ZMP
fam120c
Ensembl ID:
ZFIN ID:
Human Orthologues:
FAM120A, FAM120C
Human Descriptions:
family with sequence similarity 120A [Source:HGNC Symbol;Acc:13247]
family with sequence similarity 120C [Source:HGNC Symbol;Acc:16949]
family with sequence similarity 120C [Source:HGNC Symbol;Acc:16949]
Mouse Orthologues:
Fam120a, Fam120c
Mouse Descriptions:
family with sequence similarity 120, member A Gene [Source:MGI Symbol;Acc:MGI:2446163]
family with sequence similarity 120, member C Gene [Source:MGI Symbol;Acc:MGI:2387687]
family with sequence similarity 120, member C Gene [Source:MGI Symbol;Acc:MGI:2387687]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24291 | Essential Splice Site | Available for shipment | Available now |
sa24290 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24291
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065881 | Essential Splice Site | 256 | 1051 | 2 | 17 |
ENSDART00000135430 | Essential Splice Site | 256 | 1047 | 2 | 16 |
Genomic Location (Zv9):
Chromosome 23 (position 18579873)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 18482812 |
GRCz11 | 23 | 18409155 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCTTGGCCTCAAGACACAGCACCTGCCCATTTTTGCTGCTCTTCTTGG[T/A]AAGCGAAGCTAACATGAACATGACTTTATCTTTAAAGAACATTATTTAGT
Long Flanking Sequence:
TGCGAAGGCTTTCTCTCCTCTAATTAAATTACAGCTTAATATCTAAGAGAGTTAAGAAGTACAAGTGATATCAGTGTATTGAAAATATGCAGAAAATAAGTATTGAAATTATTTTTAAAAATCTGTGTTATTTTCATATTAATCCAAGATTATTGTCAGCAAATGTAGTATTTTCAGTTCAGATCAGTTGTAGCTTGTTGCTTAGTAAGTCACAAGAACACGTGATCACCTTCCACCCTGCTTGTGTTGTAGGTGGTGCAGACCCTGGAGGACCATCATCAGGAGGTGCTATCCCTGTACAGAGACTATGGTTTTCAGGGTCTGATTGCACAGGACTCAGAGTTTGCGCTATGCAACGTTCCGGCCTATTTCAGCTCCCACGCTCTCAAGCTCTCCTGGAATGGCAAGAATCTGACCACTCACCAGTACCTGCTATCAGAGGCGGCTCGCCAGCTTGGCCTCAAGACACAGCACCTGCCCATTTTTGCTGCTCTTCTTGG[T/A]AAGCGAAGCTAACATGAACATGACTTTATCTTTAAAGAACATTATTTAGTTCTAAATGTGGCCCTTCAAAAAAACAAACAGGTAACCACATTCTGCCAGATGAAGACTTGGCTGCCTTTCATTGGAGTCTTCTAGGCCCAGAACACCCTCTTGCCTCCCTCAAGGTGCTAAAATGATTTGTCAGTTCACACACTTTATGATATTCTCTTTTTTTTGTAGTTGTAATGGATGAGATATTTAAGCATCCTTGTGCTTTACACTTATTAGCACAACCCATACTTTATTTGTTGCTCTTTGCTTCATTATTTGTTTGTTTTTTTTTCTGCTCAGGTAAGGGCTCATCAGTTAGTCCTCCCTCCATGTGAGGTTGTTATCAAGGCTGTTTCTGAGTATGTGGCATCCATCAAAGATCTTGGGAATTTAGATTCGGTGGCCAAGGATGTTTTCAAGCAGTCACAGGTGAAGCATGCCGTGTTTACACATTTATTTGCATGTGAGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24290
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 |
---|---|---|---|---|---|
ENSDART00000065881 | Nonsense | 896 | 1051 | 14 | 17 |
ENSDART00000135430 | Nonsense | 896 | 1047 | 14 | 16 |
Genomic Location (Zv9):
Chromosome 23 (position 18564921)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 18467860 |
GRCz11 | 23 | 18394203 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTGCTTAGTGTTTTTGCTCTCTCCTTTAGGAATCCAGTCTATACCTCCC[C/T]AGGGCGGCAAACTGGAAATAGCTGGCATGGTTGTTGGTCAGTGGGCTGGA
Long Flanking Sequence:
TTCTATAATAGGAAAAATGCAATGGAAGTCAATGTTGACCATTAACCAGAAATGGTAGTCATTGGTGACCAATCATTCTGGAAATACTATTAATAATGTAATATTTACTGTAATATTTACGTGTTTTCGGAATTTTTTATATTTTTGAAACTCTGTCCCTAAAGGAGGAACTGGTTTCAAGGGTGGAGAAGATGCGTCAGGCCATTCTGGAAGGCATCAACCTGTCCCGGCCACCACCTCCACCTCCACCACTGCCACCCCCTGCATTCCTCCCACCTGCTATGGTGCCACCTTTCTACCCCATGCATCCTCTGTACCCTCCTCGCCCATTGGGCTCTATGCCTCCTCCTCCCCCTCACCATCACCACCAGCACCGACCCAGGGCCTTTCCAGGTTAGACAGTTCTGTTGTTTAGTACATTTAGTTCAGTTTCTTTACTGCACTTTCAGTGTTGCTTAGTGTTTTTGCTCTCTCCTTTAGGAATCCAGTCTATACCTCCC[C/T]AGGGCGGCAAACTGGAAATAGCTGGCATGGTTGTTGGTCAGTGGGCTGGAAACAAGCCAATTCGTGGCAAAGGGGGGTTCAACATGCAGGTGGTGTCAGTAGGAGGGAAAGGGTGAGTTTATTCAGTCTTAAAACACTTAAAACTTATTTTTGGAGGTATGGAATGCGCTTCACTACAAATGTTTTTGTTTTCCATTTGTCAATATTAACTCTTGATTGCACCACCTGCTGGTGGAGAATACCAGTAGTAGGTCGAAATCATGTTCAGCAAACTATTCAGGCTGACTGCACTGTATTTCCACTAAAATATTAGTGCTTTGACTTTCAGATGTAGTTTTCTCCCATAGAAAATTGTAGTAATATCAAACTCTGCAATGTGTCTAGTAAATATGTAGTTTAATATTTGCTAAATGTTACAATATAATATTTTCTCTGCAATGCAAAATATAATGAGCTAAATTTGAGCTGTTACAAAGATCATAAATACAGTGCATACCAGG
Associated Phenotype:
Not determined