ZMP
zgc:162193
Ensembl ID:
ZFIN ID:
Description:
Protein FAM115 [Source:UniProtKB/Swiss-Prot;Acc:A4IG42]
Human Orthologues:
FAM115A, FAM115C
Human Descriptions:
family with sequence similarity 115, member A [Source:HGNC Symbol;Acc:22201]
family with sequence similarity 115, member C [Source:HGNC Symbol;Acc:26878]
family with sequence similarity 115, member C [Source:HGNC Symbol;Acc:26878]
Mouse Orthologues:
Eapa2, Fam115a, Fam115c
Mouse Descriptions:
experimental autoimmune prostatitis antigen 2 Gene [Source:MGI Symbol;Acc:MGI:3042585]
family with sequence similarity 115, member A Gene [Source:MGI Symbol;Acc:MGI:1914665]
family with sequence similarity 115, member C Gene [Source:MGI Symbol;Acc:MGI:2385258]
family with sequence similarity 115, member A Gene [Source:MGI Symbol;Acc:MGI:1914665]
family with sequence similarity 115, member C Gene [Source:MGI Symbol;Acc:MGI:2385258]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16829 | Nonsense | Available for shipment | Available now |
sa17361 | Nonsense | Available for shipment | Available now |
sa22598 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16829
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 |
---|---|---|---|---|---|
ENSDART00000127026 | Nonsense | 102 | 912 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 15 (position 13988016)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 14273695 |
GRCz11 | 15 | 14209652 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCGGAGATGCTGGAGTTGTAGGGATTCAGAAAAGTTTACGAACWGTAGCT[G/T]AAAACTTGAACTAYAGCCCTTTCAAGACAGAACTAGGAGACTTTCAAGAT
Long Flanking Sequence:
TGAACAAAACGTTTTTAAATATGTGCAACCTTTTCCTTTCATTTTCTGTTTTTGTGTAGGAGTGAAAATTGATCACTTTCATTTTTACTGCATACACAAGCTCTGGTTGAACAATTCAAATTCTCAGACTTTCTAAAGCTGACTGTAACCAAAGAGAGTTTGTTTTGAGTCATCTTACTAAACCGAAGTAATCCACCATGGCACGTGAACAGGACTACTACACTCTCATGTCTGGTATGCAACAGCTTGATTTGCAGGGGAACGCAGTCCCCAGTGATCTTGTACTAATAGGAGAGCATGCCTTTCCACTTGCCATGAATCCAAGAGGTCAGGTGCTCATGGCTGCATCTCATTACGGTCGGGGTCGCATTGTAGTGCTGGGACATGAAGAATACTTAACACGATTTCCTGGGCTGATAGAGAATGCCATAATGTGGCTCATGCCATGTACCGGAGATGCTGGAGTTGTAGGGATTCAGAAAAGTTTACGAACAGTAGCT[G/T]AAAACTTGAACTACAGCCCTTTCAAGACAGAACTAGGAGACTTTCAAGATAGGTTCGCTATATATATCACTGATGCGTACAGTGTTGAGAGCTCTGCAAAGGATCTGATTGCTTTCCTCAAAGCTGGGGGTGGTTTGATCATTGCTGGACAAGCATGGAGTTGGTCTTATGAACACCCACAGGAAAACACTATCAGGAACTTTCCAGGAAACAAGGTGTGCAGTGTTGCAGGCATTTACTTTTCAGAGCTTGAAGGAGAAGTCGGCACCTTTCCTGTTCCTCGAAATATCCCTTCTAGTTGGCTTGCCGTGGCGTAAGTCCAGGAGACATATTTAAATATTTCCCACTGATCCTTTTTTTTTTAAATCAAAACCAACATTTGACTAATTGTGTTTATTTGCTTCTTTTCAGAATAGGCAAAGACTTTAAAGAGGACCTAGAGTTCCTGCTGGAAGGTGTGTCTGAGTTTGACACTCAAGGTGGGGCTATAGCATCAGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17361
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 |
---|---|---|---|---|---|
ENSDART00000127026 | Nonsense | 423 | 912 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 15 (position 13989077)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 14272634 |
GRCz11 | 15 | 14208591 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATAGTTGTAAACATGGGTACCACTTTCGMAGCATGCTGCAGAGATTTGCT[C/T]AGCATGTAAGCCAAGGGCAAGAGCTGACTGATCGRGAACAGGGCTGTTTG
Long Flanking Sequence:
TTGCTGGTGCCTATTATGGACAAGGGCGAGTAATTGTGGTATCCCATGAAGGGTACATGGGCCGAGACTCTCTGTCCTCTTTTATGATCAATGCTATTAAGTGGCTTGATGAGGGTCGCAAGGGTGTTGTAGGGATCGTACCCAACCTCACTGCAGCCCATACAGTACTGAGCAAATCTGGTTTAGACTGTCAATTGACCGGTTTCAGAGAAGATCTAAGCGTCTACGTCTGCACTTCCTACAGTGATGCACAGTGTGCAGAGATTCAGGAATTTGTTGCAGAAGGTGGAGGTCTTCTTATTGGGGGTCATGCCTGGTACTGGGCTCAGACCCACTGGGGCTCCAATGTGATGACTGAATACCCCGGAAATCACATTCTTAACAAGATGGGATTGTGCCTCTTGGGAAACACCTTGGGTGGAGGGTTATATAAAGCTCCAGAAATAGAGCATAGTTGTAAACATGGGTACCACTTTCGAAGCATGCTGCAGAGATTTGCT[C/T]AGCATGTAAGCCAAGGGCAAGAGCTGACTGATCGAGAACAGGGCTGTTTGAAGCAGCTGGGCACTGACTGTGCCAGTTACCTTCAAATGCGTTGTCATGACAGTGCTGCTTACACCTCAGTGGTAGCTCTTCTTAGTGACATAGTAAAGGAAGTAGGTGTTCCACAGGTGTGTAGTAACTGCCCTGTTGAAAGTCCCAAAGACCACCTGATGCTCCACATTGGTACTGAGGTCTACAAAGTGACGCCTGATCCCGACGCCCTTCTTCCCTACATCATCAAGGACAGACCCAACTTGCCAACTTTGTCAAATGCAAGAGTTCGGATTACTGCCAACACTGGAGGTACAGTTTTTGCACCAAATGTAAGGGGAAAATGTTCAAGTTTGTAATTTATGTGCACTCTAAATGTTTCAATTACTTGTTTCAGGTTGTGAAGAATGGATAAGCACAGGCTTATATCTTTCTCCTGGTATGAAGACATACATAGCAGTACCTCCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22598
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 |
---|---|---|---|---|---|
ENSDART00000127026 | Nonsense | 436 | 912 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 15 (position 13989116)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 14272595 |
GRCz11 | 15 | 14208552 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGATTTGCTCAGCATGTAAGCCAAGGGCAAGAGCTGACTGATCGAGAA[C/T]AGGGCTGTTTGAAGCAGCTGGGCACTGACTGTGCCAGTTACCTTCAAATG
Long Flanking Sequence:
TATCCCATGAAGGGTACATGGGCCGAGACTCTCTGTCCTCTTTTATGATCAATGCTATTAAGTGGCTTGATGAGGGTCGCAAGGGTGTTGTAGGGATCGTACCCAACCTCACTGCAGCCCATACAGTACTGAGCAAATCTGGTTTAGACTGTCAATTGACCGGTTTCAGAGAAGATCTAAGCGTCTACGTCTGCACTTCCTACAGTGATGCACAGTGTGCAGAGATTCAGGAATTTGTTGCAGAAGGTGGAGGTCTTCTTATTGGGGGTCATGCCTGGTACTGGGCTCAGACCCACTGGGGCTCCAATGTGATGACTGAATACCCCGGAAATCACATTCTTAACAAGATGGGATTGTGCCTCTTGGGAAACACCTTGGGTGGAGGGTTATATAAAGCTCCAGAAATAGAGCATAGTTGTAAACATGGGTACCACTTTCGAAGCATGCTGCAGAGATTTGCTCAGCATGTAAGCCAAGGGCAAGAGCTGACTGATCGAGAA[C/T]AGGGCTGTTTGAAGCAGCTGGGCACTGACTGTGCCAGTTACCTTCAAATGCGTTGTCATGACAGTGCTGCTTACACCTCAGTGGTAGCTCTTCTTAGTGACATAGTAAAGGAAGTAGGTGTTCCACAGGTGTGTAGTAACTGCCCTGTTGAAAGTCCCAAAGACCACCTGATGCTCCACATTGGTACTGAGGTCTACAAAGTGACGCCTGATCCCGACGCCCTTCTTCCCTACATCATCAAGGACAGACCCAACTTGCCAACTTTGTCAAATGCAAGAGTTCGGATTACTGCCAACACTGGAGGTACAGTTTTTGCACCAAATGTAAGGGGAAAATGTTCAAGTTTGTAATTTATGTGCACTCTAAATGTTTCAATTACTTGTTTCAGGTTGTGAAGAATGGATAAGCACAGGCTTATATCTTTCTCCTGGTATGAAGACATACATAGCAGTACCTCCAGAGATTGTTGGAAAAAATTGGCAGGTGATCTAAAAATTTTG
Associated Phenotype:
Not determined