ZMP
tubgcp2
Ensembl ID:
ZFIN ID:
Description:
gamma-tubulin complex component 2 [Source:RefSeq peptide;Acc:NP_956416]
Human Orthologue:
TUBGCP2
Human Description:
tubulin, gamma complex associated protein 2 [Source:HGNC Symbol;Acc:18599]
Mouse Orthologue:
Tubgcp2
Mouse Description:
tubulin, gamma complex associated protein 2 Gene [Source:MGI Symbol;Acc:MGI:1921487]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa22037 | Nonsense | Available for shipment | Available now |
| sa35216 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa35217 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22037
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000020192 | Nonsense | 83 | 882 | 3 | 18 |
| ENSDART00000142128 | Nonsense | 83 | 882 | 2 | 17 |
Genomic Location (Zv9):
Chromosome 12 (position 9938566)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 9146521 |
| GRCz11 | 12 | 9184364 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGATGAACTGAAGTCAAAGAATGCTCGCAACCTTGATCCACTGGTGTA[T/A]CTGCTCTCCAAACTCACTGAAGATAAAGAGGTGCAGTACCAGATTTGGTT
Long Flanking Sequence:
TCACTTAACGTTAACATCATGCAAAATAAACGTTTATATTTGACGTCCATATGTCAGCAGTTATTGTAATTACTATGTAGTGTTTGTGTAACGTTACTCATTCATTCATAGAGCTTGCTTTCTTTTCTCAATGCTCTCTCTCTCTCTCTCTCTCGGATTTCAGCTTCTGATATCATGAGTGAATTCAGGATTCATCATGATGTTAATGAACTCCTCGGGCTCCTTAATGTCCGAGGGGGAGATGGTGCAGAGGTTTATATTGATTTACTGCAGAAGAACAGGACTGGATATGTGACCACTACAGTTTCTGCACACAGCGCTAAGGTAAACAGACAGATCATGTGCTTTATTTATTGTCAGTCCATTTCTGAGTGCACTGAAACTATTTACATTGCCCTATAGGTCAAAATGGCAGAACACTCCAAAACACCTGAAGACTTCTTGAGGAAATATGATGAACTGAAGTCAAAGAATGCTCGCAACCTTGATCCACTGGTGTA[T/A]CTGCTCTCCAAACTCACTGAAGATAAAGAGGTGCAGTACCAGATTTGGTTTGCAGCCTAGAGTCCTTGTTTCATTCAGTGCCTCACAAACAAAACTCACATAGTGATAACAACAAAGGGATATAAAGACATAAAACGTAAACATAGAAAACACTCACAAAAAATACATAAATATTCACTTCAAGTAGGGCTGGGCGATAATTCGATATTGATAATTATCACAATATAATTTTTTTTGATAAATCGATAATGACAGTTCGATAATTGCTCGATAATATAAACGCACTATGCGTAACGTTGCATAAGCATTTTGCAACCTGCCCTTCCGACTGCCGCACGCCGTACAAGTTTACAGCCATACAGTGTTAGTTGCACTGAAAAGAGTAAGAAAGAAATAAGGTAAAAAAGGTCAGAGTCACAGACATTGTTGACCAGAAATGTCACTAGACTTCATGAGCTACTTAGTTTTTCGCTATCCGACACAAAAAAGAGCAACGTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35216
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 |
|---|---|---|---|---|---|
| ENSDART00000020192 | Essential Splice Site | 804 | 882 | 17 | 18 |
| ENSDART00000142128 | Essential Splice Site | 804 | 882 | 16 | 17 |
Genomic Location (Zv9):
Chromosome 12 (position 9967972)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 9175927 |
| GRCz11 | 12 | 9213770 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACTTTTAGGTGAAGTATTCCTTTAATCTGATCTGTTTGTCTTCATCTTA[G/A]TTTCTAGCTGAGCATGTGGATGCTCTTCAGTCTGACTCCGGGTTCGAGGG
Long Flanking Sequence:
AAGGGCCGCCACAGCGGAATGAACCTCAAACTTATCCAGCATATGTTGTTTGCAGCGGATGCCCTTCCAGCCATAAGCCAAGACTGGGAAACACCCAAACACTCTTGCATTCACACACATACACTACGGCCAATTTACCTTATTCAATTCACCTATAGACCATGTCTTTAGACTGTTCATGTTTTTGTCTTATGCTCAAAAATAAATGATTTAATTTGACTGTTCATCCAAAAATTGACTCATCCTCCACTTGTTCCAAACCTGTTTCTTTTCTCTGTTGAAGACAAAGGATGATATAATGAAGAATGTGGAAATAAAACAACAGAAATTGACTTCCATAGTATTTTGTCTCTACTATAAATATCAATTGCTGCTTTTTTCTAACATTTTTCAGAATATCTTGTTTTGTGTTCAACATAAGTTTGGAATGACCAGTGGTAAGGAAATATTCACTTTTAGGTGAAGTATTCCTTTAATCTGATCTGTTTGTCTTCATCTTA[G/A]TTTCTAGCTGAGCATGTGGATGCTCTTCAGTCTGACTCCGGGTTCGAGGGGACCATCAGCAAGTTTGACAGTAACTTCAGCACTTTATTGCTGGATCTTTTGGACAAGCTCAGCATTTACAGCACCAATGACTGTGAACACAGCATGATCAACATCATCTACAGGTGGGTCGCCAGAGAAACTTATCTACACTTCTTCTTTTTGTAACATCTATCAGATTTAAAGGATTAGTTCAACCCCAAAAAGAGAGAAAATTCTGTTTTAAATTACCTTCATATCATTCTAATTCCATGAGACATTTATTTATCTTCAGAACACAAATTGAGATATTTTAAATGAAATCTGAGAGTTCTCTGACCCTCCATAGACCGCAACAGTCACAAGTCAAGAAAAGGAACCAAAGCATTGTCAAAATGTTGTCTGAAAGCTCCAAGAGCACATCTGTGTGTCAAAAATCTGATGCTGTGCTTATTCATACAACATGATTTTTTTTTTTACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35217
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 |
|---|---|---|---|---|---|
| ENSDART00000020192 | Nonsense | 813 | 882 | 17 | 18 |
| ENSDART00000142128 | Nonsense | 813 | 882 | 16 | 17 |
Genomic Location (Zv9):
Chromosome 12 (position 9968000)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 9175955 |
| GRCz11 | 12 | 9213798 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATCTGTTTGTCTTCATCTTAGTTTCTAGCTGAGCATGTGGATGCTCTT[C/T]AGTCTGACTCCGGGTTCGAGGGGACCATCAGCAAGTTTGACAGTAACTTC
Long Flanking Sequence:
AACTTATCCAGCATATGTTGTTTGCAGCGGATGCCCTTCCAGCCATAAGCCAAGACTGGGAAACACCCAAACACTCTTGCATTCACACACATACACTACGGCCAATTTACCTTATTCAATTCACCTATAGACCATGTCTTTAGACTGTTCATGTTTTTGTCTTATGCTCAAAAATAAATGATTTAATTTGACTGTTCATCCAAAAATTGACTCATCCTCCACTTGTTCCAAACCTGTTTCTTTTCTCTGTTGAAGACAAAGGATGATATAATGAAGAATGTGGAAATAAAACAACAGAAATTGACTTCCATAGTATTTTGTCTCTACTATAAATATCAATTGCTGCTTTTTTCTAACATTTTTCAGAATATCTTGTTTTGTGTTCAACATAAGTTTGGAATGACCAGTGGTAAGGAAATATTCACTTTTAGGTGAAGTATTCCTTTAATCTGATCTGTTTGTCTTCATCTTAGTTTCTAGCTGAGCATGTGGATGCTCTT[C/T]AGTCTGACTCCGGGTTCGAGGGGACCATCAGCAAGTTTGACAGTAACTTCAGCACTTTATTGCTGGATCTTTTGGACAAGCTCAGCATTTACAGCACCAATGACTGTGAACACAGCATGATCAACATCATCTACAGGTGGGTCGCCAGAGAAACTTATCTACACTTCTTCTTTTTGTAACATCTATCAGATTTAAAGGATTAGTTCAACCCCAAAAAGAGAGAAAATTCTGTTTTAAATTACCTTCATATCATTCTAATTCCATGAGACATTTATTTATCTTCAGAACACAAATTGAGATATTTTAAATGAAATCTGAGAGTTCTCTGACCCTCCATAGACCGCAACAGTCACAAGTCAAGAAAAGGAACCAAAGCATTGTCAAAATGTTGTCTGAAAGCTCCAAGAGCACATCTGTGTGTCAAAAATCTGATGCTGTGCTTATTCATACAACATGATTTTTTTTTTTACTTTTGTATTTGTAATTTAGCCAACATTATC
Associated Phenotype:
Not determined