ZMP
tmem30a
Ensembl ID:
ZFIN ID:
Description:
transmembrane protein 30A [Source:RefSeq peptide;Acc:NP_997941]
Human Orthologue:
TMEM30A
Human Description:
transmembrane protein 30A [Source:HGNC Symbol;Acc:16667]
Mouse Orthologue:
Tmem30a
Mouse Description:
transmembrane protein 30A Gene [Source:MGI Symbol;Acc:MGI:106402]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39179 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12779 | Nonsense | Available for shipment | Available now |
sa23190 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39179
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 |
---|---|---|---|---|---|
ENSDART00000122747 | Essential Splice Site | 124 | 372 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 50519840)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 49905765 |
GRCz11 | 17 | 50005670 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCTGGTGACTGGATGTTATTTTAACCTCTAACTTCTTTTTTTTTTGTA[G/A]AGTAATGTTTTCATGTATTACGGACTCTCCAACTTCTATCAAAACCACAG
Long Flanking Sequence:
TATACCTCTCTGTTTGTTTATGATTATAGTAACACAGGATAATACGAAGTCACATTTTCTGAGTTTGAAAGATTTACTTATATTAAAGCACATTTAGAAATCAACATCATTGTCACTGCTACATCAGTTATTTCATTAACAAAAACCTATAAATGCATATGAAGGTATCAATGAAAAGCATAGCAAGCGTGAACTAATTTAGAGATATATTTAACTCTAGCTCCATTATGTTGTATATTTGCTTTGTCTGCTAACCGTTGGATGGTCAAACAAATCACCTAAAGTGCCATTAGCTCTCATGTATTATGCATTAGTATATTTAGAGGACGTTTTATTGATCGCACCTTTTAATATGTTAAAAATAGAATTGTTTTCCGCTCTTGTTATAACAGAGATCAGTTCAGATGATCTATAAACAACACTGAAGTAGCCTCAGTATAAAAGATTTTATGGCTGGTGACTGGATGTTATTTTAACCTCTAACTTCTTTTTTTTTTGTA[G/A]AGTAATGTTTTCATGTATTACGGACTCTCCAACTTCTATCAAAACCACAGACGTTATGTCAAATCCAGAGATGACAGTCAGCTGAATGGAGACAAAAGCTCTTTACTGGTGAGTGTTTCGACATATGCTGACTAAATGTTTGACTTTGACTTTAGTATATTATATTTAATTTTGTTTTGTGTAAACTTATAGTTTAATATTGGTGCATTTTGTGAGATCTGATGGTATGGAAATGCTTGAGGCCCAAAAGAGAAGTGGTAACAACAGCCAGTAAGTTGTTGGGAACAAAACTAAAGAGTATACTGGTAGTGTATACAAAGAAAGAGCATTACAAAAGGCTATCATGATTGTCAATGAAAGCCTTATTATATATATATTATATATATATATTTGGTGACGCGACTGACGTGACATGCTTTTCCGCTCAGAGTTTACTTTTGTTTAATTGTCGTTTGCATATTGCAAATATGTGTAATTAGTGTAAACATGGCCCTAGCAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12779
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000122747 | Nonsense | 168 | 372 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 50519245)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 49905170 |
GRCz11 | 17 | 50005075 |
KASP Assay ID:
2261-1598.1 (used for ordering genotyping assays)
KASP Sequence:
GTGTWTAAATCTTTTGTTYTACAGAATCCGAGTAAAGAGTGTGAACCGTA[T/G]CGAACAAGTGACAGGAAGCCCATYGCTCCTTGCGGCGCCATTGCTAACAG
Long Flanking Sequence:
AAAGCTCTTTACTGGTGAGTGTTTCGACATATGCTGACTAAATGTTTGACTTTGACTTTAGTATATTATATTTAATTTTGTTTTGTGTAAACTTATAGTTTAATATTGGTGCATTTTGTGAGATCTGATGGTATGGAAATGCTTGAGGCCCAAAAGAGAAGTGGTAACAACAGCCAGTAAGTTGTTGGGAACAAAACTAAAGAGTATACTGGTAGTGTATACAAAGAAAGAGCATTACAAAAGGCTATCATGATTGTCAATGAAAGCCTTATTATATATATATTATATATATATATTTGGTGACGCGACTGACGTGACATGCTTTTCCGCTCAGAGTTTACTTTTGTTTAATTGTCGTTTGCATATTGCAAATATGTGTAATTAGTGTAAACATGGCCCTAGCAAGCATACTTACTGAATTGTTGAATCGAGTTTGTACGTTGTCTTCAAGTGTTTAAATCTTTTGTTTTACAGAATCCGAGTAAAGAGTGTGAACCGTA[T/G]CGAACAAGTGACAGGAAGCCCATTGCTCCTTGCGGCGCCATTGCTAACAGTCTCTTCAACGGTAAGACTGAAGGCTCATAATACTAATAACCCAGAGGAGTAGCGGACTGGCCCGCAGGGCACGCTCCGTGGGGGGGCCCCGCGTGATTAGGGGGCCCCACGTTGTCGCGAAAATCCGGCAACCTCAATAATCAAACTCTTGAAAACAACTGTGGTCGGAACCAATGTTCACAGGTCTGTGTTCTCTGAACTCCTCTCAACCGGTGGACTACTTCATTATGATTGCCGCCGAACCGAGTCAAGCTCGGTCATAGCTCATACCATAAAGTTGACTTGATTTCAACTCTCCTCGACACTCACACAGGTGAAGACGCGCCGCGATGTTTTTCACCGCCGTTTCTCATTGAAAATGAATCACTTCTGGCTACTTTGACGCTCTCGCCGTTTTCGGTTTGTGATCGCTCCTCAGTTTGTGAAGGCTTCCCTGTGTTGTCGCCCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23190
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000122747 | Essential Splice Site | 309 | 372 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 50516446)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 49902371 |
GRCz11 | 17 | 50002276 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGACCCCAACACTACCGCCGGGAAACTACAGCCTGGAGGTCGCCTACAG[T/C]ATCCTTCACCAAACCCACACAAAGCCTTGTTCACACCAAGAATGAGCTAT
Long Flanking Sequence:
AACCCAGGAGGAAGCAACAACAACCTCTCCGTTGTTTTCCAAGGTACAACTCAGAAGTCTACTCGATCATTCGGATGTGTTTAGCAGGGCCTTTCAGCTCATGTTTCACATTTCTTTTTGATTAGATTTTTTTCAGATTTCAAGTAAAGATGTTTTATTTTTATGATTTATTTAAAATTTTAGTAGGTTTTCTATTTATTTTTTTTATATGAATACTTTCCGGATGCACTGTACATCAACACATCTCTCTTTTTTTACCCTGAGTCTGTAATGTTTGTCCTCACAGACACCAGCAAACCTGTAAACTGGCGTAAGGCTGTCTACGAGCTGGACCCGGCTGATCCCGAGAACAACGGTTTCGTCAACGAGGACTTGATCGTGTGGATGAGAACCGCTGCTCTTCCCACGTTCAGGAAACTGTACCGCATCATTCAGAAGAAGAAGGACACCATGACCCCAACACTACCGCCGGGAAACTACAGCCTGGAGGTCGCCTACAG[T/C]ATCCTTCACCAAACCCACACAAAGCCTTGTTCACACCAAGAATGAGCTATTAATGCCTTGTTTACACTGACTGGTACAGTACGGTACGGTTCGGGTCGGTACGGGTCACCTTTATCAGGCTTGCGTTTCCACTATAAAGGGTACCCTTTTGGTGGGTGTAGTGTAAGACAGAAAGTTTCAGTCGCATCATTCTCGCTCGAGGAAATGTCTACAGTAAAGCTGCACAGGTTCACGTTCACATATCATATTAAAAGCACTTCTCACAAAACAGATGCTTTACACACATAAATACTTGTGTATAAATGTTTATTACTAACTTTTCTATGAACAGGATTTGATTATAACTGCAGATCAATGACAGTGCCAAATAGCCTACTGTAACGTCTGTAATTATATAAAATAAATACATAAATGAACATATATGAACACATACAGCCCCTGACAGTCTCCGATGTTACCAACTACAGAAAAACTACACACATCAGACATTTCGTTCTTAA
Associated Phenotype:
Not determined