ZMP
zgc:86935
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100000855 [Source:RefSeq peptide;Acc:NP_001002083]
Human Orthologue:
FAM173A
Human Description:
family with sequence similarity 173, member A [Source:HGNC Symbol;Acc:14152]
Mouse Orthologue:
Fam173a
Mouse Description:
family with sequence similarity 173, member A Gene [Source:MGI Symbol;Acc:MGI:2384888]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19964 | Nonsense | Available for shipment | Available now |
sa40017 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45135 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19964
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 |
---|---|---|---|---|---|
ENSDART00000060426 | Nonsense | 24 | 213 | 3 | 7 |
ENSDART00000127738 | Nonsense | 24 | 203 | 4 | 8 |
ENSDART00000146053 | Nonsense | 24 | 167 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 3 (position 14743714)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 14989320 |
GRCz11 | 3 | 15139120 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGTGCTCTCAGAGTTCAGAGAGAAGCGTCTGGGCGGCTGGCAGATTT[T/A]GCAGCTGACGGCAGCAACAGGTCTGACGGTTTATGCAGTCTGGGCAGGAA
Long Flanking Sequence:
CTAAATAATGTACCAGATCTGTTCAGTCAAAAAGAATACTGTAGGCAGAGAAATGACATGCTGTAGTAGCTGTGCTGGATAGTTTAAGACAGTTTTTGTTTCTGATTTTGACATTGTGTTTCCTCTGGTGGCTTACAGAAACTCTTTTTCATAAACTAACTTGTACCAACACATTCTGAGCAGACAAATTTAGCTTGTTTATCCAAAACAAAAGATAAATATGAAAATCTGGAAATTTAGCAGGTAAGTGAATTGAAAGAAATATAAACCTTTTTATTATACAACCTTCAGGTCCAAACCTGGACCATACACCACTAAGGCGTTTTTCAGGGAGCAGGTGTCAACCAAATGCACAGGTATGTTTGCAATACTAAGAGGTGTAATATAAAATATGATGTATTTTAATTCTGACATCTTTATTTTTTCAGTCATGGAAGACGACATACAAGAAGAAGTGCTCTCAGAGTTCAGAGAGAAGCGTCTGGGCGGCTGGCAGATTT[T/A]GCAGCTGACGGCAGCAACAGGTCTGACGGTTTATGCAGTCTGGGCAGGAATTTTAATGCCAGGGTTTCGCCGAGTGCCGCTCAAATTACAAGTGAGGTTTAATGCAAATGCATGCTTTGATTTTACATTTGCTTTAGTTGTGTGTGCATTAATTATTATTATTAACCGCTACTGTTTCAGGTGCCTTACATACCAGCAAGCAAAGCTCAAGTTTCCAATGTTATGACTCTGATGAAGGGAAGGTCGGGAGGCATCGCTGATCTGGGATCAGGTGATGGCAGGATTGTAAGTTGTAACTTTTTCATTTATTTTTGTTTAAGCATTTGTTGCATATTTTTCATCAAGCCTATGGGAGTGAAAGTCACACAACAGAATTGATCCTTTTCACATTTCCGAGTTTCTCAGCAGCAGAGGTCATCATAGTTATGTATACTTAGAGCAGTAAATGGGAGAGGATCACAAATAAATGTTTTAGATTCCAGTTTGCCCAAGAAACTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40017
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000060426 | Nonsense | 64 | 213 | 4 | 7 |
ENSDART00000127738 | Nonsense | 64 | 203 | 5 | 8 |
ENSDART00000146053 | Nonsense | 64 | 167 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 3 (position 14743506)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 14989112 |
GRCz11 | 3 | 15138912 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTATTAACCGCTACTGTTTCAGGTGCCTTACATACCAGCAAGCAAAGCT[C/T]AAGTTTCCAATGTTATGACTCTGATGAAGGGAAGGTCGGGAGGCATCGCT
Long Flanking Sequence:
CAAAAGATAAATATGAAAATCTGGAAATTTAGCAGGTAAGTGAATTGAAAGAAATATAAACCTTTTTATTATACAACCTTCAGGTCCAAACCTGGACCATACACCACTAAGGCGTTTTTCAGGGAGCAGGTGTCAACCAAATGCACAGGTATGTTTGCAATACTAAGAGGTGTAATATAAAATATGATGTATTTTAATTCTGACATCTTTATTTTTTCAGTCATGGAAGACGACATACAAGAAGAAGTGCTCTCAGAGTTCAGAGAGAAGCGTCTGGGCGGCTGGCAGATTTTGCAGCTGACGGCAGCAACAGGTCTGACGGTTTATGCAGTCTGGGCAGGAATTTTAATGCCAGGGTTTCGCCGAGTGCCGCTCAAATTACAAGTGAGGTTTAATGCAAATGCATGCTTTGATTTTACATTTGCTTTAGTTGTGTGTGCATTAATTATTATTATTAACCGCTACTGTTTCAGGTGCCTTACATACCAGCAAGCAAAGCT[C/T]AAGTTTCCAATGTTATGACTCTGATGAAGGGAAGGTCGGGAGGCATCGCTGATCTGGGATCAGGTGATGGCAGGATTGTAAGTTGTAACTTTTTCATTTATTTTTGTTTAAGCATTTGTTGCATATTTTTCATCAAGCCTATGGGAGTGAAAGTCACACAACAGAATTGATCCTTTTCACATTTCCGAGTTTCTCAGCAGCAGAGGTCATCATAGTTATGTATACTTAGAGCAGTAAATGGGAGAGGATCACAAATAAATGTTTTAGATTCCAGTTTGCCCAAGAAACTAAAAAAAGAACTCCATGATAGTCGTTTTATGACACTCAAAAAAGTGTGAAACTGAAAATTGCAGCCAGATTAAACAACAATGTTAAATTTACTGTCCTGTCCATGAATTATGCATTACAAACACCTCGCATAAGCAATAACCTTTTAAAAATTGAAATATTGGAAAACTTTTGAGGATTTAAGATGGTTAAGATCTTTAAATCAATCTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45135
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000060426 | Nonsense | 131 | 213 | 5 | 7 |
ENSDART00000127738 | Nonsense | 131 | 203 | 6 | 8 |
ENSDART00000146053 | Nonsense | 131 | 167 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 3 (position 14741620)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 14987226 |
GRCz11 | 3 | 15137026 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACACTTTCATGCGTGGAGAGCTGGACACCATAGAAGTGTTTCTTATCGA[C/T]GAGAGGACCTCTGGAAGGTACCGTGAACATTAAAACACATAAATTTATAT
Long Flanking Sequence:
AGTTTCCTAATTGGATTTGTGTATTTTTGAATCATGTTTTGAATTTGCGAATTGTATTTGTGTATTTTTGAATTATCTTTTGTATTCAGGAATTTAATTTGTGTATTTTTTAATTATGTTTTGTTTTCAGGAATTGGATTTGTGTATTTATAAATCTTGTTTTGAATTTACGAATTGGATTTGTGTATTTTTGAATCGTGTTTTGAATTCATGAATTGGATTTGTGTATTTTTGAATCGTGTTTTGAATTCATGAATTGGATTTGTGTATTTTTGAATCGTGTTTTGTATTTACAGATTAGATTTGTAAATATATTATTTTTGAGACCAAGCTTATGAACAGTAGTGCGCATGCTGATGTATTGTAAATGTGTGCAGGTGTTAGAAGCTTGCCGTCGGGGTTTCTCTCCAGCTGTCGGTTATGAGCTCAACCCCTGGCTTGTTCGTCTTGCACACTTTCATGCGTGGAGAGCTGGACACCATAGAAGTGTTTCTTATCGA[C/T]GAGAGGACCTCTGGAAGGTACCGTGAACATTAAAACACATAAATTTATATAATACACTACACTCAGACAGAATATATACTATATAGCATCTCATAAAAATCCCCAGAGAGCTTGTCTTGTATAAATTATATATGTAAATTATAAATACATTTCCTCCAACATTTTCTGGACTGTAATATGTCTTCTCCTTTAAGGTACTTGCTCTATTTAGTTGATACATCCAGAAATGTAGTCTCCTAAAAATTGATTATATATGATATTGTTTTATTTTTTTTGAATAACTAACCTTTGCTCACCATGAATGTGAGTCAGACTTTCTTTATATACATTTTGTTTTCATAAATCATTGCAATTCGCCACTCTTTGCAATTGTCTGTACGTTTTATGGTATAGTTCACCCACAAAAAGGAAAATTATTTACTTACTTTCTGTCCTCTTGATCAAACTAGTTTAAGTTAAGTCTAGCTTTGTTGTCATTTGTGGACATGCAGTAGAAGAAA
Associated Phenotype:
Not determined