ZMP
tubgcp5
Ensembl ID:
ZFIN ID:
Description:
gamma-tubulin complex component 5 [Source:RefSeq peptide;Acc:NP_001018151]
Human Orthologue:
TUBGCP5
Human Description:
tubulin, gamma complex associated protein 5 [Source:HGNC Symbol;Acc:18600]
Mouse Orthologue:
Tubgcp5
Mouse Description:
tubulin, gamma complex associated protein 5 Gene [Source:MGI Symbol;Acc:MGI:2178836]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa842 | Nonsense | Available for shipment | Available now |
sa33903 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15200 | Nonsense | Available for shipment | Available now |
sa14709 | Essential Splice Site | Available for shipment | Available now |
sa675 | Nonsense | Available for shipment | Available now |
sa15685 | Essential Splice Site | Available for shipment | Available now |
sa40736 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa842
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065122 | Nonsense | 82 | 1015 | 4 | 24 |
ENSDART00000144812 | Nonsense | 82 | 1015 | 4 | 24 |
Genomic Location (Zv9):
Chromosome 6 (position 37575305)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37649063 |
GRCz11 | 6 | 37626957 |
KASP Assay ID:
554-0745.1 (used for ordering genotyping assays)
KASP Sequence:
ATGAGAAACTCATGGTTCACTCTGACTTGAGTAAAGCGGAGAGTTGGACA[C/T]GACTCACTGAAGAGTTTCTSACTTCGCCTCTTCCTAATACTGATGGAACA
Long Flanking Sequence:
CTTAACGTCAGGTTCTTGAGTAAATGTGTCTTGATAAAATAATTGTTTGACATTGTGCTGGAAAACAAGAGAAATTACTGAAGAACAACACTTTTTGAAATGTAAGCAGAAGGAACAGTAAAAGATAATTTCATTTTTAGCATTTGTAAACACAGGTCTTCTATTCTTGAGCTATTTTTTTGTAAAGTGAAGACAAAGTCATGGAGATTAAATCTAGTAATACAAGAAGTAGTGTTTTCAAACTCTGAGATGTTGCTTATGCAATTATATTTTGTGCTCTCTATAAAATGTCATTGAAATACCATATTGATGTTTAGCGTTTCTTTTAAATTAATCATTAAACTTCTTTACTTGAACTAAAAACATGTTTTAATGTTACATTTACCTTTATGAAACCTACTAAAACTCTAATTAAAATGATTCATTGTATTTACCTTTTTGCCAGTATTCATGAGAAACTCATGGTTCACTCTGACTTGAGTAAAGCGGAGAGTTGGACA[C/T]GACTCACTGAAGAGTTTCTCACTTCGCCTCTTCCTAATACTGATGGAACAAAGGTGAGATAACACACTGACATTATTCAGAGAAAACTGCATCTGCTGAATTAATCTAATACTTCGTCTGATTTCAGACCGACATCCATTATGGCATCCTGGCTTTGTTACTTCACCTGTCTGACTCTCCATCCAATACAAACTACTGTGAAAGACCCAGACTGAAAGAGACAGGTTAGGATTTTCTGCTGTTTACTTTTCTATTTAGTTAGACAGCTTTATCACTGTTATCAATGTGTCTACAATTATTATTATTTATTTATTTTTTCCAGAGAAAGAAGACACGTTTGACTGGGCCAAGTACCTCATGGAAGGAGAAGATTTTGATCCTGGACCTTTTCCAGACACTCCAGTGAGTGAATGTCAGATCAGTTTCTGCCTGGTCTATTGCTATTTAATAAAATGCTGAATGAGCGATGTAGCCTTATATAAATATGTCAGCCTGTATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33903
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000065122 | Essential Splice Site | 99 | 1015 | 4 | 24 |
ENSDART00000144812 | Essential Splice Site | 99 | 1015 | 4 | 24 |
Genomic Location (Zv9):
Chromosome 6 (position 37575359)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37649117 |
GRCz11 | 6 | 37627011 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACTGAAGAGTTTCTCACTTCGCCTCTTCCTAATACTGATGGAACAAAG[G/A]TGAGATAACACACTGACATTATTCAGAGAAAACTGCATCTGCTGAATTAA
Long Flanking Sequence:
GTGCTGGAAAACAAGAGAAATTACTGAAGAACAACACTTTTTGAAATGTAAGCAGAAGGAACAGTAAAAGATAATTTCATTTTTAGCATTTGTAAACACAGGTCTTCTATTCTTGAGCTATTTTTTTGTAAAGTGAAGACAAAGTCATGGAGATTAAATCTAGTAATACAAGAAGTAGTGTTTTCAAACTCTGAGATGTTGCTTATGCAATTATATTTTGTGCTCTCTATAAAATGTCATTGAAATACCATATTGATGTTTAGCGTTTCTTTTAAATTAATCATTAAACTTCTTTACTTGAACTAAAAACATGTTTTAATGTTACATTTACCTTTATGAAACCTACTAAAACTCTAATTAAAATGATTCATTGTATTTACCTTTTTGCCAGTATTCATGAGAAACTCATGGTTCACTCTGACTTGAGTAAAGCGGAGAGTTGGACACGACTCACTGAAGAGTTTCTCACTTCGCCTCTTCCTAATACTGATGGAACAAAG[G/A]TGAGATAACACACTGACATTATTCAGAGAAAACTGCATCTGCTGAATTAATCTAATACTTCGTCTGATTTCAGACCGACATCCATTATGGCATCCTGGCTTTGTTACTTCACCTGTCTGACTCTCCATCCAATACAAACTACTGTGAAAGACCCAGACTGAAAGAGACAGGTTAGGATTTTCTGCTGTTTACTTTTCTATTTAGTTAGACAGCTTTATCACTGTTATCAATGTGTCTACAATTATTATTATTTATTTATTTTTTCCAGAGAAAGAAGACACGTTTGACTGGGCCAAGTACCTCATGGAAGGAGAAGATTTTGATCCTGGACCTTTTCCAGACACTCCAGTGAGTGAATGTCAGATCAGTTTCTGCCTGGTCTATTGCTATTTAATAAAATGCTGAATGAGCGATGTAGCCTTATATAAATATGTCAGCCTGTATAAATATTCCAAAGCCTGCTAATGTAAATATTTATAGTTTTCTCTTTAAATTTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15200
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065122 | Nonsense | 177 | 1015 | 7 | 24 |
ENSDART00000144812 | Nonsense | 177 | 1015 | 7 | 24 |
Genomic Location (Zv9):
Chromosome 6 (position 37577286)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37651044 |
GRCz11 | 6 | 37628938 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTCTGAGGAGGAAAGCGAAGAAGACGACAGCCAGCAGYCCTTGAGCAGA[G/T]AGGATTCTGGGATACAGGTKGACAGAACGCCGCARGAGGACCACGAGCAG
Long Flanking Sequence:
TATACACTTGGACATGTTTGCGTAAATTTTATTCATTAACTATGTCAAAAAATTTCCAAAACATTAAAGATGAAATTATACATGTGGTGTTCATGAAATAAAAGCTGTAAACATATAAATAACATTTAAAGTGGACTTAACAGGATTTTTCCGTGAGGCGAAATGGAAAACCTGCAGTGGATCCTCAAGGGAGCGATTATACAGAAGCCTTATTAGAGAGAGGAAGATGCTTTTGCTCCTGGGCTTTGATCAGCTGGCTGAATACACAATTCGTTTCACATTATGTTAAGACCTAATCAAGCTACAATTAAGACAATTATTACAAAGCCTGGCGGGAACTCTGCAGTTGACTGAAAGCTGTTATAGCAACGAGAACTTTAATACATGTAAAGAAGTCTTGCAATAATAACAGAGCACCACTGATCACTGATGTGCTCTTTTTGCAGGAGTGGTCTGAGGAGGAAAGCGAAGAAGACGACAGCCAGCAGCCCTTGAGCAGA[G/T]AGGATTCTGGGATACAGGTGGACAGAACGCCGCAGGAGGACCACGAGCAGAACGACAAGACCGTTCAAGTCACCTGGACCGGTAGTGGACAGTATTAGCACGTTATTTTATGATAGTTGTAAACAGGTCTTAGGGGTTTTACTGATTTCCTGTTGCAGTTGGTGAGCCGGACTCCAGGGCTTGGTTGGAGCAGCATATTGTCACTTCTTATTGGGTTCCCAACTCTCCCCGTTTTCCACACAGTCTTCACCTGCACTCCAACCTCTACAACGTTTGGTATGACATCTTTGCTTTTAAAATATCTTGTTCTTAGCATGGCAGGTCCATTCATTGGGACTTTTTTATAGGTTAAATTAGATTTTTTAAAGAATGTACTATATTTTTTCTTTCTCTCCAGGGATCAGCACTTGTATAACACTGGGCCTCTCTACCTGCCTGAGGAGAAATCTTTTGTTACTGAGACACAAGTAATTCGAGAAACTCTTTGGTATGATTTGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14709
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065122 | Essential Splice Site | 304 | 1015 | 10 | 24 |
ENSDART00000144812 | Essential Splice Site | 304 | 1015 | 10 | 24 |
Genomic Location (Zv9):
Chromosome 6 (position 37579838)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37653596 |
GRCz11 | 6 | 37631490 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGGCAAGGTGACTGTRAGGAATGATGTGGTGGTCAYGCATCTAACRAAW[G/A]TAAGTTTTKACCATTTCCCAAAACTCATCCAGRGGATTTGGTAGATTTCA
Long Flanking Sequence:
TTTTCAAATTATGGATTGCAATGGCTGCGGGTTTCTTGAACATTCTTCAAGATATCGTCAACAGAACAAAAAATAAACCCATAAGCCTTTAGAACAGGCCAACTTCAGTAAATTTAGTCAATATAGTTGGATTTTTGAGGTAACCTTAAAATAGATATCCTAATAATATTTCATAATCGTGTTATGAAGATTGCAAATGTGAATATGGAATGAGATGCAAGTTGAAACCTGCAGGGAACGAGCAGTTCTGGAATGAAGATTTTCAAGATTACATCTGCACTGGTTACTGACTGTTGTATGTTTGCATACCTAGAAGAAGCTGTATCACAAATAAAACTAATTGCTCATATCCCAGTTTCCAAGGATAAAATGTGCTCTTTTATGTTATTTTATGTTCTTTCCTCAGGCTTTTCTCTGGCGTGAAGAAACTTTTCATTTTCCAGCACAATGACGGCAAGGTGACTGTAAGGAATGATGTGGTGGTCACGCATCTAACGAAT[G/A]TAAGTTTTTACCATTTCCCAAAACTCATCCAGAGGATTTGGTAGATTTCACAATCCCGTAAACGATAAATGAAAGGAGCCAGTCAGACATTAAATGCAAATCAGTGTATTTATATAATGGGATAAACTCCTTGAGATGTGACATTTTGTTTTTGAGTGGGTCCCAACATACAGTATGCAACAATCATTACATAACAGTATGTTGAGAATATATTTATCATTAAAGCAATGTGCAAAAAGCAAAAATAACAGCACATTTTTCCATTTACAACCTTAGATGTTTTCTAGTTGTATTTAAAAATGTTTAAATTGATACTTTTTACTGAGGCTAAATTAAGAACCATTCAAACCAAGAAAAATAACTGTATGAGCACAAGAAACTGCAGTATGGATACTTATTTGCTGTCATTGTTTATGTTGCGCATCTTCAGGACTCATGTGCTGTTGTAGTTATATGGACTCTGATATTTTTTTAATTTTACAGTGATTTTTAGACTTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa675
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065122 | Nonsense | 579 | 1015 | 14 | 24 |
ENSDART00000144812 | Nonsense | 579 | 1015 | 14 | 24 |
Genomic Location (Zv9):
Chromosome 6 (position 37584001)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37657759 |
GRCz11 | 6 | 37635653 |
KASP Assay ID:
554-0583.1 (used for ordering genotyping assays)
KASP Sequence:
CTGGAAAATCCATGCAGCTCCTCAAGAACCTGGACTGCAAGGAGACTGAA[C/T]AATCTGATGGCTCCTCTAGAGGTAATTTTTTTTTGTTTTATTTGATGAAT
Long Flanking Sequence:
TATTTTGTATATTAAAACCAATAAACAAATAACTAAAAAAACAACAACACCTCTGACCCTATCTTTTATATGGAGTTGTATCTCGGGTATTATGTACAGTCAGTTGGTGATCACAAAATAAACCCCTTCAGGGTGATATAAGATACCTCCGTTCGTGTCATTTCAGGATGTTCATTTTGCACTCACCACAGCTATTATTCTCCTTACATCCTTAATTTGCAAATAAATTAAACCTATGCACATGTTTTTCTAGAAACAAGGATGTACCGGTAAACCACAGGGACTTCTGGTATGCCACTTACACTCTGTATAGCGTGTCTGAAATGGTGGAGAGTGAGGAGAGGCTCAGCGATGCAGCCAGTGGAAGCTCAGGTGGAGAACAGACATCCAGCAGCAGACAACACACCATGGTGTCCTTCCTCAAGCCAGTGCTCAAGCAGATCATCATGGCTGGAAAATCCATGCAGCTCCTCAAGAACCTGGACTGCAAGGAGACTGAA[C/T]AATCTGATGGCTCCTCTAGAGGTAATTTTTTTTTGTTTTATTTGATGAATTTTTTATTTTAATACATTTTTAGTGTTTCTTTGCTCTTTCTTTATTACATAAAAAACAATTAGTTCTATTTACTTACGATGACATGCTTATAAAGTGATCAAATGTAATAACAGTGTAGCACTTAGTGGAAATGTCAGCTGTAAATGTTCCAGTACTTCCACATTTAGCAGCAGCTTGGCATCATCCATGTACACACACATATGATTCAGCATCATGGACTGGATTTACAGAGATCTAGTGTCAGCTGGAGGTTTGCGTCAGATGGAGGCTTGCGTCAAAGAATAATTAGTCATCTTTGTTTTCTGTATTTGGCACAATTAGTTCAAACCACGTTTACATTTATTCACTTAGCAGATGCTTTTGTCCAAAGTCACCTACTGTTGAGGAGGCATTCAGCTTTTCAACAAGAAGAAGCAATACAGACAATAAGCAATACAGAAGAATACAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15685
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065122 | Essential Splice Site | 967 | 1015 | 22 | 24 |
ENSDART00000144812 | Essential Splice Site | 967 | 1015 | 22 | 24 |
Genomic Location (Zv9):
Chromosome 6 (position 37596607)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37670365 |
GRCz11 | 6 | 37648259 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGTTCTCATCTTCTCTGACAGATGGCAGGCTGGTTTTGGGGCCTGGAAG[T/A]AAGTNNNAAAAAKCTTACATGTATCCYTATCTCACAGCTTTCACTTCAGC
Long Flanking Sequence:
AATTTTCCTACATAAAACGTGCAGAAAGCTTGCTTTATTTGTAGTTGAGTTCAGACTGTGTTTCTAACATCTGTTTTTATTTGATTCATTTTATTCGCAGATATTGCATAGTACGGGTCTAGAGTTTCAACACCAAGTACAGGAGGCAAAAGACCTGGACCAGCTCATTAAAATCCACTACAGATACTTGTCCACCATTCATGACCGATGTCTGCTCAGAGAGAAAGTACGCTGGAATTAGACATTGAAAAAAAAAAAATCTCGAAATTTGACTTATTATTGCACAAAATTGCATGTCACGGTTGAAAATGTACTTCTGATGGGTGGCCTAGTTTTCTTAATCTTTTAAACCGGTATAGATATTTGGAATATTTCTGATCCATCAAATTGGGGTTACTGTGTCTTTGCAGGTCAGTTTTGTCAAGGAGGCCATCATGAAAGTGCTGAATTTAGTTCTCATCTTCTCTGACAGATGGCAGGCTGGTTTTGGGGCCTGGAAG[T/A]AAGTAAAAAAAATCTTACATGTATCCCTATCTCACAGCTTTCACTTCAGCTTGATGACCATGAGCTTTCACTTCTCTTTAGCTTTCTTTTTTTCCTCATGACTGTGGATTGCAATATTCACGTCTCTCTTCTTTTCCCCAGAATCGAGTCGATTGACAAAATGGAGTCGGATTTTAAAAACTGTCACATGTTTCTGGTGACCATATTAAACAAGGCTGTTTGCAGAGGCTCATTTCCTCATCGTAAGTCCTAAACTACAGTGCATTTTAAAACAATAGTGTGAAGAAAAGAAAGCATGTTTAAATGTTTGTGGATCAATTTGTGGGTTTTAAATATCAAGTATAATGTACTATTTCTTTAGCACATTTCCCAGACAAGAAGTCACAAAGTGCTTTACAGTAAAAGAAAAAAGGTTAAAATCCATGTACAAACACTACTCGACTGTAAAAACCAGCTCACCTTACTGGTAATTAAGAACTTGTGCAAAAAGATGTCTTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40736
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065122 | Nonsense | 1011 | 1015 | 24 | 24 |
ENSDART00000144812 | Nonsense | 1011 | 1015 | 24 | 24 |
Genomic Location (Zv9):
Chromosome 6 (position 37599768)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37673526 |
GRCz11 | 6 | 37651420 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTCTTTATTATTTTACAGTGGAGTCCTTGGCGATGTCACTAATGGCT[G/T]GATTTGAACAGTGTTAACCGATCGAACATGCTGTCAATCCAGAGCAGCGA
Long Flanking Sequence:
TTTTCTTCTGAAGAAAATCTTATCTGTTTTACTTCGGCTAAAATAATTTTAAGATCAATATTATTCCCCCGTAAGCAACATATACATTTTTTACAGTCTACAGTACAAACCATCATTATACAACTACTTGCCTAATTACCCTAATTAACCAAGTTAAGCTTTTAAATTGCCCTTTAAGCTGAATACTAGTATCTTGAAAAATATGTAGTAAAATATTATATACTGTCATCATGGCAAAGATAAAAGAAATCAGTTATTAGAAATGAGCTATTAAAACTACTGTTTAGAAATCTTCTTTCCGTTAAACAGAATTTGGGAAAATATACCGGGGGGGTTGGGGGCTAATAATAATTTTGACTTCAACTGTATATATAACAATTCATATAAATTAAAAATTTATAATGGAATGAAATGCTTTTACAGACCAGAATTATGTTGTTTTACCATACCTGTTTCTTTATTATTTTACAGTGGAGTCCTTGGCGATGTCACTAATGGCT[G/T]GATTTGAACAGTGTTAACCGATCGAACATGCTGTCAATCCAGAGCAGCGAACACAAGACAGATTATTTATTGTACTGCTGCATGAAGGCTACTGTACTGTTTCTCTTCATTTCTGCCAGACGTCTGACGCAAAATCACAATAGCACTCCACTGGTACAGAAGTAGCACTTTGTTTGTGTGAACAGTGAATCTTGTGTTTCGTCGTCTACTTTGTCTATAAAACAGTTGCTGCATCAAGATACTCAGTGTTACAGGTGAAAGTGTCAGATGTGAATATTAAGTGTCCTGTACGTGTAGCGGATATATGAAGCGCACATGCCAGTAATCCCAATTATGTATATAACATGCAATAGGCACGCTCGAATTTAAGTAGTGTACATAACATAAGCTAAAATCCAAAATTGTAGACTACATTTGTATGCAGTTCAAGCTTATATTTATATATGTTGTGGTTGCGTAAAGTCATTTTTCATTGTGATGAATGGGCTACTGCATATTAA
Associated Phenotype:
Not determined