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Donor Profile : Donor 5492

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Retired Donor

This donor is no longer active in the program. The number of vials available represents the remainder of the donor's inventory.

Donor ID: 5492

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Meet The Donor

Talk may be cheap, but Donor 5492 is all action. He's creative, fun, and sweet, balanced with a relentless determination. He went to college on scholarship and is an avid drummer!

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Genetic Testing Performed: Please review the list of genetic tests performed before choosing a donor because donors have different levels of testing. Genetics is very complicated and testing can only reduce but not eliminate the risk of a donor being a carrier of a particular condition.


Any potential new health information will be indicated here. Please check periodically for medical updates. This profile is current as of:
April 19, 2024 6:10 PM EST


Document ID: 8859547A55C46244485F7A3D27A91E6AD5AE3EDAB01A7A9B18741B1FC60AF568

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Donor's "Name": Phillip

Year of Birth: 1997

Marital Status: Single

Number of Children: 0

Occupation:
(last reported) Actor/Student

Education: Bachelors, Animation

Blood Type: A +

Nationality:
(self reported) Maternal: Barbadian
Paternal: Spanish

Race: Black Or African American

CMV Status: NEG
Learn More

Last Medical History Update: 09/21/2023

  • Reported Pregnancy/Birth
  • xyIdentity Disclosure
  • Available Inventory
  • Retired
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ADDITIONAL DONOR DETAILS

  • Height:
    5'11" (180.34 cm)
    Weight:
    162 lbs (73 kg)
    Eye Color:
    Brown
    Hair Color:
    Black
    Hair Texture:
    Thick
    Hair Loss:
    None
    Hair Type:
    Average
    Body Build:
    Large
    Freckles:
    None
    Skin Tone:
    Brown, Medium

  • Over the years, Xytex has expanded genetic testing of donors as genetic knowledge and technology have advanced. As a result, not all donors have been tested for the same conditions or with the same methods. For more information about genetic testing view our Genetics FAQs.

    This donor has been evaluated for carrier status of the listed conditions. A negative result reduces, but does not eliminate, the likelihood of the donor being a carrier. If you are a known carrier of a genetic condition, please use the advanced search features to find donors who have tested negative for the condition(s) that you carry. Click the relevant link below to download the donor's test reports to share with your physician and/or genetic counselor.

    This donor's carrier testing included 47 genes.

    21-Alpha-Hydroxylase-Deficient Congenital Adrenal Hyperplasia (CYP21A2)
    No disease-causing mutations detected
    3-Phosphoglycerate Dehydrogenase Deficiency, PHGDH-Related (PHGDH)
    No disease-causing mutations detected
    Abetalipoproteinemia (MTTP)
    No disease-causing mutations detected
    Alpha-Thalassemia
    Normal complete blood count and hemoglobin analysis; does not exclude silent carrier status or alpha thalassemia minor
    Alport Syndrome, COL4A3-Related (COL4A3)
    No disease-causing mutations detected
    ANO5-Related Disorders (ANO5)
    No disease-causing mutations detected
    Arthrogryposis, Mental Retardation, and Seizures (AMRS)
    No disease-causing mutations detected
    Bardet-Biedl Syndrome, BBS2-Related (BBS2)
    No disease-causing mutations detected
    Beta-Thalassemia
    Normal complete blood count and hemoglobin analysis
    Bloom Syndrome (BLM)
    No disease-causing mutations detected
    Canavan Disease (ASPA)
    No disease-causing mutations detected
    Carnitine Palmitoyltransferase II Deficiency (CPT2)
    No disease-causing mutations detected
    Chromosome Analysis (Karyotype)
    Normal male karyotype
    Cohen Syndrome (VPS13B)
    No disease-causing mutations detected
    Combined Malonic and Methylmalonic Aciduria (ACSF3)
    No disease-causing mutations detected
    Congenital Amegakaryocytic Thrombocytopenia (MPL)
    No disease-causing mutations detected
    Congenital Disorder of Glycosylation Type 1a, PMM2-Related (PMM2)
    No disease-causing mutations detected
    Cystic Fibrosis and Other CFTR-Related Disorders (CFTR)
    No disease-causing mutations detected
    Dyskeratosis Congenita, RTEL1-Related (RTEL1)
    No disease-causing mutations detected
    Ehlers-Danlos Syndrome, Type VIIC (ADAMTS2)
    No disease-causing mutations detected
    Familial Dysautonomia (IKBKAP)
    No disease-causing mutations detected
    Familial Hyperinsulinism and Other ABCC8-Related Disorders (ABCC8)
    No disease-causing mutations detected
    Fanconi Anemia Type C (FANCC)
    No disease-causing mutations detected
    FKTN-Related Disorders including Walker-Warburg Syndrome (FKTN)
    No disease-causing mutations detected
    Galactosemia, GALT-Related (GALT)
    No disease-causing mutations detected
    Gaucher Disease (GBA)
    No disease-causing mutations detected
    Glycogen Storage Disease Type Ia (G6PC)
    No disease-causing mutations detected
    Joubert Syndrome 2 (TMEM216)
    No disease-causing mutations detected
    Maple Syrup Urine Disease Type 1A (BCKDHA)
    No disease-causing mutations detected
    Maple Syrup Urine Disease Type 1B (BCKDHB)
    No disease-causing mutations detected
    Maple Syrup Urine Disease Type 3 also known as Dihyrolipoamide Dehydrogenase Deficiency (DLD)
    No disease-causing mutations detected
    Mucolipidosis Type IV (MCOLN1)
    No disease-causing mutations detected
    Multiple Sulphatase Deficiency (SUMF1)
    No disease-causing mutations detected
    Nemaline Myopathy 2 (NEB)
    No disease-causing mutations detected
    Nephrotic Syndrome, NPHS2-Related also known as Steroid-Resistant Nephrotic Syndrome (NPHS2)
    No disease-causing mutations detected
    Niemann-Pick Disease Type A/B (SMPD1)
    No disease-causing mutations detected
    Niemann-Pick Disease Type A/B (SMPD1)
    No disease-causing mutations detected
    Polycystic Kidney Disease, Autosomal Recessive (PKHD1)
    No disease-causing mutations detected
    Retinitis Pigmentosa 59 (DHDDS)
    No disease-causing mutations detected
    Sickle Cell Disease
    Normal complete blood count and hemoglobin analysis
    Smith-Lemli-Opitz Syndrome (DHCR7)
    No disease-causing mutations detected
    Spinal Muscular Atrophy (SMN1)
    No disease-causing mutations detected (2 copies detected)
    Tay-Sachs Disease also known as Hexosaminidase A Deficiency (HEXA)
    No disease-causing mutations detected
    Tyrosinemia Type 1 (FAH)
    No disease-causing mutations detected
    Usher Syndrome Type IF (PCDH15)
    No disease-causing mutations detected
    Usher Syndrome Type IIIA (CLRN1)
    No disease-causing mutations detected
    Wilson Disease (ATP7B)
    No disease-causing mutations detected
    Zellweger Spectrum Disorder, PEX2-Related (PEX2)
    No disease-causing mutations detected
  • Medication Allergy:
    No
    Food Allergy:
    No
    Pet Allergy:
    No
    Hay Fever Allergy:
    No
    Insect Allergy:
    No
    Vaccine Allergy:
    No
    Healthy Teeth:
    Yes
    Braces:
    No
    Back Problems:
    No
    Bronchitis:
    No
    Chicken Pox:
    No
    Chicken Pox Age:
    Vertigo:
    No
    Eyesight Correction:
    Yes
    Near or Far Sighted:
    Farsighted
    Skin Infection:
    No
    Gallstones:
    No
    Removed Gall Bladder:
    No
    Hernia:
    No
    Mumps:
    No
    Measles:
    No
    Measles Age:
    German Measles:
    No
    German Measles Age:
    Sinus Infection:
    No
    Stomach Ulcers:
    No

  • Skills, Hobbies and Interests:
    Acting, drumming, skateboarding, weight training

  • In School:
    Yes
    Is the donor currently enrolled in or does the donor hold an undergraduate degree?
    Yes
    Degree Earned/Working towards:
    Bachelors
    Degree Status:
    Currently enrolled
    Major:
    Animation
    Minor:
    N/A
    Is the donor currently enrolled in or does the donor hold a graduate degree?
    No
    Is the donor currently enrolled in or does the donor hold a post graduate degree?
    No
    Is the donor currently enrolled in or does the donor have any specialized training (Including Military, Police, Firefighter, EMS, Real Estate, etc.)?
    No

  • The following medical conditions apply to the donor and his BLOOD RELATIVES ONLY (grandparents, parents, aunts, uncles, cousins, brothers, sisters, nieces, nephews and children of the donor).

    If a donor answers "yes" to any high-risk question on his Medical History Questionnaire, the donor is ineligible.

    Autoimmune Diseases Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    CREST Syndrome X
    Lupus X
    Scleroderma X
    Sjogren's Syndrome X
    Blood Diseases Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Anemia X
    Fanconi Anemia X
    Hemophilia X
    Immunodeficiency X
    Leukemia X
    Sickle Cell X
    Thalassemia X
    Von Willebrand's disease X
    Cancer Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Cancer (Breast) X
    Cancer (Colon) X
    Cancer (Leukemia) X
    Cancer (Lung) X
    Cancer (Other) X
    Cancer (Skin) X
    Lymphoma X
    Melanoma X
    Prostate X
    Tumor X
    Cardio Vascular Diseases Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Congenital Heart Disease X
    Heart Attack X
    Heart Disease X
    High Blood Pressure X
    High Cholesterol/Triglycerides X
    Stroke X
    Cardio Vascular (Other) X
    Congenital Malformations Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Deviated Septum X
    Malformations (Cleft Lip) X
    Malformations (Cleft Palate) X
    Malformations (Club Foot) X
    Malformations (Hypospadias) X
    Malformations (Other) X
    Malformations (Polydactyly) X
    Undescended Testicles X
    Gastro-Intestinal Diseases Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Gallstones X
    GI (Crohn's) X
    GI (Diverticulitis) X
    GI (Other) X
    GI (Pyloric Stenosis) X
    GI (Ulcerative Colitis) X
    GI (Ulcers) X
    Hemochromatosis X
    Hepatitis X
    Kidney Disease Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Adrenal Hyperplasia X
    Born with 1 kidney X
    Kidney (Other) X
    Kidney disease or urinary tract disorder X
    Kidney Disorder X
    Polycystic Kidney Disease X
    Progressive Kidney Disease X
    Mental Health Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Anxiety disorder X
    Mental (Depression) X
    Mental (Manic Depressive) X
    Mental (Schizophrenia) X
    Mental Retardation X
    Obsessive-compulsive disorder X
    Metabolic/Endrocrine Dis. Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Diabetes (Insulin Dependent) X
    Diabetes (Non-Insulin Dependent) X
    Galactosemia X
    Gaucher's disease X
    Goiter X
    Hypoglycemia X
    Maple Syrup disease X
    PKU or Inherited Metabolic Disorder X
    Tay Sachs X
    Thyroid Disorder X
    Muscular/Bones/Joint Disease Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Achondroplasia (Dwarfism) X
    Arthritis (Other) X
    Congenital Hip Disease X
    Gout X
    Loss of Muscle Coordination X
    Marfan's Disease X
    Muscular Dystrophy X
    Osteoarthritis X
    Osteoporosis X
    Rheumatoid Arthritis X
    Scoliosis X
    Spinal Muscular Atrophy X
    Neurological Diseases Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Learning Disorder: ADD, ADHD, Dyslexia X
    Autism/ Asperger X
    Canavan's disease X
    Cerebral Palsy X
    Dementia X
    Disorders of the spinal cord X
    Dyslexia X
    Familial dysautonomia X
    Lesch-Nyhan Syndrome X
    Migraines X
    Mucolipidosis type IV X
    Neurologic (Alzheimer) X
    Neurologic (Creutzfeld-Jacob Disease) X
    Neurologic (Epilepsy) X
    Neurologic (Guillain Barre) X
    Neurologic (Huntington's) X
    Neurologic (JC Virus) X
    Neurologic (Lou Gehrig's Disease) X
    Neurologic (Multiple Sclerosis) X
    Neurologic (Neural Tube Defect) X
    Neurologic (Neurofibromatosis) X
    Neurologic (Parkinson's Disease) X
    Neurologic (Subacute Sclerosing Panencephalitis) X
    Nieman-Pick X
    Spongiform encephalopathy/prion disease X
    Tourette Syndrome X
    Other Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Alcoholism X
    Bloom syndrome X
    Cystic Fibrosis X
    Down Syndrome X
    Drug Abuse X
    Encephalitis: viral or of unknown origin X
    Fragile X X
    Klinefelter X
    Meningitis X
    Noonan or Turner Syndrome X
    Other - Early Death X
    Other - Inherited Genetic Condition X
    Other Disease/Condition X N/A
    Premature Organ Degeneration X
    Radiation Exposure X
    SIDS X
    Toxic Chemical Exposure X
    Turner's Syndrome X
    West Nile (suspected or confirmed by lab testing) X
    Respiratory Disease Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Allergies (Drug) X
    Allergies (Food) X
    Allergies (Hay Fever) X
    Allergies (Insect) X
    Allergies (Other) X
    Allergies (Pet) X
    Asthma X
    Emphysema X
    SARS X
    Tuberculosis X
    Sight/Sound/Smell Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Cataracts X
    Deafness X
    Deafness (before age 50) X
    Ear deformity X
    Eyesight (Blindness) X
    Eyesight (Red-Green Color Blindness) X
    Eyesight (Glaucoma) X
    Eyesight (Other) X
    Eyesight (Retinoblastoma) X
    Macular degeneration X
    Skin Yes No Which
    Relative    		 Father's
    Side    		 Mother's
    Side    		 Age of
    Onset
    Albinism X
    Eczema X
    Pigmentation disorders (including Vitiligo) X
    Psoriasis X
    Skin Disease X

  • Information displayed in this profile is provided by the donor. Blank fields are intentional and indicate that the information is not available.

    FAMILY MEMBER: Father
    Hair Color: Black Eyesight:
    Freckles: None Hair Texture: Fine
    Health Status: Good Skin Tone: Brown, Light Dominant Hand:
    Year of Birth: 1974 Cause of Death: Hair Loss:
    Height: 6'02" (187.96 cm) Age at Death: Body Hair:
    Weight: 210 lbs. (95 kg) Occupation: Business Owner Eye Color: Brown, Dark
    Half Siblings: No Education: High School Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision and is double jointed. He’s a great illustrator.
    FAMILY MEMBER: Mother
    Hair Color: Brown, Dark Eyesight:
    Freckles: None Hair Texture: Thick
    Health Status: Good Skin Tone: Brown, Light Dominant Hand:
    Year of Birth: 1972 Cause of Death: Hair Loss:
    Height: 5'07" (170.18 cm) Age at Death: Body Hair:
    Weight: 200 lbs. (90 kg) Occupation: Caregiver Eye Color: Brown, Dark
    Half Siblings: No Education: High School Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has long eyelashes. Enjoys arts and crafts.
    FAMILY MEMBER: Sister
    Hair Color: Brown, Dark Eyesight:
    Freckles: None Hair Texture: Thick
    Health Status: Good Skin Tone: Brown, Light Dominant Hand:
    Year of Birth: 1999 Cause of Death: Hair Loss:
    Height: 5'08" (172.72 cm) Age at Death: Body Hair:
    Weight: 122 lbs. (55 kg) Occupation: Student Eye Color: Brown, Dark
    Half Siblings: No Education: College (Some) Body Build: Medium
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision and thick eye brows. She’s going in to the medical field. Enjoys arts and crafts.

  • Information displayed in this profile is provided by the donor. Blank fields are intentional and indicate that the information is not available.

    FAMILY MEMBER: Grandfather
    Hair Color: Brown, Dark Eyesight:
    Freckles: None Hair Texture: Fine
    Health Status: Skin Tone: Brown, Light Dominant Hand:
    Year of Birth: 1949 Cause of Death: Car Accident Hair Loss:
    Height: 6'02" (187.96 cm) Age at Death: 35 Body Hair:
    Weight: 198 lbs. (89 kg) Occupation: Eye Color: Brown, Dark
    Half Siblings: Education: High School Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Had corrected vision. Enjoyed mechanical engineering.
    FAMILY MEMBER: Grandmother
    Hair Color: Brown, Dark Eyesight:
    Freckles: Hair Texture: Coarse
    Health Status: Fair Skin Tone: Dominant Hand:
    Year of Birth: 1947 Cause of Death: Hair Loss:
    Height: 5'09" (175.26 cm) Age at Death: Body Hair:
    Weight: 192 lbs. (87 kg) Occupation: Customer Service Eye Color: Black
    Half Siblings: Education: High School Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Has corrected vision. Enjoys crafts.
    FAMILY MEMBER: Aunt
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1977 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair:
    Weight: Occupation: Eye Color:
    Half Siblings: Education: Body Build:
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:

  • Information displayed in this profile is provided by the donor. Blank fields are intentional and indicate that the information is not available.

    FAMILY MEMBER: Grandfather
    Hair Color: Black Eyesight:
    Freckles: None Hair Texture: Coarse
    Health Status: Skin Tone: Brown, Dark Dominant Hand:
    Year of Birth: 1947 Cause of Death: Kidney problems Hair Loss:
    Height: 6'" (182.88 cm) Age at Death: 67 Body Hair:
    Weight: 220 lbs. (99 kg) Occupation: Eye Color: Black
    Half Siblings: Education: High School Body Build: Large
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Had nice teeth. Played the drums.
    FAMILY MEMBER: Grandmother
    Hair Color: Black Eyesight:
    Freckles: None Hair Texture: Coarse
    Health Status: Fair Skin Tone: Olive Dominant Hand:
    Year of Birth: 1944 Cause of Death: Hair Loss:
    Height: 5'06" (167.64 cm) Age at Death: Body Hair:
    Weight: Occupation: Caregiver Eye Color: Brown, Dark
    Half Siblings: Education: High School Body Build: Small
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:
    Comments: Enjoys arts and crafts.
    FAMILY MEMBER: Aunt
    Hair Color: Eyesight:
    Freckles: Hair Texture:
    Health Status: Good Skin Tone: Dominant Hand:
    Year of Birth: 1986 Cause of Death: Hair Loss:
    Height: Age at Death: Body Hair:
    Weight: Occupation: Eye Color:
    Half Siblings: Education: Body Build:
    Half Siblings Parent: Eyesight Correction: Near or Far Sighted:

Purchase Bundle Options

Purchase Bundle Options

Vial Types Available for Donor #5492

All prices shown are in USD.

$1195 per vial xyIdentity Disclosure Washed

$1195 per vial xyIdentity Disclosure Unwashed

$1000 per vial xyIdentity Disclosure ART

Due to inventory, above prices do not guarantee that listed vial types are currently available. Please contact our team to check availability.

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