Busch Lab

ZMP

madd

Ensembl ID:
ENSDARG00000003495
Human Orthologue:
MADD
Human Description:
MAP-kinase activating death domain [Source:HGNC Symbol;Acc:6766]
Mouse Orthologue:
Madd
Mouse Description:
MAP-kinase activating death domain Gene [Source:MGI Symbol;Acc:MGI:2444672]

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa13587 Nonsense Available for shipment Available now
sa40945 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa12918 Nonsense Available for shipment Available now
sa40944 Nonsense Mutation detected in F1 DNA Not yet available
sa34115 Nonsense Mutation detected in F1 DNA Not yet available
sa40943 Nonsense Mutation detected in F1 DNA Not yet available
sa44670 Nonsense Mutation detected in F1 DNA Not yet available
sa34114 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa13587
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000047208 Nonsense 7 1641 1 35
Genomic Location (Zv9):
Chromosome 7 (position 35724071)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 34114039
GRCz11 7 34385189
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATGACTTAGAGACACTCCTGATACAGAGWTGGAGAAAAAGAAAATGTG[T/A]CCCCGCCTCCTGGACTACCTGGTGGTAGTTGGAGCCAGGTAAGSAAAGCT
Long Flanking Sequence:
AATCTACATTGCATAAGTGCATTAGAAATAAACATTAACTGAATTTTAACTTTTTGTTTCAGTTTATAATCTACATGTAAATGTGCTGCCTTATGTTGTGAGTTATGATTGATTGATAGAAAATAAAGCCTAGGGTTGTCACAGAGATATTTCAGAACTCTTTTTTTCAGTGATGCTGTCATGAAATAAGCATATTTTCTGTGCGCAATCCTATTAAAAATTCATTTACAGCACCTTTAAGCTTCACAGCTGCACAGAAGGCTTCATTTCTCTGCAGAGCCTTTTGCTGTGTGATGGATTGCTTCTATAATGTTCACGGCTTCTCTTTTTTAGACCTCATTCCTGCGCACCACAGGCCGAAATGATTGGACGCTGCCTGCCTCGTTCTGTCAACTCCTAGTTCTGCTGCACCTGATTGGTCGACTGGCTGTCTGAGAGCTACTACAGTTGCCATGACTTAGAGACACTCCTGATACAGAGATGGAGAAAAAGAAAATGTG[T/A]CCCCGCCTCCTGGACTACCTGGTGGTAGTTGGAGCCAGGTAAGGAAAGCTGTTTGGTGATGTGGGTGTGTTTGTATGTGTATGGCTCTGATGTATAGCTGCTTGAGTAAACTGCTGATGAATGAAATACAGATGAATGGATTATGTGGTTTGTTTGCATGTGACCTGAGCAGGTGCTTTTCAGGGGCTTGTATTCAGGTGTACATTGTTAAATGGGTTGTGTTAAATGGGTATCATGAATAAAGTTTGTTGTAGTTTTGACAGCAGGTGACGATATGATTAATAGGAAAAGGTGGAACCTATTGGAAATATGTTTGTACAGTTTTCAGATTGACAGCAGCAGAAGGTCCAGACTCATCACAGGTTGCGTTTACCAAAGACTGCCAATGTAAAACAGCTTTAGTTTTCACAAGACTATGTCTTGACCTTCACTTACGTTGGAAAATCCACTGTTTATTTGATCATTCAAGTGTTTCTAATTTCTAAATTACACTACCTGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40945
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000047208 Essential Splice Site 113 1641 2 35
Genomic Location (Zv9):
Chromosome 7 (position 35721859)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 34111827
GRCz11 7 34382977
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACCGCTCTTTTCAAAAGGCCCACCATCGCCCAAGAGCTGAAGGAAAAGG[T/C]TAGCGGTCACTTTGGTGCAGTATTGTACTGCTTTAATCCATGTGTTTTGA
Long Flanking Sequence:
AAAAAAAAAAAAAAAAAAAAAAAGAGCAACCATATTTCACAAATTGCATTTATTCTGAAGCACAGAAATAAAAACTTAAATGAGATATTTGAAAAAGAACACCAATCAAAAGAGAACAATTTCACAATCCATCCAGATATTGGTGTTAATCTGCTGGTGTCTGGAATAGCTGACAGAAGATTCCTGTCTCTCATTTAATTATTTTTCCCCTTTCTAATCAGGCAACCCAGCAATGACAGTGTGGCACAGACACCTCAGCTGTTGCGGCGTTATCCGCTGGAGGACCACAATGACTTTCCTCTGCCACCTGATGTGGTCTTCTTCTGCCAGCCTGAGGGCTGTCTGAGCATCCGTCAGCGGCGGGTCAGTCTCCGCGATGACACCTCTTTCGTCTTCACTCTCACTGACAAAGACTCGGGCATCACTCGCTATGGAATCTGTCTCAACTTCTACCGCTCTTTTCAAAAGGCCCACCATCGCCCAAGAGCTGAAGGAAAAGG[T/C]TAGCGGTCACTTTGGTGCAGTATTGTACTGCTTTAATCCATGTGTTTTGACCTAGTATTAGGATGGTGTTGTCCACTATAGTTTTGTCACCCTTATTGAACACCACAAATGAGTACATAACCTCTACCTTATATTTTCTACATACAGGAGAAAAGCCTGCTCATACAGACACTGCAGTGGAGGCCACAGAGAAATCTGACCCCTCCACTTTGACTCTTTCAGGGGAACATTCGGCGCCCCCTGCAGGAGATGGGACTTTGCTGCCAGGCGAGCCGGGTAGCAGCGGGAAGTCTCCGCGATCTAAACGCAGTGGCCGAATAGCACCACAGAACCGCAACAGCATGTTAACATCTCTGTGTATTCTGAGCCACTACCCTTTCTTCTCAACATTCAGAGAGTGTCTGTACATCCTCAAGCGCATGGTGGACTGCTGTAGTCAGCGGCTCAACCAGAGACCCGGAGCTCCCAAATCCACACAACGGTAAGAACAGCCTTTTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12918
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000047208 Nonsense 169 1641 3 35
Genomic Location (Zv9):
Chromosome 7 (position 35721544)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 34111512
GRCz11 7 34382662
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGGCGAGCCGGGTAGCAGCGGGAAGTCTCCGCGATCTAAACGCAGTGGC[C/T]GAATAGCACCACAGAAYCGCAACAGCATGTTAACATCTCTGTGTATTCTG
Long Flanking Sequence:
GTCTTCTTCTGCCAGCCTGAGGGCTGTCTGAGCATCCGTCAGCGGCGGGTCAGTCTCCGCGATGACACCTCTTTCGTCTTCACTCTCACTGACAAAGACTCGGGCATCACTCGCTATGGAATCTGTCTCAACTTCTACCGCTCTTTTCAAAAGGCCCACCATCGCCCAAGAGCTGAAGGAAAAGGTTAGCGGTCACTTTGGTGCAGTATTGTACTGCTTTAATCCATGTGTTTTGACCTAGTATTAGGATGGTGTTGTCCACTATAGTTTTGTCACCCTTATTGAACACCACAAATGAGTACATAACCTCTACCTTATATTTTCTACATACAGGAGAAAAGCCTGCTCATACAGACACTGCAGTGGAGGCCACAGAGAAATCTGACCCCTCCACTTTGACTCTTTCAGGGGAACATTCGGCGCCCCCTGCAGGAGATGGGACTTTGCTGCCAGGCGAGCCGGGTAGCAGCGGGAAGTCTCCGCGATCTAAACGCAGTGGC[C/T]GAATAGCACCACAGAACCGCAACAGCATGTTAACATCTCTGTGTATTCTGAGCCACTACCCTTTCTTCTCAACATTCAGAGAGTGTCTGTACATCCTCAAGCGCATGGTGGACTGCTGTAGTCAGCGGCTCAACCAGAGACCCGGAGCTCCCAAATCCACACAACGGTAAGAACAGCCTTTTTTTTTTCTCTCTTGTGGATTATGCAGTTATGTAACTGCACCCTGTGATTGAGCAAGATAATTCTTGTGCATGGAAGCGGTGGCTAATGAGTGCAGTGTTTTGCAATATCTGTGAGCTTCAGAGAGTGTCAAATACTGTGGTGGTGCTGCCAGAAGACGCTATCTCTTCCTCACACCATCACAACTGGCAACATTCTACCACTCTTTTTTTTTTTTGGTTGCTGTTACTATTTGCAATGCATTTTTTATGTGTGAGTCCTGGTGATGCAATGACATGGAAATTCTTGTCAGAAAAGAATTTGTCTACTGGACCCACTAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40944
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000047208 Nonsense 350 1641 5 35
Genomic Location (Zv9):
Chromosome 7 (position 35703597)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 34089409
GRCz11 7 34360559
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTATAACGCTCTCTCAATGAGCGTCATGGCGTTTGTTTCGATGATTTA[C/A]CCTCTTGAGTACATGTTTCCTGTCATTCCACTGTTGCCCACCTGCATGGC
Long Flanking Sequence:
NNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTATATATATATATATATATATATATATATATATATATATATGATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGTAAGTTCGATTCGATAAGTTTATTTGTAGCACTAAAAGTCTTTCACTTCAAAATTTTTTATTGACGAAGTAGAACGTGCTTTTAAAAAATACACCACTGCTGTGTCAAAGATTAGTTTAATGTTCGTCTGTAGGTCTGCTTGTTCAAGCAGAGCTATTCTTCATTGCTTTGCCTATGTGGGTCACACTGACATTAACAAGGAGACTTCCTCTCACCCTCTTCTGTGTGCAGGTGGTACTGCAGTCTCGAGATTATAACGCTCTCTCAATGAGCGTCATGGCGTTTGTTTCGATGATTTA[C/A]CCTCTTGAGTACATGTTTCCTGTCATTCCACTGTTGCCCACCTGCATGGCCTCTGCAGAACAGGTAAATGACGCATCATCTCTTTTCAGTCATTTAGTCACGTCAGTATATATGCAGTATGTACAAAAAGCTCTTCTTATTTCCTTCTGACACATCTTTCTTCTTTCTAGCTCCTATTAGCACCCACTCCATACGTCATTGGTGTGCCAGCCAGTTTCTTCTTGTACAAGTGTGATTTTAAGATGCCTGATGATGTTTGGTTAGTGGATCTGGACTGCAACAAGGTATAATCATCCATCTGAACTTATGAGGCTTATGATGGTATCAAATTGTGTGTTGAGATTGGTTGCTGAAGTTTTTAAACAGCATTATACAGTATTTTTACGCTACTGGCCTAAGCTGCAAATACTTCGTGTATTGCTTTATTGCATTTACATGTTCAGAGTAAACAAATGTCTCAACCAAATTAAATTGCAAAAATATTGTTAAGTAAAATTGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34115
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000047208 Nonsense 611 1641 10 35
Genomic Location (Zv9):
Chromosome 7 (position 35696978)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 34082790
GRCz11 7 34353940
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTCTACCGCGTGTATGATGGAAACTCTCATTTAGCGGAGGCCTTGAGT[G/T]GACCCCTGCAGGATGAGACCAATGATTCAGACCCAACAGACGACAGGTTG
Long Flanking Sequence:
TCATAACAGTAAGAGACATAGATTTATTTCATCCGTTCATCTTTAATACCCCTTTTCTGTAAACCCCTTTCATGTTTGACTGTCACAGTTCTCCCCCTAGTGGCAGTTTCAATGATTTTTCATGTTTTGTTTCTTAATGAACCAATAATAAGAGCATTTTTATTTATTTATTAAGGAGTAAATGAATAATAGTTTTAAAACACCCTTCTGAAGCTGAACTGAAATCTGTATGCAGAATTTGATGTCTGCACCCAGCCCCTTCTTTAGTTTGACCATTGTACAGGCAGATTCGCACTTGTCTGGATATACAGTTTCAATCTATGGACTGTCCATTATGTACTTCCCATTTTGTGTGTAGCCAGTAATGACACTGTGTGTGTTTTTCAGATGTGTATGACCCCTCTCTAATAGGCGATAAGCCTAAGTGGTATGCCCACCAGTTACAGCCAGTATTCTACCGCGTGTATGATGGAAACTCTCATTTAGCGGAGGCCTTGAGT[G/T]GACCCCTGCAGGATGAGACCAATGATTCAGACCCAACAGACGACAGGTTGAAAACACTACTTGCAGTGCTCACTAACATGCATAGACATTCACAGAAAGTCATGTAAACGCTATTGATTATTTTATTTACAAAACAAATCAAAAGCTTATAGACCGTTTTGACAAATTGTTTTTTACTTTTACTCAACATTAATGTATTTAAAATGATCAAAAATGAAAATTAAGACATTGTAGTGTTACAGATATGCTTTCGGTTTCAAATAAATTCTTTTTGAAATATATGGACAATTAAAACATTATATTTGTACTTTATTTTTGATCAAATAAACTGCCTTTAATAAAATAAGAGACTTCCTTTACAAACCATTGAAAGATAGTATATAATGTACATGCAGTTTTCTGTTTAATCCCCTTCAATTTGATTTATTGGTTTACATTTTTTATTTTAGTGGCAGCGACAGTGAAGCATATGATGACTCCAGCTCCTCCTACTCATCTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40943
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000047208 Nonsense 881 1641 15 35
Genomic Location (Zv9):
Chromosome 7 (position 35694187)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 34079999
GRCz11 7 34351149
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGCACCAGTTTCAGTCTGTCCAGCCTGGCTCTGCCTAATAAAGCGAGA[G/T]AGAAGAACACGCCGTTTCCCAGCCTCAAAGGTACACGCATTCCCTTGGAC
Long Flanking Sequence:
GGTTAGATTGCTGGTGTGGTTGGTGTGGAGGGTTATATTGGGTGTGATTTTTCAGATAATGACGCATGTCACTCTGTCTATATTCATCATAAAAATATATTAAAATATAAATAAAATATATTTCATAAAAAATTCCTGAACATTATTTGGTGTGCATAAGTTTTTGTCTTCACTATATATTAATATTTAACTTATAATGCTGAAATGTTTGGTAGAACAGTTTGATTTACAATCCAGTTTCTTTGTCCCTTTCCAATGTTAGTTCACTGTAAGTACACTAATTAATACAAAAATAAGTGCGACCAGATGTTTTCAGATGTGCATCATTGACTGCTGAAGGTTTGGACATAAAACCTTATTAGTATTGAGACTGAAATGTTTGGTATTTTGTGTCTATCACACAAAATGTATTCTCCCTGTTCTTGTTTACAGGTAACTTGTATAAAAACCATGGCACCAGTTTCAGTCTGTCCAGCCTGGCTCTGCCTAATAAAGCGAGA[G/T]AGAAGAACACGCCGTTTCCCAGCCTCAAAGGTACACGCATTCCCTTGGACCTCATCCCATGTGACCTCCTGCTCTTCCACTCATCTGACCGTCCTGTCTCATTCCTCCAGTCTAGTCCAGTTATCTTCTCTTATTCTTCTCTTTTTTCCCTCCAAACCCCTTAATCTGTCCTTTCCCTGTCTATACTATGGCATTGTAGCTAATGCTTTAAACTGTCCTGTTAGACTCAACTTGTACTAAGGTAATTTAAGGCACAGATTAGCAGATGCCAAAATAAAAGTAGACCAGAATGAATTGATGTAAATAGATTTCTTTAAGAAAGACGTTTAAAAAATGGAAACCATTAGATTTAGGAAGACATTTTCACTTTAGTTGACTGTTTATCTTTTTCTTTTTTCACTTTTTGTCCTCTTTTTCCATTATAATTTGTGTTATGTATTTTGTTTGAAGAATATTTTAATTTTGATTTAGCAGAGGACACAGATCAAGGTTTGTGGGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44670
Status:
Mutation detected in F1 DNA
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
ENSDART00000047208 Nonsense 1274 1641 24 35
Genomic Location (Zv9):
Chromosome 7 (position 35676443)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 34062264
GRCz11 7 34333414
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATAAAGCAGCACCTGCTCCACCCGTTGAGGATGTTAGCATGAGGATCTA[T/A]CTGTGTGAGGGGCTTCTGGGTAAGAATATATCCTCCTCTTTAATCCCATC
Long Flanking Sequence:
GTTGTTGGTTTCTTAATAGTTTGAATTGTACATTTAAATAAAGGGTGACCATTTTTTGTGTTCCTTTAAATGATTCTACTTCAAATGTTAATTTACAGTTTTTAGCCTACAGTTATACGTCTCTCTCTCTCTGAAATATGTTGATTTATGGTGATGTAAAGGCTTGTCAGAAAATGGCCACTGTTATAGTTTTTTTTTTTAATGGAAGACTAAAAGTGTCAGCGTCTCCTTGCTGCTTTGTGACTTGCAAGATGTTATGGTAAAAGACTATATAATGATGTTTTGATAAAAATATAAAAGATACATTTAAATGTTCAAATTTAAGCTGAAATTGGAACTATTGAAGGATTAAATTAATATTTTAAATAATTCAATTAATTTATTTTATGCTTGATCATGTAGGGCAAGACACACAAGCTGAAGCCAGGAGTGAAGGAGCCTGTTGGTGTTAATAAAGCAGCACCTGCTCCACCCGTTGAGGATGTTAGCATGAGGATCTA[T/A]CTGTGTGAGGGGCTTCTGGGTAAGAATATATCCTCCTCTTTAATCCCATCAGCGGTCCTCTCCTTTTATTCATTTTATTTTGTTCTTGCTTTCTTTATTTTTTTCTTCTTTCATGTCCATTCTCCTAACTGATTTAGTAATCAACTTATTGTCAACTCAATAATGATTATTAACAATGTGGTGCTTTCAAAAATGGCCTCTGTTGGCTTTCCTTTATTTTAATCTTTAAAATATGTAATACTGTCCTCACAGAGTACTCTTTTAGAGCTGTCTTTTTTCAAATGATGGCATCAGATAATTCAGCATATCATGCTTGAGCACTACAAAGTCCTCTGTTAATTTGCTCATTAACTCTAAATGTGTTCTTGTTTTAACCAGTGTTGATGACTTATTGGTTTGCAAATCTCTGACAGCTTAAAGCTTTGCTTCTAACGCTCTCTTTCTAACACTTTTTGTGCCTTCTGCTCTGCGGCTACCTCCTTTCCCCTCTTCTCTCCTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34114
Status:
Mutation detected in F1 DNA
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
ENSDART00000047208 Essential Splice Site 1342 1641 26 35
Genomic Location (Zv9):
Chromosome 7 (position 35674721)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 34060542
GRCz11 7 34331692
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACGGGAAGGAATGGGAATGGATCAGGGACCACAAGAAATGATTGACAG[G/A]TTTGTGTGTGTGTTGTTAAGTGCCTGCAGGAGTTATCATGCAGCAACGAA
Long Flanking Sequence:
TACAGCTTTACATTTTGCTAATCTCAGAATTTTAAGATGTCATAAAGCAATACCTTTTTCTGTCTTGCAATTTCATGTTTATAGTCTATAAAGTTCAGTTGCAAGATGTAAAATAACAGTTCTAAGAAGTCTGAATTGTAAAATTATTTTTGCAGGAGGAAGGAAAGTTAGGATTGAAAGATAAAAATCTGTGTTTACCTTTTTTATTTCATGGCTGAAACAAGCTTCCATAGCATTTGGGTGCCTGAGGTTTCTTTGTTAATTCATTTTATAAAGGGTGCTTACTGTAATACTCTACATATTGTCATTGTCTATTCTGGCATGTTAAACTGAAGTGCCGTTTTCCTCAAGTAAAGAGTGTAAACGTGTGTATGTGTAGGTAAAGAGCGCTCAACTCTGTGGGATCAGATGCAGTTCTGGGAGGACGCCTTCCTGGATGCCGTAATGCTGGAACGGGAAGGAATGGGAATGGATCAGGGACCACAAGAAATGATTGACAG[G/A]TTTGTGTGTGTGTTGTTAAGTGCCTGCAGGAGTTATCATGCAGCAACGAAAGCAACAAATAACCACGAAATGGAAAAAGCCCAACATGAAATTGATCATTCATAATTGTCTGCTTTCAAAAGTTTGCATACCTTGATGATAGCGTACTAAGCGTATTACAGAGTTCATACTTACAAATTACAGCCATCTGAAAATGTTGAAACATTTTCCATATGTTCTGTTCTTCAGGAAAGTAGTGGAGTGTTTTTAACCAGCCTTGAGCTATAAGCTTTTTGGTCATGCTAGGGTTTAGATGTAAACTGTGATGCTCTGTTTTGATTAGTCTGTCCAAATACGACTGTGCTGTTTTATTTTCTCTCAGGTATCTTTCTCTGGGAGATCATGACCGCAAGAGACTGGAGGATGATGAGGACAGACTGCTGGCCACGCTTCTGCACAATATGATTGCTTACATGCTTATGATGAAGGTATCAACAAGCACAGTTTCATTTCTTCACATA
Associated Phenotype:
Not determined