ZMP
ankrd44
Ensembl ID:
ZFIN ID:
Human Orthologue:
ANKRD44
Human Description:
ankyrin repeat domain 44 [Source:HGNC Symbol;Acc:25259]
Mouse Orthologues:
Ankrd44, E230028L10Rik
Mouse Descriptions:
RIKEN cDNA E230028L10 gene Gene [Source:MGI Symbol;Acc:MGI:2685285]
ankyrin repeat domain 44 Gene [Source:MGI Symbol;Acc:MGI:3045243]
ankyrin repeat domain 44 Gene [Source:MGI Symbol;Acc:MGI:3045243]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25429 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15884 | Essential Splice Site | Available for shipment | Available now |
sa34678 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa6117 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25429
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 |
---|---|---|---|---|---|
ENSDART00000037182 | Essential Splice Site | 9 | 1050 | 1 | 28 |
ENSDART00000142768 | None | None | 1037 | None | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 33191569)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 32347515 |
GRCz11 | 9 | 32158261 |
KASP Assay ID:
554-7435.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGATGTCCAGTTTCACATGATATGGCTGTTCTCAAACTAGTCGACCAG[G/A]TAATTTACTAAGATTTTTTAAAATGTTTATAAAAATGAAGTTGACTTGTG
Long Flanking Sequence:
GTAGTAGGATTCCGAAATTAGCGAGGGGGGAAGCGTACAAAAACGCTGACTTCCTGTATTTTATTATAACGAATGAATACATTACGCAGAGCGTAAAGCAGTGGGGTTTCAAATCTAAAAATCGTTATCGTTTTGGATGCCACTGCTGTAAATGCGGATTGTTTACAGCACCCCTCGCATCCTTTCCTCCCTCCCCTTTTCCTCTTTCCCGGAGCGCCGGAGCGCTGGTGGTGAGGCAGCGGCTGCAGCTGCTCCCGCTGACCGAAGATAGCGCCTGCAGAACCGGCCACGGCCGTCACATCACCCCGGGCCCTTGGAGAGGGCGAACCACAGCAAAGCAGGAAGCAAGCTTTTGACGCCACATCATTGTGCAGCATCATCCTTCCGTAAAAAAAGCGCACGGCTCCTTCTGGATTTGATTAATCTACACCTTCAGGTCTTTTCAGGAGTTTGGATGTCCAGTTTCACATGATATGGCTGTTCTCAAACTAGTCGACCAG[G/A]TAATTTACTAAGATTTTTTAAAATGTTTATAAAAATGAAGTTGACTTGTGTGAAGATGAAACTGAGGAGTTACGTGAAATTAAATGTAATTTTCTGTTAATATGCTAATGATTATTGTGATGCTCCATATGCAGTATGCAACTGCAGAAACTAGCTATATTTGCAGCATATGCGTTACATGTTAAAAATGCATGAGACCACATACAAGTTTAATTTGCATAAGTCTGTTTCTGGTGTCTTGCATTTAGCAACGACATAAAAAAAAATAATAATTTTTTAGCAACGACATAATAGTCCTTGTTGGGAGACATTGGTCTTCCTGAAAACCAAAGAGCAGCAAACTGCTATTACTGATGTACAGAGTAGTGAATCAAATACTTAAATGTGCTTGAATTTACAAGTCAAATAGTTATGTGTGATAGTGTACCATTAATGATAGTAAGTCTATGATTAATAATGTGATTTACCCACACTGTTGTGTTTAGGGTAAGATAAATGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15884
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037182 | None | None | 1050 | None | 28 |
ENSDART00000142768 | Essential Splice Site | 386 | 1037 | 11 | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 33166590)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 32322536 |
GRCz11 | 9 | 32133282 |
KASP Assay ID:
2260-2022.1 (used for ordering genotyping assays)
KASP Sequence:
TCCTCTTCTGTGCACTGTATCCTTCCTCCTCATCCTTCCATTCCTCTACA[G/A]GACGGAGGTATAGCATAATGTGYCCTCTCAGTAATGACTCGGTCCTGTCT
Long Flanking Sequence:
GGAACTGTGTATAAAGAACTGCAAGTTCTAAAGAGTTTTACCGTAACCTGCTCTTAACACAAATAAAACTTTCTCACCAGCATATTTGCTTGAGCATTTAGCCTTCGACGTTCCCTGTTTAGGTCTGGCATGCCCTTATCTGCTATTTTAACTCTGACTCTTGATTGTGGGTTTGCTGCTGTATGAAATCATAGACTGTAGATCTGTTCTTTTTAAGTTGTTCTGCTTAGTTGCACACATTTTTGTTCTCACCTCTGTAAGTGATGGGTGTTTGTCTTGTCTTTCCTGTGTGCACTGTCTTTGTTTTTCCTGCACTAACATCCTTTCTCTCTCTGTGTCTCTCTTTCTCTCACACCGTCTCTTTCTTGGACTTCTTTTTCCTCCATTTCACACTTTCCCCCTACTGCGGTCTGACACTGTGGCTGTCTGCGTCTGGTTGTGGGGACACTTTCCTCTTCTGTGCACTGTATCCTTCCTCCTCATCCTTCCATTCCTCTACA[G/A]GACGGAGGTATAGCATAATGTGCCCTCTCAGTAATGACTCGGTCCTGTCTGCAGGCTTCCAAATCGATACGCCTGATGACCTGGGGAGGACATGTCTGCACGCTGCAGCCGCAGGAGGGTGAGTCTGTCAATCTGCAGATCTGATTTTTACTTGTTGAGCTGCAGAGTCAGATGGGATTGTATATAAGATGTGTGCTATATTAGAACAACTAAAGCTGGTCTGTGAACACTTGATTACTCAATTTAAATATATGTTTTTATAACTAGAGTTATAAAACTTTTTGTTTTTTCATTGTGGCTGTGGGTAATTTATAGGAATGTCAAGATCTGTTTTTTGGCCCTAGAGTCTGACTCAGTTGATTTTGAGTATCTACCGAAACCCGATCCGATACTTCTAGAGTACATAAGTTAGGTTTATTTATAAACTTATTTCGAGAGGATCACATGGCCATGATTGTTCTCAGCTGTTCCCGCATCAGCTCGCGATTGATTGTGCAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34678
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 |
---|---|---|---|---|---|
ENSDART00000037182 | Essential Splice Site | 486 | 1050 | 14 | 28 |
ENSDART00000142768 | Essential Splice Site | 495 | 1037 | 13 | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 33163946)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 32319892 |
GRCz11 | 9 | 32130638 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGGGCGCACTGCTGTTCACTACGCTGCTGCTTCCGACCTGGACAGAAG[G/A]TACGTGCATCATTAAACAAGGATTACTCTCATAATTGGTAAAAATAAAGA
Long Flanking Sequence:
ATTGCTCAGCAGTGGAGCCGATCATAACCGCAGGGACAAACATGGAAGGTGAGTTCTTGAGTTCCTGGTAAACATTTATGTCAAGGCATTTATCCAACTAATTGCTGAGTTGTCCAGTTCATCACAGACAGTATACATATCTGTGCAATTGTGTGCAGTTTTGTGCTATTCTTGGTCAGTGCTATGAAATGTAATGCAAATGGCAGCTTTTTTCAGATGTTTTCACAGCTGTTTATAGAACCACCGATCAGCACTTATTACTGCATACATTAAATGAAATCATCCCTTCTGTAGTAGTTTGTTCTATCATGCTTATATTTGTCATATTATTTCCTGTCTTTTGTTATGGATGTCGACAGGACCCCTCTTCATTATGCGGCAGCTAGTCGTCACTTTCAGTGCCTGGAGACTTTGGTGTCCTGCGGTACCTGCATTAACGCCACTGACCAGTGGGGGCGCACTGCTGTTCACTACGCTGCTGCTTCCGACCTGGACAGAAG[G/A]TACGTGCATCATTAAACAAGGATTACTCTCATAATTGGTAAAAATAAAGATACATATAAAAAAAATATTGCGCTTTAAGCTTTTTAGACTAAATATTATGACGGATTTAAAGTACACATGAAATCAAAACTAACCATACTGATTTTATTTTTATTTTAGAAAAAAATGGCTGCGTTCAAAAACCGCCTACTACTCAGTAGGTACTGCATTTGAATTTACATGTACTACTCGGCCGTTAGAAAAGTACATTCCATACAGTTTAATTGTGAGAAGTATGAATGAAATTCGGGCATACTACATCCGCCATGCGTTAGTTGCGTCGCTTCATTCCCATTCATAAATTCTCTCGCAGAGCATCATGGGATAGCGCAGCATGCATGGGATGCGCACTTCAGAATCTCGCCGGAACGAGTAAGTCATTCAGGTACTTCTCGCAATCTGATTTTTGAATTCTATGAATTCGAATGTACTACTTGGCTCACGCACTGATTTTAGCTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6117
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 |
---|---|---|---|---|---|
ENSDART00000037182 | Nonsense | 590 | 1050 | 18 | 28 |
ENSDART00000142768 | Nonsense | 577 | 1037 | 16 | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 33153234)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 32309180 |
GRCz11 | 9 | 32119926 |
KASP Assay ID:
554-3656.1 (used for ordering genotyping assays)
KASP Sequence:
GGCACGCGCAGGCTCTAGAAGTGCTCTTGGAGGGTCACTGTGAGGTGGAT[C/T]AGGGGGATGAAGTTGRTCGGACTCCACTGGCCCTTGCTGCTCTCAGGGGC
Long Flanking Sequence:
AGACAACACCTATGATTCCACACTTACACTATCATCAAACTTTGCCTTTGTTTGTTGTGAATATGTTCCCTCTAATGGCAAAATTACATAGTGAGCCTTTTAAATGTACACACACACACACACATAGTAGTAGCACATTTTTGAAAAACGTCTTTTATTCTAACTAAGAGTACATTTATTTGATGGAAATGCATTAAAACTGTATATTAAGAAATGTTTTTACACTTTAACTGTCATATCATTCTTTTAAACACGCTAAAATCAATCATAGTACCTTTAGAAACGGCTGAGCACTGTTATCTACTACCTAATGCCACATTTTTCACAGAAAAACAGAGCTTAATAGGTTTGATCACCACAGATTACTTGCTTAAATAGGAGTAATATTTGAGAACACGTTTAGAATTTGTACACCTTTCAATGTGTGTATGTGTGTCTAGGCATATCACGGGCACGCGCAGGCTCTAGAAGTGCTCTTGGAGGGTCACTGTGAGGTGGAT[C/T]AGGGGGATGAAGTTGATCGGACTCCACTGGCCCTTGCTGCTCTCAGGGGCCACACTGACTGTGCTCTCACACTTCTGAACCACGGGGCTTCCCCGAGAAGCAGAGATACTGTCAGAGGACGTACGCCCATCCACCTTGCAGGTGTGGTGGAAACTATTCTGCACTTTTTTTAATGCATTATTGTTTGTGATTGTTACGTGTTTAATTTATGTTGGATGAGATGTAACATTCAGTCTCTAATGGTGCTGGGTGAAAATGAGAAAATGTTGAGCGAGAAGATGGATAAGTGAAACAAAAATTATCAATTTATTAAACTGAGAATATCAAACAATGAATATAGAAATTTAGATTTGTACTTTTTTTGTAATTTAATCAAAAACAGGACTGTTGCCAAAACAAAGTAATAAATATATAACAAAACAATCTAACTAAACTCCAATCCACTAAACTTACCAAAGAAAAATGCAGAAACAAACCCGTAATCTTCCGCGTATGCGATG
Associated Phenotype:
Not determined