ZMP
si:ch211-181b18.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
MAN1B1
Human Description:
mannosidase, alpha, class 1B, member 1 [Source:HGNC Symbol;Acc:6823]
Mouse Orthologue:
Man1b1
Mouse Description:
mannosidase, alpha, class 1B, member 1 Gene [Source:MGI Symbol;Acc:MGI:2684954]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43604 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37256 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31055 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43604
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114715 | Nonsense | 138 | 682 | 4 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 12442016)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 14143190 |
GRCz11 | 21 | 14239919 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCAGATGTTATGCCAGAGCTTCAGAAACCCAGCATTCCATTACTTCCT[A/T]AACCTCCAGCTATGGTTAGTGGAAATGCATAATTCACTGTTATACAGTTG
Long Flanking Sequence:
ACAATCTGCATAAGCCTTGTGTGACTAAAATAGTTTTAAAACATAGCATTACCTGTCTAATATAAATACTTCAGCCATGTCATCTTCCTCCGGCATGTAAAAGTAACTCCAATATTGATTCAGGATTCAACCAACACAACAACTTATGTTAGCACGTAAAGGCTCTACCCTCTTGTGAAAAGAGACACACACTAAAATGAAATGTTTTTGCTCACACCTAAGTTTATCAGACTCCTAATTAAAGATCTGTTTTATTTCGATTTAAAATTACAAAGTGTTTATCCATAATAAACACTCACATGAGAAACATGTATCTGTCTGTTTGTTCTCCAGGTATCTCTGATCGGTCATTGAAGGAGGATTGGGATGAAGTGGATAATCGGGGTCTCAGGCCCATTCCTCCTGGCCTCATCCCAAAGCTGTCTGCAGGAGTTGGTGTTCAAGACGTCCAACCAGATGTTATGCCAGAGCTTCAGAAACCCAGCATTCCATTACTTCCT[A/T]AACCTCCAGCTATGGTTAGTGGAAATGCATAATTCACTGTTATACAGTTGAAATCAGAATTATTAGCCCCTCTGGAATATTAGCGCCCCTGTTTATTTTTTCCCAAATTTCTGTTTAACGGAAGGAAGATTTTTATTAACACATTTCTAATTATAATAGTTTTAATAACTCATCTCTAATAGCTGATTTATCTTTGTCTTTATTTTATCAAATTTGCTTAAACTAAGCATTCTAAAGTATGACTGTATTTTACAAGCAAGGATTCTGACAGAGGAACGTGAAGCAGATGCTTTACGAAAGGGGGGAAACACGTCAAATTTAATTAAACATTTGAGGGACGCAGCTTAAGGGCAGAGAAATGTTTTTGACAGCTTGCAAATTCATCTGGCACTTTCATTCACATGGACACCAATACTCAGCTTTGATGATTAAGATAATACTGATTAAGAGTTGACCATGTTAGCAGCGATTTTTGATTATCTTAAATGACCACGCGAGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37256
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 |
---|---|---|---|---|---|
ENSDART00000114715 | Nonsense | 227 | 682 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 12434755)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 14135929 |
GRCz11 | 21 | 14232658 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTTAAAGCTCTAATCTTAAAGTGTTTTATTTGTGATGCTCAGGGACAT[T/A]GAAGCCAGTGGATCGTGTGGAAGCGGTGCAGGAGGCCTTCAGGCATGCAT
Long Flanking Sequence:
CTACTGTAGAAGTCGAGTTTTTATTCGTTGCTCTTACAACTAGGATCTACCTTTTGTCAGGTAGTGTATAGTAGGTTAAGTATAGATTTAGCTTTAAATAGAGATTTTCACAGATTTTATTGACATACACCTGACTAATACATGTTTTCAGGCTTTATGAACTTTGAGTTAATTAAAACTGGCCAAACTAAAAGTCTTGTTTGTACCTGTATAGTCTTTTATCACTAAATCTTGGAATCATTGAAGAATGAAATGAACAAAAGTAAACGTTCTTCATTTGCTAAAGTTAATATCTCATGTTTTTCCTATAATGCCAGTACTGTGTTTTTAGTCCTCGGGTTTTCTGTCCTCTGTTTATACACTTTTTACTATAAAATTATTGCAGTGTACTTTGAATTCAAGTTCAGACTCCAGAACAGAGATTGACCGAATTGAAGCAAAAATAGTTTAATCTTAAAGCTCTAATCTTAAAGTGTTTTATTTGTGATGCTCAGGGACAT[T/A]GAAGCCAGTGGATCGTGTGGAAGCGGTGCAGGAGGCCTTCAGGCATGCATGGAAAGGTTATAAGGCTTTTGCATGGGGTCATGATGAGCTGAAGCCACTATCTAAGACTCATGGAGAGTGGTTTGGTCTGGGCCTCACGCTCATAGATGCACTGGACACCATGTGGATCCTTGGTCTGAAAGACGGTGAGTCTTAAGCACAATATATACTAATTAGGGGTGTAACAATACACTCAGCTCACGATACAATGTGTATCACGATGTAATGTTCACGATTCGATATGTATCACGATATTTGGAATAAAAATTGAAAATTAAACTGAAATGCAAATTTTACCAAGTAAACTATTTTTATGTATTTCTTTTGTTTCAACTTGTTAAACTGAACCTTCTTTAGGAAAATAAATTAAACAGGCCAATTAAAAAACTTCTTAAAAATATTATTGAAATGACAGAGACAAAATTAAGGAACAATTTAAGTGAAGGTGCAAAAAAAATAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31055
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114715 | Nonsense | 449 | 682 | 10 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 12428653)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 14129827 |
GRCz11 | 21 | 14226556 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCACGCGGCGAGGGGCCTTTACCCTGGGGGCCCGAGCAGACAGTTACTA[C/A]GAGTACCTGCTCAAACAGTGGCTTCAGGGCGGCAAGAAGGAGACTGAGTG
Long Flanking Sequence:
TGCAATTAAGATTAAAATAAGTTTGTCTCTCAGTTGCACGTTTCTGATTAAGAAAAAGGTCTGAATTTGAGAAGAAAAGTCCAGATTTCAAGATGTAAAGTTGCAGTTGCCTATTTTAATAATTCATTTCTGTCTTCCATTTGTTTGTCTCTTTTATTGTGTTTTAATGAGCAGACAGTTTGTCTCCAACAGTTCTAAGACAAATCTGAACTGTAAAATATAATCTTGCAATTGTGATGAAAAGGAAAAGTCACAAATGTGCTTTATTTGTCTGAAAATCCTTGCTGGAAACAAGCTTCCATAGCTTTGTCTGTCTTATTATGTCATAGCATTGCTCATTTCTCCATCTGTTCCCAGAATGCAGTGGAAGAGGTGACCAAACAGGTCCACAGATTGGAGGGGAAGCGTGATGGACTGGTGCCAATGTTCATCAACACAAACAGTGGCAAATTCACGCGGCGAGGGGCCTTTACCCTGGGGGCCCGAGCAGACAGTTACTA[C/A]GAGTACCTGCTCAAACAGTGGCTTCAGGGCGGCAAGAAGGAGACTGAGTGAGTGACACTAACAGCAGACACAAATGCAGCTTGGGCTGACGGTTCATAAATTCAGTGCTTACACCGGGTGTCAACAGCCCCTTTTAGCTAATGGTCTCCAGAGAACTGGCCATGCTCACTGAGCCTAATGCACTGAGGTTATGCTTCTGGTCACAGATGGGCTGGGATGATTGATTTGCATTGTCCGTCAGTGATAAAGAGAATTGCTCTGGGAATAGAGGGGGAAAAATGCTAAATTTAATTGTTACATAAGGATTGTGCTTTAAAAAAAAATATATGAACATGCTTCTTAGCCCTGCGGTGATAAAAGTACATGGCGCTTTTGCTGCTCTTGAAAACCTGGAGGCGACTTCAACGCAATCAGTATTAGATTATTTTATTACTATGATGTCTTAGTTATTTCTTGGTAGAATTGGTTTCAAGAGCTTTTCAATTATGTTTGAGTTTGAA
Associated Phenotype:
Not determined