ZMP
si:ch211-251m13.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens KCNH5, potassium voltage-gated channel, subfamily H (Eag-related)
Human Orthologue:
KCNH5
Human Description:
potassium voltage-gated channel, subfamily H (eag-related), member 5 [Source:HGNC Symbol;Acc:6254]
Mouse Orthologue:
Kcnh5
Mouse Description:
potassium voltage-gated channel, subfamily H (eag-related), member 5 Gene [Source:MGI Symbol;Acc:MGI
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31956 | Nonsense | Available for shipment | Available now |
sa10517 | Nonsense | Available for shipment | Available now |
sa35563 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15450 | Nonsense | Available for shipment | Available now |
sa22359 | Nonsense | Available for shipment | Available now |
sa13966 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31956
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100322 | Nonsense | 146 | 994 | 5 | 12 |
ENSDART00000138934 | Nonsense | 146 | 675 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 37767458)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37244270 |
GRCz11 | 13 | 37370160 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAAAATGTATTATGTGTCTTTCACTCAGTACGTAAATATCTTTTAGGTT[G/A]GACCAAGTTTGCACGTTTGACTCGAGCGTTGACCAACAGCAAAAGCACCA
Long Flanking Sequence:
AATAAATAAATAAAAATCTGAAATGTAAACATAAAATCTGAATTTTGGAAATTATTTCTTAAAGTTTAAAGAAAAAAGTCAATGCTGGGTTGGAATTGTGAGGTATCTAAAGTGAGAGTCAAGTCATTTTCCAAAAACATTTCAAATATACTTAAAGTTTTTATTCATCAGAGATTAGAAAAGCTTCATGTTTTAGGTAGAAATAAGAAGTGTTTTCAACATTGATGACAAATGTTTTTTGAGCACCAAATCAGCATATTAGGAGGAATTCTAGAGTATCATGTACATCATTTGTAGCATACTAGCTTAAAGATATCTTAAAAACGAGCAATACTGATACTAACATCTAAAAAACATTATTTAATATCATGGTACTTTTAAAATTTTGCTTTAAAACGTTTATTAAAGCAAAATACTAAATTGTGTTTCCATTGTACAGTTTTTTTTAGGGTAAAATGTATTATGTGTCTTTCACTCAGTACGTAAATATCTTTTAGGTT[G/A]GACCAAGTTTGCACGTTTGACTCGAGCGTTGACCAACAGCAAAAGCACCATTCAGCAGATCACGCCTGTCAGCAGAACCGACGTCACGTCACACAAACCCTCCAGACTTGCAGAGGTAAGAACACACACACACACACAGTAGCAGCATTTGCTTACATCCTTGACTGTGCAGTACAAGGTTATACAAAACTTCATCTAACGGAGGACAAACTTGTAATAGAATCACACACAGGACGCTGCTGTAACGCAATCTCACATGTGTCTGTTGGACAGCGCAAGTCTACAGTGGGCATCCAGAAGCTGCTATTAATAATTAACACTGGTGAAGAGTGGATGTGTGTGTCCCATAACCTCTGTTCACTTTTTTCGGCTTTCCTCATTTGTTACTGTCACTGCTGTGTTCAAGACAAGGTCATTGGGTTATTTTATATTATATTAATTGAGTATTGTTTTGTGTGTCAGGAAGCTTTGGATTGTCTGAATCTTATGCACTGTGAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10517
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100322 | Nonsense | 305 | 994 | 6 | 12 |
ENSDART00000138934 | Nonsense | 304 | 675 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 37762608)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37239420 |
GRCz11 | 13 | 37365310 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATTACCTCAAGACCTGGTTCGTTATAGACTTGCTGTCCTGTCTGCCCTA[T/G]GACATCATCAAYGCWTTTGAAAACGTGGATGAGGTGAGCGGACCTGTYAT
Long Flanking Sequence:
AAATGTAACCATGCATCAAATTGAACATAAATGCTAAATCAATTCATTAATATTCATAAACTTGTGAACTTTGGTGTATTTTATTTCTGTTTATCTCCTCAGAGATCCTTTATCTCTTTTTGCCTTGTTTGTCTTTCTCAGGTTCTTCAGCTGGGCTCTGATATCCTTCCGCAGTACAAGCAGGAAGCCCCCAAAACCCCGCCTCACATCATCTTACACTACTGTACCTTTAAGACCACCTGGGACTGGGTCATCCTCATTCTTACCTTCTACACTGCCATCATGGTTCCTTACAATGTCTCCTTCAAGACCAAACAGAATAACGTCACGTGGCTGGTTCTGGACAGCGTTGTGGATGTCATCTTCCTCGTAGACATCGTGCTTAACTTCCACACCACGTTTGTCGGGCCTGGAGGAGAGGTGATCTCAGACCCCAACCTGATCAGGATGAATTACCTCAAGACCTGGTTCGTTATAGACTTGCTGTCCTGTCTGCCCTA[T/G]GACATCATCAACGCTTTTGAAAACGTGGATGAGGTGAGCGGACCTGTTATTTTGTTGCTTTAGACCAGTTTCTGATACACTGTGTAAAGAAATGTTCAGTTCCACACAATTCATTTATATTGTCCCAATACAAATCGATTAAGTTAACTTAATTGTTTTAGGTTGATTGAACATAAAACAATTAAGTTGTTCCCACAAAAATCTAAAGAATTGTGTTGTTTCAACTCATTTTAAATAAACAGTTTGAACAAACAGAAAAAGTATTTTTTTGAGTGTACAAACAAAAGGAATTGACCCTTTGCTAAACCACACCCAAAAACCGCCACCCATCAATCGTGGCTTAGCAACTGTAGCCATTCGCAGGGGCTCTGTCAAGCTTTCGAGCGAGCGAAACAAGCCAAAGTGTTGTGCATGTGGATTGTGCAAATTTGAAACCTGTATCCTAAAAGTTTAGACAGGGTGGTGGAAATTTTCCCCTTTTCAAAACCTAAAACCCAAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35563
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100322 | Nonsense | 390 | 994 | 7 | 12 |
ENSDART00000138934 | Nonsense | 389 | 675 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 37748021)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37224833 |
GRCz11 | 13 | 37350723 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTATGAGGTCATTGACGAACAAACCAACACCATCAAGACTGACAGCTG[G/A]CTCTTCCAGTTAGCCACCAGCATCGGGTCCCCGTACCGCTACAATGCCAG
Long Flanking Sequence:
TTTTTCAGATGTTTACTGAATCATGAGCTGTTCAGTAGCTTTTGATGTGGAGATACTGTAAACAAAATAAACATAAAAAACATGTAAAAAAAAAAACTTATTTATAACATAAGAGCATCATAGCAGAAATTTTTTTGTGGTTTTTGACTTAAACCTTGATGCGGTAAACCTGAAAATCAGTTATCATCCCATGCCTAAAGTATATTTGTGTTGCATTACATCATTTTATTCTATTATATACTGTACTGAATGTTACTGTCTTTATTTTTCTCGTTCCAGGGCATCAGCAGCTTGTTTAGTTCTCTGAAGGTCGTCCGACTGCTCCGTTTGGGTCGTGTTGCACGTAAACTGGACCACTATCTGGAGTATGGTGCGGCTGTGCTGGTTTTACTGGTCTGTGTATTTGGATTAGTGGCCCACTGGCTGGCCTGCATCTGGTACAGCATTGGAGATTATGAGGTCATTGACGAACAAACCAACACCATCAAGACTGACAGCTG[G/A]CTCTTCCAGTTAGCCACCAGCATCGGGTCCCCGTACCGCTACAATGCCAGTGGGACCGGCCAGTGGGAGGGCGGTCCCGGTAAAGACTCTCTATATATAACCTCACTATATTTTACCATGACCAGCCTGACCACCATTGGCTTTGGAAACATCGCGCCAACAACAGATGGAGAGAAGATTTTCTCTGTGGCCATGATGATGGTCGGATGTGAGTGTTTGTCTTCTTTTGCATATTTCCCAGAACTGTCTGTGTTGTTGTTGTTGACCAGCAAAATAGACTTTAATTAATGAGATTTCAATTTTAAAACAGAAAAAATGGTTGTTGTCTTTAATTTTGGCAGATAGGCTGGATAGTTTTATGTTAATACACCAGGCATGTTGTCGTCTAAGCCAGGGGTTCTCAAAGTGGGGGTCGGGACCCCTCGAGGGGTCGCGGGACAATGAAGGAGGGTCGCCTGGTGATTTAAAAAAATCTATTTATTATTATTATTAAATCATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15450
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100322 | Nonsense | 718 | 994 | 11 | 12 |
ENSDART00000138934 | None | None | 675 | None | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 37700745)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37177557 |
GRCz11 | 13 | 37303447 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACTCACCATTCCTGTGGACCATCCAGTCCGAAAACTTTTCCAGAAGTTT[A/T]AGCAGCAGAAAGAGCTCAGAAACCAGGGCGCTTCAGCCCAGCTGGACCTG
Long Flanking Sequence:
CAGCCAATATTCATTTGTGATGAGGAAAGGCAGATTGTTGCCGAAGAACTACTGAGAGGTTTCAGCTGCTGTCTGGGATTTCACTGCCTTTCTACACCTTCCTTTCTTCATGTGTTCAACACTTTTTCCCTCTGTCATTTCATTTTATTACACATAACTTAATTTGTAAATTAATTAGATTTGATTTCTTCGCTTATATGGATTTTTTTTTGCTTGTTACCAACGTCCGATGAAAATTTCAAATGAACAGCACATTTAGAAATAATAAGTTTTCAAAGAAAATGATGACGTGTTAAAATCTTATTCCCCTCCTGTATCTAGGTCAATATTTTGATTACAAAACTTCTAACTTAATTCCTTTTTTTTTTCTCCATATTCAGTTTGTGTTCCGTAAGATCATCGATGTGAAGAAAGAGGAAGAAGAGAGGCAGCGCTCCAAGAATGAGGTCCCACTCACCATTCCTGTGGACCATCCAGTCCGAAAACTTTTCCAGAAGTTT[A/T]AGCAGCAGAAAGAGCTCAGAAACCAGGGCGCTTCAGCCCAGCTGGACCTGGAGAAGAATCAGCATCACCTACAGCAGCCCGCGCGCATGTCCAAACCTCACACCTCCCTCATGCAGAACTCACTGCACGCGGTTCAGAACGGCTCCACCAGCAGCGTGGTCACCATCTCCCAAATCACACCCATCCAGAACTGTCTGGCCTACCCAAAACCTGGAGACTCCATCAAGCAAAACAACCGCGACTTCATGGAGCTCAAACCCGCAGTGGTGACCAGTGAGCAAGTGGCAAACCGGCTCAAAGTGAACAACACGGCGAGAACCAAACCTGCAGGAGCCGCTCGTGGCTGGATGAGACTAAAAAATAACAGGGCTGCACCAGGGTCACCTCCGGAGGACGAAAGGAAGGAGGGGTTGAACAATGCAGCTAAGGCCGTTTCAATGGAGCGCATTGCATCAGAAGTCAAGGTCCAGATCGAAAATGTTGAGGACGTTGGAGGATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22359
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100322 | Nonsense | 945 | 994 | 12 | 12 |
ENSDART00000138934 | None | None | 675 | None | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 37700025)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37176837 |
GRCz11 | 13 | 37302727 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCGGATGGAGATCCAGGCTCTGAACGGAAGGATGGCAACTTTGGAAGAA[C/T]GAGTCGGACAAATTCTCAGACTTCTTTTAGACTCTTCGAAAGCCAAGTCT
Long Flanking Sequence:
CCATCAAGCAAAACAACCGCGACTTCATGGAGCTCAAACCCGCAGTGGTGACCAGTGAGCAAGTGGCAAACCGGCTCAAAGTGAACAACACGGCGAGAACCAAACCTGCAGGAGCCGCTCGTGGCTGGATGAGACTAAAAAATAACAGGGCTGCACCAGGGTCACCTCCGGAGGACGAAAGGAAGGAGGGGTTGAACAATGCAGCTAAGGCCGTTTCAATGGAGCGCATTGCATCAGAAGTCAAGGTCCAGATCGAAAATGTTGAGGACGTTGGAGGATCTAGGAAAAGTTCACTTCGTAAAACGGACTCTTTGGACAGTGGCTTGACCTACAGCGACCAAAGACTGGATAGAGTTTCAGAACCGCAGAGTCCTGTGCCTGGCACTGGTGAAGTTTACCCCAGTAGCGAAAGCTCATTCCAGGCCTCGCTGCAGGAGGCCAGGCTGGAGCTGCGGATGGAGATCCAGGCTCTGAACGGAAGGATGGCAACTTTGGAAGAA[C/T]GAGTCGGACAAATTCTCAGACTTCTTTTAGACTCTTCGAAAGCCAAGTCTAGTGAAGACTTGACTCATAGACCCAAACTCAAAGCACAGAGCAGCATCCCAGTGTCCAATCTGAGCACGCCGGACTCTGAAAAAGATGAGGGCTTGCCATGAGAAATTTAGCATTCAATGCGCATTTAAGGTTGAAGCTTTTGTAGCATCGCTGTGTTGTTTATTGATGCAATGAATAAGCTAGAAGCTACCTATAGAAGCTTGGAATTGGTTCCTAGTTTCTGATTTCAGAGGATCTCAAGATAATTATGGGAATAAGAATTGTTTTCATGAGTCAAACTAAGAGTCAAGAACTCTAAAATGATTTTTTATTTTAGTGCTTTAAATTTCAATCAGCACTTTTTGCACACTGAAGTAATGCAGGAACTACTTTCCCCTTTTTTCCTCCCTTTTTTTCAGTGCGAGTTTGTATATATTCTGCATGTCCAGCTGGGTTCTGGCTTGCCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13966
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 |
---|---|---|---|---|---|
ENSDART00000100322 | Nonsense | 957 | 994 | 12 | 12 |
ENSDART00000138934 | None | None | 675 | None | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 37699988)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37176800 |
GRCz11 | 13 | 37302690 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACTTTGGAAGAACGAGTCGGACAAATTCWCAGACTTCTTTTAGACTCTT[C/A]GAAAGCCAAGTCTAGTGAAGACTTGACTCATAGACCCAAACTCAAAKCAC
Long Flanking Sequence:
ACCCGCAGTGGTGACCAGTGAGCAAGTGGCAAACCGGCTCAAAGTGAACAACACGGCGAGAACCAAACCTGCAGGAGCCGCTCGTGGCTGGATGAGACTAAAAAATAACAGGGCTGCACCAGGGTCACCTCCGGAGGACGAAAGGAAGGAGGGGTTGAACAATGCAGCTAAGGCCGTTTCAATGGAGCGCATTGCATCAGAAGTCAAGGTCCAGATCGAAAATGTTGAGGACGTTGGAGGATCTAGGAAAAGTTCACTTCGTAAAACGGACTCTTTGGACAGTGGCTTGACCTACAGCGACCAAAGACTGGATAGAGTTTCAGAACCGCAGAGTCCTGTGCCTGGCACTGGTGAAGTTTACCCCAGTAGCGAAAGCTCATTCCAGGCCTCGCTGCAGGAGGCCAGGCTGGAGCTGCGGATGGAGATCCAGGCTCTGAACGGAAGGATGGCAACTTTGGAAGAACGAGTCGGACAAATTCTCAGACTTCTTTTAGACTCTT[C/A]GAAAGCCAAGTCTAGTGAAGACTTGACTCATAGACCCAAACTCAAAGCACAGAGCAGCATCCCAGTGTCCAATCTGAGCACGCCGGACTCTGAAAAAGATGAGGGCTTGCCATGAGAAATTTAGCATTCAATGCGCATTTAAGGTTGAAGCTTTTGTAGCATCGCTGTGTTGTTTATTGATGCAATGAATAAGCTAGAAGCTACCTATAGAAGCTTGGAATTGGTTCCTAGTTTCTGATTTCAGAGGATCTCAAGATAATTATGGGAATAAGAATTGTTTTCATGAGTCAAACTAAGAGTCAAGAACTCTAAAATGATTTTTTATTTTAGTGCTTTAAATTTCAATCAGCACTTTTTGCACACTGAAGTAATGCAGGAACTACTTTCCCCTTTTTTCCTCCCTTTTTTTCAGTGCGAGTTTGTATATATTCTGCATGTCCAGCTGGGTTCTGGCTTGCCAAAAAAATGTACAGTCCTGATTCAGTCTGTACAGTTAAAAT
Associated Phenotype:
Not determined