAGAACTGAAATTTTGCAATTTGAAATGTGGTGACAGG[A/T]AAACTGTGGAGGCAAGGTTGTTAGCGGGCAGCACTTCCCCACCCCCCAGCGTCCTCATGAAGGTGCTGAGCGGCAATACCACGGTACACCTTCCTCTGATTCATTTACAGTACATTAGTGATCAGCAAAGGTCATAAATGCTTGGAATGGGATATTTCCCTTTTATCTCAGAGGATGTAAGTCTTTGGTCTGCAAATGTCTTTGGGTTTTGTGGTAGAAATACTGAACATTCACCTTGCTGTCTTACAGAATAAAACGCTAAGTGGAGATGGGATGGACTCTGACTTACTTGTTGATGTGAGTGATGTGTTTATTACTTCATTTTAGATATATGAAGGTACAAAAGCTGTCACTTGGGTGGTACCTTTTAAAATGGTACACATTTAAGTACGTGTCTATATGTAAAACATGGATGATTTTTGTTGTCACACCCTACTACTCCTTCATGTGCTCATGACAAACATGTGCCTGTTTCTAGAGCAACGGCAAAAACTCCGCCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43398
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000063826 None None 687 2 10
ENSDART00000127654 Nonsense 178 876 6 14
Genomic Location (Zv9):
Chromosome 20 (position 13574685)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 13763931
GRCz11 20 13659911
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTTGCAATTTGAAATGTGGTGACAGGAAAACTGTGGAGGCAAGGTTGT[T/A]AGCGGGCAGCACTTCCCCACCCCCCAGCGTCCTCATGAAGGTGCTGAGCG
Long Flanking Sequence:
AATTATGAAATTCAGTTTTGCCACATATCTACAGTTAAAGGGGTAGTTCACAAAAAAGAAAATTTGCTCAATATTACTCAATATTTAAGTGATTCTAAACCTTTATGAGTTTCTTTCATCTGTTGAACACAAATAAAAAAAATGTTAAACTGTTAGAAACCTGTAACCACTGACTTCAATTGACAAATACTATTAAAGTCAATGATTAGCAGTTTTCAGCTTTTTTCAAAAAAAAAAAAAAAAAAACTTATTTTGTGTTCAACTGAAGAAAGTACTTCATCAAGGTTTCAAACAAGTAAAGAGTGATAAAATGGTGACAGACTTTTAGTTTTTGGTTAAAGCTATCTAACTTTAATGCTGCAAAAGCAAATTAACATGTTTTCTAGCTGCTCAGGCTAGTTGAGATATTTGGTTTTGTTTACTTATTTTTACAGTAGTTGCAGAACTGAAATTTTGCAATTTGAAATGTGGTGACAGGAAAACTGTGGAGGCAAGGTTGT[T/A]AGCGGGCAGCACTTCCCCACCCCCCAGCGTCCTCATGAAGGTGCTGAGCGGCAATACCACGGTACACCTTCCTCTGATTCATTTACAGTACATTAGTGATCAGCAAAGGTCATAAATGCTTGGAATGGGATATTTCCCTTTTATCTCAGAGGATGTAAGTCTTTGGTCTGCAAATGTCTTTGGGTTTTGTGGTAGAAATACTGAACATTCACCTTGCTGTCTTACAGAATAAAACGCTAAGTGGAGATGGGATGGACTCTGACTTACTTGTTGATGTGAGTGATGTGTTTATTACTTCATTTTAGATATATGAAGGTACAAAAGCTGTCACTTGGGTGGTACCTTTTAAAATGGTACACATTTAAGTACGTGTCTATATGTAAAACATGGATGATTTTTGTTGTCACACCCTACTACTCCTTCATGTGCTCATGACAAACATGTGCCTGTTTCTAGAGCAACGGCAAAAACTCCGCCCTTTCAAAAGAGTTGCATAACCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1810
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000063826 Missense 293 687 10 10
ENSDART00000127654 Missense 482 876 14 14
Genomic Location (Zv9):
Chromosome 20 (position 13565682)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 13754928
GRCz11 20 13650908
KASP Assay ID:
554-1802.1 (used for ordering genotyping assays)
KASP Sequence:
CCCAGACCTTTAACGCCTAAATTATTCTACACAGATTCAGCCTCCTTGAT[G/A]TCCCCTGATATATCTTTCGAAGTCCACCAACATGACTCTGCATACGACAG
Long Flanking Sequence:
TAATATTTTTCAGAATAATGAACAGCTGTATTTTGATGTCATGTGCATTAATGACCAGGACATATTGTAAGTCTGTTTAAGTCCACCATTCAAAGTCAATTCAAAAATTTGAATTTTAACTAACAGTAGACCTACACATAACAGTATTAGTATTGTTTTACCATATGTTTGAGAAATAACAATAATAATAGGCTACTCATATTAACCTATATTTTACATGTACAGAATTGTGAGAAAATTGTGATCTTTATTTTAAGTAAAAGAACCCTGATTCTCATTTTAGCCAGAATCCTGCAGCTCTAAAACATATTAGACCAAGTTTCACAAGACAGCTACCAAATTAGCTTGGATTTTTCTGCAGGAAAAAGTTCCTTCTGCCAACTGATGATCTTACCTATTGGCTAGTCAGCATCATTGAACAAACAGAGCATTGTAAGCATGAAAGAGCCACCCAGACCTTTAACGCCTAAATTATTCTACACAGATTCAGCCTCCTTGAT[G/A]TCCCCTGATATATCTTTCGAAGTCCACCAACATGACTCTGCATACGACAGCACAGATCCTGATGCGGATTGTGACTGTGTGGAAGCTGAGAGCTATGAAGAAGGCATGATGGCACATGGGAGCCTAGGCCTAAGCAAAAAGGGACGCTCTGACATTCAGTCTTGTTCCTCTGATGCTATATTTGACACATTCACCAAAACTTTCAGCCGACGAAGCTCTGAGCCCTCCATTTTATCTACTCTCCCTATAACGGGTTTGAGAGAGCTTGCTCGCAGCCATGATGACTTTTCAACAGAGAAGGAACACTTTGACAATCAGCCGCTTAAAAAGCAGAACTCAGATGACTCTTTCCTGCTTCCCAACCGCTCTGAGAACAGAAGATCCCTCAAAAAACTGGCTGGGAGTTTTAACATGGACTTGCCTATCATTGTGTCTTCTCCAACATCTAAGATTGGTTCCTGTCCATCATTCTGTTCCTCAGATAGCAGCTCCTCAAATCA
Associated Phenotype:
Not determined