ZMP
si:dkey-146l2.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate ankyrin repeat domain 15 (ANKRD15) [Source:UniProtKB/TrEMBL;Acc:
Human Orthologue:
KANK1
Human Description:
KN motif and ankyrin repeat domains 1 [Source:HGNC Symbol;Acc:19309]
Mouse Orthologue:
Kank1
Mouse Description:
KN motif and ankyrin repeat domains 1 Gene [Source:MGI Symbol;Acc:MGI:2147707]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa45224 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa26558 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa2231 | Nonsense | F2 line generated | Not yet available |
| sa2225 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45224
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000084370 | Nonsense | 321 | 1335 | 3 | 12 |
| ENSDART00000136521 | Nonsense | 321 | 1335 | 4 | 13 |
| ENSDART00000145299 | None | None | 187 | None | 3 |
The following transcripts of ENSDARG00000060102 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 46537682)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 44318947 |
| GRCz11 | 5 | 44919100 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGGATGTTTCAGGAAGCGCTCCTTTAGCGTTGGCAGTGCTGATCAATA[T/G]GAGCCCCTGTCCCAGATCAAGACAGGTTCTGAGCTTCACATTGAGGAGAT
Long Flanking Sequence:
CTGGAGCAGGAGCGGCTCCTGATGCAGCCACCAGTCAGTGAGCCACCTCGTAGGCGATTAGCCAGTTTTGGAGGAATGGGGTCTTCCAGTTCCCTGTCCTCTTACAGTGGGTCCTATGGACCAAGCCAGATTTCTCCCAGCTCCCATTCTTTCCAACATAATGGTCATCTAGGCAATGGGGAATACAACCCCTACTTCACATCCTCTATGGGCAGTTCAATCCGCCACAGTCCCCTGAGCTCAGGCATGACCACACCAGTGACCAATGTTAGCCCCTTGCACCTCCAGCACATTCGAGAACAGATGGTAGTAGCGCTAAAGAGACTAAAAGAGTTGGAGGAGCAGGTAAAGACAATCCCAATCCTTCAAGTCAAGATCTCAGTCTTGCAAGAAGAGAAAAGACAACTAGTATCCCAGAAGAATAACTCTAAGGTAGTGGGGCAAGGATCAGGTGGATGTTTCAGGAAGCGCTCCTTTAGCGTTGGCAGTGCTGATCAATA[T/G]GAGCCCCTGTCCCAGATCAAGACAGGTTCTGAGCTTCACATTGAGGAGATTGATAACACTGAGCAGAGCACTCAAAGGCTACAGGAGTTCAGGCAATTAACGGCTGAAGTGGAAGCCCTAGAGCGGAACATACAGGATAATGGTGAGGAAATTAAGCACAGCTTACACCAAACAGAGCTAAGATCAAACCAAAATGTCCAGCTGTGGAGCCGTGAAAGCAGGTCCATTGGTGTCGGAGCTGATGAGAACATGAACGATGTGGTGGTTTACAGGAGGTCACCTGGCAAAAACAAAGATGTGGCTGTTGGAACTGAACAGGAGGTGAGGAGCACAGGAGTTGGTGTGACTGAAGCCATGCTAGGCCTGAGCAGTGAGGCAGAAACTGAAATTGAGATGCAGCACCAGACCATCGAAGCCCTCAAAGAGAAGATTTACAGATTGGAGGTTCAACTTAAGGAGACGACCCACCAAATGGAAATGGGAAAGCTAAAGCTTCAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26558
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 |
|---|---|---|---|---|---|
| ENSDART00000084370 | Nonsense | 471 | 1335 | 3 | 12 |
| ENSDART00000136521 | Nonsense | 471 | 1335 | 4 | 13 |
| ENSDART00000145299 | None | None | 187 | None | 3 |
The following transcripts of ENSDARG00000060102 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 46538130)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 44319395 |
| GRCz11 | 5 | 44919548 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCACCAGACCATCGAAGCCCTCAAAGAGAAGATTTACAGATTGGAGGTT[C/T]AACTTAAGGAGACGACCCACCAAATGGAAATGGGAAAGCTAAAGCTTCAA
Long Flanking Sequence:
CAGGTGGATGTTTCAGGAAGCGCTCCTTTAGCGTTGGCAGTGCTGATCAATATGAGCCCCTGTCCCAGATCAAGACAGGTTCTGAGCTTCACATTGAGGAGATTGATAACACTGAGCAGAGCACTCAAAGGCTACAGGAGTTCAGGCAATTAACGGCTGAAGTGGAAGCCCTAGAGCGGAACATACAGGATAATGGTGAGGAAATTAAGCACAGCTTACACCAAACAGAGCTAAGATCAAACCAAAATGTCCAGCTGTGGAGCCGTGAAAGCAGGTCCATTGGTGTCGGAGCTGATGAGAACATGAACGATGTGGTGGTTTACAGGAGGTCACCTGGCAAAAACAAAGATGTGGCTGTTGGAACTGAACAGGAGGTGAGGAGCACAGGAGTTGGTGTGACTGAAGCCATGCTAGGCCTGAGCAGTGAGGCAGAAACTGAAATTGAGATGCAGCACCAGACCATCGAAGCCCTCAAAGAGAAGATTTACAGATTGGAGGTT[C/T]AACTTAAGGAGACGACCCACCAAATGGAAATGGGAAAGCTAAAGCTTCAACTGCAAGTTGCTGGATCTAGGAAAAAGGCAGACAAAGGCTTGATGGCAAGGCCAGAAATGTACAGCACGTCAGTGGAGGCAAGAGTGTCCACACATACCCAAGGTGTGGGCAACCATGTTGAGCTTAGTGATGCAAGCACAAACCATGTCCATCAAATGAATTCAGTGGGCATTACTTGCAGACCGGATGCAAGGCATGTTTTAGTGGGTCCAGAGTTGCCAATGGATCGATGGATTGTACAAGAACGTACTGAGGTTCAAGATCAGTGTGTCGGCAGGCATGTTGTGATGTGCAGCCAGAGTGTGGGAGTGGAATTAAGCGTATGTGAAATGGGAATCAACACGGAGTTAACAGCTGAAGGTTTAGGACTTTGCAAAAGAGAGGCTGAACAAGCCAAGGAGTTCAGGTCTATAGGATGTGGAGATTGTTCAGTGGATGTAATGGTTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2231
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000084370 | Nonsense | 609 | 1335 | 3 | 12 |
| ENSDART00000136521 | Nonsense | 609 | 1335 | 4 | 13 |
| ENSDART00000145299 | None | None | 187 | None | 3 |
The following transcripts of ENSDARG00000060102 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 46538545)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 44319810 |
| GRCz11 | 5 | 44919963 |
KASP Assay ID:
554-2916.1 (used for ordering genotyping assays)
KASP Sequence:
ATTAAGYGTATGTGAAATGGGAATCAACACGGAGTTAACAGCTGAAGGTT[T/A]AGGACTTTGCAAAAGAGAGGCTGAACAAGCCAAGGAGTTCAGGTCTATAG
Long Flanking Sequence:
CCTGAGCAGTGAGGCAGAAACTGAAATTGAGATGCAGCACCAGACCATCGAAGCCCTCAAAGAGAAGATTTACAGATTGGAGGTTCAACTTAAGGAGACGACCCACCAAATGGAAATGGGAAAGCTAAAGCTTCAACTGCAAGTTGCTGGATCTAGGAAAAAGGCAGACAAAGGCTTGATGGCAAGGCCAGAAATGTACAGCACGTCAGTGGAGGCAAGAGTGTCCACACATACCCAAGGTGTGGGCAACCATGTTGAGCTTAGTGATGCAAGCACAAACCATGTCCATCAAATGAATTCAGTGGGCATTACTTGCAGACCGGATGCAAGGCATGTTTTAGTGGGTCCAGAGTTGCCAATGGATCGATGGATTGTACAAGAACGTACTGAGGTTCAAGATCAGTGTGTCGGCAGGCATGTTGTGATGTGCAGCCAGAGTGTGGGAGTGGAATTAAGCGTATGTGAAATGGGAATCAACACGGAGTTAACAGCTGAAGGTT[T/A]AGGACTTTGCAAAAGAGAGGCTGAACAAGCCAAGGAGTTCAGGTCTATAGGATGTGGAGATTGTTCAGTGGATGTAATGGTTAGACCCATCAAGGAGATGGCAACTCGGAGTACAGGAACAGATGAAGTTCACAGAACTGACTTTGGAGTCATGGTCTTACCCATATGTGCGTCACAGTACACAAACATAGAAATTGAGACAATAGACAAGTTAACCAATACAGACAAGTTAGTTCTTACTGATACCTCCACCAATACACAATCATGCTCAAAAGACAAACAAGTCGGCACCGAACCGTTAGAGACACGTACAATCGCTGTTGGTGATGGTCTTGTAAAAGATGCGCCAGCCACATTAAAAACCCGTTCAGTTTCAGTAGGTACTACTTCATCAGACGATGCTTTTCTTGACAAGTTGCCATCTTGCAAAACCAAAGAGACTGGAATTGGCCACACAAGCATACACGAAAACTTCTTAGTCGGTCAGAAGACAAGGAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2225
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 |
|---|---|---|---|---|---|
| ENSDART00000084370 | Nonsense | 696 | 1335 | 3 | 12 |
| ENSDART00000136521 | Nonsense | 696 | 1335 | 4 | 13 |
| ENSDART00000145299 | None | None | 187 | None | 3 |
The following transcripts of ENSDARG00000060102 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 46538805)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 44320070 |
| GRCz11 | 5 | 44920223 |
KASP Assay ID:
554-2873.1 (used for ordering genotyping assays)
KASP Sequence:
AGTTAACCAATACAGACAAGTTAGTTCTTACTGATACCTCCACCAATACA[C/T]AATCATGCTCAAAAGACAAACAAGTCGGCACCGAACCGTTAGAGACACGT
Long Flanking Sequence:
TTAGTGATGCAAGCACAAACCATGTCCATCAAATGAATTCAGTGGGCATTACTTGCAGACCGGATGCAAGGCATGTTTTAGTGGGTCCAGAGTTGCCAATGGATCGATGGATTGTACAAGAACGTACTGAGGTTCAAGATCAGTGTGTCGGCAGGCATGTTGTGATGTGCAGCCAGAGTGTGGGAGTGGAATTAAGCGTATGTGAAATGGGAATCAACACGGAGTTAACAGCTGAAGGTTTAGGACTTTGCAAAAGAGAGGCTGAACAAGCCAAGGAGTTCAGGTCTATAGGATGTGGAGATTGTTCAGTGGATGTAATGGTTAGACCCATCAAGGAGATGGCAACTCGGAGTACAGGAACAGATGAAGTTCACAGAACTGACTTTGGAGTCATGGTCTTACCCATATGTGCGTCACAGTACACAAACATAGAAATTGAGACAATAGACAAGTTAACCAATACAGACAAGTTAGTTCTTACTGATACCTCCACCAATACA[C/T]AATCATGCTCAAAAGACAAACAAGTCGGCACCGAACCGTTAGAGACACGTACAATCGCTGTTGGTGATGGTCTTGTAAAAGATGCGCCAGCCACATTAAAAACCCGTTCAGTTTCAGTAGGTACTACTTCATCAGACGATGCTTTTCTTGACAAGTTGCCATCTTGCAAAACCAAAGAGACTGGAATTGGCCACACAAGCATACACGAAAACTTCTTAGTCGGTCAGAAGACAAGGAACATTGCCTGTGGCCCCTCTCAGTCTCCTACCCCCACCCACGTTAAGAGTAATTTTGAGGAATCTGTCTTAACAGAAGGGCCCAACCAGTCACAGGCTGGTGCAGGAGTTGGACTTGATCACTACATAGAGAGAGTGCAAAAGCTCTTGCAGGAACAGCAGATGTTGCTGGCTCAGAACTACAGTGAGCTGGCAGATGCATTCGGCCCACCTCAACAATCCCAGTTCAGTTCCATCAACAGTGAACTAGTCACTACTCTATCA
Associated Phenotype:
Not determined