ZMP
zgc:172359
Ensembl ID:
ZFIN ID:
Description:
HEAT repeat-containing protein 6 [Source:UniProtKB/Swiss-Prot;Acc:A9JRI0]
Human Orthologue:
HEATR6
Human Description:
HEAT repeat containing 6 [Source:HGNC Symbol;Acc:24076]
Mouse Orthologue:
Heatr6
Mouse Description:
HEAT repeat containing 6 Gene [Source:MGI Symbol;Acc:MGI:1919790]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43697 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32356 | Essential Splice Site | Available for shipment | Available now |
sa11893 | Nonsense | Available for shipment | Available now |
sa25166 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37362 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa43698 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43697
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 |
---|---|---|---|---|---|
ENSDART00000113316 | Nonsense | 126 | 1201 | 2 | 21 |
Genomic Location (Zv9):
Chromosome 21 (position 37707673)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 38699708 |
GRCz11 | 21 | 38747414 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCTCTAAGTCAAGAACATCTCATCATCAAACTCTGCCAAATGATTCAT[C/T]AACTTCTAAACCAGCTACAGGTATTTACCATAGGGTTGGGTTAAATGGTC
Long Flanking Sequence:
GTGTAAAACATATGGCAGAGTAGTTGGCGATGCATTCCCCTGTGGCGACCCCATGATAAATTAGTGACTAAGCCGAAGGAAAATTACAAAAAAATTCCCTTGTGTTAATCAGAAAAAAGTTGGTTTGAAAAACTCAAAAAAGTTTGAATTAAGTGAAGGATGAGTAAATGATGACAGATTTTATAATGCAGCATATTTTTGCCAGTGTTTTTGTTAATTAATGTGTTTGGGGATACTTTCGTTGGAATCTAACAGTGTTTATATTGAAAATTATTTGTAAAATCCTAAGTTTATTTATTTCCACTTTGACCAATTTAATGCACCACTTGTAAAAAAGAGAATTGACATATCCCAAATTTTACAACCAGTATTGTTATACAGTACATTCATGTGCATGTACATGTTTTTGATAGGTTGTGTGTGAGATTCTGGTGCAAGCAAGTCGTCTGGTTCCTCTAAGTCAAGAACATCTCATCATCAAACTCTGCCAAATGATTCAT[C/T]AACTTCTAAACCAGCTACAGGTATTTACCATAGGGTTGGGTTAAATGGTCAAAACGCATCATGTTAATAATCTTGTATTTTTTATATCAGTAGATGCAGATAATTCAATTTCTTTTCATTTTGAAGGCAGATATTTTCTCCTGAGTAAAAGCTGTTTAAAAAAAGGACAATTGTTAAATAAAAGTACATTTTATTGTCAGTAAACATGTCAACCAGATGAACCTTTTAGAAATCTAAGATCAAAAGTACTAATAATGCTAAATGTTTATGAATTATTTGTATTTTTTATGAATGGATGTAATTTTAGGTTATTGAGTAAAATGATAACATCTGTAAAAAATTGTAATATTTGGAAATTAAAATGTAAATACCTAAATATTGCCAACCATAATCATATGTAAAACCACACATATAGCACCTCATTACCATAGGGTTTCAATGATAATTGTTTGAAAAATGAAAAACGCTAATATGAATGCACTGAGTATACATACTAATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32356
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113316 | Essential Splice Site | 179 | 1201 | 3 | 21 |
Genomic Location (Zv9):
Chromosome 21 (position 37708832)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 38700867 |
GRCz11 | 21 | 38748573 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTTGCTCTTTCGTCACTGGTGTATGGCAATGGATCCAAATGCCAAAGG[G/T]TAAGAATTGCTGATATGGAAGCTCTCTCTTTTTTTTTTCTGGATGTTTTG
Long Flanking Sequence:
ACACAATATTTCTCTTGTATGTCAGTGCTGAGTTTACATCCTAATATGCAGTGATTTATTTAATTATTATTATTTTTAAGTTTGGAAAAAAAATTAAAATCCCATATGCGAAACAGACTGTTTTAACAACTAAATGCCATTGGCTGCTTTTTTAAAGGGGGAGGGGCTACTTTGTTTTGCACTGTTTTCATTTTACTTCAAGTTACGTGACACATCAAACACAAGGCATATCACATACTAAAAGTGATACTGCACAAATTATTATTAATAAAAATGATTACTTATTATTGTTACTGACACGATTCTAATCAAGGCTTTCCTATTCCTCTGAAAAAAATCTCCTGTTTTACTACTAACAGATAATAGTGGATGAACATACGCTTGATGTTTTGGTATCGTACTGCTCGCGGGCTCTGCGGACATGCAGTTCATGGACTCATTCAGAGGTGCTGCTTGCTCTTTCGTCACTGGTGTATGGCAATGGATCCAAATGCCAAAGG[G/T]TAAGAATTGCTGATATGGAAGCTCTCTCTTTTTTTTTTCTGGATGTTTTGTTTTATATTGTAATTAAATTTAAATTTTTAATCCTTCCAGTATCTTCCAGAACTTCTTGGACCAAGTGGGGTTCTGGTTAAGTATGGTGACCCCAAGCAGCCAGACATAGAGTTGCGGCGTTCAGCTGTGCATTGCATTGCTAATCTGTGTCTCAGGTCAGTTTTTGCAAATGGCTGTTATTTCAAAAAATAGATTCAGATAAATGCTGGAAAACACCACACAACAACAAAGTGCTCAGCGCCGCGACAAGGCATGCACATAATAGTTGTAAACATTACAAACCAGAAGCCCACATTCGAATGTTATTTGATATGAAACTATTTAGATGGCGCTCTGTGGTGAGACAGAAATATGAACAGTATCCTGAGTCGTGGCTGGGCGCCGCGGACAGCTACCGACTTGCGGCATTGGTGCGTGCACACTGATAGAAATCTATGTTTAGAATTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11893
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 |
---|---|---|---|---|---|
ENSDART00000113316 | Nonsense | 441 | 1201 | 9 | 21 |
Genomic Location (Zv9):
Chromosome 21 (position 37728314)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 38720349 |
GRCz11 | 21 | 38768055 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTCGTGTGCGTCAGAGTTCACTTCAGTGTTTCCTGGCTGTGGTCAAGTG[T/A]GTGGAGAAGCGAATCCTCTATGGTTACTGGTCTTCGTTTGTTCCCGACGC
Long Flanking Sequence:
AAACATTATCTTTTAAAATTTTATTTAATGTTAAAATAAACTTTATTTGGTAAACAAAACAAGTCTCTCGTATAATATATCTACTAAAAGACAGAAAATATTACTGTACAAACTGCATTGTACACAACTCAGATGAACATTTTCATATTAGTCAATAATATTACCGTAATTAATTTGAAAACTGAAAAATAATAGATTTACACACATTTACTCAAGTAAACAGAATTAATGATGGGCTGAAAATCTGCAGAATTCTGCGCACGTCTACTTATAAGTAATAATCATGTGCATGTTAAATGTTTCCTTTGTTGTCTTTTTTATTTAAAAGCACATAATTTCTGTTCAACAAAAATTTAATTTGCTGATCTAGACATGGGTGTGAACTTTTTGGAGCTGGATGTAAATCTGTGAGTATGTGCTTTCACATGTGTCTTCTCTAGGTTGTATCAAGCTCGTGTGCGTCAGAGTTCACTTCAGTGTTTCCTGGCTGTGGTCAAGTG[T/A]GTGGAGAAGCGAATCCTCTATGGTTACTGGTCTTCGTTTGTTCCCGACGCTCCTGGGATTGGAGGTCCTCCTCCTCTCACTCTTCTCACCATCGCCCTGAAAGACCCATCGCCAAAAGTAAAACGCACACACAAAAAATAATACTACAACTAAAAAAACTAAAACCAAAAAATATAGCCTATCCACATTTTCCTACTCAACTTTGTTTTAAATTGTGGTTTGCTTCTTTTCATAAGAACTAAAACTCAATAACTGAAATATTAAAATAACAAAATAGTTGAATAACAAATAATAACAAAAACTAACTTTCCTGTTGTGGCCGACGTGTGTTTAACGTGCAAAGAAATATGTATAAGTCCAAGGTAGCTCTTTTAGAAGGAAAGTTTAAAATAAAACGATTAATGTCGCATTACCAGGCTATTAAGCGTTTCCTCCAGAGTCTCATCTAATTTCGTATGTTTCGTTTTTAATCTTTCGACTTTTGTTTTAATGAAATTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25166
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 |
---|---|---|---|---|---|
ENSDART00000113316 | Nonsense | 796 | 1201 | 15 | 21 |
Genomic Location (Zv9):
Chromosome 21 (position 37739973)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 38732008 |
GRCz11 | 21 | 38779714 |
KASP Assay ID:
554-7526.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGGTGGTCCACTCATCAGTGCCTTACAGAATGAACATCATCCGACCCTT[C/T]AGACCAGCGCGTGCGACACCCTCTCCTCCATCCTGCCACAGGCCTTCAGT
Long Flanking Sequence:
AGTAGAAGATTAAAGAAGACTTTTAACGGAGTCTTTTGTCCATAGTGATTCTTATAATGGCAGTTAATGGATATAGTTTTATTTTTTATTTTTTATTAAAAATAAATAGAATAAAGGCTTGTAAAACAAACCATAATGCCTGAAATAATATAACAACTCACCGCTCAACACCCAAGATAAGTATGTGGATATGTTTATGGTTTCATTTTTAAATATTTTGGGAAACTATCCCGGACGAGCCCCCATTTTATTTTACAAACCCCAAATGTGGTCAGTCAAAGAATACAAGAGTGAAATAAATTTTAGAATGAAACCTGCATAAGCAAACGCATAATATAAATGCATTTGGGACAACTTTATCCAACACTGAACATACAAAACTGAATTGAGAGATTTTGGTGTTGATGTAAAGCTGTTGTTTTCAGGTGGTTCAGTTCTGGTCAGAGGTTTTAGGTGGTCCACTCATCAGTGCCTTACAGAATGAACATCATCCGACCCTT[C/T]AGACCAGCGCGTGCGACACCCTCTCCTCCATCCTGCCACAGGCCTTCAGTCAGCTGCCCGTGAGTGCCTGTGTAATGCAGTGTTGAGTTATTAATTGTTATTGTGGTATTCATATTCATCAATATGGATTTGTGCAGGATAAGACTCAAGTGCTGTGCATCACGATCCTGCTGGGACTGACGTACAGTGAGAACTCTCTGGTGAAGGCAGCAGCAGTCAGAGCTCTGGGGGTCTATATACTATTCCCCTGCCTGAGAGAGGTACACAGCTCTGCCCTTTCTGATAGTTAAAGATCCATCCACCCAAATGTATACCTGTATAATGACTAATAGTTTGGAATTGTAACTACAAAAATTTATTCATAATGAAAGAGCTCCACATTTAATAAAGTATTCATCCAGAGTATTAATTTCACTTAATGTAGTTTTCTTTGTCATACAAATTTTTTATGCATTTATTTTATTTATGAATTCATCCATAATTTACTTTAATGTATGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37362
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 |
---|---|---|---|---|---|
ENSDART00000113316 | Essential Splice Site | 815 | 1201 | 15 | 21 |
Genomic Location (Zv9):
Chromosome 21 (position 37740033)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 38732068 |
GRCz11 | 21 | 38779774 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTGCGACACCCTCTCCTCCATCCTGCCACAGGCCTTCAGTCAGCTGCCC[G/A]TGAGTGCCTGTGTAATGCAGTGTTGAGTTATTAATTGTTATTGTGGTATT
Long Flanking Sequence:
CAGTTAATGGATATAGTTTTATTTTTTATTTTTTATTAAAAATAAATAGAATAAAGGCTTGTAAAACAAACCATAATGCCTGAAATAATATAACAACTCACCGCTCAACACCCAAGATAAGTATGTGGATATGTTTATGGTTTCATTTTTAAATATTTTGGGAAACTATCCCGGACGAGCCCCCATTTTATTTTACAAACCCCAAATGTGGTCAGTCAAAGAATACAAGAGTGAAATAAATTTTAGAATGAAACCTGCATAAGCAAACGCATAATATAAATGCATTTGGGACAACTTTATCCAACACTGAACATACAAAACTGAATTGAGAGATTTTGGTGTTGATGTAAAGCTGTTGTTTTCAGGTGGTTCAGTTCTGGTCAGAGGTTTTAGGTGGTCCACTCATCAGTGCCTTACAGAATGAACATCATCCGACCCTTCAGACCAGCGCGTGCGACACCCTCTCCTCCATCCTGCCACAGGCCTTCAGTCAGCTGCCC[G/A]TGAGTGCCTGTGTAATGCAGTGTTGAGTTATTAATTGTTATTGTGGTATTCATATTCATCAATATGGATTTGTGCAGGATAAGACTCAAGTGCTGTGCATCACGATCCTGCTGGGACTGACGTACAGTGAGAACTCTCTGGTGAAGGCAGCAGCAGTCAGAGCTCTGGGGGTCTATATACTATTCCCCTGCCTGAGAGAGGTACACAGCTCTGCCCTTTCTGATAGTTAAAGATCCATCCACCCAAATGTATACCTGTATAATGACTAATAGTTTGGAATTGTAACTACAAAAATTTATTCATAATGAAAGAGCTCCACATTTAATAAAGTATTCATCCAGAGTATTAATTTCACTTAATGTAGTTTTCTTTGTCATACAAATTTTTTATGCATTTATTTTATTTATGAATTCATCCATAATTTACTTTAATGTATGTTCATTATTTTACTTCCTATAATGAAAAAAAGCATTTTATTTATTTACATTGTCATTTAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43698
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113316 | Essential Splice Site | 999 | 1201 | 20 | 21 |
Genomic Location (Zv9):
Chromosome 21 (position 37749729)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 38741764 |
GRCz11 | 21 | 38789470 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAACAAAAAGAAGCTGTTGGTGTCTGTAATACGTCTTTCTTCACTCTC[A/T]GGTTCTGCTGTGTGGTCTACGGAGGCTTTCTCTGCCCTGTCCTGTGTAGT
Long Flanking Sequence:
ATAATAATTAATAACTAATTTCTTTTATCTTTGTCATGATGACAATAAATAATATTTGACTAGATATTTTTTAAGATATTAATATTTAGCTTAAAGTGAGATTAAAGGCTTAACTAGATAAATTAGGTACATTAGGCAAGTTAGAGTAATTAGGCAAGTCATTGTATAATGGTTTGTATAATGGTTAAAAAATGGGAAAAAATTGCTTGAGGGGGCTTAAAAAAACTTCAAATGCTTAAAAAAAAACTGCTTTTATTCCAGCCAAAATAACACCAAAAAAACTTTCACTCGAAGAAAAAATATTATAGGAAATACTGTGTTAAATTCCTTGCTCTTTTAAACATCATTGTGAAATATTTGAAAAAGAAAAAAAACTCACAAGAGGGCTAATAATTATGACTTTATTCGTTTGTTCTTGTGTGTGTTTGTGTAAGAGTTATTTATGTAAAAAAAAACAAAAAGAAGCTGTTGGTGTCTGTAATACGTCTTTCTTCACTCTC[A/T]GGTTCTGCTGTGTGGTCTACGGAGGCTTTCTCTGCCCTGTCCTGTGTAGTAACTTCCTGCAAGAACTTCAAGGTGCGCATCAAATCTGCAGCTGCTCTTTCTGTTCCCGCGACACGAGAGTGTTACGGAGACTCTCAGCAGTTCTCAGAGGTGTGGAGATCCTTAGCTCAGGCTCTGGAACACAGCGAGGAAACCGAGGACTTCCTGGAATACCGATACTGTGCCAGCTTACGCTCACAGCTGTGCCGCGCTCTCCTGCACCTGCTGTCCCTGTGCCAGCCTGATGACCTTCCAGCGCTCGGGTCAGTATATTCAGTTCAGTTTAAATTCAAGTTTAGTTATACAGCATTTGTAATAACACCAATTATTTTAAAGCCGCATTTTAAAGTCTGAGTGAATCAGAGGTTGCTTTTCAGAATCTTTTATTTCAGTATGTTGATGTACTTCCAATGAAAGCTTATTGTTGAGTATGGACGGGGTTTTCTTTTGTCTATAATTCC
Associated Phenotype:
Not determined