ZMP
mitfb
Ensembl ID:
ZFIN ID:
Description:
microphthalmia-associated transcription factor [Source:RefSeq peptide;Acc:NP_571922]
Human Orthologue:
MITF
Human Description:
microphthalmia-associated transcription factor [Source:HGNC Symbol;Acc:7105]
Mouse Orthologue:
Mitf
Mouse Description:
microphthalmia-associated transcription factor Gene [Source:MGI Symbol;Acc:MGI:104554]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11609 | Nonsense | Available for shipment | Available now |
sa43899 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa25188 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11609
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010248 | Nonsense | 92 | 499 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 23 (position 758726)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 728061 |
GRCz11 | 23 | 740854 |
KASP Assay ID:
2261-7209.1 (used for ordering genotyping assays)
KASP Sequence:
CGGCAGATCTCCATCACACACAGCCCCGCCATCAAYGTCAGCCATCCCTG[C/A]GGCCCGCCCAGCGCCGCACAGGTGCCCATGGAGGTGCTGAAGGTAAAGCA
Long Flanking Sequence:
GGATTGTCTCCAGAACAAACCACTGTTATACAATGACTTGCCTAATTACCCTAACTTTACCCTAATTACCCTAGTGAAGCCTTTACATGTCACTGTAAGCTGAACACTAGTGTCTTGAAGAACATCTAGTCTAATATTATGTGCTGTCATCATGATGAAGAGAAAACACATCAGCTATTAGAGATAAGTTATTAACACTGTTATGATTAGAAATGTGCTGAATAAATCTGCTCTCAGTTAAACAGAAATTGGGAGAAATATATACAGAGGGGCTAATAATTGAGACTTCAACTGTATGTAACGTCCTCTGTGTTTGTGTGTGTGTGCAGTAATCCCTCAGAGCAGCAGCATGGCTCCTGTAAGCCCCCGCTGGGCTCGTCTCGAGTCCTGCTCCGCCAGCAGCTGATGCGTGAGCAGCTCCAGCAGCAGGAGCGCCGAGAGCAGCAGAAGCGGCAGATCTCCATCACACACAGCCCCGCCATCAACGTCAGCCATCCCTG[C/A]GGCCCGCCCAGCGCCGCACAGGTGCCCATGGAGGTGCTGAAGGTAAAGCAGCGCGCAGAAAGCTCATATCAAAGCACGTGTGAAATCAAAACTAGCCATAGTGATGTTGTGAGCTCACATTGCTAGTCCTGCGCTGAACAGTTCATCTGTGCATGTCATTAAGAACAAAACAATAGTTTGCCTCTGTAATCGAATATTGAAATCTGCAAATGCACTTCCTGTTTGAGGTCAGTTCAATTCTCAGGTCAGTCTGAGATAGTGGGCGGGGCTAACACACTTAACCACGCCCCTCCAGCTGTCAGTATGACATCAAACAGAAATGGTGAGCTGGAGGACTCTCTCCAAACACTTTTCCGCATCTTTCTGAATGACACGCCTACTTTACTGCATCCAATCAGCTCACAGTAGAATCAAACAAGCCACGCCCACTGCTTTCACATTTAGTATTGTGAAACTGCATCACAATATGAAAAAAATGGTCGCAGCTTCCAGTTCATGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43899
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 |
---|---|---|---|---|---|
ENSDART00000010248 | Essential Splice Site | 180 | 499 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 23 (position 740333)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 708472 |
GRCz11 | 23 | 721265 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAACAGTCCCATGGCCTTACTGACCCTCAACCCCAACTGCGAGAAAGAG[G/A]TGAGAGTGCTGACACTAGATATCTATCGCAAAATTATCGTTATCATGATA
Long Flanking Sequence:
CAGGCCAGAGAGGGAAAAAAACTTCAAAAAAGAAAACTCTCATTTATTAAAGACAAGAATAGCCTTCTACTAATGCAGCAACTTCCATTTTTCGTTTGATATTTGGCACCGGTTTATCAGGGAGTGATGATTTTGTTCTCTCTGTTCATTCACAAATGTTTTACACCAGTTTTGCGCATATCTTTGGATGGAAGCATGGTCAGTTTCAACATCAGAGCAGCACAGAAGTGAGAAACACACGTCCTGTGATTGTAATGTTTGTCTTCGTTTGTGCTCAGGTTCAGACTCATCTTGAAAACCCCACCAAGTACCACATCCAGCAGGCTCAGCGGCAGCAGGTGAAGGCGTATCTGTCCACCACTCTGGGAGGAAAGCAGGCGGTGAGTTTGCCGTGTCCTAGCCAGGCATCTGATCACGGGGGAATGCCTCCGGGGCCGGGAAACAGCGCCCCCAACAGTCCCATGGCCTTACTGACCCTCAACCCCAACTGCGAGAAAGAG[G/A]TGAGAGTGCTGACACTAGATATCTATCGCAAAATTATCGTTATCATGATAATAGTATGTGCCACACTCCGCTGTGGAGACGCCAGATTAATAAACGGACAAAGAAAATGAGTAAATGAATAAAATATTAGTGTGCAATATTTATTCATTTATTTTGTTTTCAGCTTAGTCCCTTTATTAATCCGGGGTCGCCACAGTGGAATGAACCGCCAACTTATCCAGCACGTTTTTACACAGCGGATGCCCTTCCAGCCTCATCTTTGGCAAAAGCTTATGCAGCATAACAAGCTGTTTTTAAAGTCTAGCAATCATTGACAATGAATGATAGTGGAAGTCTCGAGCCTAAGGTCTAAGGTCAATAGATCAACAAAATCCAGTCAGCTAAATGAATGATGTGTAAATAGGCAGCAGTATCATAAAGACGTTTCATTATCTGCTCATCATCATCCTGCAGCTTCACTTCAGTGTGAAACAGCTGCTGTAGACTGCGTCATGATCTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25188
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 |
---|---|---|---|---|---|
ENSDART00000010248 | Nonsense | 193 | 499 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 23 (position 739615)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 707754 |
GRCz11 | 23 | 720547 |
KASP Assay ID:
554-7887.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATTCACAACAGATGGACGATGTCATTGACGACATCATTGGTTTGGAAT[C/A]AAGTTACAGTGATGACATCATGGGACTGTCGCTGGACCCCGGACTTCAGA
Long Flanking Sequence:
CCAGCACGTTTTTACACAGCGGATGCCCTTCCAGCCTCATCTTTGGCAAAAGCTTATGCAGCATAACAAGCTGTTTTTAAAGTCTAGCAATCATTGACAATGAATGATAGTGGAAGTCTCGAGCCTAAGGTCTAAGGTCAATAGATCAACAAAATCCAGTCAGCTAAATGAATGATGTGTAAATAGGCAGCAGTATCATAAAGACGTTTCATTATCTGCTCATCATCATCCTGCAGCTTCACTTCAGTGTGAAACAGCTGCTGTAGACTGCGTCATGATCTCACACACACACACTTACACACACACACAGACCGGCAGAAGTGTTAATAGATCCGGCAGAGTTTGAGAGCAGCTCAGTGAAACGCACAGCTCTAGCGCAGGATCTGGAGATGGATTGATGGATGGTGTTTTTGACTGTTGAGTGATGCGTCGCTGACTGATCACTGCTTCTGATTCACAACAGATGGACGATGTCATTGACGACATCATTGGTTTGGAAT[C/A]AAGTTACAGTGATGACATCATGGGACTGTCGCTGGACCCCGGACTTCAGATGGCAAACACGGTAATGACATTTACGCATTACATTACACTTGTATGTGTGTGTGTGTGTGTGTGTGTATGTGTGAGTATATATATGCAGCGGGGGAAATAAGTATTGAACACCTCACCTTTTTTCTCAGAAAACATATTATATTTGGTAACAACCAAAGACATCCATATATACAGGGAAAAAGTGTTGAACACATGAAGAAAGGAAGGTGTAGTTGGGCAGTGAAAGTCCAGACAGCAGCTGAAATCTGTCAGTAGTTCTTCAGCAAGCACTCTGCCCTTCCTCAGTGTAAATGAAGATCAGCTGCTTCAGTCCATGATCCAAAACACAGCCGAGGAGACTCTCGGATCAATCAAACAAAAAAGAAAGTAGTGATTTCTAAATTGAGTTTGACTTGTATTTGACAGTCTCTATTGAAGACAGGTCGGGGCTGCAGGCAGGCAGGTCAAGT
Associated Phenotype:
Not determined