ZMP
si:ch211-263m18.3
Ensembl ID:
ZFIN ID:
Mouse Orthologue:
Ank1
Mouse Description:
ankyrin 1, erythroid Gene [Source:MGI Symbol;Acc:MGI:88024]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37288 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa917 | Essential Splice Site | Available for shipment | Available now |
sa15660 | Nonsense | Available for shipment | Available now |
sa18669 | Essential Splice Site | Available for shipment | Available now |
sa37287 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12882 | Nonsense | Available for shipment | Available now |
sa37286 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37288
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 |
---|---|---|---|---|---|
ENSDART00000065998 | Nonsense | 215 | 1923 | 6 | 42 |
ENSDART00000144361 | Nonsense | 186 | 1672 | 5 | 41 |
The following transcripts of ENSDARG00000074777 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 19907666)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 21043155 |
GRCz11 | 21 | 21079791 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTATGGCACCAAAGGAAAAGTGCGTCTGCCGGCTCTACATATCGCAGCA[C/T]GAAACGACGACACACGCACCGCTGCCGTACTCCTCCAGAACGACCCAAAC
Long Flanking Sequence:
TTAATCGAGATTCAGTCCAAGATTACAGTGAGATTAATCTAGGTTAAAAAAGTAATCTATGCCCACCTATAGTAATTACCTACTGTAACTAAAGTTCAATATCACTTTAATGTCATAATGTGACGTCCATACAATGTCAAAGGCTAACATCATAAGCAAAAATTCATTTTGACGTTGAAGTCTAACCTCAAACTGACATTAGGTTCTGACGTCAACTTGATTTTCATATACAACCAAAATTCAAGGTTAGTCTGACATTGGAGTCTAATGTCAATTTTACGCCTGTGTGACGTCTGGTGTCTGCTGGGTACATGTAAAAATTTGTACTGTAAATAACCAGGATATCACTACTATAATTTACAACTCTTGATCTCTCCCTCCAGGACGGCTTTACTCCTCTAGCAGTAGCTCTTCAGCAGGGTCACGAAAATGTGGTGGCGCTCCTGATAAACTATGGCACCAAAGGAAAAGTGCGTCTGCCGGCTCTACATATCGCAGCA[C/T]GAAACGACGACACACGCACCGCTGCCGTACTCCTCCAGAACGACCCAAACCCAGATGTCCTCAGCAAAGTATGTGTGCTTCTGCAGGATTACGCATCATGACTCACTGAGCTCAGTGCAGCCGCTCTTGGCTTGTAATTGCAGTGATGAGTATGTGACAAGATAAACAGAACTGACTTTGTTTAGATATCCGTCAGCGTAGGTGTTTTTGTTTTGTACATATACTGAATCAATGAAATGCTACACTCTATTCCGACAGACCGGATTTACCCCTCTCCACATCGCAGCTCATTATGAGAATCTCAGTGTCGCGCAGCTTTTGTTAAACAGGGGAGCCAATGTGAACTTCACACCCAAGGTCAGTTCAACTCTAATGTTAAATGCTGCTTTATAATAGATAGACTACTTGCACAATTTCTCACTTTGTCTTTTTTATTTAAGAATGGCATCACTCCATTACATATCGCTTCCAGGAGAGGGAATGTGATTATGGTGCGGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa917
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065998 | Essential Splice Site | 765 | 1923 | 19 | 42 |
ENSDART00000144361 | Essential Splice Site | 733 | 1672 | 18 | 41 |
The following transcripts of ENSDARG00000074777 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 19893064)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 21028553 |
GRCz11 | 21 | 21065189 |
KASP Assay ID:
554-0823.1 (used for ordering genotyping assays)
KASP Sequence:
GGTGAAGTTCTTACTCCAGCAGCAAGCWCACGTAAACAGCAAGACAAGAG[T/C]AAGTGTTCTACTTCTGGATGCATCATACACAGGCCTTTTCAGTGTTNNNN
Long Flanking Sequence:
CTGAAGAAAAAAGTCACCTACGTCTTCAATGGCCTGAGGGTGAGTAAATTAACTGTAAATTAAATATTTTTAGGGAACTGTCACTTTAAACATGAAATTCCTCCAGTGTATGGTGTAAAGTTTTAGGTATTATTCATGTATGTGTTGTTAACAATTTGTCTGAATATAGAACAAACTCTATCAGCATAGTAATGATATTGCTTGTTCTGGCAAACAGAGCTACTACAGATTTTATGAGATGTATTAAAATTCATCTGTGACCTTTCACCTTTTCATTATTCATTCTTCACATATTAAAATGCCACTGATCATCTATATGCATTGGAAGTACTCATTTCTTCATTCACTTCCTTTCTTTTATCATTTACACCCTTTTAAACCTCTCACTTTTCTCTCTTAGATGGGCTACACACCCTTACATGTGGCGTGCCATTACGGGAATATAAAGATGGTGAAGTTCTTACTCCAGCAGCAAGCTCACGTAAACAGCAAGACAAGAG[T/C]AAGTGTTCTACTTCTGGATGCATCATACACAGGCCTTTTCAGTGTTTCAGTGTGTACATTACGCACTTTTGCATTCTCTTTTTCCCTCATCTTCCTTTTTCAGTTGGGATACACTCCTTTACATCAAGCAGCCCAGCAGGGGCACACAGACATCGTCACCCTGCTGCTGAAACATGGAGCTCTGCCCAATGAGATCACCACTGTGAGCGGACCCTCTTACCTATACTTGAAATACAACCATTTTTACTTGCAAATAAATAAATAAAACATTGTATGAATGGTTTGTTCTCTTAAACAGTCCTGCTTTAACACATTTTTTTGCAGTAAATGCAAGCTGTTATTGAAAGGTTATAATCTTTAAAACCTTTTATAGTGCATATACTGTTATAATATAAGTTTATTTTCATTTCGTTTTATATACAATTAGATTTAAAGTGCAATAAGTTCCAAATTAATTTAAAAGGTTGAGCTAAGTATGTTGTTAATTGTAGCCCTCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15660
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 |
---|---|---|---|---|---|
ENSDART00000065998 | Nonsense | 914 | 1923 | 24 | 42 |
ENSDART00000144361 | Nonsense | 853 | 1672 | 23 | 41 |
The following transcripts of ENSDARG00000074777 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 19885226)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 21020715 |
GRCz11 | 21 | 21057351 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCWCCTGCRATTCCCAGAATTCCATGCGTGTCACCTGAAACTGTCATGT[T/A]GGACCAGGTAKAGTTGTTTTCTGTGTTATGTGCTGTAATAAGAAWTGCTT
Long Flanking Sequence:
TTCATGTTTTCCATTGGCTATGTACATATGTGTGTGTGTATGTGCTTGGACCCGGTGAACGAGTGAAGTGATGTTTGTGCTCGATTGGGAATGATGGTGGATTGCGAATGCTGAAATAACTTCTGAGCTTCTCTTCCTTCCTGTTTTTGTTCCTGCCAGTCTCTCGTATCAGTGTGTGTGACATATATTTTGTGCCGTATGTAGGTGATGAACTCCTCGGGATGGATGGGGCTCGCTATTTGAAGCTGGATGACCTGAAAGACCAGGATGATGATTTTTTGTCGCCTAAGAAAACCCTTAGAGACTTTGAGAGCGGGATGGGCACCACGTAGGTCACAACTTTAGAGCACAATCAAATCAAAGCCTTTTGGCTAAGATGCTAGAACCATCTCTTTAAAATAAAGTGATGAGTCAGATTATAACTATTTTCGTCGTTCTCTCCAGACCGTACTCACCTGCAATTCCCAGAATTCCATGCGTGTCACCTGAAACTGTCATGT[T/A]GGACCAGGTATAGTTGTTTTCTGTGTTATGTGCTGTAATAAGAAATGCTTCTTGCAGAAAGATATTTGTCTAGTGAACTTAGTTTCATTGCTTGGTTTCTGGCAGCATTTATCAACAGTTTGACAGCACCTACTGTACTGTTCACAACAACAATAAATATAATAATAATAATAATAATAATAATAATAATAATAATAATTCCTTACGTTCATATAGTGCTTTGGACACTTAAAGGGCTTTACACATTGCGGAGAATCTCCTCATCCACCACCAGTCTGCAGCATCCACTTGGATGAGGCGACGGCAGCCTAATTGCACCAGACCGCACACCACACACCAGCTGATTGGTGGAGAAGAGACCGAGTGATGAAGCTAATTATGATATAGGGATGGTTAGGAGGCCATGATGGACAGAGGCCAGTTGGCAAATTTGGCCATTTGGGATTTTTAACGACCACACGGAGTCTCACCAGAAAGTTGGTGTTTATTGAGTCTTCATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18669
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065998 | Essential Splice Site | 1220 | 1923 | 29 | 42 |
ENSDART00000144361 | Essential Splice Site | 1159 | 1672 | 28 | 41 |
The following transcripts of ENSDARG00000074777 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 19877171)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 21012660 |
GRCz11 | 21 | 21049296 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTGGAGAGGGGGACRCCACCAGYCTCCGMCTCCTCTGCAGTGTTATTGG[T/A]ACAGTCCGAYTCTCATYCATTTCAAAGCAAACATTRTYTGAAAATGATAT
Long Flanking Sequence:
AGCAATGACTTGGAGGAGAGGGGCACAACAAAGGCCAAACCGATTTAAAAGGGGGCCGGTCCCCCTGTGGCCCCACCTATAGATATTACTCTGATATTACCTAAAGAAGAATAAAATGAATGTATGTATTATAAATAGCTGTAATAATTATTATTATCAGTTTTAAAAATCTGTTCTAAGGTCAGTGCAAAAATAAAAGAGACTTAAAGGAGACTTAAAAATAAAAAAAACTTGAACTAATCTCATTATTAAATGAAAAATTAATCTTTTGTTTCTTCTCTTGTCATCACCCAGGCCCAGCCAATTCCAGATGAGCTGCTGACTCGGCAGTTAGGAAACCAGGCCACATTCAGTCCCGTTGTGACAGTAGAGCCTCGTCGGCGCAAATTCCACCGCCCAATCGGTCTGCGCATCCCATTACCTCCATCCTGGAGGGAGAGTCCACGAGACGCTGGAGAGGGGGACACCACCAGCCTCCGCCTCCTCTGCAGTGTTATTGG[T/A]ACAGTCCGATTCTCATCCATTTCAAAGCAAACATTGTCTGAAAATGATATCTGTGATCTGGAGAATGGCAGTTTTTCCTGAACGCCAGTCTTTTTCAGCCTTTTGTTTTCTGCCAAGCTGCTTGGATAAGGGCTGAAACAGACTAGTGTCCTGCCTGGAGAGGGACACTGGGATAAAGATAGATTTAGCAAGTTCATTCCAGATGGTGTTGGTTGCAAAAAAAAGGGATTTTATAAAAAGCTGTAAACTTTCTGCAGGTGGCACTGCTCCTGCTCAGTGGGAAGACATCACTGGCACTACCAAGCTCATGTATTCCCACAACTGTGCCAACTTCACCACCAATGTGTCCGCAAGGTGAGAGATAAAAGCACTCAAGGGCACACCGGGATCAATTTATTGAACAGTAAAACTAATTTTTGCATGGTGTTTTACACAAAAACATGCTAATTTATTGTTTTTTATTATCTTTTAAGCAATTATAAACTGTTTTAACCAATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37287
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065998 | Nonsense | 1377 | 1923 | 33 | 42 |
ENSDART00000144361 | Nonsense | 1320 | 1672 | 32 | 41 |
The following transcripts of ENSDARG00000074777 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 19872113)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 21007602 |
GRCz11 | 21 | 21044238 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCCTCTGCCTCTCCATTTCCCCTGGCTCGTCAGGTGAGAGATGCTAAT[A/T]AGGAAGCCAGTGGGTTCCTGTCCTTCCTACGCAAGTCCACCAAGTATGAG
Long Flanking Sequence:
AGCTGTCTGTCTGTCTGTCTGTCTGTGTCTCTGTCTGTCCTCTTGTCTTCTTCATCTCTTCATCTGTGGTCGTGGCTTCACTCTGTCAGCCTCAGACGAGCTGCTGATCTGTGCTGTGGTGTAGTAATAGTTGTATTAGTGTCGTGCGCATGCCCTTAACTCTTTCACCTTCTAGCCTGCCCGCCCGCCTGTCCGTATGTCTGTCTCACTGTCTCTCTCTCTCTCACTGTCTGATCTCACAGACGGCCAGGTAAAAGTGAAGGTAAATCTCTCTCTCTGTCTCTCGCCTGCCTGTGGACTGCTTCCCTCCATCCCCTTCCCTGCTCCCCTGTTTGAGTCTCAGCCGCCAGCTGCTCTGTCTAACACTCTTTTTTTGGTCTTTCTCTTTCTCTTCATTCATTTCCCCCTCTTTTGTTCTCCCGTTTGCATCCGGTTCTCCTCTCCCCATCTGTTCCTCTGCCTCTCCATTTCCCCTGGCTCGTCAGGTGAGAGATGCTAAT[A/T]AGGAAGCCAGTGGGTTCCTGTCCTTCCTACGCAAGTCCACCAAGTATGAGGACACGCAGCACGTCCTGTGTAACCTCAACATCACCATGCCTCCCTGCGTCAAGGTGACGTACATCACTCATACTTGTGCATCAACTCATAAAAACACTGTTTTTTTCTGCATGCCACTTTTAGGGGATTTTGGCTTGGAGCATTTTGGCTTTTTTCTGTCAGACTAAAAAAAAATAATTTAATTATATTTGTAAAAAATAGATTCTTTAATCTGAGCTGTTGACTTGGTTAATTAATTCTATATATATTATATAAAAGTTTACCATTTAAAAACACCAAAAAAGATTCAACAAAATTAAGTGGTTTATAAAATCCTTGATTTTTCTCTTTGCCCAAAAATAGGCACCCACAAGAAATGGAGGGGGAAATATTCAAATTCAAAGCATTTTTAAAAAATTTGTCCATTCATTCATTTTCTTTCCGGCTTTATCCTTTTATTAATCTGGGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12882
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 |
---|---|---|---|---|---|
ENSDART00000065998 | Nonsense | 1699 | 1923 | 38 | 42 |
ENSDART00000144361 | None | None | 1672 | None | 41 |
The following transcripts of ENSDARG00000074777 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 19856951)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 20992440 |
GRCz11 | 21 | 21029076 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAGACGACATACAGCACGAGCCGGTGTCTGCRAGTGCAGAAAAAGCATG[G/A]GCCAGCGGTGCYGTCCCAAAGGCTAACTATAATGGGCAGGCTGGAGGTCA
Long Flanking Sequence:
CCTTTTTGAGAGGGTCAAAACTCCCCTTGTTACCCCCACTCCTTCTGTGTGGTGTTAGCGTTGCCTTTCTTGTCTGGCCATTCCTCAGGTTACGGGCTGGTGCAGGAGGAGCTGCTCTCCCCCGCTTCCATGCAGTATAGCCTGCCTTCTCCGCTGGGCGTCGAGCCCTACTGGCAGGAGGTGTCGAGCCTGGAGTGTGCGCCCATCGCCACCACTGAGGAGGACACCATGCTGGAGATGTCAGACGTGCAGGTATGGCCAGCAGGGGTCAGTCCATCCCTGGTGACTGTCGAGGACTCGTCACTGGATGGTAGCAGTCGTGCAGATGACTCAGAGGGCAACACGTTGAGCTTACCCTGCAGCAGTTTGGGAAGGCCTAGCAGCGGAGCCAGTGGGGCAAGTGGCTCCATAATGGAGCTGGAGGAGGAGGAAGAGGAAGAGGAGATTGAAGAAGACGACATACAGCACGAGCCGGTGTCTGCAAGTGCAGAAAAAGCATG[G/A]GCCAGCGGTGCTGTCCCAAAGGCTAACTATAATGGGCAGGCTGGAGGTCAGAGGTCGGAGGGCAAGAGGACAGATGCGGCGGCGGGCAGCAGTATGACAAGTGTAGCTAGAGGAGGAGGAAAGGGTGGAAAAGGGGCAAGTTCAGAGGAAAAGTTTTCTGTTCTTACAGGGCAGCAGCTCTATGCTCAGTTGTGCGAGAGAACCGGACTGACCCGATCCCTAGAACACAATGGGGACAGGTATGGATCATGTTAGTATAGCATGTTATGCTGCAATTATTAAGGCTCGTTCACACCAAGAACGATAACTATAGCGTTTACGCCATTGTGTCCACAACAGTGCAACAATTTGGCCAACCAAAATCAGCAACTTTCTTTACCTCATGCAAAATTCCCAGTTGTGCAGATTTCTTTTGGAGTAACAGTGACCAATGTGGCTGCAGCTTAAAGTTATTGTTCTATTTGTTGTTGGTGTGAACGATCCTTTAGACAACAAGTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37286
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 |
---|---|---|---|---|---|
ENSDART00000065998 | Nonsense | 1819 | 1923 | 39 | 42 |
ENSDART00000144361 | Nonsense | 1568 | 1672 | 38 | 41 |
The following transcripts of ENSDARG00000074777 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 19856302)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 20991791 |
GRCz11 | 21 | 21028427 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCCAGGCAGACCATGGAGACCATGATGTCATCGTCCCCGGACCACAAT[C/T]AGTCACGTGTAGCACAGGAGGCCCTGCTTACACCGGTATGTGATACAGGC
Long Flanking Sequence:
AAAAGTTTTCTGTTCTTACAGGGCAGCAGCTCTATGCTCAGTTGTGCGAGAGAACCGGACTGACCCGATCCCTAGAACACAATGGGGACAGGTATGGATCATGTTAGTATAGCATGTTATGCTGCAATTATTAAGGCTCGTTCACACCAAGAACGATAACTATAGCGTTTACGCCATTGTGTCCACAACAGTGCAACAATTTGGCCAACCAAAATCAGCAACTTTCTTTACCTCATGCAAAATTCCCAGTTGTGCAGATTTCTTTTGGAGTAACAGTGACCAATGTGGCTGCAGCTTAAAGTTATTGTTCTATTTGTTGTTGGTGTGAACGATCCTTTAGACAACAAGTGTTTACACTTTCTTTGTCTGTACCTACTCTCAGGCTCGGCAGCGGTGCCTTCCAGCCTTACTCGCAGGAGAAAGACTCCCTCCACAGCTGGTCTCAACCCAAACCCAGGCAGACCATGGAGACCATGATGTCATCGTCCCCGGACCACAAT[C/T]AGTCACGTGTAGCACAGGAGGCCCTGCTTACACCGGTATGTGATACAGGCCATTCGGAGGTCCTGCGGGGGCGTCTACTGGGCACTCAGCCCTTTGATAAAGGGCTGGGTTTCTCCCATCAGGAGGGGGAATTACGGGCATGGGACCAGGAAAGACGGAAGGCACAGGTGTGTCCCCTGAGCCTGTCCAGTCTGAGCAAAGAGCATGTTTTGGGCACGGTCTTGACTTGAGTTATTCAATAATGATAATTAATGCAAGCAATATTTTCTCCTTACAGAAGGATGATCCAGTAGATCTCAGCAGTGATCTTCTACATGAAGAGCAGTTCACTGATGAGCATGGGAATGTTGTGACCAAGGTGGGTCATCTCTTTTCTTTCCGATTCATAATAGTGTTTTGTGTAGTTGTTGTTGTTGAACGCAATGATTCAGTCAATTTGACCCCATCCTTCTTTTCTCCAGTTGGGTGTGGATGTGAAAAAGGATGTCCAGACCGTGAAG
Associated Phenotype:
Not determined