ZMP
zgc:113131
Ensembl ID:
ZFIN ID:
Description:
Protein FAM73B [Source:UniProtKB/Swiss-Prot;Acc:Q5BLE2]
Human Orthologue:
FAM73B
Human Description:
family with sequence similarity 73, member B [Source:HGNC Symbol;Acc:23621]
Mouse Orthologue:
Fam73b
Mouse Description:
family with sequence similarity 73, member B Gene [Source:MGI Symbol;Acc:MGI:1922035]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa29498 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12133 | Nonsense | Available for shipment | Available now |
sa37215 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa29498
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000122699 | Nonsense | 266 | 565 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 4307108)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 3707727 |
GRCz11 | 21 | 3870737 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGTGACTTCAACTGTATGTGATGTCACTTCCCTTTCTGGTTTTGCAGT[T/A]GTTTGAGACGTTTTCTCTTGAGGACTCGTTTCATCTGCTGAAGCCGGCCG
Long Flanking Sequence:
CATAATATTTGACTAGATATTTTTTAAGACACTAGTATTCAGCTTAATGTGACATTTAAAGGCTTAACTAGGTTAATTAGGCAATTCATTGTATAACAGTGGTTGGTTCTGTTGACAATCCAAAGCAAATATTGCTTAAAAAGAGCTAATAATATGGACCTTAAATGGTTTATAAAAATTAAAAACTGTTCTTGTCGAAATAAAACAAATAAGACTTCCTCCAGAAGAAAAAATAATATAGGAATTACTGTGAAAATTTTCTGAATTAAAACATCATCTGAGAAATATAAAAATAATATAATAATAATGAGCTTTCCCAGTGATGGTTGCAGCTGGAAGGTCATCCGCTGCGTAAAACATATGCTAGATAAGTTGGCGATTTATTCCGCTGTGGCGACCCCAGATTAATAAAGGGACTAAACCAAAAAGAAAATCTAATCTAAGCTACTAATTGTGACTTCAACTGTATGTGATGTCACTTCCCTTTCTGGTTTTGCAGT[T/A]GTTTGAGACGTTTTCTCTTGAGGACTCGTTTCATCTGCTGAAGCCGGCCGCTCTCTATGAAGAAGCTCTGAGTTTGGTGAAAGATGGAGACGTGGCCTGCAGATCACTGAGGTAGAGCATATTAACATGATTAACTCTGCACACTGGATGTTATTGGGATAGTTTAGATGTTCTGCTTTCTCCTGGGATTTGAGGCTTTCCGCTGTAGCTCAGGGAGCAGAGACTGATGGGAACACACACACACAGTGTTATTTCGGTGTGTCTGTTACAGAACTGAACTGCTGGAGTGTTACAGCGATCAGGACTTCCTCGCTAAACTGCACTGCGTACGACAGGCATTCCAGGTCAGCACTCTCTCACACACCATTACACACACGCACATGCACATGCCCACATGACTACACACGCATGTTGACATGATTAAAAATGGACACAAATGCACACACCATTACACAAACACACAGACACACACACACACGGTTACACGCACACACATTCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12133
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 |
---|---|---|---|---|---|
ENSDART00000122699 | Nonsense | 285 | 565 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 4307050)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 3707785 |
GRCz11 | 21 | 3870795 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGTTTTCTCTTGAGGACTCGTTTCATCTGCTGAAGCCRGCCGCTCTCTA[T/A]GAAGAAGCTCTGASTTTGGTGAAAGATGGAGACGTGGCCTGCAGATCACT
Long Flanking Sequence:
AAGGCTTAACTAGGTTAATTAGGCAATTCATTGTATAACAGTGGTTGGTTCTGTTGACAATCCAAAGCAAATATTGCTTAAAAAGAGCTAATAATATGGACCTTAAATGGTTTATAAAAATTAAAAACTGTTCTTGTCGAAATAAAACAAATAAGACTTCCTCCAGAAGAAAAAATAATATAGGAATTACTGTGAAAATTTTCTGAATTAAAACATCATCTGAGAAATATAAAAATAATATAATAATAATGAGCTTTCCCAGTGATGGTTGCAGCTGGAAGGTCATCCGCTGCGTAAAACATATGCTAGATAAGTTGGCGATTTATTCCGCTGTGGCGACCCCAGATTAATAAAGGGACTAAACCAAAAAGAAAATCTAATCTAAGCTACTAATTGTGACTTCAACTGTATGTGATGTCACTTCCCTTTCTGGTTTTGCAGTTGTTTGAGACGTTTTCTCTTGAGGACTCGTTTCATCTGCTGAAGCCGGCCGCTCTCTA[T/A]GAAGAAGCTCTGAGTTTGGTGAAAGATGGAGACGTGGCCTGCAGATCACTGAGGTAGAGCATATTAACATGATTAACTCTGCACACTGGATGTTATTGGGATAGTTTAGATGTTCTGCTTTCTCCTGGGATTTGAGGCTTTCCGCTGTAGCTCAGGGAGCAGAGACTGATGGGAACACACACACACAGTGTTATTTCGGTGTGTCTGTTACAGAACTGAACTGCTGGAGTGTTACAGCGATCAGGACTTCCTCGCTAAACTGCACTGCGTACGACAGGCATTCCAGGTCAGCACTCTCTCACACACCATTACACACACGCACATGCACATGCCCACATGACTACACACGCATGTTGACATGATTAAAAATGGACACAAATGCACACACCATTACACAAACACACAGACACACACACACACGGTTACACGCACACACATTCCCACATGATTACAAATGCACTCATATGCATACATAGACACACACACACATACAAATGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37215
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 |
---|---|---|---|---|---|
ENSDART00000122699 | Nonsense | 492 | 565 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 4297138)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 3717690 |
GRCz11 | 21 | 3880700 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATAAAGCGACCCTTGAGCTAATATCCCATTCTCCTTTACTCTCCACAG[C/T]AACAGATTGTTCAGTATCTGAAGGACATGTTTGACCATGATAAGGTGCGT
Long Flanking Sequence:
CCTACCCAATTCACCTGTATTGCATGTCTTTGGACTGTGGGGGAAACCGTAGCACCCGGAGGAAACCCACGCGAAGGCAGGGAGAACATGCAAACTCCACACAGAAACGCCAACTGAGCCGAGGTTCGAACCAGTGACCCAGTGACCTTCTTGCTGTGAGGCGACAGCACTACCCACTGCGCCACTGCCTCGCCCACATACCATCATACTAACAATATACTAATCCATACTAGAAACATGCTAATAAATGTGTACTTTTCTATCTCTGCCAACTGTTGCACACTTCTTAAAACTACTTAAATTATTTAAACTTTGAAACGACTTCAAACTTTCAGACTAGCCACCATAAAGTTTGTCAATGAACTTCACTTTTCTAGTTTGCTTTTAGGTTTGTACAGAACAGTGGCCAACAACTGTTGTTTTATTGTGCTTTATAAATAAATAAACCAACTATAAAGCGACCCTTGAGCTAATATCCCATTCTCCTTTACTCTCCACAG[C/T]AACAGATTGTTCAGTATCTGAAGGACATGTTTGACCATGATAAGGTGCGTTTCACATCCGTCCCATCTCTGGCTGAAGACATCCTCCGCCTGTCCCACAGACGAGCAGATATCCTGATGGGTTACCTAGGCATCGAAAATCTACCTGAGACCAATGGAGCTTTACCCAAGAGCCCCTGCCAAGCGGAAAGCGGGAATCTGGACGCCAGCGGACAGCAAGACTGAGCTTTAAGGTTGTTCTTCATTTAGCTCTTTATCATCAGACCAATCAAAAGCGTTCGCAGATTTACATTCGAGACCTTAGTTTTGTAGAATATACTGAGAGATCAACCACTACTGAGGTCAACCGAGGCCTTTTCTTCAGCTCTTTCTGCAAACTTTCCACCAAAATATCAAACGTTTTGTCACCGTAATCCAGCGCTGCTATTTATCCACCTTAATTTTATCAGGAAGACTCCATCATAACCCAAATGAACTGAATAAAACTCATCTTTTAGCCAA
Associated Phenotype:
Not determined