ZMP
si:ch73-138n13.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
KIAA1671
Human Description:
KIAA1671 [Source:HGNC Symbol;Acc:29345]
Mouse Orthologue:
2900026A02Rik
Mouse Description:
RIKEN cDNA 2900026A02 gene Gene [Source:MGI Symbol;Acc:MGI:1920194]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21360 | Nonsense | Available for shipment | Available now |
| sa21359 | Nonsense | Available for shipment | Available now |
| sa12854 | Nonsense | Available for shipment | Available now |
| sa14470 | Nonsense | Available for shipment | Available now |
| sa45332 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa41276 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa13366 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21360
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 |
|---|---|---|---|---|---|
| ENSDART00000111894 | Nonsense | 40 | 1823 | 1 | 11 |
| ENSDART00000132229 | Nonsense | 40 | 302 | 3 | 6 |
| ENSDART00000137258 | None | None | 36 | None | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 44736008)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 42688790 |
| GRCz11 | 8 | 42695577 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTCATAGACTCTAGCACCACGAGCTTAATGGAGAGTTCAGGTGCCCCC[C/T]AGGGGCCACTTATTAATGTCTCGGAGCCTAGCAAACCTGTCCTGGGCCCC
Long Flanking Sequence:
ATTGGCCAGTGGGTTCAATTGAATATAGACTTGTCCTGCCAACCTAAAGGAGGATTTGCACTGGCAGTGATGAGGTTCAATAAGGCAAACTGTTTTAGTGAGAGCCTGTGATTTGTACTGAAGACTGACTGTTGACAGTGAGGCAGTGTTGAGCAGAGCTTAACTGTATGCACATTATGAGAAAAGGATTTGGCAACAAACAAAGGCTGTCAGGAAATGATTCACTTGACTACCATACAGTGTCAGGCTACGTTCTACAAACCAACAGCCTACAGACTCTTCACTATCTAGAGATTTGATCACACTCATGTTAAATTATTCATAGAAGTGATTATTATCTAAATAAATTAATTTTTATGTTTTTAATTGTTTCAGGTGGTCCAATGGCTGCCCAGGTTGAGGTTGATACTGGGCGGCCATGTGTGGTCGGGAGTCGTCTGCACCTTAGTGCTCTCATAGACTCTAGCACCACGAGCTTAATGGAGAGTTCAGGTGCCCCC[C/T]AGGGGCCACTTATTAATGTCTCGGAGCCTAGCAAACCTGTCCTGGGCCCCAAGCCCAGACTTACTCCGAAACCATACACTGTGGAAAAAAATCCTTCTATACGCCCCATTCTTGCTCCCAAACCACATCCAAAACCTAGGTCTGAGTCCACTCGACCAGTTTCCTACAAGCCAGACCTACCCAGCACACCTAAACCTCAGCCAGCCAGTAAACCTAGTCTGCCATCTGCCTCTAAAATGGGCCCCAAGCCCAGCGGACAAACAAACAAACTTGTGGCACAACCCTTTAAACCAGCACCTACTATTGCCTCTGTGGATTCCAACAAGTCTAGAACCTCTTATTCTGGAGCCATGCTAAGAAGAACAAGTTTTGGAAACAAAACCGATAGTCATGCCTCCACTCCTGGTGCTGAATGGCCATTTTTATCTCGGAAAAAGCAGTCTGGCCCTTCAATCACTCGTGCTAAATCATTAGGTTTCTTATCAGAGATTGGACTCAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21359
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 |
|---|---|---|---|---|---|
| ENSDART00000111894 | Nonsense | 361 | 1823 | 1 | 11 |
| ENSDART00000132229 | None | None | 302 | None | 6 |
| ENSDART00000137258 | None | None | 36 | None | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 44735044)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 42687826 |
| GRCz11 | 8 | 42694613 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTGAGGATACAGGAGGTAGCATTATAAAGAGACGCATCAGCCTGCTCT[T/A]GGACTCTTCTTCCTCATCCTTCTCAACTGTGCGTGTAGATATGTCAGGGA
Long Flanking Sequence:
TAAATCATTAGGTTTCTTATCAGAGATTGGACTCAATTATGAGGACTGTAAAGAGGAGACTGGTGCCAAGGATGAAAACTCTCCAACTGTTCTTCGGCCCCAAACTAAAGGTTCCAGACCAAGACCAGTTTCAGCTGTGTTTCTTCAAAACTCTGCACAGTCTGAGCCTCAGGTTATACCCCCTACACCTGCTCCTCGTTGGGGAAAAGCACGACCCCTTTCATCTGACCTTACCTCAAAGTTTGAGTCAATTGGTCTTTCCCTAAACCGGCGAGCAGCCCAAGAGGATGGGAAAGAAAACACTCCTGAAACACCAGAGGCTGTTAAAGTTGTACCTCAAGAGAAACAATATGGTGCTGATGGGGCGGAAATGCTAAAAAAGGCCTCTTTGCCAGAGAATAGGACTCAGAAGATAAATCTGAAAGATGAGGACTCCGGAAAGGACCCTAAAGCTGAGGATACAGGAGGTAGCATTATAAAGAGACGCATCAGCCTGCTCT[T/A]GGACTCTTCTTCCTCATCCTTCTCAACTGTGCGTGTAGATATGTCAGGGACGGAACCTCTTTCACCTGGGCTTTCTCTCTCTGAAACTGATGGAGCAATGGGAGTAAAACAGCGAGTCAAAGAATTGAACGATGAAGTACCTACTACACTGTCACAACCCCAGAAGCCACAATATAAGCCACGGAACCCAATATCCGACCGCACTAAAAAGTAAGGCCCAGTGAATTTGCAACATTCATTGTAGAGGTCTGCTATGTTGATGCTGTAGCTCAGAACAATGCCTTTACCGTTTGACATATGTCTTTAAGAATTTGTAACATTCAAGAGGTTTTGGCCAGAATCAAATTAATGTCTTTGGAACTCTCTGTTTTTCTTTTTTTACTTTTACACTTAGGTAGTATTTTAGCTCTTATGCATCAAAATGCATAGTAAATGTTATTATTTTGTTTACCTTTTTTTTTTTTTTGTAAAAGTGGGTAACACTTTATTTTGGTGGTCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12854
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 |
|---|---|---|---|---|---|
| ENSDART00000111894 | Nonsense | 711 | 1823 | 3 | 11 |
| ENSDART00000132229 | None | None | 302 | None | 6 |
| ENSDART00000137258 | None | None | 36 | None | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 44731398)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 42684180 |
| GRCz11 | 8 | 42690967 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGCAGAAAGGAAGAAATGGTCAGAAGCACAAAGAGACATKGAAAGGGAA[C/T]GAGAGGAAGTTGCAGCACCCAAAAGGCCTAAGATGCTAGATGCAGAAGAC
Long Flanking Sequence:
CCTTTAATGCTTCTGAAGATGATGATCCTGGTAGCTTGGTCAAAGCGACCTATAGAGAACAAGTTTCTCCTTCTAGCCCTGTACGTGTGGAGCATGTCTTTGACACTGTGGCTTTGTCTGGAGAGAGTCGTGCTGTAAGTGAGGCTTTGCCAACTGCTCAACTTGAGGACAGAGCACTTACCCTACGTTCACGGCGATCAGCTCCTCAAGTGGAAAAGGGAAAACCTACCCATGAGATTACTAATTATCTGAAGGATGATGCAACCATGCCACGTTACCTCAGAGTTGGGGCACTACAGAAATGGAATGCCACAGAGACGGATATAGAGTTTGAAGCTGAGAGGGAGCGACAGAAAGAGATGGTAAAAAATATGGAAGAAGAAATAAGGAGACAAACGGAATTGCACATTGCTGCAGCAGCAGCACTCGAGGAAGAAGAGAAAGAGAGCAAAGCAGAAAGGAAGAAATGGTCAGAAGCACAAAGAGACATGGAAAGGGAA[C/T]GAGAGGAAGTTGCAGCACCCAAAAGGCCTAAGATGCTAGATGCAGAAGACCAGACGAACAAACCTAGAGCCACTTACTTTGCTCTGACTGGTCAGATTCAGGAGCCTGTTTATCAAGGTGAGCGAGTGCAGGAGGAAGCAGTCTTCAGGAGAGGTATACACAGAGAAGTGGGTGAAGAGGCCAGTGGCATAAATCATGAGGTTCCATTTGATGACTTCGCTATTAGGTCAGGGCAGTGGAGTCCACAGATTTCAATTGCTCCATTTAGAAGAAATCCTTCATTAGATGCAGCAATGCAGAGGGATTCGCTGGAGAATAAAAATGAAGCAGGACCAATAACAGATACCAAATTACAAGAAAGGGAACGGCAGAAAGCAGTTAGGGAAGGATTTGAAATAGACAGACAAATGATAGCAGAAATTGAAAAAGAAAAAGAGTTAGAAAGGCAGCGAGAAATGAAGAGACAACGAGACTTGGAGATAGAGAAACAAAGCAAAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14470
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 |
|---|---|---|---|---|---|
| ENSDART00000111894 | Nonsense | 914 | 1823 | 3 | 11 |
| ENSDART00000132229 | None | None | 302 | None | 6 |
| ENSDART00000137258 | None | None | 36 | None | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 44730789)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 42683571 |
| GRCz11 | 8 | 42690358 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGAAAGACAGAGAGAGCAAGAGAGGGAGAGACAGAGACAGATAGAGAGA[C/T]AAAGAGAAATTGAACGYCAGAAACTGAAGCAAATWGAATATGAGCGAATG
Long Flanking Sequence:
TTTATCAAGGTGAGCGAGTGCAGGAGGAAGCAGTCTTCAGGAGAGGTATACACAGAGAAGTGGGTGAAGAGGCCAGTGGCATAAATCATGAGGTTCCATTTGATGACTTCGCTATTAGGTCAGGGCAGTGGAGTCCACAGATTTCAATTGCTCCATTTAGAAGAAATCCTTCATTAGATGCAGCAATGCAGAGGGATTCGCTGGAGAATAAAAATGAAGCAGGACCAATAACAGATACCAAATTACAAGAAAGGGAACGGCAGAAAGCAGTTAGGGAAGGATTTGAAATAGACAGACAAATGATAGCAGAAATTGAAAAAGAAAAAGAGTTAGAAAGGCAGCGAGAAATGAAGAGACAACGAGACTTGGAGATAGAGAAACAAAGCAAAATTGAAAGAGAGAAAAGGAGGGAGGCTGAAATACAGAAAGAAAAAGAAAGGCAAAAGGAGTTGGAAAGACAGAGAGAGCAAGAGAGGGAGAGACAGAGACAGATAGAGAGA[C/T]AAAGAGAAATTGAACGTCAGAAACTGAAGCAAATTGAATATGAGCGAATGAAGGCTGCAGAAAGAGAACTTGAACAGCAGAGAGAGTTTGAGAGGCAACGGCAAAAAGAGTTTGAGCGGGAAAAAGAGAGAATGCTTGAGCAAGAGAGGCTTAGGCTTAGAGAATTTGAAAAACAGAAGGAGATTGAGAAAGAAAGGGAGAGACAGCTGGAGTTGGAGAGACAGAGGGAAATTGAAAGACAAAAACAAAGAGAACTGGAAAAACAAAGAGAGATAGAGAGGCAAAAGGAGATCGAAAGACAGCGAGAATTGCAGAGGCAGCGAGAGCTGGAGAAACAAAAAGAGCAGGAAAGGGAAAAACAGAGACACTTAGAAAGGCAGAAAGAATTGGACAGGCAAAGGGAACTTGAAAGGCAACGAGAATTGGAGAGACAGCTTGAGATTGAAAGACAGAAGGAGATTGAAAAGCAGAAAGAATTTGAAAGACAGAAGCAGATGGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45332
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111894 | Nonsense | 927 | 1823 | 3 | 11 |
| ENSDART00000132229 | None | None | 301 | None | 6 |
| ENSDART00000137258 | None | None | 36 | None | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 44730748)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 42683530 |
| GRCz11 | 8 | 42690317 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAGAGAGACAAAGAGAAATTGAACGTCAGAAACTGAAGCAAATTGAATA[T/A]GAGCGAATGAAGGCTGCAGAAAGAGAACTTGAACAGCAGAGAGAGTTTGA
Long Flanking Sequence:
AGAGGTATACACAGAGAAGTGGGTGAAGAGGCCAGTGGCATAAATCATGAGGTTCCATTTGATGACTTCGCTATTAGGTCAGGGCAGTGGAGTCCACAGATTTCAATTGCTCCATTTAGAAGAAATCCTTCATTAGATGCAGCAATGCAGAGGGATTCGCTGGAGAATAAAAATGAAGCAGGACCAATAACAGATACCAAATTACAAGAAAGGGAACGGCAGAAAGCAGTTAGGGAAGGATTTGAAATAGACAGACAAATGATAGCAGAAATTGAAAAAGAAAAAGAGTTAGAAAGGCAGCGAGAAATGAAGAGACAACGAGACTTGGAGATAGAGAAACAAAGCAAAATTGAAAGAGAGAAAAGGAGGGAGGCTGAAATACAGAAAGAAAAAGAAAGGCAAAAGGAGTTGGAAAGACAGAGAGAGCAAGAGAGGGAGAGACAGAGACAGATAGAGAGACAAAGAGAAATTGAACGTCAGAAACTGAAGCAAATTGAATA[T/A]GAGCGAATGAAGGCTGCAGAAAGAGAACTTGAACAGCAGAGAGAGTTTGAGAGGCAACGGCAAAAAGAGTTTGAGCGGGAAAAAGAGAGAATGCTTGAGCAAGAGAGGCTTAGGCTTAGAGAATTTGAAAAACAGAAGGAGATTGAGAAAGAAAGGGAGAGACAGCTGGAGTTGGAGAGACAGAGGGAAATTGAAAGACAAAAACAAAGAGAACTGGAAAAACAAAGAGAGATAGAGAGGCAAAAGGAGATCGAAAGACAGCGAGAATTGCAGAGGCAGCGAGAGCTGGAGAAACAAAAAGAGCAGGAAAGGGAAAAACAGAGACACTTAGAAAGGCAGAAAGAATTGGACAGGCAAAGGGAACTTGAAAGGCAACGAGAATTGGAGAGACAGCTTGAGATTGAAAGACAGAAGGAGATTGAAAAGCAGAAAGAATTTGAAAGACAGAAGCAGATGGACCTGGATATTGAGAGATGGACTCGACAAAAAGCAGAGGAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41276
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 |
|---|---|---|---|---|---|
| ENSDART00000111894 | Nonsense | 1455 | 1823 | 3 | 11 |
| ENSDART00000132229 | None | None | 302 | None | 6 |
| ENSDART00000137258 | None | None | 36 | None | 3 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 44729165)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 42681947 |
| GRCz11 | 8 | 42688734 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTGCAGCACCTATACTGGCTCCAGAGAGATGCTGGACCTCAGTACCTT[T/G]AAATGTAGGGTCAATTGGAGATTCAGTTTCTTCTCCCCCAACACCATTAT
Long Flanking Sequence:
ACGTATGAGAACTCAACTCCCTCCACCTCTGCAACCCCAAGTTCTGCACCAAACCCAACCTATGTCAAACGCATATGCTACAGAAAAACCTAGGCCACAACCTCACTCATTAATTGACACCTCAGATTGGGCCTTTGGCGCTCAGCAATCCATCTCAGCTTTGCCACCTGATCAAACCAGTGTTTGGGCTCATTCTGAAACAGAGTTGACTGTAGATGAACCTCTTTGGGTATCACCCATGGAGGGATCCAGAAGGCCAATTAGCACCAGACCAGGTGGTTTTGAGCAACAATTTTTGCGGCCAGAGGATAGAGGTTTAAGTAACATTTTGGCGCCCAGTTCAACCTCTTGCATGGGTCCAATCTTTACTCCTGTACAGTATTCCACTCTTGCACCACCCATGGTTCAAATTCAAACCCCTATGATGACTGCACAACCAAATCTTGGACCCAGTGCAGCACCTATACTGGCTCCAGAGAGATGCTGGACCTCAGTACCTT[T/G]AAATGTAGGGTCAATTGGAGATTCAGTTTCTTCTCCCCCAACACCATTATCTAGAAAAGAAACTTCAAGACCCAGAAGTCAAGCCTCAGCCCTGTCTGTTTCTGATCCTATATGGACTCCAAACTGGGAGCTGGCTTCCCAGGGACAGAGAGAGAACCGTACCTCACACAGGGACAAAGTACAGCAGGTGAGGAAGAAACTCTATACACCACCTGACACTGGTCAGTTTGATGCAGAACCACCCAACTATTGGGTTTAGCAAATTATTTTCCTGTCATGTTGCATTCTTTATCACATGAATACACAGAGGAAACTTGACTTTTTATCTGTGTGTTTGTGTAGAAACGTTCAAGGAGTATGTGTCGAAGATCTGCCCCAACAGAAAGCTCTGCCGATGGTCCGGTTGCCCATGTGAGAACTCGCAGAAGTCGCAGTGCACACAAAGAAAGAGATGGAGAAAGATCGGTAAGAAAAAGCATGCTTTGATTATAGATTATTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13366
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 |
|---|---|---|---|---|---|
| ENSDART00000111894 | Nonsense | 1471 | 1823 | 3 | 11 |
| ENSDART00000132229 | None | None | 302 | None | 6 |
| ENSDART00000137258 | None | None | 36 | None | 3 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 44729117)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 42681899 |
| GRCz11 | 8 | 42688686 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTRAATGTAGGGTCAATTGGAGATTCAGTTTCTTCTCCCCCAACACCAT[T/A]ATCTAGAAAAGAAACTTCAAGACCCAGAAGTCAAGCCTCAGCCCTGTCTG
Long Flanking Sequence:
CCAAACCCAACCTATGTCAAACGCATATGCTACAGAAAAACCTAGGCCACAACCTCACTCATTAATTGACACCTCAGATTGGGCCTTTGGCGCTCAGCAATCCATCTCAGCTTTGCCACCTGATCAAACCAGTGTTTGGGCTCATTCTGAAACAGAGTTGACTGTAGATGAACCTCTTTGGGTATCACCCATGGAGGGATCCAGAAGGCCAATTAGCACCAGACCAGGTGGTTTTGAGCAACAATTTTTGCGGCCAGAGGATAGAGGTTTAAGTAACATTTTGGCGCCCAGTTCAACCTCTTGCATGGGTCCAATCTTTACTCCTGTACAGTATTCCACTCTTGCACCACCCATGGTTCAAATTCAAACCCCTATGATGACTGCACAACCAAATCTTGGACCCAGTGCAGCACCTATACTGGCTCCAGAGAGATGCTGGACCTCAGTACCTTTAAATGTAGGGTCAATTGGAGATTCAGTTTCTTCTCCCCCAACACCAT[T/A]ATCTAGAAAAGAAACTTCAAGACCCAGAAGTCAAGCCTCAGCCCTGTCTGTTTCTGATCCTATATGGACTCCAAACTGGGAGCTGGCTTCCCAGGGACAGAGAGAGAACCGTACCTCACACAGGGACAAAGTACAGCAGGTGAGGAAGAAACTCTATACACCACCTGACACTGGTCAGTTTGATGCAGAACCACCCAACTATTGGGTTTAGCAAATTATTTTCCTGTCATGTTGCATTCTTTATCACATGAATACACAGAGGAAACTTGACTTTTTATCTGTGTGTTTGTGTAGAAACGTTCAAGGAGTATGTGTCGAAGATCTGCCCCAACAGAAAGCTCTGCCGATGGTCCGGTTGCCCATGTGAGAACTCGCAGAAGTCGCAGTGCACACAAAGAAAGAGATGGAGAAAGATCGGTAAGAAAAAGCATGCTTTGATTATAGATTATTATTTGGGTTTAGTATTTGAATCACCATTTCTTTAACCTACGGCAAAGTGA
Associated Phenotype:
Not determined