ZMP
fam151a
Ensembl ID:
ZFIN ID:
Description:
Protein FAM151A [Source:UniProtKB/Swiss-Prot;Acc:A5PN38]
Human Orthologue:
FAM151A
Human Description:
family with sequence similarity 151, member A [Source:HGNC Symbol;Acc:25032]
Mouse Orthologue:
Fam151a
Mouse Description:
family with sequence simliarity 151, member A Gene [Source:MGI Symbol;Acc:MGI:2657115]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa8552 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa44522 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19689 | Essential Splice Site | Available for shipment | Available now |
sa31261 | Nonsense | Available for shipment | Available now |
sa15963 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa8552
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 |
---|---|---|---|---|---|
ENSDART00000081026 | Essential Splice Site | 163 | 599 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 2 (position 10870157)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 11295253 |
GRCz11 | 2 | 11078852 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGACAACACTCTGGAGGAATGGCTGGATGCTGTRCTCAAGTCWAAGAAAG[G/A]TAAACAACATTGTCTGTTTTTCATACTCTGATGACATTGCGAACATTTGY
Long Flanking Sequence:
TATTGTGGGCCCCCAGACTATCTAAAAAAATAATAAATCAAGAAGGATTTTGTAGACAAAGCAAAAATTCTTGTTTTTAGAAAAAAATTATGTGAGTTTCTCCTTAAAACAAGCAAAATAATGTGCCAGTTGGGTAAATAACAATAAACAATTTTATTTTGCTTCTCCCATTTGCACATTATTTTGCCTGTTATTTTTAAAACTTGCTTAAAAATAGCTTTTTTATGAAAAATAAATCTAGTCTAGAAAATGCTTCTTGATTTAAGAACTATTAGATATTTGGACTAGAAACAAGACAAAACCTCTTAGTAGAAAAATCATTTTGTGCTGTGTAACTGTTTACATTGCAGGTGATGTGATGATCCTAGAGGCTGATGTAAATGTACAAGGTCATAACACAGTCAATGAAACCAATATTCCCATCATGGCCCATCCGCCAGACATTTACAGTGACAACACTCTGGAGGAATGGCTGGATGCTGTGCTCAAGTCAAAGAAAG[G/A]TAAACAACATTGTCTGTTTTTCATACTCTGATGACATTGCGAACATTTGTTATGTGGCTGTCCTTCATTAGGGGTAAAGCTGGATTTTAAGAGTATCAGTGCTGTGGAGCCCTCATTGGATCTGCTGAGAGCGAAAAACCAAACGGGGATCAACAGGCCGGTGTGGATAAATGCAGATATTCTTCCTGGTCCTAATGTCCCTGAGTTCTGGCCAGTGGTCAATGCTTCAGAGTAAGAGTTTCATTTTATTGCTAACAATTAATTGCTTTTTAGGCTGCATTCACACTAGTGCATGTTTTGTTTTAAAACAGTGTTGCAGAATAATTATTCTCATACAGACATCCGTTTTTACTAAGTTTCAGAAAAACTATCTCTGTCAGTATTATACATGAAAACACAAGATACGTGACCAGTTACGCTTACTGGCATGTAAATATGTTGCAGGCATTCATAAAATACTTCCCGATTCCCGTCAGTGTAATGGTCATAAGGGGTTTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44522
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081026 | Nonsense | 285 | 599 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 2 (position 10866266)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 11291362 |
GRCz11 | 2 | 11074961 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCCTGTTCATGCTCTGATGGCCAAGAATGGCTGGCCGCATCTGAGCTG[G/A]CTGCTCAGTCAGTCTTCAAGGTATAACTAAAGGTCAGCTCAATCATTTCA
Long Flanking Sequence:
GTAGCAATTTTACCCTGTAAGTGCATGGATAATATCTTCTGATATTTAAATAGTCAATCCAATGAACTTAAATGATCAAAAACTGCAACAAATATTTTTTGGAGACCTGAACTGCTAAACCAACCTTTAATACCAGCCAATACAATTCATAAGGGTTCTCAAACTCTGTCCTGCAGATTTTAGCTTCAACTTGCCCCAAAAGACCTGCACAGATGTTTCTAGAAAGCCTAGTAAGAGCTTGATTATCTAGCTTGTGTCTGATTGGGGTCGGTTTTCAGTTGTTGTTTTTTTTCCAGGTTTTTTGAGCTCATTCAGCTAAAATTTCCTGACGTCACCATCTCTCCAGGGTGGAAGGTTCTTTATCTTTCCATCTTCCCCAATGTGACTTACACCCGCAGTATGGTGGAGCAGATGTACTCCACCATAAGACACCTTCCACAGAAAATTACCTTCCCTGTTCATGCTCTGATGGCCAAGAATGGCTGGCCGCATCTGAGCTG[G/A]CTGCTCAGTCAGTCTTCAAGGTATAACTAAAGGTCAGCTCAATCATTTCAGAGTGGGAGATGAAGGCAATGTCCATATTTTGTCTTGATTATGATGCAGGTACAGTTTAACCCTGTGGCAAGGAAAGGAAAATCCCACTTTGAATGATCTCCTCTTCATTAGAGACAACAGCAACCCTCAGCGCATCTACTATGACATCTATGAGCCTGTGCTCTCACAGTTCAGAGAAGCTGCAAGTGAGTGACGTCTTGCATACTGTACCACACTTCACATGTAATGCACAATATTTCCTTATCTGATAAGTTTGTTATTTATTTACTGGCTTTGGTTGAAACTAAATGTTTTACAGATAAAACTATACTAAATGCCTCACAGCAAGAAGGTCACTGGTTCAAGCCCTGGCTGGGTCAGTTGGCATTTCTGTGTGGAGTTTGCATGTTCTCCCCGCGTTGGCCTGGGTTTCCTTCGGGTGTTTTTCCCACTGTCTAAAGACATGCGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19689
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081026 | Essential Splice Site | 383 | 599 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 2 (position 10861206)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 11286302 |
GRCz11 | 2 | 11069901 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAAATGCATAGATCCTGTTAAAATATAATACTTTTTTGTTGTCATTTC[A/C]GATAGTCCTGGAGGAATGCTGGTGATTCCAGTAAAATCCAGTGATGGTCA
Long Flanking Sequence:
TCATCAAAACAACATTTTTTAAAGGTTTATTTAATCTTTTTGGATCAAAACAGAGTTTATTGTGTTATAAGTTTTATAATATTGCTTCTCAGTTTTGGACATAAGTTTTATATGAGTGTATTTATTTCGTATATTACAAGATCTGCTGTTGTGTTTTCTTAGAGATTAAAGACAGACCCAGAAGATTCTATCCTGGTGGAGACATTGTTGACTATTTCAGACCAGCGGACAGTGATGGACTCAACATCCAGTGGGACACAGTGAATGATAAAGATTCCTTACTATCTCTGCTTGAAGGTGTCATTTTAACCCTTTATAGCGCTCTCAATCAAATAACAATGGAAAAACAAGAGTGTTACCGAGGGGTTCTTTCAACACTTTTGTTTTTACATTAATAATGGCTTAAAAAACATTGAATGATTCCTCTACAGCTTCTCTGGATTGATACAGTTTAAATGCATAGATCCTGTTAAAATATAATACTTTTTTGTTGTCATTTC[A/C]GATAGTCCTGGAGGAATGCTGGTGATTCCAGTAAAATCCAGTGATGGTCACCCAAACATTCCTATTATTGACGGGTCTGAAATGCCTCTTAAGGATTGCCTGGATTTGATTCTTGCCTCTACAAAGCCGTGGGGAATCTACTTACAGATAAAATCCCAGAATCAGCTGAGCCTCTCACTGGAGCTCCTCCGTCAGGCTTATGACATAGACTTGCTGCATCACCCCACCTGGGTCAACATGGACATATCCCACGGAGCTGTCCACATCCAAGGCTACATGACAGGAGAAGAGTTTTTGAGAACCGTTGATCGAATCTTCCCACATGTGACTCTGGCTCCGAGTTGGCCTAAAGAAGCTTTGGTTGAAGGCTACACACCAGAGATGCTGGAGCCCATGGTGCAGCTCTTCCACAGGGCCTGGCAGGATGTTTCACTGCAGCTGCAGGCTGAGGCTCTGGACAGATCTGAGACTTGGAGACTTGTCCTAGTACAACCCCGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31261
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081026 | Nonsense | 394 | 599 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 2 (position 10861172)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 11286268 |
GRCz11 | 2 | 11069867 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTGTTGTCATTTCAGATAGTCCTGGAGGAATGCTGGTGATTCCAGTA[A/T]AATCCAGTGATGGTCACCCAAACATTCCTATTATTGACGGGTCTGAAATG
Long Flanking Sequence:
TCTTTTTGGATCAAAACAGAGTTTATTGTGTTATAAGTTTTATAATATTGCTTCTCAGTTTTGGACATAAGTTTTATATGAGTGTATTTATTTCGTATATTACAAGATCTGCTGTTGTGTTTTCTTAGAGATTAAAGACAGACCCAGAAGATTCTATCCTGGTGGAGACATTGTTGACTATTTCAGACCAGCGGACAGTGATGGACTCAACATCCAGTGGGACACAGTGAATGATAAAGATTCCTTACTATCTCTGCTTGAAGGTGTCATTTTAACCCTTTATAGCGCTCTCAATCAAATAACAATGGAAAAACAAGAGTGTTACCGAGGGGTTCTTTCAACACTTTTGTTTTTACATTAATAATGGCTTAAAAAACATTGAATGATTCCTCTACAGCTTCTCTGGATTGATACAGTTTAAATGCATAGATCCTGTTAAAATATAATACTTTTTTGTTGTCATTTCAGATAGTCCTGGAGGAATGCTGGTGATTCCAGTA[A/T]AATCCAGTGATGGTCACCCAAACATTCCTATTATTGACGGGTCTGAAATGCCTCTTAAGGATTGCCTGGATTTGATTCTTGCCTCTACAAAGCCGTGGGGAATCTACTTACAGATAAAATCCCAGAATCAGCTGAGCCTCTCACTGGAGCTCCTCCGTCAGGCTTATGACATAGACTTGCTGCATCACCCCACCTGGGTCAACATGGACATATCCCACGGAGCTGTCCACATCCAAGGCTACATGACAGGAGAAGAGTTTTTGAGAACCGTTGATCGAATCTTCCCACATGTGACTCTGGCTCCGAGTTGGCCTAAAGAAGCTTTGGTTGAAGGCTACACACCAGAGATGCTGGAGCCCATGGTGCAGCTCTTCCACAGGGCCTGGCAGGATGTTTCACTGCAGCTGCAGGCTGAGGCTCTGGACAGATCTGAGACTTGGAGACTTGTCCTAGTACAACCCCGCTTTTCACTGACCGTGGAGCATCAAACAGAGAACAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15963
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 |
---|---|---|---|---|---|
ENSDART00000081026 | Nonsense | 431 | 599 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 2 (position 10861061)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 11286157 |
GRCz11 | 2 | 11069756 |
KASP Assay ID:
2259-1651.1 (used for ordering genotyping assays)
KASP Sequence:
ATTGCCTGGATTTGATTCTTGCYTCTACAAAGCYGTGGGGAATMTACTTA[C/T]AGATAAAATCCCAGAATCAGCTGAGCCTCTCACTGGAGCTCCTCCGTCAG
Long Flanking Sequence:
CTGTTGTGTTTTCTTAGAGATTAAAGACAGACCCAGAAGATTCTATCCTGGTGGAGACATTGTTGACTATTTCAGACCAGCGGACAGTGATGGACTCAACATCCAGTGGGACACAGTGAATGATAAAGATTCCTTACTATCTCTGCTTGAAGGTGTCATTTTAACCCTTTATAGCGCTCTCAATCAAATAACAATGGAAAAACAAGAGTGTTACCGAGGGGTTCTTTCAACACTTTTGTTTTTACATTAATAATGGCTTAAAAAACATTGAATGATTCCTCTACAGCTTCTCTGGATTGATACAGTTTAAATGCATAGATCCTGTTAAAATATAATACTTTTTTGTTGTCATTTCAGATAGTCCTGGAGGAATGCTGGTGATTCCAGTAAAATCCAGTGATGGTCACCCAAACATTCCTATTATTGACGGGTCTGAAATGCCTCTTAAGGATTGCCTGGATTTGATTCTTGCCTCTACAAAGCCGTGGGGAATCTACTTA[C/T]AGATAAAATCCCAGAATCAGCTGAGCCTCTCACTGGAGCTCCTCCGTCAGGCTTATGACATAGACTTGCTGCATCACCCCACCTGGGTCAACATGGACATATCCCACGGAGCTGTCCACATCCAAGGCTACATGACAGGAGAAGAGTTTTTGAGAACCGTTGATCGAATCTTCCCACATGTGACTCTGGCTCCGAGTTGGCCTAAAGAAGCTTTGGTTGAAGGCTACACACCAGAGATGCTGGAGCCCATGGTGCAGCTCTTCCACAGGGCCTGGCAGGATGTTTCACTGCAGCTGCAGGCTGAGGCTCTGGACAGATCTGAGACTTGGAGACTTGTCCTAGTACAACCCCGCTTTTCACTGACCGTGGAGCATCAAACAGAGAACAAAGACATCAATGCTGGGATTGAAAGCTTAATGGCCATCCGAGCAGCAAACAGACAACGGAGCTTTTATAATATTCCTAAAATGTACAGAGAGCATATAACAGATCTATCAGTT
Associated Phenotype:
Not determined